| Math5 defines the ganglion cell competence state in a subpopulation of retinal progenitor cells exiting the cell cycle JA Brzezinski IV, L Prasov, T Glaser Developmental biology 365 (2), 395-413, 2012 | 141 | 2012 |
| Nanophthalmos: a review of the clinical spectrum and genetics PC Carricondo, T Andrade, L Prasov, BM Ayres, SE Moroi Journal of ophthalmology 2018 (1), 2735465, 2018 | 92 | 2018 |
| ATOH7 mutations cause autosomal recessive persistent hyperplasia of the primary vitreous L Prasov, T Masud, S Khaliq, SQ Mehdi, A Abid, ER Oliver, ED Silva, ... Human molecular genetics 21 (16), 3681-3694, 2012 | 79 | 2012 |
| Variants in myelin regulatory factor (MYRF) cause autosomal dominant and syndromic nanophthalmos in humans and retinal degeneration in mice SJ Garnai, ML Brinkmeier, B Emery, TS Aleman, LC Pyle, B Veleva-Rotse, ... PLoS genetics 15 (5), e1008130, 2019 | 55 | 2019 |
| The repeat-in-toxin family member TosA mediates adherence of uropathogenic Escherichia coli and survival during bacteremia PD Vigil, TJ Wiles, MD Engstrom, L Prasov, MA Mulvey, HLT Mobley Infection and immunity 80 (2), 493-505, 2012 | 54 | 2012 |
| Pushing the envelope of retinal ganglion cell genesis: context dependent function of Math5 (Atoh7) L Prasov, T Glaser Developmental biology 368 (2), 214-230, 2012 | 47 | 2012 |
| Math5 (Atoh7) gene dosage limits retinal ganglion cell genesis L Prasov, M Nagy, DD Rudolph, T Glaser Neuroreport 23 (10), 631-634, 2012 | 37 | 2012 |
| Dynamic expression of ganglion cell markers in retinal progenitors during the terminal cell cycle L Prasov, T Glaser Molecular and Cellular Neuroscience 50 (2), 160-168, 2012 | 32 | 2012 |
| DDX58 (RIG-I)-related disease is associated with tissue-specific interferon pathway activation L Prasov, BL Bohnsack, AS El Husny, LC Tsoi, B Guan, JM Kahlenberg, ... Journal of medical genetics 59 (3), 294-304, 2022 | 20 | 2022 |
| Novel TMEM98, MFRP, PRSS56 variants in a large United States high hyperopia and nanophthalmos cohort L Prasov, B Guan, E Ullah, SM Archer, BM Ayres, CG Besirli, ... Scientific reports 10 (1), 19986, 2020 | 19 | 2020 |
| A critical analysis of Atoh7 (Math5) mRNA splicing in the developing mouse retina L Prasov, NL Brown, T Glaser PloS one 5 (8), e12315, 2010 | 19 | 2010 |
| Functional specificity of artificial transcriptional activators CY Majmudar, JK Lum, L Prasov, AK Mapp Chemistry & biology 12 (3), 313-321, 2005 | 19 | 2005 |
| Phenotypic Variation in a Four‐Generation Family with Aniridia Carrying a Novel PAX6 Mutation GM Wang, L Prasov, H Al-Hasani, CER Marrs, S Tolia, ... Journal of Ophthalmology 2018 (1), 5978293, 2018 | 17 | 2018 |
| Glaucoma syndromes: insights into glaucoma genetics and pathogenesis from monogenic syndromic disorders DA Balikov, A Jacobson, L Prasov Genes 12 (9), 1403, 2021 | 16 | 2021 |
| Expanding the genotypic spectrum of Jalili syndrome: Novel CNNM4 variants and uniparental isodisomy in a north American patient cohort L Prasov, E Ullah, AE Turriff, BM Warner, J Conley, PR Mark, RB Hufnagel, ... American Journal of Medical Genetics Part A 182 (3), 493-497, 2020 | 9 | 2020 |
| Clinical features of optic disc drusen in an ophthalmic genetics cohort JY Serpen, L Prasov, WM Zein, CA Cukras, D Cunningham, EC Murphy, ... Journal of Ophthalmology 2020 (1), 5082706, 2020 | 7 | 2020 |
| Novel ophthalmic findings and deep phenotyping in Williams-Beuren syndrome LA Huryn, T Flaherty, R Nolen, L Prasov, WM Zein, CA Cukras, S Osgood, ... British Journal of Ophthalmology 107 (10), 1554-1559, 2023 | 5 | 2023 |
| MYRF-Related Cardiac Urogenital Syndrome JD Kaplan, B Stewart, L Prasov, LC Pyle | 5 | 2022 |
| Nanophthalmos: a review of the clinical spectrum and genetics. J Ophthalmol. 2018; 2018: 2735465 PC Carricondo, T Andrade, L Prasov, BM Ayres, SE Moroi | 4 | |
| Design and Outcomes of a Novel Multidisciplinary Ophthalmic Genetics Clinic B Parekh, A Beil, B Blevins, A Jacobson, P Williams, JW Innis, ... Genes 14 (3), 726, 2023 | 3 | 2023 |
Robert B HufnagelInvestigator, National Eye Institute (NEI/NIH)在 nih.gov 的电子邮件经过验证
