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Maxime Hebrard

Showing results (11-20 of 21) with videos related to

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Research Square|March 27, 2026
Epigenome-Wide Association Study in Asian Cohort Identifies Novel DNA Methylation Markers for Carotid Intima-Media ThicknessKonstanze Tan, Sarah E Harris, Jane Maddock, et al.
American Journal of Human Genetics|September 3, 2013
Mutations in IMPG1 cause vitelliform macular dystrophiesGaël Manes, Isabelle Meunier, Almudena Avila-Fernández, et al.
Ophthalmic Epidemiology|January 29, 2013
Relative frequencies of inherited retinal dystrophies and optic neuropathies in Southern France: assessment of 21-year data managementBeatrice Bocquet, Annie Lacroux, Marie-Odile Surget, et al.
Nature Communications|November 4, 2024
A Catalogue of Structural Variation across Ancestrally Diverse Asian GenomesJoanna Hui Juan Tan, Zhihui Li, Mar Gonzalez Porta, et al.
American Journal of Human Genetics|November 24, 2015
Recessive Mutations in RTN4IP1 Cause Isolated and Syndromic Optic NeuropathiesClaire Angebault, Pierre-Olivier Guichet, Yasmina Talmat-Amar, et al.
Cell|February 1, 2024
SMARCAL1 is a dual regulator of innate immune signaling and PD-L1 expression that promotes tumor immune evasionGiuseppe Leuzzi, Alessandro Vasciaveo, Angelo Taglialatela, et al.
Nature Communications|November 6, 2022
Analysis of clinically relevant variants from ancestrally diverse Asian genomesSock Hoai Chan, Yasmin Bylstra, Jing Xian Teo, et al.
Iscience|May 1, 2023
A five-safes approach to a secure and scalable genomics data repositoryChih Chuan Shih, Jieqi Chen, Ai Shan Lee, et al.
Nature Communications|June 9, 2026
Genomic landscape of drug binding and pharmacogenetic variation across diverse populations using SNPdrug3DAshar J Malik, Dimitar Kenanov, Cheng-Shoong Chong, et al.
Nature Communications|December 30, 2025
The Health for Life in Singapore (HELIOS) Study: delivering precision medicine research for Asian populationsXiaoyan Wang, Theresia Mina, Nilanjana Sadhu, et al.
Pageof 3

Showing results (11-20 of 21) with videos related to

Sort By:
Pageof 3
Research Square|March 27, 2026
Epigenome-Wide Association Study in Asian Cohort Identifies Novel DNA Methylation Markers for Carotid Intima-Media ThicknessKonstanze Tan, Sarah E Harris, Jane Maddock, et al.
American Journal of Human Genetics|September 3, 2013
Mutations in IMPG1 cause vitelliform macular dystrophiesGaël Manes, Isabelle Meunier, Almudena Avila-Fernández, et al.
Ophthalmic Epidemiology|January 29, 2013
Relative frequencies of inherited retinal dystrophies and optic neuropathies in Southern France: assessment of 21-year data managementBeatrice Bocquet, Annie Lacroux, Marie-Odile Surget, et al.
Nature Communications|November 4, 2024
A Catalogue of Structural Variation across Ancestrally Diverse Asian GenomesJoanna Hui Juan Tan, Zhihui Li, Mar Gonzalez Porta, et al.
American Journal of Human Genetics|November 24, 2015
Recessive Mutations in RTN4IP1 Cause Isolated and Syndromic Optic NeuropathiesClaire Angebault, Pierre-Olivier Guichet, Yasmina Talmat-Amar, et al.
Cell|February 1, 2024
SMARCAL1 is a dual regulator of innate immune signaling and PD-L1 expression that promotes tumor immune evasionGiuseppe Leuzzi, Alessandro Vasciaveo, Angelo Taglialatela, et al.
Nature Communications|November 6, 2022
Analysis of clinically relevant variants from ancestrally diverse Asian genomesSock Hoai Chan, Yasmin Bylstra, Jing Xian Teo, et al.
Iscience|May 1, 2023
A five-safes approach to a secure and scalable genomics data repositoryChih Chuan Shih, Jieqi Chen, Ai Shan Lee, et al.
Nature Communications|June 9, 2026
Genomic landscape of drug binding and pharmacogenetic variation across diverse populations using SNPdrug3DAshar J Malik, Dimitar Kenanov, Cheng-Shoong Chong, et al.
Nature Communications|December 30, 2025
The Health for Life in Singapore (HELIOS) Study: delivering precision medicine research for Asian populationsXiaoyan Wang, Theresia Mina, Nilanjana Sadhu, et al.
Pageof 3