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 |
Precision medicine: personalized proteomics for the diagnosis and treatment of idiopathic inflammatory disease G Velez, CN Roybal, D Colgan, SH Tsang, AG Bassuk, VB Mahajan JAMA ophthalmology 134 (4), 444-448, 2016 | 74 | 2016 |
Paracrine WNT5A signaling inhibits expansion of tumor-initiating cells N Borcherding, D Kusner, R Kolb, Q Xie, W Li, F Yuan, G Velez, ... Cancer research 75 (10), 1972-1982, 2015 | 70 | 2015 |
BESTROPHIN1 mutations cause defective chloride conductance in patient stem cell-derived RPE Y Moshfegh, G Velez, Y Li, AG Bassuk, VB Mahajan, SH Tsang Human molecular genetics 25 (13), 2672-2680, 2016 | 55 | 2016 |
Extracellular superoxide dismutase (SOD3) regulates oxidative stress at the vitreoretinal interface KJ Wert, G Velez, MR Cross, BA Wagner, ML Teoh-Fitzgerald, ... Free Radical Biology and Medicine 124, 408-419, 2018 | 50 | 2018 |
Ocular hypertension after intravitreal dexamethasone (ozurdex) sustained-release implant EK Chin, DRP Almeida, G Velez, K Xu, M Peraire, M Corbella, ... Retina 37 (7), 1345-1351, 2017 | 50 | 2017 |
Personalized proteomics in proliferative vitreoretinopathy implicate hematopoietic cell recruitment and mTOR as a therapeutic target CN Roybal, G Velez, MA Toral, SH Tsang, AG Bassuk, VB Mahajan American journal of ophthalmology 186, 152-163, 2018 | 48 | 2018 |
Proteomic analysis of the human retina reveals region-specific susceptibilities to metabolic-and oxidative stress-related diseases G Velez, DA Machlab, PH Tang, Y Sun, SH Tsang, AG Bassuk, ... PLoS One 13 (2), e0193250, 2018 | 45 | 2018 |
Personalized proteomics for precision health: identifying biomarkers of vitreoretinal disease G Velez, PH Tang, T Cabral, GY Cho, DA Machlab, SH Tsang, AG Bassuk, ... Translational vision science & technology 7 (5), 12-12, 2018 | 44 | 2018 |
Metabolite therapy guided by liquid biopsy proteomics delays retinal neurodegeneration KJ Wert, G Velez, VL Kanchustambham, V Shankar, LP Evans, ... EBioMedicine 52, 2020 | 42 | 2020 |
Gene Therapy Restores Mfrp and Corrects Axial Eye Length G Velez, SH Tsang, YT Tsai, CW Hsu, A Gore, AH Abdelhakim, ... Scientific Reports 7 (1), 16151, 2017 | 41 | 2017 |
Calpain-5 expression in the retina localizes to photoreceptor synapses KA Schaefer, MA Toral, G Velez, AJ Cox, SA Baker, NC Borcherding, ... Investigative ophthalmology & visual science 57 (6), 2509-2521, 2016 | 36 | 2016 |
Gain-of-function mutations in a member of the Src family kinases cause autoinflammatory bone disease in mice and humans K Abe, A Cox, N Takamatsu, G Velez, RM Laxer, SML Tse, VB Mahajan, ... Proceedings of the National Academy of Sciences 116 (24), 11872-11877, 2019 | 35 | 2019 |
Therapeutic drug repositioning using personalized proteomics of liquid biopsies G Velez, AG Bassuk, D Colgan, SH Tsang, VB Mahajan JCI insight 2 (24), 2017 | 34 | 2017 |
Liquid biopsy proteomics of uveal melanoma reveals biomarkers associated with metastatic risk G Velez, HV Nguyen, T Chemudupati, CA Ludwig, M Toral, S Reddy, ... Molecular Cancer 20, 1-5, 2021 | 29 | 2021 |
Role for Krüppel-like transcription factor 11 in mesenchymal cell function and fibrosis A Mathison, A Grzenda, G Lomberk, G Velez, N Buttar, P Tietz, ... PloS one 8 (9), e75311, 2013 | 27 | 2013 |
Structure-based phylogeny identifies avoralstat as a TMPRSS2 inhibitor that prevents SARS-CoV-2 infection in mice YJ Sun, G Velez, DE Parsons, K Li, ME Ortiz, S Sharma, PB McCray, ... The Journal of clinical investigation 131 (10), 2021 | 26 | 2021 |
A novel de novo CAPN5 mutation in a patient with inflammatory vitreoretinopathy, hearing loss, and developmental delay G Velez, AG Bassuk, KA Schaefer, B Brooks, L Gakhar, MA Mahajan, ... Molecular Case Studies 4 (3), a002519, 2018 | 26 | 2018 |
Evidence supporting the existence of a NUPR1-like family of helix-loop-helix chromatin proteins related to, yet distinct from, AT hook-containing HMG proteins R Urrutia, G Velez, M Lin, G Lomberk, JL Neira, J Iovanna Journal of molecular modeling 20, 1-20, 2014 | 24 | 2014 |
Structural modeling of a novel SLC38A8 mutation that causes foveal hypoplasia MA Toral, G Velez, K Boudreault, KA Schaefer, Y Xu, N Saffra, AG Bassuk, ... Molecular genetics & genomic medicine 5 (3), 202-209, 2017 | 23 | 2017 |