| A method for constructing radiation hybrid maps of whole genomes MA Walter, DJ Spillett, P Thomas, J Weissenbach, PN Goodfellow Nature genetics 7 (1), 22-28, 1994 | 481 | 1994 |
| The forkhead/winged helix gene Mf1 is disrupted in the pleiotropic mouse mutation congenital hydrocephalus T Kume, KY Deng, V Winfrey, DB Gould, MA Walter, BLM Hogan Cell 93 (6), 985-996, 1998 | 427 | 1998 |
| Mutations of the forkhead/winged-helix gene, FKHL7, in patients with Axenfeld-Rieger anomaly AJ Mears, T Jordan, F Mirzayans, S Dubois, T Kume, M Parlee, R Ritch, ... The American Journal of Human Genetics 63 (5), 1316-1328, 1998 | 389 | 1998 |
| FOXC1 is a potential prognostic biomarker with functional significance in basal-like breast cancer PS Ray, J Wang, Y Qu, MS Sim, J Shamonki, SP Bagaria, X Ye, B Liu, ... Cancer research 70 (10), 3870-3876, 2010 | 271 | 2010 |
| Roles for the winged helix transcription factors MF1 and MFH1 in cardiovascular development revealed by nonallelic noncomplementation of null alleles GE Winnier, T Kume, K Deng, R Rogers, J Bundy, C Raines, MA Walter, ... Developmental biology 213 (2), 418-431, 1999 | 206 | 1999 |
| Molecular genetics of Axenfeld–Rieger malformations MA Lines, K Kozlowski, MA Walter Human molecular genetics 11 (10), 1177-1187, 2002 | 202 | 2002 |
| Genotype-phenotype correlations in Axenfeld-Rieger malformation and glaucoma patients with FOXC1 and PITX2 mutations MH Strungaru, I Dinu, MA Walter Investigative ophthalmology & visual science 48 (1), 228-237, 2007 | 188 | 2007 |
| Functional interactions between FOXC1 and PITX2 underlie the sensitivity to FOXC1 gene dose in Axenfeld–Rieger syndrome and anterior segment dysgenesis FB Berry, MA Lines, JM Oas, T Footz, DA Underhill, PJ Gage, MA Walter Human molecular genetics 15 (6), 905-919, 2006 | 170 | 2006 |
| Mutation of the bone morphogenetic protein GDF3 causes ocular and skeletal anomalies M Ye, KM Berry-Wynne, M Asai-Coakwell, P Sundaresan, T Footz, ... Human molecular genetics 19 (2), 287-298, 2010 | 168 | 2010 |
| Mutation in the RIEG1 Gene in Patients with Iridogoniodysgenesis Syndrome SC Kulak, K Kozlowski, EV Semina, WG Pearce, MA Walter Human Molecular Genetics 7 (7), 1113-1117, 1998 | 162 | 1998 |
| Variation in residual PITX2 activity underlies the phenotypic spectrum of anterior segment developmental disorders K Kozlowski, MA Walter Human molecular genetics 9 (14), 2131-2139, 2000 | 159 | 2000 |
| SOX genes: architects of development HM Prior, MA Walter Molecular medicine 2, 405-412, 1996 | 154 | 1996 |
| Axenfeld-Rieger syndrome resulting from mutation of the FKHL7 gene on chromosome 6p25 F Mirzayans, DB Gould, E Heon, GD Billingsley, JC Cheung, AJ Mears, ... European Journal of Human Genetics 8 (1), 71-74, 2000 | 150 | 2000 |
| Complete physical map of the human immunoglobulin heavy chain constant region gene complex. MH Hofker, MA Walter, DW Cox Proceedings of the National Academy of Sciences 86 (14), 5567-5571, 1989 | 140 | 1989 |
| Analyses of the effects that disease-causing missense mutations have on the structure and function of the winged-helix protein FOXC1 RA Saleem, S Banerjee-Basu, FB Berry, AD Baxevanis, MA Walter The American Journal of Human Genetics 68 (3), 627-641, 2001 | 139 | 2001 |
| Phenotypic heterogeneity of CYP1B1: mutations in a patient with Peters' anomaly A Vincent, G Billingsley, M Priston, D Williams-Lyn, J Sutherland, T Glaser, ... Journal of medical genetics 38 (5), 324-326, 2001 | 137 | 2001 |
| The interactions of genes, age, and environment in glaucoma pathogenesis LP Doucette, A Rasnitsyn, M Seifi, MA Walter Survey of ophthalmology 60 (4), 310-326, 2015 | 135 | 2015 |
| FOXC1 transcriptional regulation is mediated by N-and C-terminal activation domains and contains a phosphorylated transcriptional inhibitory domain FB Berry, RA Saleem, MA Walter Journal of Biological Chemistry 277 (12), 10292-10297, 2002 | 131 | 2002 |
| FOXC1 is required for cell viability and resistance to oxidative stress in the eye through the transcriptional regulation of FOXO1A FB Berry, JM Skarie, F Mirzayans, Y Fortin, TJ Hudson, V Raymond, ... Human molecular genetics 17 (4), 490-505, 2008 | 126 | 2008 |
| Genomics and anterior segment dysgenesis: a review YA Ito, MA Walter Clinical & experimental ophthalmology 42 (1), 13-24, 2014 | 123 | 2014 |
