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JCI Insight
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October 5, 2016
Tissue-specific metabolic reprogramming drives nutrient flux in diabetic complications
Kelli M Sas, Pradeep Kayampilly, Jaeman Byun, et al.
Genetic Epidemiology
|
November 11, 2017
Identification of 16q21 as a modifier of nonsyndromic orofacial cleft phenotypes
Jenna C Carlson, Jennifer Standley, Aline Petrin, et al.
Medrxiv : the Preprint Server for Health Sciences
|
March 27, 2026
Trio-based GWAS reveals novel loci associated with different forms of isolated cleft lip
Noah Herrick, Zeynep Erdogan-Yildirim, Myoung Keun Lee, et al.
Cardiology in the Young
|
December 30, 2017
Nomenclature for congenital and paediatric cardiac disease: the International Paediatric and Congenital Cardiac Code (IPCCC) and the Eleventh Iteration of the International Classification of Diseases (ICD-11)
Rodney C G Franklin, Marie J Béland, Steven D Colan, et al.
American Journal of Human Genetics
|
March 3, 2009
Mutations in BMP4 are associated with subepithelial, microform, and overt cleft lip
Satoshi Suzuki, Mary L Marazita, Margaret E Cooper, et al.
Medrxiv : the Preprint Server for Health Sciences
|
December 23, 2024
Multi-ancestry Genome Wide Association Study Meta-analysis of Non-syndromic Orofacial Clefts
Zhonglin Jia, Nandita Mukhopadhyay, Zhenglin Yang, 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 peridermopathy
Kelsey Robinson, Sunil K Singh, Rachel B Walkup, 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 explanation
Nandita Mukhopadhyay, Eleanor E Feingold, Harrison Brand, et al.
Journal of Dental Research
|
August 24, 2022
Phenotype Harmonization in the GLIDE2 Oral Health Genomics Consortium
K Divaris, S Haworth, J R Shaffer, et al.
American Journal of Human Genetics
|
June 24, 2020
Genome-wide Enrichment of De Novo Coding Mutations in Orofacial Cleft Trios
Madison R Bishop, Kimberly K Diaz Perez, Miranda Sun, et al.
Page
of 102
Search research articles
Search
Showing results (761-770 of 1,015) with videos related to
Sort By:
Page
of 102
JCI Insight
|
October 5, 2016
Tissue-specific metabolic reprogramming drives nutrient flux in diabetic complications
Kelli M Sas, Pradeep Kayampilly, Jaeman Byun, et al.
Genetic Epidemiology
|
November 11, 2017
Identification of 16q21 as a modifier of nonsyndromic orofacial cleft phenotypes
Jenna C Carlson, Jennifer Standley, Aline Petrin, et al.
Medrxiv : the Preprint Server for Health Sciences
|
March 27, 2026
Trio-based GWAS reveals novel loci associated with different forms of isolated cleft lip
Noah Herrick, Zeynep Erdogan-Yildirim, Myoung Keun Lee, et al.
Cardiology in the Young
|
December 30, 2017
Nomenclature for congenital and paediatric cardiac disease: the International Paediatric and Congenital Cardiac Code (IPCCC) and the Eleventh Iteration of the International Classification of Diseases (ICD-11)
Rodney C G Franklin, Marie J Béland, Steven D Colan, et al.
American Journal of Human Genetics
|
March 3, 2009
Mutations in BMP4 are associated with subepithelial, microform, and overt cleft lip
Satoshi Suzuki, Mary L Marazita, Margaret E Cooper, et al.
Medrxiv : the Preprint Server for Health Sciences
|
December 23, 2024
Multi-ancestry Genome Wide Association Study Meta-analysis of Non-syndromic Orofacial Clefts
Zhonglin Jia, Nandita Mukhopadhyay, Zhenglin Yang, 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 peridermopathy
Kelsey Robinson, Sunil K Singh, Rachel B Walkup, 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 explanation
Nandita Mukhopadhyay, Eleanor E Feingold, Harrison Brand, et al.
Journal of Dental Research
|
August 24, 2022
Phenotype Harmonization in the GLIDE2 Oral Health Genomics Consortium
K Divaris, S Haworth, J R Shaffer, et al.
American Journal of Human Genetics
|
June 24, 2020
Genome-wide Enrichment of De Novo Coding Mutations in Orofacial Cleft Trios
Madison R Bishop, Kimberly K Diaz Perez, Miranda Sun, et al.
Page
of 102