Works matching IS 03406717 AND DT 2014 AND VI 133 AND IP 9

Results: 11

HLA alleles associated with the adaptive immune response to smallpox vaccine: a replication study.

Published in:

Human Genetics, 2014, v. 133, n. 9, p. 1083, doi. 10.1007/s00439-014-1449-x

By:

Ovsyannikova, Inna;
Pankratz, V.;
Salk, Hannah;
Kennedy, Richard;
Poland, Gregory

Publication type:

Article

Validated context-dependent associations of coronary heart disease risk with genotype variation in the chromosome 9p21 region: the Atherosclerosis Risk in Communities study.

Published in:

Human Genetics, 2014, v. 133, n. 9, p. 1105, doi. 10.1007/s00439-014-1451-3

By:

Lusk, Christine;
Dyson, Greg;
Clark, Andrew;
Ballantyne, Christie;
Frikke-Schmidt, Ruth;
Tybjærg-Hansen, Anne;
Boerwinkle, Eric;
Sing, Charles

Publication type:

Article

Identification of methylation quantitative trait loci (mQTLs) influencing promoter DNA methylation of alcohol dependence risk genes.

Published in:

Human Genetics, 2014, v. 133, n. 9, p. 1093, doi. 10.1007/s00439-014-1452-2

By:

Zhang, Huiping;
Wang, Fan;
Kranzler, Henry;
Yang, Can;
Xu, Hongqin;
Wang, Zuoheng;
Zhao, Hongyu;
Gelernter, Joel

Publication type:

Article

A genetic association study detects haplotypes associated with obstructive heart defects.

Published in:

Human Genetics, 2014, v. 133, n. 9, p. 1127, doi. 10.1007/s00439-014-1453-1

By:

Li, Ming;
Cleves, Mario;
Mallick, Himel;
Erickson, Stephen;
Tang, Xinyu;
Nick, Todd;
Macleod, Stewart;
Hobbs, Charlotte

Publication type:

Article

A single codon insertion in PICALM is associated with development of familial subvalvular aortic stenosis in Newfoundland dogs.

Published in:

Human Genetics, 2014, v. 133, n. 9, p. 1139, doi. 10.1007/s00439-014-1454-0

By:

Stern, Joshua;
White, Stephen;
Lehmkuhl, Linda;
Reina-Doreste, Yamir;
Ferguson, Jordan;
Nascone-Yoder, Nanette;
Meurs, Kathryn

Publication type:

Article

Opposite effects on facial morphology due to gene dosage sensitivity.

Published in:

Human Genetics, 2014, v. 133, n. 9, p. 1117, doi. 10.1007/s00439-014-1455-z

By:

Hammond, Peter;
McKee, Shane;
Suttie, Michael;
Allanson, Judith;
Cobben, Jan-Maarten;
Maas, Saskia;
Quarrell, Oliver;
Smith, Ann;
Lewis, Suzanne;
Tassabehji, May;
Sisodiya, Sanjay;
Mattina, Teresa;
Hennekam, Raoul

Publication type:

Article

Hennekam syndrome can be caused by FAT4 mutations and be allelic to Van Maldergem syndrome.

Published in:

Human Genetics, 2014, v. 133, n. 9, p. 1161, doi. 10.1007/s00439-014-1456-y

By:

Alders, Mariëlle;
Al-Gazali, Lihadh;
Cordeiro, Isabelle;
Dallapiccola, Bruno;
Garavelli, Livia;
Tuysuz, Beyhan;
Salehi, Faranak;
Haagmans, Martin;
Mook, Olaf;
Majoie, Charles;
Mannens, Marcel;
Hennekam, Raoul

Publication type:

Article

Mitochondrial DNA copy number in peripheral blood cells declines with age and is associated with general health among elderly.

Published in:

Human Genetics, 2014, v. 133, n. 9, p. 1149, doi. 10.1007/s00439-014-1458-9

By:

Mengel-From, Jonas;
Thinggaard, Mikael;
Dalgård, Christine;
Kyvik, Kirsten;
Christensen, Kaare;
Christiansen, Lene

Publication type:

Article

The population genomic landscape of human genetic structure, admixture history and local adaptation in Peninsular Malaysia.

Published in:

Human Genetics, 2014, v. 133, n. 9, p. 1169, doi. 10.1007/s00439-014-1459-8

By:

Deng, Lian;
Hoh, Boon;
Lu, Dongsheng;
Fu, Ruiqing;
Phipps, Maude;
Li, Shilin;
Nur-Shafawati, Ab;
Hatin, Wan;
Ismail, Endom;
Mokhtar, Siti;
Jin, Li;
Zilfalil, Bin;
Marshall, Christian;
Scherer, Stephen;
Al-Mulla, Fahd;
Xu, Shuhua

Publication type:

Article

Host genetics and viral load in primary HIV-1 infection: clear evidence for gene by sex interactions.

Published in:

Human Genetics, 2014, v. 133, n. 9, p. 1187, doi. 10.1007/s00439-014-1465-x

By:

Li, Xuelin;
Price, Matthew;
He, Dongning;
Kamali, Anatoli;
Karita, Etienne;
Lakhi, Shabir;
Sanders, Eduard;
Anzala, Omu;
Amornkul, Pauli;
Allen, Susan;
Hunter, Eric;
Kaslow, Richard;
Gilmour, Jill;
Tang, Jianming

Publication type:

Article

Amniotic fluid RNA gene expression profiling provides insights into the phenotype of Turner syndrome.

Published in:

Human Genetics, 2014, v. 133, n. 9, p. 1075, doi. 10.1007/s00439-014-1448-y

By:

Massingham, Lauren;
Johnson, Kirby;
Scholl, Thomas;
Slonim, Donna;
Wick, Heather;
Bianchi, Diana

Publication type:

Article