Author

Hillary R. Raynes

Observed names: H. Raynes, Hillary Raynes, Raynes, Hillary, Raynes, Hillary R.

Institution: Icahn School of Medicine at Mount Sinai

Observed institutions: Albert Einstein College of Medicine, Mount Sinai Health System, Mount Sinai Hospital, Montefiore Medical Center, Yeshiva University, Seoul National University Hospital, Icahn School of Medicine at Mount Sinai

ORCID: 0000-0002-8522-5860

Observed ORCID: 0000-0002-8522-5860

OpenAlex ID: A5037229334

Exome sequencing of 20,979 individuals with epilepsy reveals shared and distinct ultra-rare genetic risk across disorder subtypes

2024 · Epi25 Collaborative, Siwei Chen, et al. · Nature Neuroscience · 68

Joubert Syndrome: Monozygotic Twins With Discordant Phenotypes

1999 · Hillary R. Raynes, Alan Shanske, et al. · Journal of Child Neurology · 38

Epilepsy surgery in patients with autism

2016 · Malgosia A. Kokoszka, Patricia E. McGoldrick, et al. · Journal of Neurosurgery Pediatrics · 26

Cyclosporine-induced neurotoxicity during treatment of Crohn's disease: lack of correlation with previously reported risk factors

2001 · Richard Rosencrantz, Aeri Moon, et al. · The American Journal of Gastroenterology · 26

Fatal cerebral infarct in a child with COVID-19

2020 · Shingo Kihira, Peter F. Morgenstern, et al. · Pediatric Radiology · 22

Diagnosis and Supportive Management of Fucosidosis: A Case Report

2019 · Arpanjeet Kaur, Arshdeep S Dhaliwal, et al. · Cureus · 12

Case report: A novel biallelic FTO variant causing multisystem anomalies with severe epilepsy, widening the spectrum of FTO syndrome

2023 · Naomi Mayman, Jiangbo Wei, et al. · SAGE Open Medical Case Reports · 3

Cardiac transplant outcomes in a pediatric patient with novel homozygous variants in TOP3Α causing mitochondrial dysfunction

2025 · J. Ganesh, C. Donnelly, et al. · Molecular Genetics and Metabolism · 1

Homozygosity for a Clinically Significant GALC Haplotype Associated with Late-Infantile Krabbe Disease Detected on Newborn Screening: Implications for Clinical Management and Genetic Counseling

2026 · Daniel R. Schecter, Colleen Donnelly, et al. · International Journal of Neonatal Screening

Exome sequencing of 20,979 individuals with epilepsy reveals shared and distinct ultra-rare genetic risk across disorder subtypes

2024 · Epi25 Collaborative, Chen, Siwei, et al. · RWTH Publications (RWTH Aachen)

ODP310 Early Onset Adrenal Dysfunction in Infants with Adrenoleukodystrophy

2022 · Sruti Patel, Hillary Raynes, et al. · Journal of the Endocrine Society

Increased Intracranial Pressure As The Presentation Of Evans Syndrome In A 4-Year-Old Boy

2022 · Lauren Herschbein, Hillary Raynes, et al.

Joubert Syndrome: Monozygotic Twins with Discordant Phenotype

1999 · Hillary Raynes, Alan L Shanske, et al. · Pediatric Research

Works count: 16

Citation count: 196

H-index: 6

I10-index: 6