Display Settings:

Format
Items per page
Sort by

Send to:

Choose Destination

Results: 1 to 20 of 80

1.

Estimation of the multiple testing burden for genomewide association studies of nearly all common variants.

Pe'er I, Yelensky R, Altshuler D, Daly MJ.

Genet Epidemiol. 2008 May;32(4):381-5. doi: 10.1002/gepi.20303.

PMID:
18348202
[PubMed - indexed for MEDLINE]
2.

A multiple testing correction method for genetic association studies using correlated single nucleotide polymorphisms.

Gao X, Starmer J, Martin ER.

Genet Epidemiol. 2008 May;32(4):361-9. doi: 10.1002/gepi.20310.

PMID:
18271029
[PubMed - indexed for MEDLINE]
3.

Geography and genography: prediction of continental origin using randomly selected single nucleotide polymorphisms.

Allocco DJ, Song Q, Gibbons GH, Ramoni MF, Kohane IS.

BMC Genomics. 2007 Mar 10;8:68.

PMID:
17349058
[PubMed - indexed for MEDLINE]
Free PMC Article
4.

Variants of DENND1B associated with asthma in children.

Sleiman PM, Flory J, Imielinski M, Bradfield JP, Annaiah K, Willis-Owen SA, Wang K, Rafaels NM, Michel S, Bonnelykke K, Zhang H, Kim CE, Frackelton EC, Glessner JT, Hou C, Otieno FG, Santa E, Thomas K, Smith RM, Glaberson WR, Garris M, Chiavacci RM, Beaty TH, Ruczinski I, Orange JS, Allen J, Spergel JM, Grundmeier R, Mathias RA, Christie JD, von Mutius E, Cookson WO, Kabesch M, Moffatt MF, Grunstein MM, Barnes KC, Devoto M, Magnusson M, Li H, Grant SF, Bisgaard H, Hakonarson H.

N Engl J Med. 2010 Jan 7;362(1):36-44. doi: 10.1056/NEJMoa0901867. Epub 2009 Dec 23. Erratum in: N Engl J Med. 2012 Feb 16;366(7):672. Orange, Jordan M [corrected to Orange, Jordan S]. N Engl J Med. 2010 Sep 2;363(10):994.

PMID:
20032318
[PubMed - indexed for MEDLINE]
Free Article
5.

Similarity in recombination rate and linkage disequilibrium at CYP2C and CYP2D cytochrome P450 gene regions among Europeans indicates signs of selection and no advantage of using tagSNPs in population isolates.

Pimenoff VN, Laval G, Comas D, Palo JU, Gut I, Cann H, Excoffier L, Sajantila A.

Pharmacogenet Genomics. 2012 Dec;22(12):846-57. doi: 10.1097/FPC.0b013e32835a3a6d.

PMID:
23089684
[PubMed - indexed for MEDLINE]
6.

Efficient computation of significance levels for multiple associations in large studies of correlated data, including genomewide association studies.

Dudbridge F, Koeleman BP.

Am J Hum Genet. 2004 Sep;75(3):424-35. Epub 2004 Jul 19.

PMID:
15266393
[PubMed - indexed for MEDLINE]
Free PMC Article
7.

A genomewide admixture mapping panel for Hispanic/Latino populations.

Mao X, Bigham AW, Mei R, Gutierrez G, Weiss KM, Brutsaert TD, Leon-Velarde F, Moore LG, Vargas E, McKeigue PM, Shriver MD, Parra EJ.

Am J Hum Genet. 2007 Jun;80(6):1171-8. Epub 2007 Apr 20.

PMID:
17503334
[PubMed - indexed for MEDLINE]
Free PMC Article
8.

Common variants in Mendelian kidney disease genes and their association with renal function.

Parsa A, Fuchsberger C, Köttgen A, O'Seaghdha CM, Pattaro C, de Andrade M, Chasman DI, Teumer A, Endlich K, Olden M, Chen MH, Tin A, Kim YJ, Taliun D, Li M, Feitosa M, Gorski M, Yang Q, Hundertmark C, Foster MC, Glazer N, Isaacs A, Rao M, Smith AV, O'Connell JR, Struchalin M, Tanaka T, Li G, Hwang SJ, Atkinson EJ, Lohman K, Cornelis MC, Johansson A, Tönjes A, Dehghan A, Couraki V, Holliday EG, Sorice R, Kutalik Z, Lehtimäki T, Esko T, Deshmukh H, Ulivi S, Chu AY, Murgia F, Trompet S, Imboden M, Kollerits B, Pistis G, Harris TB, Launer LJ, Aspelund T, Eiriksdottir G, Mitchell BD, Boerwinkle E, Schmidt H, Hofer E, Hu F, Demirkan A, Oostra BA, Turner ST, Ding J, Andrews JS, Freedman BI, Giulianini F, Koenig W, Illig T, Döring A, Wichmann HE, Zgaga L, Zemunik T, Boban M, Minelli C, Wheeler HE, Igl W, Zaboli G, Wild SH, Wright AF, Campbell H, Ellinghaus D, Nöthlings U, Jacobs G, Biffar R, Ernst F, Homuth G, Kroemer HK, Nauck M, Stracke S, Völker U, Völzke H, Kovacs P, Stumvoll M, Mägi R, Hofman A, Uitterlinden AG, Rivadeneira F, Aulchenko YS, Polasek O, Hastie N, Vitart V, Helmer C, Wang JJ, Stengel B, Ruggiero D, Bergmann S, Kähönen M, Viikari J, Nikopensius T, Province M, Colhoun H, Doney A, Robino A, Krämer BK, Portas L, Ford I, Buckley BM, Adam M, Thun GA, Paulweber B, Haun M, Sala C, Mitchell P, Ciullo M, Vollenweider P, Raitakari O, Metspalu A, Palmer C, Gasparini P, Pirastu M, Jukema JW, Probst-Hensch NM, Kronenberg F, Toniolo D, Gudnason V, Shuldiner AR, Coresh J, Schmidt R, Ferrucci L, van Duijn CM, Borecki I, Kardia SL, Liu Y, Curhan GC, Rudan I, Gyllensten U, Wilson JF, Franke A, Pramstaller PP, Rettig R, Prokopenko I, Witteman J, Hayward C, Ridker PM, Bochud M, Heid IM, Siscovick DS, Fox CS, Kao WL, Böger CA.

J Am Soc Nephrol. 2013 Dec;24(12):2105-17. doi: 10.1681/ASN.2012100983. Epub 2013 Sep 12.

PMID:
24029420
[PubMed - indexed for MEDLINE]
9.

ATRIUM: testing untyped SNPs in case-control association studies with related individuals.

Wang Z, McPeek MS.

Am J Hum Genet. 2009 Nov;85(5):667-78. doi: 10.1016/j.ajhg.2009.10.006.

PMID:
19913122
[PubMed - indexed for MEDLINE]
Free PMC Article
10.

Characterization of genome-wide association-identified variants for atrial fibrillation in African Americans.

Delaney JT, Jeff JM, Brown NJ, Pretorius M, Okafor HE, Darbar D, Roden DM, Crawford DC.

PLoS One. 2012;7(2):e32338. doi: 10.1371/journal.pone.0032338. Epub 2012 Feb 23.

PMID:
22384221
[PubMed - indexed for MEDLINE]
Free PMC Article
11.

Signatures of positive selection in genes associated with human skin pigmentation as revealed from analyses of single nucleotide polymorphisms.

Lao O, de Gruijter JM, van Duijn K, Navarro A, Kayser M.

Ann Hum Genet. 2007 May;71(Pt 3):354-69. Epub 2007 Jan 18.

PMID:
17233754
[PubMed - indexed for MEDLINE]
12.

Mapping of disease-associated variants in admixed populations.

Shriner D, Adeyemo A, Ramos E, Chen G, Rotimi CN.

Genome Biol. 2011;12(5):223. doi: 10.1186/gb-2011-12-5-223. Epub 2011 May 30. Review.

PMID:
21635713
[PubMed - indexed for MEDLINE]
Free PMC Article
13.

Human population genetic diversity as a function of SNP type from HapMap data.

Garte S.

Am J Hum Biol. 2010 May-Jun;22(3):297-300. doi: 10.1002/ajhb.20984.

PMID:
19743305
[PubMed - indexed for MEDLINE]
14.

Larger genetic differences within africans than between Africans and Eurasians.

Yu N, Chen FC, Ota S, Jorde LB, Pamilo P, Patthy L, Ramsay M, Jenkins T, Shyue SK, Li WH.

Genetics. 2002 May;161(1):269-74.

PMID:
12019240
[PubMed - indexed for MEDLINE]
Free PMC Article
15.

Estimation of significance thresholds for genomewide association scans.

Dudbridge F, Gusnanto A.

Genet Epidemiol. 2008 Apr;32(3):227-34. doi: 10.1002/gepi.20297.

PMID:
18300295
[PubMed - indexed for MEDLINE]
Free PMC Article
16.

Additive genetic variation in schizophrenia risk is shared by populations of African and European descent.

de Candia TR, Lee SH, Yang J, Browning BL, Gejman PV, Levinson DF, Mowry BJ, Hewitt JK, Goddard ME, O'Donovan MC, Purcell SM, Posthuma D; International Schizophrenia Consortium; Molecular Genetics of Schizophrenia Collaboration, Visscher PM, Wray NR, Keller MC.

Am J Hum Genet. 2013 Sep 5;93(3):463-70. doi: 10.1016/j.ajhg.2013.07.007. Epub 2013 Aug 15.

PMID:
23954163
[PubMed - indexed for MEDLINE]
Free PMC Article
17.

RFMix: a discriminative modeling approach for rapid and robust local-ancestry inference.

Maples BK, Gravel S, Kenny EE, Bustamante CD.

Am J Hum Genet. 2013 Aug 8;93(2):278-88. doi: 10.1016/j.ajhg.2013.06.020. Epub 2013 Aug 1.

PMID:
23910464
[PubMed - indexed for MEDLINE]
Free PMC Article
18.

The structure of haplotype blocks in the human genome.

Gabriel SB, Schaffner SF, Nguyen H, Moore JM, Roy J, Blumenstiel B, Higgins J, DeFelice M, Lochner A, Faggart M, Liu-Cordero SN, Rotimi C, Adeyemo A, Cooper R, Ward R, Lander ES, Daly MJ, Altshuler D.

Science. 2002 Jun 21;296(5576):2225-9. Epub 2002 May 23.

PMID:
12029063
[PubMed - indexed for MEDLINE]
Free Article
19.

Genome-wide ancestry association testing identifies a common European variant on 6q14.1 as a risk factor for asthma in African American subjects.

Torgerson DG, Capurso D, Ampleford EJ, Li X, Moore WC, Gignoux CR, Hu D, Eng C, Mathias RA, Busse WW, Castro M, Erzurum SC, Fitzpatrick AM, Gaston B, Israel E, Jarjour NN, Teague WG, Wenzel SE, Rodríguez-Santana JR, Rodríguez-Cintrón W, Avila PC, Ford JG, Barnes KC, Burchard EG, Howard TD, Bleecker ER, Meyers DA, Cox NJ, Ober C, Nicolae DL.

J Allergy Clin Immunol. 2012 Sep;130(3):622-629.e9. doi: 10.1016/j.jaci.2012.03.045. Epub 2012 May 18.

PMID:
22607992
[PubMed - indexed for MEDLINE]
Free PMC Article
20.

Sensitive and accurate detection of copy number variants using read depth of coverage.

Yoon S, Xuan Z, Makarov V, Ye K, Sebat J.

Genome Res. 2009 Sep;19(9):1586-92. doi: 10.1101/gr.092981.109. Epub 2009 Aug 5.

PMID:
19657104
[PubMed - indexed for MEDLINE]
Free PMC Article

Display Settings:

Format
Items per page
Sort by

Send to:

Choose Destination

Supplemental Content

Write to the Help Desk