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Matthew E Hurles

Showing results (61-70 of 188) with videos related to

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Human Molecular Genetics|September 11, 2012
DECIPHER: web-based, community resource for clinical interpretation of rare variants in developmental disordersGanesh J Swaminathan, Eugene Bragin, Eleni A Chatzimichali, et al.
Genome Research|June 23, 2019
Exome-wide assessment of the functional impact and pathogenicity of multinucleotide mutationsJoanna Kaplanis, Nadia Akawi, Giuseppe Gallone, et al.
Nature|March 24, 2022
Reduced reproductive success is associated with selective constraint on human genesEugene J Gardner, Matthew D C Neville, Kaitlin E Samocha, et al.
Plos Genetics|May 31, 2014
A genome-wide assessment of the role of untagged copy number variants in type 1 diabetesManuela Zanda, Suna Onengut-Gumuscu, Neil Walker, et al.
Genetics|February 21, 2006
Male demography in East Asia: a north-south contrast in human population expansion timesYali Xue, Tatiana Zerjal, Weidong Bao, et al.
American Journal of Human Genetics|September 2, 2008
Adaptive evolution of UGT2B17 copy-number variationYali Xue, Donglin Sun, Allan Daly, et al.
Communications Biology|June 27, 2019
Paternal exposure to benzo(a)pyrene induces genome-wide mutations in mouse offspringMarc A Beal, Matthew J Meier, Andrew Williams, et al.
Fetal Diagnosis and Therapy|February 7, 2021
The Diagnostic Yield of Prenatal Genetic Technologies in Congenital Heart Disease: A Prospective Cohort StudyFionnuala Mone, Bethany K Stott, Susan Hamilton, et al.
Nature|September 3, 2013
Cerebral organoids model human brain development and microcephalyMadeline A Lancaster, Magdalena Renner, Carol-Anne Martin, et al.
Nature Communications|June 10, 2023
Rare genetic variants impact muscle strengthYunfeng Huang, Dora Bodnar, Chia-Yen Chen, et al.
Pageof 19

Showing results (61-70 of 188) with videos related to

Sort By:
Pageof 19
Human Molecular Genetics|September 11, 2012
DECIPHER: web-based, community resource for clinical interpretation of rare variants in developmental disordersGanesh J Swaminathan, Eugene Bragin, Eleni A Chatzimichali, et al.
Genome Research|June 23, 2019
Exome-wide assessment of the functional impact and pathogenicity of multinucleotide mutationsJoanna Kaplanis, Nadia Akawi, Giuseppe Gallone, et al.
Nature|March 24, 2022
Reduced reproductive success is associated with selective constraint on human genesEugene J Gardner, Matthew D C Neville, Kaitlin E Samocha, et al.
Plos Genetics|May 31, 2014
A genome-wide assessment of the role of untagged copy number variants in type 1 diabetesManuela Zanda, Suna Onengut-Gumuscu, Neil Walker, et al.
Genetics|February 21, 2006
Male demography in East Asia: a north-south contrast in human population expansion timesYali Xue, Tatiana Zerjal, Weidong Bao, et al.
American Journal of Human Genetics|September 2, 2008
Adaptive evolution of UGT2B17 copy-number variationYali Xue, Donglin Sun, Allan Daly, et al.
Communications Biology|June 27, 2019
Paternal exposure to benzo(a)pyrene induces genome-wide mutations in mouse offspringMarc A Beal, Matthew J Meier, Andrew Williams, et al.
Fetal Diagnosis and Therapy|February 7, 2021
The Diagnostic Yield of Prenatal Genetic Technologies in Congenital Heart Disease: A Prospective Cohort StudyFionnuala Mone, Bethany K Stott, Susan Hamilton, et al.
Nature|September 3, 2013
Cerebral organoids model human brain development and microcephalyMadeline A Lancaster, Magdalena Renner, Carol-Anne Martin, et al.
Nature Communications|June 10, 2023
Rare genetic variants impact muscle strengthYunfeng Huang, Dora Bodnar, Chia-Yen Chen, et al.
Pageof 19