Match tier
Listed
Presence
Current · Arkansas
Last published
2021
Sources
OpenAlex · ORCID
Refreshed
2026-10-09
J
Jill Kelsay
Researchers
Also affiliated: University of Cincinnati (2005)
4 h-index
5 pubs
123 cited
Research Areas
Biomedical Subjects
Biography and Research Information
OverviewAI-generated summary
Jill Kelsay's research investigates the genetic underpinnings of neurodevelopmental conditions. 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 neurological disorders.
Metrics
- h-index: 4
- Publications: 5
- Citations: 123
Positions
-
Researchers publications 2010–2021University of Arkansas for Medical Sciences Institution web page
Selected Publications
-
De novo variants in H3-3A and H3-3B are associated with neurodevelopmental delay, dysmorphic features, and structural brain abnormalities (2021)
-
Phelan‐McDermid syndrome and cancer predisposition: The value of a karyotype (2017)
-
Low bone turnover and low bone density in a cohort of adults with Down syndrome (2012)
-
Male infertility associated with hereditary leiomyomatosis and renal cell carcinoma (2010)
Collaboration Network
Top Collaborators
Kent D. McKelvey
University of Arkansas Medical Center (US)
3 shared publications
- Low bone turnover and low bone density in a cohort of adults with Down syndrome
- Male infertility associated with hereditary leiomyomatosis and renal cell carcinoma
- Phelan‐McDermid syndrome and cancer predisposition: The value of a karyotype
Tristan W. Fowler
University of Arkansas for Medical Sciences (US)
1 shared publication
- Low bone turnover and low bone density in a cohort of adults with Down syndrome
Nisreen S. Akel
University of Arkansas for Medical Sciences
1 shared publication
In database
- Low bone turnover and low bone density in a cohort of adults with Down syndrome
Dana Gaddy
University of Arkansas for Medical Sciences (US)
1 shared publication
- Low bone turnover and low bone density in a cohort of adults with Down syndrome
Galen R. Wenger
University of Arkansas for Medical Sciences
1 shared publication
In database
- Low bone turnover and low bone density in a cohort of adults with Down syndrome
Larry J. Suva
University of Arkansas for Medical Sciences (US)
1 shared publication
- Low bone turnover and low bone density in a cohort of adults with Down syndrome
Seema Siraj
University of Arkansas for Medical Sciences (US)
1 shared publication
- Male infertility associated with hereditary leiomyomatosis and renal cell carcinoma
Francisco Batres
Arkansas Cardiology (US)
1 shared publication
- Male infertility associated with hereditary leiomyomatosis and renal cell carcinoma
Carol J. Trana
University of Arkansas Medical Center (US)
1 shared publication
- Phelan‐McDermid syndrome and cancer predisposition: The value of a karyotype
Jeffrey R. Sawyer
University of Arkansas for Medical Sciences (US)
1 shared publication
- Phelan‐McDermid syndrome and cancer predisposition: The value of a karyotype
Jeffrey L. Clothier
Psychiatric Medical Center
1 shared publication
In database
- Phelan‐McDermid syndrome and cancer predisposition: The value of a karyotype
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
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
Liesbeth Vossaert
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
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
Similar Researchers
Based on overlapping research topics
Aixa Gonzalez Garcia
University of Arkansas for Medical Sciences
Genomics and Rare Diseases
Metabolism and Genetic Disorders
Neurological disorders and treatments
Alexandrea F. Wadley
University of Arkansas for Medical Sciences
Genomics and Rare Diseases
Metabolism and Genetic Disorders
Neurological disorders and treatments
Vikki Stefans
University of Arkansas for Medical Sciences
Genomics and Rare Diseases
Metabolism and Genetic Disorders
Neurological disorders and treatments
Sandra T. Cooper
University of Arkansas for Medical Sciences
Genomics and Rare Diseases
Metabolism and Genetic Disorders
Disease Mechanisms Research
Elizabeth A. Sellars
University of Arkansas for Medical Sciences
Genomics and Rare Diseases
Metabolism and Genetic Disorders
Neurological disorders and treatments
Katie Bosanko
University of Arkansas for Medical Sciences
Metabolism and Genetic Disorders
Neurological disorders and treatments
Disease Mechanisms Research