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Brendan O'Fallon
Brendan O'Fallon
Verified email at aruplab.com
Title
Cited by
Cited by
Year
BMP9 mutations cause a vascular-anomaly syndrome with phenotypic overlap with hereditary hemorrhagic telangiectasia
WL Wooderchak-Donahue, J McDonald, B O’Fallon, PD Upton, W Li, ...
The American Journal of Human Genetics 93 (3), 530-537, 2013
3262013
The genomic and phenotypic diversity of Schizosaccharomyces pombe
DC Jeffares, C Rallis, A Rieux, D Speed, M Převorovský, T Mourier, ...
Nature genetics 47 (3), 235-241, 2015
1722015
Native Americans experienced a strong population bottleneck coincident with European contact
BD O'Fallon, L Fehren-Schmitz
Proceedings of the National Academy of Sciences 108 (51), 20444-20448, 2011
1612011
A continuous-state coalescent and the impact of weak selection on the structure of gene genealogies
BD O'Fallon, J Seger, FR Adler
Molecular biology and evolution 27 (5), 1162-1172, 2010
592010
Vascular anomalies caused by abnormal signaling within endothelial cells: targets for novel therapies
HL Nguyen, LM Boon, M Vikkula
Seminars in interventional radiology 34 (03), 233-238, 2017
582017
Phenotype of CM-AVM2 caused by variants in EPHB4: how much overlap with hereditary hemorrhagic telangiectasia (HHT)?
WL Wooderchak-Donahue, G Akay, K Whitehead, E Briggs, ...
Genetics in Medicine 21 (9), 2007-2014, 2019
532019
A support vector machine for identification of single-nucleotide polymorphisms from next-generation sequencing data
BD O’Fallon, W Wooderchak-Donahue, DK Crockett
Bioinformatics 29 (11), 1361-1366, 2013
522013
A direct comparison of next generation sequencing enrichment methods using an aortopathy gene panel-clinical diagnostics perspective
WL Wooderchak-Donahue, B O’Fallon, LV Furtado, JD Durtschi, P Plant, ...
BMC medical genomics 5, 1-10, 2012
512012
Population structure, levels of selection, and the evolution of intracellular symbionts
B O'Fallon
Evolution 62 (2), 361-373, 2008
472008
ACG: rapid inference of population history from recombining nucleotide sequences
BD O'Fallon
BMC bioinformatics 14, 1-9, 2013
212013
A method to correct for the effects of purifying selection on genealogical inference
BD O'Fallon
Molecular biology and evolution 27 (10), 2406-2416, 2010
192010
TreesimJ: a flexible, forward time population genetic simulator
B O'Fallon
Bioinformatics 26 (17), 2200-2201, 2010
192010
Quasi-species evolution in subdivided populations favours maximally deleterious mutations
BD O'Fallon, FR Adler, SR Proulx
Proceedings of the Royal Society B: Biological Sciences 274 (1629), 3159-3164, 2007
152007
Variant Tool Chest: an improved tool to analyze and manipulate variant call format (VCF) files
MTW Ebbert, ME Wadsworth, KL Boehme, KL Hoyt, AR Sharp, ...
BMC bioinformatics 15, 1-5, 2014
112014
Purifying selection causes widespread distortions of genealogical structure on the human X chromosome
B O’Fallon
Genetics 194 (2), 485-492, 2013
92013
VarRanker: rapid prioritization of sequence variations associated with human disease
BD O'Fallon, W Wooderchak-Donahue, P Bayrak-Toydemir, D Crockett
BMC bioinformatics 14, 1-8, 2013
82013
Topically applied etamsylate: a new orphan drug for HHT-derived epistaxis (antiangiogenesis through FGF pathway inhibition)
V Albiñana, G Giménez-Gallego, A García-Mato, P Palacios, ...
TH Open 3 (03), e230-e243, 2019
62019
Two optimal mutation rates in obligate pathogens subject to deleterious mutation
B O’Fallon
Journal of theoretical biology 276 (1), 150-158, 2011
52011
A method for accurate inference of population size from serially sampled genealogies distorted by selection
BD O'Fallon
Molecular biology and evolution 28 (11), 3171-3181, 2011
42011
Stochasticity, complex spatial structure, and the feasibility of the shifting balance theory
B O'Fallon, FR Adler
Evolution 60 (3), 448-459, 2006
42006
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