Biography and Research Information
OverviewAI-generated summary
Jill Kelsay's research focuses on the genetic underpinnings of developmental disorders. Her work has identified de novo variants in H3-3A and H3-3B genes as contributors to neurodevelopmental delay, dysmorphic features, and structural brain abnormalities. This research contributes to understanding the molecular basis of complex congenital conditions.
Metrics
- h-index: 4
- Publications: 5
- Citations: 119
Selected Publications
-
De novo variants in H3-3A and H3-3B are associated with neurodevelopmental delay, dysmorphic features, and structural brain abnormalities (2021)
Collaboration Network
Top Collaborators
Volkan Okur
Baylor College of Medicine (US)
1 shared publication
- De novo variants in H3-3A and H3-3B are associated with neurodevelopmental delay, dysmorphic features, and structural brain abnormalities
Zefu Chen
Peking Union Medical College Hospital (CN)
1 shared publication
- De novo variants in H3-3A and H3-3B are associated with neurodevelopmental delay, dysmorphic features, and structural brain abnormalities
Liesbeth Vossaert
Baylor Genetics (US)
1 shared publication
- De novo variants in H3-3A and H3-3B are associated with neurodevelopmental delay, dysmorphic features, and structural brain abnormalities
Sandra Peacock
Baylor College of Medicine (US)
1 shared publication
- De novo variants in H3-3A and H3-3B are associated with neurodevelopmental delay, dysmorphic features, and structural brain abnormalities
Jill A. Rosenfeld
Baylor College of Medicine (US)
1 shared publication
- De novo variants in H3-3A and H3-3B are associated with neurodevelopmental delay, dysmorphic features, and structural brain abnormalities
Lina Zhao
Peking Union Medical College Hospital (CN)
1 shared publication
- De novo variants in H3-3A and H3-3B are associated with neurodevelopmental delay, dysmorphic features, and structural brain abnormalities
Haowei Du
Baylor College of Medicine (US)
1 shared publication
- De novo variants in H3-3A and H3-3B are associated with neurodevelopmental delay, dysmorphic features, and structural brain abnormalities
Emily Calamaro
University of Rochester (US)
1 shared publication
- De novo variants in H3-3A and H3-3B are associated with neurodevelopmental delay, dysmorphic features, and structural brain abnormalities
Amanda Gerard
Texas Children's Hospital (US)
1 shared publication
- De novo variants in H3-3A and H3-3B are associated with neurodevelopmental delay, dysmorphic features, and structural brain abnormalities
Sen Zhao
Chinese Academy of Medical Sciences & Peking Union Medical College (CN)
1 shared publication
- De novo variants in H3-3A and H3-3B are associated with neurodevelopmental delay, dysmorphic features, and structural brain abnormalities
Ashley Lahr
Children's Hospital of Pittsburgh (US)
1 shared publication
- De novo variants in H3-3A and H3-3B are associated with neurodevelopmental delay, dysmorphic features, and structural brain abnormalities
Chloe Mighton
Lunenfeld-Tanenbaum Research Institute (CA)
1 shared publication
- De novo variants in H3-3A and H3-3B are associated with neurodevelopmental delay, dysmorphic features, and structural brain abnormalities
Hillary M. Porter
Children's National (US)
1 shared publication
- De novo variants in H3-3A and H3-3B are associated with neurodevelopmental delay, dysmorphic features, and structural brain abnormalities
Amy Siemon
Nationwide Children's Hospital (US)
1 shared publication
- De novo variants in H3-3A and H3-3B are associated with neurodevelopmental delay, dysmorphic features, and structural brain abnormalities
Josh Silver
Mount Sinai Hospital (CA)
1 shared publication
- De novo variants in H3-3A and H3-3B are associated with neurodevelopmental delay, dysmorphic features, and structural brain abnormalities
Similar Researchers
Based on overlapping research topics
N Rowley
University of Arkansas for Medical Sciences
Genetics and Neurodevelopmental Disorders
Genomics and Phylogenetic Studies
Birth, Development, and Health
Elizabeth A. Sellars
University of Arkansas for Medical Sciences
Genetics and Neurodevelopmental Disorders
Genomics and Phylogenetic Studies
Birth, Development, and Health
Tess McCrary
University of Arkansas at Fayetteville
Genomics and Phylogenetic Studies
Birth, Development, and Health
P.A.L. Wight
University of Arkansas for Medical Sciences
Genetics and Neurodevelopmental Disorders
Birth, Development, and Health
Neurological disorders and treatments
Justin Vestal
Arkansas State University
Genomics and Phylogenetic Studies
Birth, Development, and Health
Luke Smith
Arkansas State University
Genomics and Phylogenetic Studies
Birth, Development, and Health