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Michael A Simpson

Showing results (81-90 of 168) with videos related to

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Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 25, 2018
Noncardiac genetic predisposition in sudden infant death syndromeBelinda Gray, David J Tester, Leonie Ch Wong, et al.
The Journal of Investigative Dermatology|August 5, 2017
Tissue and Circulating MicroRNA Co-expression Analysis Shows Potential Involvement of miRNAs in the Pathobiology of Frontal Fibrosing AlopeciaChristos Tziotzios, Chrysanthi Ainali, Susan Holmes, et al.
The Journal of Clinical Investigation|August 18, 2015
SLFN14 mutations underlie thrombocytopenia with excessive bleeding and platelet secretion defectsSarah J Fletcher, Ben Johnson, Gillian C Lowe, et al.
Journal of the American College of Cardiology|March 17, 2018
Cardiac Genetic Predisposition in Sudden Infant Death SyndromeDavid J Tester, Leonie C H Wong, Pritha Chanana, et al.
American Journal of Human Genetics|February 7, 2008
Sequence alterations within CYP7B1 implicate defective cholesterol homeostasis in motor-neuron degenerationMaria K Tsaousidou, Karim Ouahchi, Tom T Warner, et al.
Cancer Discovery|April 16, 2015
Germline Mutations in the CDKN2B Tumor Suppressor Gene Predispose to Renal Cell CarcinomaMariam Jafri, Naomi C Wake, David B Ascher, et al.
The Journal of Investigative Dermatology|February 21, 2025
Genetic Risk Factors in Childhood PsoriasisChristopher Willy Schwarz, Christoffer Blegvad, David Baudry, et al.
Plos One|August 31, 2013
An in-depth characterization of the major psoriasis susceptibility locus identifies candidate susceptibility alleles within an HLA-C enhancer elementAlex Clop, Anna Bertoni, Sarah L Spain, et al.
Scientific Reports|December 3, 2021
Application of information theoretic feature selection and machine learning methods for the development of genetic risk prediction modelsFarideh Jalali-Najafabadi, Michael Stadler, Nick Dand, et al.
American Journal of Human Genetics|October 26, 2010
Defective mitochondrial mRNA maturation is associated with spastic ataxiaAndrew H Crosby, Heema Patel, Barry A Chioza, et al.
Pageof 17

Showing results (81-90 of 168) with videos related to

Sort By:
Pageof 17
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 25, 2018
Noncardiac genetic predisposition in sudden infant death syndromeBelinda Gray, David J Tester, Leonie Ch Wong, et al.
The Journal of Investigative Dermatology|August 5, 2017
Tissue and Circulating MicroRNA Co-expression Analysis Shows Potential Involvement of miRNAs in the Pathobiology of Frontal Fibrosing AlopeciaChristos Tziotzios, Chrysanthi Ainali, Susan Holmes, et al.
The Journal of Clinical Investigation|August 18, 2015
SLFN14 mutations underlie thrombocytopenia with excessive bleeding and platelet secretion defectsSarah J Fletcher, Ben Johnson, Gillian C Lowe, et al.
Journal of the American College of Cardiology|March 17, 2018
Cardiac Genetic Predisposition in Sudden Infant Death SyndromeDavid J Tester, Leonie C H Wong, Pritha Chanana, et al.
American Journal of Human Genetics|February 7, 2008
Sequence alterations within CYP7B1 implicate defective cholesterol homeostasis in motor-neuron degenerationMaria K Tsaousidou, Karim Ouahchi, Tom T Warner, et al.
Cancer Discovery|April 16, 2015
Germline Mutations in the CDKN2B Tumor Suppressor Gene Predispose to Renal Cell CarcinomaMariam Jafri, Naomi C Wake, David B Ascher, et al.
The Journal of Investigative Dermatology|February 21, 2025
Genetic Risk Factors in Childhood PsoriasisChristopher Willy Schwarz, Christoffer Blegvad, David Baudry, et al.
Plos One|August 31, 2013
An in-depth characterization of the major psoriasis susceptibility locus identifies candidate susceptibility alleles within an HLA-C enhancer elementAlex Clop, Anna Bertoni, Sarah L Spain, et al.
Scientific Reports|December 3, 2021
Application of information theoretic feature selection and machine learning methods for the development of genetic risk prediction modelsFarideh Jalali-Najafabadi, Michael Stadler, Nick Dand, et al.
American Journal of Human Genetics|October 26, 2010
Defective mitochondrial mRNA maturation is associated with spastic ataxiaAndrew H Crosby, Heema Patel, Barry A Chioza, et al.
Pageof 17