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Plos One
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April 30, 2016
A Protein Domain and Family Based Approach to Rare Variant Association Analysis
Tom G Richardson, Hashem A Shihab, Manuel A Rivas, et al.
Biomed Research International
|
June 25, 2015
Identifying Highly Penetrant Disease Causal Mutations Using Next Generation Sequencing: Guide to Whole Process
A Mesut Erzurumluoglu, Santiago Rodriguez, Hashem A Shihab, et al.
Annals of Clinical Biochemistry
|
August 25, 2016
Frequency of KLK3 gene deletions in the general population
Santiago Rodriguez, Osama A Al-Ghamdi, Philip Ai Guthrie, et al.
Bioinformatics (Oxford, England)
|
January 14, 2015
An integrative approach to predicting the functional effects of non-coding and coding sequence variation
Hashem A Shihab, Mark F Rogers, Julian Gough, et al.
Human Mutation
|
October 4, 2012
Predicting the functional, molecular, and phenotypic consequences of amino acid substitutions using hidden Markov models
Hashem A Shihab, Julian Gough, David N Cooper, et al.
Diabetes
|
March 2, 2017
Role of DNA Methylation in Type 2 Diabetes Etiology: Using Genotype as a Causal Anchor
Hannah R Elliott, Hashem A Shihab, Gabrielle A Lockett, et al.
International Journal of Epidemiology
|
April 10, 2015
Maternal pre-pregnancy BMI and gestational weight gain, offspring DNA methylation and later offspring adiposity: findings from the Avon Longitudinal Study of Parents and Children
Gemma C Sharp, Debbie A Lawlor, Rebecca C Richmond, et al.
Genome Biology
|
April 3, 2016
Systematic identification of genetic influences on methylation across the human life course
Tom R Gaunt, Hashem A Shihab, Gibran Hemani, et al.
Human Molecular Genetics
|
August 26, 2016
Collapsed methylation quantitative trait loci analysis for low frequency and rare variants
Tom G Richardson, Hashem A Shihab, Gibran Hemani, et al.
Elife
|
May 31, 2018
The MR-Base platform supports systematic causal inference across the human phenome
Gibran Hemani, Jie Zheng, Benjamin Elsworth, et al.
Page
of 3
Search research articles
Search
Showing results (11-20 of 25) with videos related to
Sort By:
Page
of 3
Plos One
|
April 30, 2016
A Protein Domain and Family Based Approach to Rare Variant Association Analysis
Tom G Richardson, Hashem A Shihab, Manuel A Rivas, et al.
Biomed Research International
|
June 25, 2015
Identifying Highly Penetrant Disease Causal Mutations Using Next Generation Sequencing: Guide to Whole Process
A Mesut Erzurumluoglu, Santiago Rodriguez, Hashem A Shihab, et al.
Annals of Clinical Biochemistry
|
August 25, 2016
Frequency of KLK3 gene deletions in the general population
Santiago Rodriguez, Osama A Al-Ghamdi, Philip Ai Guthrie, et al.
Bioinformatics (Oxford, England)
|
January 14, 2015
An integrative approach to predicting the functional effects of non-coding and coding sequence variation
Hashem A Shihab, Mark F Rogers, Julian Gough, et al.
Human Mutation
|
October 4, 2012
Predicting the functional, molecular, and phenotypic consequences of amino acid substitutions using hidden Markov models
Hashem A Shihab, Julian Gough, David N Cooper, et al.
Diabetes
|
March 2, 2017
Role of DNA Methylation in Type 2 Diabetes Etiology: Using Genotype as a Causal Anchor
Hannah R Elliott, Hashem A Shihab, Gabrielle A Lockett, et al.
International Journal of Epidemiology
|
April 10, 2015
Maternal pre-pregnancy BMI and gestational weight gain, offspring DNA methylation and later offspring adiposity: findings from the Avon Longitudinal Study of Parents and Children
Gemma C Sharp, Debbie A Lawlor, Rebecca C Richmond, et al.
Genome Biology
|
April 3, 2016
Systematic identification of genetic influences on methylation across the human life course
Tom R Gaunt, Hashem A Shihab, Gibran Hemani, et al.
Human Molecular Genetics
|
August 26, 2016
Collapsed methylation quantitative trait loci analysis for low frequency and rare variants
Tom G Richardson, Hashem A Shihab, Gibran Hemani, et al.
Elife
|
May 31, 2018
The MR-Base platform supports systematic causal inference across the human phenome
Gibran Hemani, Jie Zheng, Benjamin Elsworth, et al.
Page
of 3