Literature DB >> 17293879

Human genetics: variants in common diseases.

Nelson B Freimer, Chiara Sabatti.   

Abstract

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Year:  2007        PMID： 17293879     DOI： 10.1038/nature05568

Source DB:  PubMed          Journal:  Nature        ISSN： 0028-0836            Impact factor:   49.962


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  19 in total

1.  Pathway-based approaches for analysis of genomewide association studies.

Authors:  Kai Wang; Mingyao Li; Maja Bucan
Journal:  Am J Hum Genet       Date:  2007-12       Impact factor: 11.025

2.  Prep1 deficiency induces protection from diabetes and increased insulin sensitivity through a p160-mediated mechanism.

Authors:  Francesco Oriente; Luis Cesar Fernandez Diaz; Claudia Miele; Salvatore Iovino; Silvia Mori; Victor Manuel Diaz; Giancarlo Troncone; Angela Cassese; Pietro Formisano; Francesco Blasi; Francesco Beguinot
Journal:  Mol Cell Biol       Date:  2008-07-21       Impact factor: 4.272

3.  Gene ontology analysis of GWA study data sets provides insights into the biology of bipolar disorder.

Authors:  Peter Holmans; Elaine K Green; Jaspreet Singh Pahwa; Manuel A R Ferreira; Shaun M Purcell; Pamela Sklar; Michael J Owen; Michael C O'Donovan; Nick Craddock
Journal:  Am J Hum Genet       Date:  2009-06-18       Impact factor: 11.025

4.  Genome-wide association study of cardiac structure and systolic function in African Americans: the Candidate Gene Association Resource (CARe) study.

Authors:  Ervin R Fox; Solomon K Musani; Maja Barbalic; Honghuang Lin; Bing Yu; Kofo O Ogunyankin; Nicholas L Smith; Abdullah Kutlar; Nicole L Glazer; Wendy S Post; Dina N Paltoo; Daniel L Dries; Deborah N Farlow; Christine W Duarte; Sharon L Kardia; Kristin J Meyers; Yan V Sun; Donna K Arnett; Amit A Patki; Jin Sha; Xiangqui Cui; Tandaw E Samdarshi; Alan D Penman; Kirsten Bibbins-Domingo; Petra Bůžková; Emelia J Benjamin; David A Bluemke; Alanna C Morrison; Gerardo Heiss; J Jeffrey Carr; Russell P Tracy; Thomas H Mosley; Herman A Taylor; Bruce M Psaty; Susan R Heckbert; Thomas P Cappola; Ramachandran S Vasan
Journal:  Circ Cardiovasc Genet       Date:  2012-12-28

Review 5.  Atrial fibrillation: current knowledge and future directions in epidemiology and genomics.

Authors:  Jared W Magnani; Michiel Rienstra; Honghuang Lin; Moritz F Sinner; Steven A Lubitz; David D McManus; Josée Dupuis; Patrick T Ellinor; Emelia J Benjamin
Journal:  Circulation       Date:  2011-11-01       Impact factor: 29.690

Review 6.  Evolutionary evidence of the effect of rare variants on disease etiology.

Authors:  I P Gorlov; O Y Gorlova; M L Frazier; M R Spitz; C I Amos
Journal:  Clin Genet       Date:  2010-09-10       Impact factor: 4.438

7.  Polymorphic length of FOXE1 alanine stretch: evidence for genetic susceptibility to thyroid dysgenesis.

Authors:  Aurore Carré; Mireille Castanet; Sylvia Sura-Trueba; Gabor Szinnai; Guy Van Vliet; Delphine Trochet; Jeanne Amiel; Juliane Léger; Paul Czernichow; Virginie Scotet; Michel Polak
Journal:  Hum Genet       Date:  2007-08-24       Impact factor: 4.132

8.  Interaction between fibrinogen and IL-6 genetic variants and associations with cardiovascular disease risk in the Cardiovascular Health Study.

Authors:  Cara L Carty; Patrick Heagerty; Susan R Heckbert; Gail P Jarvik; Leslie A Lange; Mary Cushman; Russell P Tracy; Alexander P Reiner
Journal:  Ann Hum Genet       Date:  2010-01       Impact factor: 1.670

9.  Replication study of candidate genes/loci associated with osteoporosis based on genome-wide screening.

Authors:  Y-P Zhang; F-Y Deng; Y Chen; Y-F Pei; Y Fang; Y-F Guo; X Guo; X-G Liu; Q Zhou; Y-J Liu; H-W Deng
Journal:  Osteoporos Int       Date:  2009-07-24       Impact factor: 4.507

Review 10.  Eating disorders: the current status of molecular genetic research.

Authors:  Susann Scherag; Johannes Hebebrand; Anke Hinney
Journal:  Eur Child Adolesc Psychiatry       Date:  2009-12-24       Impact factor: 4.785
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