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Human Mutation
|
May 21, 2019
Integration of multiple epigenomic marks improves prediction of variant impact in saturation mutagenesis reporter assay
Dustin Shigaki, Orit Adato, Aashish N Adhikari, et al.
Communications Medicine
|
August 21, 2025
Leveraging sequences missing from the human genome to diagnose cancer
Ilias Georgakopoulos-Soares, Ofer Yizhar-Barnea, Ioannis Mouratidis, et al.
Biorxiv : the Preprint Server for Biology
|
March 22, 2023
TAD Evolutionary and functional characterization reveals diversity in mammalian TAD boundary properties and function
Mariam Okhovat, Jake VanCampen, Ana C Lima, et al.
Biorxiv : the Preprint Server for Biology
|
November 24, 2025
Large-scale discovery of neural enhancers for cis-regulation therapies
Troy A McDiarmid, Nicholas F Page, Florence M Chardon, et al.
Biorxiv : the Preprint Server for Biology
|
June 9, 2023
Association of genetic variation in
Hao Yu, Anas M Khanshour, Aki Ushiki, et al.
Elife
|
January 26, 2024
Association of genetic variation in <i>COL11A1</i> with adolescent idiopathic scoliosis
Hao Yu, Anas M Khanshour, Aki Ushiki, et al.
Human Molecular Genetics
|
November 6, 2018
Genome-wide meta-analysis and replication studies in multiple ethnicities identify novel adolescent idiopathic scoliosis susceptibility loci
Anas M Khanshour, Ikuyo Kou, Yanhui Fan, et al.
Nature Communications
|
December 7, 2023
TAD evolutionary and functional characterization reveals diversity in mammalian TAD boundary properties and function
Mariam Okhovat, Jake VanCampen, Kimberly A Nevonen, et al.
Nature
|
December 10, 2025
Publisher Correction: CRISPR activation for SCN2A-related neurodevelopmental disorders
Serena Tamura, Andrew D Nelson, Perry W E Spratt, et al.
Nature
|
September 17, 2025
CRISPR activation for SCN2A-related neurodevelopmental disorders
Serena Tamura, Andrew D Nelson, Perry W E Spratt, et al.
Page
of 19
Search research articles
Search
Showing results (171-180 of 184) with videos related to
Sort By:
Page
of 19
Human Mutation
|
May 21, 2019
Integration of multiple epigenomic marks improves prediction of variant impact in saturation mutagenesis reporter assay
Dustin Shigaki, Orit Adato, Aashish N Adhikari, et al.
Communications Medicine
|
August 21, 2025
Leveraging sequences missing from the human genome to diagnose cancer
Ilias Georgakopoulos-Soares, Ofer Yizhar-Barnea, Ioannis Mouratidis, et al.
Biorxiv : the Preprint Server for Biology
|
March 22, 2023
TAD Evolutionary and functional characterization reveals diversity in mammalian TAD boundary properties and function
Mariam Okhovat, Jake VanCampen, Ana C Lima, et al.
Biorxiv : the Preprint Server for Biology
|
November 24, 2025
Large-scale discovery of neural enhancers for cis-regulation therapies
Troy A McDiarmid, Nicholas F Page, Florence M Chardon, et al.
Biorxiv : the Preprint Server for Biology
|
June 9, 2023
Association of genetic variation in
Hao Yu, Anas M Khanshour, Aki Ushiki, et al.
Elife
|
January 26, 2024
Association of genetic variation in <i>COL11A1</i> with adolescent idiopathic scoliosis
Hao Yu, Anas M Khanshour, Aki Ushiki, et al.
Human Molecular Genetics
|
November 6, 2018
Genome-wide meta-analysis and replication studies in multiple ethnicities identify novel adolescent idiopathic scoliosis susceptibility loci
Anas M Khanshour, Ikuyo Kou, Yanhui Fan, et al.
Nature Communications
|
December 7, 2023
TAD evolutionary and functional characterization reveals diversity in mammalian TAD boundary properties and function
Mariam Okhovat, Jake VanCampen, Kimberly A Nevonen, et al.
Nature
|
December 10, 2025
Publisher Correction: CRISPR activation for SCN2A-related neurodevelopmental disorders
Serena Tamura, Andrew D Nelson, Perry W E Spratt, et al.
Nature
|
September 17, 2025
CRISPR activation for SCN2A-related neurodevelopmental disorders
Serena Tamura, Andrew D Nelson, Perry W E Spratt, et al.
Page
of 19