Works matching IS 03406717 AND DT 2009 AND VI 126 AND IP 6

Results: 11

Mathew B. Hamilton: Population genetics.

Published in:

2009

By:

Krawczak, Michael

Publication type:

Book Review

Assessment of association of rs2200733 on chromosome 4q25 with atrial fibrillation and ischemic stroke in a Chinese Han population.

Published in:

Human Genetics, 2009, v. 126, n. 6, p. 843, doi. 10.1007/s00439-009-0737-3

By:

Lisong Shi;
Cong Li;
Chuchu Wang;
Yunlong Xia;
Gang Wu;
Fan Wang;
Chengqi Xu;
Pengyun Wang;
Xiuchun Li;
Dan Wang;
Xin Xiong;
Ying Bai;
Mugen Liu;
Jingyu Liu;
Xiang Ren;
Lianjun Gao;
Binbin Wang;
Qiutang Zeng;
Bo Yang;
Xu Ma

Publication type:

Article

Intron 7 conserved sequence elements regulate the splicing of the SMN genes.

Published in:

Human Genetics, 2009, v. 126, n. 6, p. 833, doi. 10.1007/s00439-009-0733-7

By:

Gladman, Jordan T.;
Chandler, Dawn S.

Publication type:

Article

Comprehensive resequence analysis of a 97 kb region of chromosome 10q11.2 containing the MSMB gene associated with prostate cancer.

Published in:

Human Genetics, 2009, v. 126, n. 6, p. 743, doi. 10.1007/s00439-009-0723-9

By:

Yeager, Meredith;
Zuoming Deng;
Boland, Joseph;
Matthews, Casey;
Bacior, Jennifer;
Lonsberry, Victor;
Hutchinson, Amy;
Burdett, Laura A.;
Liqun Qi;
Jacobs, Kevin B.;
Gonzalez-Bosquet, Jesus;
Berndt, Sonja I.;
Hayes, Richard B.;
Hoover, Robert N.;
Thomas, Gilles;
Hunter, David J.;
Dean, Michael;
Chanock, Stephen J.

Publication type:

Article

Reduced TFAP2A function causes variable optic fissure closure and retinal defects and sensitizes eye development to mutations in other morphogenetic regulators.

Published in:

Human Genetics, 2009, v. 126, n. 6, p. 791, doi. 10.1007/s00439-009-0730-x

By:

Gestri, Gaia;
Osborne, Robert J.;
Wyatt, Alexander W.;
Gerrelli, Dianne;
Gribble, Susan;
Stewart, Helen;
Fryer, Alan;
Bunyan, David J.;
Prescott, Katrina;
Collin, J. Richard O.;
Fitzgerald, Tomas;
Robinson, David;
Carter, Nigel P.;
Wilson, Stephen W.;
Ragge, Nicola K.

Publication type:

Article

The combined impact of metabolic gene polymorphisms on elite endurance athlete status and related phenotypes.

Published in:

Human Genetics, 2009, v. 126, n. 6, p. 751, doi. 10.1007/s00439-009-0728-4

By:

Ahmetov, Ildus I.;
Williams, Alun G.;
Popov, Daniil V.;
Lyubaeva, Ekaterina V.;
Hakimullina, Albina M.;
Fedotovskaya, Olga N.;
Mozhayskaya, Irina A.;
Vinogradova, Olga L.;
Astratenkova, Irina V.;
Montgomery, Hugh E.;
Rogozkin, Viktor A.

Publication type:

Article

The molecular genetics of blood group polymorphism.

Published in:

Human Genetics, 2009, v. 126, n. 6, p. 729, doi. 10.1007/s00439-009-0738-2

By:

Daniels, Geoff

Publication type:

Article

Genetic analysis of diabetic nephropathy on chromosome 18 in African Americans: linkage analysis and dense SNP mapping.

Published in:

Human Genetics, 2009, v. 126, n. 6, p. 805, doi. 10.1007/s00439-009-0732-8

By:

McDonough, Caitrin W.;
Bostrom, Meredith A.;
Lingyi Lu;
Hicks, Pamela J.;
Langefeld, Carl D.;
Divers, Jasmin;
Mychaleckyj, Josyf C.;
Freedman, Barry I.;
Bowden, Donald W.

Publication type:

Article

Infantile hypertrophic pyloric stenosis: evaluation of three positional candidate genes, TRPC1, TRPC5 and TRPC6, by association analysis and re-sequencing.

Published in:

Human Genetics, 2009, v. 126, n. 6, p. 819, doi. 10.1007/s00439-009-0735-5

By:

Everett, Kate V.;
Chioza, Barry A.;
Georgoula, Christina;
Reece, Ashley;
Gardiner, R. Mark;
Chung, Eddie M. K.

Publication type:

Article

Modifier gene study of meconium ileus in cystic fibrosis: statistical considerations and gene mapping results.

Published in:

Human Genetics, 2009, v. 126, n. 6, p. 763, doi. 10.1007/s00439-009-0724-8

By:

Dorfman, Ruslan;
Weili Li;
Lei Sun;
Fan Lin;
Yongqian Wang;
Sandford, Andrew;
Paré, Peter;
McKay, Karen;
Kayserova, Hana;
Piskackova, Tereza;
Macek, Milan;
Czerska, Kamila;
Sands, Dorota;
Tiddens, Harm;
Margarit, Sonia;
Repetto, Gabriela;
Sontag, Marci;
Accurso, Frank;
Blackman, Scott;
Cutting, Garry

Publication type:

Article

K<sub>ATP</sub> channel Kir6.2 E23K variant overrepresented in human heart failure is associated with impaired exercise stress response.

Published in:

Human Genetics, 2009, v. 126, n. 6, p. 779, doi. 10.1007/s00439-009-0731-9

By:

Reyes, Santiago;
Sungjo Park;
Johnson, Bruce D.;
Terzic, Andre;
Olson, Timothy M.

Publication type:

Article