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Jonathan P Tyrer

Showing results (1-10 of 88) with videos related to

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BMC Bioinformatics|June 7, 2013
The admixture maximum likelihood test to test for association between rare variants and disease phenotypesJonathan P Tyrer, Qi Guo, Douglas F Easton, et al.
STAR Protocols|July 3, 2026
Protocol for constructing multi-ancestry polygenic models using S4-MultiPing-Hung Lai, Jonathan P Tyrer, John Baierl, et al.
Communications Biology|April 29, 2025
Characterizing somatic mutations in ovarian cancer germline risk regionsPing-Hung Lai, Jonathan P Tyrer, Paul Pharoah, et al.
BMC Genomics|September 18, 2024
Improving on polygenic scores across complex traits using select and shrink with summary statistics (S4) and LDpred2Jonathan P Tyrer, Pei-Chen Peng, Amber A DeVries, et al.
American Journal of Human Genetics|March 12, 2025
The contribution of coding variants to the heritability of multiple cancer types using UK Biobank whole-exome sequencing dataNaomi Wilcox, Jonathan P Tyrer, Joe Dennis, et al.
Genetic Epidemiology|January 3, 2025
Using Family History Data to Improve the Power of Association Studies: Application to Cancer in UK BiobankNaomi Wilcox, Jonathan P Tyrer, Joe Dennis, et al.
HGG Advances|November 28, 2025
S4-multi: Enhancing polygenic score prediction in ancestrally diverse populationsJohn Baierl, Jonathan P Tyrer, Ping-Hung Lai, et al.
Archives of Dermatology|February 23, 2005
Clinical features of multiple cutaneous and uterine leiomyomatosis: an underdiagnosed tumor syndromeN Afrina Alam, Ella Barclay, Andrew J Rowan, et al.
Carcinogenesis|January 5, 2008
Association of single-nucleotide polymorphisms in the cell cycle genes with breast cancer in the British populationKristy E Driver, Honglin Song, Fabienne Lesueur, et al.
Human Molecular Genetics|April 15, 2014
The contribution of deleterious germline mutations in BRCA1, BRCA2 and the mismatch repair genes to ovarian cancer in the populationHonglin Song, Mine S Cicek, Ed Dicks, et al.
Pageof 9

Showing results (1-10 of 88) with videos related to

Sort By:
Pageof 9
BMC Bioinformatics|June 7, 2013
The admixture maximum likelihood test to test for association between rare variants and disease phenotypesJonathan P Tyrer, Qi Guo, Douglas F Easton, et al.
STAR Protocols|July 3, 2026
Protocol for constructing multi-ancestry polygenic models using S4-MultiPing-Hung Lai, Jonathan P Tyrer, John Baierl, et al.
Communications Biology|April 29, 2025
Characterizing somatic mutations in ovarian cancer germline risk regionsPing-Hung Lai, Jonathan P Tyrer, Paul Pharoah, et al.
BMC Genomics|September 18, 2024
Improving on polygenic scores across complex traits using select and shrink with summary statistics (S4) and LDpred2Jonathan P Tyrer, Pei-Chen Peng, Amber A DeVries, et al.
American Journal of Human Genetics|March 12, 2025
The contribution of coding variants to the heritability of multiple cancer types using UK Biobank whole-exome sequencing dataNaomi Wilcox, Jonathan P Tyrer, Joe Dennis, et al.
Genetic Epidemiology|January 3, 2025
Using Family History Data to Improve the Power of Association Studies: Application to Cancer in UK BiobankNaomi Wilcox, Jonathan P Tyrer, Joe Dennis, et al.
HGG Advances|November 28, 2025
S4-multi: Enhancing polygenic score prediction in ancestrally diverse populationsJohn Baierl, Jonathan P Tyrer, Ping-Hung Lai, et al.
Archives of Dermatology|February 23, 2005
Clinical features of multiple cutaneous and uterine leiomyomatosis: an underdiagnosed tumor syndromeN Afrina Alam, Ella Barclay, Andrew J Rowan, et al.
Carcinogenesis|January 5, 2008
Association of single-nucleotide polymorphisms in the cell cycle genes with breast cancer in the British populationKristy E Driver, Honglin Song, Fabienne Lesueur, et al.
Human Molecular Genetics|April 15, 2014
The contribution of deleterious germline mutations in BRCA1, BRCA2 and the mismatch repair genes to ovarian cancer in the populationHonglin Song, Mine S Cicek, Ed Dicks, et al.
Pageof 9