Lisa M Vincent

Lisa M Vincent

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Lisa M Vincent

Lisa M Vincent

Publications by authors named "Lisa M Vincent"

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15Publications

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National Scouting Combine Scores as Performance Predictors in the National Football League.

J Strength Cond Res 2019 Jan;33(1):104-111

Human Performance Laboratory, Department of Kinesiology, University of Rhode Island, Kingston, Rhode Island.

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http://dx.doi.org/10.1519/JSC.0000000000002937DOI Listing
January 2019

Reclassification of the p.Ile208Val variant by case-level data sharing.

Cold Spring Harb Mol Case Stud 2018 10 1;4(5). Epub 2018 Oct 1.

Laboratory for Molecular Medicine, Partners Healthcare Personalized Medicine, Cambridge, Massachusetts 02139, USA.

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http://molecularcasestudies.cshlp.org/lookup/doi/10.1101/mcs
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http://dx.doi.org/10.1101/mcs.a002675DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6169827PMC
October 2018

Reassessment of Genomic Sequence Variation to Harmonize Interpretation for Personalized Medicine.

Am J Hum Genet 2016 Nov 27;99(5):1140-1149. Epub 2016 Oct 27.

Department of Human Genetics, Emory University School of Medicine, Atlanta, GA 30322, USA; Emory Genetics Laboratory, Decatur, GA 30033, USA. Electronic address:

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http://dx.doi.org/10.1016/j.ajhg.2016.09.015DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5097932PMC
November 2016

Coagulation factor V(A2440G) causes east Texas bleeding disorder via TFPIα.

J Clin Invest 2013 Sep 27;123(9):3777-87. Epub 2013 Aug 27.

Department of Internal Medicine, Division of Medical Genetics, University of Texas Health Science Center at Houston, Houston, Texas 77030, USA.

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http://dx.doi.org/10.1172/JCI69091DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3754264PMC
September 2013

Novel 47.5-kb deletion in RAB27A results in severe Griscelli Syndrome Type 2.

Mol Genet Metab 2010 Sep 10;101(1):62-5. Epub 2010 Jun 10.

Section on Human Biochemical Genetics, Medical Genetics Branch, NHGRI, NIH, Bethesda, MD 20892, USA.

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http://dx.doi.org/10.1016/j.ymgme.2010.05.015DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2922439PMC
September 2010

Hermansky-Pudlak syndrome type 1 in patients of Indian descent.

Mol Genet Metab 2009 Jul 2;97(3):227-33. Epub 2009 Apr 2.

Section on Human Biochemical Genetics, Medical Genetics Branch, NHGRI, NIH, 10 Center Drive, Bldg. 10, Rm 10C107, MSC1851, Bethesda, MD 20892-1851, USA.

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http://dx.doi.org/10.1016/j.ymgme.2009.03.011DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2694228PMC
July 2009

Hermansky-Pudlak syndrome in two African-American brothers.

Am J Med Genet A 2009 May;149A(5):987-92

Section on Human Biochemical Genetics, Medical Genetics Branch, National Human Genome Research Institute, National Institutes of Health, Bethesda, Maryland 20892-1851, USA.

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http://dx.doi.org/10.1002/ajmg.a.32757DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2788939PMC
May 2009