| Comparison of multifrequency bioelectrical impedance analysis with dual-energy X-ray absorptiometry for assessment of percentage body fat in a large, healthy population G Sun, CR French, GR Martin, B Younghusband, RC Green, Y Xie, ... The American journal of clinical nutrition 81 (1), 74-78, 2005 | 528 | 2005 |
| 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 of FOXC1 and PITX2 induces cerebral small-vessel disease CR French, S Seshadri, AL Destefano, M Fornage, CR Arnold, PJ Gage, ... The Journal of clinical investigation 124 (11), 4877-4881, 2014 | 151 | 2014 |
| GDF6, a novel locus for a spectrum of ocular developmental anomalies M Asai-Coakwell, CR French, KM Berry, M Ye, R Koss, M Somerville, ... The American Journal of Human Genetics 80 (2), 306-315, 2007 | 130 | 2007 |
| Identification of additional risk loci for stroke and small vessel disease: a meta-analysis of genome-wide association studies G Chauhan, CR Arnold, AY Chu, M Fornage, A Reyahi, JC Bis, ... The Lancet Neurology 15 (7), 695-707, 2016 | 128 | 2016 |
| Incomplete penetrance and phenotypic variability characterize Gdf6-attributable oculo-skeletal phenotypes M Asai-Coakwell, CR French, M Ye, K Garcha, K Bigot, AG Perera, ... Human molecular genetics 18 (6), 1110-1121, 2009 | 115 | 2009 |
| Gdf6a is required for the initiation of dorsal–ventral retinal patterning and lens development CR French, T Erickson, DV French, DB Pilgrim, AJ Waskiewicz Developmental Biology 333 (1), 37-47, 2009 | 85 | 2009 |
| Contribution of growth differentiation factor 6-dependent cell survival to early-onset retinal dystrophies M Asai-Coakwell, L March, XH Dai, M DuVal, I Lopez, CR French, ... Human molecular genetics 22 (7), 1432-1442, 2013 | 76 | 2013 |
| Changes in the transcriptome of abdominal subcutaneous adipose tissue in response to short-term overfeeding in lean and obese men J Shea, CR French, J Bishop, G Martin, B Roebothan, D Pace, ... The American journal of clinical nutrition 89 (1), 407-415, 2009 | 58 | 2009 |
| Meis1 specifies positional information in the retina and tectum to organize the zebrafish visual system T Erickson, CR French, AJ Waskiewicz Neural Development 5, 1-22, 2010 | 57 | 2010 |
| Pbx homeodomain proteins pattern both the zebrafish retina and tectum CR French, T Erickson, D Callander, KM Berry, R Koss, DW Hagey, ... BMC developmental biology 7, 1-12, 2007 | 43 | 2007 |
| foxc1 is required for embryonic head vascular smooth muscle differentiation in zebrafish TR Whitesell, PW Chrystal, JR Ryu, N Munsie, A Grosse, CR French, ... Developmental biology 453 (1), 34-47, 2019 | 36 | 2019 |
| Apoptotic and proliferative defects characterize ocular development in a microphthalmic BMP model CR French, TR Stach, LD March, OJ Lehmann, AJ Waskiewicz Investigative ophthalmology & visual science 54 (7), 4636-4647, 2013 | 33 | 2013 |
| Aberrant forebrain signaling during early development underlies the generation of holoprosencephaly and coloboma PA Gongal, CR French, AJ Waskiewicz Biochimica et Biophysica Acta (BBA)-Molecular Basis of Disease 1812 (3), 390-401, 2011 | 30 | 2011 |
| Molecular mechanisms regulating ocular apoptosis in zebrafish gdf6a mutants SD Pant, LD March, JK Famulski, CR French, OJ Lehmann, ... Investigative ophthalmology & visual science 54 (8), 5871-5879, 2013 | 18 | 2013 |
| Loss of foxc1 in zebrafish reduces optic nerve size and cell number in the retinal ganglion cell layer J Umali, A Hawkey-Noble, CR French Vision Research 156, 66-72, 2019 | 16 | 2019 |
| Mechanistic Insights into Axenfeld–Rieger Syndrome from Zebrafish foxc1 and pitx2 Mutants CR French International Journal of Molecular Sciences 22 (18), 10001, 2021 | 13 | 2021 |
| A pathogenic deletion in Forkhead Box L1 (FOXL1) identifies the first otosclerosis (OTSC) gene N Abdelfatah, AA Mostafa, CR French, LP Doucette, C Penney, MB Lucas, ... Human Genetics, 1-15, 2022 | 10 | 2022 |
| Autosomal dominant non-syndromic hearing loss maps to DFNA33 (13q34) and co-segregates with splice and frameshift variants in ATP11A, a phospholipid … JA Pater, C Penney, DD O’Rielly, A Griffin, L Kamal, Z Brownstein, B Vona, ... Human Genetics 141 (3), 431-444, 2022 | 9 | 2022 |
| The Axenfeld–Rieger Syndrome Gene FOXC1 Contributes to Left–Right Patterning PW Chrystal, CR French, F Jean, S Havrylov, S van Baarle, AM Peturson, ... Genes 12 (2), 170, 2021 | 8 | 2021 |
