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Curtis R. French

Observed names: C. R. French, Curtis French, Curtis R French, Curtis R. French (17215444), French, Curtis R, French, Curtis Robert
ORCID: 0000-0001-8135-0309
Observed ORCID: 0000-0001-8135-0309
OpenAlex ID: A5003960852
Comparison of multifrequency bioelectrical impedance analysis with dual-energy X-ray absorptiometry for assessment of percentage body fat in a large, healthy population
2005 · Guang Sun, Curtis R French, et al. · American Journal of Clinical Nutrition · 377
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Identification of additional risk loci for stroke and small vessel disease: a meta-analysis of genome-wide association studies
2016 · Ganesh Chauhan, Corey R Arnold, et al. · The Lancet Neurology · 172
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Mutation of the bone morphogenetic protein GDF3 causes ocular and skeletal anomalies
2009 · M. Ye, K. M. Berry-Wynne, et al. · Human Molecular Genetics · 156
Mutation of FOXC1 and PITX2 induces cerebral small-vessel disease
2014 · Curtis R. French, Sudha Seshadri, et al. · Journal of Clinical Investigation · 147
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GDF6, a Novel Locus for a Spectrum of Ocular Developmental Anomalies
2007 · Mika Asai-Coakwell, Curtis R. French, et al. · The American Journal of Human Genetics · 111
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Incomplete penetrance and phenotypic variability characterize Gdf6-attributable oculo-skeletal phenotypes
2009 · Mika Asai-Coakwell, Curtis R. French, et al. · Human Molecular Genetics · 104
Gdf6a is required for the initiation of dorsal–ventral retinal patterning and lens development
2009 · Curtis R. French, Timothy Erickson, et al. · Developmental Biology · 79
foxc1 is required for embryonic head vascular smooth muscle differentiation in zebrafish
2019 · Thomas R. Whitesell, Paul W. Chrystal, et al. · Developmental Biology · 67
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Contribution of growth differentiation factor 6-dependent cell survival to early-onset retinal dystrophies
2013 · Mika Asai-Coakwell, Lindsey March, et al. · Human Molecular Genetics · 65
Changes in the transcriptome of abdominal subcutaneous adipose tissue in response to short-term overfeeding in lean and obese men
2008 · Jennifer Shea, Curtis R French, et al. · American Journal of Clinical Nutrition · 52
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Genetic and lifestyle risk factors for MRI-defined brain infarcts in a population-based setting
2019 · Ganesh Chauhan, Hieab H.H. Adams, et al. · Neurology · 47
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Meis1 specifies positional information in the retina and tectum to organize the zebrafish visual system
2010 · Timothy Erickson, Curtis R French, et al. · Neural Development · 46
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Pbx homeodomain proteins pattern both the zebrafish retina and tectum
2007 · Curtis R French, Timothy Erickson, et al. · BMC Developmental Biology · 38
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Aberrant forebrain signaling during early development underlies the generation of holoprosencephaly and coloboma
2010 · Patricia A. Gongal, Curtis R. French, et al. · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease · 30
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Apoptotic and Proliferative Defects Characterize Ocular Development in a Microphthalmic BMP Model
2013 · Curtis R. French, Tara R. Stach, et al. · Investigative Ophthalmology & Visual Science · 27
Autosomal dominant non-syndromic hearing loss maps to DFNA33 (13q34) and co-segregates with splice and frameshift variants in ATP11A, a phospholipid flippase gene
2022 · Justin A. Pater, Cindy Penney, et al. · Human Genetics · 26
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Loss of foxc1 in zebrafish reduces optic nerve size and cell number in the retinal ganglion cell layer
2019 · Jurgienne Umali, Alexia Hawkey-Noble, et al. · Vision Research · 22
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Mechanistic Insights into Axenfeld–Rieger Syndrome from Zebrafish foxc1 and pitx2 Mutants
2021 · Curtis R. French · International Journal of Molecular Sciences · 21
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A pathogenic deletion in Forkhead Box L1 (FOXL1) identifies the first otosclerosis (OTSC) gene
2021 · Nelly Abdelfatah, Ahmed A. Mostafa, et al. · Human Genetics · 15
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Molecular Mechanisms Regulating Ocular Apoptosis in Zebrafish gdf6a Mutants
2013 · Sameer D. Pant, Lindsey D. March, et al. · Investigative Ophthalmology & Visual Science · 13
Phytocannabinoids Reduce Seizures in Larval Zebrafish and Affect Endocannabinoid Gene Expression
2023 · Roshni Kollipara, Evan Langille, et al. · Biomolecules · 12
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Mutation of foxl1 Results in Reduced Cartilage Markers in a Zebrafish Model of Otosclerosis
2022 · Alexia Hawkey-Noble, Justin A. Pater, et al. · Genes · 11
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The Axenfeld–Rieger Syndrome Gene FOXC1 Contributes to Left–Right Patterning
2021 · Paul W. Chrystal, Curtis R. French, et al. · Genes · 8
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Genetic Diseases of Fucosylation: Insights from Model Organisms
2025 · Muhammad T. Ameen, Curtis R. French · Genes · 7
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Protein fucosylation is required for Notch dependent vascular integrity in zebrafish
2021 · Gerissa Fowler, Danielle V. French, et al. · Developmental Biology · 7
Works count: 53
Citation count: 1,680
H-index: 18
I10-index: 22
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