Works matching IS 10184813 AND DT 2006 AND VI 14 AND IP 6

Results: 19

Haplotype-based association analysis of 56 functional candidate genes in the IBD6 locus on chromosome 19.

Published in:

European Journal of Human Genetics, 2006, v. 14, n. 6, p. 780, doi. 10.1038/sj.ejhg.5201612

By:

Tello-Ruiz, Marcela Karey;
Curley, Christine;
DelMonte, Terrye;
Giallourakis, Cosmas;
Kirby, Andrew;
Miller, Kathryn;
Wild, Gary;
Cohen, Albert;
Langelier, Diane;
Latiano, Anna;
Wedemeyer, Neils;
Lander, Eric;
Schreiber, Stefan;
Annese, Vito;
Daly, Mark J.;
Rioux, John D.

Publication type:

Article

Genetics of intelligence.

Published in:

European Journal of Human Genetics, 2006, v. 14, n. 6, p. 690, doi. 10.1038/sj.ejhg.5201588

By:

Deary, Ian J.;
Spinath, Frank M.;
Bates, Timothy C.

Publication type:

Article

Genetics and pathophysiology of mental retardation.

Published in:

European Journal of Human Genetics, 2006, v. 14, n. 6, p. 701, doi. 10.1038/sj.ejhg.5201595

By:

Chelly, Jamel;
Khelfaoui, Malik;
Francis, Fiona;
Chérif, Beldjord;
Bienvenu, Thierry

Publication type:

Article

Molecular genetics of the fruit-fly circadian clock.

Published in:

European Journal of Human Genetics, 2006, v. 14, n. 6, p. 729, doi. 10.1038/sj.ejhg.5201547

By:

Rosato, Ezio;
Tauber, Eran;
Kyriacou, Charalambos P.

Publication type:

Article

The role of mutagenesis in defining genes in behaviour.

Published in:

European Journal of Human Genetics, 2006, v. 14, n. 6, p. 651, doi. 10.1038/sj.ejhg.5201545

By:

Godinho, Sofia I. H.;
Nolan, Patrick M.

Publication type:

Article

Genetics of affective (mood) disorders.

Published in:

European Journal of Human Genetics, 2006, v. 14, n. 6, p. 660, doi. 10.1038/sj.ejhg.5201549

By:

Craddock, Nick;
Forty, Liz

Publication type:

Article

Huntington's Disease: A transcriptional report card from the peripheral blood: Can it measure disease progression in Huntington's disease?

Published in:

European Journal of Human Genetics, 2006, v. 14, n. 6, p. 649, doi. 10.1038/sj.ejhg.5201562

By:

Tabchy, Adel;
Housman, David

Publication type:

Article

The genetic basis of emotional behaviour in mice.

Published in:

European Journal of Human Genetics, 2006, v. 14, n. 6, p. 721, doi. 10.1038/sj.ejhg.5201569

By:

Willis-Owen, Saffron A. G;
Flint, Jonathan

Publication type:

Article

Molecular genetic studies of schizophrenia.

Published in:

European Journal of Human Genetics, 2006, v. 14, n. 6, p. 669, doi. 10.1038/sj.ejhg.5201571

By:

Riley, Brien;
Kendler, Kenneth S.

Publication type:

Article

The genetics of developmental dyslexia.

Published in:

European Journal of Human Genetics, 2006, v. 14, n. 6, p. 681, doi. 10.1038/sj.ejhg.5201575

By:

Williams, Julie;
O'Donovan, Michael C.

Publication type:

Article

Molecular analysis of a human PAX6 homeobox mutant.

Published in:

European Journal of Human Genetics, 2006, v. 14, n. 6, p. 744, doi. 10.1038/sj.ejhg.5201579

By:

D'elia, Angela Valentina;
Puppin, Cinzia;
Pellizzari, Lucia;
Pianta, Annalisa;
Bregant, Elisa;
Lonigro, Renata;
Tell, Gianluca;
Fogolari, Federico;
van Heyningen, Veronica;
Damante, Giuseppe

Publication type:

Article

Identification of cis- and trans-acting factors possibly modifying the risk of epimutations on chromosome 15.

Published in:

European Journal of Human Genetics, 2006, v. 14, n. 6, p. 752, doi. 10.1038/sj.ejhg.5201602

By:

Zogel, Corinna;
Böhringer, Stefan;
Groß, Stephanie;
Varon, Raymonda;
Buiting, Karin;
Horsthemke, Bernhard

Publication type:

Article

Focus on behavioural genetics.

Published in:

European Journal of Human Genetics, 2006, v. 14, n. 6, p. 647, doi. 10.1038/sj.ejhg.5201599

By:

Flint, Jonathan;
Monaco, Anthony P.

Publication type:

Article

Genetics of autism spectrum disorder.

Published in:

European Journal of Human Genetics, 2006, v. 14, n. 6, p. 714, doi. 10.1038/sj.ejhg.5201610

By:

Klauck, Sabine M.

Publication type:

Article

Deletions of 2q14 that include the homeobox engrailed 1 (EN1) transcription factor are compatible with a normal phenotype.

Published in:

European Journal of Human Genetics, 2006, v. 14, n. 6, p. 739, doi. 10.1038/sj.ejhg.5201605

By:

Barber, John C. K.;
Maloney, Viv K.;
Bewes, Beverley;
Wakeling, Emma

Publication type:

Article

Confirmation of the R653Q polymorphism of the trifunctional C1-synthase enzyme as a maternal risk for neural tube defects in the Irish population.

Published in:

European Journal of Human Genetics, 2006, v. 14, n. 6, p. 768, doi. 10.1038/sj.ejhg.5201603

By:

Parle-McDermott, Anne;
Kirke, Peadar N.;
Mills, James L.;
Molloy, Anne M.;
Cox, Christopher;
O'Leary, Valerie B.;
Pangilinan, Faith;
Conley, Mary;
Cleary, Laura;
Brody, Lawrence C.;
Scott, John M.

Publication type:

Article

Interstitial 9q22.3 microdeletion: clinical and molecular characterisation of a newly recognised overgrowth syndrome.

Published in:

European Journal of Human Genetics, 2006, v. 14, n. 6, p. 759, doi. 10.1038/sj.ejhg.5201613

By:

Redon, Richard;
Baujat, Geneviève;
Sanlaville, Damien;
Le Merrer, Martine;
Vekemans, Michel;
Munnich, Arnold;
Carter, Nigel P.;
Cormier-Daire, Valérie;
Colleaux, Laurence

Publication type:

Article

SLC26A4 gene is frequently involved in nonsyndromic hearing impairment with enlarged vestibular aqueduct in Caucasian populations.

Published in:

European Journal of Human Genetics, 2006, v. 14, n. 6, p. 773, doi. 10.1038/sj.ejhg.5201611

By:

Albert, Sébastien;
Blons, Hélène;
Jonard, Laurence;
Feldmann, Delphine;
Chauvin, Pierre;
Loundon, Nathalie;
Sergent-Allaoui, Annie;
Houang, Muriel;
Joannard, Alain;
Schmerber, Sébastien;
Delobel, Bruno;
Leman, Jacques;
Journel, Hubert;
Catros, Hélène;
Dollfus, Hélène;
Eliot, Marie-Madeleine;
David, Albert;
Calais, Catherine;
Drouin-Garraud, Valérie;
Obstoy, Marie-Françoise

Publication type:

Article

Evidence from autoimmune thyroiditis of skewed X-chromosome inactivation in female predisposition to autoimmunity.

Published in:

European Journal of Human Genetics, 2006, v. 14, n. 6, p. 791, doi. 10.1038/sj.ejhg.5201614

By:

Ozcelik, Tayfun;
Uz, Elif;
Akyerli, Cemaliye B;
Bagislar, Sevgi;
Mustafa, Chigdem A;
Gursoy, Alptekin;
Akarsu, Nurten;
Toruner, Gokce;
Kamel, Nuri;
Gullu, Sevim

Publication type:

Article