Works matching IS 10184813 AND DT 2007 AND VI 15 AND IP 9

Results: 14

Support for involvement of the AHI1 locus in schizophrenia.

Published in:

European Journal of Human Genetics, 2007, v. 15, n. 9, p. 988, doi. 10.1038/sj.ejhg.5201848

By:

Ingason, Andres;
Sigmundsson, Thordur;
Steinberg, Stacy;
Sigurdsson, Engilbert;
Haraldsson, Magnus;
Magnusdottir, Brynja B.;
Frigge, Michael L.;
Kong, Augustine;
Gulcher, Jeffrey;
Thorsteinsdottir, Unnur;
Stefansson, Kari;
Petursson, Hannes;
Stefansson, Hreinn

Publication type:

Article

ALOX5AP gene variants and risk of coronary artery disease: an angiography-based study.

Published in:

European Journal of Human Genetics, 2007, v. 15, n. 9, p. 959, doi. 10.1038/sj.ejhg.5201854

By:

Girelli, Domenico;
Martinelli, Nicola;
Trabetti, Elisabetta;
Olivieri, Oliviero;
Cavallari, Ugo;
Malerba, Giovanni;
Busti, Fabiana;
Friso, Simonetta;
Pizzolo, Francesca;
Pignatti, Pier Franco;
Corrocher, Roberto

Publication type:

Article

No association of ERCC1 C8092A and T19007C polymorphisms to cancer risk: a meta-analysis.

Published in:

European Journal of Human Genetics, 2007, v. 15, n. 9, p. 967, doi. 10.1038/sj.ejhg.5201855

By:

Yuanchun Li;
Shaohua Gu;
Qihan Wu;
Yao Li;
Xuping Fu;
Yumin Mao;
Yan Huang;
Yi Xie

Publication type:

Article

The MRE11/RAD50/NBS1 complex destabilization in Lynch-syndrome patients.

Published in:

European Journal of Human Genetics, 2007, v. 15, n. 9, p. 922, doi. 10.1038/sj.ejhg.5201858

By:

Alemayehu, Aster;
Fridrichova, Ivana

Publication type:

Article

Identification of novel deletions of 15q11q13 in Angelman syndrome by array-CGH: molecular characterization and genotype–phenotype correlations.

Published in:

European Journal of Human Genetics, 2007, v. 15, n. 9, p. 943, doi. 10.1038/sj.ejhg.5201859

By:

Sahoo, Trilochan;
Bacino, Carlos A.;
German, Jennifer R.;
Shaw, Chad A.;
Bird, Lynne M.;
Kimonis, Virginia;
Anselm, Irinia;
Waisbren, Susan;
Beaudet, Arthur L.;
Peters, Sarika U.

Publication type:

Article

Homozygosity for a FBN1 missense mutation: clinical and molecular evidence for recessive Marfan syndrome.

Published in:

European Journal of Human Genetics, 2007, v. 15, n. 9, p. 930, doi. 10.1038/sj.ejhg.5201865

By:

de Vries, Bert B. A.;
Pals, Gerard;
Odink, Roelof;
Hamel, Ben C. J.

Publication type:

Article

Confirmation of associations between ion channel gene SNPs and QTc interval duration in healthy subjects.

Published in:

European Journal of Human Genetics, 2007, v. 15, n. 9, p. 974, doi. 10.1038/sj.ejhg.5201866

By:

Gouas, L.;
Nicaud, V.;
Chaouch, S.;
Berthet, M.;
Forhan, A.;
Tichet, J.;
Tiret, L.;
Balkau, B.;
Guicheney, P.

Publication type:

Article

How can genetic tests be evaluated for clinical use? Experience of the UK Genetic Testing Network.

Published in:

European Journal of Human Genetics, 2007, v. 15, n. 9, p. 917, doi. 10.1038/sj.ejhg.5201867

By:

Kroese, Mark;
Zimmern, Ron L.;
Farndon, Peter;
Stewart, Fiona;
Whittaker, Joanne

Publication type:

Article

Linkage disequilibrium analysis of two genes mapping on OFC3: PVR and PVRL2.

Published in:

European Journal of Human Genetics, 2007, v. 15, n. 9, p. 992, doi. 10.1038/sj.ejhg.5201868

By:

Pezzetti, Furio;
Palmieri, Annalisa;
Martinelli, Marcella;
Scapoli, Luca;
Arlotti, Marzia;
Baciliero, Ugo;
Padula, Ernesto;
Carinci, Paolo;
Caramelli, Elisabetta;
Carinci, Francesco

Publication type:

Article

Population genetics of familial Mediterranean fever: a review.

Published in:

European Journal of Human Genetics, 2007, v. 15, n. 9, p. 911, doi. 10.1038/sj.ejhg.5201869

By:

Yepiskoposyan, Levon;
Harutyunyan, Ashot

Publication type:

Article

A comprehensive screen for SNP associations on chromosome region 5q31–33 in Swedish/Norwegian celiac disease families.

Published in:

European Journal of Human Genetics, 2007, v. 15, n. 9, p. 980, doi. 10.1038/sj.ejhg.5201870

By:

Amundsen, Silja Svanstrøm;
Adamovic, Svetlana;
Hellqvist, Åsa;
Nilsson, Staffan;
Gudjónsdóttir, Audur H.;
Ascher, Henry;
Ek, Johan;
Larsson, Kristina;
Wahlström, Jan;
Lie, Benedicte A.;
Sollid, Ludvig M.;
Naluai, Åsa Torinsson

Publication type:

Article

Candidate genes for congenital diaphragmatic hernia from animal models: sequencing of FOG2 and PDGFRα reveals rare variants in diaphragmatic hernia patients.

Published in:

European Journal of Human Genetics, 2007, v. 15, n. 9, p. 950, doi. 10.1038/sj.ejhg.5201872

By:

Bleyl, S. B.;
Moshrefi, A.;
Shaw, G. M.;
Saijoh, Y.;
Schoenwolf, G. C.;
Pennacchio, L. A.;
Slavotinek, A. M.

Publication type:

Article

Functional analysis of pancreatitis-associated missense mutations in the pancreatic secretory trypsin inhibitor (SPINK1) gene.

Published in:

European Journal of Human Genetics, 2007, v. 15, n. 9, p. 936, doi. 10.1038/sj.ejhg.5201873

By:

Boulling, Arnaud;
Le Maréchal, Cédric;
Trouvé, Pascal;
Raguénès, Odile;
Jian-Min Chen;
Férec, Claude

Publication type:

Article

Genetics of the ECG: QT or not QT- A genetic analysis of a complex electrophysiological trait confirms several previously detected associations.

Published in:

European Journal of Human Genetics, 2007, v. 15, n. 9, p. 909, doi. 10.1038/sj.ejhg.5201877

By:

Pfeufer, Arne

Publication type:

Article