Works matching IS 07410395 AND DT 2008 AND VI 32 AND IP 6

Results: 12

Analysis of multiple SNPs in a candidate gene or region.

Published in:

Genetic Epidemiology, 2008, v. 32, n. 6, p. 560, doi. 10.1002/gepi.20330

By:

Chapman, Juliet;
Whittaker, John

Publication type:

Article

Enhanced detection of genetic association of hypertensive heart disease by analysis of latent phenotypes.

Published in:

Genetic Epidemiology, 2008, v. 32, n. 6, p. 528, doi. 10.1002/gepi.20326

By:

Charles Gu, C.;
Flores, Hubert R.;
de las Fuentes, Lisa;
Dávila-Román, Victor G.

Publication type:

Article

Inference from genome-wide association studies using a novel Markov model.

Published in:

Genetic Epidemiology, 2008, v. 32, n. 6, p. 497, doi. 10.1002/gepi.20322

By:

Hosking, Fay J.;
Sterne, Jonathan A. C.;
Smith, George Davey;
Green, Peter J.

Publication type:

Article

Erratum.

Published in:

Genetic Epidemiology, 2008, v. 32, n. 6, p. 586, doi. 10.1002/gepi.20332

By:

Kulle, B.;
Frigessi, A.;
Edvardsen, H.;
Kristensen, V.;
Wojnowski, L.

Publication type:

Article

Simple association analysis combining data from trios/sibships and unrelated controls.

Published in:

Genetic Epidemiology, 2008, v. 32, n. 6, p. 520, doi. 10.1002/gepi.20325

By:

Chen, Yi-Hau;
Lin, Hui-Wen

Publication type:

Article

Fragile X-associated primary ovarian insufficiency: evidence for additional genetic contributions to severity.

Published in:

Genetic Epidemiology, 2008, v. 32, n. 6, p. 553, doi. 10.1002/gepi.20329

By:

Hunter, Jessica Ezzell;
Epstein, Michael P.;
Tinker, Stuart W.;
Charen, Krista H.;
Sherman, Stephanie L.

Publication type:

Article

On multiple-testing correction in genome-wide association studies.

Published in:

Genetic Epidemiology, 2008, v. 32, n. 6, p. 567, doi. 10.1002/gepi.20331

By:

Moskvina, Valentina;
Schmidt, Karl Michael

Publication type:

Article

Calculation of IBD probabilities with dense SNP or sequence data.

Published in:

Genetic Epidemiology, 2008, v. 32, n. 6, p. 513, doi. 10.1002/gepi.20324

By:

Keith, Jonathan M.;
McRae, Allan;
Duffy, David;
Mengersen, Kerrie;
Visscher, Peter M.

Publication type:

Article

Does strong linkage disequilibrium guarantee redundant association results?

Published in:

Genetic Epidemiology, 2008, v. 32, n. 6, p. 546, doi. 10.1002/gepi.20328

By:

Nielsen, Dahlia M.;
Suchindran, Sunil;
Smith, Christopher P.

Publication type:

Article

Quantifying the contribution of genetic variants for survival phenotypes.

Published in:

Genetic Epidemiology, 2008, v. 32, n. 6, p. 574, doi. 10.1002/gepi.20333

By:

Müller, Martina;
Döring, Angela;
Küchenhoff, Helmut;
Lamina, Claudia;
Malzahn, Dörthe;
Bickeböller, Heike;
Vollmert, Caren;
Klopp, Norman;
Meisinger, Christa;
Heinrich, Joachim;
Kronenberg, Florian;
Erich Wichmann, H.;
Heid, Iris M.

Publication type:

Article

Differential parental transmission of markers in RUNX2 among cleft case-parent trios from four populations.

Published in:

Genetic Epidemiology, 2008, v. 32, n. 6, p. 505, doi. 10.1002/gepi.20323

By:

Sull, Jae Woong;
Liang, Kung-Yee;
Hetmanski, Jacqueline B.;
Fallin, Margaret Daniele;
Ingersoll, Roxann G.;
Park, Jiwan;
Wu-Chou, Yah-Huei;
Chen, Philip K.;
Chong, Samuel S.;
Cheah, Felicia;
Yeow, Vincent;
Park, Beyoung Yun;
Jee, Sun Ha;
Jabs, Ethylin Wang;
Redett, Richard;
Jung, Euiju;
Ruczinski, Ingo;
Scott, Alan F.;
Beaty, Terri H.

Publication type:

Article

CLUMPHAP: a simple tool for performing haplotype-based association analysis.

Published in:

Genetic Epidemiology, 2008, v. 32, n. 6, p. 539, doi. 10.1002/gepi.20327

By:

Knight, Jo;
Curtis, David;
Sham, Pak C.

Publication type:

Article