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Anna Wilsdon

Showing results (1-10 of 16) with videos related to

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Advances in Experimental Medicine and Biology|June 17, 2024
Human Genetics of Congenital Heart DefectsAnna Wilsdon, Siobhan Loughna
F1000Research|July 1, 2017
Recent advances in congenital heart disease genomicsAnna Wilsdon, Alejandro Sifrim, Marc-Phillip Hitz, et al.
Journal of Anatomy|November 18, 2024
Cyclin-dependent kinase 13 is indispensable for normal mouse heart developmentQazi Waheed-Ullah, Anna Wilsdon, Aseel Abbad, et al.
Journal of Anatomy|February 29, 2024
Effect of deletion of the protein kinase PRKD1 on development of the mouse embryonic heartQazi Waheed-Ullah, Anna Wilsdon, Aseel Abbad, et al.
Journal of Medical Genetics|October 29, 2025
Multicentre audit reviewing reporting and management of patients with incidentally identified structural aberrations involving high actionability cancer susceptibility genesKate Richardson, Emma Douglas, Nour Elkhateeb, et al.
Journal of Human Genetics|March 21, 2014
An emerging phenotype of Xq22 microdeletions in females with severe intellectual disability, hypotonia and behavioral abnormalitiesToshiyuki Yamamoto, Anna Wilsdon, Shelagh Joss, et al.
Genome Medicine|August 30, 2020
Systems genetics analysis identifies calcium-signaling defects as novel cause of congenital heart diseaseJose M G Izarzugaza, Sabrina G Ellesøe, Canan Doganli, et al.
Journal of Medical Genetics|August 9, 2023
Use of genome sequencing to hunt for cryptic second-hit variants: analysis of 31 cases recruited to the 100 000 Genomes ProjectA Rachel Moore, Jing Yu, Yang Pei, et al.
NPJ Genomic Medicine|June 2, 2026
Assessing the contribution of rare variants to congenital heart disease through a large-scale case-control exome studyEnrique Audain, Anna Wilsdon, Gregor Dombrowsky, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 22, 2020
Germline variants in HEY2 functional domains lead to congenital heart defects and thoracic aortic aneurysmsEva S van Walree, Gregor Dombrowsky, Iris E Jansen, et al.
Pageof 2

Showing results (1-10 of 16) with videos related to

Sort By:
Pageof 2
Advances in Experimental Medicine and Biology|June 17, 2024
Human Genetics of Congenital Heart DefectsAnna Wilsdon, Siobhan Loughna
F1000Research|July 1, 2017
Recent advances in congenital heart disease genomicsAnna Wilsdon, Alejandro Sifrim, Marc-Phillip Hitz, et al.
Journal of Anatomy|November 18, 2024
Cyclin-dependent kinase 13 is indispensable for normal mouse heart developmentQazi Waheed-Ullah, Anna Wilsdon, Aseel Abbad, et al.
Journal of Anatomy|February 29, 2024
Effect of deletion of the protein kinase PRKD1 on development of the mouse embryonic heartQazi Waheed-Ullah, Anna Wilsdon, Aseel Abbad, et al.
Journal of Medical Genetics|October 29, 2025
Multicentre audit reviewing reporting and management of patients with incidentally identified structural aberrations involving high actionability cancer susceptibility genesKate Richardson, Emma Douglas, Nour Elkhateeb, et al.
Journal of Human Genetics|March 21, 2014
An emerging phenotype of Xq22 microdeletions in females with severe intellectual disability, hypotonia and behavioral abnormalitiesToshiyuki Yamamoto, Anna Wilsdon, Shelagh Joss, et al.
Genome Medicine|August 30, 2020
Systems genetics analysis identifies calcium-signaling defects as novel cause of congenital heart diseaseJose M G Izarzugaza, Sabrina G Ellesøe, Canan Doganli, et al.
Journal of Medical Genetics|August 9, 2023
Use of genome sequencing to hunt for cryptic second-hit variants: analysis of 31 cases recruited to the 100 000 Genomes ProjectA Rachel Moore, Jing Yu, Yang Pei, et al.
NPJ Genomic Medicine|June 2, 2026
Assessing the contribution of rare variants to congenital heart disease through a large-scale case-control exome studyEnrique Audain, Anna Wilsdon, Gregor Dombrowsky, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 22, 2020
Germline variants in HEY2 functional domains lead to congenital heart defects and thoracic aortic aneurysmsEva S van Walree, Gregor Dombrowsky, Iris E Jansen, et al.
Pageof 2