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Author

Robert Rigobello

Institution: Baylor Genetics
ORCID: 0009-0009-2505-9694
Observed ORCID: 0009-0009-2505-9694
OpenAlex ID: A5014456967
Distinct rates of VUS reclassification are observed when subclassifying VUS by evidence level
2025 · Gwendolyn Bennett, Izabela Karbassi, et al. · Genetics in Medicine · 33
Pharmacogenomic education among genetic counseling training programs in North America
2021 · Elizabeth Loudon, Stuart A. Scott, et al. · Journal of Genetic Counseling · 26
Clinical Pharmacogenetic Testing and the Posttest Counseling Conundrum
2020 · Robert Rigobello, Shahad Rahawi, et al. · Clinical Pharmacology & Therapeutics · 8
Clinical Pharmacogenomic MT‐RNR1 Screening for Aminoglycoside‐Induced Ototoxicity and the Post‐Test Counseling Conundrum
2023 · Robert Rigobello, Jay Shaw, et al. · Clinical Pharmacology & Therapeutics · 7
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Experiences from dual genome next-generation sequencing panel testing for mitochondrial disorders: a comprehensive molecular diagnosis
2025 · Elizabeth Gorman, Hongzheng Dai, et al. · Frontiers in Genetics · 5
CffDNA screening for Niemann–pick disease, type C1: a case series
2024 · Sydney A. Lau, Romy I. Fawaz, et al. · Frontiers in Medicine · 3
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A role for EHMT2 in a novel autosomal recessive neurodevelopmental syndrome? A case report
2026 · Dmitrijs Rots, Beatriz Cristina de Oliveira, et al. · Frontiers in Genetics · 2
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Targeted reflex RNA sequencing for enhanced variant classification on exome and genome sequencing improves patient outcomes
2026 · Xiaonan Zhao, Robert Rigobello, et al. · npj Genomic Medicine · 2
Genetic Counselor Drift: Exploring contributors to the recent growth of non-clinical genetic counseling positions and the resulting impact on the profession.
2017 · Maki Kaneko, Robert Rigobello · Digital Commons-Sarah Lawrence (Sarah Lawrence College) · 1
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Diagnostic yield of genome sequencing for children with intellectual disability and developmental delay
2026 · Robert Rigobello, Morgan Driver, et al. · Frontiers in Neurology
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Clinical significance of mRNA nonstop decay in rare disease diagnosis and recommendations for its application in variant classification
2026 · Yue Zhou, Dandan He, et al. · Research Square
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O46: Diagnostic yield of rapid genome sequencing in critically ill infants with cardiac indications
2026 · Xiaonan Zhao, Liesbeth Vossaert, et al. · Genetics in Medicine Open
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P581: The utility of genome sequencing as a diagnostic tool for children with ataxia
2026 · Xiaonan Zhao, Wilson CW Wu, et al. · Genetics in Medicine Open
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P710: Diagnostic utility of genome and transcriptome sequencing in identifying PIGL variants associated with atypical CHIME syndrome
2026 · Mumine Senturk, Yuan Liu, et al. · Genetics in Medicine Open
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P177: Prevalence of incidental findings in pharmacogenomic panel testing
2026 · Yue Wang, Yue Zhou, et al. · Genetics in Medicine Open
P696: Genome sequencing diagnoses atypical 7q11.23 region deletion in an adult patient
2026 · Madelyn Gillentine, Maruhen Datsch Silveira, et al. · Genetics in Medicine Open
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P561: Expanding the genotypic spectrum for ReNU syndrome: A clinical laboratory experience*
2026 · Eileen Barr, Morgan Driver, et al. · Genetics in Medicine Open
P564: Genome and exome sequencing reanalysis: Improvement to diagnostic yield and classification of variants over time*
2026 · Morgan Driver, Liesbeth Vossaert, et al. · Genetics in Medicine Open
P661: Uniparental disomy detection in a clinical trio genome sequencing cohort
2026 · Yuan Liu, Pengfei Liu, et al. · Genetics in Medicine Open
P501: Demographic and geographic considerations in pediatric genome sequencing: A diagnostic laboratory review
2026 · Chad Moretz, Robert Rigobello, et al. · Genetics in Medicine Open
P645: Reflex RNA sequencing for enhanced variant classification on ES/GS improves patient outcomes
2025 · Mei Ling Chong, Robert Rigobello, et al. · Genetics in Medicine Open
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P722: Low-level large deletions in mitochondria genomes: A potential diagnosis of mitochondrial diseases
2024 · Jun Yang, Tiansheng Chen, et al. · Genetics in Medicine Open
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Works count: 22
Citation count: 87
H-index: 5
I10-index: 2
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