Works matching IS 03406717 AND DT 2007 AND VI 121 AND IP 6

Results: 15

A novel genetic locus for juvenile myoclonic epilepsy at chromosome 5q12–q14.

Published in:

Human Genetics, 2007, v. 121, n. 6, p. 655, doi. 10.1007/s00439-007-0360-0

By:

Kapoor, Ashish;
Ratnapriya, R.;
Kuruttukulam, Gigy;
Anand, Anuranjan

Publication type:

Article

Extreme individual marker F<sub>ST </sub>values do not imply population-specific selection in humans: the NRG1 example.

Published in:

Human Genetics, 2007, v. 121, n. 6, p. 759, doi. 10.1007/s00439-007-0364-9

By:

Gardner, Michelle;
Williamson, Scott;
Casals, Ferran;
Bosch, Elena;
Navarro, Arcadi;
Calafell, Francesc;
Bertranpetit, Jaume;
Comas, David

Publication type:

Article

Mortality and cancer incidence in males with Y polysomy in Britain: a cohort study.

Published in:

Human Genetics, 2007, v. 121, n. 6, p. 691, doi. 10.1007/s00439-007-0365-8

By:

Higgins, Craig;
Swerdlow, Anthony;
Schoemaker, Minouk;
Wright, Alan;
Jacobs, Patricia

Publication type:

Article

Genetic association of IRF5 with SLE in Mexicans: higher frequency of the risk haplotype and its homozygozity than Europeans.

Published in:

Human Genetics, 2007, v. 121, n. 6, p. 721, doi. 10.1007/s00439-007-0367-6

By:

Reddy, M. V. Prasad Linga;
Velázquez-Cruz, Rafael;
Baca, Vicente;
Lima, Guadalupe;
Granados, Julio;
Orozco, Lorena;
Alarcón-Riquelme, Marta E.

Publication type:

Article

Linkage and association analysis of candidate genes for TB and TNFα cytokine expression: evidence for association with IFNGR1, IL-10, and TNF receptor 1 genes.

Published in:

Human Genetics, 2007, v. 121, n. 6, p. 663, doi. 10.1007/s00439-007-0357-8

By:

Stein, Catherine M.;
Zalwango, Sarah;
Chiunda, Allan B.;
Millard, Christopher;
Leontiev, Dmitry;
Horvath, Amanda L.;
Cartier, Kevin C.;
Chervenak, Keith;
Boom, W. Henry;
Elston, Robert C.;
Mugerwa, Roy D.;
Whalen, Christopher C.;
Iyengar, Sudha K.

Publication type:

Article

Intragenic deletion in the LARGE gene causes Walker-Warburg syndrome.

Published in:

Human Genetics, 2007, v. 121, n. 6, p. 685, doi. 10.1007/s00439-007-0362-y

By:

van Reeuwijk, Jeroen;
Grewal, Prabhjit K.;
Salih, Mustafa A. M.;
de Bernabé, Daniel Beltrán-Valero;
McLaughlan, Jenny M.;
Michielse, Caroline B.;
Herrmann, Ralf;
Ewitt, Jane E.;
Steinbrecher, Alice;
Seidahmed, Mohamed Z.;
Shaheed, Mohamed M.;
Abomelha, Abdullah;
Brunner, Han G.;
van Bokhoven, Hans;
Voit, Thomas

Publication type:

Article

Evidence for a pleiotropic QTL on chromosome 5q13 influencing both time to asthma onset and asthma score in French EGEA families.

Published in:

Human Genetics, 2007, v. 121, n. 6, p. 711, doi. 10.1007/s00439-007-0363-x

By:

Bouzigon, Emmanuelle;
Ulgen, Ayse;
Dizier, Marie-Hélène;
Siroux, Valérie;
Lathrop, Mark;
Kauffmann, Francine;
Pin, Isabelle;
Demenais, Florence

Publication type:

Article

The P239S palladin variant does not account for a significant fraction of hereditary or early onset pancreas cancer.

Published in:

2007

By:

Zogopoulos, George;
Rothenmund, Heidi;
Eppel, Ayelet;
Ash, Colleen;
Akbari, Mohammad;
Hedley, David;
Narod, Steven A.;
Gallinger, Steven

Publication type:

Correction Notice

Genome-wide linkage scan of prostate cancer Gleason score and confirmation of chromosome 19q.

Published in:

Human Genetics, 2007, v. 121, n. 6, p. 729, doi. 10.1007/s00439-007-0368-5

By:

Schaid, Daniel J.;
Stanford, Janet L.;
McDonnell, Shannon K.;
Suuriniemi, Miia;
McIntosh, Laura;
Karyadi, Danielle M.;
Carlson, Erin E.;
Deutsch, Kerry;
Janer, Marta;
Hood, Lee;
Ostrander, Elaine A.

Publication type:

Article

Bivariate linkage confirms genetic contribution to fetal origins of childhood growth and cardiovascular disease risk in Hispanic children.

Published in:

Human Genetics, 2007, v. 121, n. 6, p. 737, doi. 10.1007/s00439-007-0366-7

By:

Guowen Cai;
Cole, Shelley A.;
Haack, Karin;
Butte, Nancy F.;
Comuzzie, Anthony G.

Publication type:

Article

Detlev Ganten, Klaus Ruckpaul: Encyclopedic reference of genomics and proteomics in molecular medicine.

Published in:

2007

By:

Read, Andrew

Publication type:

Book Review

Parent–child pair design for detecting gene–environment interactions in complex diseases.

Published in:

Human Genetics, 2007, v. 121, n. 6, p. 745, doi. 10.1007/s00439-007-0369-4

By:

Yuan-De Tan;
Fornage, Myriam;
George, Varghese;
Hongyan Xu

Publication type:

Article

Joe T. R. Clarke: A clinical guide to inherited metabolic diseases.

Published in:

2007

By:

Moat, Stuart

Publication type:

Book Review

Genetic liability to schizophrenia in Oceanic Palau: a search in the affected and maternal generation.

Published in:

Human Genetics, 2007, v. 121, n. 6, p. 675, doi. 10.1007/s00439-007-0358-7

By:

Devlin, Bernie;
Klei, Lambertus;
Myles-Worsley, Marina;
Tiobech, Josepha;
Otto, Caleb;
Byerley, William;
Roeder, Kathryn

Publication type:

Article

Complex chromosome 17p rearrangements associated with low-copy repeats in two patients with congenital anomalies.

Published in:

Human Genetics, 2007, v. 121, n. 6, p. 697, doi. 10.1007/s00439-007-0359-6

By:

Vissers, L. E. L. M.;
Stankiewicz, P.;
Yatsenko, S. A.;
Crawford, E.;
Creswick, H.;
Proud, V. K.;
de Vries, B. B. A.;
Pfundt, R.;
Marcelis, C. L. M.;
Zackowski, J.;
Bi, W.;
van Kessel, A. Guerst;
Lupski, J. R.;
Veltman, J. A.

Publication type:

Article