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C. Templin · SciRah

Researcher profile · Semantic Scholar

C. Templin

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C. Templin — researcher profile on SciRah

h-index: 8
Works: 17
Citations: 268

Most-cited papers

Are p.I148T, p.R74W and p.D1270N cystic fibrosis causing mutations ?
M. Claustres, J. Altieri, C. Guittard, C. Templin +2 more
2004BMC Medical Genetics60 citations Open access
Semantic Scholar
Large genomic rearrangements in the CFTR gene contribute to CBAVD
M. Taulan, A. Girardet, C. Guittard, J. Altieri +4 more
2007BMC Medical Genetics53 citations Open access
Semantic Scholar
Comprehensive and rapid genotyping of mutations and haplotypes in congenital bilateral absence of the vas deferens and other cystic fibrosis transmembrane conductance regulator-related disorders.
C. Bareil, C. Guittard, J. Altieri, C. Templin +2 more
2007Journal of Molecular Diagnostics35 citations Open access
Semantic Scholar
High heterogeneity of CFTR mutations and unexpected low incidence of cystic fibrosis in the Mediterranean France.
M. Des Georges, C. Guittard, J. Altieri, C. Templin +3 more
2004Journal of Cystic Fibrosis29 citations Open access
Semantic Scholar
Variants in CFTR untranslated regions are associated with congenital bilateral absence of the vas deferens
E. Lopez, V. Viart, C. Guittard, C. Templin +6 more
2010Journal of Medical Genetics28 citations
Semantic Scholar
Cystic fibrosis transmembrane conductance regulator mutation spectrum in patients with cystic fibrosis in Tunisia.
S. Fredj, T. Messaoud, C. Templin, M. Des Georges +2 more
2009Genetic Testing and Molecular Biomarkers25 citations
Semantic Scholar
WGA allows the molecular characterization of a novel large CFTR rearrangement in a black South African cystic fibrosis patient.
M. Des Georges, C. Guittard, C. Templin, J. Altieri +3 more
2008Journal of Molecular Diagnostics13 citations Open access
Semantic Scholar
Identification of a novel duplication CFTRdup2 and functional impact of large rearrangements identified in the CFTR gene.
M. Taulan, V. Viart, C. Thèze, C. Guittard +5 more
2012Gene10 citations
Semantic Scholar
Negative genetic neonatal screening for cystic fibrosis caused by compound heterozygosity for two large CFTR rearrangements.
A. Girardet, C. Guittard, J. Altieri, C. Templin +4 more
2007Clinical Genetics8 citations Open access
Semantic Scholar
Negative genetic neonatal screening for cystic fibrosis caused by compound heterozygosity for two large CFTR rearrangements
A. Girardet, C. Guittard, J. Altieri, C. Templin +4 more
20076 citations
Semantic Scholar
Preimplantation genetic diagnosis for cystic fibrosis
C. Fernandez, C. Guittard, M. D. Georges, J. Altieri +3 more
20091 citations Open access
Semantic Scholar
WS8.7 Preimplantation genetic diagnosis for cystic fibrosis using multiplex fluorescent PCR
A. Girardet, C. Templin, F. Saguet, S. Plaza +3 more
20120 citations Open access
Semantic Scholar
Search for population-specific CFTR mutations: How to avoid the identification of unclassified variants
J. Altieri, C. Templin, C. Guittard, M. Claustres +1 more
20090 citations Open access
Semantic Scholar
3* Spectrum of CFTR mutations in a group of black patients from South Africa: Identification of a novel large rearrangement
M. D. Georges, M. Ramsay, C. Guittard, J. Altieri +4 more
20070 citations Open access
Semantic Scholar
12 Rapid and reliable analysis of the CFTR locus in CBAVD patients
M. D. Georges, C. Guittard, J. Altieri, C. Templin +2 more
20060 citations Open access
Semantic Scholar
Molecular epidemiology of DFNB1 deafness in France
A. Roux, N. Pallares-Ruiz, A. Vielle, V. Faugère +8 more
2004BMC Medical Genetics0 citations Open access
Semantic Scholar
Molecular epidemiology of deafness in France reclassifies mutations as common polymorphisms in the GJB 2 gene
A. Roux, N. Pallares-Ruiz, A. Vielle, V. Faugère +8 more
20030 citations
Semantic Scholar

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