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Full-genome scan for linkage in 50 families segregating the bipolar affective disease phenotype.
Friddle C, Koskela R, Ranade K, Hebert J, Cargill M, Clark CD, McInnis M, Simpson S, McMahon F, Stine OC, Meyers D, Xu J, MacKinnon D, Swift-Scanlan T, Jamison K, Folstein S, Daly M, Kruglyak L, Marr T, DePaulo JR, Botstein D. Friddle C, et al. Among authors: meyers d. Am J Hum Genet. 2000 Jan;66(1):205-15. doi: 10.1086/302697. Am J Hum Genet. 2000. PMID: 10631152 Free PMC article.
Initial genomic scan of the NIMH genetics initiative bipolar pedigrees: chromosomes 3, 5, 15, 16, 17, and 22.
Edenberg HJ, Foroud T, Conneally PM, Sorbel JJ, Carr K, Crose C, Willig C, Zhao J, Miller M, Bowman E, Mayeda A, Rau NL, Smiley C, Rice JP, Goate A, Reich T, Stine OC, McMahon F, DePaulo JR, Meyers D, Detera-Wadleigh SD, Goldin LR, Gershon ES, Blehar MC, Nurnberger JI Jr. Edenberg HJ, et al. Among authors: meyers d. Am J Med Genet. 1997 May 31;74(3):238-46. Am J Med Genet. 1997. PMID: 9184305
Evidence for a prostate cancer susceptibility locus on the X chromosome.
Xu J, Meyers D, Freije D, Isaacs S, Wiley K, Nusskern D, Ewing C, Wilkens E, Bujnovszky P, Bova GS, Walsh P, Isaacs W, Schleutker J, Matikainen M, Tammela T, Visakorpi T, Kallioniemi OP, Berry R, Schaid D, French A, McDonnell S, Schroeder J, Blute M, Thibodeau S, Grönberg H, Emanuelsson M, Damber JE, Bergh A, Jonsson BA, Smith J, Bailey-Wilson J, Carpten J, Stephan D, Gillanders E, Amundson I, Kainu T, Freas-Lutz D, Baffoe-Bonnie A, Van Aucken A, Sood R, Collins F, Brownstein M, Trent J. Xu J, et al. Among authors: meyers d. Nat Genet. 1998 Oct;20(2):175-9. doi: 10.1038/2477. Nat Genet. 1998. PMID: 9771711
Description of the Genetic Analysis Workshop 10 bipolar disorder linkage data sets.
Goldin LR, Gershon ES, Berrettini WH, Stine OC, DePaulo R, McMahon F, Meyers D, Nothen M, Propping P, Cichon S, Fimmers R, Baur M, Albus M, Franzek E, Kreiner R, Maier W, Rietschel M, Baron M, Knowles J, Gilliam C, Endicott J, Gurling H, Curtis D, Smyth C, Kelsoe J. Goldin LR, et al. Among authors: meyers d. Genet Epidemiol. 1997;14(6):563-8. doi: 10.1002/(SICI)1098-2272(1997)14:6<563::AID-GEPI2>3.0.CO;2-0. Genet Epidemiol. 1997. PMID: 9433543 No abstract available.
Germline mutations in the ribonuclease L gene in families showing linkage with HPC1.
Carpten J, Nupponen N, Isaacs S, Sood R, Robbins C, Xu J, Faruque M, Moses T, Ewing C, Gillanders E, Hu P, Bujnovszky P, Makalowska I, Baffoe-Bonnie A, Faith D, Smith J, Stephan D, Wiley K, Brownstein M, Gildea D, Kelly B, Jenkins R, Hostetter G, Matikainen M, Schleutker J, Klinger K, Connors T, Xiang Y, Wang Z, De Marzo A, Papadopoulos N, Kallioniemi OP, Burk R, Meyers D, Grönberg H, Meltzer P, Silverman R, Bailey-Wilson J, Walsh P, Isaacs W, Trent J. Carpten J, et al. Among authors: meyers d. Nat Genet. 2002 Feb;30(2):181-4. doi: 10.1038/ng823. Epub 2002 Jan 22. Nat Genet. 2002. PMID: 11799394
1,071 results