Literature DB >> 19371834

Kinesin family member 6 variant Trp719Arg does not associate with angiographically defined coronary artery disease in the Ottawa Heart Genomics Study.

Alexandre F R Stewart, Sonny Dandona, Li Chen, Olivia Assogba, Melanie Belanger, Gwen Ewart, Rosemary LaRose, Heather Doelle, Kathryn Williams, George A Wells, Ruth McPherson, Robert Roberts.   

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Year:  2009        PMID: 19371834     DOI: 10.1016/j.jacc.2008.12.051

Source DB:  PubMed          Journal:  J Am Coll Cardiol        ISSN: 0735-1097            Impact factor:   24.094


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  41 in total

1.  Identification of germline genomic copy number variation in familial pancreatic cancer.

Authors:  Wigdan Al-Sukhni; Sarah Joe; Anath C Lionel; Nora Zwingerman; George Zogopoulos; Christian R Marshall; Ayelet Borgida; Spring Holter; Aaron Gropper; Sara Moore; Melissa Bondy; Alison P Klein; Gloria M Petersen; Kari G Rabe; Ann G Schwartz; Sapna Syngal; Stephen W Scherer; Steven Gallinger
Journal:  Hum Genet       Date:  2012-06-05       Impact factor: 4.132

2.  Design of the Coronary ARtery DIsease Genome-Wide Replication And Meta-Analysis (CARDIoGRAM) Study: A Genome-wide association meta-analysis involving more than 22 000 cases and 60 000 controls.

Authors:  Michael Preuss; Inke R König; John R Thompson; Jeanette Erdmann; Devin Absher; Themistocles L Assimes; Stefan Blankenberg; Eric Boerwinkle; Li Chen; L Adrienne Cupples; Alistair S Hall; Eran Halperin; Christian Hengstenberg; Hilma Holm; Reijo Laaksonen; Mingyao Li; Winfried März; Ruth McPherson; Kiran Musunuru; Christopher P Nelson; Mary Susan Burnett; Stephen E Epstein; Christopher J O'Donnell; Thomas Quertermous; Daniel J Rader; Robert Roberts; Arne Schillert; Kari Stefansson; Alexandre F R Stewart; Gudmar Thorleifsson; Benjamin F Voight; George A Wells; Andreas Ziegler; Sekar Kathiresan; Muredach P Reilly; Nilesh J Samani; Heribert Schunkert
Journal:  Circ Cardiovasc Genet       Date:  2010-10-05

3.  Severe intellectual disability and autistic features associated with microduplication 2q23.1.

Authors:  Brian H Y Chung; Sureni Mullegama; Christian R Marshall; Anath C Lionel; Rosanna Weksberg; Lucie Dupuis; Lauren Brick; Chumei Li; Stephen W Scherer; Swaroop Aradhya; D James Stavropoulos; Sarah H Elsea; Roberto Mendoza-Londono
Journal:  Eur J Hum Genet       Date:  2011-11-16       Impact factor: 4.246

Review 4.  Cardiovascular drugs and the genetic response.

Authors:  Sonny Dandona
Journal:  Methodist Debakey Cardiovasc J       Date:  2014 Jan-Mar

5.  Rare deletions at the neurexin 3 locus in autism spectrum disorder.

Authors:  Andrea K Vaags; Anath C Lionel; Daisuke Sato; McKinsey Goodenberger; Quinn P Stein; Sarah Curran; Caroline Ogilvie; Joo Wook Ahn; Irene Drmic; Lili Senman; Christina Chrysler; Ann Thompson; Carolyn Russell; Aparna Prasad; Susan Walker; Dalila Pinto; Christian R Marshall; Dimitri J Stavropoulos; Lonnie Zwaigenbaum; Bridget A Fernandez; Eric Fombonne; Patrick F Bolton; David A Collier; Jennelle C Hodge; Wendy Roberts; Peter Szatmari; Stephen W Scherer
Journal:  Am J Hum Genet       Date:  2011-12-29       Impact factor: 11.025

6.  Evaluation of non-synonymous NPPA single nucleotide polymorphisms in atrial fibrillation.

Authors:  Jason D Roberts; Robert W Davies; Steven A Lubitz; Isabelle L Thibodeau; Pablo B Nery; David H Birnie; Emelia J Benjamin; Robert Lemery; Patrick T Ellinor; Michael H Gollob
Journal:  Europace       Date:  2010-06-12       Impact factor: 5.214

7.  Prospective study of insulin-like growth factor-I, insulin-like growth factor-binding protein 3, genetic variants in the IGF1 and IGFBP3 genes and risk of coronary artery disease.

Authors:  Sally L Ricketts; Katrijn L Rensing; Jeff M Holly; Li Chen; Elizabeth H Young; Robert Luben; Sofie Ashford; Kijoung Song; Xin Yuan; Abbas Dehghan; Benjamin J Wright; Dawn M Waterworth; Vincent Mooser; Gérard Waeber; Peter Vollenweider; Stephen E Epstein; Mary S Burnett; Joseph M Devaney; Hakon H Hakonarson; Daniel J Rader; Muredach P Reilly; John Danesh; Simon G Thompson; Alison M Dunning; Cornelia M van Duijn; Nilesh J Samani; Ruth McPherson; Nicholas J Wareham; Kay-Tee Khaw; S Matthijs Boekholdt; Manjinder S Sandhu
Journal:  Int J Mol Epidemiol Genet       Date:  2011-08-03

8.  SHANK1 Deletions in Males with Autism Spectrum Disorder.

Authors:  Daisuke Sato; Anath C Lionel; Claire S Leblond; Aparna Prasad; Dalila Pinto; Susan Walker; Irene O'Connor; Carolyn Russell; Irene E Drmic; Fadi F Hamdan; Jacques L Michaud; Volker Endris; Ralph Roeth; Richard Delorme; Guillaume Huguet; Marion Leboyer; Maria Rastam; Christopher Gillberg; Mark Lathrop; Dimitri J Stavropoulos; Evdokia Anagnostou; Rosanna Weksberg; Eric Fombonne; Lonnie Zwaigenbaum; Bridget A Fernandez; Wendy Roberts; Gudrun A Rappold; Christian R Marshall; Thomas Bourgeron; Peter Szatmari; Stephen W Scherer
Journal:  Am J Hum Genet       Date:  2012-04-12       Impact factor: 11.025

9.  KIF6 p.Trp719Arg Testing to Assess Risk of Coronary Artery Disease and/or Statin Response.

Authors:  Diane Allingham-Hawkins; Andrew Lea; Susan Levine
Journal:  PLoS Curr       Date:  2010-10-21

10.  Investigation of KIF6 Trp719Arg in a case-control study of myocardial infarction: a Costa Rican population.

Authors:  Lance A Bare; Edward A Ruiz-Narvaéz; Carmen H Tong; Andre R Arellano; Charles M Rowland; Joseph J Catanese; Frank M Sacks; James J Devlin; Hannia Campos
Journal:  PLoS One       Date:  2010-09-29       Impact factor: 3.240

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