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Seth M Weinberg

Showing results (81-90 of 181) with videos related to

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Plos Genetics|July 9, 2021
Pleiotropy method reveals genetic overlap between orofacial clefts at multiple novel loci from GWAS of multi-ethnic triosDebashree Ray, Sowmya Venkataraghavan, Wanying Zhang, et al.
Plos One|April 15, 2025
Change is never easy: Exploring the transition from undergraduate to dental student in a U.S.-based programTaiana C Leite, Christine R Wankiiri-Hale, Nilesh H Shah, et al.
Briefings in Bioinformatics|March 10, 2025
Optimized phenotyping of complex morphological traits: enhancing discovery of common and rare genetic variantsMeng Yuan, Seppe Goovaerts, Myoung K Lee, et al.
Genes|August 28, 2025
Gene-by-Environment Interactions Involving Maternal Exposures with Orofacial Cleft Risk in FilipinosZeynep Erdogan-Yildirim, Jenna C Carlson, Nandita Mukhopadhyay, et al.
Medrxiv : the Preprint Server for Health Sciences|April 10, 2023
Rare genetic variants in <i>SEC24D</i> modify orofacial cleft phenotypesSarah W Curtis, Jenna C Carlson, Terri H Beaty, et al.
Bioinformatics (Oxford, England)|March 22, 2025
Clustering individuals using INMTD: a novel versatile multi-view embedding framework integrating omics and imaging dataZuqi Li, Sam F L Windels, Noël Malod-Dognin, et al.
Medrxiv : the Preprint Server for Health Sciences|February 17, 2023
Rare variants found in multiplex families with orofacial clefts: Does expanding the phenotype make a difference?Kimberly K Diaz Perez, Sydney Chung, S Taylor Head, et al.
Plos One|April 27, 2018
Mapping genetic variants for cranial vault shape in humansJasmien Roosenboom, Myoung Keun Lee, Jacqueline T Hecht, et al.
Human Genetics|September 7, 2023
Rare variant modifier analysis identifies variants in SEC24D associated with orofacial cleft subtypesSarah W Curtis, Jenna C Carlson, Terri H Beaty, et al.
American Journal of Medical Genetics. Part A|June 23, 2023
Rare variants found in multiplex families with orofacial clefts: Does expanding the phenotype make a difference?Kimberly K Diaz Perez, Sydney Chung, S Taylor Head, et al.
Pageof 19

Showing results (81-90 of 181) with videos related to

Sort By:
Pageof 19
Plos Genetics|July 9, 2021
Pleiotropy method reveals genetic overlap between orofacial clefts at multiple novel loci from GWAS of multi-ethnic triosDebashree Ray, Sowmya Venkataraghavan, Wanying Zhang, et al.
Plos One|April 15, 2025
Change is never easy: Exploring the transition from undergraduate to dental student in a U.S.-based programTaiana C Leite, Christine R Wankiiri-Hale, Nilesh H Shah, et al.
Briefings in Bioinformatics|March 10, 2025
Optimized phenotyping of complex morphological traits: enhancing discovery of common and rare genetic variantsMeng Yuan, Seppe Goovaerts, Myoung K Lee, et al.
Genes|August 28, 2025
Gene-by-Environment Interactions Involving Maternal Exposures with Orofacial Cleft Risk in FilipinosZeynep Erdogan-Yildirim, Jenna C Carlson, Nandita Mukhopadhyay, et al.
Medrxiv : the Preprint Server for Health Sciences|April 10, 2023
Rare genetic variants in <i>SEC24D</i> modify orofacial cleft phenotypesSarah W Curtis, Jenna C Carlson, Terri H Beaty, et al.
Bioinformatics (Oxford, England)|March 22, 2025
Clustering individuals using INMTD: a novel versatile multi-view embedding framework integrating omics and imaging dataZuqi Li, Sam F L Windels, Noël Malod-Dognin, et al.
Medrxiv : the Preprint Server for Health Sciences|February 17, 2023
Rare variants found in multiplex families with orofacial clefts: Does expanding the phenotype make a difference?Kimberly K Diaz Perez, Sydney Chung, S Taylor Head, et al.
Plos One|April 27, 2018
Mapping genetic variants for cranial vault shape in humansJasmien Roosenboom, Myoung Keun Lee, Jacqueline T Hecht, et al.
Human Genetics|September 7, 2023
Rare variant modifier analysis identifies variants in SEC24D associated with orofacial cleft subtypesSarah W Curtis, Jenna C Carlson, Terri H Beaty, et al.
American Journal of Medical Genetics. Part A|June 23, 2023
Rare variants found in multiplex families with orofacial clefts: Does expanding the phenotype make a difference?Kimberly K Diaz Perez, Sydney Chung, S Taylor Head, et al.
Pageof 19