Emergence of wheat blast in Bangladesh was caused by a South American lineage of Magnaporthe oryzae MT Islam, D Croll, P Gladieux, DM Soanes, A Persoons, P Bhattacharjee, ... BMC biology 14, 1-11, 2016 | 496 | 2016 |
Association of mutations in the NALP3/CIAS1/PYPAF1 gene with a broad phenotype including recurrent fever, cold sensitivity, sensorineural deafness, and AA … E Aganna, F Martinon, PN Hawkins, JB Ross, DC Swan, DR Booth, ... Arthritis & Rheumatism 46 (9), 2445-2452, 2002 | 438 | 2002 |
A mutation in the 5′-UTR of IFITM5 creates an in-frame start codon and causes autosomal-dominant osteogenesis imperfecta type V with hyperplastic callus O Semler, L Garbes, K Keupp, D Swan, K Zimmermann, J Becker, S Iden, ... The American Journal of Human Genetics 91 (2), 349-357, 2012 | 315 | 2012 |
The Molecular Phenotype of Heparan Sulfate in theHs2st−/− Mutant Mouse CLR Merry, SL Bullock, DC Swan, AC Backen, M Lyon, RSP Beddington, ... Journal of Biological Chemistry 276 (38), 35429-35434, 2001 | 236 | 2001 |
A variation in the ghrelin gene increases weight and decreases insulin secretion in tall, obese children M Korbonits, M Gueorguiev, E O’Grady, C Lecoeur, DC Swan, CA Mein, ... The Journal of Clinical Endocrinology & Metabolism 87 (8), 4005-4008, 2002 | 227 | 2002 |
DNA methylation patterns in cord blood DNA and body size in childhood CL Relton, A Groom, B St. Pourcain, AE Sayers, DC Swan, ND Embleton, ... PloS one 7 (3), e31821, 2012 | 184 | 2012 |
The Genome of the Obligate Intracellular Parasite Trachipleistophora hominis: New Insights into Microsporidian Genome Dynamics and Reductive Evolution E Heinz, TA Williams, S Nakjang, CJ Noel, DC Swan, AV Goldberg, ... PLoS pathogens 8 (10), e1002979, 2012 | 172 | 2012 |
Improving and correcting the contiguity of long-read genome assemblies of three plant species using optical mapping and chromosome conformation capture data WB Jiao, GG Accinelli, B Hartwig, C Kiefer, D Baker, E Severing, ... Genome research 27 (5), 778-786, 2017 | 150 | 2017 |
Mutations in three genes encoding proteins involved in hair shaft formation cause uncombable hair syndrome FBÜ Basmanav, L Cau, A Tafazzoli, MC Méchin, S Wolf, MT Romano, ... The American Journal of Human Genetics 99 (6), 1292-1304, 2016 | 145 | 2016 |
Induction of the mammalian node requires Arkadia function in the extraembryonic lineages V Episkopou, R Arkell, PM Timmons, JJ Walsh, RL Andrew, D Swan Nature 410 (6830), 825-830, 2001 | 128 | 2001 |
BioStar: an online question & answer resource for the bioinformatics community LD Parnell, P Lindenbaum, K Shameer, GM Dall'Olio, DC Swan, ... PLoS computational biology 7 (10), e1002216, 2011 | 122 | 2011 |
What do natural antisense transcripts regulate? A Werner, M Carlile, D Swan RNA biology 6 (1), 43-48, 2009 | 104 | 2009 |
The supposed tumor suppressor gene WWOX is mutated in an early lethal microcephaly syndrome with epilepsy, growth retardation and retinal degeneration G Abdel-Salam, M Thoenes, HH Afifi, F Körber, D Swan, HJ Bolz Orphanet journal of rare diseases 9, 1-7, 2014 | 98 | 2014 |
Identification of the pathogenic pathways in osteoarthritic hip cartilage: commonality and discord between hip and knee OA Y Xu, MJ Barter, DC Swan, KS Rankin, AD Rowan, M Santibanez-Koref, ... Osteoarthritis and cartilage 20 (9), 1029-1038, 2012 | 97 | 2012 |
A CD4 T cell gene signature for early rheumatoid arthritis implicates interleukin 6-mediated STAT3 signalling, particularly in anti-citrullinated peptide antibody-negative disease AG Pratt, DC Swan, S Richardson, G Wilson, CMU Hilkens, DA Young, ... Annals of the rheumatic diseases 71 (8), 1374-1381, 2012 | 93 | 2012 |
Python for information theoretic analysis of neural data RAA Ince, RS Petersen, DC Swan, S Panzeri Frontiers in neuroinformatics 3, 385, 2009 | 84 | 2009 |
Selenium alters miRNA profile in an intestinal cell line: Evidence that miR‐185 regulates expression of GPX2 and SEPSH2 A Maciel‐Dominguez, D Swan, D Ford, J Hesketh Molecular nutrition & food research 57 (12), 2195-2205, 2013 | 70 | 2013 |
Postnatal Growth and DNA Methylation Are Associated With Differential Gene Expression of the TACSTD2 Gene and Childhood Fat Mass A Groom, C Potter, DC Swan, G Fatemifar, DM Evans, SM Ring, V Turcot, ... Diabetes 61 (2), 391-400, 2012 | 64 | 2012 |
Comparative gene expression profiling of human umbilical vein endothelial cells and ocular vascular endothelial cells AC Browning, EP Halligan, EA Stewart, DC Swan, R Dove, ... British journal of ophthalmology 96 (1), 128-132, 2012 | 54 | 2012 |
Autosomal dominant SCA5 and autosomal recessive infantile SCA are allelic conditions resulting from SPTBN2 mutations SM Elsayed, R Heller, M Thoenes, MS Zaki, D Swan, E Elsobky, C Zühlke, ... European Journal of Human Genetics 22 (2), 286-288, 2014 | 53 | 2014 |