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

Results: 17

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
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
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
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
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
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
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
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
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
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
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