Works matching IS 09646906 AND DT 2011 AND VI 20 AND IP R2

Results: 19

Subscription Page.

Published in:: Human Molecular Genetics, 2011, v. 20, n. R2, p. NP, doi. 10.1093/hmg/ddr444
Publication type:: Article

Editorial Board.

Published in:: Human Molecular Genetics, 2011, v. 20, n. R2, p. NP, doi. 10.1093/hmg/ddr443
Publication type:: Article

Cover Page.

Published in:: Human Molecular Genetics, 2011, v. 20, n. R2, p. NP, doi. 10.1093/hmg/ddr442
Publication type:: Article

Contents Page.

Published in:: Human Molecular Genetics, 2011, v. 20, n. R2, p. NP, doi. 10.1093/hmg/ddr441
Publication type:: Article

Africa: the next frontier for human disease gene discovery?

Published in:

Human Molecular Genetics, 2011, v. 20, n. R2, p. R214, doi. 10.1093/hmg/ddr401

By:

Ramsay, Michèle;
Tiemessen, Caroline T.;
Choudhury, Ananyo;
Soodyall, Himla

Publication type:

Article

Multi-ethnic studies in complex traits.

Published in:

Human Molecular Genetics, 2011, v. 20, n. R2, p. R206, doi. 10.1093/hmg/ddr386

By:

Fu, Jingyuan;
Festen, Eleonora A.M.;
Wijmenga, Cisca

Publication type:

Article

Thirty-five common variants for coronary artery disease: the fruits of much collaborative labour.

Published in:

Human Molecular Genetics, 2011, v. 20, n. R2, p. R198, doi. 10.1093/hmg/ddr384

By:

Peden, John F.;
Farrall, Martin

Publication type:

Article

Keratin disorders: from gene to therapy.

Published in:

Human Molecular Genetics, 2011, v. 20, n. R2, p. R189, doi. 10.1093/hmg/ddr379

By:

McLean, W.H. Irwin;
Moore, C.B. Tara

Publication type:

Article

Genetic risk prediction in complex disease.

Published in:

Human Molecular Genetics, 2011, v. 20, n. R2, p. R182, doi. 10.1093/hmg/ddr378

By:

Jostins, Luke;
Barrett, Jeffrey C.

Publication type:

Article

Structure and evolutionary history of DISC1.

Published in:

Human Molecular Genetics, 2011, v. 20, n. R2, p. R175, doi. 10.1093/hmg/ddr374

By:

Sanchez-Pulido, Luis;
Ponting, Chris P.

Publication type:

Article

Mitochondrial DNA disease: new options for prevention.

Published in:

Human Molecular Genetics, 2011, v. 20, n. R2, p. R168, doi. 10.1093/hmg/ddr373

By:

Craven, Lyndsey;
Elson, Joanna L.;
Irving, Laura;
Tuppen, Helen A.;
Lister, Lisa M.;
Greggains, Gareth D.;
Byerley, Samantha;
Murdoch, Alison P.;
Herbert, Mary;
Turnbull, Doug

Publication type:

Article

The ADAMTS(L) family and human genetic disorders.

Published in:

Human Molecular Genetics, 2011, v. 20, n. R2, p. R163, doi. 10.1093/hmg/ddr361

By:

Le Goff, Carine;
Cormier-Daire, Valérie

Publication type:

Article

A generalizable hypothesis for the genetic architecture of disease: pleomorphic risk loci.

Published in:

Human Molecular Genetics, 2011, v. 20, n. R2, p. R158, doi. 10.1093/hmg/ddr358

By:

Singleton, Andrew;
Hardy, John

Publication type:

Article

Scrutinizing ciliopathies by unraveling ciliary interaction networks.

Published in:

Human Molecular Genetics, 2011, v. 20, n. R2, p. R149, doi. 10.1093/hmg/ddr354

By:

van Reeuwijk, Jeroen;
Arts, Heleen H.;
Roepman, Ronald

Publication type:

Article

The human metagenome: our other genome?

Published in:

Human Molecular Genetics, 2011, v. 20, n. R2, p. R142, doi. 10.1093/hmg/ddr353

By:

Brüls, Thomas;
Weissenbach, Jean

Publication type:

Article

Direct-to-consumer personalized genomic testing.

Published in:

Human Molecular Genetics, 2011, v. 20, n. R2, p. R132, doi. 10.1093/hmg/ddr349

By:

Bloss, Cinnamon S.;
Darst, Burcu F.;
Topol, Eric J.;
Schork, Nicholas J.

Publication type:

Article

Stroke genetics.

Published in:

Human Molecular Genetics, 2011, v. 20, n. R2, p. R124, doi. 10.1093/hmg/ddr345

By:

Markus, Hugh S.

Publication type:

Article

Induced pluripotent stem cells (iPSCs) and neurological disease modeling: progress and promises.

Published in:

Human Molecular Genetics, 2011, v. 20, n. R2, p. R109, doi. 10.1093/hmg/ddr336

By:

Marchetto, Maria C.;
Brennand, Kristen J.;
Boyer, Leah F.;
Gage, Fred H.

Publication type:

Article

Myotonic dystrophy, when simple repeats reveal complex pathogenic entities: new findings and future challenges.

Published in:

Human Molecular Genetics, 2011, v. 20, n. R2, p. R116, doi. 10.1093/hmg/ddr343

By:

Sicot, Géraldine;
Gourdon, Geneviève;
Gomes-Pereira, Mário

Publication type:

Article