Author

Regan Klatt

Observed names: R. Klatt, Regan EM Klatt, Regan Elizabeth Marie Klatt

Institutions: University of Toronto, Hospital for Sick Children

Observed institutions: University of Toronto, Hospital for Sick Children, University of Cincinnati

OpenAlex ID: A5032950082

Improved diagnostic yield compared with targeted gene sequencing panels suggests a role for whole-genome sequencing as a first-tier genetic test

2017 · Anath C. Lionel, Gregory Costain, et al. · Genetics in Medicine · 557

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Genotype–phenotype analysis of the branchio‐oculo‐facial syndrome

2010 · Jeff M. Milunsky, Tom M. Maher, et al. · American Journal of Medical Genetics Part A · 67

Molecular diagnosis of 22q11.2 deletion and duplication by multiplex ligation dependent probe amplification

2007 · Andrea C. Stachon, Berivan Baskin, et al. · American Journal of Medical Genetics Part A · 55

Disease Rarity, Carrier Status, and Gender: A Triple Disadvantage for Women with Fabry Disease

2008 · Andrea L. Gibas, Regan Klatt, et al. · Journal of Genetic Counseling · 39

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A Survey of the Pain Experienced by Males and Females with Fabry Disease

2006 · Andrea L Gibas, Regan Klatt, et al. · Pain Research and Management · 28

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A deletion of FGFR2 creating a chimeric IIIb/IIIc exon in a child with Apert syndrome

2011 · Aimee L Fenwick, Sarah C Bowdin, et al. · BMC Medical Genetics · 23

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Expanding the clinical spectrum of ocular anomalies in Noonan syndrome: Axenfeld‐anomaly in a child with PTPN11 mutation

2014 · Andrea Guerin, Joyce So, et al. · American Journal of Medical Genetics Part A · 9

Molecular breakpoint mapping of 6q11‐q14 interstitial deletions in seven patients

2009 · Jia‐Chi Wang, Linda Dang, et al. · American Journal of Medical Genetics Part A · 8

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Insights into the effects of subretinal voretigene neparvovec-rzyl in RPE65-associated Leber congenital amaurosis

2025 · Alaa Tayyib, Deepika C. Parameswarappa, et al. · Canadian Journal of Ophthalmology · 4

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Middle and inner ear malformations in mutation‐proven branchio‐oculo‐facial (BOF) syndrome: Case series and review of the literature

2012 · Melissa T. Carter, Susan Blaser, et al. · American Journal of Medical Genetics Part A · 4

Vacuolated lymphocytes: a diagnostic biomarker for CLN3-related Batten disease

2025 · Miguel Cruz-Pimentel, Deepika C. Parameswarappa, et al. · Canadian Journal of Ophthalmology · 1

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Rod bipolar cell dysfunction in POLG retinopathy

2020 · Kit Green Sanderson, Eoghan Millar, et al. · Documenta Ophthalmologica · 1

Biallelic Pathogenic Variants in PYGM Impair Retinal Glycogenolysis Causing a Range of Phenotypes

2026 · Rowaida Hussein, Alaa Tayyib, et al. · Investigative Ophthalmology & Visual Science

Genetic Spectrum of Negative Electroretinograms in a Predominantly Pediatric Cohort of 177 Patients

2025 · Kirill Zaslavsky, Anupreet Tumber, et al. · Investigative Ophthalmology & Visual Science

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Genotype Correlations With Pulmonary Arteriovenous Malformations

2010 · Deena Godfrey, Vikram Prabhudesai, et al.

Neuropathic pain: human

2004 · A. Gibas, R. Klatt, et al. · Journal of Pain

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Hyperactivity and Inattention in Children With Isolated Cleft Lip and Palate or Isolated Cleft Palate

2002 · Regan Elizabeth Marie Klatt · OhioLink ETD Center (Ohio Library and Information Network)

Works count: 17

Citation count: 796

H-index: 8

I10-index: 6