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Jennifer L. Stallworth

Behavioral profiles in Rett syndrome: Data from the natural history study
2018 · Caroline B. Buchanan, Jennifer L. Stallworth, et al. · Brain and Development · 66
Genetic variants in the KDM6B gene are associated with neurodevelopmental delays and dysmorphic features
2019 · Elliot S. Stolerman, Elizabeth Francisco, et al. · American Journal of Medical Genetics Part A · 51
Neurobiologically-based treatments in Rett syndrome: opportunities and challenges
2016 · Walter E. Kaufmann, Jennifer L. Stallworth, et al. · Expert Opinion on Orphan Drugs · 50
Hand stereotypies
2019 · Jennifer L. Stallworth, Marisela E. Dy, et al. · Neurology · 46
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Certain heterozygous variants in the kinase domain of the serine/threonine kinase NEK8 can cause an autosomal dominant form of polycystic kidney disease
2023 · Laura R. Claus, Chuan Chen, et al. · Kidney International · 43
Anxiety-like behavior and anxiolytic treatment in the Rett syndrome natural history study
2022 · Caroline B. Buchanan, Jennifer L. Stallworth, et al. · Journal of Neurodevelopmental Disorders · 40
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Vitamin K Deficiency Embryopathy from Hyperemesis Gravidarum
2015 · Andrew S. Lane, Jennifer L. Stallworth, et al. · Case Reports in Obstetrics and Gynecology · 16
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Descriptive analysis of seizures and comorbidities associated with fragile X syndrome
2022 · Igor Albizua, Krista Charen, et al. · Molecular Genetics & Genomic Medicine · 10
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Mosaicism of common pathogenic MECP2 variants identified in two males with a clinical diagnosis of Rett syndrome
2022 · Jessica A. Cooley Coleman, Timothy Fee, et al. · American Journal of Medical Genetics Part A · 6
Abstracts of the 53rd ESPN Annual Meeting, Amsterdam, The Netherlands, September 2021
2021 · Claus, Laura R., Stallworth, Jennifer, et al. · Pediatric Nephrology · 3
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FC044: Heterozygous Variants in Kinase Domain of NEK8 cause an Autosomal-Dominant Ciliopathy
2022 · Laura Claus, Jennifer Stallworth, et al. · Nephrology Dialysis Transplantation · 2
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RNA analysis of the GALNS transcript reveals novel pathogenic mechanisms associated with Morquio syndrome A
2022 · Young Bae Sohn, Curtis Rogers, et al. · Molecular Genetics and Metabolism Reports · 1
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Heterozygous Variants in NEK8 Kinase Domain Cause an Autosomal-Dominant Ciliopathy
2021 · Laura R. Claus, Jennifer Stallworth, et al. · Journal of the American Society of Nephrology
Works count: 14
Citation count: 334
H-index: 8
I10-index: 8
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