Literature DB >> 15678133

Genewindow: an interactive tool for visualization of genomic variation.

Brian Staats, Liqun Qi, Michael Beerman, Hugues Sicotte, Laura A Burdett, Bernice Packer, Stephen J Chanock, Meredith Yeager.   

Abstract

Mesh：

Year:  2005        PMID： 15678133     DOI： 10.1038/ng0205-109

Source DB:  PubMed          Journal:  Nat Genet        ISSN： 1061-4036            Impact factor:   38.330


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  9 in total

1.  Nicotine withdrawal sensitivity, linkage to chr6q26, and association of OPRM1 SNPs in the SMOking in FAMilies (SMOFAM) sample.

Authors:  Jill Hardin; Yungang He; Harold S Javitz; Jennifer Wessel; Ruth E Krasnow; Elizabeth Tildesley; Hyman Hops; Gary E Swan; Andrew W Bergen
Journal:  Cancer Epidemiol Biomarkers Prev       Date:  2009-12       Impact factor: 4.254

2.  SimplevisGrid: grid services for visualization of diverse biomedical knowledge and molecular systems data.

Authors:  Todd H Stokes; May D Wang
Journal:  Conf Proc IEEE Eng Med Biol Soc       Date:  2009

3.  Gross deletions involving IGHM, BTK, or Artemis: a model for genomic lesions mediated by transposable elements.

Authors:  Menno C van Zelm; Corinne Geertsema; Nicole Nieuwenhuis; Dick de Ridder; Mary Ellen Conley; Claudine Schiff; Ilhan Tezcan; Ewa Bernatowska; Nico G Hartwig; Elisabeth A M Sanders; Jiri Litzman; Irina Kondratenko; Jacques J M van Dongen; Mirjam van der Burg
Journal:  Am J Hum Genet       Date:  2008-02       Impact factor: 11.025

4.  Dopamine genes and nicotine dependence in treatment-seeking and community smokers.

Authors:  Andrew W Bergen; David V Conti; David Van Den Berg; Wonho Lee; Jinghua Liu; Dalin Li; Nan Guo; Huaiyu Mi; Paul D Thomas; Christina N Lessov-Schlaggar; Ruth Krasnow; Yungang He; Denise Nishita; Ruhong Jiang; Jennifer B McClure; Elizabeth Tildesley; Hyman Hops; Rachel F Tyndale; Neal L Benowitz; Caryn Lerman; Gary E Swan
Journal:  Neuropsychopharmacology       Date:  2009-06-03       Impact factor: 7.853

5.  Detection of somatic mutations by high-resolution DNA melting (HRM) analysis in multiple cancers.

Authors:  Jesus Gonzalez-Bosquet; Jacob Calcei; Jun S Wei; Montserrat Garcia-Closas; Mark E Sherman; Stephen Hewitt; Joseph Vockley; Jolanta Lissowska; Hannah P Yang; Javed Khan; Stephen Chanock
Journal:  PLoS One       Date:  2011-01-17       Impact factor: 3.240

6.  SNP-VISTA: an interactive SNP visualization tool.

Authors:  Nameeta Shah; Michael V Teplitsky; Simon Minovitsky; Len A Pennacchio; Philip Hugenholtz; Bernd Hamann; Inna L Dubchak
Journal:  BMC Bioinformatics       Date:  2005-12-08       Impact factor: 3.169

7.  SNP500Cancer: a public resource for sequence validation, assay development, and frequency analysis for genetic variation in candidate genes.

Authors:  Bernice R Packer; Meredith Yeager; Laura Burdett; Robert Welch; Michael Beerman; Liqun Qi; Hugues Sicotte; Brian Staats; Mekhala Acharya; Andrew Crenshaw; Andrew Eckert; Vinita Puri; Daniela S Gerhard; Stephen J Chanock
Journal:  Nucleic Acids Res       Date:  2006-01-01       Impact factor: 16.971

8.  Cis sequence effects on gene expression.

Authors:  Andrew W Bergen; Andrea Baccarelli; Timothy K McDaniel; Kenneth Kuhn; Ruth Pfeiffer; Jerry Kakol; Patrick Bender; Kevin Jacobs; Bernice Packer; Stephen J Chanock; Meredith Yeager
Journal:  BMC Genomics       Date:  2007-08-29       Impact factor: 3.969

9.  VariVis: a visualisation toolkit for variation databases.

Authors:  Timothy D Smith; Richard G H Cotton
Journal:  BMC Bioinformatics       Date:  2008-04-23       Impact factor: 3.169
  9 in total

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