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Tomas W Fitzgerald

Showing results (11-20 of 22) with videos related to

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Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 12, 2018
Making new genetic diagnoses with old data: iterative reanalysis and reporting from genome-wide data in 1,133 families with developmental disordersCaroline F Wright, Jeremy F McRae, Stephen Clayton, et al.
Medrxiv : the Preprint Server for Health Sciences|September 29, 2025
Ophthalmic imaging as a measure of cardiovascular and neurological health: a multi-omic analysis of deep-learning derived phenotypesThomas H Julian, Haoran Dou, Jinming Duan, et al.
Nature Cardiovascular Research|June 16, 2026
Multi-omic analysis of deep learning-derived phenotypes links ophthalmic imaging to cardiovascular and neurological traitsThomas H Julian, Haoran Dou, Jinming Duan, et al.
Human Genetics|May 11, 2015
Copy number variation in the human Y chromosome in the UK populationWei Wei, Tomas W Fitzgerald, Tomas Fitzgerald, et al.
Lancet (London, England)|December 23, 2014
Genetic diagnosis of developmental disorders in the DDD study: a scalable analysis of genome-wide research dataCaroline F Wright, Tomas W Fitzgerald, Wendy D Jones, et al.
Plos Genetics|May 12, 2021
Genetic variation affects morphological retinal phenotypes extracted from UK Biobank optical coherence tomography imagesHannah Currant, Pirro Hysi, Tomas W Fitzgerald, et al.
Plos Genetics|October 18, 2021
Correction: Genetic variation affects morphological retinal phenotypes extracted from UK Biobank optical coherence tomography imagesHannah Currant, Pirro Hysi, Tomas W Fitzgerald, et al.
Nature Genetics|October 6, 2015
Discovery of four recessive developmental disorders using probabilistic genotype and phenotype matching among 4,125 familiesNadia Akawi, Jeremy McRae, Morad Ansari, et al.
Nature Genetics|April 26, 2016
Punctuated bursts in human male demography inferred from 1,244 worldwide Y-chromosome sequencesG David Poznik, Yali Xue, Fernando L Mendez, et al.
Plos Genetics|September 21, 2021
Correction: Integrative analysis of genomic variants reveals new associations of candidate haploinsufficient genes with congenital heart diseaseEnrique Audain, Anna Wilsdon, Jeroen Breckpot, et al.
Pageof 3

Showing results (11-20 of 22) with videos related to

Sort By:
Pageof 3
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 12, 2018
Making new genetic diagnoses with old data: iterative reanalysis and reporting from genome-wide data in 1,133 families with developmental disordersCaroline F Wright, Jeremy F McRae, Stephen Clayton, et al.
Medrxiv : the Preprint Server for Health Sciences|September 29, 2025
Ophthalmic imaging as a measure of cardiovascular and neurological health: a multi-omic analysis of deep-learning derived phenotypesThomas H Julian, Haoran Dou, Jinming Duan, et al.
Nature Cardiovascular Research|June 16, 2026
Multi-omic analysis of deep learning-derived phenotypes links ophthalmic imaging to cardiovascular and neurological traitsThomas H Julian, Haoran Dou, Jinming Duan, et al.
Human Genetics|May 11, 2015
Copy number variation in the human Y chromosome in the UK populationWei Wei, Tomas W Fitzgerald, Tomas Fitzgerald, et al.
Lancet (London, England)|December 23, 2014
Genetic diagnosis of developmental disorders in the DDD study: a scalable analysis of genome-wide research dataCaroline F Wright, Tomas W Fitzgerald, Wendy D Jones, et al.
Plos Genetics|May 12, 2021
Genetic variation affects morphological retinal phenotypes extracted from UK Biobank optical coherence tomography imagesHannah Currant, Pirro Hysi, Tomas W Fitzgerald, et al.
Plos Genetics|October 18, 2021
Correction: Genetic variation affects morphological retinal phenotypes extracted from UK Biobank optical coherence tomography imagesHannah Currant, Pirro Hysi, Tomas W Fitzgerald, et al.
Nature Genetics|October 6, 2015
Discovery of four recessive developmental disorders using probabilistic genotype and phenotype matching among 4,125 familiesNadia Akawi, Jeremy McRae, Morad Ansari, et al.
Nature Genetics|April 26, 2016
Punctuated bursts in human male demography inferred from 1,244 worldwide Y-chromosome sequencesG David Poznik, Yali Xue, Fernando L Mendez, et al.
Plos Genetics|September 21, 2021
Correction: Integrative analysis of genomic variants reveals new associations of candidate haploinsufficient genes with congenital heart diseaseEnrique Audain, Anna Wilsdon, Jeroen Breckpot, et al.
Pageof 3