Works matching IS 03406717 AND DT 2010 AND VI 127 AND IP 6

Results: 15

Evidence for inheritance in patients with VACTERL association.

Published in:

2010

By:

Solomon, Benjamin D.;
Pineda-Alvarez, Daniel E.;
Raam, Manu S.;
Cummings, Derek A. T.

Publication type:

Report

Replication and extension of association of choline acetyltransferase with nicotine dependence in European and African American smokers.

Published in:

Human Genetics, 2010, v. 127, n. 6, p. 691, doi. 10.1007/s00439-010-0818-3

By:

Jinxue Wei;
Ma, Jennie Z.;
Payne, Thomas J.;
Wenyan Cui;
Ray, Riju;
Mitra, Nandita;
Lerman, Caryn;
Li, Ming D.

Publication type:

Article

Malcolm Collins: Medicine and Sports Science, Vol. 54: Genetics and Sports.

Published in:

2010

By:

Rawal, Jaikirty Singh

Publication type:

Book Review

Fine mapping of the 9q31 Hirschsprung’s disease locus.

Published in:

Human Genetics, 2010, v. 127, n. 6, p. 675, doi. 10.1007/s00439-010-0813-8

By:

Tang, C. S.;
Sribudiani, Y.;
Miao, X. P.;
Vries, A. R.;
Burzynski, G.;
So, M. T.;
Leon, Y. Y.;
Yip, B. H.;
Osinga, J.;
Hui, K. J. W. S.;
Verheij, J. B. G. M.;
Cherny, S. S.;
Tam, P. K. H.;
Sham, P. C.;
Hofstra, R. M. W.;
Garcia-Barceló, M. M.

Publication type:

Article

Power analysis for case–control association studies of samples with known family histories.

Published in:

Human Genetics, 2010, v. 127, n. 6, p. 699, doi. 10.1007/s00439-010-0824-5

By:

Bo Peng;
Biao Li;
Younghun Han;
Amos, Christopher I.

Publication type:

Article

A novel loss-of-function mutation in OTX2 in a patient with anophthalmia and isolated growth hormone deficiency.

Published in:

Human Genetics, 2010, v. 127, n. 6, p. 721, doi. 10.1007/s00439-010-0820-9

By:

Ashkenazi-Hoffnung, Liat;
Lebenthal, Yael;
Wyatt, Alexander W.;
Ragge, Nicola K.;
Dateki, Sumito;
Fukami, Maki;
Ogata, Tsutomu;
Phillip, Moshe;
Gat-Yablonski, Galia

Publication type:

Article

West African and Amerindian ancestry and risk of myocardial infarction and metabolic syndrome in the Central Valley population of Costa Rica.

Published in:

Human Genetics, 2010, v. 127, n. 6, p. 629, doi. 10.1007/s00439-010-0803-x

By:

Ruiz-Narváez, Edward A.;
Bare, Lance;
Arellano, Andre;
Catanese, Joseph;
Campos, Hannia

Publication type:

Article

Comparison of the DNA methylation profiles of human peripheral blood cells and transformed B-lymphocytes.

Published in:

Human Genetics, 2010, v. 127, n. 6, p. 651, doi. 10.1007/s00439-010-0810-y

By:

Sun, Yan V.;
Turner, Stephen T.;
Smith, Jennifer A.;
Hammond, Pamela I.;
Lazarus, Alicia;
Van De Rostyne, Jodie L.;
Cunningham, Julie M.;
Kardia, Sharon L. R.

Publication type:

Article

Philippe Collas (ed): Chromatin immunoprecipitation assays: methods and protocols.

Published in:

2010

By:

Waters, Ray

Publication type:

Book Review

Ethnic diversity of DNA methylation in the OPRM1 promoter region in lymphocytes of heroin addicts.

Published in:

Human Genetics, 2010, v. 127, n. 6, p. 639, doi. 10.1007/s00439-010-0807-6

By:

Nielsen, David A.;
Hamon, Sara;
Yuferov, Vadim;
Jackson, Colin;
Ho, Ann;
Ott, Jurg;
Kreek, Mary Jeanne

Publication type:

Article

Linkage and association analyses identify a candidate region for apoB level on chromosome 4q32.3 in FCHL families.

Published in:

Human Genetics, 2010, v. 127, n. 6, p. 705, doi. 10.1007/s00439-010-0819-2

By:

Wijsman, Ellen M.;
Rothstein, Joseph H.;
Igo Jr., Robert P.;
Brunzell, John D.;
Motulsky, Arno G.;
Jarvik, Gail P.

Publication type:

Article

Two-stage case–control designs for rare genetic variants.

Published in:

Human Genetics, 2010, v. 127, n. 6, p. 659, doi. 10.1007/s00439-010-0811-x

By:

Schaid, Daniel J.;
Sinnwell, Jason P.

Publication type:

Article

Heritability of chronic venous disease.

Published in:

Human Genetics, 2010, v. 127, n. 6, p. 669, doi. 10.1007/s00439-010-0812-9

By:

Fiebig, Andreas;
Krusche, Petra;
Wolf, Andreas;
Krawczak, Michael;
Timm, Birgitt;
Nikolaus, Susanna;
Frings, Norbert;
Schreiber, Stefan

Publication type:

Article

Molecular pathogenesis of a novel mutation, G108D, in short-chain acyl-CoA dehydrogenase identified in subjects with short-chain acyl-CoA dehydrogenase deficiency.

Published in:

Human Genetics, 2010, v. 127, n. 6, p. 619, doi. 10.1007/s00439-010-0822-7

By:

Shirao, Kenichiro;
Okada, Satoshi;
Tajima, Go;
Tsumura, Miyuki;
Hara, Keiichi;
Yasunaga, Shin'ichiro;
Ohtsubo, Motoaki;
Hata, Ikue;
Sakura, Nobuo;
Shigematsu, Yosuke;
Takihara, Yoshihiro;
Kobayashi, Masao

Publication type:

Article

A single nucleotide polymorphism in the FADS1/ FADS2 gene is associated with plasma lipid profiles in two genetically similar Asian ethnic groups with distinctive differences in lifestyle.

Published in:

Human Genetics, 2010, v. 127, n. 6, p. 685, doi. 10.1007/s00439-010-0815-6

By:

Nakayama, Kazuhiro;
Bayasgalan, Tumenbayer;
Tazoe, Fumiko;
Yanagisawa, Yoshiko;
Gotoh, Takaya;
Yamanaka, Kazuhiro;
Ogawa, Ayumi;
Munkhtulga, Lkhagvasuren;
Chimedregze, Ulziiburen;
Kagawa, Yasuo;
Ishibashi, Shun;
Iwamoto, Sadahiko

Publication type:

Article