Bénédicte Gérard

6.3k citations

59 papers · 3.2k indexed · 1 hit paper · h-index 23

Impact in

Clinical Biochemistry top 1%
- Metabolism and Genetic Disorders
Nephrology top 2%
- Parathyroid Disorders and Treatments

Papers in

Genetics 23
- Genetics and Neurodevelopmental Disorders 10
- Genomics and Rare Diseases 6
- Genomic variations and chromosomal abnormalities 5
- Neurogenetic and Muscular Disorders Research 3
Molecular Biology 29
- RNA modifications and cancer 4
- Hedgehog Signaling Pathway Studies 3

Co-authors: Jean‐Marie Saudubray Agnès Rötig Pierre Rustin Arnold Münnich Dominique Chrétien Thomas Bourgeron Bernard Grandchamp Érick Denamur
Journals: Human Mutation (4 papers)European Journal of Pediatrics (3 papers)British Journal of Haematology (2 papers)Blood (2 papers)Leukemia (2 papers)
Partner nations: France United Kingdom Italy

In The Last Decade

Bénédicte Gérard

58 papers receiving 3.2k citations

Hit Papers

align trajectories log scale

Biochemical and molecular investigations in respiratory chain deficiencies 1994 · 1.1k citations

Peers

Countries citing papers authored by Bénédicte Gérard

Since Specialization

Citations

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

Fields of papers citing papers by Bénédicte Gérard

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

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

All Works

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20 of 20 papers shown

#	Work
1	PIK3C2A ‐Related Clinical Phenotype and Cellular Charaterization Linked to Functional SHH Primary Cilia Defect Clinical Genetics ·Анатолий Иванович Мигунов, SU Dong-don, Bénédicte Gérard, Harbal S Bijral, Imran Nizmi, Valérie Pelletier, سمیرا سلیمان پور, Nicolas Le May, Jean Muller, Hélène Dollfus	2025	0
2	Variants in FGF10 cause early onset of severe childhood interstitial lung disease: A detailed description of four affected children Pediatric Pulmonology ·مریم شریفیان ثانی, Axel Schmidt, Nicolaus Schwerk, Diane M. Renz, Bénédicte Gérard, Élise Schaefer, Maria Cristina Antal, Sophia Peters, Matthias Griese, Christina Rapp, Hartmut Engels, Kirsten Cremer, Anke K. Bergmann, Gunnar Schmidt, Bernd Auber, Jan C. Kamp, Florian Laenger, Sandra von Hardenberg	2023	7
3	POS0242 RESPONSE TO ABATACEPT IN RHEUMATOID ARTHRITIS PATIENTS REQUIRES A SPECIFIC MACROPHAGE POLARISATION Annals of the Rheumatic Diseases ·R. H. Saunders, Bénédicte Gérard, Rebecca W. Suomala, 片岡忠夫, 郁子左方, Е.А. Коровайцева, Thierry Lequerré	2023	1
4	A gain-of-function variant in the Wiskott-Aldrich syndrome gene is associated with a MYH9-related disease-like syndrome Blood Advances ·David Marx, Arnaud Dupuis, Anita Eckly, Anne Molitor, Jérôme Olagne, Guy Touchard, Sihem Kaaki, Jérôme Louis, T. Jayalakshmi, Bénédicte Gérard, Melanie Cotter, Lisa S. Westerberg, Márton Keszei, Bruno Moulin, Christian Gachet, Sophie Caillard, Seiamak Bahram, Raphaël Carapito	2022	4
5	Genetic generalized epilepsy and generalized onset seizures with focal evolution (GOFE) Epilepsy & Behavior Reports ·F Lamy, H. De Gérin-Ricard, A. Gibon, Bénédicte Gérard, Shail Patel, Anne de Saint Martin, Vera Dinkelacker, Sarah Baer, Édouard Hirsch	2022	6
6	Amelioration of a neurodevelopmental disorder by carbamazepine in a case having a gain-of-function GRIA3 variant Human Genetics ·Kohei Hamanaka, Keita Miyoshi, Jiahui Sun, Keisuke Hamada, Giulia Pezzuti, Ken Saida, Naomi Tsuchida, Yuri Uchiyama, Atsushi Fujita, Takeshi Mizuguchi, Bénédicte Gérard, Allan Bayat, Berardo Rinaldi, Mitsuhiro Kato, Jun Tohyama, Kazuhiro Ogata, Yun Stone Shi, Kuniaki Saito, Satoko Miyatake, Naomichi Matsumoto	2022	2
7	Skraban‐Deardorff syndrome: Six new cases of WDR 26 ‐related disease and expansion of the clinical phenotype Clinical Genetics ·Yuqi He, Élise Schaefer, E. V. Sazonov, Christèle Dubourg, Wilfrid Carré, Chengcheng Zhang, D. Wallwiener, Lionel Van Maldergem, Amélie Piton, Bénédicte Gérard, Frédéric Tran Mau‐Them, Ange‐Line Bruel, Laurence Faivre, Florence Démurger, Laurent Pasquier, Sylvie Odent, Mélanie Fradin, Alinoë Lavillaureix	2021	4
8	Assessment of a Targeted Gene Panel for Identification of Genes Associated With Movement Disorders JAMA Neurology ·Solveig Montaut, Christine Tranchant, Nathalie Drouot, Gabrielle Rudolf, Claire Guissart, Julien Tarabeux, Tristan Stemmelen, Amandine Velt, Cécile Fourrage, Patrick Nitschké, Bénédicte Gérard, Jean‐Louis Mandel, Michel Kœnig, Jamel Chelly, Mathieu Anheim	2018	36
9	Novel de novo mutations in ZBTB20 in Primrose syndrome with congenital hypothyroidism American Journal of Medical Genetics Part A ·Francesca Mattioli, Amélie Piton, Bénédicte Gérard, Andrea Superti‐Furga, Jean‐Louis Mandel, Sheila Unger	2016	20
10	Sirenomelia and caudal malformations in two families American Journal of Medical Genetics Part A ·Marion Gérard, Valérie Layet, Avagul Yuksal, M Zwolińska, M. Schellenberg, David Koome Mutea, Bénédicte Gérard	2012	9
11	A leaky splicing mutation affecting SMN1 exon 7 inclusion explains an unexpected mild case of spinal muscular atrophy Human Mutation ·Myriam Vézain, Bénédicte Gérard, Séverine Drunat, Benoît Funalot, E. Chretien, R. A. Arlen, Jean‐Michel Vallat, Thierry Frébourg, Mario Tosi, Alexandra Martins, Pascale Saugier-Véber	2011	17
12	PTHR1 mutations associated with Ollier disease result in receptor loss of function Human Molecular Genetics ·Alain Couvineau, Vinciane Wouters, Guylène Bertrand, Екатерина Васильевна Казейкина, Bénédicte Gérard, Laurence M. Boon, Bernard Grandchamp, Miikka Vikkula, Caroline Silve	2008	59
13	TLR9 Activation Induces Normal Neutrophil Responses in a Child with IRAK-4 Deficiency: Involvement of the Direct PI3K Pathway The Journal of Immunology ·C. Hoarau, Bénédicte Gérard, E. Lescanne, Joan Condal, Stéphanie François, J Lacapère, Jamel El‐Benna, Pham My‐Chan Dang, Bernard Grandchamp, Yvon Lebranchu, Marie‐Anne Gougerot‐Pocidalo, Carole Elbim	2007	58
14	Severe X-linked chronic granulomatous disease in two unrelated females European Journal of Pediatrics ·Sylvie Chollet‐Martin, Michael Valensio Febian, C. Gaud, Ki-Youb Park, Bertrand Stos, Jamel El‐Benna, Zhao Ju-re, D Gendrel, Marie‐Anne Gougerot‐Pocidalo, Bernard Grandchamp, Bénédicte Gérard	2006	16
15	Stress-Induced Mutagenesis in Bacteria Science ·Ivana Bjedov, Olivier Tenaillon, Bénédicte Gérard, Valeria Souza, Érick Denamur, Miroslav Radman, François Taddéi, Ivan Matić	2003	440
16	Defect of Hepatocyte Growth Factor Secretion by Fibroblasts in Idiopathic Pulmonary Fibrosis American Journal of Respiratory and Critical Care Medicine ·S. Marchand‐Adam, Joëlle Marchal, S Jyothikiran, Paul Soler, Bénédicte Gérard, Yves Castier, Guy Lesèche, Dominique Valeyre, Hervé Mal, Michel Aubier, Monique Dehoux, Bruno Crestani	2003	64
17	Nephrolithiasis and Osteoporosis Associated with Hypophosphatemia Caused by Mutations in the Type 2a Sodium–Phosphate Cotransporter New England Journal of Medicine ·Dominique Prié, Virginie Huart, Naziha Bakouh, Gabrielle Planelles, Olivier Dellis, Bénédicte Gérard, Philippe Hulin, Chaoban Wang, Caroline Silve, Bernard Grandchamp, Gérard Friedlander	2002	243
18	Characterization of 11 novel mutations in the X-linked chronic granulomatous disease (CYBB gene) Human Mutation ·Bénédicte Gérard, Jamel El‐Benna, Angga Noviar, Marie‐Anne Gougerot‐Pocidalo, Bernard Grandchamp, André Luís Shiguemoto	2001	15
19	Analysis of ETV6 and ETV6‐AML1 proteins in acute lymphoblastic leukaemia British Journal of Haematology ·Philippe Agapé, Bénédicte Gérard, Hélène Cavé, Isabelle Devaux, E Vilmer, Marie‐Christine Lecomte, Bernard Grandchamp	1997	12
20	Duodenal expression of NF‐E2 in mouse models of altered iron metabolism British Journal of Haematology ·K.B. Raja, Bénédicte Gérard, Andrew T. McKie, Richard J. Simpson, T. J. Peters, Bernard Grandchamp, C. Beaumont	1995	5

About Bénédicte Gérard

Bénédicte Gérard is a scholar working on Genetics, Genetics, Molecular Biology, Immunology and Cell Biology, having authored 59 papers that have together received 3.2k indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (10 papers), Genomics and Rare Diseases (6 papers), Neutrophil, Myeloperoxidase and Oxidative Mechanisms (6 papers), Genomic variations and chromosomal abnormalities (5 papers), RNA modifications and cancer (4 papers), Hedgehog Signaling Pathway Studies (3 papers), melanin and skin pigmentation (3 papers) and Neurogenetic and Muscular Disorders Research (3 papers). The work is most often cited by research in Clinical Biochemistry (407 citations), Nephrology (302 citations), Genetics (764 citations), Molecular Biology (1.7k citations) and Biological Psychiatry (44 citations). Bénédicte Gérard has collaborated with scholars based in France, United Kingdom and Italy. Frequent co-authors include Jean‐Marie Saudubray, Agnès Rötig, Pierre Rustin, Arnold Münnich, Dominique Chrétien, Thomas Bourgeron, Bernard Grandchamp, Érick Denamur, Miroslav Radman and Ivan Matić. Their work appears in journals such as Human Mutation, European Journal of Pediatrics, British Journal of Haematology, Blood and Leukemia.

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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