Bénédicte Duban‐Bedu

1.9k citations

12 papers · 214 indexed · h-index 10

Co-authors: Bruno Delobel Joris Andrieux Sonia Bouquillon Sylvie Manouvrier‐Hanu Florence Petit Julie Vogt Alisdair McNeill Charu Deshpande
Topics: Genomic variations and chromosomal abnormalities (7 papers)Genetics and Neurodevelopmental Disorders (5 papers)Congenital heart defects research (4 papers)
Cited by: Genetics Pediatrics, Perinatology and Child Health Molecular Biology
Journals: PLoS Genetics Obesity Human Genetics
Partner nations: France United Kingdom United States

In The Last Decade

Bénédicte Duban‐Bedu

12 papers receiving 167 citations

Peers

Countries citing papers authored by Bénédicte Duban‐Bedu

Since Specialization

Citations

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

Fields of papers citing papers by Bénédicte Duban‐Bedu

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Bénédicte Duban‐Bedu

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

All Works

Sort: Min cites: Since: Top N: Style:

12 of 12 papers shown

#	Work	Indexed citations
1	Neurodevelopmental phenotype associated with CHD8-SUPT16H duplication 2019 ·Neurogenetics ·Thomas Smol,C. Thuillier,(unknown),Anne Dieux‐Coëslier,Bénédicte Duban‐Bedu,Roseline Caumes,Sonia Bouquillon,Sylvie Manouvrier‐Hanu,Catherine Roche‐Lestienne,Jamal Ghoumid	9
2	A heterozygous microdeletion of 20q13.13 encompassing ADNP gene in a child with Helsmoortel–van der Aa syndrome 2018 ·European Journal of Human Genetics ·(unknown),(unknown),(unknown),C. Thuillier,Bruno Delobel,Bénédicte Duban‐Bedu,(unknown)	8
3	MYT1L mutations cause intellectual disability and variable obesity by dysregulating gene expression and development of the neuroendocrine hypothalamus 2017 ·PLoS Genetics ·Patricia Blanchet,Martina Bebin,(unknown),Gregory M. Cooper,Michelle L. Thompson,Bénédicte Duban‐Bedu,Bénédicte Gérard,Amélie Piton,(unknown),Charu Deshpande,Virginia Clowes,Julie Vogt,Peter D. Turnpenny,Michael P. Williamson,Yves Alembik,Eric Glasgow,Alisdair McNeill	49
4	Chromosome 22q12.1 microdeletions: confirmation of the MN1 gene as a candidate gene for cleft palate 2015 ·European Journal of Human Genetics ·Jeroen Breckpot,Britt‐Marie Anderlid,Yasemin Alanay,Moira Blyth,(unknown),Bénédicte Duban‐Bedu,(unknown),Helen V. Firth,M. Cengiz Yakıcıer,Greet Hens,Maissa Rayyan,Eric Legius,Joris Vermeesch,Koenraad Devriendt	20
5	Molecular and clinical analyses of 16q24.1 duplications involving FOXF1 identify an evolutionarily unstable large minisatellite 2014 ·BMC Medical Genetics ·Avinash V. Dharmadhikari,Tomasz Gambin,Przemysław Szafrański,Wenjian Cao,Frank J. Probst,Weihong Jin,Ping Fang,Krzysztof Gogolewski,Anna Gambin,(unknown),Sailaja Golla,(unknown),Bénédicte Duban‐Bedu,Bruno Delobel,Joris Andrieux,Kerstin Becker,Elke Holinski‐Feder,Sau Wai Cheung,Paweł Stankiewicz	21
6	Identification of two novel loss-of-function SIM1 mutations in two overweight children with developmental delay 2014 ·Obesity ·(unknown),Anne Raimondo,Bruno Delobel,Bénédicte Duban‐Bedu,(unknown),Aurélie Dechaume,David C. Bersten,Stephen Eyre,Murray L. Whitelaw,Philippe Froguel,Amélie Bonnefond	14
7	Trichoépithéliomes multiples familiaux : nouvelle mutation du gène CYLD 2013 ·Annales de Dermatologie et de Vénéréologie ·(unknown),(unknown),(unknown),Bénédicte Duban‐Bedu,(unknown),P. Modiano	3
8	Genotype–phenotype analysis of 18q12.1-q12.2 copy number variation in autism 2013 ·European Journal of Medical Genetics ·Peter Wang,Prescilla Carrion,Ying Qiao,Christine Tyson,Monica Hrynchak,Kristina Calli,Elena Lopez‐Rangel,Joris Andrieux,Bruno Delobel,Bénédicte Duban‐Bedu,Ann‐Charlotte Thuresson,Göran Annerén,Xudong Liu,Evica Rajcan‐Separovic,M. E. Suzanne Lewis	18
9	High resolution mapping of OCA2 intragenic rearrangements and identification of a founder effect associated with a deletion in Polish albino patients 2010 ·Human Genetics ·Caroline Rooryck,Fanny Morice‐Picard,Eulalie Lasseaux,Dorothée Cailley,Hélène Dollfus,(unknown),Bénédicte Duban‐Bedu,Thomy de Ravel,Alain Taı̈eb,Didier Lacombe,Benoı̂t Arveiler	12
10	A 5.3 Mb deletion in chromosome 18q12.3 as the smallest region of overlap in two patients with expressive speech delay 2010 ·European Journal of Medical Genetics ·Sonia Bouquillon,Joris Andrieux,Emilie Landais,Bénédicte Duban‐Bedu,(unknown),(unknown),Louis Vallée,Teresinha Leal,Martine Doco‐Fenzy,Bruno Delobel	21
11	Trisomy 7 mosaicism prenatally misdiagnosed and maternal uniparental disomy in a child with pigmentary mosaicism and Russell– Silver syndrome 2010 ·Clinical Genetics ·Florence Petit,Muriel Holder‐Espinasse,Bénédicte Duban‐Bedu,Sonia Bouquillon,Odile Boute‐Bénéjean,Anne Bazin,(unknown),Sylvie Manouvrier‐Hanu,B Delobel	28
12	Characterization by array-CGH of an interstitial de novo tandem 6p21.2p22.1 duplication in a boy with epilepsy and developmental delay 2008 ·European Journal of Medical Genetics ·Joris Andrieux,Steven Richebourg,Bénédicte Duban‐Bedu,Florence Petit,Frédéric Leprêtre,Sylvie Sukno,(unknown),Bruno Delobel	11

About Bénédicte Duban‐Bedu

Bénédicte Duban‐Bedu is a scholar working on Genetics, Genetics and Dermatology, having authored 12 papers that have together received 214 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (7 papers), Genetics and Neurodevelopmental Disorders (5 papers) and Congenital heart defects research (4 papers). The work is most often cited by research in Genetics (154 citations), Pediatrics, Perinatology and Child Health (39 citations) and Molecular Biology (93 citations). Bénédicte Duban‐Bedu has collaborated with scholars based in France, United Kingdom and United States. Frequent co-authors include Bruno Delobel, Joris Andrieux, Sonia Bouquillon, Sylvie Manouvrier‐Hanu, Florence Petit, Julie Vogt, Alisdair McNeill, Charu Deshpande, Bénédicte Gérard and B Delobel. Their work appears in journals such as PLoS Genetics, Obesity and Human Genetics.

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.

Explore authors with similar magnitude of impact