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Page 1
Polymorphisms in the GRIA1 gene region in psychotic bipolar disorder.
Kerner B, Jasinska AJ, DeYoung J, Almonte M, Choi OW, Freimer NB. Kerner B, et al. Among authors: deyoung j. Am J Med Genet B Neuropsychiatr Genet. 2009 Jan 5;150B(1):24-32. doi: 10.1002/ajmg.b.30780. Am J Med Genet B Neuropsychiatr Genet. 2009. PMID: 18484081 Free PMC article.
Genetic and morphological findings in progressive familial intrahepatic cholestasis (Byler disease [PFIC-1] and Byler syndrome): evidence for heterogeneity.
Bull LN, Carlton VE, Stricker NL, Baharloo S, DeYoung JA, Freimer NB, Magid MS, Kahn E, Markowitz J, DiCarlo FJ, McLoughlin L, Boyle JT, Dahms BB, Faught PR, Fitzgerald JF, Piccoli DA, Witzleben CL, O'Connell NC, Setchell KD, Agostini RM Jr, Kocoshis SA, Reyes J, Knisely AS. Bull LN, et al. Among authors: deyoung ja. Hepatology. 1997 Jul;26(1):155-64. doi: 10.1002/hep.510260121. Hepatology. 1997. PMID: 9214465
Fine-resolution mapping by haplotype evaluation: the examples of PFIC1 and BRIC.
Bull LN, Juijn JA, Liao M, van Eijk MJ, Sinke RJ, Stricker NL, DeYoung JA, Carlton VE, Baharloo S, Klomp LW, Abukawa D, Barton DE, Bass NM, Bourke B, Drumm B, Jankowska I, Lovisetto P, McQuaid S, Pawlowska J, Tazawa Y, Villa E, Tygstrup N, Berger R, Knisely AS, Freimer NB, et al. Bull LN, et al. Among authors: deyoung ja. Hum Genet. 1999 Mar;104(3):241-8. doi: 10.1007/pl00008714. Hum Genet. 1999. PMID: 10323248
Hereditary vascular retinopathy, cerebroretinal vasculopathy, and hereditary endotheliopathy with retinopathy, nephropathy, and stroke map to a single locus on chromosome 3p21.1-p21.3.
Ophoff RA, DeYoung J, Service SK, Joosse M, Caffo NA, Sandkuijl LA, Terwindt GM, Haan J, van den Maagdenberg AM, Jen J, Baloh RW, Barilla-LaBarca ML, Saccone NL, Atkinson JP, Ferrari MD, Freimer NB, Frants RR. Ophoff RA, et al. Among authors: deyoung j. Am J Hum Genet. 2001 Aug;69(2):447-53. doi: 10.1086/321975. Epub 2001 Jun 28. Am J Hum Genet. 2001. PMID: 11438888 Free PMC article.
Magnitude and distribution of linkage disequilibrium in population isolates and implications for genome-wide association studies.
Service S, DeYoung J, Karayiorgou M, Roos JL, Pretorious H, Bedoya G, Ospina J, Ruiz-Linares A, Macedo A, Palha JA, Heutink P, Aulchenko Y, Oostra B, van Duijn C, Jarvelin MR, Varilo T, Peddle L, Rahman P, Piras G, Monne M, Murray S, Galver L, Peltonen L, Sabatti C, Collins A, Freimer N. Service S, et al. Among authors: deyoung j. Nat Genet. 2006 May;38(5):556-60. doi: 10.1038/ng1770. Epub 2006 Apr 2. Nat Genet. 2006. PMID: 16582909
Results of a SNP genome screen in a large Costa Rican pedigree segregating for severe bipolar disorder.
Service S, Molina J, Deyoung J, Jawaheer D, Aldana I, Vu T, Araya C, Araya X, Bejarano J, Fournier E, Ramirez M, Mathews CA, Davanzo P, Macaya G, Sandkuijl L, Sabatti C, Reus V, Freimer N. Service S, et al. Among authors: deyoung j. Am J Med Genet B Neuropsychiatr Genet. 2006 Jun 5;141B(4):367-73. doi: 10.1002/ajmg.b.30323. Am J Med Genet B Neuropsychiatr Genet. 2006. PMID: 16652356
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