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Holly Corbitt

Observed name: Corbitt, Holly
ORCID: 0000-0002-9247-6131
Observed ORCID: 0000-0002-9247-6131
OpenAlex ID: A5065581376
TIMP3 and TIMP1 are risk genes for bicuspid aortic valve and aortopathy in Turner syndrome
2018 · Holly Corbitt, Shaine A. Morris, et al. · PLoS Genetics · 88
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The genetic basis of Turner syndrome aortopathy
2019 · Holly Corbitt, Jacob Gutierrez, et al. · American Journal of Medical Genetics Part C Seminars in Medical Genetics · 37
Identifying genetic factors that contribute to the increased risk of congenital heart defects in infants with Down syndrome
2020 · Cristina E. Trevino, Aaron M. Holleman, et al. · Scientific Reports · 23
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Allometric considerations when assessing aortic aneurysms in Turner syndrome: Implications for activity recommendations and medical decision‐making
2017 · Holly Corbitt, Cheryl Maslen, et al. · American Journal of Medical Genetics Part A · 14
Closing the gap: Solving complex medically relevant genes at scale
2024 · Medhat Mahmoud, John Harting, et al. · medRxiv · 12
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Sensitive detection of somatic mutations in GC-rich cancer gene promoters
2026 · Meifang Qi, Preshita Sanjay Dave, et al. · NAR Cancer
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Abstract 6009: An end-to-end workflow for improved methylation detection
2023 · Lydia Bonar, Kristin Butcher, et al. · Cancer Research
P478: Simultaneous analysis of 50+ different repeat expansions with twist target enrichment and PacBio HiFi sequencing
2023 · Tina Han, Holly Corbitt, et al. · Genetics in Medicine Open
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Author Correction: Identifying genetic factors that contribute to the increased risk of congenital heart defects in infants with Down syndrome (Scientific Reports, (2020), 10, 1, (18051), 10.1038/s41598-020-74650-4)
2021 · Cristina E. Trevino, Aaron M. Holleman, et al. · Newcastle University ePrints (Newcastle Univesity)
Author Correction: Identifying genetic factors that contribute to the increased risk of congenital heart defects in infants with Down syndrome
2021 · Cristina E. Trevino, Aaron M. Holleman, et al. · Scientific Reports
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Abstract 12066: TIMP3 and CHADL Mutations Are Common in Turner Syndrome Aortopathy
2016 · Michael Silberbach, Holly Corbitt, et al. · Circulation
Works count: 12
Citation count: 174
H-index: 5
I10-index: 5
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