Works matching IS 10184813 AND DT 2007 AND VI 15 AND IP 3

Results: 21

Are genome-wide association studies all that we need to dissect the genetic component of complex human diseases?

Published in:

European Journal of Human Genetics, 2007, v. 15, n. 3, p. 260, doi. 10.1038/sj.ejhg.5201753

By:

Bourgain, Catherine;
Génin, Emmanuelle;
Cox, Nancy;
Clerget-Darpoux, Françoise

Publication type:

Article

Sotos syndrome.

Published in:

European Journal of Human Genetics, 2007, v. 15, n. 3, p. 264, doi. 10.1038/sj.ejhg.5201686

By:

Tatton-Brown, Katrina;
Rahman, Nazneen

Publication type:

Article

Cystic Fibrosis: Cystic fibrosis and lactase persistence: a possible correlation.

Published in:

European Journal of Human Genetics, 2007, v. 15, n. 3, p. 255, doi. 10.1038/sj.ejhg.5201749

By:

Modiano, Guido;
Ciminelli, Bianca M.;
Pignatti, Pier F.

Publication type:

Article

Significant variation in haplotype block structure but conservation in tagSNP patterns among global populations.

Published in:

European Journal of Human Genetics, 2007, v. 15, n. 3, p. 302, doi. 10.1038/sj.ejhg.5201751

By:

Sheng Gu;
Pakstis, Andrew J.;
Hui Li;
Speed, William C.;
Kidd, Judith R.;
Kidd, Kenneth K.

Publication type:

Article

Enhanced linkage of a locus on chromosome 2 to premature coronary artery disease in the absence of hypercholesterolemia.

Published in:

European Journal of Human Genetics, 2007, v. 15, n. 3, p. 313, doi. 10.1038/sj.ejhg.5201752

By:

Nsengimana, Jérémie;
Samani, Nilesh J.;
Hall, Alistair S.;
Balmforth, Anthony J.;
Mangino, Massimo;
Yuldasheva, Nadira;
Maqbool, Azhar;
Braund, Peter;
Burton, Paul;
Bishop, D. Timothy;
Ball, Stephen G.;
Barrett, Jennifer H.

Publication type:

Article

No contribution of angiotensin-converting enzyme (ACE) gene variants to severe obesity: a model for comprehensive case/control and quantitative cladistic analysis of ACE in human diseases.

Published in:

European Journal of Human Genetics, 2007, v. 15, n. 3, p. 320, doi. 10.1038/sj.ejhg.5201754

By:

Bell, Christopher G.;
Meyre, David;
Petretto, Enrico;
Levy-Marchal, Claire;
Hercberg, Serge;
Charles, Marie Aline;
Boyle, Cliona;
Weill, Jacques;
Tauber, Maïte;
Mein, Charles A.;
Aitman, Timothy J.;
Froguel, Philippe;
Walley, Andrew J.

Publication type:

Article

Refined genomic localization and ethnic differences observed for the IBD5 association with Crohn's disease.

Published in:

European Journal of Human Genetics, 2007, v. 15, n. 3, p. 328, doi. 10.1038/sj.ejhg.5201756

By:

Silverberg, Mark S.;
Duerr, Richard H.;
Brant, Steven R.;
Bromfield, Gillian;
Datta, Lisa W.;
Jani, Niraj;
Kane, Sunanda V.;
Rotter, Jerome I.;
Schumm, L. Philip;
Steinhart, A. Hillary;
Taylor, Kent D.;
Yang, Huiying;
Cho, Judy H.;
Rioux, John D.;
Daly, Mark J.

Publication type:

Article

Functional analysis of human S-adenosylhomocysteine hydrolase isoforms SAHH-2 and SAHH-3.

Published in:

European Journal of Human Genetics, 2007, v. 15, n. 3, p. 347, doi. 10.1038/sj.ejhg.5201757

By:

Ksenija Fumić;
Belužić, Robert;
Ćuk, Mario;
Pavkov, Tea;
Kloor, Doris;
Barić, Ivo;
Mijić, Ivana;
Vugrek, Oliver

Publication type:

Article

Mutation screening of brain-expressed X-chromosomal miRNA genes in 464 patients with nonsyndromic X-linked mental retardation.

Published in:

European Journal of Human Genetics, 2007, v. 15, n. 3, p. 375, doi. 10.1038/sj.ejhg.5201758

By:

Wei Chen;
Jensen, Lars R.;
Gecz, Jozef;
Fryns, Jean-Pierre;
Moraine, Claude;
de Brouwer, Arjan;
Chelly, Jamel;
Moser, Bettina;
Ropers, H Hilger;
Kuss, Andreas W.

Publication type:

Article

Methylation analysis of the intergenic differentially methylated region of DLK1-GTL2 in human.

Published in:

European Journal of Human Genetics, 2007, v. 15, n. 3, p. 352, doi. 10.1038/sj.ejhg.5201759

By:

Geuns, Elke;
De Temmerman, Nele;
Hilven, Pierre;
Van Steirteghem, André;
Liebaers, Inge;
De Rycke, Martine

Publication type:

Article

Multiple mutations responsible for frequent genetic diseases in isolated populations.

Published in:

European Journal of Human Genetics, 2007, v. 15, n. 3, p. 272, doi. 10.1038/sj.ejhg.5201760

By:

Zlotogora, Joël

Publication type:

Article

A seventh locus for otosclerosis, OTSC7, maps to chromosome 6q13–16.1.

Published in:

European Journal of Human Genetics, 2007, v. 15, n. 3, p. 362, doi. 10.1038/sj.ejhg.5201761

By:

Thys, Melissa;
Van Den Bogaert, Kris;
Iliadou, Vassiliki;
Vanderstraeten, Kathleen;
Dieltjens, Nele;
Schrauwen, Isabelle;
Chen, Wenjie;
Eleftheriades, Nikolaos;
Grigoriadou, Maria;
Pauw, Robert Jan;
Cremers, Cor R. W. J.;
Smith, Richard J. H.;
Petersen, Michael B.;
Van Camp, Guy

Publication type:

Article

FGF10 missense mutations in aplasia of lacrimal and salivary glands (ALSG).

Published in:

European Journal of Human Genetics, 2007, v. 15, n. 3, p. 379, doi. 10.1038/sj.ejhg.5201762

By:

Entesarian, Miriam;
Dahlqvist, Johanna;
Shashi, Vandana;
Stanley, Christy S.;
Falahat, Babak;
Reardon, William;
Dahl, Niklas

Publication type:

Article

Dopamine transporter, gender, and number of sexual partners among young adults.

Published in:

European Journal of Human Genetics, 2007, v. 15, n. 3, p. 279, doi. 10.1038/sj.ejhg.5201763

By:

Guang Guo;
Yuying Tong;
Cui-Wei Xie;
Lange, Leslie A.

Publication type:

Article

Partial duplications of the MSH2 and MLH1 genes in hereditary nonpolyposis colorectal cancer.

Published in:

European Journal of Human Genetics, 2007, v. 15, n. 3, p. 383, doi. 10.1038/sj.ejhg.5201765

By:

Baert-Desurmont, Stephanie;
Buisine, Marie-Pierre;
Bessenay, Emilie;
Frerot, Stephanie;
Lovecchio, Tonio;
Martin, Cosette;
Olschwang, Sylviane;
Qing Wang;
Frebourg, Thierry

Publication type:

Article

Haplotypes in the human Foxo1a and Foxo3a genes; impact on disease and mortality at old age.

Published in:

European Journal of Human Genetics, 2007, v. 15, n. 3, p. 294, doi. 10.1038/sj.ejhg.5201766

By:

Kuningas, Maris;
Mägi, Reedik;
Westendorp, Rudi G. J.;
Slagboom, P. Eline;
Remm, Maido;
van Heemst, Diana

Publication type:

Article

Association of PDCD1 polymorphisms with childhood-onset systemic lupus erythematosus.

Published in:

European Journal of Human Genetics, 2007, v. 15, n. 3, p. 336, doi. 10.1038/sj.ejhg.5201767

By:

Velázquez-Cruz, Rafael;
Orozco, Lorena;
Espinosa-Rosales, Francisco;
Carreño-Manjarrez, Roberto;
Solís-Vallejo, Eunice;
López-Lara, Norma D.;
Ruiz-López, Ivon K.;
Rodríguez-Lozano, Ana L.;
Estrada-Gil, Jesús K.;
Jiménez-Sénchez, Gerardo;
Baca, Vicente

Publication type:

Article

Africans in Yorkshire? The deepest-rooting clade of the Y phylogeny within an English genealogy.

Published in:

European Journal of Human Genetics, 2007, v. 15, n. 3, p. 288, doi. 10.1038/sj.ejhg.5201771

By:

Turi E.King;
Parkin, Emma J.;
Swinfield, Geoff;
Cruciani, Fulvio;
Scozzari, Rosaria;
Rosa, Alexandra;
Si-Keun Lim;
Yali Xue;
Tyler-Smith, Chris;
Jobling, Mark A.

Publication type:

Article

Progranulin mutations in Dutch familial frontotemporal lobar degeneration.

Published in:

European Journal of Human Genetics, 2007, v. 15, n. 3, p. 369, doi. 10.1038/sj.ejhg.5201772

By:

Bronner, Iraad F.;
Rizzu, Patrizia;
Seelaar, Harro;
van Mil, Saskia E.;
Anar, Burcu;
Azmani, Asma;
Kaat, Laura Donker;
Rosso, Sonia;
Heutink, Peter;
van Swieten, John C.

Publication type:

Article

TCF7L2 polymorphisms are associated with type 2 diabetes in northern Sweden.

Published in:

European Journal of Human Genetics, 2007, v. 15, n. 3, p. 342, doi. 10.1038/sj.ejhg.5201773

By:

Mayans, Sofia;
Lackovic, Kurt;
Lindgren, Petter;
Ruikka, Karin;
Ågren, Åsa;
Eliasson, Mats;
Holmberg, Dan

Publication type:

Article

AHI1, a pivotal neurodevelopmental gene, and C6orf217 are associated with susceptibility to schizophrenia.

Published in:

2007

By:

Amann-Zalcenstein, Daniela;
Avidan, Nili;
Kanyas, Kyra;
Ebstein, Richard P.;
Kohn, Yoav;
Hamdan, Adnan;
Ben-Asher, Edna;
Karni, Osnat;
Mujaheed, Muhammed;
Segman, Ronnen H.;
Maier, Wolfgang;
Macciardi, Fabio;
Beckmann, Jacques S.;
Lancet, Doron;
Lerer, Bernard

Publication type:

Correction Notice