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Items: 27

1.

Genetic and genomic stability across lymphoblastoid cell line expansions.

Scheinfeldt LB, Hodges K, Pevsner J, Berlin D, Turan N, Gerry NP.

BMC Res Notes. 2018 Aug 3;11(1):558. doi: 10.1186/s13104-018-3664-3.

2.

The molecular epidemiology of Huntington disease is related to intermediate allele frequency and haplotype in the general population.

Kay C, Collins JA, Wright GEB, Baine F, Miedzybrodzka Z, Aminkeng F, Semaka AJ, McDonald C, Davidson M, Madore SJ, Gordon ES, Gerry NP, Cornejo-Olivas M, Squitieri F, Tishkoff S, Greenberg JL, Krause A, Hayden MR.

Am J Med Genet B Neuropsychiatr Genet. 2018 Apr;177(3):346-357. doi: 10.1002/ajmg.b.32618. Epub 2018 Feb 20.

PMID:
29460498
3.

Precision Military Medicine: Conducting a multi-site clinical utility study of genomic and lifestyle risk factors in the United States Air Force.

Delaney SK, Brenner R, Schmidlen TJ, Dempsey MP, London KE, Gordon ES, Bellafante M, Nasuti A, Scheinfeldt LB, Rajula KD, Jose L, Jarvis JP, Gerry NP, Christman MF.

NPJ Genom Med. 2017 Jan 19;2:2. doi: 10.1038/s41525-016-0004-1. eCollection 2017.

4.

Challenges in Translating GWAS Results to Clinical Care.

Scheinfeldt LB, Schmidlen TJ, Gerry NP, Christman MF.

Int J Mol Sci. 2016 Aug 4;17(8). pii: E1267. doi: 10.3390/ijms17081267.

5.

An expanded pharmacogenomics warfarin dosing table with utility in generalised dosing guidance.

Shahabi P, Scheinfeldt LB, Lynch DE, Schmidlen TJ, Perreault S, Keller MA, Kasper R, Wawak L, Jarvis JP, Gerry NP, Gordon ES, Christman MF, Dubé MP, Gharani N.

Thromb Haemost. 2016 Aug 1;116(2):337-48. doi: 10.1160/TH15-12-0955. Epub 2016 Apr 28.

6.

Using the Coriell Personalized Medicine Collaborative Data to conduct a genome-wide association study of sleep duration.

Scheinfeldt LB, Gharani N, Kasper RS, Schmidlen TJ, Gordon ES, Jarvis JP, Delaney S, Kronenthal CJ, Gerry NP, Christman MF.

Am J Med Genet B Neuropsychiatr Genet. 2015 Dec;168(8):697-705. doi: 10.1002/ajmg.b.32362. Epub 2015 Sep 3.

7.

A dynamic database of microarray-characterized cell lines with various cytogenetic and genomic backgrounds.

Tang Z, Berlin DS, Toji L, Toruner GA, Beiswanger C, Kulkarni S, Martin CL, Emanuel BS, Christman M, Gerry NP.

G3 (Bethesda). 2013 Jul 8;3(7):1143-9. doi: 10.1534/g3.113.006577. Erratum in: G3 (Bethesda). 2013 Sep;3(9):1617.

8.

Multiple loci associated with renal function in African Americans.

Shriner D, Herbert A, Doumatey AP, Zhou J, Huang H, Erdos MR, Chen G, Gerry NP, Christman MF, Adeyemo A, Rotimi CN.

PLoS One. 2012;7(9):e45112. doi: 10.1371/journal.pone.0045112. Epub 2012 Sep 13.

9.

Transferability and fine mapping of genome-wide associated loci for lipids in African Americans.

Adeyemo A, Bentley AR, Meilleur KG, Doumatey AP, Chen G, Zhou J, Shriner D, Huang H, Herbert A, Gerry NP, Christman MF, Rotimi CN.

BMC Med Genet. 2012 Sep 21;13:88. doi: 10.1186/1471-2350-13-88.

10.

C-reactive protein (CRP) promoter polymorphisms influence circulating CRP levels in a genome-wide association study of African Americans.

Doumatey AP, Chen G, Tekola Ayele F, Zhou J, Erdos M, Shriner D, Huang H, Adeleye J, Balogun W, Fasanmade O, Johnson T, Oli J, Okafor G, Amoah A, Eghan BA, Agyenim-Boateng K, Acheampong J, Adebamowo C, Gerry NP, Christman MF, Adeyemo A, Rotimi CN.

Hum Mol Genet. 2012 Jul 1;21(13):3063-72. doi: 10.1093/hmg/dds133. Epub 2012 Apr 5.

11.

UGT1A1 is a major locus influencing bilirubin levels in African Americans.

Chen G, Ramos E, Adeyemo A, Shriner D, Zhou J, Doumatey AP, Huang H, Erdos MR, Gerry NP, Herbert A, Bentley AR, Xu H, Charles BA, Christman MF, Rotimi CN.

Eur J Hum Genet. 2012 Apr;20(4):463-8. doi: 10.1038/ejhg.2011.206. Epub 2011 Nov 16.

12.

A genome-wide association study of serum uric acid in African Americans.

Charles BA, Shriner D, Doumatey A, Chen G, Zhou J, Huang H, Herbert A, Gerry NP, Christman MF, Adeyemo A, Rotimi CN.

BMC Med Genomics. 2011 Feb 4;4:17. doi: 10.1186/1755-8794-4-17.

13.

Replication of genome-wide association studies (GWAS) loci for fasting plasma glucose in African-Americans.

Ramos E, Chen G, Shriner D, Doumatey A, Gerry NP, Herbert A, Huang H, Zhou J, Christman MF, Adeyemo A, Rotimi C.

Diabetologia. 2011 Apr;54(4):783-8. doi: 10.1007/s00125-010-2002-7. Epub 2010 Dec 25.

14.

Development of admixture mapping panels for African Americans from commercial high-density SNP arrays.

Chen G, Shriner D, Zhou J, Doumatey A, Huang H, Gerry NP, Herbert A, Christman MF, Chen Y, Dunston GM, Faruque MU, Rotimi CN, Adeyemo A.

BMC Genomics. 2010 Jul 5;11:417. doi: 10.1186/1471-2164-11-417.

15.

Coriell Personalized Medicine Collaborative®: a prospective study of the utility of personalized medicine.

Keller MA, Gordon ES, Stack CB, Gharani N, Sill CJ, Schmidlen TJ, Joseph M, Pallies J, Gerry NP, Christman MF.

Per Med. 2010 May;7(3):301-317. doi: 10.2217/pme.10.13.

PMID:
29776223
16.

Transferability and fine-mapping of genome-wide associated loci for adult height across human populations.

Shriner D, Adeyemo A, Gerry NP, Herbert A, Chen G, Doumatey A, Huang H, Zhou J, Christman MF, Rotimi CN.

PLoS One. 2009 Dec 22;4(12):e8398. doi: 10.1371/journal.pone.0008398.

17.

Gene expression abnormalities in histologically normal breast epithelium of breast cancer patients.

Tripathi A, King C, de la Morenas A, Perry VK, Burke B, Antoine GA, Hirsch EF, Kavanah M, Mendez J, Stone M, Gerry NP, Lenburg ME, Rosenberg CL.

Int J Cancer. 2008 Apr 1;122(7):1557-66.

18.

Open-access database of candidate associations from a genome-wide SNP scan of the Framingham Heart Study.

Herbert A, Lenburg ME, Ulrich D, Gerry NP, Schlauch K, Christman MF.

Nat Genet. 2007 Feb;39(2):135-6. No abstract available.

PMID:
17262019
19.

A common genetic variant is associated with adult and childhood obesity.

Herbert A, Gerry NP, McQueen MB, Heid IM, Pfeufer A, Illig T, Wichmann HE, Meitinger T, Hunter D, Hu FB, Colditz G, Hinney A, Hebebrand J, Koberwitz K, Zhu X, Cooper R, Ardlie K, Lyon H, Hirschhorn JN, Laird NM, Lenburg ME, Lange C, Christman MF.

Science. 2006 Apr 14;312(5771):279-83.

20.

Applications of the universal DNA microarray in molecular medicine.

Favis R, Gerry NP, Cheng YW, Barany F.

Methods Mol Med. 2005;114:25-58.

PMID:
16156096
21.
22.

Harmonized microarray/mutation scanning analysis of TP53 mutations in undissected colorectal tumors.

Favis R, Huang J, Gerry NP, Culliford A, Paty P, Soussi T, Barany F.

Hum Mutat. 2004 Jul;24(1):63-75.

PMID:
15221790
23.

Pharmacogenomic identification of targets for adjuvant therapy with the topoisomerase poison camptothecin.

Carson JP, Zhang N, Frampton GM, Gerry NP, Lenburg ME, Christman MF.

Cancer Res. 2004 Mar 15;64(6):2096-104.

24.

Previously unidentified changes in renal cell carcinoma gene expression identified by parametric analysis of microarray data.

Lenburg ME, Liou LS, Gerry NP, Frampton GM, Cohen HT, Christman MF.

BMC Cancer. 2003 Nov 27;3:31.

25.

Microarray-based detection of select cardiovascular disease markers.

Witowski NE, Leiendecker-Foster C, Gerry NP, McGlennen RC, Barany G.

Biotechniques. 2000 Nov;29(5):936-8, 940, 942 passim. No abstract available.

26.

Universal DNA array detection of small insertions and deletions in BRCA1 and BRCA2.

Favis R, Day JP, Gerry NP, Phelan C, Narod S, Barany F.

Nat Biotechnol. 2000 May;18(5):561-4.

PMID:
10802632
27.

Universal DNA microarray method for multiplex detection of low abundance point mutations.

Gerry NP, Witowski NE, Day J, Hammer RP, Barany G, Barany F.

J Mol Biol. 1999 Sep 17;292(2):251-62.

PMID:
10493873

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