Works matching IS 03406717 AND DT 2012 AND VI 131 AND IP 3

Results: 20

Review of Aaron Gillette, Eugenics and the nature-nurture debate in the twentieth century 2007, paperback edition, 2011, New York: Palgrave Macmillan.

Published in:

2012

By:

Dupré, John

Publication type:

Book Review

Associations between gene polymorphisms in fatty acid metabolism pathway and preterm delivery in a US urban black population.

Published in:

Human Genetics, 2012, v. 131, n. 3, p. 341, doi. 10.1007/s00439-011-1079-5

By:

Liu, Xin;
Wang, Guoying;
Hong, Xiumei;
Tsai, Hui-Ju;
Liu, Rong;
Zhang, Shanchun;
Wang, Hongjian;
Pearson, Colleen;
Ortiz, Katherin;
Wang, Deli;
Hirsch, Emmet;
Zuckerman, Barry;
Wang, Xiaobin

Publication type:

Article

Sex differences in disease risk from reported genome-wide association study findings.

Published in:

Human Genetics, 2012, v. 131, n. 3, p. 353, doi. 10.1007/s00439-011-1081-y

By:

Liu, Linda;
Schaub, Marc;
Sirota, Marina;
Butte, Atul

Publication type:

Article

The 18p11.22 locus is associated with never smoker non-small cell lung cancer susceptibility in Korean populations.

Published in:

Human Genetics, 2012, v. 131, n. 3, p. 365, doi. 10.1007/s00439-011-1080-z

By:

Ahn, Myung-Ju;
Won, Hong-Hee;
Lee, Jeeyun;
Lee, Seung-Tae;
Sun, Jong-Mu;
Park, Yeon;
Ahn, Jin;
Kwon, O;
Kim, Hojoong;
Shim, Young;
Kim, Jhingook;
Kim, Kwhanmien;
Kim, Yeul;
Park, Jae;
Kim, Jong-Won;
Park, Keunchil

Publication type:

Article

Ion channels and schizophrenia: a gene set-based analytic approach to GWAS data for biological hypothesis testing.

Published in:

Human Genetics, 2012, v. 131, n. 3, p. 373, doi. 10.1007/s00439-011-1082-x

By:

Askland, Kathleen;
Read, Cynthia;
O'Connell, Chloe;
Moore, Jason

Publication type:

Article

Expression signature of epidermolysis bullosa simplex.

Published in:

Human Genetics, 2012, v. 131, n. 3, p. 393, doi. 10.1007/s00439-011-1077-7

By:

Bchetnia, Mbarka;
Tremblay, Marie-Lou;
Leclerc, Georgette;
Dupérée, Audrey;
Powell, Julie;
McCuaig, Catherine;
Morin, Charles;
Legendre-Guillemin, Valérie;
Laprise, Catherine

Publication type:

Article

Novel Alu retrotransposon insertion leading to Alström syndrome.

Published in:

Human Genetics, 2012, v. 131, n. 3, p. 407, doi. 10.1007/s00439-011-1083-9

By:

Taşkesen, Mustafa;
Collin, Gayle;
Evsikov, Alexei;
Güzel, Ayşegül;
Özgül, R.;
Marshall, Jan;
Naggert, Jürgen

Publication type:

Article

Genetic mapping of an autosomal recessive postaxial polydactyly type A to chromosome 13q13.3-q21.2 and screening of the candidate genes.

Published in:

Human Genetics, 2012, v. 131, n. 3, p. 415, doi. 10.1007/s00439-011-1085-7

By:

Umm-e-Kalsoom;
Basit, Sulman;
Kamran-ul-Hassan Naqvi, Syed;
Ansar, Muhammad;
Ahmad, Wasim

Publication type:

Article

High altitude adaptation in Daghestani populations from the Caucasus.

Published in:

Human Genetics, 2012, v. 131, n. 3, p. 423, doi. 10.1007/s00439-011-1084-8

By:

Pagani, Luca;
Ayub, Qasim;
MacArthur, Daniel;
Xue, Yali;
Baillie, J.;
Chen, Yuan;
Kozarewa, Iwanka;
Turner, Daniel;
Tofanelli, Sergio;
Bulayeva, Kazima;
Kidd, Kenneth;
Paoli, Giorgio;
Tyler-Smith, Chris

Publication type:

Article

Exome sequencing identifies GCDH (glutaryl-CoA dehydrogenase) mutations as a cause of a progressive form of early-onset generalized dystonia.

Published in:

Human Genetics, 2012, v. 131, n. 3, p. 435, doi. 10.1007/s00439-011-1086-6

By:

Marti-Masso, Jose;
Ruiz-Martínez, Javier;
Makarov, Vladimir;
Munain, Adolfo;
Gorostidi, Ana;
Bergareche, Alberto;
Yoon, Seungtai;
Buxbaum, Joseph;
Paisán-Ruiz, Coro

Publication type:

Article

The genetics of kidney transplantation.

Published in:

Human Genetics, 2012, v. 131, n. 3, p. 317, doi. 10.1007/s00439-011-1092-8

By:

Pallet, Nicolas;
Thervet, Eric

Publication type:

Article

Association study of the KCNJ3 gene as a susceptibility candidate for schizophrenia in the Chinese population.

Published in:

Human Genetics, 2012, v. 131, n. 3, p. 443, doi. 10.1007/s00439-011-1089-3

By:

Yamada, Kazuo;
Iwayama, Yoshimi;
Toyota, Tomoko;
Ohnishi, Tetsuo;
Ohba, Hisako;
Maekawa, Motoko;
Yoshikawa, Takeo

Publication type:

Article

Genome-wide association study identifies HMGN3 locus for spine bone size variation in Chinese.

Published in:

Human Genetics, 2012, v. 131, n. 3, p. 463, doi. 10.1007/s00439-011-1093-7

By:

Lei, Shu-Feng;
Shen, Hui;
Yang, Tie-Lin;
Guo, Yan;
Dong, Shan-Shan;
Xu, Xiang-Hong;
Deng, Fei-Yan;
Tian, Qing;
Liu, Yong-Jun;
Liu, Yao-Zhong;
Li, Jian;
Deng, Hong-Wen

Publication type:

Article

SLC39A2 and FSIP1 polymorphisms as potential modifiers of arsenic-related bladder cancer.

Published in:

Human Genetics, 2012, v. 131, n. 3, p. 453, doi. 10.1007/s00439-011-1090-x

By:

Karagas, Margaret;
Andrew, Angeline;
Nelson, Heather;
Li, Zhongze;
Punshon, Tracy;
Schned, Alan;
Marsit, Carmen;
Morris, J.;
Moore, Jason;
Tyler, Anna;
Gilbert-Diamond, Diane;
Guerinot, Mary-Lou;
Kelsey, Karl

Publication type:

Article

Exome sequencing and subsequent association studies identify five amino acid-altering variants influencing human height.

Published in:

Human Genetics, 2012, v. 131, n. 3, p. 471, doi. 10.1007/s00439-011-1096-4

By:

Kim, Jae-Jung;
Park, Young-Mi;
Baik, Kyu-Heum;
Choi, Hye-Yeon;
Yang, Gap-Seok;
Koh, InSong;
Hwang, Jung-Ah;
Lee, Jieun;
Lee, Yeon-Su;
Rhee, Hwanseok;
Kwon, Tae;
Han, Bok-Ghee;
Heath, Karen;
Inoue, Hiroshi;
Yoo, Han-Wook;
Park, Kiejung;
Lee, Jong-Keuk

Publication type:

Article

Fine mapping of 14q24.1 breast cancer susceptibility locus.

Published in:

Human Genetics, 2012, v. 131, n. 3, p. 479, doi. 10.1007/s00439-011-1088-4

By:

Lee, Phoebe;
Fu, Yi-Ping;
Figueroa, Jonine;
Prokunina-Olsson, Ludmila;
Gonzalez-Bosquet, Jesus;
Kraft, Peter;
Wang, Zhaoming;
Jacobs, Kevin;
Yeager, Meredith;
Horner, Marie-Josèphe;
Hankinson, Susan;
Hutchinson, Amy;
Chatterjee, Nilanjan;
Garcia-Closas, Montserrat;
Ziegler, Regina;
Berg, Christine;
Buys, Saundra;
McCarty, Catherine;
Feigelson, Heather;
Thun, Michael

Publication type:

Article

Functional analysis of Waardenburg syndrome-associated PAX3 and SOX10 mutations: report of a dominant-negative SOX10 mutation in Waardenburg syndrome type II.

Published in:

Human Genetics, 2012, v. 131, n. 3, p. 491, doi. 10.1007/s00439-011-1098-2

By:

Zhang, Hua;
Chen, Hongsheng;
Luo, Hunjin;
An, Jing;
Sun, Lin;
Mei, Lingyun;
He, Chufeng;
Jiang, Lu;
Jiang, Wen;
Xia, Kun;
Li, Jia-Da;
Feng, Yong

Publication type:

Article

Associations between common variants in GC and DHCR7/ NADSYN1 and vitamin D concentration in Chinese Hans.

Published in:

Human Genetics, 2012, v. 131, n. 3, p. 505, doi. 10.1007/s00439-011-1099-1

By:

Lu, Ling;
Sheng, Hongguang;
Li, Huaixing;
Gan, Wei;
Liu, Chen;
Zhu, Jingwen;
Loos, Ruth;
Lin, Xu

Publication type:

Article

Clinical utility of chromosomal microarray analysis in invasive prenatal diagnosis.

Published in:

Human Genetics, 2012, v. 131, n. 3, p. 513, doi. 10.1007/s00439-011-1095-5

By:

Armengol, Lluís;
Nevado, Julián;
Serra-Juhé, Clara;
Plaja, Alberto;
Mediano, Carmen;
García-Santiago, Fe;
García-Aragonés, Manel;
Villa, Olaya;
Mansilla, Elena;
Preciado, Cristina;
Fernández, Luis;
Mori, María;
García-Pérez, Lidia;
Lapunzina, Pablo;
Pérez-Jurado, Luis

Publication type:

Article

Facioscapulohumeral muscular dystrophy (FSHD): an enigma unravelled?

Published in:

Human Genetics, 2012, v. 131, n. 3, p. 325, doi. 10.1007/s00439-011-1100-z

By:

Richards, Mark;
Coppée, Frédérique;
Thomas, Nick;
Belayew, Alexandra;
Upadhyaya, Meena

Publication type:

Article