Chrystel Leroy

843 total citations
9 papers, 337 citations indexed

About

Chrystel Leroy is a scholar working on Molecular Biology, Genetics and Genetics. According to data from OpenAlex, Chrystel Leroy has authored 9 papers receiving a total of 337 indexed citations (citations by other indexed papers that have themselves been cited), including 3 papers in Molecular Biology, 3 papers in Genetics and 2 papers in Genetics. Recurrent topics in Chrystel Leroy's work include Genomics and Rare Diseases (2 papers), Hypothalamic control of reproductive hormones (2 papers) and Cystic Fibrosis Research Advances (2 papers). Chrystel Leroy is often cited by papers focused on Genomics and Rare Diseases (2 papers), Hypothalamic control of reproductive hormones (2 papers) and Cystic Fibrosis Research Advances (2 papers). Chrystel Leroy collaborates with scholars based in France, Switzerland and Réunion. Chrystel Leroy's co-authors include Corinne Fouveaut, Catherine Dodé, Jean‐Pierre Hardelin, Asma Chaoui, Véronique Pingault, Séverine Marcos, Delphine Dupin‐Deguine, Jérôme Bertherat, Jacques Young and Sandrine Marlin and has published in prestigious journals such as Scientific Reports, The American Journal of Human Genetics and European Journal of Endocrinology.

In The Last Decade

Chrystel Leroy

9 papers receiving 328 citations

Peers

Countries citing papers authored by Chrystel Leroy

Since Specialization

Citations

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

Fields of papers citing papers by Chrystel Leroy

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Chrystel Leroy

This figure shows the co-authorship network connecting the top 25 collaborators of Chrystel Leroy. A scholar is included among the top collaborators of Chrystel Leroy 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 Chrystel Leroy. Chrystel Leroy is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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9 of 9 papers shown

#	Work	Indexed citations
1	Evaluation of a saliva molecular point of care for the detection of SARS-CoV-2 in ambulatory care 2021 ·Scientific Reports ·Jérôme LeGoff, Solen Kernéis, Caroline Elie, Séverine Mercier‐Delarue, Nabil Gastli, Laure Choupeaux, Jacques Fourgeaud, (unknown), P. Quentin, Juliette Pavie, Patricia Brazille, (unknown), (unknown), Audrey Gabassi, Chrystel Leroy, Béatrice Parfait, Jean‐Marc Tréluyer, Constance Delaugerre	16
2	Phenotypic Variability in a Family with Acrodysostosis Type 2 Caused by a Novel PDE4D Mutation Affecting the Serine Target of Protein Kinase-A Phosphorylation 2017 ·Journal of Clinical Research in Pediatric Endocrinology ·(unknown), Julia Gesing, Caroline Silve, Chrystel Leroy, Astrid Bertsche, W. Hirsch, Wieland Kieß, Roland Pfäffle, Volker Schuster	5
3	Neurofibromatosis type 1 molecular diagnosis: what can NGS do for you when you have a large gene with loss of function mutations? 2014 ·European Journal of Human Genetics ·Éric Pasmant, Béatrice Parfait, Armelle Luscan, P. Goussard, Audrey Briand‐Suleau, Ingrid Laurendeau, Corinne Fouveaut, Chrystel Leroy, (unknown), P. Wolkenstein, Michel Vidaud, Dominique Vidaud	75
4	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
5	Greater prevalence of PROKR2 mutations in Kallmann syndrome patients from the Maghreb than in European patients 2013 ·European Journal of Endocrinology ·Julie Sarfati, Corinne Fouveaut, Chrystel Leroy, Marc Jeanpierre, Jean‐Pierre Hardelin, Catherine Dodé	24
6	Loss-of-Function Mutations in SOX10 Cause Kallmann Syndrome with Deafness 2013 ·The American Journal of Human Genetics ·Véronique Pingault, (unknown), Viviane Baral, Séverine Marcos, Yuli Watanabe, Asma Chaoui, Corinne Fouveaut, Chrystel Leroy, O. Vérier‐Mine, Christine Francannet, Delphine Dupin‐Deguine, F. Archambeaud, (unknown), Jacques Young, Jérôme Bertherat, Sandrine Marlin, Michel Goossens, Jean‐Pierre Hardelin, Catherine Dodé, Nadège Bondurand	142
7	Biallelic mutations in the prokineticin-2 gene in two sporadic cases of Kallmann syndrome 2008 ·European Journal of Human Genetics ·Chrystel Leroy, Corinne Fouveaut, (unknown), Sébastien Jacquemont, Hélène Du Boullay, James Lespinasse, Marc Delpech, Jean‐Michel Dupont, Jean‐Pierre Hardelin, Catherine Dodé	44
8	ENaCβ and γ genes as modifier genes in cystic fibrosis 2007 ·Journal of Cystic Fibrosis ·(unknown), Chrystel Leroy, D. Hubert, Isabelle Fajac, Thierry Bienvenu	14
9	A Frequent Large Rearrangement in the CFTR Gene in Cystic Fibrosis Patients from Reunion Island 2006 ·Genetic Testing ·Juliette Nectoux, (unknown), (unknown), Chrystel Leroy, Odile Raguénès, Claude Férec, (unknown), (unknown), Michel Renouil, François Cartault, T. Bienvenu	3

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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