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Nucleic Acids Research
|
May 6, 2024
Imputation Server PGS: an automated approach to calculate polygenic risk scores on imputation servers
Lukas Forer, Daniel Taliun, Jonathon LeFaive, et al.
American Journal of Human Genetics
|
September 29, 2020
Cancer PRSweb: An Online Repository with Polygenic Risk Scores for Major Cancer Traits and Their Evaluation in Two Independent Biobanks
Lars G Fritsche, Snehal Patil, Lauren J Beesley, et al.
Nature Genetics
|
January 19, 2026
Exploring and visualizing stratified GWAS results with PheWeb2
Justin Bellavance, Hongyu Xiao, Le Chang, et al.
Journal of Medical Genetics
|
June 22, 2011
Linkage and association analysis of hyperthyrotropinaemia in an Alpine population reveal two novel loci on chromosomes 3q28-29 and 6q26-27
Claudia B Volpato, Alessandro De Grandi, Martin Gögele, et al.
Nucleic Acids Research
|
May 16, 2025
CRISPR-BEasy: a free web-based service for designing sgRNA tiling libraries for CRISPR-dependent base editing screens
Vincent Chapdelaine-Trépanier, Shamika Shenoy, Wardah Masud, et al.
G3 (Bethesda, Md.)
|
August 23, 2018
Imputation-Aware Tag SNP Selection To Improve Power for Large-Scale, Multi-ethnic Association Studies
Genevieve L Wojcik, Christian Fuchsberger, Daniel Taliun, et al.
Nature Genetics
|
June 7, 2020
Exploring and visualizing large-scale genetic associations by using PheWeb
Sarah A Gagliano Taliun, Peter VandeHaar, Andrew P Boughton, et al.
American Journal of Human Genetics
|
October 31, 2025
Using the ancestral recombination graph to study the history of rare variants in founder populations
Alejandro Mejia-Garcia, Alex Diaz-Papkovich, Guillaume Sillon, et al.
Medrxiv : the Preprint Server for Health Sciences
|
August 12, 2025
Frequency enrichment of coding variants in a French-Canadian founder population and its implication for inflammatory bowel diseases
Claude Bhérer, Jean-Christophe Grenier, Justin Pelletier, et al.
NPJ Genomic Medicine
|
February 7, 2024
A cost-effective sequencing method for genetic studies combining high-depth whole exome and low-depth whole genome
Claude Bhérer, Robert Eveleigh, Katerina Trajanoska, et al.
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Search research articles
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Showing results (11-20 of 44) with videos related to
Sort By:
Page
of 5
Nucleic Acids Research
|
May 6, 2024
Imputation Server PGS: an automated approach to calculate polygenic risk scores on imputation servers
Lukas Forer, Daniel Taliun, Jonathon LeFaive, et al.
American Journal of Human Genetics
|
September 29, 2020
Cancer PRSweb: An Online Repository with Polygenic Risk Scores for Major Cancer Traits and Their Evaluation in Two Independent Biobanks
Lars G Fritsche, Snehal Patil, Lauren J Beesley, et al.
Nature Genetics
|
January 19, 2026
Exploring and visualizing stratified GWAS results with PheWeb2
Justin Bellavance, Hongyu Xiao, Le Chang, et al.
Journal of Medical Genetics
|
June 22, 2011
Linkage and association analysis of hyperthyrotropinaemia in an Alpine population reveal two novel loci on chromosomes 3q28-29 and 6q26-27
Claudia B Volpato, Alessandro De Grandi, Martin Gögele, et al.
Nucleic Acids Research
|
May 16, 2025
CRISPR-BEasy: a free web-based service for designing sgRNA tiling libraries for CRISPR-dependent base editing screens
Vincent Chapdelaine-Trépanier, Shamika Shenoy, Wardah Masud, et al.
G3 (Bethesda, Md.)
|
August 23, 2018
Imputation-Aware Tag SNP Selection To Improve Power for Large-Scale, Multi-ethnic Association Studies
Genevieve L Wojcik, Christian Fuchsberger, Daniel Taliun, et al.
Nature Genetics
|
June 7, 2020
Exploring and visualizing large-scale genetic associations by using PheWeb
Sarah A Gagliano Taliun, Peter VandeHaar, Andrew P Boughton, et al.
American Journal of Human Genetics
|
October 31, 2025
Using the ancestral recombination graph to study the history of rare variants in founder populations
Alejandro Mejia-Garcia, Alex Diaz-Papkovich, Guillaume Sillon, et al.
Medrxiv : the Preprint Server for Health Sciences
|
August 12, 2025
Frequency enrichment of coding variants in a French-Canadian founder population and its implication for inflammatory bowel diseases
Claude Bhérer, Jean-Christophe Grenier, Justin Pelletier, et al.
NPJ Genomic Medicine
|
February 7, 2024
A cost-effective sequencing method for genetic studies combining high-depth whole exome and low-depth whole genome
Claude Bhérer, Robert Eveleigh, Katerina Trajanoska, et al.
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of 5