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Denise M Kay

Showing results (61-70 of 73) with videos related to

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The Lancet. Neurology|June 10, 2008
Phenotype, genotype, and worldwide genetic penetrance of LRRK2-associated Parkinson's disease: a case-control studyDaniel G Healy, Mario Falchi, Sean S O'Sullivan, et al.
Plos Genetics|August 31, 2011
Genome-wide gene-environment study identifies glutamate receptor gene GRIN2A as a Parkinson's disease modifier gene via interaction with coffeeTaye H Hamza, Honglei Chen, Erin M Hill-Burns, et al.
Birth Defects Research|July 11, 2024
Exome sequencing identifies novel genes underlying primary congenital glaucoma in the National Birth Defects Prevention StudyElizabeth E Blue, Kristin J Moore, Kari E North, et al.
Birth Defects Research|March 11, 2022
Exome sequencing identifies variants in infants with sacral agenesisGeorgia Pitsava, Marcia L Feldkamp, Nathan Pankratz, et al.
HGG Advances|September 4, 2023
Rare variants in <i>CAPN2</i> increase risk for isolated hypoplastic left heart syndromeElizabeth E Blue, Janson J White, Michael K Dush, et al.
Birth Defects Research|July 23, 2019
Exome sequencing of family trios from the National Birth Defects Prevention Study: Tapping into a rich resource of genetic and environmental dataMary M Jenkins, Lynn M Almli, Faith Pangilinan, et al.
JAMA Network Open|January 29, 2026
Universal Newborn Screening for Congenital Cytomegalovirus Using Dried Blood Spot SpecimensNorma P Tavakoli, Virginia Sack, Andrew S Handel, et al.
Birth Defects Research|April 30, 2025
Exome Sequencing to Identify Novel Susceptibility Genes for Nonsyndromic Split-Hand/Ft Malformation: A Report From the National Birth Defects Prevention StudyTonia C Carter, Denise M Kay, Faith Pangilinan, et al.
Nature Genetics|November 20, 2012
A genome-wide association study identifies susceptibility loci for nonsyndromic sagittal craniosynostosis near BMP2 and within BBS9Cristina M Justice, Garima Yagnik, Yoonhee Kim, et al.
American Journal of Medical Genetics. Part A|March 21, 2023
Exome-wide assessment of isolated biliary atresia: A report from the National Birth Defects Prevention Study using child-parent trios and a case-control design to identify novel rare variantsPagna Sok, Aniko Sabo, Lynn M Almli, et al.
Pageof 8

Showing results (61-70 of 73) with videos related to

Sort By:
Pageof 8
The Lancet. Neurology|June 10, 2008
Phenotype, genotype, and worldwide genetic penetrance of LRRK2-associated Parkinson's disease: a case-control studyDaniel G Healy, Mario Falchi, Sean S O'Sullivan, et al.
Plos Genetics|August 31, 2011
Genome-wide gene-environment study identifies glutamate receptor gene GRIN2A as a Parkinson's disease modifier gene via interaction with coffeeTaye H Hamza, Honglei Chen, Erin M Hill-Burns, et al.
Birth Defects Research|July 11, 2024
Exome sequencing identifies novel genes underlying primary congenital glaucoma in the National Birth Defects Prevention StudyElizabeth E Blue, Kristin J Moore, Kari E North, et al.
Birth Defects Research|March 11, 2022
Exome sequencing identifies variants in infants with sacral agenesisGeorgia Pitsava, Marcia L Feldkamp, Nathan Pankratz, et al.
HGG Advances|September 4, 2023
Rare variants in <i>CAPN2</i> increase risk for isolated hypoplastic left heart syndromeElizabeth E Blue, Janson J White, Michael K Dush, et al.
Birth Defects Research|July 23, 2019
Exome sequencing of family trios from the National Birth Defects Prevention Study: Tapping into a rich resource of genetic and environmental dataMary M Jenkins, Lynn M Almli, Faith Pangilinan, et al.
JAMA Network Open|January 29, 2026
Universal Newborn Screening for Congenital Cytomegalovirus Using Dried Blood Spot SpecimensNorma P Tavakoli, Virginia Sack, Andrew S Handel, et al.
Birth Defects Research|April 30, 2025
Exome Sequencing to Identify Novel Susceptibility Genes for Nonsyndromic Split-Hand/Ft Malformation: A Report From the National Birth Defects Prevention StudyTonia C Carter, Denise M Kay, Faith Pangilinan, et al.
Nature Genetics|November 20, 2012
A genome-wide association study identifies susceptibility loci for nonsyndromic sagittal craniosynostosis near BMP2 and within BBS9Cristina M Justice, Garima Yagnik, Yoonhee Kim, et al.
American Journal of Medical Genetics. Part A|March 21, 2023
Exome-wide assessment of isolated biliary atresia: A report from the National Birth Defects Prevention Study using child-parent trios and a case-control design to identify novel rare variantsPagna Sok, Aniko Sabo, Lynn M Almli, et al.
Pageof 8