C. Maubaret

Association of telomere length with type 2 diabetes, oxidative stress and UCP2 gene variation

Klelia D. Salpea, Philippa J. Talmud, Jackie A. Cooper et al. · Atherosclerosis · 2009 · 281 citations · Full text

Metabolic Syndrome, Genetic Determinant, Genetics +6

A common allele in RPGRIP1L is a modifier of retinal degeneration in ciliopathies

Hemant Khanna, Erica E. Davis, Carlos Murga‐Zamalloa et al. · Nature Genetics · 2009 · 267 citations · Full text

Ocular Disease, Common Allele, Retina +7

Health and aging in elderly farmers: the AMI cohort

Karine Pérès, Fanny Matharan, Michèle Allard et al. · BMC Public Health · 2012 · 83 citations · Full text

Mutations in TOPORS Cause Autosomal Dominant Retinitis Pigmentosa with Perivascular Retinal Pigment Epithelium Atrophy

Christina Chakarova, Myrto Papaioannou, Hemant Khanna et al. · The American Journal of Human Genetics · 2007 · 79 citations · Full text

Ocular Disease, Retina, Ophthalmology +7

Loss of lysophosphatidylcholine acyltransferase 1 leads to photoreceptor degeneration in <i>rd11</i> mice

James S. Friedman, Bo Chang, Daniel S. Krauth et al. · Proceedings of the National Academy of Sciences · 2010 · 64 citations · Full text

Ocular Disease, Lysosomal Storage Disease, Genetics +32