Works matching IS 03406717 AND DT 2013 AND VI 132 AND IP 12

Results: 12

How meaningful are heritability estimates of liability?
Published in:
Human Genetics, 2013, v. 132, n. 12, p. 1351, doi. 10.1007/s00439-013-1334-z
By:
- Benchek, Penny H.;
- Morris, Nathan J.
Publication type:
Article
HLA-DPB1*04:01 allele is associated with non-obstructive azoospermia in Japanese patients.
Published in:
Human Genetics, 2013, v. 132, n. 12, p. 1405, doi. 10.1007/s00439-013-1347-7
By:
- Jinam, Timothy A.;
- Nakaoka, Hirofumi;
- Hosomichi, Kazuyoshi;
- Mitsunaga, Shigeki;
- Okada, Hiroyuki;
- Tanaka, Atsushi;
- Tanaka, Kenichi;
- Inoue, Ituro
Publication type:
Article
Bayes’ rule, medical genetics and the wider world. A review of: the theory that would not die. How Bayes’ rule cracked the Enigma code, hunted down Russian submarines, and emerged triumphant from two centuries of controversy: by Sharon Bertsch McGrayne: New Haven, Yale University Press (2011; revised paperback edition 2012)
Published in:
2013
By:
- Harper, Peter S.
Publication type:
Book Review
Genetics of healthy aging and longevity.
Published in:
Human Genetics, 2013, v. 132, n. 12, p. 1323, doi. 10.1007/s00439-013-1342-z
By:
- Brooks-Wilson, Angela R.
Publication type:
Article
Disorders with similar clinical phenotypes reveal underlying genetic interaction: SATB2 acts as an activator of the UPF3B gene.
Published in:
Human Genetics, 2013, v. 132, n. 12, p. 1383, doi. 10.1007/s00439-013-1345-9
By:
- Leoyklang, Petcharat;
- Suphapeetiporn, Kanya;
- Srichomthong, Chalurmpon;
- Tongkobpetch, Siraprapa;
- Fietze, Stefanie;
- Dorward, Heidi;
- Cullinane, Andrew R.;
- Gahl, William A.;
- Huizing, Marjan;
- Shotelersuk, Vorasuk
Publication type:
Article
Erratum to: The success of pharmacogenomics in moving genetic association studies from bench to bedside: study design and implementation of precision medicine in the post-GWAS era.
Published in:
2013
By:
- Ritchie, Marylyn D.
Publication type:
Correction Notice
No evidence of interaction between known lipid-associated genetic variants and smoking in the multi-ethnic PAGE population.
Published in:
Human Genetics, 2013, v. 132, n. 12, p. 1427, doi. 10.1007/s00439-013-1375-3
By:
- Dumitrescu, Logan;
- Carty, Cara L.;
- Franceschini, Nora;
- Hindorff, Lucia A.;
- Cole, Shelley A.;
- Bůžková, Petra;
- Schumacher, Fredrick R.;
- Eaton, Charles B.;
- Goodloe, Robert J.;
- Duggan, David J.;
- Haessler, Jeff;
- Cochran, Barbara;
- Henderson, Brian E.;
- Cheng, Iona;
- Johnson, Karen C.;
- Carlson, Chris S.;
- Love, Shelly-Anne;
- Brown-Gentry, Kristin;
- Nato, Alejandro Q.;
- Quibrera, Miguel
Publication type:
Article
A novel method for identifying nonlinear gene–environment interactions in case–control association studies.
Published in:
Human Genetics, 2013, v. 132, n. 12, p. 1413, doi. 10.1007/s00439-013-1350-z
By:
- Wu, Cen;
- Cui, Yuehua
Publication type:
Article
A functional variant of pre-miRNA-196a2 confers risk for Behcet’s disease but not for Vogt–Koyanagi–Harada syndrome or AAU in ankylosing spondylitis.
Published in:
Human Genetics, 2013, v. 132, n. 12, p. 1395, doi. 10.1007/s00439-013-1346-8
By:
- Qi, Jian;
- Hou, Shengping;
- Zhang, Qi;
- Liao, Dan;
- Wei, Lin;
- Fang, Jing;
- Zhou, Yan;
- Kijlstra, Aize;
- Yang, Peizeng
Publication type:
Article
Variants in BET1L and TNRC6B associate with increasing fibroid volume and fibroid type among European Americans.
Published in:
Human Genetics, 2013, v. 132, n. 12, p. 1361, doi. 10.1007/s00439-013-1340-1
By:
- Edwards, Todd L.;
- Hartmann, Katherine E.;
- Velez Edwards, Digna R.
Publication type:
Article
Gene–smoking interactions in multiple Rho-GTPase pathway genes in an early-onset coronary artery disease cohort.
Published in:
Human Genetics, 2013, v. 132, n. 12, p. 1371, doi. 10.1007/s00439-013-1339-7
By:
- Ward-Caviness, Cavin;
- Haynes, Carol;
- Blach, Colette;
- Dowdy, Elaine;
- Gregory, Simon G.;
- Shah, Svati H.;
- Horne, Benjamin D.;
- Kraus, William E.;
- Hauser, Elizabeth R.
Publication type:
Article
Genome-wide copy number variation analysis of a Branchio-oto-renal syndrome cohort identifies a recombination hotspot and implicates new candidate genes.
Published in:
Human Genetics, 2013, v. 132, n. 12, p. 1339, doi. 10.1007/s00439-013-1338-8
By:
- Brophy, Patrick D.;
- Alasti, Fatemeh;
- Darbro, Benjamin W.;
- Clarke, Jason;
- Nishimura, Carla;
- Cobb, Bryan;
- Smith, Richard J.;
- Manak, J. Robert
Publication type:
Article

Works matching IS 03406717 AND DT 2013 AND VI 132 AND IP 12

How meaningful are heritability estimates of liability?

HLA-DPB1*04:01 allele is associated with non-obstructive azoospermia in Japanese patients.

Genetics of healthy aging and longevity.

Disorders with similar clinical phenotypes reveal underlying genetic interaction: SATB2 acts as an activator of the <i>UPF3B</i> gene.

Erratum to: The success of pharmacogenomics in moving genetic association studies from bench to bedside: study design and implementation of precision medicine in the post-GWAS era.

No evidence of interaction between known lipid-associated genetic variants and smoking in the multi-ethnic PAGE population.

A novel method for identifying nonlinear gene–environment interactions in case–control association studies.

A functional variant of pre-miRNA-196a2 confers risk for Behcet’s disease but not for Vogt–Koyanagi–Harada syndrome or AAU in ankylosing spondylitis.

Variants in <i>BET1L</i> and <i>TNRC6B</i> associate with increasing fibroid volume and fibroid type among European Americans.

Gene–smoking interactions in multiple Rho-GTPase pathway genes in an early-onset coronary artery disease cohort.

Genome-wide copy number variation analysis of a Branchio-oto-renal syndrome cohort identifies a recombination hotspot and implicates new candidate genes.