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Richard Gibbs

Showing results (81-90 of 99) with videos related to

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Nature Communications|September 30, 2023
Deleterious heteroplasmic mitochondrial mutations are associated with an increased risk of overall and cancer-specific mortalityYun Soo Hong, Stephanie L Battle, Wen Shi, et al.
Human Mutation|November 7, 2019
A diagnostic ceiling for exome sequencing in cerebellar ataxia and related neurological disordersKathie J Ngo, Jessica E Rexach, Hane Lee, et al.
Nature Genetics|December 27, 2011
Frequent somatic mutations in MAP3K5 and MAP3K9 in metastatic melanoma identified by exome sequencingMitchell S Stark, Susan L Woods, Michael G Gartside, et al.
Nature Communications|December 2, 2010
Deep resequencing reveals excess rare recent variants consistent with explosive population growthAlex Coventry, Lara M Bull-Otterson, Xiaoming Liu, et al.
Genetics|June 22, 2023
Genetic control of mRNA splicing as a potential mechanism for incomplete penetrance of rare coding variantsJonah Einson, Dafni Glinos, Eric Boerwinkle, et al.
Biorxiv : the Preprint Server for Biology|February 13, 2023
Genetic control of mRNA splicing as a potential mechanism for incomplete penetrance of rare coding variantsJonah Einson, Dafni Glinos, Eric Boerwinkle, et al.
Genome Biology|September 16, 2011
The functional spectrum of low-frequency coding variationGabor T Marth, Fuli Yu, Amit R Indap, et al.
JAMA Surgery|June 14, 2023
Outcomes After Endovascular Aortic Intervention in Patients With Connective Tissue DiseaseKarl Wilhelm Olsson, Kevin Mani, Anne Burdess, et al.
Nature Genetics|March 30, 2007
Recommendations of the 2006 Human Variome Project meetingRichard G H Cotton, , William Appelbe, et al.
Human Molecular Genetics|September 5, 2014
Association of exome sequences with plasma C-reactive protein levels in >9000 participantsUrsula M Schick, Paul L Auer, Joshua C Bis, et al.
Pageof 10

Showing results (81-90 of 99) with videos related to

Sort By:
Pageof 10
Nature Communications|September 30, 2023
Deleterious heteroplasmic mitochondrial mutations are associated with an increased risk of overall and cancer-specific mortalityYun Soo Hong, Stephanie L Battle, Wen Shi, et al.
Human Mutation|November 7, 2019
A diagnostic ceiling for exome sequencing in cerebellar ataxia and related neurological disordersKathie J Ngo, Jessica E Rexach, Hane Lee, et al.
Nature Genetics|December 27, 2011
Frequent somatic mutations in MAP3K5 and MAP3K9 in metastatic melanoma identified by exome sequencingMitchell S Stark, Susan L Woods, Michael G Gartside, et al.
Nature Communications|December 2, 2010
Deep resequencing reveals excess rare recent variants consistent with explosive population growthAlex Coventry, Lara M Bull-Otterson, Xiaoming Liu, et al.
Genetics|June 22, 2023
Genetic control of mRNA splicing as a potential mechanism for incomplete penetrance of rare coding variantsJonah Einson, Dafni Glinos, Eric Boerwinkle, et al.
Biorxiv : the Preprint Server for Biology|February 13, 2023
Genetic control of mRNA splicing as a potential mechanism for incomplete penetrance of rare coding variantsJonah Einson, Dafni Glinos, Eric Boerwinkle, et al.
Genome Biology|September 16, 2011
The functional spectrum of low-frequency coding variationGabor T Marth, Fuli Yu, Amit R Indap, et al.
JAMA Surgery|June 14, 2023
Outcomes After Endovascular Aortic Intervention in Patients With Connective Tissue DiseaseKarl Wilhelm Olsson, Kevin Mani, Anne Burdess, et al.
Nature Genetics|March 30, 2007
Recommendations of the 2006 Human Variome Project meetingRichard G H Cotton, , William Appelbe, et al.
Human Molecular Genetics|September 5, 2014
Association of exome sequences with plasma C-reactive protein levels in >9000 participantsUrsula M Schick, Paul L Auer, Joshua C Bis, et al.
Pageof 10