Works matching IS 03406717 AND DT 2007 AND VI 120 AND IP 6

Results: 17

Mitochondrial haplogroup N9b is protective against myocardial infarction in Japanese males.

Published in:

Human Genetics, 2007, v. 120, n. 6, p. 827, doi. 10.1007/s00439-006-0269-z

By:

Nishigaki, Yutaka;
Yamada, Yoshiji;
Fuku, Noriyuki;
Matsuo, Hitoshi;
Segawa, Tomonori;
Watanabe, Sachiro;
Kato, Kimihiko;
Yokoi, Kiyoshi;
Yamaguchi, Sachiyo;
Nozawa, Yoshinori;
Tanaka, Masashi

Publication type:

Article

Evidence for statistical epistasis between catechol- O-methyltransferase (COMT) and polymorphisms in RGS4, G72 (DAOA), GRM3, and DISC1: influence on risk of schizophrenia.

Published in:

Human Genetics, 2007, v. 120, n. 6, p. 889, doi. 10.1007/s00439-006-0257-3

By:

Nicodemus, Kristin K.;
Kolachana, Bhaskar S.;
Vakkalanka, Radhakrishna;
Straub, Richard E.;
Giegling, Ina;
Egan, Michael F.;
Rujescu, Dan;
Weinberger, Daniel R.

Publication type:

Article

Identification of a regulatory SNP in the retinol binding protein 4 gene associated with type 2 diabetes in Mongolia.

Published in:

Human Genetics, 2007, v. 120, n. 6, p. 879, doi. 10.1007/s00439-006-0264-4

By:

Munkhtulga, Lkhagvasuren;
Nakayama, Kazuhiro;
Utsumi, Nanami;
Yanagisawa, Yoshiko;
Gotoh, Takaya;
Omi, Toshinori;
Kumada, Maki;
Erdenebulgan, Batmunkh;
Zolzaya, Khadbaatar;
Lkhagvasuren, Tserenkhuu;
Iwamoto, Sadahiko

Publication type:

Article

Subsets of SNPs define rare genotype classes that predict ischemic heart disease.

Published in:

Human Genetics, 2007, v. 120, n. 6, p. 865, doi. 10.1007/s00439-006-0233-y

By:

Frikke-Schmidt, Ruth;
Sing, Charles F.;
Nordestgaard, Børge G.;
Steffensen, Rolf;
Tybjærg-Hansen, Anne

Publication type:

Article

The LRRK2 Gly2385Arg variant is associated with Parkinson’s disease: genetic and functional evidence.

Published in:

Human Genetics, 2007, v. 120, n. 6, p. 857, doi. 10.1007/s00439-006-0268-0

By:

Tan, E. K.;
Zhao, Y.;
Skipper, L.;
Tan, M. G.;
Di Fonzo, A.;
Sun, L.;
Fook-Chong, S.;
Tang, S.;
Chua, E.;
Yuen, Y.;
Tan, L.;
Pavanni, R.;
Wong, M. C.;
Kolatkar, P.;
Lu, C. S.;
Bonifati, V.;
Liu, J. J.

Publication type:

Article

Cytogenetically balanced translocations are associated with focal copy number alterations.

Published in:

Human Genetics, 2007, v. 120, n. 6, p. 795, doi. 10.1007/s00439-006-0251-9

By:

Watson, Spencer K.;
deLeeuw, Ronald J.;
Horsman, Doug E.;
Squire, Jeremy A.;
Lam, Wan L.

Publication type:

Article

Sequence variant in the laminin γ1 ( LAMC1) gene associated with familial pelvic organ prolapse.

Published in:

Human Genetics, 2007, v. 120, n. 6, p. 847, doi. 10.1007/s00439-006-0267-1

By:

Nikolova, Ganka;
Lee, Hane;
Berkovitz, Suzanne;
Nelson, Stanley;
Sinsheimer, Janet;
Vilain, Eric;
Rodríguez, Larissa V.

Publication type:

Article

Molecular characterization of deletion breakpoints in adults with 22q11 deletion syndrome.

Published in:

Human Genetics, 2007, v. 120, n. 6, p. 837, doi. 10.1007/s00439-006-0242-x

By:

Weksberg, Rosanna;
Stachon, Andrea C.;
Squire, Jeremy A.;
Moldovan, Laura;
Bayani, Jane;
Meyn, Stephen;
Chow, Eva;
Bassett, Anne S.

Publication type:

Article

The possible role of 10398A and 16189C mtDNA variants in providing susceptibility toT2DM in two North Indian populations: a replicative study.

Published in:

Human Genetics, 2007, v. 120, n. 6, p. 821, doi. 10.1007/s00439-006-0272-4

By:

Bhat, Audesh;
Koul, Anil;
Sharma, Swarkar;
Rai, Ekta;
Bukhari, S. I. A.;
Dhar, M. K.;
Bamezai, R. N. K.

Publication type:

Article

Autosomal recessive nonsyndromic deafness locus DFNB63 at chromosome 11q13.2–q13.3.

Published in:

Human Genetics, 2007, v. 120, n. 6, p. 789, doi. 10.1007/s00439-006-0275-1

By:

Khan, Shahid Y.;
Riazuddin, Saima;
Tariq, Muhammad;
Anwar, Saima;
Shabbir, Muhammad I.;
Riazuddin, S. Amer;
Khan, Shaheen N.;
Husnain, Tayyab;
Ahmed, Zubair M.;
Friedman, Thomas B.;
Riazuddin, Sheikh

Publication type:

Article

Admixture in Mexico City: implications for admixture mapping of Type 2 diabetes genetic risk factors.

Published in:

Human Genetics, 2007, v. 120, n. 6, p. 807, doi. 10.1007/s00439-006-0273-3

By:

Martinez-Marignac, Veronica L.;
Valladares, Adan;
Cameron, Emily;
Chan, Andrea;
Perera, Arjuna;
Globus-Goldberg, Rachel;
Wacher, Niels;
Kumate, Jesús;
McKeigue, Paul;
O’Donnell, David;
Shriver, Mark D.;
Cruz, Miguel;
Parra, Esteban J.

Publication type:

Article

Structural divergence between the human and chimpanzee genomes.

Published in:

Human Genetics, 2007, v. 120, n. 6, p. 759, doi. 10.1007/s00439-006-0270-6

By:

Kehrer-Sawatzki, Hildegard;
Cooper, David N.

Publication type:

Article

A novel polymorphism associated with lactose tolerance in Africa: multiple causes for lactase persistence?

Published in:

Human Genetics, 2007, v. 120, n. 6, p. 779, doi. 10.1007/s00439-006-0291-1

By:

Ingram, Catherine J. E.;
Elamin, Mohamed F.;
Mulcare, Charlotte A.;
Weale, Michael E.;
Tarekegn, Ayele;
Oljira Raga, Tamiru;
Bekele, Endashaw;
Elamin, Farouk M.;
Thomas, Mark G.;
Bradman, Neil;
Swallow, Dallas M.

Publication type:

Article

My last visit with Friedrich Vogel: a personal remembrance.

Published in:

2007

By:

Rappold, Gudrun

Publication type:

Obituary

Obituary: Prof. Dr. med. Dr. h. c. Friedrich Vogel (1925–2006).

Published in:

2007

By:

Sperling, Karl

Publication type:

Obituary

Friedrich Vogel 1925–2006.

Published in:

2007

By:

Propping, Peter;
Bartram, Claus R.

Publication type:

Obituary

Novel human pathological mutations.

Published in:: Human Genetics, 2007, v. 120, n. 6, p. 907, doi. 10.1007/s00439-006-0247-5
Publication type:: Article