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Genome Biology
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January 24, 2014
MutPred Splice: machine learning-based prediction of exonic variants that disrupt splicing
Matthew Mort, Timothy Sterne-Weiler, Biao Li, et al.
Human Mutation
|
December 17, 2021
Distinct sequence features underlie microdeletions and gross deletions in the human genome
Mengling Qi, Peter D Stenson, Edward V Ball, et al.
Human Genetics
|
March 29, 2017
The Human Gene Mutation Database: towards a comprehensive repository of inherited mutation data for medical research, genetic diagnosis and next-generation sequencing studies
Peter D Stenson, Matthew Mort, Edward V Ball, et al.
The Journal of General Virology
|
June 4, 2010
Genetic characterization of slow bee paralysis virus of the honeybee (Apis mellifera L.)
Joachim R de Miranda, Benjamin Dainat, Barbara Locke, et al.
Human Mutation
|
May 20, 2003
Human Gene Mutation Database (HGMD): 2003 update
Peter D Stenson, Edward V Ball, Matthew Mort, et al.
Neuropsychologia
|
August 30, 2025
No evidence for a targeted memory reactivation effect on word-meaning priming
Lewis V Ball, Eva Kimel, Vanessa G Keller, et al.
Human Mutation
|
May 28, 2010
Genes, mutations, and human inherited disease at the dawn of the age of personalized genomics
David N Cooper, Jian-Min Chen, Edward V Ball, et al.
Arthritis and Rheumatism
|
September 1, 1985
Pure red cell aplasia and protein-losing enteropathy in a patient with systemic lupus erythematosus
L W Heck, G S Alarcón, G V Ball, et al.
American Journal of Human Genetics
|
December 11, 2012
Deleterious- and disease-allele prevalence in healthy individuals: insights from current predictions, mutation databases, and population-scale resequencing
Yali Xue, Yuan Chen, Qasim Ayub, et al.
Human Genetics
|
June 30, 2020
The Human Gene Mutation Database (HGMD<sup>®</sup>): optimizing its use in a clinical diagnostic or research setting
Peter D Stenson, Matthew Mort, Edward V Ball, et al.
Page
of 13
Search research articles
Search
Showing results (111-120 of 130) with videos related to
Sort By:
Page
of 13
Genome Biology
|
January 24, 2014
MutPred Splice: machine learning-based prediction of exonic variants that disrupt splicing
Matthew Mort, Timothy Sterne-Weiler, Biao Li, et al.
Human Mutation
|
December 17, 2021
Distinct sequence features underlie microdeletions and gross deletions in the human genome
Mengling Qi, Peter D Stenson, Edward V Ball, et al.
Human Genetics
|
March 29, 2017
The Human Gene Mutation Database: towards a comprehensive repository of inherited mutation data for medical research, genetic diagnosis and next-generation sequencing studies
Peter D Stenson, Matthew Mort, Edward V Ball, et al.
The Journal of General Virology
|
June 4, 2010
Genetic characterization of slow bee paralysis virus of the honeybee (Apis mellifera L.)
Joachim R de Miranda, Benjamin Dainat, Barbara Locke, et al.
Human Mutation
|
May 20, 2003
Human Gene Mutation Database (HGMD): 2003 update
Peter D Stenson, Edward V Ball, Matthew Mort, et al.
Neuropsychologia
|
August 30, 2025
No evidence for a targeted memory reactivation effect on word-meaning priming
Lewis V Ball, Eva Kimel, Vanessa G Keller, et al.
Human Mutation
|
May 28, 2010
Genes, mutations, and human inherited disease at the dawn of the age of personalized genomics
David N Cooper, Jian-Min Chen, Edward V Ball, et al.
Arthritis and Rheumatism
|
September 1, 1985
Pure red cell aplasia and protein-losing enteropathy in a patient with systemic lupus erythematosus
L W Heck, G S Alarcón, G V Ball, et al.
American Journal of Human Genetics
|
December 11, 2012
Deleterious- and disease-allele prevalence in healthy individuals: insights from current predictions, mutation databases, and population-scale resequencing
Yali Xue, Yuan Chen, Qasim Ayub, et al.
Human Genetics
|
June 30, 2020
The Human Gene Mutation Database (HGMD<sup>®</sup>): optimizing its use in a clinical diagnostic or research setting
Peter D Stenson, Matthew Mort, Edward V Ball, et al.
Page
of 13