| Year |
Citation |
Score |
| 2020 |
Seabra CM, Aneichyk T, Erdin S, Tai DJC, De Esch CEF, Razaz P, An Y, Manavalan P, Ragavendran A, Stortchevoi A, Abad C, Young JI, Maciel P, Talkowski ME, Gusella JF. Transcriptional consequences of MBD5 disruption in mouse brain and CRISPR-derived neurons. Molecular Autism. 11: 45. PMID 32503625 DOI: 10.1186/S13229-020-00354-1 |
0.567 |
|
| 2018 |
Long JD, Lee JM, Aylward EH, Gillis T, Mysore JS, Abu Elneel K, Chao MJ, Paulsen JS, MacDonald ME, Gusella JF. Genetic Modification of Huntington Disease Acts Early in the Prediagnosis Phase. American Journal of Human Genetics. PMID 30122542 DOI: 10.1016/J.Ajhg.2018.07.017 |
0.303 |
|
| 2017 |
Lee JM, Chao MJ, Harold D, Abu Elneel K, Gillis T, Holmans P, Jones L, Orth M, Myers RH, Kwak S, Wheeler VC, MacDonald ME, Gusella JF. A modifier of Huntington's disease onset at the MLH1 locus. Human Molecular Genetics. 26: 3859-3867. PMID 28934397 DOI: 10.1093/Hmg/Ddx286 |
0.321 |
|
| 2017 |
Seabra CM, Szoko N, Erdin S, Ragavendran A, Stortchevoi A, Maciel P, Lundberg K, Schlatzer D, Smith J, Talkowski ME, Gusella JF, Natowicz MR. A novel microduplication of ARID1B: Clinical, genetic, and proteomic findings. American Journal of Medical Genetics. Part A. PMID 28691782 DOI: 10.1002/Ajmg.A.38327 |
0.594 |
|
| 2016 |
Maussion G, Cruceanu C, Rosenfeld JA, Bell SC, Jollant F, Szatkiewicz J, Collins RL, Hanscom C, Kolobova I, de Champfleur NM, Blumenthal I, Chiang C, Ota V, Hultman C, O'Dushlaine C, ... ... Gusella JF, et al. Implication of LRRC4C and DPP6 in neurodevelopmental disorders. American Journal of Medical Genetics. Part A. PMID 27759917 DOI: 10.1002/Ajmg.A.38021 |
0.431 |
|
| 2016 |
Rodan LH, Cohen J, Fatemi A, Gillis T, Lucente D, Gusella J, Picker JD. A novel neurodevelopmental disorder associated with compound heterozygous variants in the huntingtin gene. European Journal of Human Genetics : Ejhg. PMID 27329733 DOI: 10.1038/Ejhg.2016.74 |
0.357 |
|
| 2015 |
Ramos EM, Gillis T, Mysore JS, Lee JM, Gögele M, D'Elia Y, Pichler I, Sequeiros J, Pramstaller PP, Gusella JF, MacDonald ME, Alonso I. Haplotype analysis of the 4p16.3 region in Portuguese families with Huntington's disease. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 168: 135-43. PMID 25656686 DOI: 10.1002/Ajmg.B.32289 |
0.307 |
|
| 2015 |
Quintero-Rivera F, Xi QJ, Keppler-Noreuil KM, Lee JH, Higgins AW, Anchan RM, Roberts AE, Seong IS, Fan X, Lage K, Lu LY, Tao J, Hu X, Berezney R, Gelb BD, ... ... Gusella JF, et al. MATR3 disruption in human and mouse associated with bicuspid aortic valve, aortic coarctation and patent ductus arteriosus. Human Molecular Genetics. 24: 2375-89. PMID 25574029 DOI: 10.1093/Hmg/Ddv004 |
0.47 |
|
| 2015 |
Lee JM, Wheeler VC, Chao MJ, Vonsattel JPG, Pinto RM, Lucente D, Abu-Elneel K, Ramos EM, Mysore JS, Gillis T, MacDonald ME, Gusella JF, Harold D, Stone TC, Escott-Price V, et al. Identification of Genetic Factors that Modify Clinical Onset of Huntington's Disease Cell. 162: 516-526. DOI: 10.1016/J.Cell.2015.07.003 |
0.305 |
|
| 2014 |
Jones L, Gusella J, MacDonald M, Wheeler V, Lee J, Myers R, Latourelle J, Harold D, Holmans P, Orth M, Kwak S. A03 Genetic Modifiers Affecting The Age At Motor Onset In Huntington’s Disease Journal of Neurology, Neurosurgery, and Psychiatry. 85. DOI: 10.1136/Jnnp-2014-309032.3 |
0.338 |
|
| 2012 |
Talkowski ME, Maussion G, Crapper L, Rosenfeld JA, Blumenthal I, Hanscom C, Chiang C, Lindgren A, Pereira S, Ruderfer D, Diallo AB, Lopez JP, Turecki G, Chen ES, Gigek C, ... ... Gusella JF, et al. Disruption of a large intergenic noncoding RNA in subjects with neurodevelopmental disabilities. American Journal of Human Genetics. 91: 1128-34. PMID 23217328 DOI: 10.1016/J.Ajhg.2012.10.016 |
0.414 |
|
| 2012 |
Hooli BV, Mohapatra G, Mattheisen M, Parrado AR, Roehr JT, Shen Y, Gusella JF, Moir R, Saunders AJ, Lange C, Tanzi RE, Bertram L. Role of common and rare APP DNA sequence variants in Alzheimer disease. Neurology. 78: 1250-7. PMID 22491860 DOI: 10.1212/Wnl.0B013E3182515972 |
0.463 |
|
| 2012 |
Mattis V, Svendsen S, Ebert A, Svendsen C, King A, Casale M, Winokur S, Batugedara G, Vawter M, Donovan P, Lock L, Thompson L, Zhu Y, Fossale E, Atwal R, ... ... Gusella J, et al. A11 Induced pluripotent stem cells for basic and translational research on HD Journal of Neurology, Neurosurgery & Psychiatry. 83: A3.2-A4. DOI: 10.1136/Jnnp-2012-303524.11 |
0.341 |
|
| 2011 |
Myre MA, Lumsden AL, Thompson MN, Wasco W, MacDonald ME, Gusella JF. Deficiency of huntingtin has pleiotropic effects in the social amoeba Dictyostelium discoideum. Plos Genetics. 7: e1002052. PMID 21552328 DOI: 10.1371/Journal.Pgen.1002052 |
0.611 |
|
| 2011 |
Engler D, Shen Y, Gusella J, Betensky RA. Comparison of clinical subgroup aCGH profiles through pseudolikelihood ratio tests Statistical Applications in Genetics and Molecular Biology. 10. DOI: 10.2202/1544-6115.1407 |
0.302 |
|
| 2010 |
Ramos EM, Gillis T, Mysore J, Abuelneel K, Gusella J, MacDonald M, Lee J, Alonso I, Sequeiros J. C03 Modifiers of instability and age at onset in HD: haplotype study in the Portuguese population Journal of Neurology, Neurosurgery & Psychiatry. 81: A16.3-A17. DOI: 10.1136/Jnnp.2010.222588.3 |
0.431 |
|
| 2010 |
MacDonald M, Lee JM, Seong IS, Fossale E, Anderson M, Wheeler V, Gusella J. Poster 16: Genetic Approach to Huntington's Disease Therapeutics Neurotherapeutics. 7: 143-143. DOI: 10.1016/J.Nurt.2009.09.018 |
0.371 |
|
| 2009 |
Weiss LA, Arking DE, Daly MJ, Chakravarti A, Brune CW, West K, O'Connor A, Hilton G, Tomlinson RL, West AB, Cook EH, Green T, Chang SC, Gabriel S, Gates C, ... ... Gusella J, et al. A genome-wide linkage and association scan reveals novel loci for autism Nature. 461: 802-808. PMID 19812673 DOI: 10.1038/Nature08490 |
0.54 |
|
| 2008 |
Higgins AW, Alkuraya FS, Bosco AF, Brown KK, Bruns GA, Donovan DJ, Eisenman R, Fan Y, Farra CG, Ferguson HL, Gusella JF, Harris DJ, Herrick SR, Kelly C, Kim HG, et al. Characterization of apparently balanced chromosomal rearrangements from the developmental genome anatomy project. American Journal of Human Genetics. 82: 712-22. PMID 18319076 DOI: 10.1016/J.Ajhg.2008.01.011 |
0.3 |
|
| 2008 |
Weiss LA, Shen Y, Korn JM, Arking DE, Miller DT, Fossdal R, Saemundsen E, Stefansson H, Ferreira MA, Green T, Platt OS, Ruderfer DM, Walsh CA, Altshuler D, Chakravarti A, ... ... Gusella JF, et al. Association between microdeletion and microduplication at 16p11.2 and autism. The New England Journal of Medicine. 358: 667-75. PMID 18184952 DOI: 10.1056/Nejmoa075974 |
0.44 |
|
| 2007 |
Lu W, van Eerde AM, Fan X, Quintero-Rivera F, Kulkarni S, Ferguson H, Kim HG, Fan Y, Xi Q, Li QG, Sanlaville D, Andrews W, Sundaresan V, Bi W, Yan J, ... ... Gusella JF, et al. Disruption of ROBO2 is associated with urinary tract anomalies and confers risk of vesicoureteral reflux. American Journal of Human Genetics. 80: 616-32. PMID 17357069 DOI: 10.1086/512735 |
0.453 |
|
| 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 |
0.43 |
|
| 2006 |
Pichler I, Marroni F, Volpato CB, Gusella JF, Klein C, Casari G, De Grandi A, Pramstaller PP. Linkage analysis identifies a novel locus for restless legs syndrome on chromosome 2q in a South Tyrolean population isolate. American Journal of Human Genetics. 79: 716-23. PMID 16960808 DOI: 10.1086/507875 |
0.306 |
|
| 2005 |
Nunes F, Shen Y, Niida Y, Beauchamp R, Stemmer-Rachamimov AO, Ramesh V, Gusella J, MacCollin M. Inactivation patterns of NF2 and DAL-1/4.1B (EPB41L3) in sporadic meningioma. Cancer Genetics and Cytogenetics. 162: 135-9. PMID 16213361 DOI: 10.1016/J.Cancergencyto.2005.04.003 |
0.315 |
|
| 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, ... ... Gusella J, 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 |
0.525 |
|
| 2003 |
Scherer SW, Cheung J, MacDonald JR, Osborne LR, Nakabayashi K, Herbrick JA, Carson AR, Parker-Katiraee L, Skaug J, Khaja R, Zhang J, Hudek AK, Li M, Haddad M, Duggan GE, ... ... Gusella JF, et al. Human chromosome 7: DNA sequence and biology. Science (New York, N.Y.). 300: 767-72. PMID 12690205 DOI: 10.1126/Science.1083423 |
0.314 |
|
| 2002 |
Gusella J, MacDonald M. No post-genetics era in human disease research. Nature Reviews. Genetics. 3: 72-9. PMID 11823793 DOI: 10.1038/Nrg706 |
0.333 |
|
| 1999 |
Castells A, Ino Y, Louis DN, Ramesh V, Gusella JF, Rustgi AK. Mapping of a target region of allelic loss to a 0.5-cM interval on chromosome 22q13 in human colorectal cancer. Gastroenterology. 117: 831-7. PMID 10500065 DOI: 10.1016/S0016-5085(99)70341-0 |
0.316 |
|
| 1999 |
Slaugenhaupt SA, Acierno JS, Helbling LA, Bove C, Goldin E, Bach G, Schiffmann R, Gusella JF. Mapping of the mucolipidosis type IV gene to chromosome 19p and definition of founder haplotypes. American Journal of Human Genetics. 65: 773-8. PMID 10441585 DOI: 10.1086/302549 |
0.348 |
|
| 1999 |
Blumenfeld A, Slaugenhaupt SA, Liebert CB, Temper V, Maayan C, Gill S, Lucente DE, Idelson M, MacCormack K, Monahan MA, Mull J, Leyne M, Mendillo M, Schiripo T, Mishori E, ... ... Gusella JF, et al. Precise genetic mapping and haplotype analysis of the familial dysautonomia gene on human chromosome 9q31. American Journal of Human Genetics. 64: 1110-8. PMID 10090896 DOI: 10.1086/302339 |
0.335 |
|
| 1998 |
Chishti AH, Kim AC, Marfatia SM, Lutchman M, Hanspal M, Jindal H, Liu SC, Low PS, Rouleau GA, Mohandas N, Chasis JA, Conboy JG, Gascard P, Takakuwa Y, Huang SC, ... ... Gusella JF, et al. The FERM domain: a unique module involved in the linkage of cytoplasmic proteins to the membrane. Trends in Biochemical Sciences. 23: 281-2. PMID 9757824 DOI: 10.1016/S0968-0004(98)01237-7 |
0.303 |
|
| 1997 |
Jacoby LB, Jones D, Davis K, Kronn D, Short MP, Gusella J, MacCollin M. Molecular analysis of the NF2 tumor-suppressor gene in schwannomatosis. American Journal of Human Genetics. 61: 1293-302. PMID 9399891 DOI: 10.1086/301633 |
0.319 |
|
| 1997 |
Ozelius LJ, Hewett J, Kramer P, Bressman SB, Shalish C, de Leon D, Rutter M, Risch N, Brin MF, Markova ED, Limborska SA, Ivanova-Smolenskaya IA, McCormick MK, Fahn S, Buckler AJ, ... Gusella JF, et al. Fine localization of the torsion dystonia gene (DYT1) on human chromosome 9q34: YAC map and linkage disequilibrium. Genome Research. 7: 483-94. PMID 9149944 DOI: 10.1101/Gr.7.5.483 |
0.34 |
|
| 1995 |
Yong WH, Ueki K, Chou D, Reeves SA, von Deimling A, Gusella JF, Mohrenweiser HW, Buckler AJ, Louis DN. Cloning of a highly conserved human protein serine-threonine phosphatase gene from the glioma candidate region on chromosome 19q13.3. Genomics. 29: 533-6. PMID 8666404 DOI: 10.1006/Geno.1995.9972 |
0.328 |
|
| 1995 |
Trofatter JA, Long KR, Murrell JR, Stotler CJ, Gusella JF, Buckler AJ. An expression-independent catalog of genes from human chromosome 22. Genome Research. 5: 214-24. PMID 8593609 DOI: 10.1101/GR.5.3.214 |
0.305 |
|
| 1995 |
Oddoux C, Reich E, Axelrod F, Blumenfeld A, Maayan C, Slaugenhaupt S, Gusella J, Ostrer H. Prenatal diagnostic testing for familial dysautonomia using linked genetic markers Prenatal Diagnosis. 15: 817-826. PMID 8559751 DOI: 10.1002/Pd.1970150905 |
0.386 |
|
| 1995 |
Kozman HM, Keith TP, Donis-Keller H, White RL, Weissenbach J, Dean M, Vergnaud G, Kidd K, Gusella J, Royle NJ. The CEPH consortium linkage map of human chromosome 16. Genomics. 25: 44-58. PMID 7774955 DOI: 10.1016/0888-7543(95)80108-X |
0.376 |
|
| 1995 |
Locke PA, Conneally PM, Tanzi RE, Gusella JF, Haines JL. Apolipoprotein E4 allele and Alzheimer disease: examination of allelic association and effect on age at onset in both early- and late-onset cases. Genetic Epidemiology. 12: 83-92. PMID 7713402 DOI: 10.1002/Gepi.1370120108 |
0.391 |
|
| 1995 |
Duyao MP, Auerbach AB, Ryan A, Persichetti F, Barnes GT, McNeil SM, Ge P, Vonsattel JP, Gusella JF, Joyner AL. Inactivation of the mouse Huntington's disease gene homolog Hdh. Science (New York, N.Y.). 269: 407-10. PMID 7618107 DOI: 10.1126/Science.7618107 |
0.351 |
|
| 1995 |
Slaugenhaupt SA, Roca AL, Liebert CB, Altherr MR, Gusella JF, Reppert SM. Mapping of the gene for the Mel1a-melatonin receptor to human chromosome 4 (MTNR1A) and mouse chromosome 8 (Mtnr1a). Genomics. 27: 355-7. PMID 7558006 DOI: 10.1006/Geno.1995.1056 |
0.308 |
|
| 1995 |
Blumenfeld A, Lucente DE, Trofatter JA, Lerner T, Slaugenhaupt SA, Liebert CB, Monahan M, Haines JL, Gusella JF, Breakefield XO, Parysek LM. Peripherin gene is linked to keratin 18 gene on human chromosome 12. Somatic Cell and Molecular Genetics. 21: 83-8. PMID 7541564 DOI: 10.1007/BF02255825 |
0.3 |
|
| 1994 |
Lerner TJ, Boustany RM, MacCormack K, Gleitsman J, Schlumpf K, Breakefield XO, Gusella JF, Haines JL. Linkage disequilibrium between the juvenile neuronal ceroid lipofuscinosis gene and marker loci on chromosome 16p 12.1. American Journal of Human Genetics. 54: 88-94. PMID 8279474 |
0.319 |
|
| 1994 |
Attwood J, Chiano M, Collins A, Donis-Keller H, Dracopoli N, Fountain J, Falk C, Goudie D, Gusella J, Haines J, Armour JAL, Jeffreys AJ, Kwiatkowski D, Lathrop M, Matise T, et al. CEPH Consortium Map of Chromosome 9 Genomics. 19: 203-214. PMID 8188250 DOI: 10.1006/Geno.1994.1049 |
0.351 |
|
| 1994 |
Hummerich H, Baxendale S, Mott R, Kirby SF, MacDonald ME, Gusella J, Lehrach H, Bates GP. Distribution of trinucleotide repeat sequences across a 2 Mbp region containing the Huntington's disease gene. Human Molecular Genetics. 3: 73-8. PMID 8162055 DOI: 10.1093/Hmg/3.1.73 |
0.366 |
|
| 1994 |
Bush AI, Pettingell WH, Multhaup G, d Paradis M, Vonsattel JP, Gusella JF, Beyreuther K, Masters CL, Tanzi RE. Rapid induction of Alzheimer A beta amyloid formation by zinc. Science (New York, N.Y.). 265: 1464-7. PMID 8073293 DOI: 10.1126/Science.8073293 |
0.504 |
|
| 1994 |
Rubio MP, Correa KM, Ueki K, Mohrenweiser HW, Gusella JF, von Deimling A, Louis DN. The putative glioma tumor suppressor gene on chromosome 19q maps between APOC2 and HRC. Cancer Research. 54: 4760-3. PMID 8062276 |
0.302 |
|
| 1994 |
MacCollin M, Peterfreund R, MacDonald M, Fink JS, Gusella J. Mapping of a human A2a adenosine receptor (ADORA2) to chromosome 22. Genomics. 20: 332-3. PMID 8020991 DOI: 10.1006/Geno.1994.1181 |
0.399 |
|
| 1994 |
Ali G, Wasco W, Cai X, Szabo P, Sheu KF, Cooper AJ, Gaston SM, Gusella JF, Tanzi RE, Blass JP. Isolation, characterization, and mapping of gene encoding dihydrolipoyl succinyltransferase (E2k) of human alpha-ketoglutarate dehydrogenase complex. Somatic Cell and Molecular Genetics. 20: 99-105. PMID 8009371 DOI: 10.1007/Bf02290679 |
0.717 |
|
| 1994 |
Barnes GT, Duyao MP, Ambrose CM, McNeil S, Persichetti F, Srinidhi J, Gusella JF, MacDonald ME. Mouse Huntington's disease gene homolog (Hdh). Somatic Cell and Molecular Genetics. 20: 87-97. PMID 8009370 DOI: 10.1007/Bf02290678 |
0.315 |
|
| 1994 |
Hubert R, Macdonald M, Gusella J, Arnheim N. High resolution localization of recombination hot spots using sperm typing Nature Genetics. 7: 420-424. PMID 7920662 DOI: 10.1038/Ng0794-420 |
0.373 |
|
| 1994 |
Grosson CL, MacDonald ME, Duyao MP, Ambrose CM, Roffler-Tarlov S, Gusella JF. Synteny conservation of the Huntington's disease gene and surrounding loci on mouse Chromosome 5. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 5: 424-8. PMID 7919654 DOI: 10.1007/Bf00357002 |
0.314 |
|
| 1994 |
Gasser T, Wszolek ZK, Trofatter J, Ozelius L, Uitti RJ, Lee CS, Gusella J, Pfeiffer RF, Calne DB, Breakefield XO. Genetic linkage studies in autosomal dominant parkinsonism: evaluation of seven candidate genes. Annals of Neurology. 36: 387-96. PMID 7915897 DOI: 10.1002/Ana.410360310 |
0.365 |
|
| 1994 |
Rosen DR, Sapp P, O'Regan J, McKenna-Yasek D, Schlumpf KS, Haines JL, Gusella JF, Horvitz HR, Brown RH. Genetic linkage analysis of familial amyotrophic lateral sclerosis using human chromosome 21 microsatellite DNA markers. American Journal of Medical Genetics. 51: 61-9. PMID 7913294 DOI: 10.1002/Ajmg.1320510114 |
0.301 |
|
| 1994 |
Kieburtz K, MacDonald M, Shih C, Feigin A, Steinberg K, Bordwell K, Zimmerman C, Srinidhi J, Sotack J, Gusella J. Trinucleotide repeat length and progression of illness in Huntington's disease. Journal of Medical Genetics. 31: 872-4. PMID 7853373 DOI: 10.1136/Jmg.31.11.872 |
0.39 |
|
| 1994 |
Menon AG, Gusella JF, Seizinger BR. Progress toward the isolation and characterization of the genes causing neurofibromatosis. Brain Pathology (Zurich, Switzerland). 1: 33-40. PMID 1669691 DOI: 10.1111/J.1750-3639.1990.Tb00636.X |
0.323 |
|
| 1993 |
MacCollin M, Romano D, Budarf M, Denny C, Trofatter J, Menon A, Rouleau G, Fontaine B, Emanuel B, Gusella J. A set of STS assays targeting the chromosome 22 physical framework markers. Genomics. 15: 680-3. PMID 8468063 DOI: 10.1006/Geno.1993.1125 |
0.513 |
|
| 1993 |
Yan W, Boustany RM, Konradi C, Ozelius L, Lerner T, Trofatter JA, Julier C, Breakefield XO, Gusella JF, Haines JL. Localization of juvenile, but not late-infantile, neuronal ceroid lipofuscinosis on chromosome 16. American Journal of Human Genetics. 52: 89-95. PMID 8434611 |
0.339 |
|
| 1993 |
Pericak-Vance MA, St George-Hyslop PH, Gaskell PC, Growdon J, Crain BJ, Hulette C, Gusella JF, Yamaoka L, Tanzi RE, Roses AD. Linkage analysis in familial Alzheimer disease: description of the Duke and Boston data sets. Genetic Epidemiology. 10: 361-4. PMID 8314027 DOI: 10.1002/Gepi.1370100605 |
0.451 |
|
| 1993 |
Rogaev EI, Lukiw WJ, Vaula G, Haines JL, Rogaeva EA, Tsuda T, Alexandrova N, Liang Y, Mortilla M, Amaducci L, Bergamini L, Bruni AC, Foncin JF, Macciardi F, Montesi M, ... ... Gusella JF, et al. Analysis of the c-FOS gene on chromosome 14 and the promoter of the amyloid precursor protein gene in familial Alzheimer's disease. Neurology. 43: 2275-9. PMID 8232942 DOI: 10.1212/Wnl.43.11.2275 |
0.458 |
|
| 1993 |
Watanabe M, Kondo I, Nissato S, Wakisaka A, Toda T, Ikeda J, Wasmuth JJ, Gusella JF, Kanazawa I. A linkage study with DNA markers (D4S95, D4S115, and D4S111) in Japanese Huntington disease families. The Japanese Journal of Human Genetics. 38: 193-201. PMID 8102909 DOI: 10.1007/BF01883710 |
0.352 |
|
| 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 |
0.486 |
|
| 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 |
0.468 |
|
| 1992 |
Allitto BA, McClatchey AI, Barnes G, Altherr M, Wasmuth J, Frischauf AM, MacDonald ME, Gusella J. Assay by polymerase chain reaction (PCR) of multi-allele polymorphisms in the Huntington's disease region of chromosome 4. Molecular and Cellular Probes. 6: 513-20. PMID 1480191 DOI: 10.1016/0890-8508(92)90048-3 |
0.394 |
|
| 1992 |
Ozelius LJ, Kwiatkowski DJ, Schuback DE, Breakefield XO, Wexler NS, Gusella JF, Haines JL. A genetic linkage map of human chromosome 9q. Genomics. 14: 715-20. PMID 1427899 DOI: 10.1016/S0888-7543(05)80173-9 |
0.314 |
|
| 1992 |
Tanzi RE, Romano DM, Berger R, Buraczynska MJ, Gaston SM, Kurnit DM, Patterson D, Gusella JF, Stewart GD. Sequence-tagged sites (STSs) for a set of mapped markers on chromosome 21. Genomics. 14: 498-502. PMID 1427866 DOI: 10.1016/S0888-7543(05)80251-4 |
0.52 |
|
| 1992 |
Ramesh V, Cheng SV, Kozak CA, Herron BJ, Shih VE, Taylor BA, Gusella JF. Mapping of ornithine aminotransferase gene sequences to mouse chromosomes 7, X, and 3. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 3: 17-22. PMID 1349842 DOI: 10.1007/Bf00355836 |
0.305 |
|
| 1992 |
Ozelius LJ, Kramer PL, de Leon D, Risch N, Bressman SB, Schuback DE, Brin MF, Kwiatkowski DJ, Burke RE, Gusella JF. Strong allelic association between the torsion dystonia gene (DYT1) andloci on chromosome 9q34 in Ashkenazi Jews. American Journal of Human Genetics. 50: 619-28. PMID 1347197 |
0.313 |
|
| 1992 |
Tanzi RE, Watkins PC, Stewart GD, Wexler NS, Gusella JF, Haines JL. A genetic linkage map of human chromosome 21: analysis of recombination as a function of sex and age. American Journal of Human Genetics. 50: 551-8. PMID 1347193 |
0.504 |
|
| 1992 |
Haines JL, Trofatter JA, Tanzi RE, Watkins P, Wexler NS, Conneally PM, Gusella JF. Chromosome 21 genetic linkage data set based on the Venezuelan reference pedigree. Cytogenetics and Cell Genetics. 59: 88-9. PMID 1346592 DOI: 10.1159/000133208 |
0.461 |
|
| 1992 |
Kwiatkowski DJ, Henske EP, Weimer K, Ozelius L, Gusella JF, Haines J. Construction of a GT polymorphism map of human 9q. Genomics. 12: 229-40. PMID 1339384 DOI: 10.1016/0888-7543(92)90370-8 |
0.309 |
|
| 1992 |
McCombie WR, Martin-Gallardo A, Gocayne JD, FitzGerald M, Dubnick M, Kelley JM, Castilla L, Liu LI, Wallace S, Trapp S, Tagle D, Whaley WL, Cheng S, Gusella J, Frischauf AM, et al. Expressed genes, Alu repeats and polymorphisms in cosmids sequenced from chromosome 4p16.3 Nature Genetics. 1: 348-353. PMID 1338771 DOI: 10.1038/Ng0892-348 |
0.4 |
|
| 1992 |
St George-Hyslop P, Haines J, Rogaev E, Mortilla M, Vaula G, Pericak-Vance M, Foncin JF, Montesi M, Bruni A, Sorbi S, Rainero I, Pinessi L, Pollen D, Polinsky R, Nee L, ... ... Gusella J, et al. Genetic evidence for a novel familial Alzheimer's disease locus on chromosome 14. Nature Genetics. 2: 330-4. PMID 1303289 DOI: 10.1038/Ng1292-330 |
0.588 |
|
| 1992 |
Wasco W, Bupp K, Magendantz M, Gusella JF, Tanzi RE, Solomon F. Identification of a mouse brain cDNA that encodes a protein related to the Alzheimer disease-associated amyloid beta protein precursor. Proceedings of the National Academy of Sciences of the United States of America. 89: 10758-62. PMID 1279693 DOI: 10.1073/Pnas.89.22.10758 |
0.671 |
|
| 1991 |
Fontaine B, Rouleau GA, Seizinger BR, Menon AG, Jewell AF, Martuza RL, Gusella JF. Molecular genetics of neurofibromatosis 2 and related tumors (acoustic neuroma and meningioma). Annals of the New York Academy of Sciences. 615: 338-43. PMID 2039155 DOI: 10.1111/J.1749-6632.1991.Tb37776.X |
0.412 |
|
| 1991 |
Tanzi RE, George-Hyslop PS, Gusella JF. Molecular genetics of Alzheimer disease amyloid. The Journal of Biological Chemistry. 266: 20579-82. PMID 1939107 |
0.408 |
|
| 1991 |
Brown RH, Horvitz HR, Rouleau GA, McKenna-Yasek D, Beard C, Sapp P, Haines JL, Gusella JF, Figlewicz DA. Gene linkage in familial amyotrophic lateral sclerosis: a progress report. Advances in Neurology. 56: 215-26. PMID 1853758 |
0.375 |
|
| 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 DOI: 10.1007/Bf01233171 |
0.538 |
|
| 1991 |
MacDonald ME, Scott HS, Whaley WL, Pohl T, Wasmuth JJ, Lehrach H, Morris CP, Frischauf AM, Hopwood JJ, Gusella JF. Huntington disease-linked locus D4S111 exposed as the alpha-L-iduronidase gene. Somatic Cell and Molecular Genetics. 17: 421-5. PMID 1832239 DOI: 10.1007/Bf01233067 |
0.33 |
|
| 1991 |
Fontaine B, Trofatter J, Rouleau GA, Khurana TS, Haines J, Brown R, Gusella JF. Different gene loci for hyperkalemic and hypokalemic periodic paralysis. Neuromuscular Disorders : Nmd. 1: 235-8. PMID 1822800 DOI: 10.1016/0960-8966(91)90095-A |
0.384 |
|
| 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 |
0.521 |
|
| 1990 |
St George-Hyslop PH, Haines JL, Farrer LA, Polinsky R, Van Broeckhoven C, Goate A, McLachlan DR, Orr H, Bruni AC, Sorbi S, Rainero I, Foncin JF, Pollen D, Cantu JM, Tupler R, ... ... Gusella JF, et al. Genetic linkage studies suggest that Alzheimer's disease is not a single homogeneous disorder. Nature. 347: 194-7. PMID 2395471 DOI: 10.1038/347194A0 |
0.33 |
|
| 1990 |
Rouleau GA, Bazanowski A, Gusella JF, Haines JL. A genetic map of chromosome 1: comparison of different data sets and linkage programs. Genomics. 7: 313-8. PMID 2365352 DOI: 10.1016/0888-7543(90)90163-O |
0.406 |
|
| 1990 |
Tanzi RE, Haines JL, Gusella JF. Detailed genetic linkage map of human chromosome 21: patterns of recombination according to age and sex. Progress in Clinical and Biological Research. 360: 15-26. PMID 2247506 |
0.526 |
|
| 1990 |
Fontaine B, Rouleau GA, Seizinger B, Jewell AF, Hanson MP, Martuza RL, Gusella JF. Equal parental origin of chromosome 22 losses in human sporadic meningioma: no evidence for genomic imprinting. American Journal of Human Genetics. 47: 823-7. PMID 2220822 |
0.437 |
|
| 1990 |
Rouleau GA, Seizinger BR, Wertelecki W, Haines JL, Superneau DW, Martuza RL, Gusella JF. Flanking markers bracket the neurofibromatosis type 2 (NF2) gene on chromosome 22. American Journal of Human Genetics. 46: 323-8. PMID 2105641 |
0.483 |
|
| 1990 |
Palmert MR, Podlisny MB, Golde TE, Cohen ML, Kovacs DM, Tanzi RE, Gusella JF, Whitehouse PJ, Witker DS, Oltersdorf T. Analysis of the beta-amyloid protein precursor of Alzheimer's disease: mRNAs and protein products. Advances in Neurology. 51: 181-4. PMID 2104687 |
0.567 |
|
| 1990 |
Grafton ST, Mazziotta JC, Pahl JJ, St George-Hyslop P, Haines JL, Gusella J, Hoffman JM, Baxter LR, Phelps ME. A comparison of neurological, metabolic, structural, and genetic evaluations in persons at risk for Huntington's disease. Annals of Neurology. 28: 614-21. PMID 1979723 DOI: 10.1002/Ana.410280503 |
0.335 |
|
| 1990 |
Fontaine B, Hanson MP, Liou HC, Glimcher LH, Rouleau GA, Gusella JF. BanI polymorphism at the XBP1 locus. Nucleic Acids Research. 18: 5578. PMID 1977120 DOI: 10.1093/Nar/18.18.5578-A |
0.339 |
|
| 1990 |
Kondo I, Ohta H, Yazaki M, Ikeda JE, Gusella JF, Kanazawa I. Exclusion mapping of the hereditary dentatorubropallidoluysian atrophy gene from the Huntington's disease locus. Journal of Medical Genetics. 27: 105-8. PMID 1969487 DOI: 10.1136/jmg.27.2.105 |
0.313 |
|
| 1989 |
St George-Hyslop PH, Tanzi RE, Haines JL, Polinsky RJ, Farrer L, Myers RH, Gusella JF. Molecular genetics of familial Alzheimer's disease. European Neurology. 29: 25-7. PMID 2693103 DOI: 10.1159/000116477 |
0.498 |
|
| 1989 |
St George-Hyslop PH, Myers RH, Haines JL, Farrer LA, Tanzi RE, Abe K, James MF, Conneally PM, Polinsky RJ, Gusella JF. Familial Alzheimer's disease: progress and problems. Neurobiology of Aging. 10: 417-25. PMID 2682321 DOI: 10.1016/0197-4580(89)90082-1 |
0.441 |
|
| 1989 |
St George-Hyslop PH, Haines JL, Polinsky RJ, Tanzi RE, Farrer L, Myers RH, Gusella JF. Molecular genetics of familial Alzheimer's disease. The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques. 16: 465-7. PMID 2680005 DOI: 10.1017/S0317167100029772 |
0.459 |
|
| 1989 |
Youngman S, Sarfarazi M, Bucan M, MacDonald M, Smith B, Zimmer M, Gilliam C, Frischauf AM, Wasmuth JJ, Gusella JF, Lehrach H, Harper PS, Shaw DJ. A new DNA marker (D4S90) is located terminally on the short arm of chromosome 4, close to the Huntington disease gene Genomics. 5: 802-809. PMID 2574148 DOI: 10.1016/0888-7543(89)90122-5 |
0.33 |
|
| 1989 |
Gusella JF. Location cloning strategy for characterizing genetic defects in Huntington's disease and Alzheimer's disease. Faseb Journal : Official Publication of the Federation of American Societies For Experimental Biology. 3: 2036-41. PMID 2568302 DOI: 10.1096/fasebj.3.9.2568302 |
0.34 |
|
| 1989 |
Kwiatkowski DJ, Ozelius L, Schuback D, Gusella J, Breakefield XO. The gelsolin (GSN) cDNA clone, from 9q32-34, identifies BclI and StuI RFLPs. Nucleic Acids Research. 17: 4425. PMID 2567988 DOI: 10.1093/Nar/17.11.4425 |
0.322 |
|
| 1989 |
Rouleau GA, Haines JL, Bazanowski A, Colella-Crowley A, Trofatter JA, Wexler NS, Conneally PM, Gusella JF. A genetic linkage map of the long arm of human chromosome 22. Genomics. 4: 1-6. PMID 2563348 DOI: 10.1016/0888-7543(89)90306-6 |
0.503 |
|
| 1989 |
Van Keuren ML, Stewart GD, Bradley CM, Kurnit DM, Neve RL, Watkins PC, Tanzi RE, Gusella JF, Patterson D. Characterization of an unusual and complex chromosome 21 rearrangement using somatic cell genetics and cloned DNA probes. American Journal of Medical Genetics. 33: 369-75. PMID 2529766 DOI: 10.1002/Ajmg.1320330316 |
0.505 |
|
| 1989 |
Palmert MR, Podlisny MB, Golde TE, Cohen ML, Kovacs DM, Tanzi RE, Gusella JF, Whitehouse PJ, Witker DS, Oltersdorf T. The beta amyloid protein precursor: mRNAs, membrane-associated forms, and soluble derivatives. Progress in Clinical and Biological Research. 317: 971-84. PMID 2513588 |
0.558 |
|
| 1989 |
Tanzi RE, St George-Hyslop PH, Gusella JF. Molecular genetic approaches to Alzheimer's disease. Trends in Neurosciences. 12: 152-8. PMID 2470173 DOI: 10.1016/0166-2236(89)90055-6 |
0.409 |
|
| 1988 |
Sacchi N, Cheng SV, Tanzi RE, Gusella JF, Drabkin HA, Patterson D, Haines JH, Papas TS. The ETS genes on chromosome 21 are distal to the breakpoint of the acute myelogenous leukemia translocation (8;21). Genomics. 3: 110-6. PMID 3267212 DOI: 10.1016/0888-7543(88)90140-1 |
0.519 |
|
| 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 |
0.538 |
|
| 1988 |
Graw S, Davidson J, Gusella J, Watkins P, Tanzi R, Neve R, Patterson D. Irradiation-reduced human chromosome 21 hybrids. Somatic Cell and Molecular Genetics. 14: 233-42. PMID 3163426 DOI: 10.1007/Bf01534584 |
0.567 |
|
| 1988 |
Wertelecki W, Rouleau GA, Superneau DW, Forehand LW, Williams JP, Haines JL, Gusella JF. Neurofibromatosis 2: clinical and DNA linkage studies of a large kindred. The New England Journal of Medicine. 319: 278-83. PMID 3134615 DOI: 10.1056/NEJM198808043190505 |
0.427 |
|
| 1988 |
Patterson D, Gardiner K, Kao FT, Tanzi R, Watkins P, Gusella JF. Mapping of the gene encoding the beta-amyloid precursor protein and its relationship to the Down syndrome region of chromosome 21. Proceedings of the National Academy of Sciences of the United States of America. 85: 8266-70. PMID 2973063 DOI: 10.1073/Pnas.85.21.8266 |
0.519 |
|
| 1988 |
Tanzi RE, Haines JL, Watkins PC, Stewart GD, Wallace MR, Hallewell R, Wong C, Wexler NS, Conneally PM, Gusella JF. Genetic linkage map of human chromosome 21. Genomics. 3: 129-36. PMID 2906323 DOI: 10.1016/0888-7543(88)90143-7 |
0.556 |
|
| 1988 |
Rouleau GA, Bazanowski A, Cohen EH, Guellaen G, Gusella JF. Gamma-glutamyl transferase locus (GGT) displays a PvuII polymorphism. Nucleic Acids Research. 16: 11848. PMID 2905445 DOI: 10.1093/Nar/16.24.11848 |
0.337 |
|
| 1988 |
Phelan MC, Morton CC, Stevenson RE, Tanzi RE, Stewart GD, Watkins PC, Gusella JF, Amos JA. Molecular and cytogenetic characterization of a de novo t(5p;21q) in a patient previously diagnosed as monosomy 21. American Journal of Human Genetics. 43: 511-9. PMID 2902789 |
0.49 |
|
| 1988 |
Richards JE, Gilliam TC, Cole JL, Drumm ML, Wasmuth JJ, Gusella JF, Collins FS. Chromosome jumping from D4S10 (G8) toward the Huntington disease gene. Proceedings of the National Academy of Sciences of the United States of America. 85: 6437-41. PMID 2901098 DOI: 10.1073/Pnas.85.17.6437 |
0.345 |
|
| 1988 |
Cheng SV, Nadeau JH, Tanzi RE, Watkins PC, Jagadesh J, Taylor BA, Haines JL, Sacchi N, Gusella JF. Comparative mapping of DNA markers from the familial Alzheimer disease and Down syndrome regions of human chromosome 21 to mouse chromosomes 16 and 17. Proceedings of the National Academy of Sciences of the United States of America. 85: 6032-6. PMID 2901095 DOI: 10.1073/Pnas.85.16.6032 |
0.53 |
|
| 1988 |
Sacchi N, Gusella JF, Perroni L, Bricarelli FD, Papas TS. Lack of evidence for association of meiotic nondisjunction with particular DNA haplotypes on chromosome 21. Proceedings of the National Academy of Sciences of the United States of America. 85: 4794-8. PMID 2898783 DOI: 10.1073/PNAS.85.13.4794 |
0.304 |
|
| 1988 |
Rouleau GA, Kurnit DM, Neve RL, Bazanowsky A, Patterson D, Gusella JF. D22S15--a fetal brain cDNA with BanII and SacI RFLP. Nucleic Acids Research. 16: 1646. PMID 2894636 DOI: 10.1093/Nar/16.4.1646 |
0.323 |
|
| 1988 |
Tanzi RE, McClatchey AI, Lamperti ED, Villa-Komaroff L, Gusella JF, Neve RL. Protease inhibitor domain encoded by an amyloid protein precursor mRNA associated with Alzheimer's disease. Nature. 331: 528-30. PMID 2893290 DOI: 10.1038/331528A0 |
0.451 |
|
| 1988 |
Martuza RL, Seizinger BR, Jacoby LB, Rouleau GA, Gusella JF. The molecular biology of human glial tumors. Trends in Neurosciences. 11: 22-7. PMID 2469150 DOI: 10.1016/0166-2236(88)90045-8 |
0.361 |
|
| 1988 |
Palmert MR, Golde TE, Cohen ML, Kovacs DM, Tanzi RE, Gusella JF, Usiak MF, Younkin LH, Younkin SG. Amyloid protein precursor messenger RNAs: differential expression in Alzheimer's disease. Science (New York, N.Y.). 241: 1080-4. PMID 2457949 |
0.561 |
|
| 1988 |
PALMERT MR, GOLDE TE, COHEN ML, KOVACS DM, TANZI RE, GUSELLA JF, USIAK MF, YOUNKIN LH, YOUNKIN SG. AMYLOID PROTEIN PRECURSOR mRNA LACKING THE KUNITZ PROTEASE INHIBITOR SEQUENCE INCREASES IN AD NUCLEUS BASALIS AND LOCUS CERULEUS NEURONS Alzheimer Disease & Associated Disorders. 2: 401. DOI: 10.1097/00002093-198802040-00031 |
0.377 |
|
| 1988 |
TANZI RE, GUSELLA JF. GENETIC ANALYSIS OF THE ALZHEIMER??S ASSOCIATED AMYLOID BETA PEPTIDE GENE Alzheimer Disease & Associated Disorders. 2: 277. DOI: 10.1097/00002093-198802030-00126 |
0.407 |
|
| 1988 |
Tanzi RE, Gusella JF, Watkins PC, Bruns GA, St.-George HP, Van Keuren ML, Patterson D, Pagan S, Kurnit DM, Neve RL. Amyloid β protein gene Alzheimer Disease & Associated Disorders. 2: 135. DOI: 10.1097/00002093-198802020-00013 |
0.365 |
|
| 1987 |
Seizinger BR, Martuza RL, Rouleau G, Breakefield XO, Gusella JF. Models for inherited susceptibility to cancer in the nervous system: a molecular-genetic approach to neurofibromatosis. Developmental Neuroscience. 9: 144-53. PMID 3119309 DOI: 10.1159/000111618 |
0.413 |
|
| 1987 |
Seizinger BR, Rouleau G, Ozelius LJ, Lane AH, St George-Hyslop P, Huson S, Gusella JF, Martuza RL. Common pathogenetic mechanism for three tumor types in bilateral acoustic neurofibromatosis. Science (New York, N.Y.). 236: 317-9. PMID 3105060 DOI: 10.1126/Science.3105060 |
0.522 |
|
| 1987 |
Seizinger BR, de la Monte S, Atkins L, Gusella JF, Martuza RL. Molecular genetic approach to human meningioma: loss of genes on chromosome 22. Proceedings of the National Academy of Sciences of the United States of America. 84: 5419-23. PMID 3037550 DOI: 10.1073/Pnas.84.15.5419 |
0.326 |
|
| 1987 |
Cheng SV, Gross Lugo T, Tanzi RE, Whitney JB, Fournier RE, Gusella JF. Chromosomal localization of the mouse homolog of the Huntington's disease linked G8 (D4S10) marker. Dna (Mary Ann Liebert, Inc.). 6: 401-7. PMID 2890502 |
0.517 |
|
| 1987 |
MacDonald ME, Anderson MA, Lockyer JL, Milstien S, Hobbs WJ, Faryniarz AG, Kaufman S, Ledley FD, Woo SL, Gusella JF. Physical and genetic localization of quinonoid dihydropteridine reductase gene (QDPR) on short arm of chromosome 4. Somatic Cell and Molecular Genetics. 13: 569-74. PMID 2889272 DOI: 10.1007/Bf01534498 |
0.347 |
|
| 1987 |
Rouleau GA, Wertelecki W, Haines JL, Hobbs WJ, Trofatter JA, Seizinger BR, Martuza RL, Superneau DW, Conneally PM, Gusella JF. Genetic linkage of bilateral acoustic neurofibromatosis to a DNA marker on chromosome 22. Nature. 329: 246-8. PMID 2888021 DOI: 10.1038/329246A0 |
0.498 |
|
| 1987 |
Tanzi RE, St George-Hyslop PH, Haines JL, Polinsky RJ, Nee L, Foncin JF, Neve RL, McClatchey AI, Conneally PM, Gusella JF. The genetic defect in familial Alzheimer's disease is not tightly linked to the amyloid beta-protein gene. Nature. 329: 156-7. PMID 2888020 DOI: 10.1038/329156A0 |
0.517 |
|
| 1987 |
Ramesh V, Eddy R, Bruns GA, Shih VE, Shows TB, Gusella JF. Localization of the ornithine aminotransferase gene and related sequences on two human chromosomes. Human Genetics. 76: 121-6. PMID 2886418 DOI: 10.1007/Bf00284906 |
0.335 |
|
| 1987 |
Watkins PC, Eddy R, Beck AK, Vellucci V, Leverone B, Tanzi RE, Gusella JF, Shows TB. DNA sequence and regional assignment of the human follicle-stimulating hormone beta-subunit gene to the short arm of human chromosome 11. Dna (Mary Ann Liebert, Inc.). 6: 205-12. PMID 2885163 |
0.498 |
|
| 1987 |
Watkins PC, Tanzi RE, Cheng SV, Gusella JF. Molecular genetics of human chromosome 21. Journal of Medical Genetics. 24: 257-70. PMID 2884319 DOI: 10.1136/Jmg.24.5.257 |
0.542 |
|
| 1987 |
Gilliam TC, Healey ST, MacDonald ME, Stewart GD, Wasmuth JJ, Tanzi RE, Roy JC, Gusella JF. Isolation of polymorphic DNA fragments from human chromosome 4. Nucleic Acids Research. 15: 1445-58. PMID 2881276 DOI: 10.1093/Nar/15.4.1445 |
0.514 |
|
| 1986 |
Seizinger BR, Tanzi RE, Gilliam TC, Bader JL, Parry DM, Spence MA, Marazita ML, Gibbons K, Hobbs W, Gusella JF. Genetic linkage analysis of neurofibromatosis with DNA markers. Annals of the New York Academy of Sciences. 486: 304-10. PMID 3105395 DOI: 10.1111/J.1749-6632.1986.Tb48083.X |
0.432 |
|
| 1986 |
Seizinger BR, Martuza RL, Gusella JF. Loss of genes on chromosome 22 in tumorigenesis of human acoustic neuroma. Nature. 322: 644-7. PMID 3092103 DOI: 10.1038/322644a0 |
0.312 |
|
| 1986 |
Youngman S, Sarfarazi M, Quarrell OWJ, Conneally PM, Gibbons K, Harper PS, Shaw DJ, Tanzi RE, Wallace MR, Gusella JF. Studies of a DNA marker (G8) genetically linked to Huntington disease in British families Human Genetics. 73: 333-339. PMID 3017842 DOI: 10.1007/Bf00279096 |
0.455 |
|
| 1986 |
Zabel BU, Naylor SL, Sakaguchi AY, Gusella JF. Mapping of the DNA locus D4S10 and the linked Huntington's disease gene to 4p16----p15. Cytogenetics and Cell Genetics. 42: 187-90. PMID 2944714 DOI: 10.1159/000132276 |
0.332 |
|
| 1986 |
Gusella JF, Gilliam TC, Tanzi RE, MacDonald ME, Cheng SV, Wallace M, Haines J, Conneally PM, Wexler NS. Molecular genetics of Huntington's disease. Cold Spring Harbor Symposia On Quantitative Biology. 51: 359-64. PMID 2884064 DOI: 10.1101/Sqb.1986.051.01.043 |
0.511 |
|
| 1986 |
Watkins PC, Eddy R, Hoffman N, Stanislovitis P, Beck AK, Galli J, Vellucci V, Gusella JF, Shows TB. Regional assignment of the erythropoietin gene to human chromosome region 7pter----q22. Cytogenetics and Cell Genetics. 42: 214-8. PMID 2875851 DOI: 10.1159/000132281 |
0.316 |
|
| 1985 |
Gusella JF. Genetic linkage of the Huntington's disease gene to a DNA marker. The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques. 11: 421-5. PMID 6240313 DOI: 10.1017/S0317167100045947 |
0.323 |
|
| 1985 |
Wexler NS, Conneally PM, Housman D, Gusella JF. A DNA Polymorphism for Huntington's Disease Marks the Future Archives of Neurology. 42: 20-24. PMID 3155610 DOI: 10.1001/Archneur.1985.04060010026009 |
0.476 |
|
| 1985 |
Harper PS, Youngman S, Anderson MA, Sarfarazi M, Quarrell O, Tanzi R, Shaw D, Wallace P, Conneally PM, Gusella JF. Genetic linkage between Huntington's disease and the DNA polymorphism G8 in South Wales families Journal of Medical Genetics. 22: 447-450. PMID 3001311 DOI: 10.1136/Jmg.22.6.447 |
0.449 |
|
| 1985 |
Stewart GD, Tanzi RE, Gusella JF. RFLPS at the D21S19 locus of human chromosome 21. Nucleic Acids Research. 13: 7168. PMID 2997741 DOI: 10.1093/Nar/13.19.7168 |
0.474 |
|
| 1985 |
Gusella JF, Tanzi RE, Bader PI, Phelan MC, Stevenson R, Hayden MR, Hofman KJ, Faryniarz AG, Gibbons K. Deletion of Huntington's disease-linked G8 (D4S10) locus in Wolf-Hirschhorn syndrome. Nature. 318: 75-8. PMID 2997623 DOI: 10.1038/318075A0 |
0.524 |
|
| 1985 |
Gusella JF, Tanzi RE, Watkins PC, Gibbons KT, Hobbs WJ, Faryniarz AG, Healey ST, Anderson MA. Genetic linkage map for chromosome 21. Annals of the New York Academy of Sciences. 450: 25-31. PMID 2990310 DOI: 10.1111/J.1749-6632.1985.Tb21480.X |
0.473 |
|
| 1985 |
Kittur S, Antonarakis S, Tanzi R, Meyers D, Chakravarti A, Groner Y, Phillips J, Watkins P, Gusella J, Kazazian H. A linkage map of three anonymous human DNA fragments and SOD-1 on chromosome 21. The Embo Journal. 4: 2257-2260. DOI: 10.1002/J.1460-2075.1985.Tb03923.X |
0.511 |
|
| 1984 |
Fisher JH, Gusella JF, Scoggin CH. Molecular hybridization under conditions of high stringency permits cloned DNA segments containing reiterated DNA sequences to be assigned to specific chromosomal locations. Proceedings of the National Academy of Sciences of the United States of America. 81: 520-4. PMID 6582508 DOI: 10.1073/PNAS.81.2.520 |
0.301 |
|
| 1984 |
Minden M, Gusella J, Housman D. Chromosome-mediated transfer of the malignant phenotype by human acute myelogenous leukemic cells Blood. 64: 842-846. DOI: 10.1182/Blood.V64.4.842.Bloodjournal644842 |
0.542 |
|
| 1982 |
Gusella JF, Jones C, Kao FT, Housman D, Puck TT. Genetic fine-structure mapping in human chromosome 11 by use of repetitive DNA sequences. Proceedings of the National Academy of Sciences of the United States of America. 79: 7804-8. PMID 6961451 DOI: 10.1073/Pnas.79.24.7804 |
0.539 |
|
| 1982 |
Gusella JF, Tsiftsoglou AS, Volloch V, Weil SC, Neumann J, Housman DE. Dissociation of hemoglobin accumulation and commitment during murine erythroleukemia cell differentiation by treatment with imidazole. Journal of Cellular Physiology. 113: 179-85. PMID 6957412 DOI: 10.1002/JCP.1041130127 |
0.417 |
|
| 1982 |
Housman D, Kidd K, Gusella JF. Recombinant DNA approach to neurogenetic disorders Trends in Neurosciences. 5: 320-323. DOI: 10.1016/0166-2236(82)90192-8 |
0.475 |
|
| 1981 |
Housman D, Levenson R, Volloch V, Tsiftsoglou A, Gusella J, Parker D, Kernen J, Mitrani A, Weeks V, Witte O, Besmer P. Control of proliferation and differentiation in cells transformed by Friend virus. Cold Spring Harbor Symposia On Quantitative Biology. 1177-85. PMID 6933050 DOI: 10.1101/Sqb.1980.044.01.127 |
0.572 |
|
| 1981 |
Bruns GAP, Gusella JF, Keys C, Housman D, Gerald PS. 704 ISOLATION OF DNA SEGMENTS FROM THE HUMAN X CHROMOSOME Pediatric Research. 15: 559-559. DOI: 10.1203/00006450-198104001-00727 |
0.475 |
|
| 1980 |
Gusella JF, Keys C, VarsanyiBreiner A, Kao FT, Jones C, Puck TT, Housman D. Isolation and localization of DNA segments from specific human chromosomes. Proceedings of the National Academy of Sciences of the United States of America. 77: 2829-33. PMID 6930670 DOI: 10.1073/Pnas.77.5.2829 |
0.519 |
|
| 1980 |
Gusella J, Weil S, Tsiftsoglou A, Volloch V, Neumann J, Keys C, Housman D. Hemin does not cause commitment of murine erythroleukemia (MEL) cells to terminal differentiation Blood. 56: 481-487. DOI: 10.1182/Blood.V56.3.481.481 |
0.477 |
|
| 1980 |
Gusella J, Weil S, Tsiftsoglou A, Volloch V, Neumann J, Keys C, Housman D. Hemin does not cause commitment of murine erythroleukemia (MEL) cells to terminal differentiation Blood. 56: 481-487. DOI: 10.1182/BLOOD.V56.3.481.481 |
0.412 |
|
| 1979 |
Gusella J, Varsanyi-Breiner A, Kao FT, Jones C, Puck TT, Keys C, Orkin S, Housman D. Precise localization of human beta-globin gene complex on chromosome 11. Proceedings of the National Academy of Sciences of the United States of America. 76: 5239-42. PMID 291941 DOI: 10.1073/Pnas.76.10.5239 |
0.595 |
|
| 1979 |
Varsanyi-Breiner A, Gusella JF, Keys C, Housman DE, Sullivan D, Brisson N, Verma DP. The organization of a nuclear DNA sequence from a higher plant: molecular cloning and characterization of soybean ribosomal DNA. Gene. 7: 317-34. PMID 160361 DOI: 10.1016/0378-1119(79)90051-9 |
0.443 |
|
| 1976 |
Gusella J, Geller R, Clarke B, Weeks V, Housman D. Commitment to erythroid differentiation by friend erythroleukemia cells: a stochastic analysis Cell. 9: 221-229. PMID 975244 DOI: 10.1016/0092-8674(76)90113-6 |
0.477 |
|
| 1976 |
Gusella JF, Housman D. Induction of erythroid differentiation in vitro by purines and purine analogues. Cell. 8: 263-9. PMID 971485 DOI: 10.1016/0092-8674(76)90010-6 |
0.389 |
|
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