Sylvain Briault

5.2k citations

64 papers · 3.1k · 2 hit papers · h-index 23

Impact in

Genetics top 1%
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
Developmental Neuroscience top 5%

Papers in

Genetics 47
- Genetics and Neurodevelopmental Disorders 39
- Genomic variations and chromosomal abnormalities 20
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 5
Molecular Biology 31
- Congenital heart defects research 7
- RNA modifications and cancer 6
- Retinal Development and Disorders 5

Co-authors: Claude Moraine (19 shared papers)Nathalie Ronce (12 shared papers)Frédéric Laumonnier (10 shared papers)Ben C.J. Hamel (3 shared papers)Martine Raynaud (10 shared papers)Jamel Chelly (5 shared papers)Jean‐Pierre Fryns (2 shared papers)Christian Andrés (4 shared papers)
Journals: Prenatal Diagnosis (4 papers)Experimental Eye Research (4 papers)European Journal of Human Genetics (3 papers)The American Journal of Human Genetics (2 papers)Frontiers in Behavioral Neuroscience (2 papers)
Partner nations: France United States Germany

In The Last Decade

Sylvain Briault

64 papers receiving 3.0k citations

Sylvain Briault's Hit Papers

align trajectories log scale

STING agonist diABZI induces PANoptosis and DNA mediated acute respiratory distress syndrome (ARDS) 2022 · 175 citations

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if any of the following hold:

it has ≥500 total citations;
it reaches ≥1.5× the top-1% citation threshold for papers in the same subfield and year (the threshold is the minimum needed to enter the top 1%, not the average within it);
it reaches the top citation threshold in at least one of its specific research topics.

2022 Cell Death and Disease
2004 The American Journal of Human Genetics

Peers

Countries citing papers authored by Sylvain Briault

Since Specialization

Citations

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

Fields of papers citing papers by Sylvain Briault

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside Sylvain Briault, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Sylvain Briault Line = papers co-authored together Sylvain Briault links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

Showing the 20 most-cited of 64 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	X-Linked Mental Retardation and Autism Are Associated with a Mutation in the NLGN4 Gene, a Member of the Neuroligin Family The American Journal of Human Genetics ·Frédéric Laumonnier, Frédérique Bonnet‐Brilhault, Marie Gomot, Romuald Blanc, Albert David, Marie‐Pierre Moizard, Martine Raynaud, Nathalie Ronce, Éric Lemonnier, Patrick Calvas, Béatrice Laudier, Jamel Chelly, Jean‐Pierre Fryns, Hans‐Hilger Ropers, Ben C.J. Hamel, Christian Andrés, Catherine Barthélémy, Claude Moraine, Sylvain Briault Hit paper breakdown →	2004	553
2	Oligophrenin-1 encodes a rhoGAP protein involved in X-linked mental retardation Nature ·Pierre Billuart, T Bienvenu, Nathalie Ronce, Vincent des Portes, Marie Claude Vinet, Ramzi Zemni, Hugues Roest Crollius, Alain Carrié, Fabien Fauchereau, Michele Cherry, Sylvain Briault, Ben C.J. Hamel, Jean‐Pierre Fryns, Chérif Beldjord, Axel Kahn, Claude Moraine, Jamel Chelly	1998	382
3	Transcription Factor SOX3 Is Involved in X-Linked Mental Retardation with Growth Hormone Deficiency The American Journal of Human Genetics ·Frédéric Laumonnier, Nathalie Ronce, Ben C.J. Hamel, Paul Q. Thomas, James Lespinasse, Martine Raynaud, Christine Paringaux, Hans van Bokhoven, Vera M. Kalscheuer, Jean‐Pierre Fryns, Jamel Chelly, Claude Moraine, Sylvain Briault	2002	232
4	STING agonist diABZI induces PANoptosis and DNA mediated acute respiratory distress syndrome (ARDS) Cell Death and Disease ·Yasmine Messaoud‐Nacer, Elodie Culerier, Stéphanie Rose, Isabelle Maillet, Nathalie Rouxel, Sylvain Briault, Bernhard Ryffel, Valérie Quesniaux, Dieudonnée Togbe Hit paper breakdown →	2022	175
5	Chromosomal factors of infertility in candidate couples for ICSI: an equal risk of constitutional aberrations in women and men* Human Reproduction ·Jean Gekas, F. Thépot, C Turleau, JP Siffroi, J. P. Dadoune, Sylvain Briault, Marlène Rio, G Bourouillou, F. Carré‐Pigeon, Richard Wasels, Brigitte Benzacken	2001	172
6	Homozygous silencing of T-box transcription factor EOMES leads to microcephaly with polymicrogyria and corpus callosum agenesis Nature Genetics ·Lekbir Baala, Sylvain Briault, Heather Etchevers, Frédéric Laumonnier, Abdelhafid Natiq, Jeanne Amiel, Nathalie Boddaert, Capucine Pïcard, Aziza Sbiti, A. Asermouh, Tania Attié‐Bitach, Férechté Encha‐Razavi, Arnold Münnich, Abdelaziz Sefiani, Stanislas Lyonnet	2007	148
7	Nuclear envelope alterations in fibroblasts from patients with muscular dystrophy, cardiomyopathy, and partial lipodystrophy carrying lamin A/C gene mutations Muscle & Nerve ·Antoine Muchir, Jacques Médioni, M. Laluc, Catherine Massart, Takuro Arimura, Anneke J. van der Kooi, Isabelle Desguerre, M. Mayer, Xavier Ferrer, Sylvain Briault, Michio Hirano, Howard J. Worman, Audrey Mallet, Manfred Wehnert, K Schwartz, Gisèle Bonne	2004	139
8	Truncating Neurotrypsin Mutation in Autosomal Recessive Nonsyndromic Mental Retardation Science ·Florence Molinari, Marlène Rio, Virginia Meskenaïte, Férechté Encha-Razavi, Joëlle Augé, Delphine Bacq, Sylvain Briault, Michel Vekemans, Arnold Münnich, Tania Attié‐Bitach, P. Sonderegger, Laurence Colleaux	2002	138
9	Association of a Functional Deficit of the BK _Ca Channel, a Synaptic Regulator of Neuronal Excitability, With Autism and Mental Retardation American Journal of Psychiatry ·Frédéric Laumonnier, Sébastien Roger, Pascaline Guérin, Florence Molinari, Ridha Mrad, Dominique Cahard, A. Belhadj, M.B. Halayem, Antonio M. Persico, Maurizio Elia, Valentino Romano, Sébastien Holbert, Christian Andrés, Habiba Chaâbouni, Laurence Colleaux, Jacques Constant, Jean-Yves Le Guennec, Sylvain Briault	2006	135
10	Mutations of the UPF3B gene, which encodes a protein widely expressed in neurons, are associated with nonspecific mental retardation with or without autism Molecular Psychiatry ·Frédéric Laumonnier, Cheryl Shoubridge, Catherine Antar, Lam Son Nguyen, Hilde Van Esch, Tjitske Kleefstra, Sylvain Briault, J. P. Fryns, B Hamel, Jamel Chelly, Hans‐Hilger Ropers, Nathalie Ronce, S. Blesson, Claude Moraine, Jozef Gécz, Martine Raynaud	2009	89
11	Rescue of fragile X syndrome phenotypes in Fmr1KO mice by a BKCa channel opener molecule Orphanet Journal of Rare Diseases ·Betty Hébert, Susanna Pietropaolo, Sandra Même, Béatrice Laudier, Anthony Laugeray, Nicolas Doisne, Angélique Quartier, Sandrine Lefeuvre, Laurence Got, Dominique Cahard, Frédéric Laumonnier, Wim E. Crusio, Jacques Pichon, Arnaud Menuet, Olivier Perche, Sylvain Briault	2014	75
12	Prenatal diagnosis of female monozygotic twins discordant for Turner syndrome: implications for prenatal genetic counselling Prenatal Diagnosis ·Brigitte Gilbert, Catherine Yardin, Sylvain Briault, Valérie Belin, Anne Lienhardt, Y. Aubard, J Battin, M Servaud, H.-J. Philippe, Didier Lacombe	2002	53
13	Autism and Nonsyndromic Mental Retardation Associated with a De Novo Mutation in the NLGN4X Gene Promoter Causing an Increased Expression Level Biological Psychiatry ·Hussein Daoud, Frédérique Bonnet‐Brilhault, Sylviane Védrine, Marie-Véronique Demattei, Patrick Vourc’h, Nadia Bayou, Christian Andrés, Catherine Barthélémy, Frédéric Laumonnier, Sylvain Briault	2009	48
14	Increased Dosage of RAB39B Affects Neuronal Development and Could Explain the Cognitive Impairment in Male Patients with Distal Xq28 Copy Number Gains Human Mutation ·Lieselot Vanmarsenille, Maila Giannandrea, Nathalie Fieremans, Jelle Verbeeck, Stefanie Belet, Martine Raynaud, Annick Vogels, Katrin Männik, Katrin Õunap, Jacqueline Vigneron, Sylvain Briault, Hilde Van Esch, Patrizia D’Adamo, Guy Froyen	2013	47
15	Specific clinical and brain MRI features in mentally retarded patients with mutations in the Oligophrenin‐1 gene American Journal of Medical Genetics Part A ·Vincent des Portes, Nathalie Boddaert, Silvia Sacco, Sylvain Briault, Kim Maincent, Nadia Bahi, Marie Gomot, Nathalie Ronce, Joseph Bursztyn, C. Adamsbaum, Mônica Zilbovicius, Jamel Chelly, Claude Moraine	2003	45
16	Isotypy of serum monoclonal immunoglobulins in human immunodeficiency virus-infected adults. PubMed ·Sylvain Briault, M Courtois-Capella, Françoise Duarte, Pièrre Aucouturier, J L Preud'homme	1988	41
17	Apical Left Ventricular Aneurysm Without Atrio-Ventricular Block Due to a Lamin A/C Gene Mutation European Journal of Heart Failure ·J.-F. Forissier, Gisèle Bonne, Christiane Bouchier, Laëtitia Duboscq-Bidot, Pascale Richard, Claudine Wisnewski, Sylvain Briault, Claude Moraine, Olivier Dubourg, Ketty Schwartz, Michel Komajda	2003	38
18	A gene for FG syndrome maps in the Xq12-q21.31 region American Journal of Medical Genetics ·Sylvain Briault, Ruth F. Hill, Antony E. Shrimpton, Danping Zhu, Marianne Till, Nathalie Ronce, Patricia Margaritte‐Jeannin, M Baraitser, Helen Middleton‐Price, Sue Malcolm, Elizabeth Thompson, Joe J. Hoo, Golder N. Wilson, Corrado Romano, Agnès Guichet, Marcus Pembrey, Michel Fontés, Annemarie Poustka, Claude Moraine	1997	38
19	Hippocampal interleukin-33 mediates neuroinflammation-induced cognitive impairments Journal of Neuroinflammation ·Flora Reverchon, Vidian de Concini, Vanessa Larrigaldie, Sulayman Benmerzoug, Sylvain Briault, Dieudonnée Togbe, Bernhard Ryffel, Valérie Quesniaux, Arnaud Menuet	2020	36
20	Visual Sensorial Impairments in Neurodevelopmental Disorders: Evidence for a Retinal Phenotype in Fragile X Syndrome PLoS ONE ·Rafaëlle Rossignol, Isabelle Ranchon‐Cole, Arnaud Pâris, Améziane Herzine, Astrid Perche, David Laurenceau, Pauline Coti Bertrand, C. Cercy, Jacques Pichon, Stéphane Mortaud, Sylvain Briault, Arnaud Menuet, Olivier Perche	2014	32

About Sylvain Briault

Sylvain Briault is a scholar working on Genetics, Molecular Biology, Cognitive Neuroscience, Pediatrics, Perinatology and Child Health and Surgery, having authored 64 papers that have together received 3.1k indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (39 papers), Genomic variations and chromosomal abnormalities (20 papers), Autism Spectrum Disorder Research (14 papers), Congenital heart defects research (7 papers), Prenatal Screening and Diagnostics (7 papers), RNA modifications and cancer (6 papers), Retinal Development and Disorders (5 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (5 papers). The work is most often cited by research in Genetics (1.6k citations), Developmental Neuroscience (153 citations), Cognitive Neuroscience (610 citations), Molecular Biology (1.8k citations) and Cellular and Molecular Neuroscience (426 citations). Sylvain Briault has collaborated with scholars based in France, United States and Germany. Frequent co-authors include Claude Moraine, Nathalie Ronce, Frédéric Laumonnier, Ben C.J. Hamel, Martine Raynaud, Jamel Chelly, Jean‐Pierre Fryns, Christian Andrés, Béatrice Laudier and Hans‐Hilger Ropers. Their work appears in journals such as Prenatal Diagnosis, Experimental Eye Research, European Journal of Human Genetics, The American Journal of Human Genetics and Frontiers in Behavioral Neuroscience.

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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