Author

Taylor Warner

Observed name: Taylor C. Warner

Institutions: University of Iowa, University of Iowa Hospitals and Clinics, University of Iowa Stead Family Children’s Hospital

Observed institutions: University of Iowa, University of Iowa Hospitals and Clinics, University of Iowa Stead Family Children’s Hospital

OpenAlex ID: A5023608789

WDR26 Haploinsufficiency Causes a Recognizable Syndrome of Intellectual Disability, Seizures, Abnormal Gait, and Distinctive Facial Features

2017 · Cara M. Skraban, Constance F. Wells, et al. · The American Journal of Human Genetics · 95

Leveraging Next-Generation Phenotyping in Dysmorphology to Support Variant Interpretation in Mowat-Wilson Syndrome

2026 · Tzung-Chien Hsieh, Dylan Todd, et al. · Neurology Genetics · 1

P145: Paradigm shift in Occam’s Razor and the need for genotype driven reverse phenotyping in rare diseases with complex phenotypes*

2024 · Moon Ley Tung, Bharatendu Chandra, et al. · Genetics in Medicine Open · 1

A novel de novo intragenic duplication in FBN1 associated with early‐onset Marfan syndrome in a 16‐month‐old: A case report and review of the literature

2023 · Anthony Piscopo, Taylor Warner, et al. · American Journal of Medical Genetics Part A · 1

Brugada Syndrome: New Implications for Heterozygous Carriers of the Pathogenic SCN5A c. 689T >C(p. Ile230Thr ) Variant

2026 · Shayla Shojaat, Benjamin Hale, et al. · American Journal of Medical Genetics Part A

eP263: A pathogenic deletion at 13q32.1q33.1 presenting with bilateral sensorineural hearing loss and pigmentation anomalies, mimicking Waardenburg syndrome

2022 · Moon Ley Tung, Taylor Warner, et al. · Genetics in Medicine

eP262: De novo heterozygous variant in the RAB11B gene presenting with combined cardiac defect and neurodevelopmental disorder: A case report

2022 · Moon Ley Tung, Shelby Romoser, et al. · Genetics in Medicine

eP095: A family-based study of hereditary spastic paraplegia type 46 in two siblings due to a novel GBA2 variant

2022 · Bharatendu Chandra, Shelby Romoser, et al. · Genetics in Medicine

Works count: 8

Citation count: 98

H-index: 1

I10-index: 1