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M Weinberg

Showing results (741-750 of 1,015) with videos related to

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Nature Genetics|February 21, 2018
Genome-wide mapping of global-to-local genetic effects on human facial shapePeter Claes, Jasmien Roosenboom, Julie D White, et al.
Human Molecular Genetics|October 31, 2025
Haploinsufficiency of GRHL2 is associated with orofacial clefting in humansSarah W Curtis, Cinderella Yang, Alba Sanchis-Juan, et al.
American Journal of Human Genetics|October 7, 2025
Distinguishing syndromic and nonsyndromic cleft palate through analysis of protein-altering de novo variants in 818 triosKelsey R Robinson, Sarah W Curtis, Justin E Paschall, et al.
Human Genetics|January 6, 2017
Genome-wide meta-analyses of nonsyndromic orofacial clefts identify novel associations between FOXE1 and all orofacial clefts, and TP63 and cleft lip with or without cleft palateElizabeth J Leslie, Jenna C Carlson, John R Shaffer, et al.
Frontiers in Cell and Developmental Biology|April 26, 2021
Genome-Wide Association Study of Non-syndromic Orofacial Clefts in a Multiethnic Sample of Families and Controls Identifies Novel RegionsNandita Mukhopadhyay, Eleanor Feingold, Lina Moreno-Uribe, et al.
Plos Genetics|August 19, 2021
Genome scans of facial features in East Africans and cross-population comparisons reveal novel associationsChenxing Liu, Myoung Keun Lee, Sahin Naqvi, et al.
Frontiers in Genetics|March 11, 2021
The Intersection of the Genetic Architectures of Orofacial Clefts and Normal Facial VariationKarlijne Indencleef, Hanne Hoskens, Myoung Keun Lee, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 12, 2014
Synchronized renal tubular cell death involves ferroptosisAndreas Linkermann, Rachid Skouta, Nina Himmerkus, et al.
Genetic Epidemiology|February 22, 2022
Genome-wide association study of multiethnic nonsyndromic orofacial cleft families identifies novel loci specific to family and phenotypic subtypesNandita Mukhopadhyay, Eleanor Feingold, Lina Moreno-Uribe, et al.
Genetic Epidemiology|June 8, 2019
A systematic genetic analysis and visualization of phenotypic heterogeneity among orofacial cleft GWAS signalsJenna C Carlson, Deepti Anand, Azeez Butali, et al.
Pageof 102

Showing results (741-750 of 1,015) with videos related to

Sort By:
Pageof 102
Nature Genetics|February 21, 2018
Genome-wide mapping of global-to-local genetic effects on human facial shapePeter Claes, Jasmien Roosenboom, Julie D White, et al.
Human Molecular Genetics|October 31, 2025
Haploinsufficiency of GRHL2 is associated with orofacial clefting in humansSarah W Curtis, Cinderella Yang, Alba Sanchis-Juan, et al.
American Journal of Human Genetics|October 7, 2025
Distinguishing syndromic and nonsyndromic cleft palate through analysis of protein-altering de novo variants in 818 triosKelsey R Robinson, Sarah W Curtis, Justin E Paschall, et al.
Human Genetics|January 6, 2017
Genome-wide meta-analyses of nonsyndromic orofacial clefts identify novel associations between FOXE1 and all orofacial clefts, and TP63 and cleft lip with or without cleft palateElizabeth J Leslie, Jenna C Carlson, John R Shaffer, et al.
Frontiers in Cell and Developmental Biology|April 26, 2021
Genome-Wide Association Study of Non-syndromic Orofacial Clefts in a Multiethnic Sample of Families and Controls Identifies Novel RegionsNandita Mukhopadhyay, Eleanor Feingold, Lina Moreno-Uribe, et al.
Plos Genetics|August 19, 2021
Genome scans of facial features in East Africans and cross-population comparisons reveal novel associationsChenxing Liu, Myoung Keun Lee, Sahin Naqvi, et al.
Frontiers in Genetics|March 11, 2021
The Intersection of the Genetic Architectures of Orofacial Clefts and Normal Facial VariationKarlijne Indencleef, Hanne Hoskens, Myoung Keun Lee, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 12, 2014
Synchronized renal tubular cell death involves ferroptosisAndreas Linkermann, Rachid Skouta, Nina Himmerkus, et al.
Genetic Epidemiology|February 22, 2022
Genome-wide association study of multiethnic nonsyndromic orofacial cleft families identifies novel loci specific to family and phenotypic subtypesNandita Mukhopadhyay, Eleanor Feingold, Lina Moreno-Uribe, et al.
Genetic Epidemiology|June 8, 2019
A systematic genetic analysis and visualization of phenotypic heterogeneity among orofacial cleft GWAS signalsJenna C Carlson, Deepti Anand, Azeez Butali, et al.
Pageof 102