Works matching IS 03406717 AND DT 2013 AND VI 132 AND IP 7

Results: 12

Replication of genetic loci for sarcoidosis in US black women: data from the Black Women's Health Study.

Published in:

Human Genetics, 2013, v. 132, n. 7, p. 803, doi. 10.1007/s00439-013-1292-5

By:

Cozier, Yvette;
Ruiz-Narvaez, Edward;
McKinnon, Craig;
Berman, Jeffrey;
Rosenberg, Lynn;
Palmer, Julie

Publication type:

Article

Erratum to: Sex- and age-dependent DNA methylation at the 17q12-q21 locus associated with childhood asthma.

Published in:

2013

By:

Naumova, Anna;
Al Tuwaijri, Abeer;
Morin, Andréanne;
Vaillancourt, Vanessa;
Madore, Anne-Marie;
Berlivet, Soizik;
Kohan-Ghadr, Hamid-Reza;
Moussette, Sanny;
Laprise, Catherine

Publication type:

Correction Notice

Victor McKusick and the history of medical genetics.

Published in:

2013

By:

Hall, Judith

Publication type:

Book Review

Confirming genes influencing risk to cleft lip with/without cleft palate in a case-parent trio study.

Published in:

Human Genetics, 2013, v. 132, n. 7, p. 771, doi. 10.1007/s00439-013-1283-6

By:

Beaty, T.;
Taub, M.;
Scott, A.;
Murray, J.;
Marazita, M.;
Schwender, H.;
Parker, M.;
Hetmanski, J.;
Balakrishnan, P.;
Mansilla, M.;
Mangold, E.;
Ludwig, K.;
Noethen, M.;
Rubini, M.;
Elcioglu, N.;
Ruczinski, I.

Publication type:

Article

Sex- and age-dependent DNA methylation at the 17q12-q21 locus associated with childhood asthma.

Published in:

Human Genetics, 2013, v. 132, n. 7, p. 811, doi. 10.1007/s00439-013-1298-z

By:

Naumova, Anna;
Al Tuwaijri, Abeer;
Morin, Andréanne;
Vaillancout, Vanessa;
Madore, Anne-Marie;
Berlivet, Soizik;
Kohan-Ghadr, Hamid-Reza;
Moussette, Sanny;
Laprise, Catherine

Publication type:

Article

Obesity-related genetic variants, human pigmentation, and risk of melanoma.

Published in:

Human Genetics, 2013, v. 132, n. 7, p. 793, doi. 10.1007/s00439-013-1293-4

By:

Li, Xin;
Liang, Liming;
Zhang, Mingfeng;
Song, Fengju;
Nan, Hongmei;
Wang, Li-E;
Wei, Qingyi;
Lee, Jeffrey;
Amos, Christopher;
Qureshi, Abrar;
Han, Jiali

Publication type:

Article

Genome-wide scan revealed that polymorphisms in the PNPLA3, SAMM50, and PARVB genes are associated with development and progression of nonalcoholic fatty liver disease in Japan.

Published in:

Human Genetics, 2013, v. 132, n. 7, p. 783, doi. 10.1007/s00439-013-1294-3

By:

Kitamoto, Takuya;
Kitamoto, Aya;
Yoneda, Masato;
Hyogo, Hideyuki;
Ochi, Hidenori;
Nakamura, Takahiro;
Teranishi, Hajime;
Mizusawa, Seiho;
Ueno, Takato;
Chayama, Kazuaki;
Nakajima, Atsushi;
Nakao, Kazuwa;
Sekine, Akihiro;
Hotta, Kikuko

Publication type:

Article

Next-generation sequencing diagnostics for neurological diseases/disorders: from a clinical perspective.

Published in:

Human Genetics, 2013, v. 132, n. 7, p. 721, doi. 10.1007/s00439-013-1287-2

By:

Foo, Jia;
Liu, Jianjun;
Tan, Eng-King

Publication type:

Article

Recursive organizer (ROR): an analytic framework for sequence-based association analysis.

Published in:

Human Genetics, 2013, v. 132, n. 7, p. 745, doi. 10.1007/s00439-013-1285-4

By:

Zhao, Lue;
Huang, Xin

Publication type:

Article

Whole exome sequencing in dominant cataract identifies a new causative factor, CRYBA2, and a variety of novel alleles in known genes.

Published in:

Human Genetics, 2013, v. 132, n. 7, p. 761, doi. 10.1007/s00439-013-1289-0

By:

Reis, Linda;
Tyler, Rebecca;
Muheisen, Sanaa;
Raggio, Victor;
Salviati, Leonardo;
Han, Dennis;
Costakos, Deborah;
Yonath, Hagith;
Hall, Sarah;
Power, Patricia;
Semina, Elena

Publication type:

Article

Dissecting the genotype in syndromic intellectual disability using whole exome sequencing in addition to genome-wide copy number analysis.

Published in:

Human Genetics, 2013, v. 132, n. 7, p. 825, doi. 10.1007/s00439-013-1296-1

By:

Classen, Carl;
Riehmer, Vera;
Landwehr, Christina;
Kosfeld, Anne;
Heilmann, Stefanie;
Scholz, Caroline;
Kabisch, Sarah;
Engels, Hartmut;
Tierling, Sascha;
Zivicnjak, Miroslav;
Schacherer, Frank;
Haffner, Dieter;
Weber, Ruthild

Publication type:

Article

Association between common alcohol dehydrogenase gene ( ADH) variants and schizophrenia and autism.

Published in:

Human Genetics, 2013, v. 132, n. 7, p. 735, doi. 10.1007/s00439-013-1277-4

By:

Zuo, Lingjun;
Wang, Kesheng;
Zhang, Xiang-Yang;
Pan, Xinghua;
Wang, Guilin;
Tan, Yunlong;
Zhong, Chunlong;
Krystal, John;
State, Matthew;
Zhang, Heping;
Luo, Xingguang

Publication type:

Article