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Showing results (31-40 of 45) with videos related to

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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.
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 Heredity|February 16, 2022
Genetic Analyses of Enamel Hypoplasia in Multiethnic CohortsRasha N Alotaibi, Brian J Howe, Lina M Moreno Uribe, et al.
Dentistry Journal|July 25, 2022
Tooth Agenesis Patterns in Orofacial Clefting Using Tooth Agenesis Code: A Meta-AnalysisBrian J Howe, Chandler Pendleton, Miyuraj Harishchandra Hikkaduwa Withanage, et al.
HGG Advances|September 18, 2023
Trio-based GWAS identifies novel associations and subtype-specific risk factors for cleft palateKelsey Robinson, Trenell J Mosley, Kenneth S Rivera-González, et al.
Medrxiv : the Preprint Server for Health Sciences|April 17, 2023
Trio-based GWAS identifies novel associations and subtype-specific risk factors for cleft palateKelsey Robinson, Trenell J Mosley, Kenneth S Rivera-González, et al.
Genetic Epidemiology|November 11, 2017
Identification of 16q21 as a modifier of nonsyndromic orofacial cleft phenotypesJenna C Carlson, Jennifer Standley, Aline Petrin, et al.
Medrxiv : the Preprint Server for Health Sciences|February 6, 2026
Is 7p14.1 an orofacial cleft risk locus? Genome-wide study of copy number variation in multiple populations provides both a replication of previous studies and an alternative explanationNandita Mukhopadhyay, Eleanor E Feingold, Harrison Brand, et al.
Medrxiv : the Preprint Server for Health Sciences|January 27, 2025
Rare variants in <i>PRKCI</i> cause Van der Woude syndrome and other features of peridermopathyKelsey Robinson, Sunil K Singh, Rachel B Walkup, et al.
Medrxiv : the Preprint Server for Health Sciences|December 23, 2024
Multi-ancestry Genome Wide Association Study Meta-analysis of Non-syndromic Orofacial CleftsZhonglin Jia, Nandita Mukhopadhyay, Zhenglin Yang, et al.
Pageof 5

Showing results (31-40 of 45) with videos related to

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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.
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 Heredity|February 16, 2022
Genetic Analyses of Enamel Hypoplasia in Multiethnic CohortsRasha N Alotaibi, Brian J Howe, Lina M Moreno Uribe, et al.
Dentistry Journal|July 25, 2022
Tooth Agenesis Patterns in Orofacial Clefting Using Tooth Agenesis Code: A Meta-AnalysisBrian J Howe, Chandler Pendleton, Miyuraj Harishchandra Hikkaduwa Withanage, et al.
HGG Advances|September 18, 2023
Trio-based GWAS identifies novel associations and subtype-specific risk factors for cleft palateKelsey Robinson, Trenell J Mosley, Kenneth S Rivera-González, et al.
Medrxiv : the Preprint Server for Health Sciences|April 17, 2023
Trio-based GWAS identifies novel associations and subtype-specific risk factors for cleft palateKelsey Robinson, Trenell J Mosley, Kenneth S Rivera-González, et al.
Genetic Epidemiology|November 11, 2017
Identification of 16q21 as a modifier of nonsyndromic orofacial cleft phenotypesJenna C Carlson, Jennifer Standley, Aline Petrin, et al.
Medrxiv : the Preprint Server for Health Sciences|February 6, 2026
Is 7p14.1 an orofacial cleft risk locus? Genome-wide study of copy number variation in multiple populations provides both a replication of previous studies and an alternative explanationNandita Mukhopadhyay, Eleanor E Feingold, Harrison Brand, et al.
Medrxiv : the Preprint Server for Health Sciences|January 27, 2025
Rare variants in <i>PRKCI</i> cause Van der Woude syndrome and other features of peridermopathyKelsey Robinson, Sunil K Singh, Rachel B Walkup, et al.
Medrxiv : the Preprint Server for Health Sciences|December 23, 2024
Multi-ancestry Genome Wide Association Study Meta-analysis of Non-syndromic Orofacial CleftsZhonglin Jia, Nandita Mukhopadhyay, Zhenglin Yang, et al.
Pageof 5