T. Conrad Gilliam - Publications

Columbia University, New York, NY 
 University of Chicago, Chicago, IL 

95 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2017 Bainer RO, Trendowski MR, Cheng C, Pei D, Yang W, Paugh SW, Goss KH, Skol AD, Pavlidis P, Pui CH, Gilliam TC, Evans WE, Onel K. A p53-regulated apoptotic gene signature predicts treatment response and outcome in pediatric acute lymphoblastic leukemia. Cancer Management and Research. 9: 397-410. PMID 28979163 DOI: 10.2147/Cmar.S139864  0.4
2015 Sulakhe D, Xie B, Taylor A, D'Souza M, Balasubramanian S, Hashemifar S, White S, Dave UJ, Agam G, Xu J, Wang S, Gilliam TC, Maltsev N. Lynx: a knowledge base and an analytical workbench for integrative medicine. Nucleic Acids Research. PMID 26590263 DOI: 10.1093/nar/gkv1257  0.96
2015 Xie B, Agam G, Balasubramanian S, Xu J, Gilliam TC, Maltsev N, Börnigen D. Disease gene prioritization using network and feature. Journal of Computational Biology : a Journal of Computational Molecular Cell Biology. 22: 313-23. PMID 25844670 DOI: 10.1089/cmb.2015.0001  0.96
2014 Dubchak I, Balasubramanian S, Wang S, Meyden C, Sulakhe D, Poliakov A, Börnigen D, Xie B, Taylor A, Ma J, Paciorkowski AR, Mirzaa GM, Dave P, Agam G, Xu J, ... ... Gilliam TC, et al. An integrative computational approach for prioritization of genomic variants. Plos One. 9: e114903. PMID 25506935 DOI: 10.1371/journal.pone.0114903  0.96
2014 Sulakhe D, Taylor A, Balasubramanian S, Feng B, Xie B, Börnigen D, Dave UJ, Foster IT, Gilliam TC, Maltsev N. Lynx web services for annotations and systems analysis of multi-gene disorders. Nucleic Acids Research. 42: W473-7. PMID 24948611 DOI: 10.1093/nar/gku517  0.96
2014 Sulakhe D, Balasubramanian S, Xie B, Berrocal E, Feng B, Taylor A, Chitturi B, Dave U, Agam G, Xu J, Börnigen D, Dubchak I, Gilliam TC, Maltsev N. High-throughput translational medicine: challenges and solutions. Advances in Experimental Medicine and Biology. 799: 39-67. PMID 24292961 DOI: 10.1007/978-1-4614-8778-4_3  0.96
2014 Sulakhe D, Balasubramanian S, Xie B, Feng B, Taylor A, Wang S, Berrocal E, Dave U, Xu J, Börnigen D, Gilliam TC, Maltsev N. Lynx: a database and knowledge extraction engine for integrative medicine. Nucleic Acids Research. 42: D1007-12. PMID 24270788 DOI: 10.1093/nar/gkt1166  0.96
2012 Xie B, Sulakhe D, Chitturi B, Agam G, Maltsev N, Gilliam TC. Prediction of candidate genes for neuropsychiatric disorders using feature-based enrichment 2012 Acm Conference On Bioinformatics, Computational Biology and Biomedicine, Bcb 2012. 564-566. DOI: 10.1145/2382936.2383022  0.96
2010 Strug LJ, Suresh R, Fyer AJ, Talati A, Adams PB, Li W, Hodge SE, Gilliam TC, Weissman MM. Panic disorder is associated with the serotonin transporter gene (SLC6A4) but not the promoter region (5-HTTLPR). Molecular Psychiatry. 15: 166-76. PMID 18663369 DOI: 10.1038/Mp.2008.79  0.96
2008 Iossifov I, Zheng T, Baron M, Gilliam TC, Rzhetsky A. Genetic-linkage mapping of complex hereditary disorders to a whole-genome molecular-interaction network. Genome Research. 18: 1150-62. PMID 18417725 DOI: 10.1101/Gr.075622.107  0.96
2008 Christian SL, Brune CW, Sudi J, Kumar RA, Liu S, Karamohamed S, Badner JA, Matsui S, Conroy J, McQuaid D, Gergel J, Hatchwell E, Gilliam TC, Gershon ES, Nowak NJ, et al. Novel submicroscopic chromosomal abnormalities detected in autism spectrum disorder. Biological Psychiatry. 63: 1111-7. PMID 18374305 DOI: 10.1016/J.Biopsych.2008.01.009  0.96
2008 Ponder CA, Huded CP, Munoz MB, Gulden FO, Gilliam TC, Palmer AA. Rapid selection response for contextual fear conditioning in a cross between C57BL/6J and A/J: behavioral, QTL and gene expression analysis. Behavior Genetics. 38: 277-91. PMID 18363093 DOI: 10.1007/S10519-008-9203-6  0.96
2008 Kumar RA, KaraMohamed S, Sudi J, Conrad DF, Brune C, Badner JA, Gilliam TC, Nowak NJ, Cook EH, Dobyns WB, Christian SL. Recurrent 16p11.2 microdeletions in autism. Human Molecular Genetics. 17: 628-38. PMID 18156158 DOI: 10.1093/Hmg/Ddm376  0.96
2007 Ponder CA, Munoz M, Gilliam TC, Palmer AA. Genetic architecture of fear conditioning in chromosome substitution strains: relationship to measures of innate (unlearned) anxiety-like behavior. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 18: 221-8. PMID 17492333 DOI: 10.1007/S00335-007-9013-9  0.96
2007 Sebat J, Lakshmi B, Malhotra D, Troge J, Lese-Martin C, Walsh T, Yamrom B, Yoon S, Krasnitz A, Kendall J, Leotta A, Pai D, Zhang R, Lee YH, Hicks J, ... ... Gilliam TC, et al. Strong association of de novo copy number mutations with autism. Science (New York, N.Y.). 316: 445-9. PMID 17363630 DOI: 10.1126/Science.1138659  0.96
2007 Szatmari P, Paterson AD, Zwaigenbaum L, Roberts W, Brian J, Liu XQ, Vincent JB, Skaug JL, Thompson AP, Senman L, Feuk L, Qian C, Bryson SE, Jones MB, ... ... Gilliam TC, et al. Mapping autism risk loci using genetic linkage and chromosomal rearrangements. Nature Genetics. 39: 319-28. PMID 17322880 DOI: 10.1038/Ng1985  0.96
2007 Ponder CA, Kliethermes CL, Drew MR, Muller J, Das K, Risbrough VB, Crabbe JC, Gilliam TC, Palmer AA. Selection for contextual fear conditioning affects anxiety-like behaviors and gene expression. Genes, Brain, and Behavior. 6: 736-49. PMID 17309658 DOI: 10.1111/J.1601-183X.2007.00306.X  0.96
2007 Xu H, Kellendonk CB, Simpson EH, Keilp JG, Bruder GE, Polan HJ, Kandel ER, Gilliam TC. DRD2 C957T polymorphism interacts with the COMT Val158Met polymorphism in human working memory ability. Schizophrenia Research. 90: 104-7. PMID 17113268 DOI: 10.1016/j.schres.2006.10.001  0.96
2006 Cheng R, Juo SH, Loth JE, Nee J, Iossifov I, Blumenthal R, Sharpe L, Kanyas K, Lerer B, Lilliston B, Smith M, Trautman K, Gilliam TC, Endicott J, Baron M. Genome-wide linkage scan in a large bipolar disorder sample from the National Institute of Mental Health genetics initiative suggests putative loci for bipolar disorder, psychosis, suicide, and panic disorder. Molecular Psychiatry. 11: 252-60. PMID 16402137 DOI: 10.1038/sj.mp.4001778  0.96
2006 Yonan AL, Palmer AA, Gilliam TC. Hardy-Weinberg disequilibrium identified genotyping error of the serotonin transporter (SLC6A4) promoter polymorphism. Psychiatric Genetics. 16: 31-4. PMID 16395127 DOI: 10.1097/01.Ypg.0000174393.79883.05  0.96
2006 Cheng R, Park N, Juo SH, Liu J, Loth JE, Endicott J, Gilliam TC, Baron M. Psychosis and the genetic spectrum of bipolar disorder: evidence from linkage analysis. Molecular Psychiatry. 11: 3-5. PMID 16172609 DOI: 10.1038/sj.mp.4001745  0.96
2005 McQueen MB, Devlin B, Faraone SV, Nimgaonkar VL, Sklar P, Smoller JW, Abou Jamra R, Albus M, Bacanu SA, Baron M, Barrett TB, Berrettini W, Blacker D, Byerley W, Cichon S, ... ... Gilliam TC, et al. Combined analysis from eleven linkage studies of bipolar disorder provides strong evidence of susceptibility loci on chromosomes 6q and 8q. American Journal of Human Genetics. 77: 582-95. PMID 16175504 DOI: 10.1086/491603  0.96
2005 Palmer AA, Verbitsky M, Suresh R, Kamens HM, Reed CL, Li N, Burkhart-Kasch S, McKinnon CS, Belknap JK, Gilliam TC, Phillips TJ. Gene expression differences in mice divergently selected for methamphetamine sensitivity. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 16: 291-305. PMID 16104378 DOI: 10.1007/S00335-004-2451-8  0.96
2005 Bruder GE, Keilp JG, Xu H, Shikhman M, Schori E, Gorman JM, Gilliam TC. Catechol-O-methyltransferase (COMT) genotypes and working memory: associations with differing cognitive operations. Biological Psychiatry. 58: 901-7. PMID 16043133 DOI: 10.1016/j.biopsych.2005.05.010  0.96
2005 Alarcón M, Yonan AL, Gilliam TC, Cantor RM, Geschwind DH. Quantitative genome scan and Ordered-Subsets Analysis of autism endophenotypes support language QTLs. Molecular Psychiatry. 10: 747-57. PMID 15824743 DOI: 10.1038/sj.mp.4001666  0.96
2005 Park N, Cheng R, Juo SH, Liu J, Loth JE, Endicott J, Gilliam TC, Baron M. Absence of psychosis may influence linkage results for bipolar disorder. Molecular Psychiatry. 10: 235-7. PMID 15570316 DOI: 10.1038/sj.mp.4001623  0.96
2004 Krauthammer M, Kaufmann CA, Gilliam TC, Rzhetsky A. Molecular triangulation: bridging linkage and molecular-network information for identifying candidate genes in Alzheimer's disease. Proceedings of the National Academy of Sciences of the United States of America. 101: 15148-53. PMID 15471992 DOI: 10.1073/pnas.0404315101  0.96
2004 Stone JL, Merriman B, Cantor RM, Yonan AL, Gilliam TC, Geschwind DH, Nelson SF. Evidence for sex-specific risk alleles in autism spectrum disorder. American Journal of Human Genetics. 75: 1117-23. PMID 15467983 DOI: 10.1086/426034  0.96
2004 Tadin-Strapps M, Warburton D, Baumeister FA, Fischer SG, Yonan J, Gilliam TC, Christiano AM. Cloning of the breakpoints of a de novo inversion of chromosome 8, inv (8)(p11.2q23.1) in a patient with Ambras syndrome. Cytogenetic and Genome Research. 107: 68-76. PMID 15305058 DOI: 10.1159/000079573  0.96
2004 Garcia Arocena D, Louis ED, Tassone F, Gilliam TC, Ottman R, Jacquemont S, Hagerman PJ. Screen for expanded FMR1 alleles in patients with essential tremor. Movement Disorders : Official Journal of the Movement Disorder Society. 19: 930-3. PMID 15300658 DOI: 10.1002/Mds.20043  0.96
2004 Sebat J, Lakshmi B, Troge J, Alexander J, Young J, Lundin P, MÃ¥nér S, Massa H, Walker M, Chi M, Navin N, Lucito R, Healy J, Hicks J, Ye K, ... ... Gilliam TC, et al. Large-scale copy number polymorphism in the human genome. Science (New York, N.Y.). 305: 525-8. PMID 15273396 DOI: 10.1126/Science.1098918  0.96
2004 Park N, Juo SH, Cheng R, Liu J, Loth JE, Lilliston B, Nee J, Grunn A, Kanyas K, Lerer B, Endicott J, Gilliam TC, Baron M. Linkage analysis of psychosis in bipolar pedigrees suggests novel putative loci for bipolar disorder and shared susceptibility with schizophrenia. Molecular Psychiatry. 9: 1091-9. PMID 15241432 DOI: 10.1038/sj.mp.4001541  0.96
2004 Morabia A, Ross BM, Costanza MC, Cayanis E, Flaherty MS, Alvin GB, Das K, James R, Yang AS, Evagrafov O, Gilliam TC. Population-based study of SR-BI genetic variation and lipid profile. Atherosclerosis. 175: 159-68. PMID 15186961 DOI: 10.1016/J.Atherosclerosis.2004.03.014  0.96
2004 Verbitsky M, Yonan AL, Malleret G, Kandel ER, Gilliam TC, Pavlidis P. Altered hippocampal transcript profile accompanies an age-related spatial memory deficit in mice. Learning & Memory (Cold Spring Harbor, N.Y.). 11: 253-60. PMID 15169854 DOI: 10.1101/lm.68204  0.96
2004 Ottman R, Winawer MR, Kalachikov S, Barker-Cummings C, Gilliam TC, Pedley TA, Hauser WA. LGI1 mutations in autosomal dominant partial epilepsy with auditory features. Neurology. 62: 1120-6. PMID 15079011  0.96
2003 Martinez-Mir A, Zlotogorski A, Londono D, Gordon D, Grunn A, Uribe E, Horev L, Ruiz IM, Davalos NO, Alayan O, Liu J, Gilliam TC, Salas-Alanis JC, Christiano AM. Identification of a locus for type I punctate palmoplantar keratoderma on chromosome 15q22-q24. Journal of Medical Genetics. 40: 872-8. PMID 14684683 DOI: 10.1136/jmg.40.12.872  0.32
2003 Kim S, Ruparel HD, Gilliam TC, Ju J. Digital genotyping using molecular affinity and mass spectrometry. Nature Reviews. Genetics. 4: 1001-8. PMID 14631360 DOI: 10.1038/Nrg1230  0.96
2003 Yonan AL, Palmer AA, Smith KC, Feldman I, Lee HK, Yonan JM, Fischer SG, Pavlidis P, Gilliam TC. Bioinformatic analysis of autism positional candidate genes using biological databases and computational gene network prediction. Genes, Brain, and Behavior. 2: 303-20. PMID 14606695 DOI: 10.1034/J.1601-183X.2003.00041.X  0.96
2003 Yonan AL, Alarcón M, Cheng R, Magnusson PK, Spence SJ, Palmer AA, Grunn A, Juo SH, Terwilliger JD, Liu J, Cantor RM, Geschwind DH, Gilliam TC. A genomewide screen of 345 families for autism-susceptibility loci. American Journal of Human Genetics. 73: 886-97. PMID 13680528 DOI: 10.1086/378778  0.96
2003 Morabia A, Cayanis E, Costanza MC, Ross BM, Flaherty MS, Alvin GB, Das K, Gilliam TC. Association of extreme blood lipid profile phenotypic variation with 11 reverse cholesterol transport genes and 10 non-genetic cardiovascular disease risk factors. Human Molecular Genetics. 12: 2733-43. PMID 12966036 DOI: 10.1093/hmg/ddg314  0.96
2003 Chen A, Muzzio IA, Malleret G, Bartsch D, Verbitsky M, Pavlidis P, Yonan AL, Vronskaya S, Grody MB, Cepeda I, Gilliam TC, Kandel ER. Inducible enhancement of memory storage and synaptic plasticity in transgenic mice expressing an inhibitor of ATF4 (CREB-2) and C/EBP proteins. Neuron. 39: 655-69. PMID 12925279 DOI: 10.1016/S0896-6273(03)00501-4  0.96
2003 Kljuic A, Bazzi H, Sundberg JP, Martinez-Mir A, O'Shaughnessy R, Mahoney MG, Levy M, Montagutelli X, Ahmad W, Aita VM, Gordon D, Uitto J, Whiting D, Ott J, Fischer S, ... Gilliam TC, et al. Desmoglein 4 in hair follicle differentiation and epidermal adhesion: evidence from inherited hypotrichosis and acquired pemphigus vulgaris. Cell. 113: 249-60. PMID 12705872 DOI: 10.1016/S0092-8674(03)00273-3  0.96
2003 Morabia A, Cayanis E, Costanza MC, Ross BM, Bernstein MS, Flaherty MS, Alvin GB, Das K, Morris MA, Penchaszadeh GK, Zhang P, Gilliam TC. Association between lipoprotein lipase (LPL) gene and blood lipids: a common variant for a common trait? Genetic Epidemiology. 24: 309-21. PMID 12687649 DOI: 10.1002/gepi.10229  0.96
2003 Liu J, Juo SH, Dewan A, Grunn A, Tong X, Brito M, Park N, Loth JE, Kanyas K, Lerer B, Endicott J, Penchaszadeh G, Knowles JA, Ott J, Gilliam TC, et al. Evidence for a putative bipolar disorder locus on 2p13-16 and other potential loci on 4q31, 7q34, 8q13, 9q31, 10q21-24, 13q32, 14q21 and 17q11-12. Molecular Psychiatry. 8: 333-42. PMID 12660806 DOI: 10.1038/sj.mp.4001254  0.32
2003 Zhang P, Sheng H, Morabia A, Gilliam TC. Optimal step length EM algorithm (OSLEM) for the estimation of haplotype frequency and its application in lipoprotein lipase genotyping. Bmc Bioinformatics. 4: 3. PMID 12529185 DOI: 10.1186/1471-2105-4-3  0.96
2002 Winawer MR, Martinelli Boneschi F, Barker-Cummings C, Lee JH, Liu J, Mekios C, Gilliam TC, Pedley TA, Hauser WA, Ottman R. Four new families with autosomal dominant partial epilepsy with auditory features: clinical description and linkage to chromosome 10q24. Epilepsia. 43: 60-7. PMID 11879388 DOI: 10.1046/j.1528-1157.2002.45001.x  0.96
2002 Martinez-Mir A, Liu J, Gordon D, Weiner MS, Ahmad W, Fine JD, Ott J, Gilliam TC, Christiano AM. EB simplex superficialis resulting from a mutation in the type VII collagen gene. The Journal of Investigative Dermatology. 118: 547-9. PMID 11874498 DOI: 10.1046/j.0022-202x.2001.01702.x  0.96
2002 Kalachikov S, Evgrafov O, Ross B, Winawer M, Barker-Cummings C, Martinelli Boneschi F, Choi C, Morozov P, Das K, Teplitskaya E, Yu A, Cayanis E, Penchaszadeh G, Kottmann AH, Pedley TA, ... ... Gilliam TC, et al. Mutations in LGI1 cause autosomal-dominant partial epilepsy with auditory features. Nature Genetics. 30: 335-41. PMID 11810107 DOI: 10.1038/ng832  0.96
2002 Alarcón M, Cantor RM, Liu J, Gilliam TC, Geschwind DH. Evidence for a language quantitative trait locus on chromosome 7q in multiplex autism families. American Journal of Human Genetics. 70: 60-71. PMID 11741194 DOI: 10.1086/338241  0.96
2002 Liu J, Juo SH, Holopainen P, Terwilliger J, Tong X, Grunn A, Brito M, Green P, Mustalahti K, Mäki M, Gilliam TC, Partanen J. Genomewide linkage analysis of celiac disease in Finnish families. American Journal of Human Genetics. 70: 51-9. PMID 11715113 DOI: 10.1086/338453  0.96
2001 Liu J, Nyholt DR, Magnussen P, Parano E, Pavone P, Geschwind D, Lord C, Iversen P, Hoh J, Ott J, Gilliam TC. A genomewide screen for autism susceptibility loci. American Journal of Human Genetics. 69: 327-40. PMID 11452361 DOI: 10.1086/321980  0.96
2001 Liu J, Juo SH, Terwilliger JD, Grunn A, Tong X, Brito M, Loth JE, Kanyas K, Lerer B, Endicott J, Penchaszadeh G, Gilliam TC, Baron M. A follow-up linkage study supports evidence for a bipolar affective disorder locus on chromosome 21q22. American Journal of Medical Genetics. 105: 189-94. PMID 11304836 DOI: 10.1002/ajmg.1195  0.32
2000 Ranta S, Zhang Y, Ross B, Takkunen E, Hirvasniemi A, de la Chapelle A, Gilliam TC, Lehesjoki AE. Positional cloning and characterisation of the human DLGAP2 gene and its exclusion in progressive epilepsy with mental retardation. European Journal of Human Genetics : Ejhg. 8: 381-4. PMID 10854099 DOI: 10.1038/sj.ejhg.5200440  0.96
2000 Aita VM, Ahmad W, Panteleyev AA, Kozlowska U, Kozlowska A, Gilliam TC, Jablonska S, Christiano AM. A novel missense mutation (C622G) in the zinc-finger domain of the human hairless gene associated with congenital atrichia with papular lesions. Experimental Dermatology. 9: 157-62. PMID 10772391 DOI: 10.1034/j.1600-0625.2000.009002157.x  0.96
1999 Aita VM, Christiano AM, Gilliam TC. Mapping complex traits in diseases of the hair and skin. Experimental Dermatology. 8: 439-52. PMID 10597133 DOI: 10.1111/J.1600-0625.1999.TB00302.X  0.96
1999 Ranta S, Zhang Y, Ross B, Lonka L, Takkunen E, Messer A, Sharp J, Wheeler R, Kusumi K, Mole S, Liu W, Soares MB, Bonaldo MDF, Hirvasniemi A, De La Chapelle A, ... Gilliam TC, et al. The neuronal ceroid lipofuscinoses in human EPMR and mnd mutant mice are associated with mutations in CLN8 Nature Genetics. 23: 233-236. PMID 10508524 DOI: 10.1038/13868  0.96
1999 Larin D, Mekios C, Das K, Ross B, Yang AS, Gilliam TC. Characterization of the interaction between the Wilson and Menkes disease proteins and the cytoplasmic copper chaperone, HAH1p Journal of Biological Chemistry. 274: 28497-28504. PMID 10497213 DOI: 10.1074/Jbc.274.40.28497  0.96
1999 Buiakova OI, Xu J, Lutsenko S, Zeitlin S, Das K, Das S, Ross BM, Mekios C, Scheinberg IH, Gilliam TC. Null mutation of the murine ATP7B (Wilson disease) gene results in intracellular copper accumulation and late-onset hepatic nodular transformation. Human Molecular Genetics. 8: 1665-71. PMID 10441329 DOI: 10.1093/hmg/8.9.1665  0.96
1999 Lewis CA, Batlle IR, Batlle KG, Banerjee P, Cideciyan AV, Huang J, Alemán TS, Huang Y, Ott J, Gilliam TC, Knowles JA, Jacobson SG. Tubby-like protein 1 homozygous splice-site mutation causes early-onset severe retinal degeneration. Investigative Ophthalmology & Visual Science. 40: 2106-14. PMID 10440267  0.96
1999 Aita VM, Liang XH, Murty VV, Pincus DL, Yu W, Cayanis E, Kalachikov S, Gilliam TC, Levine B. Cloning and genomic organization of beclin 1, a candidate tumor suppressor gene on chromosome 17q21. Genomics. 59: 59-65. PMID 10395800 DOI: 10.1006/geno.1999.5851  0.96
1998 Gavrilov DK, Shi X, Das K, Gilliam TC, Wang CH. Differential SMN2 expression associated with SMA severity. Nature Genetics. 20: 230-1. PMID 9806538 DOI: 10.1038/3030  0.96
1998 Frucht S, Sun D, Schiff N, Eidelberg D, Gilliam TC. Arm tremor secondary to Wilson's disease Movement Disorders. 13: 351-353. PMID 9539354 DOI: 10.1002/mds.870130227  0.96
1998 Knowles JA, Rao PA, Cox-Matise T, Loth JE, de Jesus GM, Levine L, Das K, Penchaszadeh GK, Alexander JR, Lerer B, Endicott J, Ott J, Gilliam TC, Baron M. No evidence for significant linkage between bipolar affective disorder and chromosome 18 pericentromeric markers in a large series of multiplex extended pedigrees. American Journal of Human Genetics. 62: 916-24. PMID 9529343 DOI: 10.1086/301785  0.96
1998 Banerjee P, Lewis CA, Kleyn PW, Shugart YY, Ross BM, Penchaszadeh GK, Ott J, Jacobson SG, Gilliam TC, Knowles JA. Homozygosity and physical mapping of the autosomal recessive retinitis pigmentosa locus (RP14) on chromosome 6p21.3. Genomics. 48: 171-7. PMID 9521870 DOI: 10.1006/Geno.1997.5174  0.96
1997 Lutsenko S, Petrukhin K, Gilliam TC, Kaplan JH. Heterologous expression of the metal-binding domains of human copper-transporting ATPases (P1-ATPases). Annals of the New York Academy of Sciences. 834: 155-7. PMID 9405803 DOI: 10.1111/j.1749-6632.1997.tb52246.x  0.96
1997 Ranta S, Lehesjoki AE, de Fatima Bonaldo M, Knowles JA, Hirvasniemi A, Ross B, de Jong PJ, Soares MB, de la Chapelle A, Gilliam TC. High-resolution mapping and transcript identification at the progressive epilepsy with mental retardation locus on chromosome 8p. Genome Research. 7: 887-96. PMID 9314494 DOI: 10.1101/gr.7.9.887  0.96
1997 Shah AB, Chernov I, Zhang HT, Ross BM, Das K, Lutsenko S, Parano E, Pavone L, Evgrafov O, Ivanova-Smolenskaya IA, Annerén G, Westermark K, Urrutia FH, Penchaszadeh GK, Sternlieb I, ... ... Gilliam TC, et al. Identification and analysis of mutations in the Wilson disease gene (ATP7B): population frequencies, genotype-phenotype correlation, and functional analyses. American Journal of Human Genetics. 61: 317-28. PMID 9311736 DOI: 10.1086/514864  0.96
1997 Wang CH, Carter TA, Das K, Xu J, Ross BM, Penchaszadeh GK, Gilliam TC. Extensive DNA deletion associated with severe disease alleles on spinal muscular atrophy homologues. Annals of Neurology. 42: 41-9. PMID 9225684 DOI: 10.1002/ana.410420109  0.96
1997 Carter TA, Bönnemann CG, Wang CH, Obici S, Parano E, De Fatima Bonaldo M, Ross BM, Penchaszadeh GK, Mackenzie A, Soares MB, Kunkel LM, Gilliam TC. A multicopy transcription-repair gene, BTF2p44, maps to the SMA region and demonstrates SMA associated deletions. Human Molecular Genetics. 6: 229-36. PMID 9063743 DOI: 10.1093/hmg/6.2.229  0.96
1996 Ferenci P, Gilliam TC, Gitlin JD, Packman S, Schilsky ML, Sokol RJ, Sternlieb I. An international symposium on Wilson's and Menkes' diseases. Hepatology (Baltimore, Md.). 24: 952-8. PMID 8855204 DOI: 10.1002/hep.510240433  0.96
1996 Wang CH, Xu J, Carter TA, Ross BM, Dominski MK, Bellcross CA, Penchaszadeh GK, Munsat TL, Gilliam TC. Characterization of survival motor neuron (SMNT) gene deletions in asymptomatic carriers of spinal muscular atrophy. Human Molecular Genetics. 5: 359-65. PMID 8852661 DOI: 10.1093/hmg/5.3.359  0.96
1996 Ranta S, Lehesjoki AE, Hirvasniemi A, Weissenbach J, Ross B, Leal SM, de la Chapelle A, Gilliam TC. Genetic and physical mapping of the progressive epilepsy with mental retardation (EPMR) locus on chromosome 8p. Genome Research. 6: 351-60. PMID 8743986  0.96
1996 Wilhelmsen KC, Blake DM, Lynch T, Mabutas J, De Vera M, Neystat M, Bernstein M, Hirano M, Gilliam TC, Murphy PL, Sola MD, Bonilla E, Schotland DL, Hays AP, Rowland LP. Chromosome 12-linked autosomal dominant scapuloperoneal muscular dystrophy. Annals of Neurology. 39: 507-20. PMID 8619529 DOI: 10.1002/Ana.410390413  0.96
1995 Brzustowicz LM, Wang CH, Matseoane D, Kleyn PW, Vitale E, Das K, Penchaszadeh GK, Munsat TL, Hausmanowa-Petrusewicz I, Gilliam TC. Linkage disequilibrium and haplotype analysis among Polish families with Spinal Muscular Atrophy American Journal of Human Genetics. 56: 210-215. PMID 7825580  0.96
1995 Huang TH, Yeh PL, Martin MB, Straub RE, Gilliam TC, Caldwell CW, Skibba JL. Genetic alterations of microsatellites on chromosome 18 in human breast carcinoma. Diagnostic Molecular Pathology : the American Journal of Surgical Pathology, Part B. 4: 66-72. PMID 7735559  0.96
1995 Selig S, Bruno S, Scharf JM, Wang CH, Vitale E, Gilliam TC, Kunkel LM. Expressed cadherin pseudogenes are localized to the critical region of the spinal muscular atrophy gene. Proceedings of the National Academy of Sciences of the United States of America. 92: 3702-6. PMID 7731968 DOI: 10.1073/Pnas.92.9.3702  0.96
1995 Boylan KB, Cornblath DR, Glass JD, Alderson K, Kuncl RW, Kleyn PW, Gilliam TC. Autosomal dominant distal spinal muscular atrophy in four generations. Neurology. 45: 699-704. PMID 7723957 DOI: 10.1212/WNL.45.4.699  0.96
1995 Shugart YY, Banerjee P, Knowles JA, Lewis CA, Jacobson SG, Matise TC, Penchaszadeh G, Gilliam TC, Ott J. Fine genetic mapping of a gene for autosomal recessive retinitis pigmentosa on chromosome 6p21. American Journal of Human Genetics. 57: 499-502. PMID 7668276  0.96
1995 Gilliam TC. Is the spinal muscular atrophy gene found? Nature Medicine. 1: 124-7. PMID 7585007 DOI: 10.1038/nm0295-124  0.96
1994 Mérette C, Brzustowicz LM, Daniels RJ, Davies KE, Gilliam TC, Melki J, Munnich A, Pericak-Vance MA, Siddique T, Voosen B. An investigation of genetic heterogeneity and linkage disequilibrium in 161 families with spinal muscular atrophy. Genomics. 21: 27-33. PMID 8088801 DOI: 10.1006/Geno.1994.1220  0.96
1994 Baron M, Straub RE, Lehner T, Endicott J, Ott J, Gilliam TC, Lerer B. Bipolar disorder and linkage to Xq28. Nature Genetics. 7: 461-2. PMID 7951314 DOI: 10.1038/ng0894-461a  0.96
1994 Petrukhin K, Gilliam TC. Genetic disorders of copper metabolism. Current Opinion in Pediatrics. 6: 698-701. PMID 7849817  0.96
1994 Petrukhin K, Lutsenko S, Chernov I, Ross BM, Kaplan JH, Gilliam TC. Characterization of the Wilson disease gene encoding a P-type copper transporting ATPase: genomic organization, alternative splicing, and structure/function predictions. Human Molecular Genetics. 3: 1647-56. PMID 7833924 DOI: 10.1093/hmg/3.9.1647  0.96
1993 Soares VM, Brzustowicz LM, Kleyn PW, Knowles JA, Palmer DA, Asokan S, Penchaszadeh GK, Munsat TL, Gilliam TC. Refinement of the spinal muscular atrophy locus to the interval between D5S435 and MAP1B. Genomics. 15: 365-71. PMID 8449502 DOI: 10.1006/geno.1993.1069  0.96
1993 Petrukhin KE, Speer MC, Cayanis E, Bonaldo MdF, Tantravahi U, Soares MB, Fischer SG, Warburton D, Gilliam TC, Ott J. A Microsatellite Genetic Linkage Map of Human Chromosome 13 Genomics. 15: 76-85. PMID 8432553 DOI: 10.1006/geno.1993.1012  0.96
1993 Thompson TG, Morrison KE, Kleyn P, Bengtsson U, Gilliam TC, Davies KE, Wasmuth JJ, McPherson JD. High resolution physical map of the region surrounding the spinal muscular atrophy gene. Human Molecular Genetics. 2: 1169-76. PMID 8401498 DOI: 10.1093/hmg/2.8.1169  0.96
1993 Nygaard TG, Wilhelmsen KC, Risch NJ, Brown DL, Trugman JM, Gilliam TC, Fahn S, Weeks DE. Linkage mapping of dopa-responsive dystonia (DRD) to chromosome 14q. Nature Genetics. 5: 386-91. PMID 8298648 DOI: 10.1038/ng1293-386  0.96
1993 Kleyn PW, Gilliam TC. Progress toward cloning of the gene responsible for childhood spinal muscular atrophy. Seminars in Neurology. 13: 276-82. PMID 8272599 DOI: 10.1055/s-2008-1041135  0.96
1993 Brzustowicz LM, Mérette C, Xie X, Townsend L, Gilliam TC, Ott J. Molecular and statistical approaches to the detection and correction of errors in genotype databases. American Journal of Human Genetics. 53: 1137-45. PMID 8213837  0.96
1993 Le Beau MM, Overhauser J, Straub RE, Silverman G, Gilliam TC, Ott J, O'Connell P, Francke U, Geurts van Kessel A. Report of the first international workshop on human chromosome 18 mapping. Cytogenetics and Cell Genetics. 63: 78-96. PMID 8096808  0.96
1993 Locke PA, MacDonald ME, Srinidhi J, Gilliam TC, Tanzi RE, Conneally PM, Wexler NS, Haines JL, Gusella JF. A genetic linkage map of the chromosome 4 short arm. Somatic Cell and Molecular Genetics. 19: 95-101. PMID 8096345 DOI: 10.1007/Bf01233958  0.96
1993 Straub RE, Speer MC, Luo Y, Rojas K, Overhauser J, Ott J, Gilliam TC. A microsatellite genetic linkage map of human chromosome 18. Genomics. 15: 48-56. PMID 8094374 DOI: 10.1006/geno.1993.1008  0.96
1993 Brzustowicz LM, Merette C, Kleyn PW, Lehner T, Castilla LH, Penchaszadeh GK, Das K, Munsat TL, Ott J, Gilliam TC. Assessment of nonallelic genetic heterogeneity of chronic (Type II and III) spinal muscular atrophy Human Heredity. 43: 380-387. PMID 7904586 DOI: 10.1159/000154164  0.96
1992 Knowles JA, Vieland VJ, Gilliam TC. Perils of gene mapping with microsatellite markers. American Journal of Human Genetics. 51: 905-9. PMID 1415237  0.96
1992 Ben Othmane K, Ben Hamida M, Pericak-Vance MA, Ben Hamida C, Blel S, Carter SC, Bowcock AM, Petruhkin K, Gilliam TC, Roses AD. Linkage of Tunisian autosomal recessive Duchenne-like muscular dystrophy to the pericentromeric region of chromosome 13q. Nature Genetics. 2: 315-7. PMID 1303286 DOI: 10.1038/Ng1292-315  0.96
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