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A MacRae

Showing results (581-590 of 599) with videos related to

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Cardiovascular Research|January 25, 2020
Impact of functional studies on exome sequence variant interpretation in early-onset cardiac conduction system diseasesKenshi Hayashi, Ryota Teramoto, Akihiro Nomura, et al.
Journal of Medical Genetics|October 21, 2022
Germline mutations in <i>WNK2</i> could be associated with serrated polyposis syndromeYasmin Soares de Lima, Coral Arnau-Collell, Jenifer Muñoz, et al.
Genome Biology|February 4, 2020
The Deep Genome ProjectK C Kent Lloyd, David J Adams, Gareth Baynam, et al.
Medrxiv : the Preprint Server for Health Sciences|March 13, 2023
A tumor focused approach to resolving the etiology of DNA mismatch repair deficient tumors classified as suspected Lynch syndromeRomy Walker, Khalid Mahmood, Jihoon E Joo, et al.
NPJ Genomic Medicine|August 23, 2018
An integrated clinical program and crowdsourcing strategy for genomic sequencing and Mendelian disease gene discoveryAlireza Haghighi, Joel B Krier, Agnes Toth-Petroczy, et al.
Journal of Translational Medicine|April 26, 2023
A tumor focused approach to resolving the etiology of DNA mismatch repair deficient tumors classified as suspected Lynch syndromeRomy Walker, Khalid Mahmood, Jihoon E Joo, et al.
BMC Genomics|July 29, 2008
Analysis of expressed sequence tags from Actinidia: applications of a cross species EST database for gene discovery in the areas of flavor, health, color and ripeningRoss N Crowhurst, Andrew P Gleave, Elspeth A MacRae, et al.
Nature Communications|June 6, 2022
Identifying colorectal cancer caused by biallelic MUTYH pathogenic variants using tumor mutational signaturesPeter Georgeson, Tabitha A Harrison, Bernard J Pope, et al.
Medrxiv : the Preprint Server for Health Sciences|April 24, 2023
Genotoxic colibactin mutational signature in colorectal cancer is associated with clinicopathological features, specific genomic alterations and better survivalPeter Georgeson, Robert S Steinfelder, Tabitha A Harrison, et al.
Nature Genetics|February 23, 2010
Common variants in KCNN3 are associated with lone atrial fibrillationPatrick T Ellinor, Kathryn L Lunetta, Nicole L Glazer, et al.
Pageof 60

Showing results (581-590 of 599) with videos related to

Sort By:
Pageof 60
Cardiovascular Research|January 25, 2020
Impact of functional studies on exome sequence variant interpretation in early-onset cardiac conduction system diseasesKenshi Hayashi, Ryota Teramoto, Akihiro Nomura, et al.
Journal of Medical Genetics|October 21, 2022
Germline mutations in <i>WNK2</i> could be associated with serrated polyposis syndromeYasmin Soares de Lima, Coral Arnau-Collell, Jenifer Muñoz, et al.
Genome Biology|February 4, 2020
The Deep Genome ProjectK C Kent Lloyd, David J Adams, Gareth Baynam, et al.
Medrxiv : the Preprint Server for Health Sciences|March 13, 2023
A tumor focused approach to resolving the etiology of DNA mismatch repair deficient tumors classified as suspected Lynch syndromeRomy Walker, Khalid Mahmood, Jihoon E Joo, et al.
NPJ Genomic Medicine|August 23, 2018
An integrated clinical program and crowdsourcing strategy for genomic sequencing and Mendelian disease gene discoveryAlireza Haghighi, Joel B Krier, Agnes Toth-Petroczy, et al.
Journal of Translational Medicine|April 26, 2023
A tumor focused approach to resolving the etiology of DNA mismatch repair deficient tumors classified as suspected Lynch syndromeRomy Walker, Khalid Mahmood, Jihoon E Joo, et al.
BMC Genomics|July 29, 2008
Analysis of expressed sequence tags from Actinidia: applications of a cross species EST database for gene discovery in the areas of flavor, health, color and ripeningRoss N Crowhurst, Andrew P Gleave, Elspeth A MacRae, et al.
Nature Communications|June 6, 2022
Identifying colorectal cancer caused by biallelic MUTYH pathogenic variants using tumor mutational signaturesPeter Georgeson, Tabitha A Harrison, Bernard J Pope, et al.
Medrxiv : the Preprint Server for Health Sciences|April 24, 2023
Genotoxic colibactin mutational signature in colorectal cancer is associated with clinicopathological features, specific genomic alterations and better survivalPeter Georgeson, Robert S Steinfelder, Tabitha A Harrison, et al.
Nature Genetics|February 23, 2010
Common variants in KCNN3 are associated with lone atrial fibrillationPatrick T Ellinor, Kathryn L Lunetta, Nicole L Glazer, et al.
Pageof 60