Bérénice Herve

653 total citations
14 papers, 72 citations indexed

About

Bérénice Herve is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Bérénice Herve has authored 14 papers receiving a total of 72 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Genetics, 6 papers in Molecular Biology and 5 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Bérénice Herve's work include Genomic variations and chromosomal abnormalities (8 papers), Prenatal Screening and Diagnostics (4 papers) and Chromosomal and Genetic Variations (3 papers). Bérénice Herve is often cited by papers focused on Genomic variations and chromosomal abnormalities (8 papers), Prenatal Screening and Diagnostics (4 papers) and Chromosomal and Genetic Variations (3 papers). Bérénice Herve collaborates with scholars based in France, Italy and United Kingdom. Bérénice Herve's co-authors include François Vialard, Denise Molina‐Gomes, Delphine Fauvert, Thibaud Quibel, J. Roume, Patrice Clément, Guillaume Legendre, D. Subtil, J. Nizard and Marianne Till and has published in prestigious journals such as Gene, European Journal of Human Genetics and European Journal of Obstetrics & Gynecology and Reproductive Biology.

In The Last Decade

Bérénice Herve

14 papers receiving 59 citations

Peers

Countries citing papers authored by Bérénice Herve

Since Specialization

Citations

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

Fields of papers citing papers by Bérénice Herve

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Bérénice Herve

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

All Works

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14 of 14 papers shown

#	Work	Indexed citations
1	From Dominant Assumptions to Recessive Trait: Rethinking BMP15 in Ovarian Dysfunction 2025 ·Reproductive Sciences ·Bérénice Herve, (unknown), (unknown), (unknown), (unknown), (unknown), Deirdre A. Hill, (unknown), (unknown), (unknown), Anne Bachelot, Jean‐Michel Dupont, Sophie Christin‐Maître, Geneviève Plu‐Bureau, Thierry Bienvenu	1
2	The clinical value of optical genome mapping in the rapid characterization of RB1 duplication and 15q23q24.2 triplication, for more appropriate prenatal genetic counselling 2024 ·Molecular Genetics & Genomic Medicine ·(unknown), Denise Molina‐Gomes, (unknown), Bérénice Herve, (unknown), (unknown), (unknown), Marion Gauthier‐Villars, Valérie Serazin, Thibaud Quibel, Rodolphe Dard, François Vialard	2
3	Revisiting GDF9 variants in primary ovarian insufficiency: A shift from dominant to recessive pathogenicity? 2024 ·Gene ·(unknown), (unknown), Bérénice Herve, (unknown), Valérie Bernard, (unknown), (unknown), Aude Brac de la Perrière, Virginie Grouthier, (unknown), Philippe Touraine, Corinne Fouveaut, Geneviève Plu‐Bureau, Jean‐Michel Dupont, Anne Bachelot, Sophie Christin‐Maître, Thierry Bienvenu	1
4	2p25.3 microduplications involving MYT1L: further phenotypic characterization through an assessment of 16 new cases and a literature review 2023 ·European Journal of Human Genetics ·(unknown), Matthieu Egloff, Jonathan Lévy, Nicolas Chatron, Laura Bernardini, Gwenaël Le Guyader, Anne‐Claude Tabet, Caroline Schluth‐Bolard, Francesco Brancati, Maria Grazia Giuffrida, Rodolphe Dard, (unknown), (unknown), François Vialard, Bérénice Herve	1
5	Effects of the implementation of second-line prenatal cell-free DNA testing on termination of pregnancy in a French perinatal network 2021 ·European Journal of Obstetrics & Gynecology and Reproductive Biology ·(unknown), Rodolphe Dard, Bérénice Herve, Camille Cohen, François Vialard, Thibaud Quibel	1
6	A high level of tetrasomy 9p mosaicism but no clinical manifestations other than moderate oligozoospermia with chromosomally balanced sperm: a case report 2020 ·Journal of Assisted Reproduction and Genetics ·(unknown), Bérénice Herve, (unknown), (unknown), François Vialard, Marine Poulain	6
7	Prenatal findings in 1p36 deletion syndrome: New cases and a literature review 2019 ·Prenatal Diagnosis ·(unknown), Claire Bénéteau, Sylvia Redon, Céline Dupont, Chantal Missirian, (unknown), Bérénice Herve, (unknown), Nathalie Douet‐Guilbert, Marianne Till, Anne‐Claude Tabet, Kamran Moradkhani, Valérie Malan, (unknown), François Vialard	11
8	First prenatal diagnosis of a ‘pure’ 9q34.3 deletion (Kleefstra syndrome): A case report and literature review 2017 ·Journal of obstetrics and gynaecology research ·(unknown), Bérénice Herve, Julie Rivière, Delphine Fauvert, Patrice Clément, François Vialard	7
9	The emerging microduplication 3q13.31: Expanding the genotype-phenotype correlations of the reciprocal microdeletion 3q13.31 syndrome 2016 ·European Journal of Medical Genetics ·Bérénice Herve, Delphine Fauvert, Rodolphe Dard, J. Roume, (unknown), Didier Goidin, (unknown), Denise Molina‐Gomes, François Vialard	4
10	DNA ligase IV deficiency: Immunoglobulin class deficiency depends on the genotype 2016 ·Pediatric Allergy and Immunology ·Rodolphe Dard, Bérénice Herve, Thierry Leblanc, Jean‐Pierre de Villartay, Laura C. Collopy, (unknown), Séverine Drunat, (unknown), (unknown), Pierre‐François Souchon, (unknown), (unknown), (unknown), Alain Verloès, Martine Doco‐Fenzy	5
11	Low-level mosaicism of a de novo derivative chromosome 9 from a t(5;9)(q35.1;q34.3) has a major phenotypic impact 2015 ·European Journal of Medical Genetics ·Bérénice Herve, J. Roume, (unknown), Delphine Fauvert, Denise Molina‐Gomes, François Vialard	7
12	Are de novo rea(21;21) chromosomes really de novo? 2015 ·Clinical Case Reports ·Bérénice Herve, Thibaud Quibel, (unknown), (unknown), Denise Molina‐Gomes, François Vialard	17
13	Fausses couches précoces « à répétition » : bilan et prise en charge 2014 ·Journal de gynécologie, obstétrique et biologie de la reproduction. Supplément ·V. Gallot, (unknown), P. Capmas, Guillaume Legendre, (unknown), D. Subtil, J. Nizard, (unknown), X. Deffieux, Bérénice Herve, François Vialard	8
14	Gravité et transport de masse dans les mélanges liquides 2001 ·Journal de Physique IV (Proceedings) ·Jean Colombani, Bérénice Herve, Julien Bert	1

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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