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Matthew Hurles

Showing results (1-10 of 33) with videos related to

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Human Genomics|October 4, 2005
How homologous recombination generates a mutable genomeMatthew Hurles
Nature Genetics|October 30, 2012
Older males beget more mutationsMatthew Hurles
F1000Research|July 1, 2017
Recent advances in congenital heart disease genomicsAnna Wilsdon, Alejandro Sifrim, Marc-Phillip Hitz, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 20, 2002
Mitochondrial DNA and the origins of the domestic horseThomas Jansen, Peter Forster, Marsha A Levine, et al.
Bipolar Disorders|October 17, 2013
Reduced burden of very large and rare CNVs in bipolar affective disorderDetelina Grozeva, George Kirov, Donald F Conrad, et al.
Schizophrenia Research|December 2, 2011
Independent estimation of the frequency of rare CNVs in the UK population confirms their role in schizophreniaDetelina Grozeva, Donald F Conrad, Chris P Barnes, et al.
Human Mutation|July 13, 2017
"Matching" consent to purpose: The example of the Matchmaker ExchangeStephanie O M Dyke, Bartha M Knoppers, Ada Hamosh, et al.
Viruses|July 19, 2011
Genomic analysis of hepatitis B virus reveals antigen state and genotype as sources of evolutionary rate variationAbby Harrison, Philippe Lemey, Matthew Hurles, et al.
Plos Genetics|July 11, 2014
Cis and trans effects of human genomic variants on gene expressionJulien Bryois, Alfonso Buil, David M Evans, et al.
Nature Communications|November 3, 2025
Complex de novo structural variants are an underestimated cause of rare disordersHyunchul Jung, Tsun-Po Yang, Susan Walker, et al.
Pageof 4

Showing results (1-10 of 33) with videos related to

Sort By:
Pageof 4
Human Genomics|October 4, 2005
How homologous recombination generates a mutable genomeMatthew Hurles
Nature Genetics|October 30, 2012
Older males beget more mutationsMatthew Hurles
F1000Research|July 1, 2017
Recent advances in congenital heart disease genomicsAnna Wilsdon, Alejandro Sifrim, Marc-Phillip Hitz, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 20, 2002
Mitochondrial DNA and the origins of the domestic horseThomas Jansen, Peter Forster, Marsha A Levine, et al.
Bipolar Disorders|October 17, 2013
Reduced burden of very large and rare CNVs in bipolar affective disorderDetelina Grozeva, George Kirov, Donald F Conrad, et al.
Schizophrenia Research|December 2, 2011
Independent estimation of the frequency of rare CNVs in the UK population confirms their role in schizophreniaDetelina Grozeva, Donald F Conrad, Chris P Barnes, et al.
Human Mutation|July 13, 2017
"Matching" consent to purpose: The example of the Matchmaker ExchangeStephanie O M Dyke, Bartha M Knoppers, Ada Hamosh, et al.
Viruses|July 19, 2011
Genomic analysis of hepatitis B virus reveals antigen state and genotype as sources of evolutionary rate variationAbby Harrison, Philippe Lemey, Matthew Hurles, et al.
Plos Genetics|July 11, 2014
Cis and trans effects of human genomic variants on gene expressionJulien Bryois, Alfonso Buil, David M Evans, et al.
Nature Communications|November 3, 2025
Complex de novo structural variants are an underestimated cause of rare disordersHyunchul Jung, Tsun-Po Yang, Susan Walker, et al.
Pageof 4