| Frequent mutation of BAP1 in metastasizing uveal melanomas JW Harbour, MD Onken, EDO Roberson, S Duan, L Cao, LA Worley, ... Science 330 (6009), 1410-1413, 2010 | 1549 | 2010 |
| Early-onset lymphoproliferation and autoimmunity caused by germline STAT3 gain-of-function mutations JD Milner, TP Vogel, L Forbes, CA Ma, A Stray-Pedersen, JE Niemela, ... Blood, The Journal of the American Society of Hematology 125 (4), 591-599, 2015 | 561 | 2015 |
| Recurrent mutations at codon 625 of the splicing factor SF3B1 in uveal melanoma JW Harbour, EDO Roberson, H Anbunathan, MD Onken, LA Worley, ... Nature genetics 45 (2), 133-135, 2013 | 537 | 2013 |
| PSORS2 is due to mutations in CARD14 CT Jordan, L Cao, EDO Roberson, KC Pierson, CF Yang, CE Joyce, ... The American Journal of Human Genetics 90 (5), 784-795, 2012 | 476 | 2012 |
| Rare and common variants in CARD14, encoding an epidermal regulator of NF-kappaB, in psoriasis CT Jordan, L Cao, EDO Roberson, S Duan, CA Helms, RP Nair, KC Duffin, ... The American Journal of Human Genetics 90 (5), 796-808, 2012 | 395 | 2012 |
| Psoriasis genetics: breaking the barrier EDO Roberson, AM Bowcock Trends in Genetics 26 (9), 415-423, 2010 | 326 | 2010 |
| Retinal ganglion cells downregulate gene expression and lose their axons within the optic nerve head in a mouse glaucoma model I Soto, E Oglesby, BP Buckingham, JL Son, EDO Roberson, MR Steele, ... Journal of Neuroscience 28 (2), 548-561, 2008 | 305 | 2008 |
| Mutations in the gene PRRT2 cause paroxysmal kinesigenic dyskinesia with infantile convulsions. HY Lee, Y Huang, N Bruneau, P Roll, ED Roberson, M Hermann, E Quinn, ... | 295 | 2012 |
| A subset of methylated CpG sites differentiate psoriatic from normal skin EDO Roberson, Y Liu, C Ryan, CE Joyce, S Duan, L Cao, A Martin, ... Journal of investigative dermatology 132 (3), 583-592, 2012 | 174 | 2012 |
| Inference of relationships in population data using identity-by-descent and identity-by-state EL Stevens, G Heckenberg, EDO Roberson, JD Baugher, TJ Downey, ... PLoS genetics 7 (9), e1002287, 2011 | 119 | 2011 |
| A mucosal imprint left by prior Escherichia coli bladder infection sensitizes to recurrent disease VP O'brien, TJ Hannan, L Yu, J Livny, E Roberson, DJ Schwartz, S Souza, ... Nature microbiology 2 (1), 1-10, 2016 | 95 | 2016 |
| Rare variants in the functional domains of complement factor H are associated with age-related macular degeneration MP Triebwasser, EDO Roberson, Y Yu, EC Schramm, EK Wagner, ... Investigative ophthalmology & visual science 56 (11), 6873-6878, 2015 | 71 | 2015 |
| Dynamic immunoglobulin responses to gut bacteria during inflammatory bowel disease S Rengarajan, EE Vivio, M Parkes, DA Peterson, EDO Roberson, ... Gut Microbes 11 (3), 405-420, 2020 | 61 | 2020 |
| Genomic analysis of partial 21q monosomies with variable phenotypes E Roberson, ES Wohler, JE Hoover-Fong, E Lisi, EL Stevens, GH Thomas, ... European Journal of Human Genetics 19 (2), 235-238, 2011 | 59 | 2011 |
| Visualization of shared genomic regions and meiotic recombination in high-density SNP data EDO Roberson, J Pevsner PloS one 4 (8), e6711, 2009 | 53 | 2009 |
| Visualization of uniparental inheritance, Mendelian inconsistencies, deletions, and parent of origin effects in single nucleotide polymorphism trio data with SNPtrio JC Ting, EDO Roberson, ND Miller, A Lysholm‐Bernacchi, DA Stephan, ... Human mutation 28 (12), 1225-1235, 2007 | 50 | 2007 |
| Mucosal infection rewires TNFɑ signaling dynamics to skew susceptibility to recurrence L Yu, VP O'Brien, J Livny, D Dorsey, N Bandyopadhyay, M Colonna, ... Elife 8, e46677, 2019 | 31 | 2019 |
| Protective low-frequency variants for preeclampsia in the Fms related tyrosine kinase 1 gene in the Finnish population AI Lokki, E Daly, M Triebwasser, MI Kurki, EDO Roberson, P Häppölä, ... Hypertension 70 (2), 365-371, 2017 | 31 | 2017 |
| STING gain-of-function disrupts lymph node organogenesis and innate lymphoid cell development in mice BG Bennion, CA Croft, TL Ai, W Qian, AM Menos, CA Miner, ML Frémond, ... Cell reports 31 (11), 2020 | 23 | 2020 |
| Nicastrin haploinsufficiency alters expression of type I interferon‐stimulated genes: the relationship to familial hidradenitis suppurativa L Cao, DJ Morales‐Heil, EDO Roberson Clinical and experimental dermatology 44 (4), e118-e125, 2019 | 22 | 2019 |
Hima AnbunathanStanford UniversityVerified email at stanford.edu
