David Housman - Publications

Affiliations: 
Massachusetts Institute of Technology, Cambridge, MA, United States 
Area:
Human Genetics, Huntington's disease, Myotonic dystrophy, Fragile-X syndrome

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Year Citation  Score
2016 Crittenden JR, Tillberg PW, Riad MH, Shima Y, Gerfen CR, Curry J, Housman DE, Nelson SB, Boyden ES, Graybiel AM. Striosome-dendron bouquets highlight a unique striatonigral circuit targeting dopamine-containing neurons. Proceedings of the National Academy of Sciences of the United States of America. PMID 27647894 DOI: 10.1073/pnas.1613337113  0.36
2016 Ouyang Q, Nakayama T, Baytas O, Davidson SM, Yang C, Schmidt M, Lizarraga SB, Mishra S, Ei-Quessny M, Niaz S, Gul Butt M, Imran Murtaza S, Javed A, Chaudhry HR, Vaughan DJ, ... ... Housman DE, et al. Mutations in mitochondrial enzyme GPT2 cause metabolic dysfunction and neurological disease with developmental and progressive features. Proceedings of the National Academy of Sciences of the United States of America. PMID 27601654 DOI: 10.1073/pnas.1609221113  0.4
2014 Ochaba J, Lukacsovich T, Csikos G, Zheng S, Margulis J, Salazar L, Mao K, Lau AL, Yeung SY, Humbert S, Saudou F, Klionsky DJ, Finkbeiner S, Zeitlin SO, Marsh JL, ... Housman DE, et al. Potential function for the Huntingtin protein as a scaffold for selective autophagy. Proceedings of the National Academy of Sciences of the United States of America. 111: 16889-94. PMID 25385587 DOI: 10.1073/pnas.1420103111  0.4
2014 Bugiardini E, Meola G, Alvarez C, Angeard N, Bassez G, Day JW, Dent G, Ekström AB, Eymard B, Fossati B, Gagnon C, Gomes-Pereira M, Gourdon G, Heatwole C, Housman DE, et al. Consensus on cerebral involvement in myotonic dystrophy. Workshop report: May 24-27, 2013, Ferrere (AT), Italy Neuromuscular Disorders. 24: 445-452. PMID 24613228 DOI: 10.1016/j.nmd.2014.01.013  0.4
2013 Gipson TA, Neueder A, Wexler NS, Bates GP, Housman D. Aberrantly spliced HTT, a new player in Huntington's disease pathogenesis. Rna Biology. 10: 1647-52. PMID 24256709 DOI: 10.4161/rna.26706  0.4
2013 Boissonneault KR, Henningsen BM, Bates SS, Robertson DL, Milton S, Pelletier J, Hogan DA, Housman DE. Gene expression studies for the analysis of domoic acid production in the marine diatom Pseudo-nitzschia multiseries. Bmc Molecular Biology. 14: 25. PMID 24180290 DOI: 10.1186/1471-2199-14-25  0.32
2013 Vashishtha M, Ng CW, Yildirim F, Gipson TA, Kratter IH, Bodai L, Song W, Lau A, Labadorf A, Vogel-Ciernia A, Troncosco J, Ross CA, Bates GP, Krainc D, Sadri-Vakili G, ... ... Housman DE, et al. Targeting H3K4 trimethylation in Huntington disease. Proceedings of the National Academy of Sciences of the United States of America. 110: E3027-36. PMID 23872847 DOI: 10.1073/pnas.1311323110  0.4
2013 Sontag EM, Joachimiak LA, Tan Z, Tomlinson A, Housman DE, Glabe CG, Potkin SG, Frydman J, Thompson LM. Exogenous delivery of chaperonin subunit fragment ApiCCT1 modulates mutant Huntingtin cellular phenotypes. Proceedings of the National Academy of Sciences of the United States of America. 110: 3077-82. PMID 23365139 DOI: 10.1073/pnas.1222663110  0.4
2013 Ng CW, Yildirim F, Yap YS, Dalin S, Matthews BJ, Velez PJ, Labadorf A, Housman DE, Fraenkel E. Extensive changes in DNA methylation are associated with expression of mutant huntingtin. Proceedings of the National Academy of Sciences of the United States of America. 110: 2354-9. PMID 23341638 DOI: 10.1073/pnas.1221292110  0.4
2013 Sathasivam K, Neueder A, Gipson TA, Landles C, Benjamin AC, Bondulich MK, Smith DL, Faull RL, Roos RA, Howland D, Detloff PJ, Housman DE, Bates GP. Aberrant splicing of HTT generates the pathogenic exon 1 protein in Huntington disease. Proceedings of the National Academy of Sciences of the United States of America. 110: 2366-70. PMID 23341618 DOI: 10.1073/pnas.1221891110  0.4
2012 Janas MM, Wang E, Love T, Harris AS, Stevenson K, Semmelmann K, Shaffer JM, Chen PH, Doench JG, Yerramilli SV, Neuberg DS, Iliopoulos D, Housman DE, Burge CB, Novina CD. Reduced expression of ribosomal proteins relieves microRNA-mediated repression. Molecular Cell. 46: 171-86. PMID 22541556 DOI: 10.1016/j.molcel.2012.04.008  0.4
2012 Crook ZR, Housman DE. Dysregulation of dopamine receptor D2 as a sensitive measure for Huntington disease pathology in model mice. Proceedings of the National Academy of Sciences of the United States of America. 109: 7487-92. PMID 22529362 DOI: 10.1073/pnas.1204542109  0.4
2011 Acquaviva J, Jun HJ, Lessard J, Ruiz R, Zhu H, Donovan M, Woolfenden S, Boskovitz A, Raval A, Bronson RT, Pfannl R, Whittaker CA, Housman DE, Charest A. Chronic activation of wild-type epidermal growth factor receptor and loss of Cdkn2a cause mouse glioblastoma formation. Cancer Research. 71: 7198-206. PMID 21987724 DOI: 10.1158/0008-5472.CAN-11-1514  0.4
2011 Crook ZR, Housman D. Huntington's disease: can mice lead the way to treatment? Neuron. 69: 423-35. PMID 21315254 DOI: 10.1016/j.neuron.2010.12.035  0.4
2010 Williams AL, Housman DE, Rinard MC, Gifford DK. Rapid haplotype inference for nuclear families. Genome Biology. 11: R108. PMID 21034477 DOI: 10.1186/gb-2010-11-10-r108  0.4
2010 Crittenden JR, Dunn DE, Merali FI, Woodman B, Yim M, Borkowska AE, Frosch MP, Bates GP, Housman DE, Lo DC, Graybiel AM. CalDAG-GEFI down-regulation in the striatum as a neuroprotective change in Huntington's disease. Human Molecular Genetics. 19: 1756-65. PMID 20147317 DOI: 10.1093/hmg/ddq055  0.4
2010 Wooten EC, Iyer LK, Montefusco MC, Hedgepeth AK, Payne DD, Kapur NK, Housman DE, Mendelsohn ME, Huggins GS. Application of gene network analysis techniques identifies AXIN1/PDIA2 and endoglin haplotypes associated with bicuspid aortic valve. Plos One. 5: e8830. PMID 20098615 DOI: 10.1371/journal.pone.0008830  0.4
2009 Weiss A, Abramowski D, Bibel M, Bodner R, Chopra V, DiFiglia M, Fox J, Kegel K, Klein C, Grueninger S, Hersch S, Housman D, Régulier E, Rosas HD, Stefani M, et al. Single-step detection of mutant huntingtin in animal and human tissues: a bioassay for Huntington's disease. Analytical Biochemistry. 395: 8-15. PMID 19664996 DOI: 10.1016/j.ab.2009.08.001  0.4
2009 Paganetti P, Weiss A, Trapp M, Hammerl I, Bleckmann D, Bodner RA, Coven-Easter S, Housman DE, Parker CN. Development of a method for the high-throughput quantification of cellular proteins. Chembiochem : a European Journal of Chemical Biology. 10: 1678-88. PMID 19492395 DOI: 10.1002/cbic.200900131  0.4
2009 Jun HJ, Woolfenden S, Coven S, Lane K, Bronson R, Housman D, Charest A. Epigenetic regulation of c-ROS receptor tyrosine kinase expression in malignant gliomas. Cancer Research. 69: 2180-4. PMID 19276365 DOI: 10.1158/0008-5472.CAN-08-3351  0.4
2009 Zhu H, Acquaviva J, Ramachandran P, Boskovitz A, Woolfenden S, Pfannl R, Bronson RT, Chen JW, Weissleder R, Housman DE, Charest A. Oncogenic EGFR signaling cooperates with loss of tumor suppressor gene functions in gliomagenesis. Proceedings of the National Academy of Sciences of the United States of America. 106: 2712-6. PMID 19196966 DOI: 10.1073/pnas.0813314106  0.4
2009 Peter I, Kelley-Hedgepeth A, Huggins GS, Housman DE, Mendelsohn ME, Vita JA, Vasan RS, Levy D, Benjamin EJ, Mitchell GF. Association between arterial stiffness and variations in oestrogen-related genes. Journal of Human Hypertension. 23: 636-44. PMID 19194457 DOI: 10.1038/jhh.2009.1  0.4
2009 Kelley-Hedgepeth A, Peter I, Montefusco MC, Levy D, Benjamin EJ, Vasan RS, Mendelsohn ME, Housman D, Huggins GS, Mitchell GF. The KCNMB1 E65K variant is associated with reduced central pulse pressure in the community-based Framingham Offspring Cohort. Journal of Hypertension. 27: 55-60. PMID 19050450 DOI: 10.1097/HJH.0b013e328317c8ae  0.4
2009 Brocklebank D, Gayán J, Andresen JM, Roberts SA, Young AB, Snodgrass SR, Penney JB, Ramos-Arroyo MA, Cha JJ, Rosas HD, Hersch SM, Feigin A, Cherny SS, Wexler NS, Housman DE, et al. Repeat instability in the 27-39 CAG range of the HD gene in the Venezuelan kindreds: Counseling implications. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 150: 425-9. PMID 18712713 DOI: 10.1002/ajmg.b.30826  0.4
2008 Williams BR, Prabhu VR, Hunter KE, Glazier CM, Whittaker CA, Housman DE, Amon A. Aneuploidy affects proliferation and spontaneous immortalization in mammalian cells. Science (New York, N.Y.). 322: 703-9. PMID 18974345 DOI: 10.1126/science.1160058  0.4
2008 Mills JR, Hippo Y, Robert F, Chen SM, Malina A, Lin CJ, Trojahn U, Wendel HG, Charest A, Bronson RT, Kogan SC, Nadon R, Housman DE, Lowe SW, Pelletier J. mTORC1 promotes survival through translational control of Mcl-1. Proceedings of the National Academy of Sciences of the United States of America. 105: 10853-8. PMID 18664580 DOI: 10.1073/pnas.0804821105  0.4
2008 Gayán J, Brocklebank D, Andresen JM, Alkorta-Aranburu G, Zameel Cader M, Roberts SA, Cherny SS, Wexler NS, Cardon LR, Housman DE. Genomewide linkage scan reveals novel loci modifying age of onset of Huntington's disease in the Venezuelan HD kindreds. Genetic Epidemiology. 32: 445-53. PMID 18481795 DOI: 10.1002/gepi.20317  0.4
2008 Peter I, Kelley-Hedgepeth A, Fox CS, Cupples LA, Huggins GS, Housman DE, Karas RH, Mendelsohn ME, Levy D, Murabito JM. Variation in estrogen-related genes associated with cardiovascular phenotypes and circulating estradiol, testosterone, and dehydroepiandrosterone sulfate levels. The Journal of Clinical Endocrinology and Metabolism. 93: 2779-85. PMID 18445666 DOI: 10.1210/jc.2008-0106  0.4
2008 Kelley-Hedgepeth A, Peter I, Kip K, Montefusco M, Kogan S, Cox D, Ordovas J, Levy D, Reis S, Mendelsohn M, Housman D, Huggins G. The protective effect of KCNMB1 E65K against hypertension is restricted to blood pressure treatment with beta-blockade. Journal of Human Hypertension. 22: 512-5. PMID 18418400 DOI: 10.1038/jhh.2008.23  0.4
2007 Chopra V, Fox JH, Lieberman G, Dorsey K, Matson W, Waldmeier P, Housman DE, Kazantsev A, Young AB, Hersch S. A small-molecule therapeutic lead for Huntington's disease: preclinical pharmacology and efficacy of C2-8 in the R6/2 transgenic mouse. Proceedings of the National Academy of Sciences of the United States of America. 104: 16685-9. PMID 17925440 DOI: 10.1073/pnas.0707842104  0.4
2007 Bergmeier W, Goerge T, Wang HW, Crittenden JR, Baldwin AC, Cifuni SM, Housman DE, Graybiel AM, Wagner DD. Mice lacking the signaling molecule CalDAG-GEFI represent a model for leukocyte adhesion deficiency type III. The Journal of Clinical Investigation. 117: 1699-707. PMID 17492052 DOI: 10.1172/JCI30575  0.4
2007 Coufal M, Maxwell MM, Russel DE, Amore AM, Altmann SM, Hollingsworth ZR, Young AB, Housman DE, Kazantsev AG. Discovery of a novel small-molecule targeting selective clearance of mutant huntingtin fragments. Journal of Biomolecular Screening. 12: 351-60. PMID 17379859 DOI: 10.1177/1087057107299428  0.4
2007 Peter I, Huggins GS, Shearman AM, Pollak A, Schmid CH, Cupples LA, Demissie S, Patten RD, Karas RH, Housman DE, Mendelsohn ME, Vasan RS, Benjamin EJ. Age-related changes in echocardiographic measurements: association with variation in the estrogen receptor-alpha gene. Hypertension. 49: 1000-6. PMID 17372038 DOI: 10.1161/HYPERTENSIONAHA.106.083790  0.4
2007 Andresen JM, Gayán J, Djoussé L, Roberts S, Brocklebank D, Cherny SS, Cardon LR, Gusella JF, MacDonald ME, Myers RH, Housman DE, Wexler NS. The relationship between CAG repeat length and age of onset differs for Huntington's disease patients with juvenile onset or adult onset. Annals of Human Genetics. 71: 295-301. PMID 17181545 DOI: 10.1111/j.1469-1809.2006.00335.x  0.4
2007 Andresen JM, Gayán J, Cherny SS, Brocklebank D, Alkorta-Aranburu G, Addis EA, Cardon LR, Housman DE, Wexler NS. Replication of twelve association studies for Huntington's disease residual age of onset in large Venezuelan kindreds. Journal of Medical Genetics. 44: 44-50. PMID 17018562 DOI: 10.1136/jmg.2006.045153  0.4
2006 Horiuchi K, Umetani M, Minami T, Okayama H, Takada S, Yamamoto M, Aburatani H, Reid PC, Housman DE, Hamakubo T, Kodama T. Wilms' tumor 1-associating protein regulates G2/M transition through stabilization of cyclin A2 mRNA. Proceedings of the National Academy of Sciences of the United States of America. 103: 17278-83. PMID 17088532 DOI: 10.1073/pnas.0608357103  0.4
2006 Charest A, Wilker EW, McLaughlin ME, Lane K, Gowda R, Coven S, McMahon K, Kovach S, Feng Y, Yaffe MB, Jacks T, Housman D. ROS fusion tyrosine kinase activates a SH2 domain-containing phosphatase-2/phosphatidylinositol 3-kinase/mammalian target of rapamycin signaling axis to form glioblastoma in mice. Cancer Research. 66: 7473-81. PMID 16885344 DOI: 10.1158/0008-5472.CAN-06-1193  0.4
2006 Bodner RA, Housman DE, Kazantsev AG. New directions for neurodegenerative disease therapy: using chemical compounds to boost the formation of mutant protein inclusions. Cell Cycle (Georgetown, Tex.). 5: 1477-80. PMID 16861893  0.4
2006 Tabchy A, Housman D. Huntington's disease: A transcriptional report card from the peripheral blood: can it measure disease progression in Huntington's disease? European Journal of Human Genetics : Ejhg. 14: 649-50. PMID 16538227 DOI: 10.1038/sj.ejhg.5201562  0.4
2006 Bodner RA, Outeiro TF, Altmann S, Maxwell MM, Cho SH, Hyman BT, McLean PJ, Young AB, Housman DE, Kazantsev AG. Pharmacological promotion of inclusion formation: a therapeutic approach for Huntington's and Parkinson's diseases. Proceedings of the National Academy of Sciences of the United States of America. 103: 4246-51. PMID 16537516 DOI: 10.1073/pnas.0511256103  0.4
2006 Shearman AM, Cooper JA, Kotwinski PJ, Miller GJ, Humphries SE, Ardlie KG, Jordan B, Irenze K, Lunetta KL, Schuit SC, Uitterlinden AG, Pols HA, Demissie S, Cupples LA, Mendelsohn ME, ... ... Housman DE, et al. Estrogen receptor alpha gene variation is associated with risk of myocardial infarction in more than seven thousand men from five cohorts. Circulation Research. 98: 590-2. PMID 16484614 DOI: 10.1161/01.RES.0000210578.62102.a6  0.4
2006 Demissie S, Cupples LA, Shearman AM, Gruenthal KM, Peter I, Schmid CH, Karas RH, Housman DE, Mendelsohn ME, Ordovas JM. Estrogen receptor-alpha variants are associated with lipoprotein size distribution and particle levels in women: the Framingham Heart Study. Atherosclerosis. 185: 210-8. PMID 16005459 DOI: 10.1016/j.atherosclerosis.2005.06.008  0.4
2005 Peter I, Shearman AM, Vasan RS, Zucker DR, Schmid CH, Demissie S, Cupples LA, Kuvin JT, Karas RH, Mendelsohn ME, Housman DE, Benjamin EJ. Association of estrogen receptor beta gene polymorphisms with left ventricular mass and wall thickness in women. American Journal of Hypertension. 18: 1388-95. PMID 16280269 DOI: 10.1016/j.amjhyper.2005.05.023  0.4
2005 Peter I, Shearman AM, Zucker DR, Schmid CH, Demissie S, Cupples LA, Larson MG, Vasan RS, D'Agostino RB, Karas RH, Mendelsohn ME, Housman DE, Levy D. Variation in estrogen-related genes and cross-sectional and longitudinal blood pressure in the Framingham Heart Study. Journal of Hypertension. 23: 2193-200. PMID 16269961  0.4
2005 Shearman AM, Cooper JA, Kotwinski PJ, Humphries SE, Mendelsohn ME, Housman DE, Miller GJ. Estrogen receptor alpha gene variation and the risk of stroke. Stroke; a Journal of Cerebral Circulation. 36: 2281-2. PMID 16179580 DOI: 10.1161/01.STR.0000181088.76518.ec  0.4
2005 Fox CS, Yang Q, Cupples LA, Guo CY, Atwood LD, Murabito JM, Levy D, Mendelsohn ME, Housman DE, Shearman AM. Sex-specific association between estrogen receptor-alpha gene variation and measures of adiposity: the Framingham Heart Study. The Journal of Clinical Endocrinology and Metabolism. 90: 6257-62. PMID 16144952 DOI: 10.1210/jc.2005-0670  0.4
2005 Prawitt D, Enklaar T, Gärtner-Rupprecht B, Spangenberg C, Lausch E, Reutzel D, Fees S, Korzon M, Brozek I, Limon J, Housman DE, Pelletier J, Zabel B. Microdeletion and IGF2 loss of imprinting in a cascade causing Beckwith-Wiedemann syndrome with Wilms' tumor. Nature Genetics. 37: 785-6; author reply . PMID 16049499 DOI: 10.1038/ng0805-785  0.4
2005 Shearman AM, Demissie S, Cupples LA, Peter I, Schmid CH, Ordovas JM, Mendelsohn ME, Housman DE. Tobacco smoking, estrogen receptor alpha gene variation and small low density lipoprotein level. Human Molecular Genetics. 14: 2405-13. PMID 16014638 DOI: 10.1093/hmg/ddi242  0.4
2005 Yang Q, Lai CQ, Parnell L, Cupples LA, Adiconis X, Zhu Y, Wilson PW, Housman DE, Shearman AM, D'Agostino RB, Ordovas JM. Genome-wide linkage analyses and candidate gene fine mapping for HDL3 cholesterol: the Framingham Study. Journal of Lipid Research. 46: 1416-25. PMID 15805549 DOI: 10.1194/jlr.M400382-JLR200  0.4
2005 Prawitt D, Enklaar T, Gärtner-Rupprecht B, Spangenberg C, Oswald M, Lausch E, Schmidtke P, Reutzel D, Fees S, Lucito R, Korzon M, Brozek I, Limon J, Housman DE, Pelletier J, et al. Microdeletion of target sites for insulator protein CTCF in a chromosome 11p15 imprinting center in Beckwith-Wiedemann syndrome and Wilms' tumor. Proceedings of the National Academy of Sciences of the United States of America. 102: 4085-90. PMID 15743916 DOI: 10.1073/pnas.0500037102  0.4
2005 Zhang X, Smith DL, Meriin AB, Engemann S, Russel DE, Roark M, Washington SL, Maxwell MM, Marsh JL, Thompson LM, Wanker EE, Young AB, Housman DE, Bates GP, Sherman MY, et al. A potent small molecule inhibits polyglutamine aggregation in Huntington's disease neurons and suppresses neurodegeneration in vivo. Proceedings of the National Academy of Sciences of the United States of America. 102: 892-7. PMID 15642944 DOI: 10.1073/pnas.0408936102  0.4
2005 McCarty JH, Lacy-Hulbert A, Charest A, Bronson RT, Crowley D, Housman D, Savill J, Roes J, Hynes RO. Selective ablation of alphav integrins in the central nervous system leads to cerebral hemorrhage, seizures, axonal degeneration and premature death. Development (Cambridge, England). 132: 165-76. PMID 15576410 DOI: 10.1242/dev.01551  0.4
2004 Crittenden JR, Bergmeier W, Zhang Y, Piffath CL, Liang Y, Wagner DD, Housman DE, Graybiel AM. CalDAG-GEFI integrates signaling for platelet aggregation and thrombus formation. Nature Medicine. 10: 982-6. PMID 15334074 DOI: 10.1038/nm1098  0.4
2004 Shearman AM, Karasik D, Gruenthal KM, Demissie S, Cupples LA, Housman DE, Kiel DP. Estrogen receptor beta polymorphisms are associated with bone mass in women and men: the Framingham Study. Journal of Bone and Mineral Research : the Official Journal of the American Society For Bone and Mineral Research. 19: 773-81. PMID 15068501 DOI: 10.1359/JBMR.0301258  0.4
2004 Natoli TA, Alberta JA, Bortvin A, Taglienti ME, Menke DB, Loring J, Jaenisch R, Page DC, Housman DE, Kreidberg JA. Wt1 functions in the development of germ cells in addition to somatic cell lineages of the testis. Developmental Biology. 268: 429-40. PMID 15063178 DOI: 10.1016/j.ydbio.2003.12.033  0.4
2004 Wexler NS, Lorimer J, Porter J, Gomez F, Moskowitz C, Shackell E, Marder K, Penchaszadeh G, Roberts SA, Gayán J, Brocklebank D, Cherny SS, Cardon LR, Gray J, Dlouhy SR, ... ... Housman DE, et al. Venezuelan kindreds reveal that genetic and environmental factors modulate Huntington's disease age of onset. Proceedings of the National Academy of Sciences of the United States of America. 101: 3498-503. PMID 14993615 DOI: 10.1073/pnas.0308679101  0.4
2004 Tian XL, Kadaba R, You SA, Liu M, Timur AA, Yang L, Chen Q, Szafranski P, Rao S, Wu L, Housman DE, DiCorleto PE, Driscoll DJ, Borrow J, Wang Q. Identification of an angiogenic factor that when mutated causes susceptibility to Klippel-Trenaunay syndrome. Nature. 427: 640-5. PMID 14961121 DOI: 10.1038/nature02320  0.4
2003 Shearman AM, Cupples LA, Demissie S, Peter I, Schmid CH, Karas RH, Mendelsohn ME, Housman DE, Levy D. Association between estrogen receptor alpha gene variation and cardiovascular disease. Jama. 290: 2263-70. PMID 14600184 DOI: 10.1001/jama.290.17.2263  0.4
2003 Fluiter K, Housman D, Ten Asbroek AL, Baas F. Killing cancer by targeting genes that cancer cells have lost: allele-specific inhibition, a novel approach to the treatment of genetic disorders. Cellular and Molecular Life Sciences : Cmls. 60: 834-43. PMID 12827273 DOI: 10.1007/s00018-003-3043-6  0.4
2003 Apostol BL, Kazantsev A, Raffioni S, Illes K, Pallos J, Bodai L, Slepko N, Bear JE, Gertler FB, Hersch S, Housman DE, Marsh JL, Thompson LM. A cell-based assay for aggregation inhibitors as therapeutics of polyglutamine-repeat disease and validation in Drosophila. Proceedings of the National Academy of Sciences of the United States of America. 100: 5950-5. PMID 12730384 DOI: 10.1073/pnas.2628045100  0.4
2003 Charest A, Lane K, McMahon K, Park J, Preisinger E, Conroy H, Housman D. Fusion of FIG to the receptor tyrosine kinase ROS in a glioblastoma with an interstitial del(6)(q21q21). Genes, Chromosomes & Cancer. 37: 58-71. PMID 12661006 DOI: 10.1002/gcc.10207  0.4
2003 Osman A, Jordan B, Lessard PA, Muhammad N, Haron MR, Riffin NM, Sinskey AJ, Rha C, Housman DE. Genetic diversity of Eurycoma longifolia inferred from single nucleotide polymorphisms. Plant Physiology. 131: 1294-301. PMID 12644679 DOI: 10.1104/pp.012492  0.4
2003 Charest A, Kheifets V, Park J, Lane K, McMahon K, Nutt CL, Housman D. Oncogenic targeting of an activated tyrosine kinase to the Golgi apparatus in a glioblastoma. Proceedings of the National Academy of Sciences of the United States of America. 100: 916-21. PMID 12538861 DOI: 10.1073/pnas.242741799  0.4
2003 Alberta JA, Springett GM, Rayburn H, Natoli TA, Loring J, Kreidberg JA, Housman D. Role of the WT1 tumor suppressor in murine hematopoiesis. Blood. 101: 2570-4. PMID 12468434 DOI: 10.1182/blood-2002-06-1656  0.4
2002 Dash AB, Williams IR, Kutok JL, Tomasson MH, Anastasiadou E, Lindahl K, Li S, Van Etten RA, Borrow J, Housman D, Druker B, Gilliland DG. A murine model of CML blast crisis induced by cooperation between BCR/ABL and NUP98/HOXA9. Proceedings of the National Academy of Sciences of the United States of America. 99: 7622-7. PMID 12032333 DOI: 10.1073/pnas.102583199  0.4
2002 Natoli TA, McDonald A, Alberta JA, Taglienti ME, Housman DE, Kreidberg JA. A mammal-specific exon of WT1 is not required for development or fertility. Molecular and Cellular Biology. 22: 4433-8. PMID 12024052 DOI: 10.1128/MCB.22.12.4433-4438.2002  0.4
2002 Kazantsev A, Walker HA, Slepko N, Bear JE, Preisinger E, Steffan JS, Zhu YZ, Gertler FB, Housman DE, Marsh JL, Thompson LM. A bivalent Huntingtin binding peptide suppresses polyglutamine aggregation and pathogenesis in Drosophila. Nature Genetics. 30: 367-76. PMID 11925563 DOI: 10.1038/ng864  0.4
2002 Jordan B, Charest A, Dowd JF, Blumenstiel JP, Yeh Rf RF, Osman A, Housman DE, Landers JE. Genome complexity reduction for SNP genotyping analysis. Proceedings of the National Academy of Sciences of the United States of America. 99: 2942-7. PMID 11880640 DOI: 10.1073/pnas.261710699  0.4
2001 Steffan JS, Bodai L, Pallos J, Poelman M, McCampbell A, Apostol BL, Kazantsev A, Schmidt E, Zhu YZ, Greenwald M, Kurokawa R, Housman DE, Jackson GR, Marsh JL, Thompson LM. Histone deacetylase inhibitors arrest polyglutamine-dependent neurodegeneration in Drosophila. Nature. 413: 739-43. PMID 11607033 DOI: 10.1038/35099568  0.4
2001 Toki S, Kawasaki H, Tashiro N, Housman DE, Graybiel AM. Guanine nucleotide exchange factors CalDAG-GEFI and CalDAG-GEFII are colocalized in striatal projection neurons. The Journal of Comparative Neurology. 437: 398-407. PMID 11503142 DOI: 10.1002/cne.1291  0.4
2001 Guillemette C, De Vivo I, Hankinson SE, Haiman CA, Spiegelman D, Housman DE, Hunter DJ. Association of genetic polymorphisms in UGT1A1 with breast cancer and plasma hormone levels. Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association For Cancer Research, Cosponsored by the American Society of Preventive Oncology. 10: 711-4. PMID 11401924  0.4
2001 Charest A, Lane K, McMahon K, Housman DE. Association of a novel PDZ domain-containing peripheral Golgi protein with the Q-SNARE (Q-soluble N-ethylmaleimide-sensitive fusion protein (NSF) attachment protein receptor) protein syntaxin 6. The Journal of Biological Chemistry. 276: 29456-65. PMID 11384996 DOI: 10.1074/jbc.M104137200  0.4
2001 Lecerf JM, Shirley TL, Zhu Q, Kazantsev A, Amersdorfer P, Housman DE, Messer A, Huston JS. Human single-chain Fv intrabodies counteract in situ huntingtin aggregation in cellular models of Huntington's disease. Proceedings of the National Academy of Sciences of the United States of America. 98: 4764-9. PMID 11296304 DOI: 10.1073/pnas.071058398  0.4
2001 Ten Asbroek AL, Olsen J, Housman D, Baas F, Stanton V. Genetic variation in mRNA coding sequences of highly conserved genes. Physiological Genomics. 5: 113-8. PMID 11285364  0.4
2000 Pulver AE, Mulle J, Nestadt G, Swartz KL, Blouin JL, Dombroski B, Liang KY, Housman DE, Kazazian HH, Antonarakis SE, Lasseter VK, Wolyniec PS, Thornquist MH, McGrath JA. Genetic heterogeneity in schizophrenia: stratification of genome scan data using co-segregating related phenotypes. Molecular Psychiatry. 5: 650-3. PMID 11126395  0.4
2000 Volkert MR, Elliott NA, Housman DE. Functional genomics reveals a family of eukaryotic oxidation protection genes. Proceedings of the National Academy of Sciences of the United States of America. 97: 14530-5. PMID 11114193 DOI: 10.1073/pnas.260495897  0.4
2000 Guillemette C, Ritter JK, Auyeung DJ, Kessler FK, Housman DE. Structural heterogeneity at the UDP-glucuronosyltransferase 1 locus: functional consequences of three novel missense mutations in the human UGT1A7 gene. Pharmacogenetics. 10: 629-44. PMID 11037804 DOI: 10.1097/00008571-200010000-00006  0.4
2000 Chattopadhyay S, Kaul R, Charest A, Housman D, Chen J. SMAR1, a novel, alternatively spliced gene product, binds the Scaffold/Matrix-associated region at the T cell receptor beta locus. Genomics. 68: 93-6. PMID 10950932 DOI: 10.1006/geno.2000.6279  0.4
2000 Woolley AT, Guillemette C, Li Cheung C, Housman DE, Lieber CM. Direct haplotyping of kilobase-size DNA using carbon nanotube probes. Nature Biotechnology. 18: 760-3. PMID 10888845 DOI: 10.1038/77332  0.4
2000 Steffan JS, Kazantsev A, Spasic-Boskovic O, Greenwald M, Zhu YZ, Gohler H, Wanker EE, Bates GP, Housman DE, Thompson LM. The Huntington's disease protein interacts with p53 and CREB-binding protein and represses transcription. Proceedings of the National Academy of Sciences of the United States of America. 97: 6763-8. PMID 10823891 DOI: 10.1073/pnas.100110097  0.4
2000 Shearman AM, Ordovas JM, Cupples LA, Schaefer EJ, Harmon MD, Shao Y, Keen JD, DeStefano AL, Joost O, Wilson PW, Housman DE, Myers RH. Evidence for a gene influencing the TG/HDL-C ratio on chromosome 7q32.3-qter: a genome-wide scan in the Framingham study. Human Molecular Genetics. 9: 1315-20. PMID 10814713  0.4
2000 Ashizawa T, Gonzales I, Ohsawa N, Singer RH, Devillers M, Balasubramanyam A, Cooper TA, Khajavi M, Lia-Baldini AS, Miller G, Philips AV, Timchenko LT, Waring J, Yamagata H, Barbet JP, ... ... Housman DE, et al. New nomenclature and DNA testing guidelines for myotonic dystrophy type 1 (DM1) Neurology. 54: 1218-1221. PMID 10746587  0.4
2000 Guillemette C, Millikan RC, Newman B, Housman DE. Genetic polymorphisms in uridine diphospho-glucuronosyltransferase 1A1 and association with breast cancer among African Americans. Cancer Research. 60: 950-6. PMID 10706110  0.4
1999 Dzau V, Frank M, Reich M, Austin MJ, Aebersold R, Cowley A, Housman D, Mulligan R, Rosenberg R. Constants and scientific progress. Physiological Genomics. 1: 107. PMID 11015568  0.4
1999 Dzau VJ, Austin MJ, Brown P, Cowley A, Housman D, Mulligan R, Rosenberg R. Revolution and renaissance. Physiological Genomics. 1: 1-2. PMID 11015554  0.4
1999 Saba S, Vanderbrink BA, Luciano B, Aronovitz MJ, Berul CI, Reddy S, Housman D, Mendelsohn ME, Estes NA, Wang PJ. Localization of the sites of conduction abnormalities in a mouse model of myotonic dystrophy. Journal of Cardiovascular Electrophysiology. 10: 1214-20. PMID 10517654  0.4
1999 Kazantsev A, Preisinger E, Dranovsky A, Goldgaber D, Housman D. Insoluble detergent-resistant aggregates form between pathological and nonpathological lengths of polyglutamine in mammalian cells. Proceedings of the National Academy of Sciences of the United States of America. 96: 11404-9. PMID 10500189 DOI: 10.1073/pnas.96.20.11404  0.4
1999 Ashworth A, Lloyd S, Brown J, Gydesen S, Sorensen SA, Brun A, Englund E, Humphreys C, Housman D, Badura M, Stanton V, Taylor K, Cameron J, Munroe D, Johansson J, et al. Molecular genetic characterisation of frontotemporal dementia on chromosome 3. Dementia and Geriatric Cognitive Disorders. 10: 93-101. PMID 10436350 DOI: 10.1159/000051222  0.4
1999 Preisinger E, Jordan BM, Kazantsev A, Housman D. Evidence for a recruitment and sequestration mechanism in Huntington's disease. Philosophical Transactions of the Royal Society of London. Series B, Biological Sciences. 354: 1029-34. PMID 10434302 DOI: 10.1098/rstb.1999.0455  0.4
1999 Basilion JP, Schievella AR, Burns E, Rioux P, Olson JC, Monia BP, Lemonidis KM, Stanton VP, Housman DE. Selective killing of cancer cells based on loss of heterozygosity and normal variation in the human genome: a new paradigm for anticancer drug therapy. Molecular Pharmacology. 56: 359-69. PMID 10419555  0.4
1999 Antonarakis SE, Blouin JL, Lasseter VK, Gehrig C, Radhakrishna U, Nestadt G, Housman DE, Kazazian HH, Kalman K, Gutman G, Fantino E, Chandy KG, Gargus JJ, Pulver AE. Lack of linkage or association between schizophrenia and the polymorphic trinucleotide repeat within the KCNN3 gene on chromosome 1q21. American Journal of Medical Genetics. 88: 348-51. PMID 10402501 DOI: 10.1002/(SICI)1096-8628(19990820)88:4<348::AID-AJMG11>3.0.CO;2-N  0.4
1999 Hunter K, Greenwood J, Yang YL, Cunningham JM, Birren B, Housman D. An integrated somatic cell hybrid, YAC, and BAC map of the Rmc1 region of mouse chromosome 1. Genomics. 58: 318-22. PMID 10373331 DOI: 10.1006/geno.1999.5841  0.4
1999 Curtis L, Blouin JL, Radhakrishna U, Gehrig C, Lasseter VK, Wolyniec P, Nestadt G, Dombroski B, Kazazian HH, Pulver AE, Housman D, Bertrand D, Antonarakis SE. No evidence for linkage between schizophrenia and markers at chromosome 15q13-14. American Journal of Medical Genetics. 88: 109-12. PMID 10206225 DOI: 10.1002/(SICI)1096-8628(19990416)88:2<109::AID-AJMG1>3.0.CO;2-3  0.4
1999 Zhang X, Tsao H, Tsuji T, Minoshima S, McBride J, Majewski P, Todd R, Shimizu N, Wong DT, Housman DE, Haluska FG. Identification and mutation analysis of DOC-1R, a DOC-1 growth suppressor-related gene. Biochemical and Biophysical Research Communications. 255: 59-63. PMID 10082655 DOI: 10.1006/bbrc.1999.0148  0.4
1999 Berul CI, Maguire CT, Aronovitz MJ, Greenwood J, Miller C, Gehrmann J, Housman D, Mendelsohn ME, Reddy S. DMPK dosage alterations result in atrioventricular conduction abnormalities in a mouse myotonic dystrophy model. The Journal of Clinical Investigation. 103: R1-7. PMID 10021468 DOI: 10.1172/JCI5346  0.4
1998 Ushijima T, Nomoto T, Sugimura T, Housman DE, Nagao M. Isolation of 48 genetic markers appropriate for high throughput genotyping of inbred rat strains by B1 repetitive sequence-representational difference analysis. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 9: 1008-12. PMID 9880669 DOI: 10.1007/s003359900916  0.4
1998 Kawasaki H, Springett GM, Mochizuki N, Toki S, Nakaya M, Matsuda M, Housman DE, Graybiel AM. A family of cAMP-binding proteins that directly activate Rap1. Science (New York, N.Y.). 282: 2275-9. PMID 9856955 DOI: 10.1126/science.282.5397.2275  0.4
1998 Nichols KE, Harkin DP, Levitz S, Krainer M, Kolquist KA, Genovese C, Bernard A, Ferguson M, Zuo L, Snyder E, Buckler AJ, Wise C, Ashley J, Lovett M, Valentine MB, ... ... Housman DE, et al. Inactivating mutations in an SH2 domain-encoding gene in X-linked lymphoproliferative syndrome. Proceedings of the National Academy of Sciences of the United States of America. 95: 13765-70. PMID 9811875 DOI: 10.1073/pnas.95.23.13765  0.4
1998 Kawasaki H, Springett GM, Toki S, Canales JJ, Harlan P, Blumenstiel JP, Chen EJ, Bany IA, Mochizuki N, Ashbacher A, Matsuda M, Housman DE, Graybiel AM. A Rap guanine nucleotide exchange factor enriched highly in the basal ganglia. Proceedings of the National Academy of Sciences of the United States of America. 95: 13278-83. PMID 9789079 DOI: 10.1073/pnas.95.22.13278  0.4
1998 Reece M, Prawitt D, Landers J, Kast C, Gros P, Housman D, Zabel BU, Pelletier J. Functional characterization of ORCTL2--an organic cation transporter expressed in the renal proximal tubules. Febs Letters. 433: 245-50. PMID 9744804  0.4
1998 Blouin JL, Dombroski BA, Nath SK, Lasseter VK, Wolyniec PS, Nestadt G, Thornquist M, Ullrich G, McGrath J, Kasch L, Lamacz M, Thomas MG, Gehrig C, Radhakrishna U, Snyder SE, ... ... Housman DE, et al. Schizophrenia susceptibility loci on chromosomes 13q32 and 8p21. Nature Genetics. 20: 70-3. PMID 9731535 DOI: 10.1038/1734  0.4
1998 Housman D, Ledley FD. Why pharmacogenomics? Why now? Nature Biotechnology. 16: 492-3. PMID 9624664 DOI: 10.1038/nbt0698-492  0.4
1998 Cooper PR, Smilinich NJ, Day CD, Nowak NJ, Reid LH, Pearsall RS, Reece M, Prawitt D, Landers J, Housman DE, Winterpacht A, Zabel BU, Pelletier J, Weissman BE, Shows TB, et al. Divergently transcribed overlapping genes expressed in liver and kidney and located in the 11p15.5 imprinted domain. Genomics. 49: 38-51. PMID 9570947 DOI: 10.1006/geno.1998.5221  0.4
1998 Karayiorgou M, Gogos JA, Galke BL, Wolyniec PS, Nestadt G, Antonarakis SE, Kazazian HH, Housman DE, Pulver AE. Identification of sequence variants and analysis of the role of the catechol-O-methyl-transferase gene in schizophrenia susceptibility. Biological Psychiatry. 43: 425-31. PMID 9532347 DOI: 10.1016/S0006-3223(97)00202-3  0.4
1998 Heesen M, Berman MA, Charest A, Housman D, Gerard C, Dorf ME. Cloning and chromosomal mapping of an orphan chemokine receptor: mouse RDC1. Immunogenetics. 47: 364-70. PMID 9510554 DOI: 10.1007/s002510050371  0.4
1998 Das M, Chu LL, Ghahremani M, Abrams-Ogg T, Roy MS, Housman D, Pelletier J. Characterization of an abundant short interspersed nuclear element (SINE) present in Canis familiaris. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 9: 64-9. PMID 9434948 DOI: 10.1007/s003359900681  0.4
1997 Rodriguez P, Munroe D, Prawitt D, Chu LL, Bric E, Kim J, Reid LH, Davies C, Nakagama H, Loebbert R, Winterpacht A, Petruzzi MJ, Higgins MJ, Nowak N, Evans G, ... ... Housman DE, et al. Functional characterization of human nucleosome assembly protein-2 (NAP1L4) suggests a role as a histone chaperone. Genomics. 44: 253-65. PMID 9325046 DOI: 10.1006/geno.1997.4868  0.4
1997 Sobulo OM, Borrow J, Tomek R, Reshmi S, Harden A, Schlegelberger B, Housman D, Doggett NA, Rowley JD, Zeleznik-Le NJ. MLL is fused to CBP, a histone acetyltransferase, in therapy-related acute myeloid leukemia with a t(11;16)(q23;p13.3). Proceedings of the National Academy of Sciences of the United States of America. 94: 8732-7. PMID 9238046 DOI: 10.1073/pnas.94.16.8732  0.4
1997 Haluska FG, Thiele C, Goldstein A, Tsao H, Benoit EP, Housman D. Lack of phospholipase A2 mutations in neuroblastoma, melanoma and colon-cancer cell lines. International Journal of Cancer. Journal International Du Cancer. 72: 337-9. PMID 9219842 DOI: 10.1002/(SICI)1097-0215(19970717)72:2<337::AID-IJC22>3.0.CO;2-B  0.4
1997 Davis BM, McCurrach ME, Taneja KL, Singer RH, Housman DE. Expansion of a CUG trinucleotide repeat in the 3' untranslated region of myotonic dystrophy protein kinase transcripts results in nuclear retention of transcripts. Proceedings of the National Academy of Sciences of the United States of America. 94: 7388-93. PMID 9207101 DOI: 10.1073/pnas.94.14.7388  0.4
1997 Reddy PS, Housman DE. The complex pathology of trinucleotide repeats. Current Opinion in Cell Biology. 9: 364-72. PMID 9159084 DOI: 10.1016/S0955-0674(97)80009-9  0.4
1997 Beckers MC, Ernst E, Diez E, Morissette C, Gervais F, Hunter K, Housman D, Yoshida S, Skamene E, Gros P. High-resolution linkage map of mouse chromosome 13 in the vicinity of the host resistance locus Lgn1. Genomics. 39: 254-63. PMID 9119362 DOI: 10.1006/geno.1996.4489  0.4
1996 Karayiorgou M, Gogos JA, Galke BL, Jeffery JA, Nestadt G, Wolyniec PS, Antonarakis SE, Kazazian HH, Housman DE, Driscoll DA, Pulver AE. Genotype and phenotype analysis at the 22q11 schizophrenia susceptibility locus. Cold Spring Harbor Symposia On Quantitative Biology. 61: 835-43. PMID 9246508  0.4
1996 Pulver AE, Wolyniec PS, Housman D, Kazazian HH, Antonarakis SE, Nestadt G, Lasseter VK, McGrath JA, Dombroski B, Karayiorgou M, Ton C, Blouin JL, Kempf L. The Johns Hopkins University Collaborative Schizophrenia Study: an epidemiologic-genetic approach to test the heterogeneity hypothesis and identify schizophrenia susceptibility genes. Cold Spring Harbor Symposia On Quantitative Biology. 61: 797-814. PMID 9246505  0.4
1996 Corless CL, Aburatani H, Fletcher JA, Housman DE, Amin MB, Weinberg DS. Papillary renal cell carcinoma: quantitation of chromosomes 7 and 17 by FISH, analysis of chromosome 3p for LOH, and DNA ploidy. Diagnostic Molecular Pathology : the American Journal of Surgical Pathology, Part B. 5: 53-64. PMID 8919546 DOI: 10.1097/00019606-199603000-00009  0.4
1996 Flores JF, Walker GJ, Glendening JM, Haluska FG, Castresana JS, Rubio MP, Pastorfide GC, Boyer LA, Kao WH, Bulyk ML, Barnhill RL, Hayward NK, Housman DE, Fountain JW. Loss of the p16INK4a and p15INK4b genes, as well as neighboring 9p21 markers, in sporadic melanoma. Cancer Research. 56: 5023-32. PMID 8895759  0.4
1996 Shearman AM, Hudson TJ, Andresen JM, Wu X, Sohn RL, Haluska F, Housman DE, Weiss JS. The gene for schnyder's crystalline corneal dystrophy maps to human chromosome 1p34.1-p36. Human Molecular Genetics. 5: 1667-72. PMID 8894705  0.4
1996 Dackowski WR, Connors TD, Bowe AE, Stanton V, Housman D, Doggett NA, Landes GM, Klinger KW. The region surrounding the PKD1 gene: a 700-kb P1 contig from a YAC-deficient interval. Genome Research. 6: 515-24. PMID 8828040  0.4
1996 Mihich E, Housman D. Seventh annual Pezcoller Symposium: cancer genes--functional aspects. Cancer Research. 56: 4282-7. PMID 8797609  0.4
1996 Borrow J, Stanton VP, Andresen JM, Becher R, Behm FG, Chaganti RS, Civin CI, Disteche C, Dubé I, Frischauf AM, Horsman D, Mitelman F, Volinia S, Watmore AE, Housman DE. The translocation t(8;16)(p11;p13) of acute myeloid leukaemia fuses a putative acetyltransferase to the CREB-binding protein. Nature Genetics. 14: 33-41. PMID 8782817 DOI: 10.1038/ng0996-33  0.4
1996 Hunter KW, Riba L, Schalkwyk L, Clark M, Resenchuk S, Beeghly A, Su J, Tinkov F, Lee P, Ramu E, Lehrach H, Housman D. Toward the construction of integrated physical and genetic maps of the mouse genome using interspersed repetitive sequence PCR (IRS-PCR) genomics. Genome Research. 6: 290-9. PMID 8723722  0.4
1996 Gill M, Vallada H, Collier D, Sham P, Holmans P, Murray R, McGuffin P, Nanko S, Owen M, Antonarakis S, Housman D, Kazazian H, Nestadt G, Pulver AE, Straub RE, et al. A combined analysis of D22S278 marker alleles in affected sib-pairs: support for a susceptibility locus for schizophrenia at chromosome 22q12. Schizophrenia Collaborative Linkage Group (Chromosome 22). American Journal of Medical Genetics. 67: 40-5. PMID 8678112 DOI: 10.1002/(SICI)1096-8628(19960216)67:1<40::AID-AJMG6>3.0.CO;2-W  0.4
1996 Reddy S, Smith DB, Rich MM, Leferovich JM, Reilly P, Davis BM, Tran K, Rayburn H, Bronson R, Cros D, Balice-Gordon RJ, Housman D. Mice lacking the myotonic dystrophy protein kinase develop a late onset progressive myopathy. Nature Genetics. 13: 325-35. PMID 8673132 DOI: 10.1038/ng0796-325  0.4
1996 Elango R, Riba L, Housman D, Hunter K. Generation and mapping of Mus spretus strain-specific markers for rapid genomic scanning. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 7: 340-3. PMID 8661719  0.4
1996 Russell MW, Munroe DJ, Bric E, Housman DE, Dietz-Band J, Riethman HC, Collins FS, Brody LC. A 500-kb physical map and contig from the Harvey ras-1 gene to the 11p telomere. Genomics. 35: 353-60. PMID 8661149 DOI: 10.1006/geno.1996.0367  0.4
1996 Aburatani H, Stanton VP, Housman DE. High-resolution physical mapping by combined Alu-hybridization/PCR screening: construction of a yeast artificial chromosome map covering 31 centimorgans in 3p21-p14. Proceedings of the National Academy of Sciences of the United States of America. 93: 4474-9. PMID 8633093 DOI: 10.1073/pnas.93.9.4474  0.4
1996 Manenti G, Gariboldi M, Elango R, Fiorino A, De Gregorio L, Falvella FS, Hunter K, Housman D, Pierotti MA, Dragani TA. Genetic mapping of a pulmonary adenoma resistance (Par1) in mouse. Nature Genetics. 12: 455-7. PMID 8630506 DOI: 10.1038/ng0496-455  0.4
1996 Qin S, Nowak NJ, Zhang J, Sait SN, Mayers PG, Higgins MJ, Cheng Y, Li L, Munroe DJ, Gerhard DS, Weber BH, Bric E, Housman DE, Evans GA, Shows TB. A high-resolution physical map of human chromosome 11. Proceedings of the National Academy of Sciences of the United States of America. 93: 3149-54. PMID 8610184 DOI: 10.1073/pnas.93.7.3149  0.4
1996 Borrow J, Shearman AM, Stanton VP, Becher R, Collins T, Williams AJ, Dubé I, Katz F, Kwong YL, Morris C, Ohyashiki K, Toyama K, Rowley J, Housman DE. The t(7;11)(p15;p15) translocation in acute myeloid leukaemia fuses the genes for nucleoporin NUP98 and class I homeoprotein HOXA9. Nature Genetics. 12: 159-67. PMID 8563754 DOI: 10.1038/ng0296-159  0.4
1996 Graeber TG, Osmanian C, Jacks T, Housman DE, Koch CJ, Lowe SW, Giaccia AJ. Hypoxia-mediated selection of cells with diminished apoptotic potential in solid tumours. Nature. 379: 88-91. PMID 8538748 DOI: 10.1038/379088a0  0.4
1996 Aburatani H, Stanton V, Housman DE. High resolution physical mapping by combined aluhybridization/sts content screening: Construction of a YAC contig covering 25 CM in 3p21-pl4 reveals inverse distribution of (CA)n and ALU-PCR Loci Japanese Journal of Human Genetics. 41: 41.  0.4
1995 Bird SJ, Housman DE. Conducting and reporting research. Professional Ethics (Gainesville, Fla.). 4: 127-54. PMID 11655035  0.4
1995 Haluska FG, Housman DE. Recent advances in the molecular genetics of malignant melanoma. Cancer Surveys. 25: 277-92. PMID 8718523  0.4
1995 Hsu SY, Kubo M, Chun SY, Haluska FG, Housman DE, Hsueh AJ. Wilms' tumor protein WT1 as an ovarian transcription factor: decreases in expression during follicle development and repression of inhibin-alpha gene promoter. Molecular Endocrinology (Baltimore, Md.). 9: 1356-66. PMID 8544844 DOI: 10.1210/mend.9.10.8544844  0.4
1995 Taneja KL, McCurrach M, Schalling M, Housman D, Singer RH. Foci of trinucleotide repeat transcripts in nuclei of myotonic dystrophy cells and tissues. The Journal of Cell Biology. 128: 995-1002. PMID 7896884 DOI: 10.1083/jcb.128.6.995  0.4
1995 Munroe DJ, Loebbert R, Bric E, Whitton T, Prawitt D, Vu D, Buckler A, Winterpacht A, Zabel B, Housman DE. Systematic screening of an arrayed cDNA library by PCR. Proceedings of the National Academy of Sciences of the United States of America. 92: 2209-13. PMID 7892249 DOI: 10.1073/pnas.92.6.2209  0.4
1995 Nakagama H, Heinrich G, Pelletier J, Housman DE. Sequence and structural requirements for high-affinity DNA binding by the WT1 gene product. Molecular and Cellular Biology. 15: 1489-98. PMID 7862142  0.4
1995 Housman DE. DNA on trial--the molecular basis of DNA fingerprinting. The New England Journal of Medicine. 332: 534-5. PMID 7830738 DOI: 10.1056/NEJM199502233320812  0.4
1995 Housman D. Human DNA polymorphism. The New England Journal of Medicine. 332: 318-20. PMID 7816069 DOI: 10.1056/NEJM199502023320508  0.4
1995 Polakiewicz RD, Munroe DJ, Sait SN, Tycowski KT, Nowak NJ, Shows TB, Housman DE, Page DC. Mapping of ribosomal protein S3 and internally nested snoRNA U15A gene to human chromosome 11q13.3-q13.5. Genomics. 25: 577-80. PMID 7789996 DOI: 10.1016/0888-7543(95)80063-R  0.4
1995 Mccarthy L, Hunter K, Schalkwyk L, Riba L, Anson S, Mott R, Newell W, Bruley C, Bar I, Ramu E, Housman D, Cox R, Lehrach H. Efficient high-resolution genetic mapping of mouse interspersed repetitive sequence PCR products, toward integrated genetic and physical mapping of the mouse genome Proceedings of the National Academy of Sciences of the United States of America. 92: 5302-5306. PMID 7777502 DOI: 10.1073/pnas.92.12.5302  0.4
1995 Cai W, Aburatani H, Stanton VP, Housman DE, Wang YK, Schwartz DC. Ordered restriction endonuclease maps of yeast artificial chromosomes created by optical mapping on surfaces. Proceedings of the National Academy of Sciences of the United States of America. 92: 5164-8. PMID 7761468 DOI: 10.1073/pnas.92.11.5164  0.4
1995 Russell MW, Dick M, Campbell RM, Hulse JE, Munroe DJ, Bric E, Housman DE, Collins FS, Brody LC. Localization of Romano-Ward long QT syndrome gene, LQT1, to the interval between tyrosine hydroxylase (TH) and D11S1349. American Journal of Human Genetics. 57: 503-7. PMID 7668277  0.4
1995 Housman D. Gain of glutamines, gain of function? Nature Genetics. 10: 3-4. PMID 7647786 DOI: 10.1038/ng0595-3  0.4
1995 Karayiorgou M, Morris MA, Morrow B, Shprintzen RJ, Goldberg R, Borrow J, Gos A, Nestadt G, Wolyniec PS, Lasseter VK. Schizophrenia susceptibility associated with interstitial deletions of chromosome 22q11. Proceedings of the National Academy of Sciences of the United States of America. 92: 7612-6. PMID 7644464 DOI: 10.1073/pnas.92.17.7612  0.4
1995 Liu J, Stanton VP, Fujiwara TM, Wang JX, Rezonzew R, Crumley MJ, Morgan K, Gros P, Housman D, Schurr E. Large-scale cloning of human chromosome 2-specific yeast artificial chromosomes (YACs) using an interspersed repetitive sequences (IRS)-PCR approach. Genomics. 26: 178-91. PMID 7601441 DOI: 10.1016/0888-7543(95)80199-V  0.4
1995 Pulver AE, Lasseter VK, Kasch L, Wolyniec P, Nestadt G, Blouin JL, Kimberland M, Babb R, Vourlis S, Chen H. Schizophrenia: a genome scan targets chromosomes 3p and 8p as potential sites of susceptibility genes. American Journal of Medical Genetics. 60: 252-60. PMID 7573181 DOI: 10.1002/ajmg.1320600316  0.4
1995 Lasseter VK, Pulver AE, Wolyniec PS, Nestadt G, Meyers D, Karayiorgou M, Housman D, Antonarakis S, Kazazian H, Kasch L. Follow-up report of potential linkage for schizophrenia on chromosome 22q: Part 3. American Journal of Medical Genetics. 60: 172-3. PMID 7485255 DOI: 10.1002/ajmg.1320600217  0.4
1995 Moffett P, Bruening W, Nakagama H, Bardeesy N, Housman D, Housman DE, Pelletier J. Antagonism of WT1 activity by protein self-association. Proceedings of the National Academy of Sciences of the United States of America. 92: 11105-9. PMID 7479946 DOI: 10.1073/pnas.92.24.11105  0.32
1995 Dong WF, Xu Y, Hu QL, Munroe D, Minowada J, Housman DE, Minden MD. Molecular characterization of a chromosome translocation breakpoint t(11;14)(p13;q11) from the cell line KOPT-K1. Leukemia. 9: 1812-7. PMID 7475267  0.4
1995 Bird SJ, Housman DE. Trust and the collection, selection, analysis and interpretation of data: A scientist's view Science and Engineering Ethics. 1: 371-382. DOI: 10.1007/BF02583255  0.4
1994 Munroe DJ, Haas M, Bric E, Whitton T, Aburatani H, Hunter K, Ward D, Housman DE. IRE-bubble PCR: a rapid method for efficient and representative amplification of human genomic DNA sequences from complex sources. Genomics. 19: 506-14. PMID 8188293 DOI: 10.1006/geno.1994.1100  0.4
1994 Glaser T, Ton CC, Mueller R, Petzl-Erler ML, Oliver C, Nevin NC, Housman DE, Maas RL. Absence of PAX6 gene mutations in Gillespie syndrome (partial aniridia, cerebellar ataxia, and mental retardation). Genomics. 19: 145-8. PMID 8188215 DOI: 10.1006/geno.1994.1024  0.4
1994 Pulver AE, Karayiorgou M, Wolyniec PS, Lasseter VK, Kasch L, Nestadt G, Antonarakis S, Housman D, Kazazian HH, Meyers D. Sequential strategy to identify a susceptibility gene for schizophrenia: report of potential linkage on chromosome 22q12-q13.1: Part 1. American Journal of Medical Genetics. 54: 36-43. PMID 8178837 DOI: 10.1002/ajmg.1320540108  0.4
1994 Lowe SW, Jacks T, Housman DE, Ruley HE. Abrogation of oncogene-associated apoptosis allows transformation of p53-deficient cells. Proceedings of the National Academy of Sciences of the United States of America. 91: 2026-30. PMID 8134344  0.4
1994 Pulver AE, Nestadt G, Goldberg R, Shprintzen RJ, Lamacz M, Wolyniec PS, Morrow B, Karayiorgou M, Antonarakis SE, Housman D. Psychotic illness in patients diagnosed with velo-cardio-facial syndrome and their relatives. The Journal of Nervous and Mental Disease. 182: 476-8. PMID 8040660  0.4
1994 Lowe SW, Bodis S, McClatchey A, Remington L, Ruley HE, Fisher DE, Housman DE, Jacks T. p53 status and the efficacy of cancer therapy in vivo. Science (New York, N.Y.). 266: 807-10. PMID 7973635  0.4
1994 Pulver AE, Karayiorgou M, Lasseter VK, Wolyniec P, Kasch L, Antonarakis S, Housman D, Kazazian HH, Meyers D, Nestadt G. Follow-up of a report of a potential linkage for schizophrenia on chromosome 22q12-q13.1: Part 2. American Journal of Medical Genetics. 54: 44-50. PMID 7909990 DOI: 10.1002/ajmg.1320540109  0.4
1994 Lowe SW, Bodis S, Bardeesy N, McClatchey A, Remington L, Ruley HE, Fisher DE, Jacks T, Pelletier J, Housman DE. Apoptosis and the prognostic significance of p53 mutation. Cold Spring Harbor Symposia On Quantitative Biology. 59: 419-26. PMID 7587096  0.4
1993 Hinds HL, Ashley CT, Sutcliffe JS, Nelson DL, Warren ST, Housman DE, Schalling M. Tissue specific expression of FMR-1 provides evidence for a functional role in fragile X syndrome. Nature Genetics. 3: 36-43. PMID 8490651 DOI: 10.1038/ng0193-36  0.4
1993 Bruhn SL, Housman DE, Lippard SJ. Isolation and characterization of cDNA clones encoding the Drosophila homolog of the HMG-box SSRP family that recognizes specific DNA structures. Nucleic Acids Research. 21: 1643-6. PMID 8479916 DOI: 10.1093/nar/21.7.1643  0.4
1993 Lowe SW, Ruley HE, Jacks T, Housman DE. p53-dependent apoptosis modulates the cytotoxicity of anticancer agents. Cell. 74: 957-67. PMID 8402885 DOI: 10.1016/0092-8674(93)90719-7  0.4
1993 Kreidberg JA, Sariola H, Loring JM, Maeda M, Pelletier J, Housman D, Jaenisch R. WT-1 is required for early kidney development. Cell. 74: 679-91. PMID 8395349 DOI: 10.1016/0092-8674(93)90515-R  0.4
1993 Fountain JW, Hudson TJ, Engelstein M, Housman DE, Dracopoli NC. Dinucleotide repeat polymorphism at the D9S126 locus (9p21). Human Molecular Genetics. 2: 823. PMID 8353508 DOI: 10.1093/hmg/2.6.823-a  0.4
1993 Duyao MP, Taylor SA, Buckler AJ, Ambrose CM, Lin C, Groot N, Church D, Barnes G, Wasmuth JJ, Housman DE. A gene from chromosome 4p16.3 with similarity to a superfamily of transporter proteins. Human Molecular Genetics. 2: 673-6. PMID 8353488  0.4
1993 Schalling M, Hudson TJ, Buetow KH, Housman DE. Direct detection of novel expanded trinucleotide repeats in the human genome. Nature Genetics. 4: 135-9. PMID 8348150 DOI: 10.1038/ng0693-135  0.4
1993 Bruening W, Gros P, Sato T, Stanimir J, Nakamura Y, Housman D, Pelletier J. Analysis of the 11p13 Wilms' tumor suppressor gene (WT1) in ovarian tumors. Cancer Investigation. 11: 393-9. PMID 8324644  0.32
1993 Hunter KW, Watson ML, Rochelle J, Ontiveros S, Munroe D, Seldin MF, Housman DE. Single-strand conformational polymorphism (SSCP) mapping of the mouse genome: integration of the SSCP, microsatellite, and gene maps of mouse chromosome 1. Genomics. 18: 510-9. PMID 8307560  0.4
1993 Church DM, Banks LT, Rogers AC, Graw SL, Housman DE, Gusella JF, Buckler AJ. Identification of human chromosome 9 specific genes using exon amplification. Human Molecular Genetics. 2: 1915-20. PMID 7506603 DOI: 10.1093/hmg/2.11.1915  0.4
1992 Oettinger MA, Stanger B, Schatz DG, Glaser T, Call K, Housman D, Baltimore D. The recombination activating genes, RAG 1 and RAG 2, are on chromosome 11p in humans and chromosome 2p in mice. Immunogenetics. 35: 97-101. PMID 1735560 DOI: 10.1007/BF00189518  0.4
1992 Hudson TJ, Engelstein M, Lee MK, Ho EC, Rubenfield MJ, Adams CP, Housman DE, Dracopoli NC. Isolation and chromosomal assignment of 100 highly informative human simple sequence repeat polymorphisms. Genomics. 13: 622-9. PMID 1639389 DOI: 10.1016/0888-7543(92)90133-D  0.4
1992 Graw SL, Schalling M, Housman D, Callen DF, Klinger K, Landes G, Lerner T. Isolation and characterization of a candidate gene for autosomal-dominant polycystic kidney disease. Contributions to Nephrology. 97: 110-7. PMID 1633711  0.4
1992 Jackson CL, Britt DE, Graw SL, Potts A, Santoro K, Buckler AJ, Housman DE, Mark HF. Construction and characterization of radiation hybrids for chromosome 9, and their use in mapping cosmid probes on the chromosome. Somatic Cell and Molecular Genetics. 18: 285-301. PMID 1496423  0.4
1992 Graw SL, Buckler AJ, Britt DE, Jackson CL, Taruscio D, Baldini A, Ward DC, Housman DE. Generation and characterization of a human chromosome 9 cosmid library. Somatic Cell and Molecular Genetics. 18: 269-84. PMID 1496422  0.4
1992 Call KM, Ito CY, Lindberg C, Memisoglu A, Petrou C, Glaser T, Jones C, Housman DE. Mapping and characterization of 129 cosmids on human chromosome 11p. Somatic Cell and Molecular Genetics. 18: 463-75. PMID 1475712 DOI: 10.1007/BF01233086  0.4
1992 Fountain JW, Karayiorgou M, Taruscio D, Graw SL, Buckler AJ, Ward DC, Dracopoli NC, Housman DE. Genetic and physical map of the interferon region on chromosome 9p. Genomics. 14: 105-12. PMID 1385297 DOI: 10.1016/S0888-7543(05)80290-3  0.4
1992 Bruhn SL, Pil PM, Essigmann JM, Housman DE, Lippard SJ. Isolation and characterization of human cDNA clones encoding a high mobility group box protein that recognizes structural distortions to DNA caused by binding of the anticancer agent cisplatin. Proceedings of the National Academy of Sciences of the United States of America. 89: 2307-11. PMID 1372440  0.4
1992 Hubert R, Stanton VP, Aburatani H, Warren J, Li H, Housman DE, Arnheim N. Sperm typing allows accurate measurement of the recombination fraction between D3S2 and D3S3 on the short arm of human chromosome 3. Genomics. 12: 683-7. PMID 1349296 DOI: 10.1016/0888-7543(92)90294-3  0.4
1992 Harley HG, Brook JD, Rundle SA, Crow S, Reardon W, Buckler AJ, Harper PS, Housman DE, Shaw DJ. Expansion of an unstable DNA region and phenotypic variation in myotonic dystrophy. Nature. 355: 545-6. PMID 1346923 DOI: 10.1038/355545a0  0.4
1992 Baird PN, Groves N, Haber DA, Housman DE, Cowell JK. Identification of mutations in the WT1 gene in tumours from patients with the WAGR syndrome. Oncogene. 7: 2141-9. PMID 1331933  0.72
1992 Haber DA, Housman DE. The genetics of Wilms' tumor. Advances in Cancer Research. 59: 41-68. PMID 1325734  0.72
1992 Haber DA, Housman DE. Role of the WT1 gene in Wilms' tumour. Cancer Surveys. 12: 105-17. PMID 1322241  0.72
1992 Haber DA, Timmers HT, Pelletier J, Sharp PA, Housman DE. A dominant mutation in the Wilms tumor gene WT1 cooperates with the viral oncogene E1A in transformation of primary kidney cells. Proceedings of the National Academy of Sciences of the United States of America. 89: 6010-4. PMID 1321431  0.72
1992 Valentijn LJ, Bolhuis PA, Zorn I, Hoogendijk JE, van den Bosch N, Hensels GW, Stanton VP, Housman DE, Fischbeck KH, Ross DA. The peripheral myelin gene PMP-22/GAS-3 is duplicated in Charcot-Marie-Tooth disease type 1A. Nature Genetics. 1: 166-70. PMID 1303229 DOI: 10.1038/ng0692-166  0.4
1992 Bruening W, Bardeesy N, Silverman BL, Cohn RA, Machin GA, Aronson AJ, Housman D, Pelletier J. Germline intronic and exonic mutations in the Wilms' tumour gene (WT1) affecting urogenital development. Nature Genetics. 1: 144-8. PMID 1302008 DOI: 10.1038/ng0592-144  0.32
1991 Pelletier J, Brook JD, Housman DE. Assignment of two of the translation initiation factor-4E (EIF4EL1 and EIF4EL2) genes to human chromosomes 4 and 20. Genomics. 10: 1079-82. PMID 1916814  0.32
1991 Cowell JK, Wadey RB, Haber DA, Call KM, Housman DE, Pritchard J. Structural rearrangements of the WT1 gene in Wilms' tumour cells. Oncogene. 6: 595-9. PMID 1851548  0.72
1991 Buckler AJ, Chang DD, Graw SL, Brook JD, Haber DA, Sharp PA, Housman DE. Exon amplification: a strategy to isolate mammalian genes based on RNA splicing. Proceedings of the National Academy of Sciences of the United States of America. 88: 4005-9. PMID 1850845  0.72
1991 Haber DA, Housman DE. Rate-limiting steps: the genetics of pediatric cancers. Cell. 64: 5-8. PMID 1846091  0.72
1991 Doucette-Stamm LA, Riba L, Handelin B, Difilippantonio M, Ward DC, Wasmuth JJ, Gusella JF, Housman DE. Generation and characterization of irradiation hybrids of human chromosome 4. Somatic Cell and Molecular Genetics. 17: 471-80. PMID 1837181  0.4
1991 Strobel SA, Doucette-Stamm LA, Riba L, Housman DE, Dervan PB. Site-specific cleavage of human chromosome 4 mediated by triple-helix formation. Science (New York, N.Y.). 254: 1639-42. PMID 1836279  0.4
1991 Geissler EN, Liao M, Brook JD, Martin FH, Zsebo KM, Housman DE, Galli SJ. Stem cell factor (SCF), a novel hematopoietic growth factor and ligand for c-kit tyrosine kinase receptor, maps on human chromosome 12 between 12q14.3 and 12qter. Somatic Cell and Molecular Genetics. 17: 207-14. PMID 1707188  0.36
1991 Goradia TM, Stanton VP, Cui XF, Aburatani H, Li HH, Lange K, Housman DE, Arnheim N. Ordering three DNA polymorphisms on human chromosome 3 by sperm typing. Genomics. 10: 748-55. PMID 1679751 DOI: 10.1016/0888-7543(91)90459-R  0.4
1991 Huff V, Miwa H, Haber DA, Call KM, Housman D, Strong LC, Saunders GF. Evidence for WT1 as a Wilms tumor (WT) gene: intragenic germinal deletion in bilateral WT. American Journal of Human Genetics. 48: 997-1003. PMID 1673293  0.72
1991 Buckler AJ, Pelletier J, Haber DA, Glaser T, Housman DE. Isolation, characterization, and expression of the murine Wilms' tumor gene (WT1) during kidney development. Molecular and Cellular Biology. 11: 1707-12. PMID 1671709  0.72
1991 Thompson LM, Plummer S, Schalling M, Altherr MR, Gusella JF, Housman DE, Wasmuth JJ. A gene encoding a fibroblast growth factor receptor isolated from the Huntington disease gene region of human chromosome 4. Genomics. 11: 1133-42. PMID 1664411 DOI: 10.1016/0888-7543(91)90041-C  0.4
1991 Haber DA, Sohn RL, Buckler AJ, Pelletier J, Call KM, Housman DE. Alternative splicing and genomic structure of the Wilms tumor gene WT1. Proceedings of the National Academy of Sciences of the United States of America. 88: 9618-22. PMID 1658787  0.72
1991 Samulski RJ, Zhu X, Xiao X, Brook JD, Housman DE, Epstein N, Hunter LA. Targeted integration of adeno-associated virus (AAV) into human chromosome 19. The Embo Journal. 10: 3941-50. PMID 1657596  0.4
1991 Schwartz CE, Haber DA, Stanton VP, Strong LC, Skolnick MH, Housman DE. Familial predisposition to Wilms tumor does not segregate with the WT1 gene. Genomics. 10: 927-30. PMID 1655633  0.72
1991 Pelletier J, Bruening W, Li FP, Haber DA, Glaser T, Housman DE. WT1 mutations contribute to abnormal genital system development and hereditary Wilms' tumour. Nature. 353: 431-4. PMID 1654525 DOI: 10.1038/353431a0  0.72
1991 Pelletier J, Schalling M, Buckler AJ, Rogers A, Haber DA, Housman D. Expression of the Wilms' tumor gene WT1 in the murine urogenital system. Genes & Development. 5: 1345-56. PMID 1651275  0.72
1991 Ton CC, Huff V, Call KM, Cohn S, Strong LC, Housman DE, Saunders GF. Smallest region of overlap in Wilms tumor deletions uniquely implicates an 11p13 zinc finger gene as the disease locus. Genomics. 10: 293-7. PMID 1646159 DOI: 10.1016/0888-7543(91)90516-H  0.4
1990 Hensold JO, Hunt CR, Calderwood SK, Housman DE, Kingston RE. DNA binding of heat shock factor to the heat shock element is insufficient for transcriptional activation in murine erythroleukemia cells. Molecular and Cellular Biology. 10: 1600-8. PMID 2320006  0.4
1990 Tam SY, Geissler EN, Graw SL, Housman DE. Functional expression of the genomic DNA sequences encoding mouse Na,K-ATPase alpha 1 gene by cotransfection of overlapping genomic DNA segments. Molecular and Cellular Biology. 10: 6619-23. PMID 2174112  0.4
1990 Pritchard-Jones K, Fleming S, Davidson D, Bickmore W, Porteous D, Gosden C, Bard J, Buckler A, Pelletier J, Housman D. The candidate Wilms' tumour gene is involved in genitourinary development. Nature. 346: 194-7. PMID 2164159 DOI: 10.1038/346194a0  0.32
1990 Haber DA, Buckler AJ, Glaser T, Call KM, Pelletier J, Sohn RL, Douglass EC, Housman DE. An internal deletion within an 11p13 zinc finger gene contributes to the development of Wilms' tumor. Cell. 61: 1257-69. PMID 2163761 DOI: 10.1016/0092-8674(90)90690-G  0.4
1990 Wilson SD, Billings PR, D'Eustachio P, Fournier RE, Geissler E, Lalley PA, Burd PR, Housman DE, Taylor BA, Dorf ME. Clustering of cytokine genes on mouse chromosome 11. The Journal of Experimental Medicine. 171: 1301-14. PMID 1969921  0.44
1990 Brilliant MH, Szabo G, Katarova Z, Kozak CA, Glaser TM, Greenspan RJ, Housman DE. Sequences homologous to glutamic acid decarboxylase cDNA are present on mouse chromosomes 2 and 10. Genomics. 6: 115-22. PMID 1968040 DOI: 10.1016/0888-7543(90)90455-4  0.4
1989 Dracopoli NC, Harnett P, Bale SJ, Stanger BZ, Tucker MA, Housman DE, Kefford RF. Loss of alleles from the distal short arm of chromosome 1 occurs late in melanoma tumor progression. Proceedings of the National Academy of Sciences of the United States of America. 86: 4614-8. PMID 2734311  0.4
1989 Bale SJ, Dracopoli NC, Tucker MA, Clark WH, Fraser MC, Stanger BZ, Green P, Donis-Keller H, Housman DE, Greene MH. Mapping the gene for hereditary cutaneous malignant melanoma-dysplastic nevus to chromosome 1p. The New England Journal of Medicine. 320: 1367-72. PMID 2716782 DOI: 10.1056/NEJM198905253202102  0.4
1989 Glaser T, Matthews KE, Hudson JW, Seth P, Housman DE, Crerar MM. Localization of the muscle, liver, and brain glycogen phosphorylase genes on linkage maps of mouse chromosomes 19, 12, and 2, respectively. Genomics. 5: 510-21. PMID 2575583 DOI: 10.1016/0888-7543(89)90017-7  0.4
1989 Emanuel JR, Graw S, Housman D, Levenson R. Identification of a region within the Na,K-ATPase alpha subunit that contributes to differential ouabain sensitivity. Molecular and Cellular Biology. 9: 3744-9. PMID 2550800  0.6
1989 Haber DA, Housman DE. MspI/HpaII polymorphism in the human multidrug resistance gene 1. Nucleic Acids Research. 17: 10142. PMID 2481261  0.72
1988 Croop JM, Gros P, Housman DE. Genetics of multidrug resistance. The Journal of Clinical Investigation. 81: 1303-9. PMID 3284909 DOI: 10.1172/JCI113455  0.4
1988 Geissler EN, Cheng SV, Gusella JF, Housman DE. Genetic analysis of the dominant white-spotting (W) region on mouse chromosome 5: identification of cloned DNA markers near W. Proceedings of the National Academy of Sciences of the United States of America. 85: 9635-9. PMID 3200849  0.4
1988 Dracopoli NC, Stanger BZ, Lager M, Housman DE. Localization of the FGR protooncogene on the genetic linkage map of human chromosome 1p. Genomics. 3: 124-8. PMID 2906322 DOI: 10.1016/0888-7543(88)90142-5  0.4
1988 Darby JK, Willems PJ, Nakashima P, Johnsen J, Ferrell RE, Wijsman EM, Gerhard DS, Dracopoli NC, Housman D, Henke J. Restriction analysis of the structural alpha-L-fucosidase gene and its linkage to fucosidosis. American Journal of Human Genetics. 43: 749-55. PMID 2903667  0.4
1988 Dracopoli NC, Stanger BZ, Ito CY, Call KM, Lincoln SE, Lander ES, Housman DE. A genetic linkage map of 27 loci from PND to FY on the short arm of human chromosome I. American Journal of Human Genetics. 43: 462-70. PMID 2902785  0.4
1988 Kent RB, Fallows DA, Emanuel JR, Lalley PA, Levenson R, Housman DE. Application of gene transfer and gene mapping techniques to functional analysis of the Na,K-ATPase. Progress in Clinical and Biological Research. 268: 97-104. PMID 2851836  0.6
1988 Emanuel JR, Schulz J, Zhou XM, Kent RB, Housman D, Cantley L, Levenson R. Expression of an ouabain-resistant Na,K-ATPase in CV-1 cells after transfection with a cDNA encoding the rat Na,K-ATPase alpha 1 subunit. The Journal of Biological Chemistry. 263: 7726-33. PMID 2836394  0.6
1988 Geissler EN, Ryan MA, Housman DE. The dominant-white spotting (W) locus of the mouse encodes the c-kit proto-oncogene. Cell. 55: 185-92. PMID 2458842 DOI: 10.1016/0092-8674(88)90020-7  0.4
1987 Kent RB, Emanuel JR, Ben Neriah Y, Levenson R, Housman DE. Ouabain resistance conferred by expression of the cDNA for a murine Na+, K+-ATPase alpha subunit. Science (New York, N.Y.). 237: 901-3. PMID 3039660  0.6
1987 Kent RB, Fallows DA, Geissler E, Glaser T, Emanuel JR, Lalley PA, Levenson R, Housman DE. Genes encoding alpha and beta subunits of Na,K-ATPase are located on three different chromosomes in the mouse. Proceedings of the National Academy of Sciences of the United States of America. 84: 5369-73. PMID 2885848  0.6
1987 Fallows D, Kent RB, Nelson DL, Emanuel JR, Levenson R, Housman DE. Chromosome-mediated transfer of the murine Na,K-ATPase alpha subunit confers ouabain resistance. Molecular and Cellular Biology. 7: 2985-7. PMID 2823111  0.6
1986 Gros P, Fallows DA, Croop JM, Housman DE. Chromosome-mediated gene transfer of multidrug resistance. Molecular and Cellular Biology. 6: 3785-90. PMID 3796594  0.44
1986 Gros P, Croop J, Housman D. Mammalian multidrug resistance gene: complete cDNA sequence indicates strong homology to bacterial transport proteins. Cell. 47: 371-80. PMID 3768958 DOI: 10.1016/0092-8674(86)90594-5  0.4
Low-probability matches
2019 Ochaba J, Fote G, Kachemov M, Thein S, Yeung SY, Lau AL, Hernandez S, Lim RG, Casale M, Neel MJ, Monuki ES, Reidling J, Housman DE, Thompson LM, Steffan JS. IKKβ slows Huntington's disease progression in R6/1 mice. Proceedings of the National Academy of Sciences of the United States of America. PMID 31088970 DOI: 10.1073/pnas.1814246116  0.24
2017 Lim RG, Quan C, Reyes-Ortiz AM, Lutz SE, Kedaigle AJ, Gipson TA, Wu J, Vatine GD, Stocksdale J, Casale MS, Svendsen CN, Fraenkel E, Housman DE, Agalliu D, Thompson LM. Huntington's Disease iPSC-Derived Brain Microvascular Endothelial Cells Reveal WNT-Mediated Angiogenic and Blood-Brain Barrier Deficits. Cell Reports. 19: 1365-1377. PMID 28514657 DOI: 10.1016/j.celrep.2017.04.021  0.24
1993 Galson DL, Hensold JO, Bishop TR, Schalling M, D'Andrea AD, Jones C, Auron PE, Housman DE. Mouse beta-globin DNA-binding protein B1 is identical to a proto-oncogene, the transcription factor Spi-1/PU.1, and is restricted in expression to hematopoietic cells and the testis. Molecular and Cellular Biology. 13: 2929-41. PMID 8474451  0.24
1991 Wexler NS, Rose EA, Housman DE. Molecular approaches to hereditary diseases of the nervous system: Huntington's disease as a paradigm. Annual Review of Neuroscience. 14: 503-29. PMID 1827708 DOI: 10.1146/annurev.ne.14.030191.002443  0.24
2018 Nath SR, Yu Z, Gipson TA, Marsh GB, Yoshidome E, Robins DM, Todi SV, Housman DE, Lieberman AP. Androgen receptor polyglutamine expansion drives age-dependent quality control defects and muscle dysfunction. The Journal of Clinical Investigation. PMID 29809168 DOI: 10.1172/JCI99042  0.2
2017 Neueder A, Gipson TA, Batterton S, Lazell HJ, Farshim PP, Paganetti P, Housman DE, Bates GP. HSF1-dependent and -independent regulation of the mammalian in vivo heat shock response and its impairment in Huntington's disease mouse models. Scientific Reports. 7: 12556. PMID 28970536 DOI: 10.1038/s41598-017-12897-0  0.2
2017 Dolzhenko E, van Vugt JJFA, Shaw RJ, Bekritsky MA, van Blitterswijk M, Narzisi G, Ajay SS, Rajan V, Lajoie B, Johnson NH, Kingsbury Z, Humphray SJ, Schellevis RD, Brands WJ, Baker M, ... ... Housman DE, et al. Detection of long repeat expansions from PCR-free whole-genome sequence data. Genome Research. PMID 28887402 DOI: 10.1101/gr.225672.117  0.2
1993 Haas M, Aburatani H, Stanton VP, Bhatt M, Housman D, Ward DC. Isolation and FISH mapping of 80 cosmid clones on the short arm of human chromosome 3. Genomics. 16: 90-6. PMID 8486389 DOI: 10.1006/geno.1993.1145  0.2
1992 Boyle AL, Feltquite DM, Dracopoli NC, Housman DE, Ward DC. Rapid physical mapping of cloned DNA on banded mouse chromosomes by fluorescence in situ hybridization. Genomics. 12: 106-15. PMID 1733847  0.2
1991 Royer-Pokora B, Ragg S, Heckl-Ostreicher B, Held M, Loos U, Call K, Glaser T, Housman D, Saunders G, Zabel B. Direct pulsed field gel electrophoresis of Wilms' tumors shows that DNA deletions in 11p13 are rare. Genes, Chromosomes & Cancer. 3: 89-100. PMID 1648959  0.2
1990 Warburton D, Gersen S, Yu MT, Jackson C, Handelin B, Housman D. Monochromosomal rodent-human hybrids from microcell fusion of human lymphoblastoid cells containing an inserted dominant selectable marker. Genomics. 6: 358-66. PMID 2307476  0.2
1990 Lichter P, Tang CJ, Call K, Hermanson G, Evans GA, Housman D, Ward DC. High-resolution mapping of human chromosome 11 by in situ hybridization with cosmid clones. Science (New York, N.Y.). 247: 64-9. PMID 2294592  0.2
1990 Glaser T, Lane J, Housman D. A mouse model of the aniridia-Wilms tumor deletion syndrome. Science (New York, N.Y.). 250: 823-7. PMID 2173141  0.2
1990 Glaser T, Rose E, Morse H, Housman D, Jones C. A panel of irradiation-reduced hybrids selectively retaining human chromosome 11p13: their structure and use to purify the WAGR gene complex. Genomics. 6: 48-64. PMID 2154397  0.2
1989 Glaser T, Housman D, Lewis WH, Gerhard D, Jones C. A fine-structure deletion map of human chromosome 11p: analysis of J1 series hybrids. Somatic Cell and Molecular Genetics. 15: 477-501. PMID 2595451  0.2
1989 Glaser T, Driscoll DJ, Antonarakis S, Valle D, Housman D. A highly polymorphic locus cloned from the breakpoint of a chromosome 11p13 deletion associated with the WAGR syndrome. Genomics. 5: 880-93. PMID 2574149  0.2
1987 Gerhard DS, Jones C, Morse HG, Handelin B, Weeks V, Housman D. Analysis of human chromosome 11 by somatic cell genetics: reexamination of derivatives of human-hamster cell line J1. Somatic Cell and Molecular Genetics. 13: 293-304. PMID 3331828  0.2
1987 Lugo TG, Handelin B, Killary AM, Housman DE, Fournier RE. Isolation of microcell hybrid clones containing retroviral vector insertions into specific human chromosomes. Molecular and Cellular Biology. 7: 2814-20. PMID 2823107  0.2
1993 Moir DT, Dorman TE, Xue F, Ma NS, Stanton VP, Housman D, Bowden DW, Noll WW, Mao J. Rapid identification of overlapping YACs in the MEN2 region of human chromosome 10 by hybridization with Alu element-mediated PCR products. Gene. 136: 177-83. PMID 7904972  0.16
1994 Coleman A, Fountain JW, Nobori T, Olopade OI, Robertson G, Housman DE, Lugo TG. Distinct deletions of chromosome 9p associated with melanoma versus glioma, lung cancer, and leukemia. Cancer Research. 54: 344-8. PMID 8275465  0.08
1993 Andersen LB, Fountain JW, Gutmann DH, Tarlé SA, Glover TW, Dracopoli NC, Housman DE, Collins FS. Mutations in the neurofibromatosis 1 gene in sporadic malignant melanoma cell lines. Nature Genetics. 3: 118-21. PMID 8499944 DOI: 10.1038/ng0293-118  0.08
1993 Petty EM, Gibson LH, Fountain JW, Bolognia JL, Yang-Feng TL, Housman DE, Bale AE. Molecular definition of a chromosome 9p21 germ-line deletion in a woman with multiple melanomas and a plexiform neurofibroma: implications for 9p tumor-suppressor gene(s). American Journal of Human Genetics. 53: 96-104. PMID 8317504  0.08
1991 Fountain JW, Dracopoli NC, Housman DE, Baldwin AS. MspI RFLP detected by a ZNF-40 cDNA sequence. Nucleic Acids Research. 19: 2514. PMID 1710360  0.08
1990 Fountain JW, Bale SJ, Housman DE, Dracopoli NC. Genetics of melanoma. Cancer Surveys. 9: 645-71. PMID 2101727  0.08
1989 Fong CT, Dracopoli NC, White PS, Merrill PT, Griffith RC, Housman DE, Brodeur GM. Loss of heterozygosity for the short arm of chromosome 1 in human neuroblastomas: correlation with N-myc amplification. Proceedings of the National Academy of Sciences of the United States of America. 86: 3753-7. PMID 2566996  0.08
1988 Dracopoli NC, Rose E, Whitfield GK, Guidon PT, Bale SJ, Chance PA, Kourides IA, Housman DE. Two thyroid hormone regulated genes, the beta-subunits of nerve growth factor (NGFB) and thyroid stimulating hormone (TSHB), are located less than 310 kb apart in both human and mouse genomes. Genomics. 3: 161-7. PMID 2906326  0.08
1987 Gerhard DS, Dracopoli NC, Bale SJ, Houghton AN, Watkins P, Payne CE, Greene MH, Housman DE. Evidence against Ha-ras-1 involvement in sporadic and familial melanoma. Nature. 325: 73-5. PMID 2879249 DOI: 10.1038/325073a0  0.08
1986 Tsiftsoglou A, Housman D, Wong W. The inhibition of commitment of mouse erythroleukemia cells by steroids involves a glucocorticoid-receptor mediated process(es) acting at the nuclear level. Biochimica Et Biophysica Acta. 889: 251-61. PMID 3465373  0.08
2012 Johnson SL, Kuske CR, Carney TD, Housman DC, Gallegos-Graves LV, Belnap J. Increased temperature and altered summer precipitation have differential effects on biological soil crusts in a dryland ecosystem Global Change Biology. 18: 2583-2593. DOI: 10.1111/j.1365-2486.2012.02709.x  0.04
2012 Reed SC, Coe KK, Sparks JP, Housman DC, Zelikova TJ, Belnap J. Changes to dryland rainfall result in rapid moss mortality and altered soil fertility Nature Climate Change. 2: 752-755. DOI: 10.1038/nclimate1596  0.04
2012 Housman DC, Killingbeck KT, Dave Evans R, Charlet TN, Smith SD. Foliar nutrient resorption in two Mojave Desert shrubs exposed to Free-Air CO 2 Enrichment (FACE) Journal of Arid Environments. 78: 26-32. DOI: 10.1016/j.jaridenv.2011.11.007  0.04
2012 Zelikova TJ, Housman DC, Grote EE, Neher DA, Belnap J. Warming and increased precipitation frequency on the Colorado Plateau: Implications for biological soil crusts and soil processes Plant and Soil. 355: 265-282. DOI: 10.1007/s11104-011-1097-z  0.04
2011 Darby BJ, Neher DA, Housman DC, Belnap J. Few apparent short-term effects of elevated soil temperature and increased frequency of summer precipitation on the abundance and taxonomic diversity of desert soil micro- and meso-fauna Soil Biology and Biochemistry. 43: 1474-1481. DOI: 10.1016/j.soilbio.2011.03.020  0.04
2010 Grote EE, Belnap J, Housman DC, Sparks JP. Carbon exchange in biological soil crust communities under differential temperatures and soil water contents: Implications for global change Global Change Biology. 16: 2763-2774. DOI: 10.1111/j.1365-2486.2010.02201.x  0.04
2007 Yeager CM, Kornosky JL, Morgan RE, Cain EC, Garcia-Pichel F, Housman DC, Belnap J, Kuske CR. Three distinct clades of cultured heterocystous cyanobacteria constitute the dominant N2-fixing members of biological soil crusts of the Colorado Plateau, USA. Fems Microbiology Ecology. 60: 85-97. PMID 17381526 DOI: 10.1111/j.1574-6941.2006.00265.x  0.04
2007 Housman DC, Yeager CM, Darby BJ, Sanford RL, Kuske CR, Neher DA, Belnap J. Heterogeneity of soil nutrients and subsurface biota in a dryland ecosystem Soil Biology and Biochemistry. 39: 2138-2149. DOI: 10.1016/j.soilbio.2007.03.015  0.04
2006 Darby BJ, Housman DC, Zaki AM, Shamout Y, Adl SM, Belnap J, Neher DA. Effects of altered temperature and precipitation on desert protozoa associated with biological soil crusts. The Journal of Eukaryotic Microbiology. 53: 507-14. PMID 17123415 DOI: 10.1111/j.1550-7408.2006.00134.x  0.04
2006 Housman DC, Powers HH, Collins AD, Belnap J. Carbon and nitrogen fixation differ between successional stages of biological soil crusts in the Colorado Plateau and Chihuahuan Desert Journal of Arid Environments. 66: 620-634. DOI: 10.1016/j.jaridenv.2005.11.014  0.04
2006 Housman DC, Naumburg E, Huxman TE, Charlet TN, Nowak RS, Smith SD. Increases in desert shrub productivity under elevated carbon dioxide vary with water availability Ecosystems. 9: 374-385. DOI: 10.1007/s10021-005-0124-4  0.04
2004 Yeager CM, Kornosky JL, Housman DC, Grote EE, Belnap J, Kuske CR. Diazotrophic community structure and function in two successional stages of biological soil crusts from the Colorado Plateau and Chihuahuan Desert. Applied and Environmental Microbiology. 70: 973-83. PMID 14766579 DOI: 10.1128/AEM.70.2.973-983.2004  0.04
2003 Housman DC, Zitzer SF, Huxman TE, Smith SD. Functional ecology of shrub seedlings after a natural recruitment event at the Nevada Desert FACE facility Global Change Biology. 9: 718-728. DOI: 10.1046/j.1365-2486.2003.00618.x  0.04
2003 Naumburg E, Housman DC, Huxman TE, Charlet TN, Loik ME, Smith SD. Photosynthetic responses of Mojave Desert shrubs to free air CO2 enrichment are greatest during wet years Global Change Biology. 9: 276-285. DOI: 10.1046/j.1365-2486.2003.00580.x  0.04
2002 Housman DC, Price MV, Redak RA. Architecture of coastal and desert Encelia farinosa (Asteraceae): Consequences of plastic and heritable variation in leaf characters American Journal of Botany. 89: 1303-1310.  0.04
2000 Smith SD, Huxman TE, Zitzer SF, Charlet TN, Housman DC, Coleman JS, Fenstermaker LK, Seemann JR, Nowak RS. Elevated CO2 increases productivity and invasive species success in an arid ecosystem. Nature. 408: 79-82. PMID 11081510 DOI: 10.1038/35040544  0.04
1992 Krolewski AS, Krolewski B, Gray M, Stanton V, Warram JH, Housman D. High-frequency DNA sequence polymorphisms in the insulin receptor gene detected by denaturing gradient gel blots. Genomics. 12: 705-9. PMID 1572644  0.04
1992 Buschman E, Arceci RJ, Croop JM, Che M, Arias IM, Housman DE, Gros P. mdr2 encodes P-glycoprotein expressed in the bile canalicular membrane as determined by isoform-specific antibodies. The Journal of Biological Chemistry. 267: 18093-9. PMID 1381362  0.04
1991 Hunter K, Housman D, Hopkins N. Isolation and characterization of irradiation fusion hybrids from mouse chromosome 1 for mapping Rmc-1, a gene encoding a cellular receptor for MCF class murine retroviruses. Somatic Cell and Molecular Genetics. 17: 169-83. PMID 2011795  0.04
1990 Raymond M, Rose E, Housman DE, Gros P. Physical mapping, amplification, and overexpression of the mouse mdr gene family in multidrug-resistant cells. Molecular and Cellular Biology. 10: 1642-51. PMID 1969609  0.04
1990 Arceci RJ, Baas F, Raponi R, Horwitz SB, Housman D, Croop JM. Multidrug resistance gene expression is controlled by steroid hormones in the secretory epithelium of the uterus. Molecular Reproduction and Development. 25: 101-9. PMID 1968749 DOI: 10.1002/mrd.1080250202  0.04
1989 Croop JM, Raymond M, Haber D, Devault A, Arceci RJ, Gros P, Housman DE. The three mouse multidrug resistance (mdr) genes are expressed in a tissue-specific manner in normal mouse tissues. Molecular and Cellular Biology. 9: 1346-50. PMID 2471060  0.04
1988 Guild BC, Mulligan RC, Gros P, Housman DE. Retroviral transfer of a murine cDNA for multidrug resistance confers pleiotropic drug resistance to cells without prior drug selection. Proceedings of the National Academy of Sciences of the United States of America. 85: 1595-9. PMID 3422751  0.04
1988 Gros P, Raymond M, Bell J, Housman D. Cloning and characterization of a second member of the mouse mdr gene family. Molecular and Cellular Biology. 8: 2770-8. PMID 3405218  0.04
1988 Arceci RJ, Croop JM, Horwitz SB, Housman D. The gene encoding multidrug resistance is induced and expressed at high levels during pregnancy in the secretory epithelium of the uterus. Proceedings of the National Academy of Sciences of the United States of America. 85: 4350-4. PMID 3380797  0.04
1987 Croop JM, Guild BC, Gros P, Housman DE. Genetics of multidrug resistance: relationship of a cloned gene to the complete multidrug resistant phenotype. Cancer Research. 47: 5982-8. PMID 3664502  0.04
1986 Roninson IB, Chin JE, Choi KG, Gros P, Housman DE, Fojo A, Shen DW, Gottesman MM, Pastan I. Isolation of human mdr DNA sequences amplified in multidrug-resistant KB carcinoma cells. Proceedings of the National Academy of Sciences of the United States of America. 83: 4538-42. PMID 3459187  0.04
1986 Gros P, Ben Neriah YB, Croop JM, Housman DE. Isolation and expression of a complementary DNA that confers multidrug resistance. Nature. 323: 728-31. PMID 3022150 DOI: 10.1038/323728a0  0.04
2018 Wang ET, Treacy D, Eichinger K, Struck A, Estabrook J, Olafson H, Wang TT, Bhatt K, Westbrook T, Sedehizadeh S, Ward A, Day J, Brook D, Berglund JA, Cooper T, ... Housman D, et al. Transcriptome alterations in myotonic dystrophy skeletal muscle and heart. Human Molecular Genetics. PMID 30561649 DOI: 10.1093/hmg/ddy432  0.01
2018 Fratta P, Sivakumar P, Humphrey J, Lo K, Ricketts T, Oliveira H, Brito-Armas JM, Kalmar B, Ule A, Yu Y, Birsa N, Bodo C, Collins T, Conicella AE, Mejia Maza A, ... ... Housman DE, et al. Mice with endogenous TDP-43 mutations exhibit gain of splicing function and characteristics of amyotrophic lateral sclerosis. The Embo Journal. PMID 29764981 DOI: 10.15252/embj.201798684  0.01
2018 Drosu NC, Edelman ER, Housman DE. Could antiretrovirals be treating EBV in MS? A case report. Multiple Sclerosis and Related Disorders. 22: 19-21. PMID 29510325 DOI: 10.1016/j.msard.2018.02.029  0.01
2017 McGinty RJ, Puleo F, Aksenova AY, Hisey JA, Shishkin AA, Pearson EL, Wang ET, Housman DE, Moore C, Mirkin SM. A Defective mRNA Cleavage and Polyadenylation Complex Facilitates Expansions of Transcribed (GAA)n Repeats Associated with Friedreich's Ataxia. Cell Reports. 20: 2490-2500. PMID 28877480 DOI: 10.1016/j.celrep.2017.08.051  0.01
2017 Taylor JY, Wright ML, Hickey KT, Housman DE. Genome Sequencing Technologies and Nursing: What Are the Roles of Nurses and Nurse Scientists? Nursing Research. 66: 198-205. PMID 28252579 DOI: 10.1097/NNR.0000000000000211  0.01
2016 Wright ML, Housman D, Taylor JY. A perspective for sequencing familial hypercholesterolaemia in African Americans. Npj Genomic Medicine. 1: 16012. PMID 29263812 DOI: 10.1038/npjgenmed.2016.12  0.01
2016 Taylor JY, Wright ML, Housman D. Lead toxicity and genetics in Flint, MI. Npj Genomic Medicine. 1. PMID 27398227 DOI: 10.1038/npjgenmed.2016.18  0.01
2015 Munson SM, Webb RH, Housman DC, Veblen KE, Nussear KE, Beever EA, Hartney KB, Miriti MN, Phillips SL, Fulton RE, Tallent NG. Long-term plant responses to climate are moderated by biophysical attributes in a North American desert Journal of Ecology. 103: 657-668. DOI: 10.1111/1365-2745.12381  0.01
2014 Scheufele E, Aronzon D, Coopersmith R, McDuffie MT, Kapoor M, Uhrich CA, Avitabile JE, Liu J, Housman D, Palchuk MB. tranSMART: An Open Source Knowledge Management and High Content Data Analytics Platform. Amia Joint Summits On Translational Science Proceedings Amia Summit On Translational Science. 2014: 96-101. PMID 25717408  0.01
2013 Crook ZR, Housman DE. In vivo identification of therapeutic constructs from pooled candidates in HD model mice. Journal of Huntington's Disease. 2: 437-41. PMID 25062730 DOI: 10.3233/JHD-130073  0.01
2013 Crook ZR, Housman DE. Surveying the landscape of Huntington's disease mechanisms, measurements, and medicines. Journal of Huntington's Disease. 2: 405-36. PMID 25062729 DOI: 10.3233/JHD-130072  0.01
2013 Katsoulakis E, Solomon SB, Maybody M, Housman D, Niyazov G, Riaz N, Lovelock M, Spratt DE, Erinjeri JP, Thornton RH, Yamada Y. Temporary organ displacement coupled with image-guided, intensity-modulated radiotherapy for paraspinal tumors. Radiation Oncology (London, England). 8: 150. PMID 23800073 DOI: 10.1186/1748-717X-8-150  0.01
2013 van Blitterswijk M, Wang ET, Friedman BA, Keagle PJ, Lowe P, Leclerc AL, van den Berg LH, Housman DE, Veldink JH, Landers JE. Characterization of FUS mutations in amyotrophic lateral sclerosis using RNA-Seq. Plos One. 8: e60788. PMID 23577159 DOI: 10.1371/journal.pone.0060788  0.01
2013 Tabchy A, Eltonsy N, Housman DE, Mills GB. Systematic identification of combinatorial drivers and targets in cancer cell lines. Plos One. 8: e60339. PMID 23577104 DOI: 10.1371/journal.pone.0060339  0.01
2013 Tabchy A, Eltonsy N, Housman DE, Mills GB. Correction: Systematic identification of combinatorial drivers and targets in cancer cell lines (PLoS ONE) Plos One. 8. DOI: 10.1371/annotation/85d86c29-4ba6-4bf0-94f6-2977b3e1c792  0.01
2012 Wang ET, Cody NA, Jog S, Biancolella M, Wang TT, Treacy DJ, Luo S, Schroth GP, Housman DE, Reddy S, Lécuyer E, Burge CB. Transcriptome-wide regulation of pre-mRNA splicing and mRNA localization by muscleblind proteins. Cell. 150: 710-24. PMID 22901804 DOI: 10.1016/j.cell.2012.06.041  0.01
2012 Parkesh R, Childs-Disney JL, Nakamori M, Kumar A, Wang E, Wang T, Hoskins J, Tran T, Housman D, Thornton CA, Disney MD. Design of a bioactive small molecule that targets the myotonic dystrophy type 1 RNA via an RNA motif-ligand database and chemical similarity searching. Journal of the American Chemical Society. 134: 4731-42. PMID 22300544 DOI: 10.1021/ja210088v  0.01
2012 Zelefsky MJ, Housman DM, Pei X, Alicikus Z, Magsanoc JM, Dauer LT, St Germain J, Yamada Y, Kollmeier M, Cox B, Zhang Z. Incidence of secondary cancer development after high-dose intensity-modulated radiotherapy and image-guided brachytherapy for the treatment of localized prostate cancer. International Journal of Radiation Oncology, Biology, Physics. 83: 953-9. PMID 22172904 DOI: 10.1016/j.ijrobp.2011.08.034  0.01
2012 Jun HJ, Acquaviva J, Chi D, Lessard J, Zhu H, Woolfenden S, Bronson RT, Pfannl R, White F, Housman DE, Iyer L, Whittaker CA, Boskovitz A, Raval A, Charest A. Acquired MET expression confers resistance to EGFR inhibition in a mouse model of glioblastoma multiforme. Oncogene. 31: 3039-50. PMID 22020333 DOI: 10.1038/onc.2011.474  0.01
2009 Abend A, Housman D, Johnson B. Integrating Clinical Data into the i2b2 Repository. Summit On Translational Bioinformatics. 2009: 1-5. PMID 21347159  0.01
2008 Siegel LC, Housman D, Newmark L, Ungar J, Ungar JP, Einbinder JS, Einbinder JS, Gandhi TK. Linking test ordering with order tracking: closing the loop in ambulatory care. Amia ... Annual Symposium Proceedings / Amia Symposium. Amia Symposium. 1131. PMID 18999233  0.01
2008 Greim J, Housman D, Lenz S, Mort E, Ferris TG, Meyer GS, Einbinder JS. Improving physician note entry rates through an incentive program. Amia ... Annual Symposium Proceedings / Amia Symposium. Amia Symposium. 939. PMID 18999141  0.01
2008 Housman D, Greim J, Morgan SJ, Nelson SM, Flanagan T, Martin K, Eskin M, Einbinder JS. Modeling pediatric vaccination guidelines in a data warehouse. Amia ... Annual Symposium Proceedings / Amia Symposium. Amia Symposium. 976. PMID 18999017  0.01
2008 Parikh RR, Housman D, Yang Q, Toppmeyer D, Wilson LD, Haffty BG. Prognostic value of triple-negative phenotype at the time of locally recurrent, conservatively treated breast cancer. International Journal of Radiation Oncology, Biology, Physics. 72: 1056-63. PMID 18676094 DOI: 10.1016/j.ijrobp.2008.02.066  0.01
2008 Fuller CD, Housman DM, Thomas CR. Radiotherapy for thymoma and thymic carcinoma. Hematology/Oncology Clinics of North America. 22: 489-507. PMID 18514129 DOI: 10.1016/j.hoc.2008.03.012  0.01
2008 Yu JB, Blitzblau RC, Decker RH, Housman DM, Wilson LD. Analysis of primary CD30+ cutaneous lymphoproliferative disease and survival from the Surveillance, Epidemiology, and End Results database. Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology. 26: 1483-8. PMID 18349400 DOI: 10.1200/JCO.2007.14.1374  0.01
2008 Weber K, Porter M, Housman D. Worked examples and concept example usage in understanding mathematical concepts and proofs Making the Connection: Research and Teaching in Undergraduate Mathematics Education. 245-252. DOI: 10.5948/UPO9780883859759.020  0.01
2007 Linder JA, Jung E, Housman D, Eskin MS, Schnipper JL, Middleton B, Einbinder JS. The Acute Respiratory Infection Quality Dashboard: a performance measurement reporting tool in an electronic health record. Amia ... Annual Symposium Proceedings / Amia Symposium. Amia Symposium. 1035. PMID 18694133  0.01
2007 Jung E, Schnipper JL, Li Q, Linder JA, Rose AF, Li R, Eskin MS, Housman D, Middleton B, Einbinder JS. The coronary artery disease quality dashboard: a chronic care disease management tool in an electronic health record. Amia ... Annual Symposium Proceedings / Amia Symposium. Amia Symposium. 999. PMID 18694098  0.01
2007 Housman DM, Decker RH, Wilson LD. Regarding adjuvant radiation therapy in merkel cell carcinoma: selection bias and its affect on overall survival. Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology. 25: 4503-4; author reply. PMID 17906216 DOI: 10.1200/JCO.2007.12.2895  0.01
2006 Jung E, Li Q, Mangalampalli A, Greim J, Eskin MS, Housman D, Isikoff J, Abend AH, Middleton B, Einbinder JS. Report Central: quality reporting tool in an electronic health record. Amia ... Annual Symposium Proceedings / Amia Symposium. Amia Symposium. 971. PMID 17238590  0.01
2006 Greim J, Housman D, Turchin A, Orlowitz B, Eskin M, Abend A, Isikoff J, Einbinder J. The quality data warehouse: delivering answers on demand. Amia ... Annual Symposium Proceedings / Amia Symposium. Amia Symposium. 934. PMID 17238553  0.01
2005 Wilson LD, Housman D, Smith BD. Merkel cell carcinoma: improved outcome with the addition of adjuvant therapy. Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology. 23: 7236-7; author reply. PMID 16192614 DOI: 10.1200/JCO.2005.02.4430  0.01
2003 Mitra RD, Butty VL, Shendure J, Williams BR, Housman DE, Church GM. Digital genotyping and haplotyping with polymerase colonies. Proceedings of the National Academy of Sciences of the United States of America. 100: 5926-31. PMID 12730373 DOI: 10.1073/pnas.0936399100  0.01
2003 Housman D, Porter M. Proof schemes and learning strategies of above-average mathematics students Educational Studies in Mathematics. 53: 139-158. DOI: 10.1023/A:1025541416693  0.01
2002 Housman DC, Price MV, Redak RA. Architecture of coastal and desert Encelia farinosa (Asteraceae): consequences of plastic and heritable variation in leaf characters. American Journal of Botany. 89: 1303-10. PMID 21665733 DOI: 10.3732/ajb.89.8.1303  0.01
2002 Housman D. Linear and symmetric allocation methods for partially defined cooperative games International Journal of Game Theory. 30: 377-404. DOI: 10.1007/s001820100086  0.01
1998 Jing J, Reed J, Huang J, Hu X, Clarke V, Edington J, Housman D, Anantharaman TS, Huff EJ, Mishra B, Porter B, Shenker A, Wolfson E, Hiort C, Kantor R, et al. Automated high resolution optical mapping using arrayed, fluid-fixed DNA molecules. Proceedings of the National Academy of Sciences of the United States of America. 95: 8046-51. PMID 9653137 DOI: 10.1073/pnas.95.14.8046  0.01
1998 Housman D, Clark L. Core and monotonic allocation methods International Journal of Game Theory. 27: 611-616.  0.01
1997 Dahlberg RP, Housman DL. Facilitating learning events through example generation Educational Studies in Mathematics. 33: 283-299.  0.01
1992 Rubin C, Rubenstein JL, Stechler G, Heeren T, Halton A, Housman D, Kasten L. Depressive affect in "normal" adolescents: relationship to life stress, family, and friends. The American Journal of Orthopsychiatry. 62: 430-41. PMID 1497108  0.01
1992 Krolewski AS, Doria A, Magre J, Warram JH, Housman D. Molecular genetic approaches to the identification of genes involved in the development of nephropathy in insulin-dependent diabetes mellitus. Journal of the American Society of Nephrology : Jasn. 3: S9-17. PMID 1457765  0.01
1992 Takahara Y, Hamada K, Housman DE. A new retrovirus packaging cell for gene transfer constructed from amplified long terminal repeat-free chimeric proviral genes. Journal of Virology. 66: 3725-32. PMID 1316479  0.01
1991 Hensold JO, Dubyak G, Housman DE. Calcium ionophore, A23187, induces commitment to differentiation but inhibits the subsequent expression of erythroid genes in murine erythroleukemia cells. Blood. 77: 1362-70. PMID 2001459  0.01
1991 Davis LM, Zabel B, Senger G, Lüdecke HJ, Metzroth B, Call K, Housman D, Claussen U, Horsthemke B, Shows TB. A tumor chromosome rearrangement further defines the 11p13 Wilms tumor locus. Genomics. 10: 588-92. PMID 1653761  0.01
1990 Baas F, Jongsma AP, Broxterman HJ, Arceci RJ, Housman D, Scheffer GL, Riethorst A, van Groenigen M, Nieuwint AW, Joenje H. Non-P-glycoprotein mediated mechanism for multidrug resistance precedes P-glycoprotein expression during in vitro selection for doxorubicin resistance in a human lung cancer cell line. Cancer Research. 50: 5392-8. PMID 1974823  0.01
1989 Rubenstein JL, Heeren T, Housman D, Rubin C, Stechler G. Suicidal behavior in "normal" adolescents: risk and protective factors. The American Journal of Orthopsychiatry. 59: 59-71. PMID 2929730  0.01
1988 Galson DL, Housman DE. Detection of two tissue-specific DNA-binding proteins with affinity for sites in the mouse beta-globin intervening sequence 2. Molecular and Cellular Biology. 8: 381-92. PMID 3422099  0.01
1988 Guild BC, Finer MH, Housman DE, Mulligan RC. Development of retrovirus vectors useful for expressing genes in cultured murine embryonal cells and hematopoietic cells in vivo. Journal of Virology. 62: 3795-801. PMID 3418785  0.01
1988 Kabnick KS, Housman DE. Determinants that contribute to cytoplasmic stability of human c-fos and beta-globin mRNAs are located at several sites in each mRNA. Molecular and Cellular Biology. 8: 3244-50. PMID 3211141  0.01
1988 Hensold JO, Housman DE. Decreased expression of the stress protein HSP70 is an early event in murine erythroleukemic cell differentiation. Molecular and Cellular Biology. 8: 2219-23. PMID 3164440  0.01
1988 Friedhoff AJ, Pickar D, Axelrod J, Creese I, Davis KL, Gallagher DW, Greengard P, Housman D, Maas JW, Richelson E. Neurochemistry and neuropharmacology. Schizophrenia Bulletin. 14: 399-412. PMID 2905525  0.01
1988 von Melchner H, Housman DE. The expression of neomycin phosphotransferase in human promyelocytic leukemia cells (HL60) delays their differentiation. Oncogene. 2: 137-40. PMID 2835723  0.01
1988 Hensold JO, Swerdlow PS, Housman DE. A transient increase in histone H2A ubiquitination is coincident with the onset of erythroleukemic cell differentiation. Blood. 71: 1153-6. PMID 2833326  0.01
1987 Housman D. Insertion of dominant selectable markers into the human genome. Somatic Cell and Molecular Genetics. 13: 441-6. PMID 3331833  0.01
1987 Arriza JL, Weinberger C, Cerelli G, Glaser TM, Handelin BL, Housman DE, Evans RM. Cloning of human mineralocorticoid receptor complementary DNA: structural and functional kinship with the glucocorticoid receptor. Science (New York, N.Y.). 237: 268-75. PMID 3037703  0.01
1987 Gerhard DS, Egeland JA, Pauls DL, Housman DE. Search for a gene that predisposes individuals to BPI disorder. Journal of Psychiatric Research. 21: 569-75. PMID 2894460  0.01
1987 Egeland JA, Gerhard DS, Pauls DL, Sussex JN, Kidd KK, Allen CR, Hostetter AM, Housman DE. Bipolar affective disorders linked to DNA markers on chromosome 11. Nature. 325: 783-7. PMID 2881209 DOI: 10.1038/325783a0  0.01
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