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Chad VanSant Webb
Chad VanSant Webb
ARUP Laboratories
Genetics
Biology
Exome
Allelic Imbalance
Molecular biology
4
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605
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NF1 Somatic Mutation in Dystrophic Scoliosis
2019
Journal of Molecular Neuroscience
Rebecca L. Margraf
Chad VanSant Webb
Rong Mao
David H. Viskochil
John C. Carey
Heather Hanson
Jacques L. D’Astous
Allie H. Grossmann
David A. Stevenson
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Citations (5)
Genome sequencing reveals a deep intronic splicing ACVRL1 mutation hotspot in Hereditary Haemorrhagic Telangiectasia
2018
Journal of Medical Genetics
Whitney Wooderchak-Donahue
Jamie McDonald
Andrew Farrell
Gulsen Akay
Matt Velinder
Peter Johnson
Chad VanSant Webb
Rebecca L. Margraf
Eric Briggs
Kevin J. Whitehead
Jennifer Thomson
Angela E. Lin
Reed E. Pyeritz
Gabor T. Marth
Pinar Bayrak-Toydemir
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Citations (6)
Utilization of Whole-Exome Next-Generation Sequencing Variant Read Frequency for Detection of Lesion-Specific, Somatic Loss of Heterozygosity in a Neurofibromatosis Type 1 Cohort with Tibial Pseudarthrosis
2017
The Journal of Molecular Diagnostics
Rebecca L. Margraf
Chad VanSant Webb
David W. Sant
John C. Carey
Heather Hanson
Jacques D'Astous
D. Viskochil
David A. Stevenson
Rong Mao
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Citations (4)
Hereditary hemorrhagic telangiectasia: Genetics and molecular diagnostics in a new era
2015
Frontiers in Genetics
Jamie McDonald
Whitney Wooderchak-Donahue
Chad VanSant Webb
Kevin J. Whitehead
David A. Stevenson
Pinar Bayrak-Toydemir
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Citations (590)
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