Works matching IS 03406717 AND DT 2013 AND VI 132 AND IP 10

Results: 8

A meta-analysis of two genome-wide association studies to identify novel loci for maximum number of alcoholic drinks.

Published in:

Human Genetics, 2013, v. 132, n. 10, p. 1141, doi. 10.1007/s00439-013-1318-z

By:

Kapoor, Manav;
Wang, Jen-Chyong;
Wetherill, Leah;
Le, Nhung;
Bertelsen, Sarah;
Hinrichs, Anthony;
Budde, John;
Agrawal, Arpana;
Bucholz, Kathleen;
Dick, Danielle;
Harari, Oscar;
Hesselbrock, Victor;
Kramer, John;
Nurnberger, John;
Rice, John;
Saccone, Nancy;
Schuckit, Marc;
Tischfield, Jay;
Porjesz, Bernice;
Edenberg, Howard

Publication type:

Article

Association, interaction, and replication analysis of genes encoding serotonin transporter and 5-HT receptor subunits A and B in alcohol dependence.

Published in:

Human Genetics, 2013, v. 132, n. 10, p. 1165, doi. 10.1007/s00439-013-1319-y

By:

Seneviratne, Chamindi;
Franklin, Jason;
Beckett, Katherine;
Ma, Jennie;
Ait-Daoud, Nassima;
Payne, Thomas;
Johnson, Bankole;
Li, Ming

Publication type:

Article

Responses to booster hepatitis B vaccination are significantly correlated with genotypes of human leukocyte antigen (HLA)- DPB1 in neonatally vaccinated adolescents.

Published in:

Human Genetics, 2013, v. 132, n. 10, p. 1131, doi. 10.1007/s00439-013-1320-5

By:

Wu, Tzu-Wei;
Chu, Chen-Chung;
Ho, Tzu-Ying;
Chang Liao, Huei-Wen;
Lin, Sheng-Kai;
Lin, Marie;
Lin, Hans;
Wang, Li-Yu

Publication type:

Article

Early medical genetics in Soviet Russia: its growth and destruction.

Published in:

2013

By:

Harper, Peter

Publication type:

Book Review

Where genotype is not predictive of phenotype: towards an understanding of the molecular basis of reduced penetrance in human inherited disease.

Published in:

Human Genetics, 2013, v. 132, n. 10, p. 1077, doi. 10.1007/s00439-013-1331-2

By:

Cooper, David;
Krawczak, Michael;
Polychronakos, Constantin;
Tyler-Smith, Chris;
Kehrer-Sawatzki, Hildegard

Publication type:

Article

The new sequencer on the block: comparison of Life Technology's Proton sequencer to an Illumina HiSeq for whole-exome sequencing.

Published in:

Human Genetics, 2013, v. 132, n. 10, p. 1153, doi. 10.1007/s00439-013-1321-4

By:

Boland, Joseph;
Chung, Charles;
Roberson, David;
Mitchell, Jason;
Zhang, Xijun;
Im, Kate;
He, Ji;
Chanock, Stephen;
Yeager, Meredith;
Dean, Michael

Publication type:

Article

The adaptive variant EDARV370A is associated with straight hair in East Asians.

Published in:

Human Genetics, 2013, v. 132, n. 10, p. 1187, doi. 10.1007/s00439-013-1324-1

By:

Tan, Jingze;
Yang, Yajun;
Tang, Kun;
Sabeti, Pardis;
Jin, Li;
Wang, Sijia

Publication type:

Article

The mitochondrial solute carrier SLC25A5 at Xq24 is a novel candidate gene for non-syndromic intellectual disability.

Published in:

Human Genetics, 2013, v. 132, n. 10, p. 1177, doi. 10.1007/s00439-013-1322-3

By:

Vandewalle, Joke;
Bauters, Marijke;
Van Esch, Hilde;
Belet, Stefanie;
Verbeeck, Jelle;
Fieremans, Nathalie;
Holvoet, Maureen;
Vento, Jodie;
Spreiz, Ana;
Kotzot, Dieter;
Haberlandt, Edda;
Rosenfeld, Jill;
Andrieux, Joris;
Delobel, Bruno;
Dehouck, Marie-Bertille;
Devriendt, Koen;
Fryns, Jean-Pierre;
Marynen, Peter;
Goldstein, Amy;
Froyen, Guy

Publication type:

Article