Works matching IS 03406717 AND DT 2010 AND VI 127 AND IP 2

Results: 13

Monoamine oxidase A gene polymorphisms and enzyme activity associated with risk of gout in Taiwan aborigines.

Published in:

Human Genetics, 2010, v. 127, n. 2, p. 223, doi. 10.1007/s00439-009-0765-z

By:

Hung-Pin Tu;
Ko, Albert Min-Shan;
Shu-Jung Wang;
Chien-Hung Lee;
Lea, Rod A.;
Shang-Lun Chiang;
Hung-Che Chiang;
Tsu-Nai Wang;
Meng-Chuan Huang;
Tsan-Teng Ou;
Gau-Tyan Lin;
Ying-Chin Ko

Publication type:

Article

Evaluation of genetic tests for susceptibility to common complex diseases: why, when and how?

Published in:

Human Genetics, 2010, v. 127, n. 2, p. 125, doi. 10.1007/s00439-009-0767-x

By:

Wright, Caroline Fiona;
Kroese, Mark

Publication type:

Article

Genetic analysis of ABCG2 gene C421A polymorphism with gout disease in Chinese Han male population.

Published in:

Human Genetics, 2010, v. 127, n. 2, p. 245, doi. 10.1007/s00439-009-0760-4

By:

Binbin Wang;
Zhimin Miao;
Shiguo Liu;
Jing Wang;
Shiyi Zhou;
Lin Han;
Dongmei Meng;
Yunlong Wang;
Changgui Li;
Xu Ma

Publication type:

Article

Transposable elements in disease-associated cryptic exons.

Published in:

Human Genetics, 2010, v. 127, n. 2, p. 135, doi. 10.1007/s00439-009-0752-4

By:

Vorechovsky, Igor

Publication type:

Article

Genetic variants in the RELN gene are associated with otosclerosis in multiple European populations.

Published in:

Human Genetics, 2010, v. 127, n. 2, p. 155, doi. 10.1007/s00439-009-0754-2

By:

Schrauwen, Isabelle;
Ealy, Megan;
Fransen, Erik;
Vanderstraeten, Kathleen;
Thys, Melissa;
Meyer, Nicole C.;
Cosgarea, Marcel;
Huber, Alex;
Mazzoli, Manuela;
Pfister, Markus;
Smith, Richard J. H.;
Van Camp, Guy

Publication type:

Article

Malaria severity and human nitric oxide synthase type 2 (NOS2) promoter haplotypes.

Published in:

Human Genetics, 2010, v. 127, n. 2, p. 163, doi. 10.1007/s00439-009-0753-3

By:

Levesque, Marc C.;
Hobbs, Maurine R.;
O'Loughlin, Charles W.;
Chancellor, Jennifer A.;
Youwei Chen;
Tkachuk, Ariana N.;
Booth, Jennifer;
Patch, Kistie B.;
Allgood, Sallie;
Pole, Ann R.;
Fernandez, Carolyn A.;
Mwaikambo, Esther D.;
Mutabingwa, Theonest K.;
Fried, Michal;
Sorensen, Bess;
Duffy, Patrick E.;
Granger, Donald L.;
Anstey, Nicholas M.;
Weinberg, J. Brice

Publication type:

Article

Genetic variation in PARL influences mitochondrial content.

Published in:

Human Genetics, 2010, v. 127, n. 2, p. 183, doi. 10.1007/s00439-009-0756-0

By:

Curran, Joanne E.;
Jowett, Jeremy B. M.;
Abraham, Lawrence J.;
Diepeveen, Luke A.;
Elliott, Katherine S.;
Dyer, Thomas D.;
Kerr-Bayles, Lyndal J.;
Johnson, Matthew P.;
Comuzzie, Anthony G.;
Moses, Eric K.;
Walder, Ken R.;
Collier, Gregory R.;
Blangero, John;
Kissebah, Ahmed H.

Publication type:

Article

Linkage and sequence analysis indicate that CCBE1 is mutated in recessively inherited generalised lymphatic dysplasia.

Published in:

Human Genetics, 2010, v. 127, n. 2, p. 231, doi. 10.1007/s00439-009-0766-y

By:

Connell, Fiona;
Kalidas, Kamini;
Ostergaard, Pia;
Brice, Glen;
Homfray, Tessa;
Roberts, Lesley;
Bunyan, David J.;
Mitton, Sally;
Mansour, Sahar;
Mortimer, Peter;
Jeffery, Steve

Publication type:

Article

A novel mutation in the connexin 29 gene may contribute to nonsyndromic hearing loss.

Published in:

Human Genetics, 2010, v. 127, n. 2, p. 191, doi. 10.1007/s00439-009-0758-y

By:

Hui-Mei Hong;
Jiann-Jou Yang;
Ching-Chyuan Su;
Juan-Yu Chang;
Tung-Cheng Li;
Shuan-Yow Li

Publication type:

Article

Common CFTR gene variants influence body composition and survival in rural Ghana.

Published in:

Human Genetics, 2010, v. 127, n. 2, p. 201, doi. 10.1007/s00439-009-0762-2

By:

Kuningas, Maris;
van Bodegom, David;
May, Linda;
Meij, Johannes J.;
Slagboom, P. Eline;
Westendorp, Rudi G. J.

Publication type:

Article

Rubella vaccine-induced cellular immunity: evidence of associations with polymorphisms in the Toll-like, vitamin A and D receptors, and innate immune response genes.

Published in:

Human Genetics, 2010, v. 127, n. 2, p. 207, doi. 10.1007/s00439-009-0763-1

By:

Ovsyannikova, Inna G.;
Dhiman, Neelam;
Haralambieva, Iana H.;
Vierkant, Robert A.;
O'Byrne, Megan M.;
Jacobson, Robert M.;
Poland, Gregory A.

Publication type:

Article

R. C. Elston and W. D. Johnson: Basic biostatistics for geneticists and epidemiologists.

Published in:

2010

By:

Holmans, Peter;
Jones, Lesley

Publication type:

Book Review

Erratum to: Linkage and sequence analysis indicate that CCBE1 is mutated in recessively inherited generalised lymphatic dysplasia.

Published in:

2010

By:

Connell, Fiona;
Kalidas, Kamini;
Ostergaard, Pia;
Brice, Glen;
Homfray, Tessa;
Roberts, Lesley;
Bunyan, David J.;
Mitton, Sally;
Mansour, Sahar;
Mortimer, Peter;
Jeffery, Steve

Publication type:

Correction Notice