Page GP - Search Results

1

The quantitative LOD score: test statistic and sample size for exclusion and linkage of quantitative traits in human sibships.

Page GP, Amos CI, Boerwinkle E. Page GP, et al. Am J Hum Genet. 1998 Apr;62(4):962-8. doi: 10.1086/301783. Am J Hum Genet. 1998. PMID: 9529341 Free PMC article.

2

Polymorphic markers in apolipoprotein C-III gene flanking regions and hypertriglyceridemia.

Surguchov AP, Page GP, Smith L, Patsch W, Boerwinkle E. Surguchov AP, et al. Among authors: page gp. Arterioscler Thromb Vasc Biol. 1996 Aug;16(8):941-7. doi: 10.1161/01.atv.16.8.941. Arterioscler Thromb Vasc Biol. 1996. PMID: 8696957

3

Comparison of linkage-disequilibrium methods for localization of genes influencing quantitative traits in humans.

Page GP, Amos CI. Page GP, et al. Am J Hum Genet. 1999 Apr;64(4):1194-205. doi: 10.1086/302331. Am J Hum Genet. 1999. PMID: 10090905 Free PMC article.

4

Assessing linkage of monoamine oxidase B in a genome-wide scan using a univariate variance components approach.

Barnholtz JS, de Andrade M, Page GP, King TM, Peterson LE, Amos CI. Barnholtz JS, et al. Among authors: page gp. Genet Epidemiol. 1999;17 Suppl 1:S49-54. doi: 10.1002/gepi.1370170709. Genet Epidemiol. 1999. PMID: 10597411

5

Genome scans for genetic predisposition to alcoholism by use of transmission disequilibrium test analyses.

Page GP, King TM, Barnholtz JS, de Andrade M, Peterson LE, Amos CI. Page GP, et al. Genet Epidemiol. 1999;17 Suppl 1:S277-81. doi: 10.1002/gepi.1370170747. Genet Epidemiol. 1999. PMID: 10597449

6

A genome-wide search for susceptibility genes linked to alcohol dependence.

Peterson LE, Barnholtz JS, Page GP, King TM, de Andrade M, Amos CI. Peterson LE, et al. Among authors: page gp. Genet Epidemiol. 1999;17 Suppl 1:S295-300. doi: 10.1002/gepi.1370170750. Genet Epidemiol. 1999. PMID: 10597452

7

Cost of linkage versus association methods.

Amos CI, Page G. Amos CI, et al. Adv Genet. 2001;42:213-21. doi: 10.1016/s0065-2660(01)42024-4. Adv Genet. 2001. PMID: 11037323

8

Evidence for linkage and association with reading disability on 6p21.3-22.

Kaplan DE, Gayán J, Ahn J, Won TW, Pauls D, Olson RK, DeFries JC, Wood F, Pennington BF, Page GP, Smith SD, Gruen JR. Kaplan DE, et al. Among authors: page gp. Am J Hum Genet. 2002 May;70(5):1287-98. doi: 10.1086/340449. Epub 2002 Apr 10. Am J Hum Genet. 2002. PMID: 11951179 Free PMC article.

9

De novo mutations across 1,465 diverse genomes reveal mutational insights and reductions in the Amish founder population.

Kessler MD, Loesch DP, Perry JA, Heard-Costa NL, Taliun D, Cade BE, Wang H, Daya M, Ziniti J, Datta S, Celedón JC, Soto-Quiros ME, Avila L, Weiss ST, Barnes K, Redline SS, Vasan RS, Johnson AD, Mathias RA, Hernandez R, Wilson JG, Nickerson DA, Abecasis G, Browning SR, Zöllner S, O'Connell JR, Mitchell BD; National Heart, Lung, and Blood Institute Trans-Omics for Precision Medicine (TOPMed) Consortium; TOPMed Population Genetics Working Group; O'Connor TD. Kessler MD, et al. Proc Natl Acad Sci U S A. 2020 Feb 4;117(5):2560-2569. doi: 10.1073/pnas.1902766117. Epub 2020 Jan 21. Proc Natl Acad Sci U S A. 2020. PMID: 31964835 Free PMC article.

10

Familial analysis of event related potentials.

King TM, Barnholtz J, Page GP. King TM, et al. Among authors: page gp. Genet Epidemiol. 1999;17 Suppl 1:S199-204. doi: 10.1002/gepi.1370170734. Genet Epidemiol. 1999. PMID: 10597436

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