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Results: 1 to 20 of 61

1.

Correcting systematic inflation in genetic association tests that consider interaction effects: application to a genome-wide association study of posttraumatic stress disorder.

Almli LM, Duncan R, Feng H, Ghosh D, Binder EB, Bradley B, Ressler KJ, Conneely KN, Epstein MP.

JAMA Psychiatry. 2014 Dec 1;71(12):1392-9. doi: 10.1001/jamapsychiatry.2014.1339.

PMID:
25354142
[PubMed - in process]
Free PMC Article
2.

Flexible and robust methods for rare-variant testing of quantitative traits in trios and nuclear families.

Jiang Y, Conneely KN, Epstein MP.

Genet Epidemiol. 2014 Sep;38(6):542-51. doi: 10.1002/gepi.21839. Epub 2014 Jul 14.

PMID:
25044337
[PubMed - indexed for MEDLINE]
Free PMC Article
3.

Analysis of gene-gene interactions using gene-trait similarity regression.

Wang X, Epstein MP, Tzeng JY.

Hum Hered. 2014;78(1):17-26. doi: 10.1159/000360161. Epub 2014 Jun 21.

PMID:
24969398
[PubMed - in process]
4.

Utilizing population controls in rare-variant case-parent association tests.

Jiang Y, Satten GA, Han Y, Epstein MP, Heinzen EL, Goldstein DB, Allen AS.

Am J Hum Genet. 2014 Jun 5;94(6):845-53. doi: 10.1016/j.ajhg.2014.04.014. Epub 2014 May 15.

PMID:
24836453
[PubMed - indexed for MEDLINE]
Free PMC Article
5.

Accounting for population stratification in DNA methylation studies.

Barfield RT, Almli LM, Kilaru V, Smith AK, Mercer KB, Duncan R, Klengel T, Mehta D, Binder EB, Epstein MP, Ressler KJ, Conneely KN.

Genet Epidemiol. 2014 Apr;38(3):231-41. doi: 10.1002/gepi.21789. Epub 2014 Jan 29.

PMID:
24478250
[PubMed - indexed for MEDLINE]
Free PMC Article
6.

Meta-analysis confirms association between TNFA-G238A variant and JIA, and between PTPN22-C1858T variant and oligoarticular, RF-polyarticular and RF-positive polyarticular JIA.

Kaalla MJ, Broadaway KA, Rohani-Pichavant M, Conneely KN, Whiting A, Ponder L, Okou DT, Angeles-Han S, Rouster-Stevens K, Brown MR, Vogler LB, Jorde LB, Bohnsack JF, Epstein MP, Prahalad S.

Pediatr Rheumatol Online J. 2013 Oct 25;11(1):40. doi: 10.1186/1546-0096-11-40.

PMID:
24160187
[PubMed]
Free PMC Article
7.

De novo mutations in epileptic encephalopathies.

Epi4K Consortium; Epilepsy Phenome/Genome Project, Allen AS, Berkovic SF, Cossette P, Delanty N, Dlugos D, Eichler EE, Epstein MP, Glauser T, Goldstein DB, Han Y, Heinzen EL, Hitomi Y, Howell KB, Johnson MR, Kuzniecky R, Lowenstein DH, Lu YF, Madou MR, Marson AG, Mefford HC, Esmaeeli Nieh S, O'Brien TJ, Ottman R, Petrovski S, Poduri A, Ruzzo EK, Scheffer IE, Sherr EH, Yuskaitis CJ, Abou-Khalil B, Alldredge BK, Bautista JF, Berkovic SF, Boro A, Cascino GD, Consalvo D, Crumrine P, Devinsky O, Dlugos D, Epstein MP, Fiol M, Fountain NB, French J, Friedman D, Geller EB, Glauser T, Glynn S, Haut SR, Hayward J, Helmers SL, Joshi S, Kanner A, Kirsch HE, Knowlton RC, Kossoff EH, Kuperman R, Kuzniecky R, Lowenstein DH, McGuire SM, Motika PV, Novotny EJ, Ottman R, Paolicchi JM, Parent JM, Park K, Poduri A, Scheffer IE, Shellhaas RA, Sherr EH, Shih JJ, Singh R, Sirven J, Smith MC, Sullivan J, Lin Thio L, Venkat A, Vining EP, Von Allmen GK, Weisenberg JL, Widdess-Walsh P, Winawer MR.

Nature. 2013 Sep 12;501(7466):217-21. doi: 10.1038/nature12439. Epub 2013 Aug 11.

PMID:
23934111
[PubMed - indexed for MEDLINE]
Free PMC Article
8.

Assessing the impact of population stratification on association studies of rare variation.

Jiang Y, Epstein MP, Conneely KN.

Hum Hered. 2013;76(1):28-35. doi: 10.1159/000353270. Epub 2013 Jul 31.

PMID:
23921847
[PubMed - indexed for MEDLINE]
9.

Modifiers of ovarian function in girls and women with classic galactosemia.

Spencer JB, Badik JR, Ryan EL, Gleason TJ, Broadaway KA, Epstein MP, Fridovich-Keil JL.

J Clin Endocrinol Metab. 2013 Jul;98(7):E1257-65. doi: 10.1210/jc.2013-1374. Epub 2013 May 20.

PMID:
23690308
[PubMed - indexed for MEDLINE]
Free PMC Article
10.

Cryptic residual GALT activity is a potential modifier of scholastic outcome in school age children with classic galactosemia.

Ryan EL, Lynch ME, Taddeo E, Gleason TJ, Epstein MP, Fridovich-Keil JL.

J Inherit Metab Dis. 2013 Nov;36(6):1049-61. doi: 10.1007/s10545-012-9575-x. Epub 2013 Jan 15.

PMID:
23319291
[PubMed - indexed for MEDLINE]
Free PMC Article
11.

SNP set association analysis for familial data.

Schifano ED, Epstein MP, Bielak LF, Jhun MA, Kardia SL, Peyser PA, Lin X.

Genet Epidemiol. 2012 Dec;36(8):797-810. doi: 10.1002/gepi.21676. Epub 2012 Sep 11.

PMID:
22968922
[PubMed - in process]
Free PMC Article
12.

A permutation procedure to correct for confounders in case-control studies, including tests of rare variation.

Epstein MP, Duncan R, Jiang Y, Conneely KN, Allen AS, Satten GA.

Am J Hum Genet. 2012 Aug 10;91(2):215-23. doi: 10.1016/j.ajhg.2012.06.004. Epub 2012 Jul 19.

PMID:
22818855
[PubMed - indexed for MEDLINE]
Free PMC Article
13.

Stratification-score matching improves correction for confounding by population stratification in case-control association studies.

Epstein MP, Duncan R, Broadaway KA, He M, Allen AS, Satten GA.

Genet Epidemiol. 2012 Apr;36(3):195-205. doi: 10.1002/gepi.21611.

PMID:
22714934
[PubMed - indexed for MEDLINE]
Free PMC Article
14.

Families or Unrelated: The Evolving Debate in Genetic Association Studies.

Fardo DW, Charnigo R, Epstein MP.

J Biom Biostat. 2012 Jun 1;3(4):e108.

PMID:
25077036
[PubMed]
Free PMC Article
15.

Depression and anxiety symptoms among women who carry the FMR1 premutation: impact of raising a child with fragile X syndrome is moderated by CRHR1 polymorphisms.

Hunter JE, Leslie M, Novak G, Hamilton D, Shubeck L, Charen K, Abramowitz A, Epstein MP, Lori A, Binder E, Cubells JF, Sherman SL.

Am J Med Genet B Neuropsychiatr Genet. 2012 Jul;159B(5):549-59. doi: 10.1002/ajmg.b.32061. Epub 2012 May 9.

PMID:
22573456
[PubMed - indexed for MEDLINE]
Free PMC Article
16.

Sparse principal component analysis for identifying ancestry-informative markers in genome-wide association studies.

Lee S, Epstein MP, Duncan R, Lin X.

Genet Epidemiol. 2012 May;36(4):293-302. doi: 10.1002/gepi.21621. Epub 2012 Apr 16.

PMID:
22508067
[PubMed - indexed for MEDLINE]
Free PMC Article
17.

The FMR1 premutation and attention-deficit hyperactivity disorder (ADHD): evidence for a complex inheritance.

Hunter JE, Epstein MP, Tinker SW, Abramowitz A, Sherman SL.

Behav Genet. 2012 May;42(3):415-22. doi: 10.1007/s10519-011-9520-z. Epub 2011 Nov 19.

PMID:
22101959
[PubMed - indexed for MEDLINE]
Free PMC Article
18.

Ovarian function in Duarte galactosemia.

Badik JR, Casta├▒eda U, Gleason TJ, Spencer JB, Epstein MP, Ficicioglu C, Fitzgerald K, Fridovich-Keil JL.

Fertil Steril. 2011 Aug;96(2):469-473.e1. doi: 10.1016/j.fertnstert.2011.05.088. Epub 2011 Jun 29.

PMID:
21719007
[PubMed - indexed for MEDLINE]
Free PMC Article
19.

Association of a polymorphism in the indoleamine- 2,3-dioxygenase gene and interferon-╬▒-induced depression in patients with chronic hepatitis C.

Smith AK, Simon JS, Gustafson EL, Noviello S, Cubells JF, Epstein MP, Devlin DJ, Qiu P, Albrecht JK, Brass CA, Sulkowski MS, McHutchinson JG, Miller AH.

Mol Psychiatry. 2012 Jul;17(8):781-9. doi: 10.1038/mp.2011.67. Epub 2011 Jun 21.

PMID:
21691274
[PubMed - indexed for MEDLINE]
Free PMC Article
20.

Associations of progesterone receptor polymorphisms with age at menarche and menstrual cycle length.

Taylor KC, Small CM, Epstein MP, Sherman SL, Tang W, Wilson MM, Bouzyk M, Marcus M.

Horm Res Paediatr. 2010;74(6):421-7. doi: 10.1159/000316961. Epub 2010 Sep 2.

PMID:
20814185
[PubMed - indexed for MEDLINE]
Free PMC Article

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