Éric Bieth

7.4k citations

73 papers · 2.3k · h-index 25

Impact in

Genetics top 5%
- Genetic Syndromes and Imprinting
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
Virology top 5%

Papers in

Molecular Biology 26
- RNA regulation and disease 4
Genetics 26
- Genetic Syndromes and Imprinting 8
- Genomic variations and chromosomal abnormalities 6
- Congenital Ear and Nasal Anomalies 5
- Neurogenetic and Muscular Disorders Research 4
- Genetics and Neurodevelopmental Disorders 4

Co-authors: Jean‐Luc Darlix (2 shared papers)Caroline Gabus (1 shared paper)Roger Mieusset (5 shared papers)M. Tauber (12 shared papers)Catherine Molinas (8 shared papers)Nicolas Chassaing (5 shared papers)Louis Bujan (4 shared papers)Safouane M. Hamdi (2 shared papers)
Journals: Human Mutation (5 papers)European Journal of Human Genetics (4 papers)European Journal of Medical Genetics (4 papers)Journal of Cystic Fibrosis (3 papers)Pacing and Clinical Electrophysiology (2 papers)
Partner nations: France United States Belgium

In The Last Decade

Éric Bieth

70 papers receiving 2.2k citations

Peers

Countries citing papers authored by Éric Bieth

Since Specialization

Citations

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

Fields of papers citing papers by Éric Bieth

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

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

All Works

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20 of 20 papers shown

Showing the 20 most-cited of 73 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	Mutations in LRP2, which encodes the multiligand receptor megalin, cause Donnai-Barrow and facio-oculo-acoustico-renal syndromes Nature Genetics ·Sibel Kantarci, Lihadh Al‐Gazali, R. Sean Hill, Dian Donnai, Graeme C. Black, Éric Bieth, Nicolas Chassaing, Didier Lacombe, Koenraad Devriendt, Ahmad S. Teebi, Marı́a Loscertales, Caroline D. Robson, Tianming Liu, David T. MacLaughlin, Kristin Noonan, Meaghan Russell, Christopher A. Walsh, Patricia K. Donahoe, Barbara R. Pober	2007	249
2	Mutations in genes in the renin-angiotensin system are associated with autosomal recessive renal tubular dysgenesis Nature Genetics ·Olivier Gribouval, Marie Gonzalès, Thomas J. Neuhaus, Jacqueline Aziza, Éric Bieth, Nicole Laurent, Jean Marie Bouton, François Feuillet, Saloua Makni, H. Ben Amar, Guido F. Laube, Anne‐Lise Delezoide, Raymonde Bouvier, Frédérique Dijoud, Elisabeth Ollagnon‐Roman, J. Roume, Madeleine Joubert, Corinne Antignac, Marie-Claire Gübler	2005	211
3	A study of the dimer formation of Rous sarcoma virus RNA and of its effect on viral protein synthesisin vitro Nucleic Acids Research ·Éric Bieth, Caroline Gabus, Jean‐Luc Darlix	1990	161
4	Highly restricted deletion of the SNORD116 region is implicated in Prader–Willi Syndrome European Journal of Human Genetics ·Éric Bieth, Sanaa Eddiry, Véronique Gaston, F. Lorenzini, Alexandre Buffet, Françoise Auriol, Catherine Molinas, Dorothée Cailley, Caroline Rooryck, Benoı̂t Arveiler, Jérôme Cavaillé, Jean‐Pierre Salles, M. Tauber	2014	132
5	Truncating Mutations in the Adhesion G Protein-Coupled Receptor G2 Gene ADGRG2 Cause an X-Linked Congenital Bilateral Absence of Vas Deferens The American Journal of Human Genetics ·Olivier Patat, A. Pagin, Aurore Siegfried, Valérie Mitchell, Nicolas Chassaing, Stanislas Faguer, Laetitia Monteil, Véronique Gaston, Louis Bujan, Monique Courtade-Saïdi, F. Marcelli, G. Lalau, Jean-Marc Rigot, Roger Mieusset, Éric Bieth	2016	108
6	Congenital bilateral absence of the vas deferens: clinical characteristics, biological parameters, cystic fibrosis transmembrane conductance regulator gene mutations, and implications for genetic counseling Fertility and Sterility ·Myriam Daudin, Éric Bieth, Louis Bujan, G. Massat, F Pontonnier, Roger Mieusset	2000	102
7	A molecular approach to dominance in hypophosphatasia Human Genetics ·Anne-Sophie Lia-Baldini, Françoise Müller, A. Taillandier, J.-F. Gibrat, M. Mouchard, Blaise Robin, Brigitte Simon‐Bouy, Justine Serre, A. Aylsworth, Éric Bieth, S. Delanote, P. Freisinger, Jingjing Hu, H P Krohn, Mark E. Nuñes, E. Mornet	2001	92
8	Early diagnosis and care is achieved but should be improved in infants with Prader-Willi syndrome Orphanet Journal of Rare Diseases ·Céline Bar, Gwénaëlle Diene, Catherine Molinas, Éric Bieth, Charlotte Casper, M. Tauber	2017	83
9	Molecular analysis of pericentrin gene (PCNT) in a series of 24 Seckel/microcephalic osteodysplastic primordial dwarfism type II (MOPD II) families Journal of Medical Genetics ·Marjorlaine Willems, D. Genevieve, Guntram Borck, Clarisse Baumann, Geneviève Baujat, Éric Bieth, Patrick Edery, Chantal Farra, M. Gerard, Delphine Héron, Bruno Leheup, M Le Merrer, Stanislas Lyonnet, Dominique Martin‐Coignard, M Mathieu, Christel Thauvin‐Robinet, Alain Verloès, Laurence Colleaux, Arnold Münnich, Valérie Cormier‐Daire	2009	81
10	Genetics of the congenital absence of the vas deferens Human Genetics ·Éric Bieth, Safouane M. Hamdi, Roger Mieusset	2020	68
11	CFTR genotypes in patients with normal or borderline sweat chloride levels Human Mutation ·Delphine Feldmann, Rémy Couderc, Marie‐Pierre Audrézet, Claude Férec, Thierry Bienvenu, Marie Desgeorges, Mireille Claustres, Herv� Mittre, Martine Blayau, Dominique Bozon, Marie‐Claire Malinge, Nicole Monnier, Jean‐Paul Bonnefont, A. Iron, Éric Bieth, Viviane Dumur, Christine Clavel, C�cile Cazeneuve, E. Girodon	2003	63
12	Assessment of Aspergillus sensitization or persistent carriage as a factor in lung function impairment in cystic fibrosis patients Scandinavian Journal of Infectious Diseases ·Judith Fillaux, François Brémont, Marlène Murris, Sophie Cassaing, J.L. Rittié, L. Têtu, Christine Segonds, M. Abbal, Éric Bieth, Antoine Berry, Bernard Pipy, Jean‐François Magnaval	2012	61
13	14q12 and severe Rett-like phenotypes: new clinical insights and physical mapping of FOXG1-regulatory elements European Journal of Human Genetics ·Lila Allou, Laëtitia Lambert, Daniel Amsallem, Éric Bieth, Patrick Edery, Anne Destrèe, François Rivier, David J. Amor, Elizabeth Thompson, Julian Nicholl, Michael Harbord, Christophe Némos, Aline Saunier, Aissa Moustaïne, Adeline Vigouroux, Philippe Jonveaux, Christophe Philippe	2012	54
14	Medical, psychological and social features in a large cohort of adults with Prader–Willi syndrome: experience from a dedicated centre in France Journal of Intellectual Disability Research ·Virginie Laurier, A. Lapeyrade, P. Copet, Geneviève Demeer, M. Silvie, Éric Bieth, Muriel Coupaye, Christine Poitou, F. Lorenzini, François Labrousse, Catherine Molinas, M. Tauber, Denise Thuilleaux, J. Jauregi	2014	50
15	Molecular mechanisms of perilipin protein function in lipid droplet metabolism FEBS Letters ·Elena Griseti, Abdoul Akim Bello, Éric Bieth, Bayane Sabbagh, Jason S. Iacovoni, Joëlle Bigay, Henrik Laurell, Alenka Čopič	2023	41
16	Growth Hormone, Insulin-Like Growth Factor-I and Insulin-Like Growth Factor Binding Protein-3 Are Regulated Differently in Small-for-Gestational-Age and Appropriate-for-Gestational-Age Neonates Neonatology ·A. Cance-Rouzaud, Sophie Laborie, Éric Bieth, J Tricoire, Michel Rolland, H. Grandjean, P Rochiccioli, M.T. Tauber	1998	38
17	Effect of Genotype and Previous GH Treatment on Adiposity in Adults With Prader-Willi Syndrome The Journal of Clinical Endocrinology & Metabolism ·Muriel Coupaye, M. Tauber, Laurence Cuisset, Virginie Laurier, Éric Bieth, Jean‐Marc Lacorte, Jean‐Michel Oppert, Karine Clément, Christine Poitou	2016	38
18	A sensitive assay for measuring SMN mRNA levels in peripheral blood and in muscle samples of patients affected with spinal muscular atrophy European Journal of Human Genetics ·Myriam Vézain, Pascale Saugier-Véber, Judith Melki, Annick Toutain, Éric Bieth, Marie Husson, Jean‐Michel Pedespan, Louis Viollet, I. Pénisson-Besnier, Séverine Fehrenbach, Jacqueline Bou, Thierry Frébourg, Mario Tosi	2007	35
19	The role of muscle biopsy in analysis of the dystrophin gene in Duchenne muscular dystrophy: experience of a national referral centre Neuromuscular Disorders ·Sylvie Tuffery‐Giraud, Céline Saquet, Sylvie Chambert, Bernard Échenne, J. Cuisset, François Rivier, Mireille Cossée, Christophe Philippe, Nicole Monnier, Éric Bieth, Dominique Récan, Marie Antoinette Voelckel, Serge Perelman, Jean-Claude Lambert, Sue Malcolm, Mireille Claustres	2004	34
20	Distal 10q monosomy: New evidence for a neurobehavioral condition? European Journal of Medical Genetics ·Julie Plaisancié, Laurence Bouneau, Claude Cancès, Christelle Garnier, Jacques Benesteau, Samantha Leonard, G. Bourrouillou, Patrick Calvas, Adeline Vigouroux, Sophie Julia, Éric Bieth	2013	32

About Éric Bieth

Éric Bieth is a scholar working on Molecular Biology, Genetics, Pulmonary and Respiratory Medicine, Genetics and Rheumatology, having authored 73 papers that have together received 2.3k indexed citations. Recurring topics across this work include Cystic Fibrosis Research Advances (12 papers), Genetic Syndromes and Imprinting (8 papers), Genomic variations and chromosomal abnormalities (6 papers), Growth Hormone and Insulin-like Growth Factors (5 papers), Congenital Ear and Nasal Anomalies (5 papers), Neurogenetic and Muscular Disorders Research (4 papers), RNA regulation and disease (4 papers) and Genetics and Neurodevelopmental Disorders (4 papers). The work is most often cited by research in Genetics (681 citations), Virology (105 citations), Pediatrics, Perinatology and Child Health (292 citations), Reproductive Medicine (125 citations) and Molecular Biology (1.0k citations). Éric Bieth has collaborated with scholars based in France, United States and Belgium. Frequent co-authors include Jean‐Luc Darlix, Caroline Gabus, Roger Mieusset, M. Tauber, Catherine Molinas, Nicolas Chassaing, Louis Bujan, Safouane M. Hamdi, Myriam Daudin and Jean‐Pierre Salles. Their work appears in journals such as Human Mutation, European Journal of Human Genetics, European Journal of Medical Genetics, Journal of Cystic Fibrosis and Pacing and Clinical Electrophysiology.

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.

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