Literature DB >> 22715278

Modifying Mendel: approaches for identification of susceptibility alleles for human cardiovascular malformations.

Kim L McBride, Stephanie M Ware.   

Abstract

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Year:  2012        PMID： 22715278     DOI： 10.1161/CIRCGENETICS.112.963579

Source DB:  PubMed          Journal:  Circ Cardiovasc Genet        ISSN： 1942-3268


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  5 in total

1.  Genetic abnormalities in FOXP1 are associated with congenital heart defects.

Authors:  Sheng-Wei Chang; Mona Mislankar; Chaitali Misra; Nianyuan Huang; Daniel G Dajusta; Steven M Harrison; Kim L McBride; Linda A Baker; Vidu Garg
Journal:  Hum Mutat       Date:  2013-07-11       Impact factor: 4.878

2.  Modifying Mendel Redux: Unbiased Approaches Can Find Modifiers.

Authors:  Kim L McBride; Stephanie M Ware
Journal:  Circ Cardiovasc Genet       Date:  2017-10

3.  Use of a targeted, combinatorial next-generation sequencing approach for the study of bicuspid aortic valve.

Authors:  Elizabeth M Bonachea; Gloria Zender; Peter White; Don Corsmeier; David Newsom; Sara Fitzgerald-Butt; Vidu Garg; Kim L McBride
Journal:  BMC Med Genomics       Date:  2014-09-26       Impact factor: 3.063

4.  The analysis of heterotaxy patients reveals new loss-of-function variants of GRK5.

Authors:  Davor Lessel; Tariq Muhammad; Teresa Casar Tena; Barbara Moepps; Martin D Burkhalter; Marc-Phillip Hitz; Okan Toka; Axel Rentzsch; Stephan Schubert; Adelheid Schalinski; Ulrike M M Bauer; Christian Kubisch; Stephanie M Ware; Melanie Philipp
Journal:  Sci Rep       Date:  2016-09-13       Impact factor: 4.379

5.  Rationale for the Cytogenomics of Cardiovascular Malformations Consortium: A Phenotype Intensive Registry Based Approach.

Authors:  Robert B Hinton; Kim L McBride; Steven B Bleyl; Neil E Bowles; William L Border; Vidu Garg; Teresa A Smolarek; Seema R Lalani; Stephanie M Ware
Journal:  J Cardiovasc Dev Dis       Date:  2015-04-29
  5 in total

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