Literature DB >> 17495150

Genome-wide association. Closing the net on common disease genes.

Jennifer Couzin, Jocelyn Kaiser.   

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Year:  2007        PMID： 17495150     DOI： 10.1126/science.316.5826.820

Source DB:  PubMed          Journal:  Science        ISSN： 0036-8075            Impact factor:   47.728


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  26 in total

1.  Medicine. The future of personal genomics.

Authors:  Amy L McGuire; Mildred K Cho; Sean E McGuire; Timothy Caulfield
Journal:  Science       Date:  2007-09-21       Impact factor: 47.728

2.  Accommodating linkage disequilibrium in genetic-association analyses via ridge regression.

Authors:  Nathalie Malo; Ondrej Libiger; Nicholas J Schork
Journal:  Am J Hum Genet       Date:  2008-02       Impact factor: 11.025

3.  Continue to study childhood ALL.

Authors:  Mary V Relling; William E Evans; Ching-Hon Pui
Journal:  Blood       Date:  2008-01-01       Impact factor: 22.113

4.  The Pathway Less Traveled: Moving from Candidate Genes to Candidate Pathways in the Analysis of Genome-Wide Data from Large Scale Pharmacogenetic Association Studies.

Authors:  R A Wilke; R K Mareedu; J H Moore
Journal:  Curr Pharmacogenomics Person Med       Date:  2008

5.  Power of deep, all-exon resequencing for discovery of human trait genes.

Authors:  Gregory V Kryukov; Alexander Shpunt; John A Stamatoyannopoulos; Shamil R Sunyaev
Journal:  Proc Natl Acad Sci U S A       Date:  2009-02-06       Impact factor: 11.205

Review 6.  The genetic study of primary biliary cirrhosis: great hope, some caution.

Authors:  Gideon M Hirschfield; E J Heathcote
Journal:  Curr Gastroenterol Rep       Date:  2008-06

7.  Using prior knowledge and genome-wide association to identify pathways involved in multiple sclerosis.

Authors:  Marylyn D Ritchie
Journal:  Genome Med       Date:  2009-06-29       Impact factor: 11.117

8.  Absolute pitch: a special group of ears.

Authors:  Dennis T Drayna
Journal:  Proc Natl Acad Sci U S A       Date:  2007-09-10       Impact factor: 11.205

9.  The common colorectal cancer predisposition SNP rs6983267 at chromosome 8q24 confers potential to enhanced Wnt signaling.

Authors:  Sari Tuupanen; Mikko Turunen; Rainer Lehtonen; Outi Hallikas; Sakari Vanharanta; Teemu Kivioja; Mikael Björklund; Gonghong Wei; Jian Yan; Iina Niittymäki; Jukka-Pekka Mecklin; Heikki Järvinen; Ari Ristimäki; Mariachiara Di-Bernardo; Phil East; Luis Carvajal-Carmona; Richard S Houlston; Ian Tomlinson; Kimmo Palin; Esko Ukkonen; Auli Karhu; Jussi Taipale; Lauri A Aaltonen
Journal:  Nat Genet       Date:  2009-06-28       Impact factor: 38.330

Review 10.  The search for genetic polymorphisms in the homocysteine/folate pathway that contribute to the etiology of human neural tube defects.

Authors:  Anne M Molloy; Lawrence C Brody; James L Mills; John M Scott; Peadar N Kirke
Journal:  Birth Defects Res A Clin Mol Teratol       Date:  2009-04
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