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David N Cooper

Showing results (181-190 of 398) with videos related to

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Genome Research|January 20, 2021
A platform for curated products from novel open reading frames prompts reinterpretation of disease variantsMatthew D C Neville, Robin Kohze, Chaitanya Erady, et al.
Human Molecular Genetics|November 29, 2015
Fine mapping of meiotic NAHR-associated crossovers causing large NF1 deletionsMorten Hillmer, David Wagner, Anna Summerer, et al.
Personalized Medicine|May 13, 2018
Critical appraisal of the views of healthcare professionals with respect to pharmacogenomics and personalized medicine in GreeceYuan Mai, Christina Mitropoulou, Xanthi E Papadopoulou, et al.
Human Mutation|June 27, 2017
Investigating DNA-, RNA-, and protein-based features as a means to discriminate pathogenic synonymous variantsMark Livingstone, Lukas Folkman, Yuedong Yang, et al.
Human Genetics|November 9, 2022
Identifying shared genetic factors underlying epilepsy and congenital heart disease in EuropeansYiming Wu, Cigdem Sevim Bayrak, Bosi Dong, et al.
Genome Medicine|April 8, 2009
The Human Gene Mutation Database: 2008 updatePeter D Stenson, Matthew Mort, Edward V Ball, et al.
Human Genetics|August 27, 2024
VCAT: an integrated variant function annotation toolsBi Huang, Cong Fan, Ken Chen, et al.
Genome Research|September 6, 2005
Independent intrachromosomal recombination events underlie the pericentric inversions of chimpanzee and gorilla chromosomes homologous to human chromosome 16Violaine Goidts, Justyna M Szamalek, Pieter J de Jong, et al.
Human Mutation|May 6, 2020
5' splice site GC>GT and GT>GC variants differ markedly in terms of their functionality and pathogenicityJin-Huan Lin, Emmanuelle Masson, Arnaud Boulling, et al.
Human Mutation|March 25, 2011
Comparative analysis of germline and somatic microlesion mutational spectra in 17 human tumor suppressor genesDobril Ivanov, Stephen E Hamby, Peter D Stenson, et al.
Pageof 40

Showing results (181-190 of 398) with videos related to

Sort By:
Pageof 40
Genome Research|January 20, 2021
A platform for curated products from novel open reading frames prompts reinterpretation of disease variantsMatthew D C Neville, Robin Kohze, Chaitanya Erady, et al.
Human Molecular Genetics|November 29, 2015
Fine mapping of meiotic NAHR-associated crossovers causing large NF1 deletionsMorten Hillmer, David Wagner, Anna Summerer, et al.
Personalized Medicine|May 13, 2018
Critical appraisal of the views of healthcare professionals with respect to pharmacogenomics and personalized medicine in GreeceYuan Mai, Christina Mitropoulou, Xanthi E Papadopoulou, et al.
Human Mutation|June 27, 2017
Investigating DNA-, RNA-, and protein-based features as a means to discriminate pathogenic synonymous variantsMark Livingstone, Lukas Folkman, Yuedong Yang, et al.
Human Genetics|November 9, 2022
Identifying shared genetic factors underlying epilepsy and congenital heart disease in EuropeansYiming Wu, Cigdem Sevim Bayrak, Bosi Dong, et al.
Genome Medicine|April 8, 2009
The Human Gene Mutation Database: 2008 updatePeter D Stenson, Matthew Mort, Edward V Ball, et al.
Human Genetics|August 27, 2024
VCAT: an integrated variant function annotation toolsBi Huang, Cong Fan, Ken Chen, et al.
Genome Research|September 6, 2005
Independent intrachromosomal recombination events underlie the pericentric inversions of chimpanzee and gorilla chromosomes homologous to human chromosome 16Violaine Goidts, Justyna M Szamalek, Pieter J de Jong, et al.
Human Mutation|May 6, 2020
5' splice site GC>GT and GT>GC variants differ markedly in terms of their functionality and pathogenicityJin-Huan Lin, Emmanuelle Masson, Arnaud Boulling, et al.
Human Mutation|March 25, 2011
Comparative analysis of germline and somatic microlesion mutational spectra in 17 human tumor suppressor genesDobril Ivanov, Stephen E Hamby, Peter D Stenson, et al.
Pageof 40