Bérénice Doray

5.2k total citations
52 papers, 1.2k citations indexed

About

Bérénice Doray is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Bérénice Doray has authored 52 papers receiving a total of 1.2k indexed citations (citations by other indexed papers that have themselves been cited), including 24 papers in Molecular Biology, 23 papers in Genetics and 19 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Bérénice Doray's work include Prenatal Screening and Diagnostics (11 papers), Genomic variations and chromosomal abnormalities (11 papers) and Renal and related cancers (6 papers). Bérénice Doray is often cited by papers focused on Prenatal Screening and Diagnostics (11 papers), Genomic variations and chromosomal abnormalities (11 papers) and Renal and related cancers (6 papers). Bérénice Doray collaborates with scholars based in France, Réunion and Canada. Bérénice Doray's co-authors include Elisabeth Flori, R. Favre, Françoise Girard‐Lemaire, B. Viville, B. Langer, Claude Stoll, Michel Dreyfus, Valérie Cormier‐Daire, Alice Goldenberg and Bernard Gasser and has published in prestigious journals such as New England Journal of Medicine, International Journal of Molecular Sciences and PLoS Biology.

In The Last Decade

Bérénice Doray

48 papers receiving 1.2k citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Bérénice Doray France 18 640 540 319 237 83 52 1.2k
Beate Albrecht Germany 23 1.0k 1.6× 862 1.6× 264 0.8× 214 0.9× 83 1.0× 45 1.7k
Robert Wallerstein United States 17 399 0.6× 410 0.8× 180 0.6× 140 0.6× 50 0.6× 66 924
Mariluce Riegel Switzerland 21 826 1.3× 523 1.0× 434 1.4× 161 0.7× 60 0.7× 86 1.5k
Donald Basel United States 17 717 1.1× 486 0.9× 188 0.6× 168 0.7× 193 2.3× 68 1.3k
Yolande van Bever Netherlands 18 441 0.7× 297 0.6× 191 0.6× 218 0.9× 56 0.7× 46 871
Emma Wakeling United Kingdom 19 903 1.4× 887 1.6× 543 1.7× 135 0.6× 62 0.7× 69 1.4k
Y. Gillerot Belgium 22 616 1.0× 740 1.4× 426 1.3× 334 1.4× 176 2.1× 74 1.8k
Frank Majewski Germany 16 755 1.2× 579 1.1× 271 0.8× 200 0.8× 99 1.2× 26 1.3k
Valérie Malan France 20 923 1.4× 733 1.4× 333 1.0× 135 0.6× 33 0.4× 69 1.4k
Christl Vermeij‐Keers Netherlands 22 727 1.1× 699 1.3× 210 0.7× 459 1.9× 116 1.4× 61 1.7k

Countries citing papers authored by Bérénice Doray

Since Specialization
Citations

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

Fields of papers citing papers by Bérénice Doray

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Bérénice Doray

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

All Works

20 of 20 papers shown
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Doray, Bérénice, et al.. (2024). Revue systématique des thérapeutiques psychomotrices validées pour les enfants présentant un trouble du spectre de l’alcoolisation fœtale. Neuropsychiatrie de l Enfance et de l Adolescence. 72(3). 135–143.
3.
4.
Jacquemont, Marie‐Line, Françoise Darcel, Jean‐Luc Alessandri, et al.. (2020). High prevalence of Bardet‐Biedl syndrome in La Réunion Island is due to a founder variant in ARL6/BBS3. Clinical Genetics. 98(2). 166–171. 11 indexed citations
5.
Baer, Sarah, Cathy Obringer, Sophie Julia, et al.. (2020). Early‐onset nucleotide excision repair disorders with neurological impairment: Clues for early diagnosis and prognostic counseling. Clinical Genetics. 98(3). 251–260. 11 indexed citations
6.
Van‐Gils, Julien, Sophie Naudion, Jérôme Toutain, et al.. (2019). Fetal phenotype of Rubinstein‐Taybi syndrome caused by CREBBP mutations. Clinical Genetics. 95(3). 420–426. 8 indexed citations
7.
Gervasini, Cristina, Silvia Russo, Anna Cereda, et al.. (2013). Cornelia de Lange individuals with new and recurrent SMC1A mutations enhance delineation of mutation repertoire and phenotypic spectrum. American Journal of Medical Genetics Part A. 161(11). 2909–2919. 24 indexed citations
8.
Fradin, Mélanie, Bernard Aral, Jean Muller, et al.. (2013). Long-Term Follow-Up and Molecular Characterization of a Patient with a RECQL4 Mutation Spectrum Disorder. Dermatology. 226(4). 353–357. 8 indexed citations
9.
Lopez, Estelle, Patrick Callier, Valérie Cormier‐Daire, et al.. (2012). Search for a gene responsible for Floating‐Harbor syndrome on chromosome 12q15q21.1. American Journal of Medical Genetics Part A. 158A(2). 333–339. 6 indexed citations
10.
Dheu, Céline, Bérénice Doray, S. Soskin, et al.. (2009). Frasier syndrome, a potential cause of end-stage renal failure in childhood. Pediatric Nephrology. 25(3). 549–552. 11 indexed citations
11.
Amor-Guéret, Mounira, Anthony Laugé, Rosine Onclercq-Delic, et al.. (2008). Three New BLM Gene Mutations Associated with Bloom Syndrome. Genetic Testing. 12(2). 257–261. 11 indexed citations
12.
Bloch, Juliette, Christine Cans, C. De Vigan, et al.. (2008). Faisabilité de la surveillance du syndrome d’alcoolisation fœtale (SAF). Archives de Pédiatrie. 15(5). 507–509. 4 indexed citations
13.
Flori, Elisabeth, Valérie Biancalana, Françoise Girard‐Lemaire, et al.. (2003). Difficulties of genetic counseling and prenatal diagnosis in a consanguineous couple segregating for the same translocation (14;15) (q11;q13) and at risk for Prader–Willi and Angelman syndromes. European Journal of Human Genetics. 12(3). 181–186. 16 indexed citations
14.
Doray, Bérénice, Françoise Girard‐Lemaire, Bernard Gasser, et al.. (2002). Pallister‐Killian syndrome: difficulties of prenatal diagnosis. Prenatal Diagnosis. 22(6). 470–477. 53 indexed citations
15.
Schluth, C, Bérénice Doray, Françoise Girard‐Lemaire, et al.. (2002). Prenatal sonographic diagnosis of the 49,XXXXY syndrome. Prenatal Diagnosis. 22(13). 1177–1180. 12 indexed citations
16.
Doray, Bérénice, R. Favre, B. Viville, et al.. (2000). Prenatal sonographic diagnosis of skeletal dysplasias. A report of 47 cases. Annales de Génétique. 43(3-4). 163–169. 74 indexed citations
17.
Doray, Bérénice, et al.. (1999). Two cases of Townes-Brocks syndrome.. PubMed. 10(4). 359–67. 4 indexed citations
18.
Doray, Bérénice, et al.. (1999). Hereditary renal adysplasia in a three generations family.. PubMed. 10(3). 251–7. 17 indexed citations
19.
20.
Bard, H, et al.. (1980). Elective delivery and the neonatal respiratory distress syndrome.. PubMed. 122(3). 307–9. 3 indexed citations

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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