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Development and translational imaging of a TP53 porcine tumorigenesis model JC Sieren, DK Meyerholz, XJ Wang, BT Davis, JD Newell, E Hammond, ... The Journal of clinical investigation 124 (9), 4052-4066, 2014 | 106 | 2014 |
Disruption of the non-canonical Wnt gene PRICKLE2 leads to autism-like behaviors with evidence for hippocampal synaptic dysfunction LP Sowers, L Loo, Y Wu, E Campbell, JD Ulrich, S Wu, L Paemka, ... Molecular psychiatry 18 (10), 1077-1089, 2013 | 103 | 2013 |
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The heritability of hemolysis in stored human red blood cells TJ Van't Erve, BA Wagner, SM Martin, CM Knudson, R Blendowski, ... Transfusion 55 (6), 1178-1185, 2015 | 79 | 2015 |
A gene implicated in activation of retinoic acid receptor targets is a novel renal agenesis gene in humans PD Brophy, M Rasmussen, M Parida, G Bonde, BW Darbro, X Hong, ... Genetics 207 (1), 215-228, 2017 | 78 | 2017 |
Recessive coding and regulatory mutations in FBLIM1 underlie the pathogenesis of chronic recurrent multifocal osteomyelitis (CRMO) AJ Cox, BW Darbro, RM Laxer, G Velez, X Bing, AL Finer, A Erives, ... PloS one 12 (3), e0169687, 2017 | 74 | 2017 |
A missense mutation in the MLKL brace region promotes lethal neonatal inflammation and hematopoietic dysfunction JM Hildebrand, M Kauppi, IJ Majewski, Z Liu, AJ Cox, S Miyake, EJ Petrie, ... Nature communications 11 (1), 3150, 2020 | 71 | 2020 |
Lactobacillus delbrueckii as the Cause of Urinary Tract Infection BW Darbro, BK Petroelje, GV Doern Journal of clinical microbiology 47 (1), 275-277, 2009 | 66 | 2009 |
Heritability of glutathione and related metabolites in stored red blood cells TJ van‘t Erve, CM Doskey, BA Wagner, JR Hess, BW Darbro, ... Free Radical Biology and Medicine 76, 107-113, 2014 | 64 | 2014 |
Mutations of the sonic hedgehog pathway underlie hypothalamic hamartoma with gelastic epilepsy MS Hildebrand, NG Griffin, JA Damiano, EJ Cops, R Burgess, E Ozturk, ... The American Journal of Human Genetics 99 (2), 423-429, 2016 | 63 | 2016 |
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PRICKLE1 interaction with SYNAPSIN I reveals a role in autism spectrum disorders L Paemka, VB Mahajan, JM Skeie, LP Sowers, SN Ehaideb, ... PloS one 8 (12), e80737, 2013 | 49 | 2013 |
Mutations in Extracellular Matrix Genes NID1 and LAMC1 Cause Autosomal Dominant Dandy–Walker Malformation and Occipital Cephaloceles BW Darbro, VB Mahajan, L Gakhar, JM Skeie, E Campbell, S Wu, X Bing, ... Human mutation 34 (8), 1075-1079, 2013 | 48 | 2013 |
A porcine model of neurofibromatosis type 1 that mimics the human disease KA White, VJ Swier, JT Cain, JL Kohlmeyer, DK Meyerholz, MR Tanas, ... JCI insight 3 (12), 2018 | 47 | 2018 |
Co-regulation of p16INK4A and migratory genes in culture conditions that lead to premature senescence in human keratinocytes BW Darbro, GB Schneider, AJ Klingelhutz Journal of investigative dermatology 125 (3), 499-509, 2005 | 46 | 2005 |
Gene expression signatures identify novel therapeutics for metastatic pancreatic neuroendocrine tumors AT Scott, M Weitz, PJ Breheny, PH Ear, B Darbro, BJ Brown, TA Braun, ... Clinical cancer research 26 (8), 2011-2021, 2020 | 44 | 2020 |
Autism linked to increased oncogene mutations but decreased cancer rate BW Darbro, R Singh, MB Zimmerman, VB Mahajan, AG Bassuk PLoS One 11 (3), e0149041, 2016 | 43 | 2016 |