Virginie Scotet

3.0k citations

55 papers · 2.0k indexed · h-index 24

Genetics top 2%
- Hemoglobinopathies and Related Disorders 12
- Congenital Ear and Nasal Anomalies 5
Hematology top 5%
- Iron Metabolism and Disorders 12
Biochemistry top 5%
Nutrition and Dietetics top 5%
- Trace Elements in Health 6
Pulmonary and Respiratory Medicine top 5%
- Cystic Fibrosis Research Advances 29
- Neonatal Respiratory Health Research 17
- Tracheal and airway disorders 8
Rheumatology
- Folate and B Vitamins Research 5

Co-authors: Claude Férec Daniel Commenges Jean‐François Dartigues S. Renaud Pascale Barberger‐Gateau Hélène Jacqmin‐Gadda Marie‐Pierre Audrézet Cédric Le Maréchal
Cited by: Genetics Hematology Biochemistry
Journals: The Lancet (1 paper)Blood (1 paper)PLoS ONE (3 papers)
Partner nations: France United States Italy

In The Last Decade

Virginie Scotet

55 papers receiving 2.0k citations

Peers

Countries citing papers authored by Virginie Scotet

Since Specialization

Citations

This map shows the geographic impact of Virginie Scotet'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 Virginie Scotet with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Virginie Scotet more than expected).

Fields of papers citing papers by Virginie Scotet

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Virginie Scotet. 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 Virginie Scotet. The network helps show where Virginie Scotet may publish in the future.

Co-authorship network

The 25 scholars most cited alongside Virginie Scotet, 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 Virginie Scotet Line = papers co-authored together Virginie Scotet links everyone, so they are left out of the graph.

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

#	Work
1	Penetrance is a critical parameter for assessing the disease liability of CFTR variants Journal of Cystic Fibrosis ·Agathe Boussaroque,M.‐P. Audrézet,Caroline Raynal,Isabelle Sermet‐Gaudelus,Thierry Bienvenu,Claude Férec,Anne Bergougnoux,Maureen Lopez,Virginie Scotet,À. Munck,Emmanuelle Girodon	2020	11
2	Do pregnancies reduce iron overload in HFE hemochromatosis women? results from an observational prospective study BMC Pregnancy and Childbirth ·Virginie Scotet,Philippe Saliou,Marianne Uguen,C. L’Hostis,Marie Christine Merour,Céline Triponey,B Chanu,Jean Baptiste Nousbaum,Gérald Le Gac,Claude Férec	2018	5
3	Highlighting the impact of cascade carrier testing in cystic fibrosis families Journal of Cystic Fibrosis ·I. Duguépéroux,C. L’Hostis,Marie‐Pierre Audrézet,G. Rault,I. Frachon,R Bernard,Philippe Parent,Martine Blayau,Sébastien Schmitt,Emmanuelle Génin,Claude Férec,Virginie Scotet	2016	10
4	Comprehensive CFTR gene analysis of the French cystic fibrosis screened newborn cohort: implications for diagnosis, genetic counseling, and mutation-specific therapy Genetics in Medicine ·Marie Pierre Audrézet,À. Munck,Virginie Scotet,Mireille Claustres,Michel Roussey,Dominique Delmas,Claude Férec,Marie Desgeorges	2014	33
5	Evidence for the High Importance of Co-Morbid Factors in HFE C282Y/H63D Patients Cared by Phlebotomies: Results from an Observational Prospective Study PLoS ONE ·Philippe Saliou,Gérald Le Gac,Anne‐Yvonne Mercier,B Chanu,Paul Guéguen,Marie-Christine Mérour,Isabelle Gourlaouen,Sandrine Autret,Cédric Le Maréchal,Karen Rouault,Jean‐Baptiste Nousbaum,Claude Férec,Virginie Scotet	2013	5
6	Cascade testing in families of carriers identified through newborn screening in Western Brittany (France) Journal of Cystic Fibrosis ·I. Duguépéroux,Marie‐Pierre Audrézet,Philippe Parent,Séverine Audebert‐Bellanger,Michel Roussey,Claude Férec,Virginie Scotet	2012	1
7	Génétique et gènes modificateurs, formes atypiques et rares Archives de Pédiatrie ·Claude Férec,Virginie Scotet,J. Beucher,Harriet Corvol	2012	4
8	Evidence for decline in the incidence of cystic fibrosis: a 35-year observational study in Brittany, France Orphanet Journal of Rare Diseases ·Virginie Scotet,I. Duguépéroux,Philippe Saliou,G. Rault,Michel Roussey,Marie‐Pierre Audrézet,Claude Férec	2012	41
9	Evidence of association between GDF5 polymorphisms and congenital dislocation of the hip in a Caucasian population Osteoarthritis and Cartilage ·Karen Rouault,Virginie Scotet,Sandrine Autret,François Gaucher,F. Dubrana,D. Tanguy,C. Yaacoub El Rassi,B. Fénoll,Claude Férec	2010	58
10	Polymorphic length of FOXE1 alanine stretch: evidence for genetic susceptibility to thyroid dysgenesis Human Genetics ·Aurore Carré,Mireille Castanet,Sylvia Sura‐Trueba,Gabor Szinnai,Guy Van Vliet,Delphine Trochet,Jeanne Amiel,Juliane Léger,Paul Czernichow,Virginie Scotet,Michel Polak	2007	47
11	Time Trends in Birth Incidence of Cystic Fibrosis in Two European Areas: Data from Newborn Screening Programs The Journal of Pediatrics ·Virginie Scotet,B.M. Assael,I. Duguépéroux,Anna Tamanini,Marie‐Pierre Audrézet,Claude Férec,Carlo Castellani	2007	13
12	A 6-year survey of HFE gene test for hemochromatosis diagnosis Genetics in Medicine ·Catherine Mura,Odile Raguénès,Virginie Scotet,Sandrine Jacolot,Anne‐Yvonne Mercier,Claude Férec	2005	7
13	Impact of HFEgenetic testing on clinical presentation of hereditary hemochromatosis: new epidemiological data BMC Medical Genetics ·Virginie Scotet,Gérald Le Gac,Marie-Christine Mérour,Anne‐Yvonne Mercier,B Chanu,Chandran Ka,Catherine Mura,Jean‐Baptiste Nousbaum,Claude Férec	2005	15
14	Early onset hereditary hemochromatosis resulting from a novel TFR2 gene nonsense mutation (R105X) in two siblings of north French descent British Journal of Haematology ·Gérald Le Gac,F. Mons,Sandrine Jacolot,Virginie Scotet,Claude Férec,Thierry Frébourg	2004	53
15	Hereditary Hemochromatosis: Effect of Excessive Alcohol Consumption on Disease Expression in Patients Homozygous for the C282Y Mutation American Journal of Epidemiology ·Virginie Scotet	2003	70
16	Quantification of CFTR splice variants in adults with disseminated bronchiectasis, using the TaqMan fluorogenic detection system Clinical Genetics ·Joris Andrieux,M.P. Audrézet,I. Frachon,Christophe Leroyer,C. Rogé,Virginie Scotet,Claude Férec	2002	11
17	Endometrial vascularity and ongoing pregnancy after IVF European Journal of Obstetrics & Gynecology and Reproductive Biology ·B. Maugey‐Laulom,M. Commenges-Ducos,Véronique Jullien,Aline Papaxanthos-Roche,Virginie Scotet,Daniel Commenges	2002	35
18	Determination of the relative contribution of three genes–the cystic fibrosis transmembrane conductance regulator gene, the cationic trypsinogen gene, and the pancreatic secretory trypsin inhibitor gene–to the etiology of idiopathic chronic pancreatitis European Journal of Human Genetics ·Marie‐Pierre Audrézet,Jian‐Min Chen,Cédric Le Maréchal,Philippe Ruszniewski,Michel Robaszkiewicz,Odile Raguénès,I. Quéré,Virginie Scotet,Claude Férec	2002	101
19	Prevalence of CFTR mutations in hypertrypsinaemia detected through neonatal screening for cystic fibrosis Clinical Genetics ·Virginie Scotet,Marc De Braekeleer,M.‐P. Audrézet,Laurence Lodé,C. Verlingue,I. Quéré,Bernard Mercier,I. Duguépéroux,Jean-Pierre Codet,Marie‐Pierre Moineau,Philippe Parent,Claude Férec	2001	28
20	Neonatal screening for cystic fibrosis in Brittany, France: assessment of 10 years' experience and impact on prenatal diagnosis The Lancet ·Virginie Scotet,Marc De Braekeleer,Michel Roussey,G. Rault,Philippe Parent,M. Dagorne,Hubert Journel,A. Lemoigne,Jean-Pierre Codet,Michel Catheline,Véronique David,André Chaventré,I. Duguépéroux,C. Verlingue,I. Quéré,Bernard Mercier,Marie‐Pierre Audrézet,Claude Férec	2000	85

About Virginie Scotet

Virginie Scotet is a scholar working on Genetics, Hematology and Pulmonary and Respiratory Medicine, having authored 55 papers that have together received 2.0k indexed citations. Recurring topics across this work include Cystic Fibrosis Research Advances (29 papers), Neonatal Respiratory Health Research (17 papers), Iron Metabolism and Disorders (12 papers), Hemoglobinopathies and Related Disorders (12 papers), Tracheal and airway disorders (8 papers), Trace Elements in Health (6 papers), Folate and B Vitamins Research (5 papers) and Congenital Ear and Nasal Anomalies (5 papers). The work is most often cited by research in Genetics (399 citations), Hematology (344 citations) and Biochemistry (157 citations). Virginie Scotet has collaborated with scholars based in France, United States and Italy. Frequent co-authors include Claude Férec, Daniel Commenges, Jean‐François Dartigues, S. Renaud, Pascale Barberger‐Gateau, Hélène Jacqmin‐Gadda, Marie‐Pierre Audrézet, Cédric Le Maréchal, Gérald Le Gac and I. Quéré. Their work appears in journals such as The Lancet, Blood and PLoS ONE.

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

Explore authors with similar magnitude of impact