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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: simpson s. Am J Hum Genet. 2000 Jan;66(1):205-15. doi: 10.1086/302697. Am J Hum Genet. 2000. PMID: 10631152 Free PMC article.
Suggestive evidence of a locus on chromosome 10p using the NIMH genetics initiative bipolar affective disorder pedigrees.
Foroud T, Castelluccio PF, Koller DL, Edenberg HJ, Miller M, Bowman E, Rau NL, Smiley C, Rice JP, Goate A, Armstrong C, Bierut LJ, Reich T, Detera-Wadleigh SD, Goldin LR, Badner JA, Guroff JJ, Gershon ES, McMahon FJ, Simpson S, MacKinnon D, McInnis M, Stine OC, DePaulo JR, Blehar MC, Nurnberger JI Jr. Foroud T, et al. Among authors: simpson s. Am J Med Genet. 2000 Feb 7;96(1):18-23. Am J Med Genet. 2000. PMID: 10686547
Linkage in a family with X-linked Charcot-Marie-Tooth disease.
Haites N, Fairweather N, Clark C, Kelly KF, Simpson S, Johnston AW. Haites N, et al. Among authors: simpson s. Clin Genet. 1989 Jun;35(6):399-403. doi: 10.1111/j.1399-0004.1989.tb02964.x. Clin Genet. 1989. PMID: 2567643
Family-based association of YWHAH in psychotic bipolar disorder.
Grover D, Verma R, Goes FS, Mahon PL, Gershon ES, McMahon FJ, Potash JB; NIMH Genetics Initiative Bipolar Disorder Collaborative, Bipolar Disorder Phenome Group; Gershon ES, McMahon FJ, Potash JB. Grover D, et al. Am J Med Genet B Neuropsychiatr Genet. 2009 Oct 5;150B(7):977-83. doi: 10.1002/ajmg.b.30927. Am J Med Genet B Neuropsychiatr Genet. 2009. PMID: 19160447 Free PMC article.
Allelic and locus heterogeneity in inherited venous malformations.
Calvert JT, Riney TJ, Kontos CD, Cha EH, Prieto VG, Shea CR, Berg JN, Nevin NC, Simpson SA, Pasyk KA, Speer MC, Peters KG, Marchuk DA. Calvert JT, et al. Among authors: simpson sa. Hum Mol Genet. 1999 Jul;8(7):1279-89. doi: 10.1093/hmg/8.7.1279. Hum Mol Genet. 1999. PMID: 10369874
Huntington disease in black African populations.
Scrimgeour EM, Simpson SA. Scrimgeour EM, et al. Among authors: simpson sa. Hum Genet. 1992 Sep-Oct;90(1-2):186-7. doi: 10.1007/BF00210775. Hum Genet. 1992. PMID: 1427779 No abstract available.
2,656 results