T. Bienvenu

1.4k citations

29 papers · 1.0k indexed · h-index 12

Impact in

Genetics top 5%
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
Cell Biology top 10%
- Cellular transport and secretion

Papers in

Genetics 6
- Genetics and Neurodevelopmental Disorders 7
- Congenital Ear and Nasal Anomalies 3
- Hemoglobinopathies and Related Disorders 2
Pulmonary and Respiratory Medicine 11
- Cystic Fibrosis Research Advances 10
- Neonatal Respiratory Health Research 7

Co-authors: Jamel Chelly P. Kamoun Annick Ankri B. Chadefaux Chérif Beldjord Philippe Couvert Patrizia D’Adamo Daniela Toniolo
Journals: European Journal of Human Genetics (2 papers)Journal of Cystic Fibrosis (2 papers)Human Mutation (2 papers)Nature Genetics (1 paper)Human Molecular Genetics (1 paper)
Partner nations: France United States Netherlands

In The Last Decade

T. Bienvenu

29 papers receiving 1.0k citations

Peers

Countries citing papers authored by T. Bienvenu

Since Specialization

Citations

This map shows the geographic impact of T. Bienvenu's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by T. Bienvenu with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites T. Bienvenu more than expected).

Fields of papers citing papers by T. Bienvenu

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by T. Bienvenu. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by T. Bienvenu. The network helps show where T. Bienvenu may publish in the future.

Co-authors

The 25 scholars most cited alongside T. Bienvenu, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with T. Bienvenu Line = papers co-authored together T. Bienvenu links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	P019 Variants in the CFTR gene: a predisposition factor to aquagenic palmoplantar keratoderma Journal of Cystic Fibrosis ·E. Girodon, Caroline Raynal, M.‐P. Audrézet, F. Cabet, A. Pagin, M Reboul, Fabienne Dufernez, Patricia Fergelot, Anne Bergougnoux, Pascale Fanen, Claude Férec, T. Bienvenu	2019	1
2	Aquagenic Palmoplantar Keratoderma as a CFTR-related Disorder Acta Dermato Venereologica ·Christelle Cabrol, T. Bienvenu, Lyse Ruaud, Emmanuelle Girodon, G Noacco, M. Delobeau, Férial Fanian, Bénédicte Richaud-Thiriez, Lionel Van Maldergem, F. Aubin	2014	11
3	The p.Gly622Asp (G622D) mutation, frequently found in Reunion Island and in black populations, is associated with a wide spectrum of CF and CFTR-RD phenotypes Journal of Cystic Fibrosis ·Marion Heller, Natacha Gaitch, Brigitte Martinez, François Cartault, Michel Renouil, C. Thèze, Girodon Emmanuelle, T. Bienvenu	2014	1
4	The p.Val66Met polymorphism in the BDNF gene protects against early seizures in Rett syndrome Neurology ·Juliette Nectoux, Nadia Bahi‐Buisson, Isabelle Guellec, Joël Coste, Nicolás de Roux, H. Rosas, Marc Tardieu, Jamel Chelly, T. Bienvenu	2008	39
5	A Frequent Large Rearrangement in the CFTR Gene in Cystic Fibrosis Patients from Reunion Island Genetic Testing ·Juliette Nectoux, Marie Pierre Audrézet, Marion Viel, Chrystel Leroy, Odile Raguénès, Claude Férec, Jean François Lesure, Nolwenne Davy, Michel Renouil, François Cartault, T. Bienvenu	2006	3
6	Duplication of the MECP2 region is a frequent cause of severe mental retardation and neurological symptoms in males Hilde Van Esch, Marijke Bauters, Jaakko Ignatius, Martine Raynaud, Karen Hollanders, Dorien Lugtenberg, T. Bienvenu, LR Jensen, C Moraine, Peter Marynen, Guido Froyen, Jean‐Pierre Fryns	2006	1
7	ARX, a novel Prd-class-homeobox gene highly expressed in the telencephalon, is mutated in X-linked mental retardation Human Molecular Genetics ·T. Bienvenu	2002	213
8	Parental origin of de novo MECP2 mutations in Rett syndrome European Journal of Human Genetics ·M Girard, Philippe Couvert, Alain Carrié, Marc Tardieu, Jamel Chelly, Chérif Beldjord, T. Bienvenu	2001	92
9	Reduction in the DAZ gene copy number in two infertile men with impaired spermatogenesis Annales de Génétique ·T. Bienvenu, Catherine Patrat, Ken Mc Elreavey, Martha de Almeida, Pierre Jouannet	2001	18
10	Missense mutation in PAK3, R67C, causes X-linked nonspecific mental retardation American Journal of Medical Genetics ·T. Bienvenu, Vincent des Portes, Nathalie McDonell, Alain Carri�, Ramzi Zemni, Philippe Couvert, Hilger H. Ropers, Claude Moraine, Hans van Bokhoven, J. P. Fryns, Kristina M. Allen, Christopher A. Walsh, Joelle Bou�, Axel Kahn, Jamel Chelly, Chérif Beldjord	2000	108
11	Analysis of the Complete Coding Region of the CFTR Gene in Ten Algerian Cystic Fibrosis Families Human Heredity ·Ourida Loumi, M. Baghriche, Marc Delpech, J.‐C. Kaplan, T. Bienvenu	1999	11
12	Mutations in GDI1 are responsible for X-linked non-specific mental retardation Nature Genetics ·Patrizia D’Adamo, Andrea Menegon, Cristiana Lo Nigro, Marina Grasso, Massimo Gulisano, Filippo Tamanini, T. Bienvenu, Ági K. Gedeon, Ben A. Oostra, Shih-Kwang Wu, Anurag Tandon, Flavia Valtorta, William E. Balch, Jamel Chelly, Daniela Toniolo	1998	264
13	Novel double mutant CF allele identified in a cystic fibrosis patient with meconium ileus. PubMed ·Julie Steffann, Dominique Vidaud, Sandrine Bousquet, M Jullien, Alain Ninot, Kaplan Jc, C. Beldjord, T. Bienvenu	1998	1
14	Oligophrenin 1 encodes a rho-GAP protein involved in X-linked mental retardation. PubMed ·Pierre Billuart, T. Bienvenu, Nathalie Ronce, V. des Portes, Marie Claude Vinet, Ramzi Zemni, Alain Carrié, C. Beldjord, A Kahn, C Moraine, Jamel Chelly	1998	33
15	Analysis of Alternative Splicing Patterns in the Cystic Fibrosis Transmembrane Conductance Regulator Gene Using mRNA Derived from Lymphoblastoid Cells of Cystic Fibrosis Patients European Journal of Human Genetics ·T. Bienvenu, Chérif Beldjord, Jamel Chelly, Núria Fonknechten, D. Hubert, Daniel Dusser, Jean Claude Kaplan	1996	10
16	A novel missense mutation in exon 16 of the cystic fibrosis transmembrane conductance regulator (CFTR) gene identified in CBAVD patients Human Mutation ·T. Bienvenu, D. Hubert, Eric Setbon, Daniel Dusser, Jean‐Claude Kaplan, Chérif Beldjord	1996	3
17	Elevated total plasma homocysteine, a risk factor for thrombosis. Relation to coagulation and fibrinolytic parameters Thrombosis Research ·T. Bienvenu, Annick Ankri, B. Chadefaux, Gilles Montalescot, P. Kamoun	1993	83
18	Use of chemical clamps in denaturing gradient gel electrophoresis: application in the detection of the most frequent Mediterranean beta-thalassemic mutations. Genome Research ·Elena Fernández Fernández, T. Bienvenu, F. Desclaux Arramond, Kheïra Beldjord, J.‐C. Kaplan, C. Beldjord	1993	23
19	Fernandez, E. et al. Use of chemical clamps in denaturing gradient gel electrophoresis: application in the detection of the most frequent Mediterranean -thalassemic mutations. PCR Methods Appl. 3, 122-124 Esteve Fernández, T. Bienvenu, F. Desclaux Arramond, Kheïra Beldjord, Joan C. Kaplan, C. Beldjord	1993	10
20	Antithrombin III Activity Is Not Related to Plasma Homocysteine Concentrations Pathophysiology of Haemostasis and Thrombosis ·T. Bienvenu, B. Chadefaux, Annick Ankri, Vincent S. Leblond, M. Coudé, Behrouz Salehian, J. L. Binet, P. Kamoun	1991	5

About T. Bienvenu

T. Bienvenu is a scholar working on Genetics, Genetics, Pulmonary and Respiratory Medicine, Internal Medicine and Rheumatology, having authored 29 papers that have together received 1.0k indexed citations. Recurring topics across this work include Cystic Fibrosis Research Advances (10 papers), Genetics and Neurodevelopmental Disorders (7 papers), Neonatal Respiratory Health Research (7 papers), Epigenetics and DNA Methylation (3 papers), Folate and B Vitamins Research (3 papers), Congenital Ear and Nasal Anomalies (3 papers), Hemoglobinopathies and Related Disorders (2 papers) and Skin and Cellular Biology Research (2 papers). The work is most often cited by research in Genetics (519 citations), Cell Biology (177 citations), Developmental Neuroscience (34 citations), Molecular Biology (556 citations) and Cognitive Neuroscience (149 citations). T. Bienvenu has collaborated with scholars based in France, United States and Netherlands. Frequent co-authors include Jamel Chelly, P. Kamoun, Annick Ankri, B. Chadefaux, Chérif Beldjord, Philippe Couvert, Patrizia D’Adamo, Daniela Toniolo, Flavia Valtorta and Cristiana Lo Nigro. Their work appears in journals such as European Journal of Human Genetics, Journal of Cystic Fibrosis, Human Mutation, Nature Genetics and Human Molecular Genetics.

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