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Jared M Evans

Showing results (11-20 of 36) with videos related to

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Journal of Cardiovascular Development and Disease|September 27, 2023
Identification of Rare Genetic Variants in Familial Spontaneous Coronary Artery Dissection and Evidence for Shared Biological PathwaysTamiel N Turley, Jeanne L Theis, Jared M Evans, et al.
Circulation. Cardiovascular Genetics|May 17, 2013
Exome sequencing and systems biology converge to identify novel mutations in the L-type calcium channel, CACNA1C, linked to autosomal dominant long QT syndromeNicole J Boczek, Jabe M Best, David J Tester, et al.
Circulation. Genomic and Precision Medicine|December 16, 2020
Genetic Association Between Hypoplastic Left Heart Syndrome and CardiomyopathiesJeanne L Theis, Jessie J Hu, Rhianna S Sundsbak, et al.
Human Molecular Genetics|May 5, 2017
Recessive TAF1A mutations reveal ribosomopathy in siblings with end-stage pediatric dilated cardiomyopathyPamela A Long, Jeanne L Theis, Yu-Huan Shih, et al.
Circulation. Cardiovascular Genetics|June 19, 2015
Recessive MYH6 Mutations in Hypoplastic Left Heart With Reduced Ejection FractionJeanne L Theis, Michael T Zimmermann, Jared M Evans, et al.
Human Genetics|July 13, 2015
Compound heterozygous NOTCH1 mutations underlie impaired cardiogenesis in a patient with hypoplastic left heart syndromeJeanne L Theis, Sybil C L Hrstka, Jared M Evans, et al.
Circulation. Genomic and Precision Medicine|March 20, 2019
Rare Missense Variants in TLN1 Are Associated With Familial and Sporadic Spontaneous Coronary Artery DissectionTamiel N Turley, Jeanne L Theis, Rhianna S Sundsbak, et al.
Journal of Psychiatric Research|October 23, 2016
Mitochondrial DNA sequence data reveals association of haplogroup U with psychosis in bipolar disorderMark A Frye, Euijung Ryu, Malik Nassan, et al.
The Application of Clinical Genetics|December 1, 2018
Association of mitochondrial DNA copy number with self-rated health statusPaul Y Takahashi, Gregory D Jenkins, Benjamin P Welkie, et al.
The EMBO Journal|July 21, 2016
Natural underlying mtDNA heteroplasmy as a potential source of intra-person hiPSC variabilityEster Perales-Clemente, Alexandra N Cook, Jared M Evans, et al.
Pageof 4

Showing results (11-20 of 36) with videos related to

Sort By:
Pageof 4
Journal of Cardiovascular Development and Disease|September 27, 2023
Identification of Rare Genetic Variants in Familial Spontaneous Coronary Artery Dissection and Evidence for Shared Biological PathwaysTamiel N Turley, Jeanne L Theis, Jared M Evans, et al.
Circulation. Cardiovascular Genetics|May 17, 2013
Exome sequencing and systems biology converge to identify novel mutations in the L-type calcium channel, CACNA1C, linked to autosomal dominant long QT syndromeNicole J Boczek, Jabe M Best, David J Tester, et al.
Circulation. Genomic and Precision Medicine|December 16, 2020
Genetic Association Between Hypoplastic Left Heart Syndrome and CardiomyopathiesJeanne L Theis, Jessie J Hu, Rhianna S Sundsbak, et al.
Human Molecular Genetics|May 5, 2017
Recessive TAF1A mutations reveal ribosomopathy in siblings with end-stage pediatric dilated cardiomyopathyPamela A Long, Jeanne L Theis, Yu-Huan Shih, et al.
Circulation. Cardiovascular Genetics|June 19, 2015
Recessive MYH6 Mutations in Hypoplastic Left Heart With Reduced Ejection FractionJeanne L Theis, Michael T Zimmermann, Jared M Evans, et al.
Human Genetics|July 13, 2015
Compound heterozygous NOTCH1 mutations underlie impaired cardiogenesis in a patient with hypoplastic left heart syndromeJeanne L Theis, Sybil C L Hrstka, Jared M Evans, et al.
Circulation. Genomic and Precision Medicine|March 20, 2019
Rare Missense Variants in TLN1 Are Associated With Familial and Sporadic Spontaneous Coronary Artery DissectionTamiel N Turley, Jeanne L Theis, Rhianna S Sundsbak, et al.
Journal of Psychiatric Research|October 23, 2016
Mitochondrial DNA sequence data reveals association of haplogroup U with psychosis in bipolar disorderMark A Frye, Euijung Ryu, Malik Nassan, et al.
The Application of Clinical Genetics|December 1, 2018
Association of mitochondrial DNA copy number with self-rated health statusPaul Y Takahashi, Gregory D Jenkins, Benjamin P Welkie, et al.
The EMBO Journal|July 21, 2016
Natural underlying mtDNA heteroplasmy as a potential source of intra-person hiPSC variabilityEster Perales-Clemente, Alexandra N Cook, Jared M Evans, et al.
Pageof 4