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Brendan O’Fallon

ARUP Laboratories

19

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473

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Phenotype of CM-AVM2 caused by variants in EPHB4: how much overlap with hereditary hemorrhagic telangiectasia (HHT)?

2019 Genetics in Medicine
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Algorithmic improvements for discovery of germline copy number variants in next-generation sequencing data

2018 bioRxiv
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TreesimJ: a flexible, forward time population genetic simulator

2016 Bioinformatics
- Brendan O’Fallon
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Reporting of Clinical Genomics Test Results

2015
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Variant Tool Chest: an improved tool to analyze and manipulate variant call format (VCF) files

2014 BMC Bioinformatics
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BMP9 Mutations Cause a Vascular-Anomaly Syndrome with Phenotypic Overlap with Hereditary Hemorrhagic Telangiectasia

2013 American Journal of Human Genetics
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VarRanker: rapid prioritization of sequence variations associated with human disease

2013 BMC Bioinformatics
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ACG: rapid inference of population history from recombining nucleotide sequences

2013 BMC Bioinformatics
- Brendan O’Fallon
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A support vector machine for identification of single-nucleotide polymorphisms from next-generation sequencing data

2013 Bioinformatics
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Purifying Selection Causes Widespread Distortions of Genealogical Structure on the Human X Chromosome

2013 Genetics
- Brendan O’Fallon
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Citations (6)