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Items: 1 to 20 of 39

1.

Postmortem Genetic Testing for Sudden Unexpected Death.

Schrodi SJ.

JAMA. 2017 Jan 17;317(3):320-321. doi: 10.1001/jama.2016.19271. No abstract available.

PMID:
28114545
2.

The Decay of Disease Association with Declining Linkage Disequilibrium: A Fine Mapping Theorem.

Maadooliat M, Bansal NK, Upadhya J, Farazi MR, Li X, He MM, Hebbring SJ, Ye Z, Schrodi SJ.

Front Genet. 2016 Dec 12;7:217. doi: 10.3389/fgene.2016.00217. eCollection 2016.

3.

Validation of a metabolite panel for early diagnosis of type 2 diabetes.

Carter TC, Rein D, Padberg I, Peter E, Rennefahrt U, David DE, McManus V, Stefanski E, Martin S, Schatz P, Schrodi SJ.

Metabolism. 2016 Sep;65(9):1399-408. doi: 10.1016/j.metabol.2016.06.007. Epub 2016 Jun 26.

PMID:
27506746
4.

Reflections on the Field of Human Genetics: A Call for Increased Disease Genetics Theory.

Schrodi SJ.

Front Genet. 2016 Jun 8;7:106. doi: 10.3389/fgene.2016.00106. eCollection 2016.

5.

Cell line donor genotype and its influence on experimental phenotype: Toll-like receptor SNPs and potential variability in innate immunity.

Tokarz SA, DeValk J, Luo W, Pattnaik BR, Schrodi SJ, Pillers DA.

Mol Genet Metab. 2016 Jul;118(3):147-52. doi: 10.1016/j.ymgme.2016.04.011. Epub 2016 Apr 22.

PMID:
27324283
6.

The Use of Multiplicity Corrections, Order Statistics and Generalized Family-Wise Statistics with Application to Genome-Wide Studies.

Schrodi SJ.

PLoS One. 2016 Apr 29;11(4):e0154472. doi: 10.1371/journal.pone.0154472. eCollection 2016.

7.

Changes in Gut and Plasma Microbiome following Exercise Challenge in Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS).

Shukla SK, Cook D, Meyer J, Vernon SD, Le T, Clevidence D, Robertson CE, Schrodi SJ, Yale S, Frank DN.

PLoS One. 2015 Dec 18;10(12):e0145453. doi: 10.1371/journal.pone.0145453. eCollection 2015.

8.

Mining Retrospective Data for Virtual Prospective Drug Repurposing: L-DOPA and Age-related Macular Degeneration.

Brilliant MH, Vaziri K, Connor TB Jr, Schwartz SG, Carroll JJ, McCarty CA, Schrodi SJ, Hebbring SJ, Kishor KS, Flynn HW Jr, Moshfeghi AA, Moshfeghi DM, Fini ME, McKay BS.

Am J Med. 2016 Mar;129(3):292-8. doi: 10.1016/j.amjmed.2015.10.015. Epub 2015 Oct 30.

9.

Complex host genetic susceptibility to Staphylococcus aureus infections.

Shukla SK, Rose W, Schrodi SJ.

Trends Microbiol. 2015 Sep;23(9):529-36. doi: 10.1016/j.tim.2015.05.008. Epub 2015 Jun 22. Review.

PMID:
26112911
10.

Differential Lipid Response to Statins Is Associated With Variants in the BUD13-APOA5 Gene Region.

OʼBrien SE, Schrodi SJ, Ye Z, Brilliant MH, Virani SS, Brautbar A.

J Cardiovasc Pharmacol. 2015 Aug;66(2):183-8. doi: 10.1097/FJC.0000000000000261.

11.

Prevalence estimation for monogenic autosomal recessive diseases using population-based genetic data.

Schrodi SJ, DeBarber A, He M, Ye Z, Peissig P, Van Wormer JJ, Haws R, Brilliant MH, Steiner RD.

Hum Genet. 2015 Jun;134(6):659-69. doi: 10.1007/s00439-015-1551-8. Epub 2015 Apr 19.

PMID:
25893794
12.

SeqHBase: a big data toolset for family based sequencing data analysis.

He M, Person TN, Hebbring SJ, Heinzen E, Ye Z, Schrodi SJ, McPherson EW, Lin SM, Peissig PL, Brilliant MH, O'Rawe J, Robison RJ, Lyon GJ, Wang K.

J Med Genet. 2015 Apr;52(4):282-8. doi: 10.1136/jmedgenet-2014-102907. Epub 2015 Jan 13.

13.

Use of an electronic medical record to create the marshfield clinic twin/multiple birth cohort.

Mayer J, Kitchner T, Ye Z, Zhou Z, He M, Schrodi SJ, Hebbring SJ.

Genet Epidemiol. 2014 Dec;38(8):692-8. doi: 10.1002/gepi.21855. Epub 2014 Sep 22.

14.

Phenome-wide association studies (PheWASs) for functional variants.

Ye Z, Mayer J, Ivacic L, Zhou Z, He M, Schrodi SJ, Page D, Brilliant MH, Hebbring SJ.

Eur J Hum Genet. 2015 Apr;23(4):523-9. doi: 10.1038/ejhg.2014.123. Epub 2014 Jul 30.

15.

Genetic-based prediction of disease traits: prediction is very difficult, especially about the future.

Schrodi SJ, Mukherjee S, Shan Y, Tromp G, Sninsky JJ, Callear AP, Carter TC, Ye Z, Haines JL, Brilliant MH, Crane PK, Smelser DT, Elston RC, Weeks DE.

Front Genet. 2014 Jun 2;5:162. doi: 10.3389/fgene.2014.00162. eCollection 2014. Review.

16.

Genome wide association study of SNP-, gene-, and pathway-based approaches to identify genes influencing susceptibility to Staphylococcus aureus infections.

Ye Z, Vasco DA, Carter TC, Brilliant MH, Schrodi SJ, Shukla SK.

Front Genet. 2014 May 9;5:125. doi: 10.3389/fgene.2014.00125. eCollection 2014.

17.

A PheWAS approach in studying HLA-DRB1*1501.

Hebbring SJ, Schrodi SJ, Ye Z, Zhou Z, Page D, Brilliant MH.

Genes Immun. 2013 Apr;14(3):187-91. doi: 10.1038/gene.2013.2. Epub 2013 Feb 7.

18.

Genetic evidence of PTPN22 effects on chronic lymphocytic leukemia.

Hebbring SJ, Slager SL, Epperla N, Mazza JJ, Ye Z, Zhou Z, Achenbach SJ, Vasco DA, Call TG, Rabe KG, Kay NE, Caporaso NE, Lanasa MC, Camp NJ, Strom SS, Goldin LR, Cerhan JR, Brilliant MH, Schrodi SJ.

Blood. 2013 Jan 3;121(1):237-8. doi: 10.1182/blood-2012-08-450221. No abstract available.

19.

Identification of 15 new psoriasis susceptibility loci highlights the role of innate immunity.

Tsoi LC, Spain SL, Knight J, Ellinghaus E, Stuart PE, Capon F, Ding J, Li Y, Tejasvi T, Gudjonsson JE, Kang HM, Allen MH, McManus R, Novelli G, Samuelsson L, Schalkwijk J, Ståhle M, Burden AD, Smith CH, Cork MJ, Estivill X, Bowcock AM, Krueger GG, Weger W, Worthington J, Tazi-Ahnini R, Nestle FO, Hayday A, Hoffmann P, Winkelmann J, Wijmenga C, Langford C, Edkins S, Andrews R, Blackburn H, Strange A, Band G, Pearson RD, Vukcevic D, Spencer CC, Deloukas P, Mrowietz U, Schreiber S, Weidinger S, Koks S, Kingo K, Esko T, Metspalu A, Lim HW, Voorhees JJ, Weichenthal M, Wichmann HE, Chandran V, Rosen CF, Rahman P, Gladman DD, Griffiths CE, Reis A, Kere J; Collaborative Association Study of Psoriasis (CASP).; Genetic Analysis of Psoriasis Consortium.; Psoriasis Association Genetics Extension.; Wellcome Trust Case Control Consortium 2., Nair RP, Franke A, Barker JN, Abecasis GR, Elder JT, Trembath RC.

Nat Genet. 2012 Dec;44(12):1341-8. doi: 10.1038/ng.2467. Epub 2012 Nov 11.

20.

Multiple Loci within the major histocompatibility complex confer risk of psoriasis.

Feng BJ, Sun LD, Soltani-Arabshahi R, Bowcock AM, Nair RP, Stuart P, Elder JT, Schrodi SJ, Begovich AB, Abecasis GR, Zhang XJ, Callis-Duffin KP, Krueger GG, Goldgar DE.

PLoS Genet. 2009 Aug;5(8):e1000606. doi: 10.1371/journal.pgen.1000606. Epub 2009 Aug 14.

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