Catherine Dodé

9.5k total citations · 1 hit paper
92 papers, 4.7k citations indexed

About

Catherine Dodé is a scholar working on Molecular Biology, Reproductive Medicine and Genetics. According to data from OpenAlex, Catherine Dodé has authored 92 papers receiving a total of 4.7k indexed citations (citations by other indexed papers that have themselves been cited), including 58 papers in Molecular Biology, 27 papers in Reproductive Medicine and 19 papers in Genetics. Recurrent topics in Catherine Dodé's work include Inflammasome and immune disorders (27 papers), Hypothalamic control of reproductive hormones (23 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (11 papers). Catherine Dodé is often cited by papers focused on Inflammasome and immune disorders (27 papers), Hypothalamic control of reproductive hormones (23 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (11 papers). Catherine Dodé collaborates with scholars based in France, United States and Switzerland. Catherine Dodé's co-authors include Jean‐Pierre Hardelin, Marc Delpech, Jacques Young, Jean-Pierre Hardelin, Gilles Grateau, Christophe Pécheux, Rajagopal Krishnamoorthy, Philippe Rondard, Laurence Cuisset and Corinne Fouveaut and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Clinical Investigation and PLoS ONE.

In The Last Decade

Catherine Dodé

89 papers receiving 4.5k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

European Consensus Statement on congenital hypogonadotropic hypogonadism—pathogenesis, diagnosis and treatment

2015 528 citations Catherine Dodé, Jean-Pierre Hardelin et al. profile →

Peers

Countries citing papers authored by Catherine Dodé

Since Specialization

Citations

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

Fields of papers citing papers by Catherine Dodé

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Catherine Dodé

This figure shows the co-authorship network connecting the top 25 collaborators of Catherine Dodé. A scholar is included among the top collaborators of Catherine Dodé based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Catherine Dodé. Catherine Dodé is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	Reconsidering olfactory bulb magnetic resonance patterns in Kallmann syndrome 2017 ·Annales d Endocrinologie ·(unknown), (unknown), (unknown), Salem Hannoun, Gérald Raverot, Michel Pugeat, Aude Brac de la Perrière, V. Lapras, (unknown), Catherine Dodé, François Cotton	6
2	Defective signaling through plexin-A1 compromises the development of the peripheral olfactory system and neuroendocrine reproductive axis in mice 2017 ·Human Molecular Genetics ·Séverine Marcos, Carine Monnier, Xavier Rovira, Corinne Fouveaut, Nelly Pitteloud, Fabrice Ango, Catherine Dodé, Jean‐Pierre Hardelin	33
3	Custom oligonucleotide array-based CGH: a reliable diagnostic tool for detection of exonic copy-number changes in multiple targeted genes 2013 ·European Journal of Human Genetics ·(unknown), (unknown), (unknown), (unknown), Aurélie Toussaint, Chrystel Leroy, (unknown), (unknown), Nathalie Deburgrave, Yoann Saillour, (unknown), Corinne Fouveaut, Chérif Beldjord, Sophie Valleix, France Leturcq, Catherine Dodé, Thierry Bienvenu, Jamel Chelly, Mireille Cossée	14
4	Genetics of Kallmann syndrome 2010 ·Catherine Dodé, Jean‐Pierre Hardelin	1
5	Kallmann Syndrome Caused by Mutations in the <i>PROK2</i> and <i>PROKR2</i> Genes: Pathophysiology and Genotype-Phenotype Correlations 2010 ·Frontiers of hormone research ·Julie Sarfati, Catherine Dodé, Jacques Young	40
6	Kallmann syndrome 2008 ·European Journal of Human Genetics ·Catherine Dodé, Jean‐Pierre Hardelin	140
7	The Complex Genetics of Kallmann Syndrome: <i>KAL1, FGFR1, FGF8, PROKR2, PROK2</i>, et al. 2008 ·Sexual Development ·Jean-Pierre Hardelin, Catherine Dodé	113
8	Psychiatric and Cognitive Difficulties as Indicators of Juvenile Huntington Disease Onset in 29 Patients 2007 ·Archives of Neurology ·Pascale Ribaı̈, Karine Nguyen, Valérie Hahn‐Barma, Isabelle Gourfinkel‐An, Marie Vidailhet, (unknown), Catherine Dodé, Alexis Brice, Alexandra Dürr	94
9	Intestinal Pseudo-Obstruction as a Manifestation of Tumor Necrosis Factor Receptor–Associated Periodic Syndrome 2006 ·Digestive Diseases and Sciences ·I. Marie, F. Hervé, Catherine Dodé, (unknown), H. Lévesque	3
10	Clinical significance of P46L and R92Q substitutions in the tumour necrosis factor superfamily 1A gene 2006 ·Annals of the Rheumatic Diseases ·N. Ravet, S. Rouaghe, Catherine Dodé, (unknown), Jérôme Stirnemann, Pierre Lévy, Marc Delpech, G Grateau	109
11	Dramatic etanercept-induced remission of relapsing febrile sciatic neuralgia related to p46l mutation of the tnfrsf1a gene 2006 ·Clinical Rheumatology ·Jacques Serratrice, J. Serratrice, P. Disdier, Catherine Dodé, Pierre‐Jean Weiller	4
12	Infevers: An evolving mutation database for auto-inflammatory syndromes 2004 ·Human Mutation ·Isabelle Touitou, Suzanne Lesage, Michael McDermott, Laurence Cuisset, Hal M. Hoffman, Catherine Dodé, Nitza G. Shoham, Ebun Aganna, Jean‐Pierre Hugot, Carol A. Wise, Hans R. Waterham, D. Pugnère, Jacques Demaille, Cyril Sarrauste de Menthière	234
13	Fièvres intermittentes héréditaires 2004 ·La Presse Médicale ·Gilles Grateau, B. Granel, Véronique Hentgen, Catherine Dodé, Laurence Cuisset, Marc Delpech	4
14	TNFRSF1A-associated periodic syndrome (TRAPS), Muckle-Wells syndrome (MWS) and renal amyloidosis 2003 ·Journal of Nephrology ·Catherine Dodé, Laurence Cuisset, Marc Delpech, Gilles Grateau	20
15	Mutational spectrum in the MEFV and TNFRSF1A genes in patients suffering from AA amyloidosis and recurrent inflammatory attacks 2002 ·Nephrology Dialysis Transplantation ·Catherine Dodé	22
16	La fièvre méditerranéenne familiale 2001 ·Gilles Grateau, Catherine Dodé, Laurence Cuisset, (unknown)	3
17	Les maladies inflammatoires récurrentes héréditaires, en dehors de la fièvre méditerranéenne familiale 2001 ·Gilles Grateau, Laurence Cuisset, Catherine Dodé, (unknown)	2
18	Autosomal-dominant periodic fever with AA amyloidosis: Novel mutation in tumor necrosis factor receptor 1 gene Rapid Communication 2001 ·Kidney International ·Michel Jadoul, Catherine Dodé, Jean‐Pierre Cosyns, Daniel Abramowicz, Bernard Georges, Marc Delpech, Yves Pirson	33
19	MEFV-Gene Analysis in Armenian Patients with Familial Mediterranean Fever: Diagnostic Value and Unfavorable Renal Prognosis of the M694V Homozygous Genotype—Genetic and Therapeutic Implications 1999 ·The American Journal of Human Genetics ·Cécile Cazeneuve, Tamara Sarkisian, Christophe Pécheux, M Dervichian, Brigitte Nédelec, Philippe Reinert, (unknown), Jean‐Claude Kouyoumdjian, (unknown), Marc Delpech, Michel Goossens, Catherine Dodé, Gilles Grateau, Serge Amselem	203
20	Neurosensory Hearing Loss in Secondary Adhalinopathy 1996 ·Neuropediatrics ·Konrad Oexle, R. Herrmann, Catherine Dodé, France Leturcq, (unknown), Kaplan Jc, Yuji Mizuno, E Ozawa, Kevin P. Campbell, Thomas Voit	10

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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