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C. Maubaret · SciRah

Researcher profile · Semantic Scholar

C. Maubaret

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C. Maubaret — researcher profile on SciRah

h-index: 18
Works: 43
Citations: 1,607

Most-cited papers

Association of telomere length with type 2 diabetes, oxidative stress and UCP2 gene variation
K. Salpea, P. Talmud, J. Cooper, C. Maubaret +3 more
2009Atherosclerosis293 citations Open access
Semantic Scholar
A common allele in RPGRIP1L is a modifier of retinal degeneration in ciliopathies
H. Khanna, E. Davis, C. Murga-Zamalloa, A. Estrada +30 more
2009Nature Genetics290 citations Open access
Semantic Scholar
Genome-wide analysis of multiethnic cohorts identifies new loci influencing intraocular pressure and susceptibility to glaucoma
P. Hysi, Ching-Yu Cheng, Henriët Springelkamp, Stuart MacGregor +87 more
2014Nature Genetics235 citations Open access
Semantic Scholar
Health and aging in elderly farmers: the AMI cohort
K. Pérès, F. Matharan, M. Allard, H. Amieva +15 more
2012BMC Public Health92 citations Open access
Semantic Scholar
Mutations in TOPORS cause autosomal dominant retinitis pigmentosa with perivascular retinal pigment epithelium atrophy.
C. Chakarova, M. Papaioannou, H. Khanna, I. Lopez +22 more
2007American Journal of Human Genetics85 citations Open access
Semantic Scholar
Loss of lysophosphatidylcholine acyltransferase 1 leads to photoreceptor degeneration in rd11 mice
J. Friedman, B. Chang, D. S. Krauth, I. Lopez +18 more
2010Proceedings of the National Academy of Sciences of the United States of America64 citations Open access
Semantic Scholar
Study of gene-targeted mouse models of splicing factor gene Prpf31 implicated in human autosomal dominant retinitis pigmentosa (RP).
K. Bujakowska, C. Maubaret, C. Chakarova, N. Tanimoto +13 more
2009Investigative Ophthalmology and Visual Science62 citations
Semantic Scholar
Genome-Wide Association Study Identifies Variants in Casein Kinase II (CSNK2A2) to be Associated With Leukocyte Telomere Length in a Punjabi Sikh Diabetic Cohort
R. Saxena, A. Bjonnes, J. Prescott, P. Dib +28 more
2014Circulation: Cardiovascular Genetics54 citations Open access
Semantic Scholar
Autosomal dominant retinitis pigmentosa with intrafamilial variability and incomplete penetrance in two families carrying mutations in PRPF8.
C. Maubaret, V. Vaclavik, R. Mukhopadhyay, N. Waseem +5 more
2011Investigative Ophthalmology and Visual Science50 citations
Semantic Scholar
Association of TERC and OBFC1 Haplotypes with Mean Leukocyte Telomere Length and Risk for Coronary Heart Disease
C. Maubaret, K. Salpea, C. Romanoski, L. Folkersen +11 more
2013PLoS ONE49 citations Open access
Semantic Scholar
Telomeres are shorter in myocardial infarction patients compared to healthy subjects: correlation with environmental risk factors
C. Maubaret, K. Salpea, Anjly Jain, J. Cooper +6 more
2010Journal of molecular medicine47 citations Open access
Semantic Scholar
The Val158Met COMT polymorphism is a modifier of the age at onset in Parkinson's disease with a sexual dimorphism
S. Klebe, J. Golmard, M. Nalls, M. Saad +29 more
2013Journal of Neurology Neurosurgery & Psychiatry45 citations Open access
Semantic Scholar
Association of HDL-Related Loci with Age-Related Macular Degeneration and Plasma Lutein and Zeaxanthin: the Alienor Study
B. Merle, C. Maubaret, J. Korobelnik, M. Delyfer +8 more
2013PLoS ONE43 citations Open access
Semantic Scholar
Prognosis for splicing factor PRPF8 retinitis pigmentosa, novel mutations and correlation between human and yeast phenotypes
Katherine V. Towns, A. Kipioti, V. Long, M. Mckibbin +16 more
2010Human Mutation42 citations Open access
Semantic Scholar
Genome-wide analysis of multi-ancestry cohorts identifies new loci influencing intraocular pressure and susceptibility to glaucoma
P. Hysi, Ching-Yu Cheng, Henriët Springelkamp, Stuart MacGregor +70 more
201432 citations
Semantic Scholar
The Effect of Pro-Inflammatory Conditioning and/or High Glucose on Telomere Shortening of Aging Fibroblasts
K. Salpea, C. Maubaret, Annegret Kathagen, Gie Ken-Dror +2 more
2013PLoS ONE21 citations Open access
Semantic Scholar
Identification of Preferentially Expressed mRNAs in Retina and Cochlea
C. Maubaret, C. Delettre, S. Solá, C. Hamel
2002DNA and Cell Biology20 citations
Semantic Scholar
Novel Mutations in MYO7A and USH2A in Usher Syndrome
C. Maubaret, J. Griffoin, B. Arnaud, C. Hamel
2005Ophthalmic Genetics19 citations
Semantic Scholar
Becoming a nonagenarian: Factors associated with survival up to 90 years old in 70+ men and women. Results from the paquid longitudinal cohort
A. Edjolo, Catherine Helmer, Pascale Barberger-Gateau, J. Dartigues +2 more
2013The Journal of Nutrition, Health & Aging17 citations Open access
Semantic Scholar
Plasma estrogen levels, estrogen receptor gene variation, and ischemic arterial disease in postmenopausal women: the three-city prospective cohort study.
V. Scarabin-Carré, S. Brailly‐Tabard, M. Ancelin, C. Maubaret +3 more
2014Journal of Clinical Endocrinology and Metabolism16 citations
Semantic Scholar
[Genetics of retinitis pigmentosa: metabolic classification and phenotype/genotype correlations].
C. Maubaret, C. Hamel
2005Journal Francais d'Ophtalmologie16 citations
Semantic Scholar
Mitochondrial uncoupling proteins regulate angiotensin‐converting enzyme expression: crosstalk between cellular and endocrine metabolic regulators suggested by RNA interference and genetic studies
Sukhbir S. Dhamrait, C. Maubaret, U. Pedersen-Bjergaard, David J. Brull +6 more
2016Bioessays7 citations Open access
Semantic Scholar
Mitochondrial uncoupling proteins regulate angiotensin‐converting enzyme expression: crosstalk between cellular and endocrine metabolic regulators suggested by RNA interference and genetic studies
S. Dhamrait, C. Maubaret, U. Pedersen-Bjergaard, D. Brull +6 more
2015Inside the Cell6 citations Open access
Semantic Scholar
Functional characterization of a novel c.614-622del rhodopsin mutation in a French pedigree with retinitis pigmentosa
C. Maubaret, M. Kosmaoglou, S. Low, C. Chakarova +6 more
2012Molecular Vision3 citations
Semantic Scholar
DOWN-REGULATION OF ACE EXPRESSION IN HUVECS USING siRNA RESULTS IN DOWN-REGULATION OF UCP2 EXPRESSION: A POTENTIAL MECHANISM OF THE CLINICAL BENEFIT OF ACE-INHIBITORS?
C. Maubaret, R. Heads, S. Dhamrait, H. Montgomery +1 more
20091 citations
Semantic Scholar
Specific learning phenomena in pitch discrimination tasks
L. Demany, C. Semal, C. Maubaret, Odon Noblia
20001 citations
Semantic Scholar
Peer Review #1 of "The leukocyte telomere length, single nucleotide polymorphisms near TERC gene and risk of COPD (v0.1)"
T. Tacheva, S. Zienolddiny, D. Dimov, D. Vlaykova +458 more
20210 citations Open access
Semantic Scholar
Mutations in TOPORS Cause Autosomal Dominant Retinitis Pigmentosa with Perivascular RPE Atrophy
C. Chakarova, M. Papaioannou, H. Khanna, I. Lopez +23 more
20180 citations
Semantic Scholar
The Val 158 Met COMT polymorphism is a modifier of the age at onset in Parkinson ' s disease with a sexual dimorphism KLEBE
S. Klebe, Jean-Louis Golmard, M. Nalls, M. Saad +29 more
20170 citations
Semantic Scholar
LIPC and LPL polymorphisms, age-related macular degeneration and plasma lutein and zeaxanthin: the Alienor Study
B. Merle, C. Maubaret, J. Korobelnik, M. Delyfer +6 more
20130 citations
Semantic Scholar
MS443 THE ARG399GLN VARIANT IN THE DNA REPAIR ENZYME XRCC1 IS ASSOCIATED WITH INCREASED GENETIC INSTABILITY IN PATIENTS WITH ATHEROSCLEROSIS
C. Federici, Ka-Wah Li, K. Salpea, C. Maubaret +2 more
20100 citations
Semantic Scholar
W56 TELOMERES ARE SHORTER IN PATIENTS WITH POLYGENIC AND MONOGENIC FORMS OF CORONARY HEART DISEASE
C. Maubaret, K. Salpea, A. Jain, J. Cooper +6 more
20100 citations
Semantic Scholar
THE COMMON FUNCTIONAL ARG399GLN VARIANT IN THE DNA REPAIR ENZYME XRCC1 IS ASSOCIATED WITH ELEVATED LEVELS OF MICRONUCLEUS CHROMOSOMAL DNA DAMAGE AND SHORTER TELOMERE LENGTH IN PATIENT WITH ATHEROSCLEROSIS
C. Federici, S. Manfredi, M. Del Fiandra, K. Salpea +3 more
20090 citations
Semantic Scholar
Abstract: P794 TELOMERES ARE SHORTER IN MI AND CABG PATIENTS COMPARED TO HEALTHY SUBJECTS; CORRELATION WITH ENVIRONMENTAL AND GENETIC RISK FACTORS
C. Maubaret, K. Salpea, J. Cooper, J. Sanders +2 more
20090 citations
Semantic Scholar
TELOMERES ARE SHORTER IN MYOCARDIAL INFARCTION PATIENTS COMPARED TO HEALTHY SUBJECTS; CORRELATION WITH ENVIRONMENTAL AND GENETIC RISK FACTORS
C. Maubaret, K. Salpea, A. Jain, J. Cooper +4 more
20090 citations
Semantic Scholar
TELOMERES ARE SHORTER IN MI AND CABG PATIENTS COMPARED TO HEALTHY SUBJECTS; CORRELATION WITH ENVIRONMENTAL AND GENETIC RISK FACTORS
C. Maubaret, K. Salpea, J. Cooper, J. Sanders +2 more
20090 citations
Semantic Scholar
Prpf31 Knock-In Mouse as a Model of Retinitis Pigmentosa 11
K. Bujakowska, C. Maubaret, N. Tanimoto, Susanne C. Beck +6 more
20080 citations
Semantic Scholar
Investigation and Characterization of PRPF31 Interacting Proteins in Retina
F. Fiocco, C. Maubaret, R. Roepman, F. Cremers +2 more
20080 citations
Semantic Scholar
A Novel Mutation in Exon 39 of PRPF8 Causes Autosomal Dominant Retinitis Pigmentosa (adRP) With Incomplete Penetrance
V. Vaclavik, C. Maubaret, N. Waseem, A. Churchill +2 more
20080 citations
Semantic Scholar
Identification of Mutations in IMPDH1 in a Cohort of 96 Recessive RP Patients
N. Waseem, A. Ortiz, C. Maubaret, A. Kennan +6 more
20060 citations
Semantic Scholar
New loci for autosomal recessive retinitis pigmentosa and macular degeneration
C. Maubaret, A. Sénéchal, G. Humbert, B. Arnaud +4 more
20040 citations
Semantic Scholar
MYOSINE 3A: Genomic Structure, Tissue Expression and Mutation Search in Usher Syndrome
C. Hamel, N. Renard, M. Surget, A. Dosé +4 more
20030 citations
Semantic Scholar
Linkage Analysis in Two French Autosomal Dominant Retinitis Pigmentosa Pedigrees: Exclusion of Known Loci
C. Maubaret, M. Surget, D. Hillaire, C. Hamel
20030 citations
Semantic Scholar

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