Brigitte Benzacken

3.1k total citations
61 papers, 1.3k citations indexed

About

Brigitte Benzacken is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Brigitte Benzacken has authored 61 papers receiving a total of 1.3k indexed citations (citations by other indexed papers that have themselves been cited), including 41 papers in Genetics, 33 papers in Molecular Biology and 22 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Brigitte Benzacken's work include Genomic variations and chromosomal abnormalities (28 papers), Prenatal Screening and Diagnostics (18 papers) and Chromosomal and Genetic Variations (11 papers). Brigitte Benzacken is often cited by papers focused on Genomic variations and chromosomal abnormalities (28 papers), Prenatal Screening and Diagnostics (18 papers) and Chromosomal and Genetic Variations (11 papers). Brigitte Benzacken collaborates with scholars based in France, United Kingdom and Italy. Brigitte Benzacken's co-authors include Alain Verloès, Eva Pipiras, Nathalie Sermondade, Céline Dupont, Rachel Lévy, C. Sifer, JP Siffroi, Anne‐Claude Tabet, Isabelle Cédrin‐Durnerin and Azzedine Aboura and has published in prestigious journals such as The Journal of Clinical Endocrinology & Metabolism, Neurology and Human Reproduction.

In The Last Decade

Brigitte Benzacken

59 papers receiving 1.2k citations

Peers

Countries citing papers authored by Brigitte Benzacken

Since Specialization

Citations

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

Fields of papers citing papers by Brigitte Benzacken

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Brigitte Benzacken

This figure shows the co-authorship network connecting the top 25 collaborators of Brigitte Benzacken. A scholar is included among the top collaborators of Brigitte Benzacken 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 Brigitte Benzacken. Brigitte Benzacken 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	New evidence that biallelic loss of function in EEF1B2 gene leads to intellectual disability 2019 ·Clinical Genetics ·Lise Larcher, Julien Buratti, (unknown), Brigitte Benzacken, Eva Pipiras, Boris Keren, Andrée Delahaye‐Duriez	7
2	EFNB2haploinsufficiency causes a syndromic neurodevelopmental disorder 2018 ·Clinical Genetics ·Jonathan Lévy, Damien Haye, Nicola Marziliano, Gavino Casu, Fabien Guimiot, Céline Dupont, N. Teissier, Brigitte Benzacken, Pierre Gressèns, Eva Pipiras, Alain Verloès, Anne‐Claude Tabet	19
3	NR4A2 haploinsufficiency is associated with intellectual disability and autism spectrum disorder 2018 ·Clinical Genetics ·Jonathan Lévy, Sarah Grotto, Cyril Mignot, A. Maruani, Andrée Delahaye‐Duriez, Brigitte Benzacken, Boris Keren, Damien Haye, (unknown), (unknown), (unknown), Alain Verloès, Céline Dupont, Eva Pipiras, Anne‐Claude Tabet	25
4	Molecular and clinical delineation of 2p15p16.1 microdeletion syndrome 2017 ·American Journal of Medical Genetics Part A ·Jonathan Lévy, Aurélie Coussement, Céline Dupont, Fabien Guimiot, Clarisse Baumann, Géraldine Viot, Sandrine Passemard, Yline Capri, Séverine Drunat, Alain Verloès, Eva Pipiras, Brigitte Benzacken, Jean‐Michel Dupont, Anne‐Claude Tabet	15
5	De novo deletion of TBL1XR1 in a child with non‐specific developmental delay supports its implication in intellectual disability 2014 ·American Journal of Medical Genetics Part A ·Anne‐Claude Tabet, (unknown), Céline Dupont, (unknown), (unknown), (unknown), Nathalie Pouvreau, Jean‐François Gadisseux, Brigitte Benzacken, Alain Verloès	24
6	Autism multiplex family with 16p11.2p12.2 microduplication syndrome in monozygotic twins and distal 16p11.2 deletion in their brother 2012 ·European Journal of Human Genetics ·Anne‐Claude Tabet, Marion Pilorge, Richard Delorme, Frédérique Amsellem, Jean-Marc Pinard, Marion Leboyer, Alain Verloès, Brigitte Benzacken, Catalina Betancur	33
7	Nail and phalangeal agenesis in a patient with 4pter and 9pter duplication 2012 ·American Journal of Medical Genetics Part A ·Jérôme Rambaud, Isabelle Marey, Céline Dupont, (unknown), Yline Capri, Anne Claude Tabet, Brigitte Benzacken, Alain Verloès, Azzedine Aboura, Marion Gérard	2
8	Pre‐ and postnatal phenotype of 6p25 deletions involving the FOXC1 gene 2012 ·American Journal of Medical Genetics Part A ·Andrée Delahaye‐Duriez, Suonavy Khung‐Savatovsky, Azzedine Aboura, Fabien Guimiot, Séverine Drunat, Jean‐Luc Alessandri, Marion Gérard, Pierre Bitoun, (unknown), Stéphanie Robin, C. Huel, (unknown), Stéphane Serero, Pierre Gressèns, Jacques Élion, Alain Verloès, Brigitte Benzacken, Anne‐Lise Delezoide, Eva Pipiras	37
9	Issue de la vitrification des embryons précoces versus congélation lente. Rapport de la première naissance française 2011 ·Gynécologie Obstétrique & Fertilité ·C. Sifer, Nathalie Sermondade, Christophe Dupont, C. Poncelet, Isabelle Cédrin‐Durnerin, Jean‐Noël Hugues, Brigitte Benzacken, Rachel Lévy	16
10	Successful childbirth after intracytoplasmic morphologically selected sperm injection without assisted oocyte activation in a patient with globozoospermia 2011 ·Human Reproduction ·Nathalie Sermondade, (unknown), Charlotte Dupont, Shaliha Bechoua, Carlos Palacios, Florence Eustache, C. Poncelet, Brigitte Benzacken, Rachel Lévy, C. Sifer	62
11	À la recherche d’une étiologie génétique chez les hommes infertiles 2010 ·Rachel Lévy, Nathalie Sermondade, (unknown), (unknown), Brigitte Benzacken, Isabelle Aknin‐Seifer	0
12	Abnormal muscle development of the diaphragm in a fetus with 2p14–p16 duplication 2009 ·American Journal of Medical Genetics Part A ·(unknown), Fabien Guimiot, Anne‐Claude Tabet, Suonavy Khung‐Savatovsky, (unknown), (unknown), Brigitte Benzacken, Alain Verloès, Jean‐François Oury, Anne‐Lise Delezoide, Azzedine Aboura	3
13	Ectodermal dysplasia‐like syndrome with mental retardation due to contiguous gene deletion: Further clinical and molecular delineation of del(2q32) syndrome 2009 ·American Journal of Medical Genetics Part A ·(unknown), (unknown), Anne‐Claude Tabet, Isabelle Bailleul‐Forestier, Brigitte Benzacken, Séverine Drunat, (unknown), Sandrine Passemard, Alain Verloès, Azzedine Aboura	24
14	Partial trisomy of chromosome 22 resulting from a supernumerary marker chromosome 22 in a child with features of cat eye syndrome 2008 ·American Journal of Medical Genetics Part A ·(unknown), Marion Gérard‐Blanluet, Stéphane Serero, (unknown), Clarisse Baumann, Marie‐Line Jacquemont, Céline Dupont, (unknown), Séverine Drunat, (unknown), (unknown), Brigitte Benzacken, Alain Verloès, Anne‐Claude Tabet, Azzedine Aboura	9
15	Molecular cytogenetic characterization of terminal 14q32 deletions in two children with an abnormal phenotype and corpus callosum hypoplasia 2008 ·European Journal of Human Genetics ·Anouck Schneider, Brigitte Benzacken, Agnès Guichet, Alain Verloès, Dominique Bonneau, Nathalie Collot, (unknown), Michel Goossens, Laurence Taine, Emilie Landais, Dominique Gaillard, Martine Doco‐Fenzy	21
16	Blepharophimosis‐mental retardation (BMR) syndromes: A proposed clinical classification of the so‐called Ohdo syndrome, and delineation of two new BMR syndromes, one X‐linked and one autosomal recessive 2006 ·American Journal of Medical Genetics Part A ·Alain Verloès, Dominique Brémond‐Gignac, Bertrand Isidor, Albert David, Clarisse Baumann, M Leroy, René Stevens, Y. Gillerot, Delphine Héron, Bénédicte Héron, Brigitte Benzacken, Didier Lacombe, Han G. Brunner, Pierre Bitoun	52
17	A New Cause of Congenital Blindness: Adenylosuccinase Lyase Deficiency 2003 ·Investigative Ophthalmology & Visual Science ·Isabelle Carchon, Pierre Bitoun, (unknown), Brigitte Benzacken, (unknown), Joseph Bursztyn, J. Gaudelus, Bénédicte Héron	0
18	Acrocentric chromosome polymorphisms: beware of cryptic translocations 2001 ·Prenatal Diagnosis ·Brigitte Benzacken, (unknown), Jean Pierre Siffroi, (unknown), (unknown), Jean Philippe Wolf	7
19	Advanced paternal age and de-novo complex chromosomal rearrangement in offspring 1998 ·Human Reproduction ·Brigitte Benzacken, Jean Pierre Siffroi, Bernd F. Straub, (unknown), (unknown), J. Gaudelus, J. P. Dadoune, Jean Philippe Wolf	5
20	PRENATAL DIAGNOSIS OF ROBERTS SYNDROME: TWO NEW CASES 1996 ·Prenatal Diagnosis ·Brigitte Benzacken, (unknown), Sylvie Manouvrier, Martine Bucourt, (unknown)	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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