Pericak-Vance MA - Search Results

1

Genome-wide association study implicates a chromosome 12 risk locus for late-onset Alzheimer disease.

Beecham GW, Martin ER, Li YJ, Slifer MA, Gilbert JR, Haines JL, Pericak-Vance MA. Beecham GW, et al. Am J Hum Genet. 2009 Jan;84(1):35-43. doi: 10.1016/j.ajhg.2008.12.008. Am J Hum Genet. 2009. PMID: 19118814 Free PMC article.

2

Genetic evidence for a novel familial Alzheimer's disease locus on chromosome 14.

St George-Hyslop P, Haines J, Rogaev E, Mortilla M, Vaula G, Pericak-Vance M, Foncin JF, Montesi M, Bruni A, Sorbi S, Rainero I, Pinessi L, Pollen D, Polinsky R, Nee L, Kennedy J, Macciardi F, Rogaeva E, Liang Y, Alexandrova N, Lukiw W, Schlumpf K, Tanzi R, Tsuda T, Farrer L, Cantu JM, Duara R, Amaducci L, Bergamini L, Gusella J, Roses A, Crapper McLachlan D, et al. St George-Hyslop P, et al. Nat Genet. 1992 Dec;2(4):330-4. doi: 10.1038/ng1292-330. Nat Genet. 1992. PMID: 1303289 Free article.

3

Regional mapping of facioscapulohumeral muscular dystrophy gene on 4q35: combined analysis of an international consortium.

Sarfarazi M, Wijmenga C, Upadhyaya M, Weiffenbach B, Hyser C, Mathews K, Murray J, Gilbert J, Pericak-Vance M, Lunt P, et al. Sarfarazi M, et al. Am J Hum Genet. 1992 Aug;51(2):396-403. Am J Hum Genet. 1992. PMID: 1642237 Free PMC article.

4

A refined genetic map of the region of chromosome 17 surrounding the von Recklinghausen neurofibromatosis (NF1) gene.

Diehl SR, Boehnke M, Erickson RP, Ploughman LM, Seiler KA, Lieberman JL, Clarke HB, Bruce MA, Schorry EK, Pericak-Vance M, et al. Diehl SR, et al. Am J Hum Genet. 1989 Jan;44(1):33-7. Am J Hum Genet. 1989. PMID: 2491779 Free PMC article.

5

No association between alpha 1-antichymotrypsin and familial Alzheimer's disease.

Haines JL, Pritchard ML, Saunders AM, Schildkraut JM, Growdon JH, Gaskell PC, Farrer LA, Auerbach SA, Gusella JF, Locke PA, Rosi BL, Yamaoka L, Small GW, Conneally PM, Roses AD, Pericak-Vance M. Haines JL, et al. Ann N Y Acad Sci. 1996 Dec 16;802:35-41. doi: 10.1111/j.1749-6632.1996.tb32596.x. Ann N Y Acad Sci. 1996. PMID: 8993482

6

Genome-wide scan for adult onset primary open angle glaucoma.

Wiggs JL, Allingham RR, Hossain A, Kern J, Auguste J, DelBono EA, Broomer B, Graham FL, Hauser M, Pericak-Vance M, Haines JL. Wiggs JL, et al. Hum Mol Genet. 2000 Apr 12;9(7):1109-17. doi: 10.1093/hmg/9.7.1109. Hum Mol Genet. 2000. PMID: 10767336

7

PTPRC (CD45) is not associated with the development of multiple sclerosis in U.S. patients.

Barcellos LF, Caillier S, Dragone L, Elder M, Vittinghoff E, Bucher P, Lincoln RR, Pericak-Vance M, Haines JL, Weiss A, Hauser SL, Oksenberg JR. Barcellos LF, et al. Nat Genet. 2001 Sep;29(1):23-4. doi: 10.1038/ng722. Nat Genet. 2001. PMID: 11528386

8

Ganglioside-induced differentiation-associated protein-1 is mutant in Charcot-Marie-Tooth disease type 4A/8q21.

Baxter RV, Ben Othmane K, Rochelle JM, Stajich JE, Hulette C, Dew-Knight S, Hentati F, Ben Hamida M, Bel S, Stenger JE, Gilbert JR, Pericak-Vance MA, Vance JM. Baxter RV, et al. Nat Genet. 2002 Jan;30(1):21-2. doi: 10.1038/ng796. Epub 2001 Dec 17. Nat Genet. 2002. PMID: 11743579

9

Association of polymorphisms in the apolipoprotein E region with susceptibility to and progression of multiple sclerosis.

Schmidt S, Barcellos LF, DeSombre K, Rimmler JB, Lincoln RR, Bucher P, Saunders AM, Lai E, Martin ER, Vance JM, Oksenberg JR, Hauser SL, Pericak-Vance MA, Haines JL; Multiple Sclerosis Genetics Group. Schmidt S, et al. Am J Hum Genet. 2002 Mar;70(3):708-17. doi: 10.1086/339269. Epub 2002 Feb 11. Am J Hum Genet. 2002. PMID: 11836653 Free PMC article.

10

Genomic screen and follow-up analysis for autistic disorder.

Shao Y, Wolpert CM, Raiford KL, Menold MM, Donnelly SL, Ravan SA, Bass MP, McClain C, von Wendt L, Vance JM, Abramson RH, Wright HH, Ashley-Koch A, Gilbert JR, DeLong RG, Cuccaro ML, Pericak-Vance MA. Shao Y, et al. Am J Med Genet. 2002 Jan 8;114(1):99-105. doi: 10.1002/ajmg.10153. Am J Med Genet. 2002. PMID: 11840513

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