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Genes, Chromosomes & Cancer
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November 2, 2018
Translating genomic risk into an early detection strategy for sarcoma
Mandy L Ballinger, Mark Pinese, David M Thomas
European Journal of Human Genetics : EJHG
|
October 15, 2025
Updated penetrance estimates for recurrent copy number variants - an improved definition and formula
Shuxiang Goh, Tracy Dudding-Byth, Mark Pinese, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
August 2, 2024
A systematic review and pooled analysis of penetrance estimates of copy-number variants associated with neurodevelopment
Shuxiang Goh, Lavvina Thiyagarajan, Tracy Dudding-Byth, et al.
American Journal of Human Genetics
|
September 3, 2024
SpliceVarDB: A comprehensive database of experimentally validated human splicing variants
Patricia J Sullivan, Julian M W Quinn, Weilin Wu, et al.
Annals of the New York Academy of Sciences
|
September 7, 2007
The effect of resveratrol on a cell model of human aging
Maurizio Stefani, M Andrea Markus, Ruby C Y Lin, et al.
American Journal of Human Genetics
|
March 8, 2025
Data-driven insights to inform splice-altering variant assessment
Patricia J Sullivan, Julian M W Quinn, Pamela Ajuyah, et al.
Nature Reviews. Clinical Oncology
|
April 19, 2019
Author Correction: Therapeutic implications of germline genetic findings in cancer
Subotheni Thavaneswaran, Emma Rath, Kathy Tucker, et al.
Nature Reviews. Clinical Oncology
|
February 21, 2019
Therapeutic implications of germline genetic findings in cancer
Subotheni Thavaneswaran, Emma Rath, Kathy Tucker, et al.
Plos One
|
April 29, 2009
Messina: a novel analysis tool to identify biologically relevant molecules in disease
Mark Pinese, Christopher J Scarlett, James G Kench, et al.
Nucleic Acids Research
|
November 10, 2011
PINA v2.0: mining interactome modules
Mark J Cowley, Mark Pinese, Karin S Kassahn, et al.
Page
of 7
Search research articles
Search
Showing results (1-10 of 63) with videos related to
Sort By:
Page
of 7
Genes, Chromosomes & Cancer
|
November 2, 2018
Translating genomic risk into an early detection strategy for sarcoma
Mandy L Ballinger, Mark Pinese, David M Thomas
European Journal of Human Genetics : EJHG
|
October 15, 2025
Updated penetrance estimates for recurrent copy number variants - an improved definition and formula
Shuxiang Goh, Tracy Dudding-Byth, Mark Pinese, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
August 2, 2024
A systematic review and pooled analysis of penetrance estimates of copy-number variants associated with neurodevelopment
Shuxiang Goh, Lavvina Thiyagarajan, Tracy Dudding-Byth, et al.
American Journal of Human Genetics
|
September 3, 2024
SpliceVarDB: A comprehensive database of experimentally validated human splicing variants
Patricia J Sullivan, Julian M W Quinn, Weilin Wu, et al.
Annals of the New York Academy of Sciences
|
September 7, 2007
The effect of resveratrol on a cell model of human aging
Maurizio Stefani, M Andrea Markus, Ruby C Y Lin, et al.
American Journal of Human Genetics
|
March 8, 2025
Data-driven insights to inform splice-altering variant assessment
Patricia J Sullivan, Julian M W Quinn, Pamela Ajuyah, et al.
Nature Reviews. Clinical Oncology
|
April 19, 2019
Author Correction: Therapeutic implications of germline genetic findings in cancer
Subotheni Thavaneswaran, Emma Rath, Kathy Tucker, et al.
Nature Reviews. Clinical Oncology
|
February 21, 2019
Therapeutic implications of germline genetic findings in cancer
Subotheni Thavaneswaran, Emma Rath, Kathy Tucker, et al.
Plos One
|
April 29, 2009
Messina: a novel analysis tool to identify biologically relevant molecules in disease
Mark Pinese, Christopher J Scarlett, James G Kench, et al.
Nucleic Acids Research
|
November 10, 2011
PINA v2.0: mining interactome modules
Mark J Cowley, Mark Pinese, Karin S Kassahn, et al.
Page
of 7