| Year |
Citation |
Score |
| 2018 |
Sulakhe D, D'Souza M, Wang S, Balasubramanian S, Athri P, Xie B, Canzar S, Agam G, Gilliam TC, Maltsev N. Exploring the functional impact of alternative splicing on human protein isoforms using available annotation sources. Briefings in Bioinformatics. PMID 29931155 DOI: 10.1093/Bib/Bby047 |
0.322 |
|
| 2018 |
Xie B, Laxman B, Hashemifar S, Stern R, Gilliam TC, Maltsev N, White SR. Chemokine expression in the early response to injury in human airway epithelial cells. Plos One. 13: e0193334. PMID 29534074 DOI: 10.1371/Journal.Pone.0193334 |
0.323 |
|
| 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 |
0.356 |
|
| 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 |
0.415 |
|
| 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 |
0.362 |
|
| 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 |
0.41 |
|
| 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 |
0.465 |
|
| 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 |
0.77 |
|
| 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 |
0.425 |
|
| 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 |
0.76 |
|
| 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 |
0.394 |
|
| 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 |
0.476 |
|
| 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 |
0.777 |
|
| 2007 |
Martinez-Mir A, Zlotogorski A, Gordon D, Petukhova L, Mo J, Gilliam TC, Londono D, Haynes C, Ott J, Hordinsky M, Nanova K, Norris D, Price V, Duvic M, Christiano AM. Genomewide scan for linkage reveals evidence of several susceptibility loci for alopecia areata. American Journal of Human Genetics. 80: 316-28. PMID 17236136 DOI: 10.1086/511442 |
0.457 |
|
| 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 |
0.32 |
|
| 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 |
0.757 |
|
| 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 |
0.441 |
|
| 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 |
0.747 |
|
| 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 |
0.778 |
|
| 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 |
0.39 |
|
| 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 |
0.781 |
|
| 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 |
0.327 |
|
| 2004 |
Sebat J, Lakshmi B, Troge J, Alexander J, Young J, Lundin P, Månér 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 |
0.413 |
|
| 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 |
0.326 |
|
| 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 |
0.754 |
|
| 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 |
0.325 |
|
| 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 |
0.791 |
|
| 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 |
0.777 |
|
| 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 |
0.371 |
|
| 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 |
0.75 |
|
| 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 |
0.731 |
|
| 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 |
0.35 |
|
| 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 |
0.334 |
|
| 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 |
0.41 |
|
| 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 |
0.355 |
|
| 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 |
0.437 |
|
| 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 |
0.398 |
|
| 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 |
0.449 |
|
| 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 |
0.418 |
|
| 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 |
0.358 |
|
| 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 |
0.743 |
|
| 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 |
0.759 |
|
| 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 |
0.362 |
|
| 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 |
0.313 |
|
| 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 |
0.762 |
|
| 1999 |
Aita VM, Liu J, Knowles JA, Terwilliger JD, Baltazar R, Grunn A, Loth JE, Kanyas K, Lerer B, Endicott J, Wang Z, Penchaszadeh G, Gilliam TC, Baron M. A comprehensive linkage analysis of chromosome 21q22 supports prior evidence for a putative bipolar affective disorder locus. American Journal of Human Genetics. 64: 210-7. PMID 9915960 DOI: 10.1086/302185 |
0.782 |
|
| 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 |
0.446 |
|
| 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 |
0.427 |
|
| 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 |
0.424 |
|
| 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 |
0.736 |
|
| 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 |
0.772 |
|
| 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 |
0.744 |
|
| 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 |
0.312 |
|
| 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 |
0.313 |
|
| 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 |
0.303 |
|
| 1995 |
Gilliam TC. Is the spinal muscular atrophy gene found? Nature Medicine. 1: 124-7. PMID 7585007 DOI: 10.1038/Nm0295-124 |
0.348 |
|
| 1994 |
Knowles JA, Shugart Y, Banerjee P, Gilliam TC, Lewis CA, Jacobson SG, Ott J. Identification of a locus, distinct from RDS-peripherin, for autosomal recessive retinitis pigmentosa on chromosome 6p. Human Molecular Genetics. 3: 1401-3. PMID 7987322 DOI: 10.1093/Hmg/3.8.1401 |
0.343 |
|
| 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 |
0.373 |
|
| 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 |
0.428 |
|
| 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 |
0.387 |
|
| 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 |
0.436 |
|
| 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 |
0.338 |
|
| 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 |
0.406 |
|
| 1992 |
Consalez GG, Stayton CL, Freimer NB, Goonewardena P, Brown WT, Gilliam TC, Warren ST. Isolation and characterization of a highly polymorphic human locus (DXS455) in proximal Xq28 Genomics. 12: 710-714. PMID 1572645 DOI: 10.1016/0888-7543(92)90299-8 |
0.467 |
|
| 1992 |
Rojas K, Straub RE, Kurtz A, Feder M, Mewar R, Gilliam TC, Overhauser J. Identification and localization of microsatellite markers covering human chromosome 18. Genomics. 14: 1095-7. PMID 1478651 DOI: 10.1016/S0888-7543(05)80136-3 |
0.405 |
|
| 1992 |
Gilliam TC. Mapping psychiatric disease genes: impact of new molecular strategies. Journal of Psychiatric Research. 26: 309-26. PMID 1362776 DOI: 10.1016/0022-3956(92)90038-P |
0.461 |
|
| 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 |
0.401 |
|
| 1989 |
Gilliam TC, Freimer NB, Kaufmann CA, Powchik PP, Bassett AS, Bengtsson U, Wasmuth JJ. Deletion mapping of DNA markers to a region of chromosome 5 that cosegregates with schizophrenia. Genomics. 5: 940-4. PMID 2591972 DOI: 10.1016/0888-7543(89)90138-9 |
0.362 |
|
| 1989 |
Bassett A, Sandkuyl L, Lehner T, Powchik P, Gilliam TC, Kaufman C. Preliminary linkage analysis of schizophrenia in Canadian pedigrees to a candidate region on chromosome 5 Schizophrenia Research. 2: 40. DOI: 10.1016/0920-9964(89)90076-5 |
0.326 |
|
| 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 |
0.322 |
|
| 1987 |
Gilliam TC, Bucan M, MacDonald ME, Zimmer M, Haines JL, Cheng SV, Pohl TM, Meyers RH, Whaley WL, Allitto BA. A DNA segment encoding two genes very tightly linked to Huntington's disease. Science (New York, N.Y.). 238: 950-2. PMID 2890209 DOI: 10.1126/Science.2890209 |
0.315 |
|
| 1987 |
Gilliam TC, Tanzi RE, Haines JL, Bonner TI, Faryniarz AG, Hobbs WJ, MacDonald ME, Cheng SV, Folstein SE, Conneally PM. Localization of the Huntington's disease gene to a small segment of chromosome 4 flanked by D4S10 and the telomere. Cell. 50: 565-71. PMID 2886227 DOI: 10.1016/0092-8674(87)90029-8 |
0.352 |
|
| 1986 |
Gusella JA, Gilliam TC, MacDonald ME, Cheng SV, Tanzi RE. Molecular genetics of human chromosome 4. Journal of Medical Genetics. 23: 193-9. PMID 2941587 |
0.32 |
|
| 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 |
0.323 |
|
| Show low-probability matches. |