| Year |
Citation |
Score |
| 2021 |
Jia X, Goes FS, Locke AE, Palmer D, Wang W, Cohen-Woods S, Genovese G, Jackson AU, Jiang C, Kvale M, Mullins N, Nguyen H, Pirooznia M, Rivera M, Ruderfer DM, ... ... Risch N, et al. Correction: Investigating rare pathogenic/likely pathogenic exonic variation in bipolar disorder. Molecular Psychiatry. PMID 33674754 DOI: 10.1038/s41380-021-01063-8 |
0.396 |
|
| 2021 |
Jia X, Goes FS, Locke AE, Palmer D, Wang W, Cohen-Woods S, Genovese G, Jackson AU, Jiang C, Kvale M, Mullins N, Nguyen H, Pirooznia M, Rivera M, Ruderfer DM, ... ... Risch N, et al. Investigating rare pathogenic/likely pathogenic exonic variation in bipolar disorder. Molecular Psychiatry. PMID 33483695 DOI: 10.1038/s41380-020-01006-9 |
0.472 |
|
| 2020 |
Nandakumar P, Lee D, Hoffmann TJ, Ehret GB, Arking D, Ranatunga D, Li M, Grove ML, Boerwinkle E, Schaefer C, Kwok PY, Iribarren C, Risch N, Chakravarti A. Analysis of putative cis-regulatory elements regulating blood pressure variation. Human Molecular Genetics. PMID 32436959 DOI: 10.1093/Hmg/Ddaa098 |
0.348 |
|
| 2020 |
Oni-Orisan A, Haldar T, Ranatunga DK, Medina MW, Schaefer C, Krauss RM, Iribarren C, Risch N, Hoffmann TJ. The impact of adjusting for baseline in pharmacogenomic genome-wide association studies of quantitative change. Npj Genomic Medicine. 5: 1. PMID 31969989 DOI: 10.1038/S41525-019-0109-4 |
0.343 |
|
| 2020 |
Claussnitzer M, Cho JH, Collins R, Cox NJ, Dermitzakis ET, Hurles ME, Kathiresan S, Kenny EE, Lindgren CM, MacArthur DG, North KN, Plon SE, Rehm HL, Risch N, Rotimi CN, et al. A brief history of human disease genetics. Nature. 577: 179-189. PMID 31915397 DOI: 10.1038/S41586-019-1879-7 |
0.383 |
|
| 2019 |
Hauser MA, Allingham RR, Aung T, Van Der Heide CJ, Taylor KD, Rotter JI, Wang SJ, Bonnemaijer PWM, Williams SE, Abdullahi SM, Abu-Amero KK, Anderson MG, Akafo S, Alhassan MB, ... ... Risch N, et al. Association of Genetic Variants With Primary Open-Angle Glaucoma Among Individuals With African Ancestry. Jama. 322: 1682-1691. PMID 31688885 DOI: 10.1001/Jama.2019.16161 |
0.363 |
|
| 2019 |
Kilpeläinen TO, Bentley AR, Noordam R, Sung YJ, Schwander K, Winkler TW, Jakupović H, Chasman DI, Manning A, Ntalla I, Aschard H, Brown MR, de Las Fuentes L, Franceschini N, Guo X, ... ... Risch N, et al. Multi-ancestry study of blood lipid levels identifies four loci interacting with physical activity. Nature Communications. 10: 376. PMID 30670697 DOI: 10.1038/S41467-018-08008-W |
0.495 |
|
| 2019 |
Schaefer C, Thai K, Jorgenson E, Banda Y, Hoffmann T, Kvale M, Risch N. ASSOCIATIONS OF POLYGENIC RISK OF SCHIZOPHRENIA AND MAJOR DEPRESSION IN STUDIES OF BIPOLAR DISORDER AND MAJOR DEPRESSION European Neuropsychopharmacology. 29: S899-S900. DOI: 10.1016/J.Euroneuro.2017.08.212 |
0.369 |
|
| 2018 |
Hoffmann TJ, Choquet H, Yin J, Banda Y, Kvale MN, Glymour M, Schaefer C, Risch N, Jorgenson E. A Large Multi-ethnic Genome-Wide Association Study of Adult Body Mass Index Identifies Novel Loci. Genetics. PMID 30108127 DOI: 10.1534/Genetics.118.301479 |
0.366 |
|
| 2018 |
Choquet H, Paylakhi S, Kneeland SC, Thai KK, Hoffmann TJ, Yin J, Kvale MN, Banda Y, Tolman NG, Williams PA, Schaefer C, Melles RB, Risch N, John SWM, Nair KS, et al. A multiethnic genome-wide association study of primary open-angle glaucoma identifies novel risk loci. Nature Communications. 9: 2278. PMID 29891935 DOI: 10.1038/S41467-018-04555-4 |
0.379 |
|
| 2018 |
Liang J, Le TH, Velez Edwards DR, Tayo BO, Gaulton KJ, Smith JA, Lu Y, Jensen RA, Chen G, Yanek LR, Schwander K, Tajuddin SM, Sofer T, Kim W, Kayima J, ... ... Risch N, et al. Correction: Single-trait and multi-trait genome-wide association analyses identify novel loci for blood pressure in African-ancestry populations. Plos Genetics. 14: e1007345. PMID 29750786 DOI: 10.1371/Journal.Pgen.1007345 |
0.335 |
|
| 2018 |
Hoffmann TJ, Theusch E, Haldar T, Ranatunga DK, Jorgenson E, Medina MW, Kvale MN, Kwok PY, Schaefer C, Krauss RM, Iribarren C, Risch N. A large electronic-health-record-based genome-wide study of serum lipids. Nature Genetics. PMID 29507422 DOI: 10.1038/S41588-018-0064-5 |
0.37 |
|
| 2018 |
Abuabara K, You Y, Margolis D, Risch N, Jorgenson E. 269 Genetic ancestry does not influence atopic dermatitis susceptibility or disease activity among African Americans Journal of Investigative Dermatology. 138: S46. DOI: 10.1016/J.Jid.2018.03.275 |
0.357 |
|
| 2017 |
Choquet H, Thai KK, Yin J, Hoffmann TJ, Kvale MN, Banda Y, Schaefer C, Risch N, Nair KS, Melles R, Jorgenson E. A large multi-ethnic genome-wide association study identifies novel genetic loci for intraocular pressure. Nature Communications. 8: 2108. PMID 29235454 DOI: 10.1038/S41467-017-01913-6 |
0.364 |
|
| 2017 |
Liang J, Le TH, Edwards DRV, Tayo BO, Gaulton KJ, Smith JA, Lu Y, Jensen RA, Chen G, Yanek LR, Schwander K, Tajuddin SM, Sofer T, Kim W, Kayima J, ... ... Risch N, et al. Single-trait and multi-trait genome-wide association analyses identify novel loci for blood pressure in African-ancestry populations. Plos Genetics. 13: e1006728. PMID 28498854 DOI: 10.1371/Journal.Pgen.1006728 |
0.371 |
|
| 2017 |
Jorgenson E, Thai KK, Hoffmann TJ, Sakoda LC, Kvale MN, Banda Y, Schaefer C, Risch N, Mertens J, Weisner C, Choquet H. Genetic contributors to variation in alcohol consumption vary by race/ethnicity in a large multi-ethnic genome-wide association study. Molecular Psychiatry. 22: 1359-1367. PMID 28485404 DOI: 10.1038/Mp.2017.101 |
0.304 |
|
| 2017 |
Hoffmann TJ, Passarelli MN, Graff RE, Emami NC, Sakoda LC, Jorgenson E, Habel LA, Shan J, Ranatunga DK, Quesenberry CP, Chao CR, Ghai NR, Aaronson D, Presti J, Nordström T, ... ... Risch N, et al. Genome-wide association study of prostate-specific antigen levels identifies novel loci independent of prostate cancer. Nature Communications. 8: 14248. PMID 28139693 DOI: 10.1038/Ncomms14248 |
0.323 |
|
| 2016 |
Hoffmann TJ, Ehret GB, Nandakumar P, Ranatunga D, Schaefer C, Kwok PY, Iribarren C, Chakravarti A, Risch N. Genome-wide association analyses using electronic health records identify new loci influencing blood pressure variation. Nature Genetics. PMID 27841878 DOI: 10.1038/Ng.3715 |
0.323 |
|
| 2016 |
Hoffmann TJ, Keats BJ, Yoshikawa N, Schaefer C, Risch N, Lustig LR. A Large Genome-Wide Association Study of Age-Related Hearing Impairment Using Electronic Health Records. Plos Genetics. 12: e1006371. PMID 27764096 DOI: 10.1371/Journal.Pgen.1006371 |
0.343 |
|
| 2016 |
Jorgenson E, Melles RB, Hoffmann TJ, Jia X, Sakoda LC, Kvale MN, Banda Y, Schaefer C, Risch N, Shen L. Common coding variants in the HLA-DQB1 region confer susceptibility to age-related macular degeneration. European Journal of Human Genetics : Ejhg. PMID 26733291 DOI: 10.1038/Ejhg.2015.247 |
0.371 |
|
| 2015 |
Kvale MN, Hesselson S, Hoffmann TJ, Cao Y, Chan D, Connell S, Croen LA, Dispensa BP, Eshragh J, Finn A, Gollub J, Iribarren C, Jorgenson E, Kushi LH, Lao R, ... ... Risch N, et al. Genotyping Informatics and Quality Control for 100,000 Subjects in the Genetic Epidemiology Research on Adult Health and Aging (GERA) Cohort. Genetics. PMID 26092718 DOI: 10.1534/Genetics.115.178905 |
0.355 |
|
| 2015 |
Banda Y, Kvale MN, Hoffmann TJ, Hesselson SE, Ranatunga D, Tang H, Sabatti C, Croen LA, Dispensa BP, Henderson M, Iribarren C, Jorgenson E, Kushi LH, Ludwig D, Olberg D, ... ... Risch N, et al. Characterizing Race/Ethnicity and Genetic Ancestry for 100,000 Subjects in the Genetic Epidemiology Research on Adult Health and Aging (GERA) Cohort. Genetics. PMID 26092716 DOI: 10.1534/Genetics.115.178616 |
0.383 |
|
| 2015 |
Hoffmann TJ, Van Den Eeden SK, Sakoda LC, Jorgenson E, Habel LA, Graff RE, Passarelli MN, Cario CL, Emami NC, Chao CR, Ghai NR, Shan J, Ranatunga DK, Quesenberry CP, Aaronson D, ... ... Risch N, et al. A Large Multiethnic Genome-Wide Association Study of Prostate Cancer Identifies Novel Risk Variants and Substantial Ethnic Differences. Cancer Discovery. PMID 26034056 DOI: 10.1158/2159-8290.Cd-15-0315 |
0.33 |
|
| 2015 |
Wen CC, Yee SW, Liang X, Hoffmann TJ, Kvale MN, Banda Y, Jorgenson E, Schaefer C, Risch N, Giacomini KM. Genome-wide association study identifies ABCG2 (BCRP) as an allopurinol transporter and a determinant of drug response. Clinical Pharmacology and Therapeutics. 97: 518-25. PMID 25676789 DOI: 10.1002/Cpt.89 |
0.358 |
|
| 2015 |
Hoffmann TJ, Sakoda LC, Shen L, Jorgenson E, Habel LA, Liu J, Kvale MN, Asgari MM, Banda Y, Corley D, Kushi LH, Quesenberry CP, Schaefer C, Van Den Eeden SK, Risch N, et al. Imputation of the rare HOXB13 G84E mutation and cancer risk in a large population-based cohort. Plos Genetics. 11: e1004930. PMID 25629170 DOI: 10.1371/Journal.Pgen.1004930 |
0.324 |
|
| 2015 |
Shetty PB, Tang H, Feng T, Tayo B, Morrison AC, Kardia SL, Hanis CL, Arnett DK, Hunt SC, Boerwinkle E, Rao DC, Cooper RS, Risch N, Zhu X. Variants for HDL-C, LDL-C, and triglycerides identified from admixture mapping and fine-mapping analysis in African American families. Circulation. Cardiovascular Genetics. 8: 106-13. PMID 25552592 DOI: 10.1161/Circgenetics.114.000481 |
0.307 |
|
| 2014 |
Hoffmann TJ, Tang H, Thornton TA, Caan B, Haan M, Millen AE, Thomas F, Risch N. Genome-wide association and admixture analysis of glaucoma in the Women's Health Initiative. Human Molecular Genetics. 23: 6634-43. PMID 25027321 DOI: 10.1093/Hmg/Ddu364 |
0.326 |
|
| 2014 |
Risch N, Hoffmann TJ, Anderson M, Croen LA, Grether JK, Windham GC. Familial recurrence of autism spectrum disorder: evaluating genetic and environmental contributions. The American Journal of Psychiatry. 171: 1206-13. PMID 24969362 DOI: 10.1176/Appi.Ajp.2014.13101359 |
0.336 |
|
| 2014 |
Fears SC, Service SK, Kremeyer B, Araya C, Araya X, Bejarano J, Ramirez M, Castrillón G, Gomez-Franco J, Lopez MC, Montoya G, Montoya P, Aldana I, Teshiba TM, Abaryan Z, ... ... Risch N, et al. Multisystem component phenotypes of bipolar disorder for genetic investigations of extended pedigrees. Jama Psychiatry. 71: 375-87. PMID 24522887 DOI: 10.1001/Jamapsychiatry.2013.4100 |
0.424 |
|
| 2013 |
Shen L, Hoffmann T, Kvale M, Sakoda L, Banda Y, Kwok P, Risch N, Jorgenson E, Schaefer C. PS3-15: Genome-Wide Association Study of Anxiety Disorders: Early Results from Kaiser Permanente's Research Program on Genes, Environment, and Health (RPGEH) Clinical Medicine & Research. 11: 149-149. DOI: 10.3121/Cmr.2013.1176.Ps3-15 |
0.33 |
|
| 2013 |
Jorgenson E, Sciortino S, Shen L, Ranatunga D, Hoffmann T, Kvale M, Banda Y, Kwok P, Walter L, Risch N, Schaefer C. B4-4: Genome-Wide Association Study of Macular Degeneration: Early Results from the Kaiser Permanente Research Program on Genes, Environment, and Health (RPGEH) Clinical Medicine & Research. 11: 146-147. DOI: 10.3121/Cmr.2013.1176.B4-4 |
0.369 |
|
| 2012 |
Thornton T, Tang H, Hoffmann TJ, Ochs-Balcom HM, Caan BJ, Risch N. Estimating kinship in admixed populations. American Journal of Human Genetics. 91: 122-38. PMID 22748210 DOI: 10.1016/J.Ajhg.2012.05.024 |
0.334 |
|
| 2011 |
Hoffmann TJ, Zhan Y, Kvale MN, Hesselson SE, Gollub J, Iribarren C, Lu Y, Mei G, Purdy MM, Quesenberry C, Rowell S, Shapero MH, Smethurst D, Somkin CP, Van den Eeden SK, ... ... Risch N, et al. Design and coverage of high throughput genotyping arrays optimized for individuals of East Asian, African American, and Latino race/ethnicity using imputation and a novel hybrid SNP selection algorithm. Genomics. 98: 422-30. PMID 21903159 DOI: 10.1016/J.Ygeno.2011.08.007 |
0.305 |
|
| 2011 |
Wynshaw-Boris A, Risch N, Motulsky A. Charles Joseph Epstein, M.D., 1933-2011, in memoriam American Journal of Human Genetics. 88: 684-688. PMID 21805720 DOI: 10.1016/J.Ajhg.2011.05.016 |
0.305 |
|
| 2011 |
Hallmayer J, Cleveland S, Torres A, Phillips J, Cohen B, Torigoe T, Miller J, Fedele A, Collins J, Smith K, Lotspeich L, Croen LA, Ozonoff S, Lajonchere C, Grether JK, ... Risch N, et al. Genetic heritability and shared environmental factors among twin pairs with autism. Archives of General Psychiatry. 68: 1095-102. PMID 21727249 DOI: 10.1001/Archgenpsychiatry.2011.76 |
0.34 |
|
| 2011 |
Hoffmann TJ, Kvale MN, Hesselson SE, Zhan Y, Aquino C, Cao Y, Cawley S, Chung E, Connell S, Eshragh J, Ewing M, Gollub J, Henderson M, Hubbell E, Iribarren C, ... ... Risch N, et al. Next generation genome-wide association tool: design and coverage of a high-throughput European-optimized SNP array. Genomics. 98: 79-89. PMID 21565264 DOI: 10.1016/J.Ygeno.2011.04.005 |
0.324 |
|
| 2011 |
Via M, Gignoux CR, Roth LA, Fejerman L, Galanter J, Choudhry S, Toro-Labrador G, Viera-Vera J, Oleksyk TK, Beckman K, Ziv E, Risch N, Burchard EG, Martínez-Cruzado JC. History shaped the geographic distribution of genomic admixture on the island of Puerto Rico. Plos One. 6: e16513. PMID 21304981 DOI: 10.1371/Journal.Pone.0016513 |
0.34 |
|
| 2011 |
Kornum BR, Kawashima M, Faraco J, Lin L, Rico TJ, Hesselson S, Axtell RC, Kuipers H, Weiner K, Hamacher A, Kassack MU, Han F, Knudsen S, Li J, Dong X, ... ... Risch N, et al. Common variants in P2RY11 are associated with narcolepsy. Nature Genetics. 43: 66-71. PMID 21170044 DOI: 10.1038/Ng.734 |
0.672 |
|
| 2011 |
Kornum BR, Kawashima M, Faraco J, Lin L, Rico TJ, Hesselson S, Axtell RC, Kuipers H, Weiner K, Hamacher A, Kassack MU, Han F, Knudsen S, Li J, Dong X, ... ... Risch N, et al. Erratum: Common variants in P2RY11 are associated with narcolepsy Nature Genetics. 43: 1040-1040. DOI: 10.1038/Ng1011-1040B |
0.657 |
|
| 2010 |
Assimes TL, Hólm H, Kathiresan S, Reilly MP, Thorleifsson G, Voight BF, Erdmann J, Willenborg C, Vaidya D, Xie C, Patterson CC, Morgan TM, Burnett MS, Li M, Hlatky MA, ... ... Risch N, et al. Lack of association between the Trp719Arg polymorphism in kinesin-like protein-6 and coronary artery disease in 19 case-control studies. Journal of the American College of Cardiology. 56: 1552-63. PMID 20933357 DOI: 10.1016/J.Jacc.2010.06.022 |
0.329 |
|
| 2010 |
Peralta CA, Li Y, Wassel C, Choudhry S, Palmas W, Seldin MF, Risch N, Siscovick D, Arnett D, Psaty B, Shlipak MG. Differences in albuminuria between Hispanics and whites: an evaluation by genetic ancestry and country of origin: the multi-ethnic study of atherosclerosis. Circulation. Cardiovascular Genetics. 3: 240-7. PMID 20445135 DOI: 10.1161/Circgenetics.109.914499 |
0.343 |
|
| 2010 |
Lomelin D, Jorgenson E, Risch N. Human genetic variation recognizes functional elements in noncoding sequence. Genome Research. 20: 311-9. PMID 20032171 DOI: 10.1101/Gr.094151.109 |
0.76 |
|
| 2010 |
Ottman R, Risch N. Study of the genetically complex epilepsies Epilepsia. 51: 57. DOI: 10.1111/J.1528-1167.2010.02843.X |
0.325 |
|
| 2009 |
Zakharia F, Basu A, Absher D, Assimes TL, Go AS, Hlatky MA, Iribarren C, Knowles JW, Li J, Narasimhan B, Sidney S, Southwick A, Myers RM, Quertermous T, Risch N, et al. Characterizing the admixed African ancestry of African Americans. Genome Biology. 10: R141. PMID 20025784 DOI: 10.1186/Gb-2009-10-12-R141 |
0.354 |
|
| 2009 |
Risch N, Choudhry S, Via M, Basu A, Sebro R, Eng C, Beckman K, Thyne S, Chapela R, Rodriguez-Santana JR, Rodriguez-Cintron W, Avila PC, Ziv E, Gonzalez Burchard E. Ancestry-related assortative mating in Latino populations. Genome Biology. 10: R132. PMID 19930545 DOI: 10.1186/Gb-2009-10-11-R132 |
0.356 |
|
| 2009 |
Poduri A, Wang Y, Gordon D, Barral-Rodriguez S, Barker-Cummings C, Ulgen A, Chitsazzadeh V, Hill RS, Risch N, Hauser WA, Pedley TA, Walsh CA, Ottman R. Novel susceptibility locus at chromosome 6q16.3-22.31 in a family with GEFS+. Neurology. 73: 1264-72. PMID 19841378 DOI: 10.1212/Wnl.0B013E3181Bd10D3 |
0.35 |
|
| 2009 |
Basu A, Tang H, Arnett D, Gu CC, Mosley T, Kardia S, Luke A, Tayo B, Cooper R, Zhu X, Risch N. Admixture mapping of quantitative trait loci for BMI in African Americans: evidence for loci on chromosomes 3q, 5q, and 15q. Obesity (Silver Spring, Md.). 17: 1226-31. PMID 19584881 DOI: 10.1038/Oby.2009.24 |
0.368 |
|
| 2009 |
Hallmayer J, Faraco J, Lin L, Hesselson S, Winkelmann J, Kawashima M, Mayer G, Plazzi G, Nevsimalova S, Bourgin P, Hong SC, Hong SS, Honda Y, Honda M, Högl B, ... ... Risch N, et al. Narcolepsy is strongly associated with the T-cell receptor alpha locus. Nature Genetics. 41: 708-11. PMID 19412176 DOI: 10.1038/Ng.372 |
0.679 |
|
| 2009 |
Hallmayer J, Faraco J, Lin L, Hesselson S, Winkelmann J, Kawashima M, Mayer G, Plazzi G, Nevsimalova S, Bourgin P, Hong SS, Honda Y, Honda M, Högl B, Longstreth WT, ... ... Risch N, et al. Erratum: Narcolepsy is strongly associated with the T-cell receptor alpha locus Nature Genetics. 41: 859-859. DOI: 10.1038/Ng0709-859B |
0.646 |
|
| 2008 |
Basu A, Tang H, Zhu X, Gu CC, Hanis C, Boerwinkle E, Risch N. Genome-wide distribution of ancestry in Mexican Americans. Human Genetics. 124: 207-14. PMID 18752003 DOI: 10.1007/S00439-008-0541-5 |
0.331 |
|
| 2008 |
Assimes TL, Knowles JW, Basu A, Iribarren C, Southwick A, Tang H, Absher D, Li J, Fair JM, Rubin GD, Sidney S, Fortmann SP, Go AS, Hlatky MA, Myers RM, ... Risch N, et al. Susceptibility locus for clinical and subclinical coronary artery disease at chromosome 9p21 in the multi-ethnic ADVANCE study. Human Molecular Genetics. 17: 2320-8. PMID 18443000 DOI: 10.1093/Hmg/Ddn132 |
0.353 |
|
| 2008 |
Assimes TL, Knowles JW, Priest JR, Basu A, Volcik KA, Southwick A, Tabor HK, Hartiala J, Allayee H, Grove ML, Tabibiazar R, Sidney S, Fortmann SP, Go A, Hlatky M, ... ... Risch N, et al. Common polymorphisms of ALOX5 and ALOX5AP and risk of coronary artery disease. Human Genetics. 123: 399-408. PMID 18369664 DOI: 10.1007/S00439-008-0489-5 |
0.348 |
|
| 2008 |
Zhu X, Tang H, Risch N. Admixture mapping and the role of population structure for localizing disease genes. Advances in Genetics. 60: 547-69. PMID 18358332 DOI: 10.1016/S0065-2660(07)00419-1 |
0.325 |
|
| 2008 |
Assimes TL, Knowles JW, Priest JR, Basu A, Borchert A, Volcik KA, Grove ML, Tabor HK, Southwick A, Tabibiazar R, Sidney S, Boerwinkle E, Go AS, Iribarren C, Hlatky MA, ... ... Risch N, et al. A near null variant of 12/15-LOX encoded by a novel SNP in ALOX15 and the risk of coronary artery disease. Atherosclerosis. 198: 136-44. PMID 17959182 DOI: 10.1016/J.Atherosclerosis.2007.09.003 |
0.336 |
|
| 2007 |
Willer CJ, Dyment DA, Cherny S, Ramagopalan SV, Herrera BM, Morrison KM, Sadovnick AD, Risch NJ, Ebers GC. A genome-wide scan in forty large pedigrees with multiple sclerosis. Journal of Human Genetics. 52: 955-62. PMID 18000641 DOI: 10.1007/S10038-007-0194-6 |
0.3 |
|
| 2007 |
Saunders-Pullman R, Raymond D, Senthil G, Kramer P, Ohmann E, Deligtisch A, Shanker V, Greene P, Tabamo R, Huang N, Tagliati M, Kavanagh P, Soto-Valencia J, Aguiar Pde C, Risch N, et al. Narrowing the DYT6 dystonia region and evidence for locus heterogeneity in the Amish-Mennonites. American Journal of Medical Genetics. Part A. 143: 2098-105. PMID 17702011 DOI: 10.1002/Ajmg.A.31887 |
0.341 |
|
| 2007 |
Dyment DA, Cader MZ, Herrera BM, Ramagopalan SV, Orton SM, Chao M, Willer CJ, Sadovnick AD, Risch N, Ebers GC. A genome scan in a single pedigree with a high prevalence of multiple sclerosis. Journal of Neurology, Neurosurgery, and Psychiatry. 79: 158-62. PMID 17550985 DOI: 10.1136/Jnnp.2007.122705 |
0.362 |
|
| 2006 |
Hsiao CF, Chiu YF, Chiang FT, Ho LT, Lee WJ, Hung YJ, Chen YD, Donlon TA, Jorgenson E, Curb D, Risch N, Hsiung CA. Genome-wide linkage analysis of lipids in nondiabetic Chinese and Japanese from the SAPPHIRe family study. American Journal of Hypertension. 19: 1270-7. PMID 17161774 DOI: 10.1016/J.Amjhyper.2006.05.004 |
0.343 |
|
| 2006 |
Gunderson EP, Tsai AL, Selby JV, Caan B, Mayer-Davis EJ, Risch N. Twins of mistaken zygosity (TOMZ): evidence for genetic contributions to dietary patterns and physiologic traits. Twin Research and Human Genetics : the Official Journal of the International Society For Twin Studies. 9: 540-9. PMID 16899161 DOI: 10.1375/183242706778025053 |
0.343 |
|
| 2006 |
Tang H, Coram M, Wang P, Zhu X, Risch N. Reconstructing genetic ancestry blocks in admixed individuals. American Journal of Human Genetics. 79: 1-12. PMID 16773560 DOI: 10.1086/504302 |
0.353 |
|
| 2006 |
Tang H, Jorgenson E, Gadde M, Kardia SL, Rao DC, Zhu X, Schork NJ, Hanis CL, Risch N. Racial admixture and its impact on BMI and blood pressure in African and Mexican Americans. Human Genetics. 119: 624-33. PMID 16738946 DOI: 10.1007/S00439-006-0175-4 |
0.327 |
|
| 2006 |
Urban TJ, Sebro R, Hurowitz EH, Leabman MK, Badagnani I, Lagpacan LL, Risch N, Giacomini KM. Functional genomics of membrane transporters in human populations. Genome Research. 16: 223-30. PMID 16354753 DOI: 10.1101/Gr.4356206 |
0.345 |
|
| 2006 |
Choudhry S, Coyle NE, Tang H, Salari K, Lind D, Clark SL, Tsai HJ, Naqvi M, Phong A, Ung N, Matallana H, Avila PC, Casal J, Torres A, Nazario S, ... ... Risch N, et al. Population stratification confounds genetic association studies among Latinos. Human Genetics. 118: 652-64. PMID 16283388 DOI: 10.1007/S00439-005-0071-3 |
0.342 |
|
| 2005 |
González Burchard E, Borrell LN, Choudhry S, Naqvi M, Tsai HJ, Rodriguez-Santana JR, Chapela R, Rogers SD, Mei R, Rodriguez-Cintron W, Arena JF, Kittles R, Perez-Stable EJ, Ziv E, Risch N. Latino populations: a unique opportunity for the study of race, genetics, and social environment in epidemiological research. American Journal of Public Health. 95: 2161-8. PMID 16257940 DOI: 10.2105/Ajph.2005.068668 |
0.342 |
|
| 2005 |
Dyment DA, Herrera BM, Cader MZ, Willer CJ, Lincoln MR, Sadovnick AD, Risch N, Ebers GC. Complex interactions among MHC haplotypes in multiple sclerosis: susceptibility and resistance. Human Molecular Genetics. 14: 2019-26. PMID 15930013 DOI: 10.1093/Hmg/Ddi206 |
0.341 |
|
| 2005 |
Chiu YF, Chuang LM, Hsiao CF, Hung YJ, Lin MW, Chen YT, Grove J, Jorgenson E, Quertermous T, Risch N, Hsiung CA. An autosomal genome-wide scan for loci linked to pre-diabetic phenotypes in nondiabetic Chinese subjects from the Stanford Asia-Pacific Program of Hypertension and Insulin Resistance Family Study. Diabetes. 54: 1200-6. PMID 15793262 DOI: 10.2337/Diabetes.54.4.1200 |
0.34 |
|
| 2005 |
Urban TJ, Giacomini KM, Risch N. Haplotype structure and ethnic-specific allele frequencies at the OCTN locus: implications for the genetics of Crohn's disease. Inflammatory Bowel Diseases. 11: 78-9. PMID 15674120 DOI: 10.1097/00054725-200501000-00014 |
0.368 |
|
| 2005 |
Zhu X, Luke A, Cooper RS, Quertermous T, Hanis C, Mosley T, Gu CC, Tang H, Rao DC, Risch N, Weder A. Admixture mapping for hypertension loci with genome-scan markers. Nature Genetics. 37: 177-81. PMID 15665825 DOI: 10.1038/Ng1510 |
0.384 |
|
| 2005 |
Jorgenson E, Tang H, Gadde M, Province M, Leppert M, Kardia S, Schork N, Cooper R, Rao DC, Boerwinkle E, Risch N. Ethnicity and human genetic linkage maps. American Journal of Human Genetics. 76: 276-90. PMID 15627237 DOI: 10.1086/427926 |
0.392 |
|
| 2004 |
Mountain JL, Risch N. Assessing genetic contributions to phenotypic differences among 'racial' and 'ethnic' groups. Nature Genetics. 36: S48-53. PMID 15508003 DOI: 10.1038/Ng1456 |
0.394 |
|
| 2004 |
Dyment DA, Steckley JL, Morrison K, Willer CJ, Cader MZ, DeLuca GC, Sadovnick AD, Risch N, Ebers GC, Paty D, Oger J, Devonshire V, Hashimoto S, Hooge J, Kastrukoff L, et al. TRC β polymorphisms and multiple sclerosis Genes and Immunity. 5: 337-342. PMID 15175643 DOI: 10.1038/Sj.Gene.6364091 |
0.332 |
|
| 2004 |
Dyment DA, Sadovnick AD, Willer CJ, Armstrong H, Cader ZM, Wiltshire S, Kalman B, Risch N, Ebers GC. An extended genome scan in 442 Canadian multiple sclerosis-affected sibships: a report from the Canadian Collaborative Study Group. Human Molecular Genetics. 13: 1005-15. PMID 15069025 DOI: 10.1093/Hmg/Ddh123 |
0.39 |
|
| 2004 |
Li J, Nguyen L, Gleason C, Lotspeich L, Spiker D, Risch N, Myers RM. Lack of evidence for an association between WNT2 and RELN polymorphisms and autism. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 126: 51-7. PMID 15048648 DOI: 10.1002/Ajmg.B.20122 |
0.393 |
|
| 2004 |
Tukel T, Shalata A, Present D, Rachmilewitz D, Mayer L, Grant D, Risch N, Desnick RJ. Crohn disease: frequency and nature of CARD15 mutations in Ashkenazi and Sephardi/Oriental Jewish families. American Journal of Human Genetics. 74: 623-36. PMID 15024686 DOI: 10.1086/382226 |
0.322 |
|
| 2004 |
Risch N. Genetic Analysis Workshop II: multiple-locus segregation analysis incorporating linkage markers. Genetic Epidemiology. 1: 207-11. PMID 14971378 DOI: 10.1002/Gepi.1370010216 |
0.388 |
|
| 2003 |
Merikangas KR, Risch N. Genomic Priorities and Public Health Science. 302: 599-601. PMID 14576422 DOI: 10.1126/Science.1091468 |
0.368 |
|
| 2003 |
Varon R, Gooding R, Steglich C, Marns L, Tang H, Angelicheva D, Yong KK, Ambrugger P, Reinhold A, Morar B, Baas F, Kwa M, Tournev I, Guerguelcheva V, Kremensky I, ... ... Risch N, et al. Partial deficiency of the C-terminal-domain phosphatase of RNA polymerase II is associated with congenital cataracts facial dysmorphism neuropathy syndrome. Nature Genetics. 35: 185-9. PMID 14517542 DOI: 10.1038/Ng1243 |
0.329 |
|
| 2003 |
Leabman MK, Huang CC, DeYoung J, Carlson EJ, Taylor TR, de la Cruz M, Johns SJ, Stryke D, Kawamoto M, Urban TJ, Kroetz DL, Ferrin TE, Clark AG, Risch N, Herskowitz I, et al. Natural variation in human membrane transporter genes reveals evolutionary and functional constraints. Proceedings of the National Academy of Sciences of the United States of America. 100: 5896-901. PMID 12719533 DOI: 10.1073/Pnas.0730857100 |
0.308 |
|
| 2003 |
Merikangas KR, Risch N. Will the genomics revolution revolutionize psychiatry? American Journal of Psychiatry. 160: 625-635. PMID 12668348 DOI: 10.1176/Appi.Ajp.160.4.625 |
0.391 |
|
| 2003 |
Risch N, Tang H, Katzenstein H, Ekstein J. Geographic distribution of disease mutations in the Ashkenazi Jewish population supports genetic drift over selection. American Journal of Human Genetics. 72: 812-22. PMID 12612865 DOI: 10.1086/373882 |
0.317 |
|
| 2003 |
Botstein D, Risch N. Discovering genotypes underlying human phenotypes: past successes for mendelian disease, future approaches for complex disease. Nature Genetics. 33: 228-37. PMID 12610532 DOI: 10.1038/Ng1090 |
0.366 |
|
| 2003 |
Kim UK, Jorgenson E, Coon H, Leppert M, Risch N, Drayna D. Positional cloning of the human quantitative trait locus underlying taste sensitivity to phenylthiocarbamide. Science (New York, N.Y.). 299: 1221-5. PMID 12595690 DOI: 10.1126/Science.1080190 |
0.406 |
|
| 2003 |
Ranade K, Hinds D, Hsiung CA, Chuang LM, Chang MS, Chen YT, Pesich R, Hebert J, Chen YD, Dzau V, Olshen R, Curb D, Botstein D, Cox DR, Risch N. A genome scan for hypertension susceptibility loci in populations of Chinese and Japanese origins. American Journal of Hypertension. 16: 158-62. PMID 12559686 DOI: 10.1016/S0895-7061(02)03245-4 |
0.325 |
|
| 2003 |
Risch N, Tang H. Selection in the Ashkenazi Jewish Population Unlikely—Reply to Zlotogora and Bach The American Journal of Human Genetics. 73: 440-441. DOI: 10.1086/377009 |
0.335 |
|
| 2002 |
Bressman SB, Raymond D, Wendt K, Saunders-Pullman R, De Leon D, Fahn S, Ozelius L, Risch N. Diagnostic criteria for dystonia in DYT1 families. Neurology. 59: 1780-2. PMID 12473770 DOI: 10.1212/01.Wnl.0000035630.12515.E0 |
0.336 |
|
| 2002 |
Shifman S, Bronstein M, Sternfeld M, Pisanté-Shalom A, Lev-Lehman E, Weizman A, Reznik I, Spivak B, Grisaru N, Karp L, Schiffer R, Kotler M, Strous RD, Swartz-Vanetik M, Knobler HY, ... ... Risch N, et al. A highly significant association between a COMT haplotype and schizophrenia. American Journal of Human Genetics. 71: 1296-302. PMID 12402217 DOI: 10.1086/344514 |
0.336 |
|
| 2002 |
Hallmayer J, Glasson EJ, Bower C, Petterson B, Croen L, Grether J, Risch N. On the twin risk in autism. American Journal of Human Genetics. 71: 941-6. PMID 12297988 DOI: 10.1086/342990 |
0.317 |
|
| 2002 |
Risch N, Burchard E, Ziv E, Tang H. Categorization of humans in biomedical research: genes, race and disease. Genome Biology. 3: comment2007. PMID 12184798 DOI: 10.1186/Gb-2002-3-7-Comment2007 |
0.334 |
|
| 2002 |
Dyment DA, Cader MZ, Willer CJ, Risch N, Sadovnick AD, Ebers GC. A multigenerational family with multiple sclerosis. Brain : a Journal of Neurology. 125: 1474-82. PMID 12076998 DOI: 10.1093/Brain/Awf158 |
0.352 |
|
| 2002 |
Dyment DA, Steckley JL, Willer CJ, Armstrong H, Sadovnick AD, Risch N, Ebers GC. No evidence to support CTLA-4 as a susceptibility gene in MS families: the Canadian Collaborative Study Journal of Neuroimmunology. 123: 193-198. PMID 11880164 DOI: 10.1016/S0165-5728(01)00493-3 |
0.349 |
|
| 2002 |
Risch N. Implications of multilocus inheritance for gene-disease association studies. Theoretical Population Biology. 60: 215-20. PMID 11855955 DOI: 10.1006/Tpbi.2001.1538 |
0.369 |
|
| 2002 |
Li J, Tabor HK, Nguyen L, Gleason C, Lotspeich LJ, Spiker D, Risch N, Myers RM. Lack of association between HoxA1 and HoxB1 gene variants and autism in 110 multiplex families. American Journal of Medical Genetics. 114: 24-30. PMID 11840501 DOI: 10.1002/Ajmg.1618 |
0.398 |
|
| 2002 |
Risch N, Piazza A, Cavalli-Sforza LL. Dropped genetics paper lacked scientific merit. Nature. 415: 115. PMID 11805804 DOI: 10.1038/415115B |
0.353 |
|
| 2002 |
Boerwinkle E, Brown CA, Carrejo M, Ferrell R, Hanis C, Hutchinson R, Kardia S, Sing C, Turner S, Weder A, Chakravarti A, Cooper R, Jacob H, NS, Hunt S, ... ... Risch N, et al. Multi-center genetic study of hypertension: The Family blood pressure program (FBPP) Hypertension. 39: 3-9. PMID 11799070 DOI: 10.1161/Hy1201.100415 |
0.314 |
|
| 2002 |
Risch N. Molecular epidemiology of Tay-Sachs disease. Advances in Genetics. 44: 233-52. PMID 11596986 DOI: 10.1016/S0065-2660(01)44083-1 |
0.34 |
|
| 2001 |
Ranade K, Shue WHH, Hung YJ, Hsuing CA, Chiang FT, Pesich R, Hebert J, Olivier M, Chen YDI, Pratt R, Olshen R, Curb D, Botstein D, Risch N, Cox DR. The glycine allele of a glycine/arginine polymorphism in the β2-adrenergic receptor gene is associated with essential hypertension in a population of Chinese origin American Journal of Hypertension. 14: 1196-1200. PMID 11775126 DOI: 10.1016/S0895-7061(01)02213-0 |
0.325 |
|
| 2001 |
Liu JS, Sabatti C, Teng J, Keats BJB, Risch N. Bayesian analysis of haplotypes for linkage disequilibrium mapping Genome Research. 11: 1716-1724. PMID 11591648 DOI: 10.1101/Gr.194801 |
0.323 |
|
| 2001 |
Ranade K, Wu KD, Hwu CM, Ting CT, Pei D, Pesich R, Hebert J, Chen YDI, Pratt R, Olshen R, Masaki K, Risch N, Cox DR, Botstein D. Genetic variation in the human urea transporter-2 is associated with variation in blood pressure Human Molecular Genetics. 10: 2157-2164. PMID 11590132 DOI: 10.1093/Hmg/10.19.2157 |
0.343 |
|
| 2001 |
Dyment DA, Willer CJ, Scott B, Armstrong H, Ligers A, Hillert J, Paty DW, Hashimoto S, Devonshire V, Hooge J, Kastrukoff L, Oger J, Metz L, Warren S, Hader W, ... ... Risch N, et al. Genetic susceptibility to MS: a second stage analysis in Canadian MS families. Neurogenetics. 3: 145-51. PMID 11523565 DOI: 10.1007/S100480100113 |
0.381 |
|
| 2001 |
Ligers A, Dyment DA, Willer CJ, Sadovnick AD, Ebers G, Risch N, Hillert J. Evidence of linkage with HLA-DR in DRB1*15-negative families with multiple sclerosis. American Journal of Human Genetics. 69: 900-3. PMID 11519010 DOI: 10.1086/323480 |
0.327 |
|
| 2001 |
Ranade K, Chang MS, Ting CT, Pei D, Hsiao CF, Olivier M, Pesich R, Hebert J, Chen YDI, Dzau VJ, Curb D, Olshen R, Risch N, Cox DR, Botstein D. High-throughput genotyping with single nucleotide polymorphisms Genome Research. 11: 1262-1268. PMID 11435409 DOI: 10.1101/Gr.157801 |
0.316 |
|
| 2001 |
Glatt CE, DeYoung JA, Delgado S, Service SK, Giacomini KM, Edwards RH, Risch N, Freimer NB. Screening a large reference sample to identify very low frequency sequence variants: comparisons between two genes. Nature Genetics. 27: 435-8. PMID 11279528 DOI: 10.1038/86948 |
0.4 |
|
| 2001 |
Mignot E, Lin L, Rogers W, Honda Y, Qiu X, Lin X, Okun M, Hohjoh H, Miki T, Hsu S, Leffell M, Grumet F, Fernandez-Vina M, Honda M, Risch N. Complex HLA-DR and -DQ interactions confer risk of narcolepsy-cataplexy in three ethnic groups. American Journal of Human Genetics. 68: 686-99. PMID 11179016 DOI: 10.1086/318799 |
0.333 |
|
| 2000 |
Ranade K, Hsuing AC, Wu KD, Chang MS, Chen YT, Hebert J, Chen YDI, Olshen R, Curb D, Dzau V, Botstein D, Cox D, Risch N. Lack of evidence for an association between α-adducin and blood pressure regulation in Asian populations American Journal of Hypertension. 13: 704-709. PMID 10912757 DOI: 10.1016/S0895-7061(00)00238-7 |
0.319 |
|
| 2000 |
Diaz GA, Gelb BD, Risch N, Nygaard TG, Frisch A, Cohen IJ, Sa Miranda C, Amaral O, Maire I, Poenaru L, Caillaud C, Weizberg M, Mistry P, Desnick RJ. Gaucher disease: The origins of the ashkenazi jewish N370S anti 84GG acid β-glucosidase mutations American Journal of Human Genetics. 66: 1821-1832. PMID 10777718 DOI: 10.1086/302946 |
0.327 |
|
| 2000 |
Steckley JL, Dyment DA, Sadovnick AD, Risch N, Hayes C, Ebers GC. Genetic analysis of vitamin D related genes in Canadian multiple sclerosis patients. Canadian Collaborative Study Group. Neurology. 54: 729-32. PMID 10680811 DOI: 10.1212/Wnl.54.3.729 |
0.317 |
|
| 1999 |
Jorgenson E, Hinds D, Risch N. Sib-pair analysis of the collaborative study on the genetics of alcoholism data set. Genetic Epidemiology. 17: S187-91. PMID 10597434 DOI: 10.1002/Gepi.1370170732 |
0.34 |
|
| 1999 |
Salmon B, Hallmayer J, Rogers T, Kalaydjieva L, Petersen PB, Nicholas P, Pingree C, McMahon W, Spiker D, Lotspeich L, Kraemer H, McCague P, Dimiceli S, Nouri N, Pitts T, ... ... Risch N, et al. Absence of linkage and linkage disequilibrium to chromosome 15q11-q13 markers in 139 multiplex families with autism. American Journal of Medical Genetics. 88: 551-6. PMID 10490715 DOI: 10.1002/(SICI)1096-8628(19991015)88:5<551::AID-AJMG21>3.0.CO;2-# |
0.336 |
|
| 1999 |
Rogers T, Kalaydjieva L, Hallmayer J, Petersen PB, Nicholas P, Pingree C, McMahon WM, Spiker D, Lotspeich L, Kraemer H, McCague P, Dimiceli S, Nouri N, Peachy T, Yang J, ... ... Risch N, et al. Exclusion of linkage to the HLA region in ninety multiplex sibships with autism. Journal of Autism and Developmental Disorders. 29: 195-201. PMID 10425582 DOI: 10.1023/A:1023075904742 |
0.414 |
|
| 1999 |
Risch N, Spiker D, Lotspeich L, Nouri N, Hinds D, Hallmayer J, Kalaydjieva L, McCague P, Dimiceli S, Pitts T, Nguyen L, Yang J, Harper C, Thorpe D, Vermeer S, et al. A genomic screen of autism: evidence for a multilocus etiology. American Journal of Human Genetics. 65: 493-507. PMID 10417292 DOI: 10.1086/302497 |
0.369 |
|
| 1999 |
Rice G, Anderson C, Risch N, Ebers G. Male homosexuality: absence of linkage to microsatellite markers at Xq28. Science (New York, N.Y.). 284: 665-7. PMID 10213693 DOI: 10.1126/Science.284.5414.665 |
0.385 |
|
| 1999 |
Teng J, Risch N. The Relative Power of Family-Based and Case-Control Designs for Linkage Disequilibrium Studies of Complex Human Diseases. II. Individual Genotyping Genome Research. 9: 234-241. DOI: 10.1101/Gr.9.3.234 |
0.302 |
|
| 1998 |
Concannon P, Gogolin-Ewens KJ, Hinds DA, Wapelhorst B, Morrison VA, Stirling B, Mitra M, Farmer J, Williams SR, Cox NJ, Bell GI, Risch N, Spielman RS. A second-generation screen of the human genome for susceptibility to insulin-dependent diabetes mellitus. Nature Genetics. 19: 292-6. PMID 9662408 DOI: 10.1038/985 |
0.406 |
|
| 1997 |
Risch N. Haemochromatosis, HFE and genetic complexity. Nature Genetics. 17: 375-6. PMID 9398831 DOI: 10.1038/Ng1297-375 |
0.33 |
|
| 1997 |
Almasy L, Bressman S, de Leon D, Risch N. Ethnic variation in the clinical expression of idiopathic torsion dystonia. Movement Disorders : Official Journal of the Movement Disorder Society. 12: 715-21. PMID 9380054 DOI: 10.1002/Mds.870120515 |
0.323 |
|
| 1997 |
Risch N. Evolving methods in genetic epidemiology. II. Genetic linkage from an epidemiologic perspective. Epidemiologic Reviews. 19: 24-32. PMID 9360899 DOI: 10.1093/Oxfordjournals.Epirev.A017942 |
0.385 |
|
| 1997 |
Mansfield TA, Simon DB, Farfel Z, Bia M, Tucci JR, Lebel M, Gutkin M, Vialettes B, Christofilis MA, Kauppinen-Makelin R, Mayan H, Risch N, Lifton RP. Multilocus linkage of familial hyperkalaemia and hypertension, pseudohypoaldosteronism type II, to chromosomes 1q31-42 and 17p11-q21. Nature Genetics. 16: 202-5. PMID 9171836 DOI: 10.1038/Ng0697-202 |
0.31 |
|
| 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, 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 |
0.363 |
|
| 1997 |
Uhl GR, Gold LH, Risch N. Genetic analyses of complex behavioral disorders. Proceedings of the National Academy of Sciences of the United States of America. 94: 2785-6. PMID 9096294 DOI: 10.1073/Pnas.94.7.2785 |
0.393 |
|
| 1996 |
Risch N, Kidd KK, Tishkoff SA. Response: genetic data and the african origin of humans. Science (New York, N.Y.). 274: 1548b-9b. PMID 17816998 DOI: 10.1126/Science.274.5292.1548B |
0.339 |
|
| 1996 |
Hallmayer J, Hebert JM, Spiker D, Lotspeich L, McMahon WM, Petersen PB, Nicholas P, Pingree C, Lin AA, Cavalli-Sforza LL, Risch N, Ciaranello RD. Autism and the X chromosome. Multipoint sib-pair analysis. Archives of General Psychiatry. 53: 985-9. PMID 8911221 DOI: 10.1001/Archpsyc.1996.01830110021003 |
0.331 |
|
| 1996 |
Devlin B, Risch N, Roeder K. Disequilibrium mapping: composite likelihood for pairwise disequilibrium. Genomics. 36: 1-16. PMID 8812410 DOI: 10.1006/Geno.1996.0419 |
0.344 |
|
| 1996 |
Risch N, Merikangas K. The future of genetic studies of complex human diseases. Science (New York, N.Y.). 273: 1516-7. PMID 8801636 DOI: 10.1126/Science.273.5281.1516 |
0.356 |
|
| 1996 |
Almasy L, Tierney C, Risch N. Use of sibling risk ratios and components of genetic variance in the characterization of a simulated oligogenic disease. Genetic Epidemiology. 12: 565-70. PMID 8787974 DOI: 10.1002/Gepi.1370120607 |
0.344 |
|
| 1996 |
Hauser ER, Boehnke M, Guo SW, Risch N. Affected-sib-pair interval mapping and exclusion for complex genetic traits: Sampling considerations Genetic Epidemiology. 13: 117-137. PMID 8722742 DOI: 10.1002/(Sici)1098-2272(1996)13:2<117::Aid-Gepi1>3.0.Co;2-5 |
0.575 |
|
| 1996 |
Wapelhorst B, Bell GI, Risch N, Spielman RS, Concannon P. Linkage and association studies in insulin-dependent diabetes with a new dinucleotide repeat polymorphism at the GAD65 locus. Autoimmunity. 21: 127-30. PMID 8679901 DOI: 10.3109/08916939508993360 |
0.412 |
|
| 1996 |
Hanis CL, Boerwinkle E, Chakraborty R, Ellsworth DL, Concannon P, Stirling B, Morrison VA, Wapelhorst B, Spielman RS, Gogolin-Ewens KJ, Shephard JM, Williams SR, Risch N, Hinds D, Iwasaki N, et al. A genome-wide search for human non-insulin-dependent (type 2) diabetes genes reveals a major susceptibility locus on chromosome 2 Nature Genetics. 13: 161-166. PMID 8640221 DOI: 10.1038/Ng0696-161 |
0.343 |
|
| 1996 |
Ottman R, Annegers JF, Risch N, Hauser WA, Susser M. Relations of genetic and environmental factors in the etiology of epilepsy Annals of Neurology. 39: 442-449. PMID 8619522 DOI: 10.1002/Ana.410390406 |
0.314 |
|
| 1996 |
Wildenauer DB, Hallmayer J, Schwab SG, Albus M, Eckstein GN, Zill P, Hönig S, Strauss M, Borrmann M, Lichtermann D, Ebstein RP, Lerer B, Risch N, Maier W. Searching for susceptibility genes in schizophrenia by genetic linkage analysis. Cold Spring Harbor Symposia On Quantitative Biology. 61: 845-850. DOI: 10.1101/Sqb.1996.061.01.083 |
0.338 |
|
| 1995 |
Devlin B, Risch N. A comparison of linkage disequilibrium measures for fine-scale mapping Genomics. 29: 311-322. PMID 8666377 DOI: 10.1006/Geno.1995.9003 |
0.349 |
|
| 1995 |
Risch N, Zhang H. Extreme discordant sib pairs for mapping quantitative trait loci in humans. Science (New York, N.Y.). 268: 1584-9. PMID 7777857 DOI: 10.1126/Science.7777857 |
0.341 |
|
| 1995 |
Risch N, de Leon D, Ozelius L, Kramer P, Almasy L, Singer B, Fahn S, Breakefield X, Bressman S. Genetic analysis of idiopathic torsion dystonia in Ashkenazi Jews and their recent descent from a small founder population. Nature Genetics. 9: 152-9. PMID 7719342 DOI: 10.1038/Ng0295-152 |
0.377 |
|
| 1995 |
Tierney C, Merikangas KR, Risch N. Feasibility of half-sibling designs for detecting a genetic component to a disease. Genetic Epidemiology. 11: 523-38. PMID 7713393 DOI: 10.1002/Gepi.1370110608 |
0.323 |
|
| 1995 |
Rowe RE, Wapelhorst B, Bell GI, Risch N, Spielman RS, Concannon P. Linkage and association between insulin-dependent diabetes mellitus (IDDM) susceptibility and markers near the glucokinase gene on chromosome 7. Nature Genetics. 10: 240-2. PMID 7663523 DOI: 10.1038/Ng0695-240 |
0.377 |
|
| 1995 |
Ottman R, Risch N, Hauser WA, Pedley TA, Lee JH, Barker-Cummings C, Lustenberger A, Nagle KJ, Lee KS, Scheuer ML. Localization of a gene for partial epilepsy to chromosome 10q. Nature Genetics. 10: 56-60. PMID 7647791 DOI: 10.1038/Ng0595-56 |
0.361 |
|
| 1995 |
Schwab SG, Albus M, Hallmayer J, Hönig S, Borrmann M, Lichtermann D, Ebstein RP, Ackenheil M, Lerer B, Risch N. Evaluation of a susceptibility gene for schizophrenia on chromosome 6p by multipoint affected sib-pair linkage analysis. Nature Genetics. 11: 325-7. PMID 7581458 DOI: 10.1038/Ng1195-325 |
0.376 |
|
| 1995 |
Risch N, DeLeon D, Fahn S, Bressman S, Ozelius L, Breakefield X, Kramer P, Almasy L, Singer B. Reply to “ITD in Ashkenazi Jews — genetic drift or selection?” Nature Genetics. 11: 14-15. DOI: 10.1038/Ng0995-14 |
0.341 |
|
| 1995 |
Ebers GC, Sadovnick AD, Risch N. Genetic susceptibility to multiple sclerosis Journal of Neuroimmunology. 56: 9-9. DOI: 10.1016/0165-5728(95)98876-D |
0.361 |
|
| 1994 |
Risch N, Merikangas KR. Linkage studies of psychiatric disorders. European Archives of Psychiatry and Clinical Neuroscience. 243: 143-9. PMID 8117757 DOI: 10.1007/Bf02190720 |
0.372 |
|
| 1994 |
Devlin B, Risch N, Roeder K. Comments on the statistical aspects of the NRC's report on DNA typing. Journal of Forensic Sciences. 39: 28-40. PMID 8113709 DOI: 10.1520/Jfs13568J |
0.339 |
|
| 1993 |
Baron M, Freimer NF, Risch N, Lerer B, Alexander JR, Straub RE, Asokan S, Das K, Peterson A, Amos J. Diminished support for linkage between manic depressive illness and X-chromosome markers in three Israeli pedigrees. Nature Genetics. 3: 49-55. PMID 8490654 DOI: 10.1038/Ng0193-49 |
0.342 |
|
| 1993 |
Mitchell LE, Risch N. Correlates of genetic risk for non-syndromic cleft lip with or without cleft palate Clinical Genetics. 43: 255-260. PMID 8375107 DOI: 10.1111/J.1399-0004.1993.Tb03813.X |
0.332 |
|
| 1993 |
Krontiris TG, Devlin B, Karp DD, Robert NJ, Risch N. An association between the risk of cancer and mutations in the HRAS1 minisatellite locus New England Journal of Medicine. 329: 517-523. PMID 8336750 DOI: 10.1056/Nejm199308193290801 |
0.322 |
|
| 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 |
0.489 |
|
| 1993 |
Mitchell LE, Risch N. The Genetics of Infantile Hypertrophic Pyloric Stenosis: A Reanalysis American Journal of Diseases of Children. 147: 1203-1211. PMID 8237916 DOI: 10.1001/Archpedi.1993.02160350077012 |
0.334 |
|
| 1992 |
Claus EB, Giuffra L, Rogers J, Risch N. Genetic relationship between nevus count or nevus density and cutaneous malignant melanoma. Cytogenetics and Cell Genetics. 59: 188-90. PMID 1737496 DOI: 10.1159/000133241 |
0.302 |
|
| 1992 |
Risch N, Sherman S. Genetic Analysis Workshop 7: summary of the melanoma workshop. Cytogenetics and Cell Genetics. 59: 148-58. PMID 1737485 DOI: 10.1159/000133230 |
0.363 |
|
| 1992 |
Risch N, Giuffra L. Model misspecification and multipoint linkage analysis. Human Heredity. 42: 77-92. PMID 1555848 DOI: 10.1159/000154047 |
0.384 |
|
| 1992 |
Risch N. Genetic linkage: interpreting lod scores. Science (New York, N.Y.). 255: 803-4. PMID 1536004 DOI: 10.1126/Science.1536004 |
0.376 |
|
| 1992 |
Breakfield XO, Ozelius L, Kramer P, De Leon D, Bressman S, Risch N, Schuback D, Brin M, Kwiatkowski D, Hewett J, Gasser T, Gusella JF, Fahn S. Principles of molecular genetics/Dystonia Movement Disorders. 7: 2-2. DOI: 10.1002/Mds.870070503 |
0.338 |
|
| 1991 |
Baron M, Hamburger R, Sandkuyl LA, Risch N, Mandel B, Endicott J, Belmaker RH, Ott J. The impact of phenotypic variation on genetic analysis: application to X-linkage in manic-depressive illness. Acta Psychiatrica Scandinavica. 82: 196-203. PMID 2248044 DOI: 10.1111/J.1600-0447.1990.Tb03052.X |
0.385 |
|
| 1990 |
Kramer PL, de Leon D, Ozelius L, Risch N, Bressman SB, Brin MF, Schuback DE, Burke RE, Kwiatkowski DJ, Shale H. Dystonia gene in Ashkenazi Jewish population is located on chromosome 9q32-34. Annals of Neurology. 27: 114-20. PMID 2317008 DOI: 10.1002/Ana.410270203 |
0.35 |
|
| 1990 |
Devlin B, Risch N, Roeder K. No excess of homozygosity at loci used for DNA fingerprinting. Science (New York, N.Y.). 249: 1416-20. PMID 2205919 DOI: 10.1126/Science.2205919 |
0.335 |
|
| 1990 |
Risch N. Genetic linkage and complex diseases, with special reference to psychiatric disorders. Genetic Epidemiology. 7: 3-16; discussion 17-. PMID 2184091 DOI: 10.1002/Gepi.1370070103 |
0.372 |
|
| 1990 |
Risch N. Genetic linkage and complex diseases: A response Genetic Epidemiology. 7: 41-45. DOI: 10.1002/Gepi.1370070111 |
0.347 |
|
| 1989 |
Bressman SB, de Leon D, Brin MF, Risch N, Burke RE, Greene PE, Shale H, Fahn S. Idiopathic dystonia among Ashkenazi Jews: evidence for autosomal dominant inheritance. Annals of Neurology. 26: 612-20. PMID 2817837 DOI: 10.1002/Ana.410260505 |
0.306 |
|
| 1989 |
Rice J, Risch N. Genetic analysis of the affective disorders: summary of GAW5. Genetic Epidemiology. 6: 161-77. PMID 2659428 DOI: 10.1002/Gepi.1370060130 |
0.377 |
|
| 1989 |
Ozelius L, Kramer PL, Moskowitz CB, Kwiatkowski DJ, Brin MF, Bressman SB, Schuback DE, Falk CT, Risch N, de Leon D. Human gene for torsion dystonia located on chromosome 9q32-q34. Neuron. 2: 1427-34. PMID 2576373 DOI: 10.1016/0896-6273(89)90188-8 |
0.333 |
|
| 1989 |
Risch N. Genetics of IDDM: evidence for complex inheritance with HLA. Genetic Epidemiology. 6: 143-8. PMID 2499501 DOI: 10.1002/Gepi.1370060127 |
0.381 |
|
| 1987 |
Risch N, Baron M, Mendlewicz J. Assessing the role of X-linked inheritance in bipolar-related major affective disorder. Journal of Psychiatric Research. 20: 275-88. PMID 3806423 DOI: 10.1016/0022-3956(86)90031-2 |
0.34 |
|
| 1987 |
Baron M, Risch N, Hamburger R, Mandel B, Kushner S, Newman M, Drumer D, Belmaker RH. Genetic linkage between X-chromosome markers and bipolar affective illness. Nature. 326: 289-92. PMID 3493438 DOI: 10.1038/326289A0 |
0.374 |
|
| 1986 |
Risch N. Genetic analysis workshop IV: Summary of the multiple sclerosis workshop Genetic Epidemiology. 3: 369-380. DOI: 10.1002/Gepi.1370030757 |
0.359 |
|
| 1985 |
Risch N, Pringle G. Segregation analysis of human hand preference. Behavior Genetics. 15: 385-400. PMID 4038240 DOI: 10.1007/Bf01070896 |
0.308 |
|
| 1985 |
Baron M, Risch N, Levitt M, Gruen R. Genetic analysis of platelet monoamine oxidase activity in families of schizophrenic patients. Journal of Psychiatric Research. 19: 9-21. PMID 3989738 DOI: 10.1016/0022-3956(85)90064-0 |
0.341 |
|
| 1985 |
Baron M, Risch N, Levitt M, Gruen R. Genetic analysis of plasma amine oxidase activity in schizophrenia. Psychiatry Research. 15: 121-32. PMID 3862144 DOI: 10.1016/0165-1781(85)90048-4 |
0.303 |
|
| 1985 |
Risch N. Genetic analysis workshop III: Simple methods for accurate gene mapping with multipoint data Genetic Epidemiology. 2: 221-222. DOI: 10.1002/Gepi.1370020221 |
0.309 |
|
| 1983 |
Baron M, Risch N, Mendlewicz J. Age at onset in bipolar-related major affective illness: clinical and genetic implications. Journal of Psychiatric Research. 17: 5-18. PMID 7183760 DOI: 10.1016/0022-3956(82)90030-9 |
0.302 |
|
| 1983 |
Baron M, Risch N. X-linkage in affective and schizoaffective disorders: genetic and diagnostic implications. Neuropsychobiology. 8: 304-11. PMID 6984491 DOI: 10.1159/000117916 |
0.327 |
|
| 1983 |
Risch N. A general model for disease-marker association. Annals of Human Genetics. 47: 245-52. PMID 6577811 DOI: 10.1111/J.1469-1809.1983.Tb00992.X |
0.325 |
|
| 1982 |
Risch N, Baron M. X-linkage and genetic heterogeneity in bipolar-related major affective illness: reanalysis of linkage data. Annals of Human Genetics. 46: 153-66. PMID 6985470 DOI: 10.1111/J.1469-1809.1982.Tb00706.X |
0.387 |
|
| 1981 |
Baron M, Rainer JD, Risch N. X-linkage in bipolar affective illness. Perspectives on genetic heterogeneity, pedigree analysis and the X-chromosome map. Journal of Affective Disorders. 3: 141-57. PMID 6454708 DOI: 10.1016/0165-0327(81)90039-2 |
0.379 |
|
| 1980 |
Risch N, Lange K. Application of a recombination model in calculating the variance of sib pair genetic identity. Annals of Human Genetics. 43: 177-86. PMID 525976 DOI: 10.1111/J.1469-1809.1979.Tb02010.X |
0.542 |
|
| 1979 |
Lange K, Risch N. Comments on lack of interference in the four strand model of crossing over. Journal of Mathematical Biology. 5: 55-9. PMID 753907 DOI: 10.1007/BF00275806 |
0.456 |
|
| 1979 |
Risch N, Lange K. An alternative model of recombination and interference. Annals of Human Genetics. 43: 61-70. PMID 496395 DOI: 10.1111/J.1469-1809.1979.Tb01549.X |
0.492 |
|
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