| 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 | 342 | 2013 |
| 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 | 180 | 2015 |
| 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 | 164 | 2011 |
| 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 | 67 | 2017 |
| 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 | 63 | 2010 |
| 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 | 60 | 2019 |
| 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 | 56 | 2013 |
| 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 | 52 | 2012 |
| Population structure, levels of selection, and the evolution of intracellular symbionts B O'Fallon Evolution 62 (2), 361-373, 2008 | 51 | 2008 |
| ACG: rapid inference of population history from recombining nucleotide sequences BD O'Fallon BMC bioinformatics 14, 1-9, 2013 | 23 | 2013 |
| 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 | 20 | 2010 |
| TreesimJ: a flexible, forward time population genetic simulator B O'Fallon Bioinformatics 26 (17), 2200-2201, 2010 | 19 | 2010 |
| 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 | 15 | 2007 |
| 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 | 12 | 2014 |
| Purifying selection causes widespread distortions of genealogical structure on the human X chromosome B O’Fallon Genetics 194 (2), 485-492, 2013 | 9 | 2013 |
| 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 | 8 | 2019 |
| 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 | 8 | 2013 |
| 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 | 5 | 2011 |
| Two optimal mutation rates in obligate pathogens subject to deleterious mutation B O’Fallon Journal of theoretical biology 276 (1), 150-158, 2011 | 5 | 2011 |
| Algorithmic improvements for discovery of germline copy number variants in next-generation sequencing data B O’Fallon, J Durtschi, A Kellogg, T Lewis, D Close, H Best BMC bioinformatics 23 (1), 285, 2022 | 4 | 2022 |
Stephen ProulxUCSBEmail verificata su lifesci.ucsb.edu