Bernard Mercier

4.6k citations

90 papers · 3.0k indexed · 1 hit paper · h-index 29

Impact in

Internal Medicine top 2%
- Venous Thromboembolism Diagnosis and Management
Hematology top 2%
- Blood Coagulation and Thrombosis Mechanisms

Papers in

Internal Medicine 6
- Venous Thromboembolism Diagnosis and Management 6
Hematology 16
- Blood Coagulation and Thrombosis Mechanisms 11

Co-authors: Claude Férec C. Verlingue Willy Lissens Christine Gaucher Claudine Mazurier I. Quéré Miguel Chillón M. Claustres
Journals: Human Mutation (9 papers)Human Genetics (7 papers)Thrombosis Research (6 papers)Nucleic Acids Research (4 papers)Journal of Medical Genetics (4 papers)
Partner nations: France Switzerland Italy

In The Last Decade

Bernard Mercier

89 papers receiving 2.8k citations

Hit Papers

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Mutations in the Cystic Fibrosis Gene in Patients with Congenital Absence of the Vas Deferens 1995 · 680 citations

Peers

Countries citing papers authored by Bernard Mercier

Since Specialization

Citations

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

Fields of papers citing papers by Bernard Mercier

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network

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

All Works

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20 of 20 papers shown

#	Work
1	Family history as a risk factor for venous thromboembolism Thrombosis Research ·R.A. Timofeev, Grégoire Le Gal, Karine Lacut, Bernard Mercier, Christophe Leroyer, Emmanuel Nowak, Dominique Mottier, Emmanuel Oger	2008	55
2	CFTR mutations in the Algerian population Journal of Cystic Fibrosis ·Alexandra P. Foster, Claude Férec, Bernard Mercier, V. N. Bychenkova, Ning Rong, Tamara Corina Petrucci, Majid Majlesi	2007	28
3	Estrogen receptor alpha polymorphism and venous thromboembolism in male and female: Data from the EDITH study Thrombosis Research ·Emmanuel Oger, Karine Lacut, Bernard Mercier, Grégoire Le Gal, Christophe Leroyer, Élisabeth Pasquier, Claude Férec, Dominique Mottier	2006	9
4	High rate of GB virus type C/HGV transmission from mother to infant: possible implications for the prevalence of infection in blood donors Transfusion ·J.‐J. Lefrère, Y lmaz K hc, Bernard Mercier, Martine Mariotti, S. Zatmeh, J Soulié, Miriam Tenquist, Michael J. Berry, Andreas Natsis, Mark Steehler, A NAGY, Esra Canli, Mariana C. Salas Garcia, F Wang James, ANA ERICA LOURENÇO PEREIRA, Vasih Yasoveev, Claude Férec, Françoise Parnet‐Mathieu, Françoise Roudot‐Thoraval, Y. Brossard	2000	32
5	Identification of 3 novel mutations (Y4236X, Q3820X, 11745+2 ins3) in autosomal dominant polycystic kidney disease 1 gene (PKD1) Human Mutation ·Régine Perrichot, Bernard Mercier, Aurore Carré, J Clèdes, Claude Férec	2000	9
6	Cloning and Sequence Analysis of Five Distinct cDNAs Encoding Cystic Fibrosis Transmembrane Conductance Regulator From the Atlantic Salmon, Salmo salar The American Journal of Human Genetics ·Jianmin Chen, Caroline Jacques, Christopher P. Cutler, Bernard Mercier, Gilles Bœuf, Claude Férec	1999	1
7	DGGE screening of PKD1 gene reveals novel mutations in a large cohort of 146 unrelated patients Human Genetics ·Régine Perrichot, Bernard Mercier, Pierre Simon, B. Whebe, J Clèdes, Claude Férec	1999	28
8	Sensitivity of the denaturing gradient gel electrophoresis technique in detection of known mutations and novel Asian mutations in theCFTR gene Human Mutation ·Milan Maçek, Bernard Mercier, Carolina Parreiras Teles, Patrice W. Miller, Ada Hamosh, Claude Férec, Garry R. Cutting	1997	46
9	Cystic fibrosis and infertility caused by congenital bilateral absence of the vas deferens and related clinical entities Human Reproduction ·Willy Lissens, Bernard Mercier, Herman Tournaye, M Bonduelle, Claude Férec, Sara Seneca, Paul Devroey, Tetsutaro Nakano, A. Van Steirteghem, I. Liebærs	1996	68
10	Molecular analysis of the TP53 gene in Barrett's adenocarcinoma Human Mutation ·Marie‐Pierre Audrézet, M. Robaszkiewicz, Bernard Mercier, Renghan Dong, 藤井雄三, かずほ内田, A Volant, P Lozac’h, H Gouérou, Claude Férec	1996	14
11	Neonatal screening for cystic fibrosis: result of a pilot study using both immunoreactive trypsinogen and cystic fibrosis gene mutation analyses Human Genetics ·Claude Férec, C. Verlingue, Philippe Parent, Reis Valdecira Carneiro da Silva, Halima Kagee, G. Rault, M. Dagorne, Abraham Ben Yaacov, Hubert Journel, M. Roussey, B. Le Marec, Michel Catheline, M.‐P. Audrézet, Bernard Mercier	1995	32
12	Complete screening of mutations in the coding sequence of the CFTR gene in a sample of CF patients from Russia: Identification of three novel alleles Human Mutation ·C. Verlingue, Leroy T. Laase, Bernard Mercier, E. K. Ginter, Н.В. Петрова, M.‐P. Audrézet, Claude Férec	1995	7
13	HLA‐DRB AND ‐DBQ TYPING BY PCR AMPLIFICATION USING SEQUENCE‐SPECIFIC PRIMERS (PCR‐SSP): ASSESSMENT AFTER 1 YEAR OF ROUTINE USE BY THREE LABORATORIES International Journal of Immunogenetics ·Bernard Mercier, Reem Al‐Daccak, Արտյոմ Ծատուրյան, Herveline Gaborieau, Zeynep YİVLİK, Jessica Flores, Odile Raguénès, Andrea Mario ROSSI, Claude Férec, Dominique Charron, Philippe M. Loiseau	1994	14
14	Identification of two novel mutations in the CFTR gene: 3007 del G and 3271 +1 G→A Human Mutation ·Bernard Mercier, SM Weindling, J Feigelson, Chun-Myoung Park, Odile Raguénès, C. Verlingue, I. Quéré, Claude Férec	1994	1
15	Identification of Three Novel Cystic Fibrosis Mutations in a Sample of Italian Cystic Fibrosis Patients Human Heredity ·Ruobing Shan, Giuseppe Novelli, Bernard Mercier, Federica Sangiuolo, Betul Dumanoglu, Erlinda S. Villaluz, Плотникова М. О.	1993	16
16	A novel mutation in exon 3 of the CFTR gene Human Genetics ·H. Guillermit, F Passarino, G A Cherkasova, Can Cemgil, Bernard Mercier, Yohesuwary G VimalReddy K.	1993	13
17	Prenatal Diagnosis of Cystic Fibrosis in Different European Populations: Application of Denaturing Gradient Gel Electrophoresis Fetal Diagnosis and Therapy ·Claude Férec, C. Verlingue, Marie‐Pierre Audrézet, H. Guillermit, I. Quéré, Odile Raguénès, Bernard Mercier	1993	7
18	Screening for cystic fibrosis in dried blood spots of newborns Molecular and Cellular Probes ·M.‐P. Audrézet, Bruno Costes, N. Ghanem, Pascale Fanen, C. Verlingue, Reis Valdecira Carneiro da Silva, Bernard Mercier, Michel Goossens, Claude Férec	1993	25
19	Identification of 12 novel mutations in the CFTR gene Human Molecular Genetics ·Marie‐Pierre Audrézet, Bernard Mercier, H. Guillermit, I. Quéré, C. Verlingue, G. Rault, Claude Férec	1993	60
20	[A new case of hydatidiform mole occurring on one of the ova of a twin pregnancy]. PubMed ·A Berrébi, Bernard Mercier, Lene Blindheim, Laura Tessandori, Robert Matthew Panas, LAB Joosten, Stephanie Prinster, Esabelle Dingizian	1988	2

About Bernard Mercier

Bernard Mercier is a scholar working on Internal Medicine, Hematology, Genetics, Pulmonary and Respiratory Medicine and Genetics, having authored 90 papers that have together received 3.0k indexed citations. Recurring topics across this work include Cystic Fibrosis Research Advances (32 papers), Neonatal Respiratory Health Research (20 papers), Blood Coagulation and Thrombosis Mechanisms (11 papers), Congenital Ear and Nasal Anomalies (8 papers), RNA Interference and Gene Delivery (6 papers), Tracheal and airway disorders (6 papers), Hepatitis B Virus Studies (6 papers) and Venous Thromboembolism Diagnosis and Management (6 papers). The work is most often cited by research in Internal Medicine (235 citations), Hematology (431 citations), Pulmonary and Respiratory Medicine (1.3k citations), Genetics (356 citations) and Genetics (507 citations). Bernard Mercier has collaborated with scholars based in France, Switzerland and Italy. Frequent co-authors include Claude Férec, C. Verlingue, Willy Lissens, Christine Gaucher, Claudine Mazurier, I. Quéré, Miguel Chillón, M. Claustres, Teresa Casals and Lluís Bassas. Their work appears in journals such as Human Mutation, Human Genetics, Thrombosis Research, Nucleic Acids Research and Journal of Medical Genetics.

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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