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Philosophical Transactions of the Royal Society of London. Series B, Biological Sciences
|
February 6, 2013
Observing micro-evolutionary processes of viral populations at multiple scales
Richard J Orton, Caroline F Wright, Marco J Morelli, et al.
Lancet (London, England)
|
December 9, 2023
Population screening requires robust evidence-genomics is no exception
Clare Turnbull, Helen V Firth, Andrew O M Wilkie, et al.
Nature
|
March 22, 2018
De novo mutations in regulatory elements in neurodevelopmental disorders
Patrick J Short, Jeremy F McRae, Giuseppe Gallone, et al.
Nature Communications
|
February 6, 2026
Whole-genome sequencing analysis of anthropometric traits in 672,976 individuals reveals convergence between rare and common genetic associations
Gareth Hawkes, Harrison I W Wright, Robin N Beaumont, et al.
JAMA Network Open
|
June 27, 2025
Medullary Thyroid Cancer Risk and Mortality in Carriers of Incidentally Identified MEN2A RET Variants
Courtney E West, Uyenlinh L Mirshahi, Katherine S Ruth, et al.
American Journal of Human Genetics
|
January 23, 2019
Assessing the Pathogenicity, Penetrance, and Expressivity of Putative Disease-Causing Variants in a Population Setting
Caroline F Wright, Ben West, Marcus Tuke, et al.
American Journal of Human Genetics
|
October 9, 2021
Detecting cryptic clinically relevant structural variation in exome-sequencing data increases diagnostic yield for developmental disorders
Eugene J Gardner, Alejandro Sifrim, Sarah J Lindsay, et al.
Msphere
|
July 14, 2021
Mutagenesis Mapping of RNA Structures within the Foot-and-Mouth Disease Virus Genome Reveals Functional Elements Localized in the Polymerase (3D<sup>pol</sup>)-Encoding Region
Lidia Lasecka-Dykes, Fiona Tulloch, Peter Simmonds, et al.
Journal of Molecular Biology
|
March 28, 2026
Gene2Phenotype: a database of structured human monogenic diseases and pathomechanisms
Sarah E Hunt, Diana Lemos, Seeta Ramaraju Pericherla, et al.
Nature Communications
|
June 1, 2019
Flexible and scalable diagnostic filtering of genomic variants using G2P with Ensembl VEP
Anja Thormann, Mihail Halachev, William McLaren, et al.
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Search research articles
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Showing results (81-90 of 128) with videos related to
Sort By:
Page
of 13
Philosophical Transactions of the Royal Society of London. Series B, Biological Sciences
|
February 6, 2013
Observing micro-evolutionary processes of viral populations at multiple scales
Richard J Orton, Caroline F Wright, Marco J Morelli, et al.
Lancet (London, England)
|
December 9, 2023
Population screening requires robust evidence-genomics is no exception
Clare Turnbull, Helen V Firth, Andrew O M Wilkie, et al.
Nature
|
March 22, 2018
De novo mutations in regulatory elements in neurodevelopmental disorders
Patrick J Short, Jeremy F McRae, Giuseppe Gallone, et al.
Nature Communications
|
February 6, 2026
Whole-genome sequencing analysis of anthropometric traits in 672,976 individuals reveals convergence between rare and common genetic associations
Gareth Hawkes, Harrison I W Wright, Robin N Beaumont, et al.
JAMA Network Open
|
June 27, 2025
Medullary Thyroid Cancer Risk and Mortality in Carriers of Incidentally Identified MEN2A RET Variants
Courtney E West, Uyenlinh L Mirshahi, Katherine S Ruth, et al.
American Journal of Human Genetics
|
January 23, 2019
Assessing the Pathogenicity, Penetrance, and Expressivity of Putative Disease-Causing Variants in a Population Setting
Caroline F Wright, Ben West, Marcus Tuke, et al.
American Journal of Human Genetics
|
October 9, 2021
Detecting cryptic clinically relevant structural variation in exome-sequencing data increases diagnostic yield for developmental disorders
Eugene J Gardner, Alejandro Sifrim, Sarah J Lindsay, et al.
Msphere
|
July 14, 2021
Mutagenesis Mapping of RNA Structures within the Foot-and-Mouth Disease Virus Genome Reveals Functional Elements Localized in the Polymerase (3D<sup>pol</sup>)-Encoding Region
Lidia Lasecka-Dykes, Fiona Tulloch, Peter Simmonds, et al.
Journal of Molecular Biology
|
March 28, 2026
Gene2Phenotype: a database of structured human monogenic diseases and pathomechanisms
Sarah E Hunt, Diana Lemos, Seeta Ramaraju Pericherla, et al.
Nature Communications
|
June 1, 2019
Flexible and scalable diagnostic filtering of genomic variants using G2P with Ensembl VEP
Anja Thormann, Mihail Halachev, William McLaren, et al.
Page
of 13