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Ryan S Dhindsa

Showing results (11-20 of 49) with videos related to

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Epilepsia|January 15, 2022
Association of ultra-rare coding variants with genetic generalized epilepsy: A case-control whole exome sequencing studyMahmoud Koko, Joshua E Motelow, Kate E Stanley, et al.
American Journal of Human Genetics|September 23, 2023
Literature-based predictions of Mendelian disease therapiesCole A Deisseroth, Won-Seok Lee, Jiyoen Kim, et al.
Science Advances|June 30, 2023
<i>Atoh1</i> drives the heterogeneity of the pontine nuclei neurons and promotes their differentiationSih-Rong Wu, Jessica C Butts, Matthew S Caudill, et al.
Communications Biology|July 11, 2023
Author Correction: DrugnomeAI is an ensemble machine-learning framework for predicting druggability of candidate drug targetsArwa Raies, Ewa Tulodziecka, James Stainer, et al.
Communications Biology|November 26, 2022
DrugnomeAI is an ensemble machine-learning framework for predicting druggability of candidate drug targetsArwa Raies, Ewa Tulodziecka, James Stainer, et al.
Plos One|August 11, 2017
Orion: Detecting regions of the human non-coding genome that are intolerant to variation using population geneticsAyal B Gussow, Brett R Copeland, Ryan S Dhindsa, et al.
American Journal of Human Genetics|February 27, 2025
Genome-wide prediction of dominant and recessive neurodevelopmental disorder-associated genesRyan S Dhindsa, Blake A Weido, Justin S Dhindsa, et al.
Plos One|January 12, 2018
Correction: Orion: Detecting regions of the human non-coding genome that are intolerant to variation using population geneticsAyal B Gussow, Brett R Copeland, Ryan S Dhindsa, et al.
Science Advances|August 26, 2022
Cancer-driving mutations are enriched in genic regions intolerant to germline variationDimitrios Vitsios, Ryan S Dhindsa, Dorota Matelska, et al.
American Journal of Human Genetics|December 2, 2022
A minimal role for synonymous variation in human diseaseRyan S Dhindsa, Quanli Wang, Dimitrios Vitsios, et al.
Pageof 5

Showing results (11-20 of 49) with videos related to

Sort By:
Pageof 5
Epilepsia|January 15, 2022
Association of ultra-rare coding variants with genetic generalized epilepsy: A case-control whole exome sequencing studyMahmoud Koko, Joshua E Motelow, Kate E Stanley, et al.
American Journal of Human Genetics|September 23, 2023
Literature-based predictions of Mendelian disease therapiesCole A Deisseroth, Won-Seok Lee, Jiyoen Kim, et al.
Science Advances|June 30, 2023
<i>Atoh1</i> drives the heterogeneity of the pontine nuclei neurons and promotes their differentiationSih-Rong Wu, Jessica C Butts, Matthew S Caudill, et al.
Communications Biology|July 11, 2023
Author Correction: DrugnomeAI is an ensemble machine-learning framework for predicting druggability of candidate drug targetsArwa Raies, Ewa Tulodziecka, James Stainer, et al.
Communications Biology|November 26, 2022
DrugnomeAI is an ensemble machine-learning framework for predicting druggability of candidate drug targetsArwa Raies, Ewa Tulodziecka, James Stainer, et al.
Plos One|August 11, 2017
Orion: Detecting regions of the human non-coding genome that are intolerant to variation using population geneticsAyal B Gussow, Brett R Copeland, Ryan S Dhindsa, et al.
American Journal of Human Genetics|February 27, 2025
Genome-wide prediction of dominant and recessive neurodevelopmental disorder-associated genesRyan S Dhindsa, Blake A Weido, Justin S Dhindsa, et al.
Plos One|January 12, 2018
Correction: Orion: Detecting regions of the human non-coding genome that are intolerant to variation using population geneticsAyal B Gussow, Brett R Copeland, Ryan S Dhindsa, et al.
Science Advances|August 26, 2022
Cancer-driving mutations are enriched in genic regions intolerant to germline variationDimitrios Vitsios, Ryan S Dhindsa, Dorota Matelska, et al.
American Journal of Human Genetics|December 2, 2022
A minimal role for synonymous variation in human diseaseRyan S Dhindsa, Quanli Wang, Dimitrios Vitsios, et al.
Pageof 5