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Showing results (271-280 of 301) with videos related to

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Nature Communications|September 23, 2017
Establishing multiple omics baselines for three Southeast Asian populations in the Singapore Integrative Omics StudyWoei-Yuh Saw, Erwin Tantoso, Husna Begum, et al.
Neurosurgery|February 5, 2026
Prenatal Closure of Myeloschisis vs Myelomeningocele: Insights From the fMMC Consortium RegistryDavid S Hersh, Amirul Anuar, Jagruti Anadkat, et al.
American Journal of Human Genetics|January 8, 2013
Deep whole-genome sequencing of 100 southeast Asian MalaysLai-Ping Wong, Rick Twee-Hee Ong, Wan-Ting Poh, et al.
American Journal of Human Genetics|June 8, 2021
De novo and bi-allelic variants in AP1G1 cause neurodevelopmental disorder with developmental delay, intellectual disability, and epilepsyMuhammad A Usmani, Zubair M Ahmed, Pamela Magini, et al.
American Journal of Human Genetics|September 21, 2021
Rare and de novo variants in 827 congenital diaphragmatic hernia probands implicate LONP1 as candidate risk geneLu Qiao, Le Xu, Lan Yu, et al.
International Journal of Cancer|March 12, 2014
Exposure to secondhand tobacco smoke and lung cancer by histological type: a pooled analysis of the International Lung Cancer Consortium (ILCCO)Claire H Kim, Yuan-Chin Amy Lee, Rayjean J Hung, et al.
American Journal of Human Genetics|September 27, 2024
Common variants increase risk for congenital diaphragmatic hernia within the context of de novo variantsLu Qiao, Carrie L Welch, Rebecca Hernan, et al.
Human Molecular Genetics|May 28, 2014
Meta-analysis of genome-wide association studies in East Asian-ancestry populations identifies four new loci for body mass indexWanqing Wen, Wei Zheng, Yukinori Okada, et al.
Nature Genetics|August 30, 2011
Genome-wide association study in individuals of South Asian ancestry identifies six new type 2 diabetes susceptibility lociJaspal S Kooner, Danish Saleheen, Xueling Sim, et al.
American Journal of Human Genetics|June 16, 2015
Polymorphisms in a Putative Enhancer at the 10q21.2 Breast Cancer Risk Locus Regulate NRBF2 ExpressionHatef Darabi, Karen McCue, Jonathan Beesley, et al.
Pageof 31

Showing results (271-280 of 301) with videos related to

Sort By:
Pageof 31
Nature Communications|September 23, 2017
Establishing multiple omics baselines for three Southeast Asian populations in the Singapore Integrative Omics StudyWoei-Yuh Saw, Erwin Tantoso, Husna Begum, et al.
Neurosurgery|February 5, 2026
Prenatal Closure of Myeloschisis vs Myelomeningocele: Insights From the fMMC Consortium RegistryDavid S Hersh, Amirul Anuar, Jagruti Anadkat, et al.
American Journal of Human Genetics|January 8, 2013
Deep whole-genome sequencing of 100 southeast Asian MalaysLai-Ping Wong, Rick Twee-Hee Ong, Wan-Ting Poh, et al.
American Journal of Human Genetics|June 8, 2021
De novo and bi-allelic variants in AP1G1 cause neurodevelopmental disorder with developmental delay, intellectual disability, and epilepsyMuhammad A Usmani, Zubair M Ahmed, Pamela Magini, et al.
American Journal of Human Genetics|September 21, 2021
Rare and de novo variants in 827 congenital diaphragmatic hernia probands implicate LONP1 as candidate risk geneLu Qiao, Le Xu, Lan Yu, et al.
International Journal of Cancer|March 12, 2014
Exposure to secondhand tobacco smoke and lung cancer by histological type: a pooled analysis of the International Lung Cancer Consortium (ILCCO)Claire H Kim, Yuan-Chin Amy Lee, Rayjean J Hung, et al.
American Journal of Human Genetics|September 27, 2024
Common variants increase risk for congenital diaphragmatic hernia within the context of de novo variantsLu Qiao, Carrie L Welch, Rebecca Hernan, et al.
Human Molecular Genetics|May 28, 2014
Meta-analysis of genome-wide association studies in East Asian-ancestry populations identifies four new loci for body mass indexWanqing Wen, Wei Zheng, Yukinori Okada, et al.
Nature Genetics|August 30, 2011
Genome-wide association study in individuals of South Asian ancestry identifies six new type 2 diabetes susceptibility lociJaspal S Kooner, Danish Saleheen, Xueling Sim, et al.
American Journal of Human Genetics|June 16, 2015
Polymorphisms in a Putative Enhancer at the 10q21.2 Breast Cancer Risk Locus Regulate NRBF2 ExpressionHatef Darabi, Karen McCue, Jonathan Beesley, et al.
Pageof 31