Works in Human Genetics, 2015, Vol 134, Issue 3

Results: 9

Is there a male-specific effect on hypertension?

Published in:

2015

By:

Dankowski, Theresa;
Schillert, Arne;
Teumer, Alexander;
Blankenberg, Stefan;
Dörr, Marcus;
Franke, Andre;
Lieb, Wolfgang;
König, Inke;
Ziegler, Andreas

Publication type:

Letter

Genome-wide association study identifies a PSMD3 variant associated with neutropenia in interferon-based therapy for chronic hepatitis C.

Published in:

Human Genetics, 2015, v. 134, n. 3, p. 279, doi. 10.1007/s00439-014-1520-7

By:

Iio, Etsuko;
Matsuura, Kentaro;
Nishida, Nao;
Maekawa, Shinya;
Enomoto, Nobuyuki;
Nakagawa, Mina;
Sakamoto, Naoya;
Yatsuhashi, Hiroshi;
Kurosaki, Masayuki;
Izumi, Namiki;
Hiasa, Yoichi;
Masaki, Naohiko;
Ide, Tatsuya;
Hino, Keisuke;
Tamori, Akihiro;
Honda, Masao;
Kaneko, Shuichi;
Mochida, Satoshi;
Nomura, Hideyuki;
Nishiguchi, Shuhei

Publication type:

Article

CDH13 promoter SNPs with pleiotropic effect on cardiometabolic parameters represent methylation QTLs.

Published in:

Human Genetics, 2015, v. 134, n. 3, p. 291, doi. 10.1007/s00439-014-1521-6

By:

Putku, Margus;
Kals, Mart;
Inno, Rain;
Kasela, Silva;
Org, Elin;
Kožich, Viktor;
Milani, Lili;
Laan, Maris

Publication type:

Article

Autosomal recessive lissencephaly with cerebellar hypoplasia is associated with a loss-of-function mutation in CDK5.

Published in:

Human Genetics, 2015, v. 134, n. 3, p. 305, doi. 10.1007/s00439-014-1522-5

By:

Magen, Daniella;
Ofir, Ayala;
Berger, Liron;
Goldsher, Dorit;
Eran, Ayelet;
Katib, Nassser;
Nijem, Yousif;
Vlodavsky, Euvgeni;
Zur, Shay;
Behar, Doron;
Fellig, Yakov;
Mandel, Hanna

Publication type:

Article

A systematic heritability analysis of the human whole blood transcriptome.

Published in:

Human Genetics, 2015, v. 134, n. 3, p. 343, doi. 10.1007/s00439-014-1524-3

By:

Huan, Tianxiao;
Liu, Chunyu;
Joehanes, Roby;
Zhang, Xiaoling;
Chen, Brian;
Johnson, Andrew;
Yao, Chen;
Courchesne, Paul;
O'Donnell, Christopher;
Munson, Peter;
Levy, Daniel

Publication type:

Article

Genome-wide methylation analysis in Silver-Russell syndrome patients.

Published in:

Human Genetics, 2015, v. 134, n. 3, p. 317, doi. 10.1007/s00439-014-1526-1

By:

Prickett, A.;
Ishida, M.;
Böhm, S.;
Frost, J.;
Puszyk, W.;
Abu-Amero, S.;
Stanier, P.;
Schulz, R.;
Moore, G.;
Oakey, R.

Publication type:

Article

Interactions between household air pollution and GWAS-identified lung cancer susceptibility markers in the Female Lung Cancer Consortium in Asia (FLCCA).

Published in:

Human Genetics, 2015, v. 134, n. 3, p. 333, doi. 10.1007/s00439-014-1528-z

By:

Hosgood, H.;
Song, Minsun;
Hsiung, Chao;
Yin, Zhihua;
Shu, Xiao-Ou;
Wang, Zhaoming;
Chatterjee, Nilanjan;
Zheng, Wei;
Caporaso, Neil;
Burdette, Laurie;
Yeager, Meredith;
Berndt, Sonja;
Landi, Maria;
Chen, Chien-Jen;
Chang, Gee-Chen;
Hsiao, Chin-Fu;
Tsai, Ying-Huang;
Chien, Li-Hsin;
Chen, Kuan-Yu;
Huang, Ming-Shyan

Publication type:

Article

Erratum to: Autosomal recessive lissencephaly with cerebellar hypoplasia is associated with a loss-of-function mutation in CDK5.

Published in:

2015

By:

Magen, Daniella;
Ofir, Ayala;
Berger, Liron;
Goldsher, Dorit;
Eran, Ayelet;
Katib, Nasser;
Nijem, Yousif;
Vlodavsky, Euvgeni;
Tzur, Shay;
Behar, Doron;
Fellig, Yakov;
Mandel, Hanna

Publication type:

Erratum

Rare germline copy number deletions of likely functional importance are implicated in endometrial cancer predisposition.

Published in:

Human Genetics, 2015, v. 134, n. 3, p. 269, doi. 10.1007/s00439-014-1507-4

By:

Moir-Meyer, Gemma;
Pearson, John;
Lose, Felicity;
Scott, Rodney;
McEvoy, Mark;
Attia, John;
Holliday, Elizabeth;
Pharoah, Paul;
Dunning, Alison;
Thompson, Deborah;
Easton, Douglas;
Spurdle, Amanda;
Walker, Logan

Publication type:

Article