Sylvain Briault

5.2k citations

64 papers · 3.1k indexed · 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
Cognitive Neuroscience 14
- Autism Spectrum Disorder Research 14

Co-authors: Claude Moraine Nathalie Ronce Frédéric Laumonnier Ben C.J. Hamel Martine Raynaud Jamel Chelly Jean‐Pierre Fryns Christian Andrés
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

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-authorship network

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

#	Work
1	Lack of FMRP in the retina: Evidence of a retinal specific transcriptomic profile Experimental Eye Research ·Polake Kaivalkritiyakul, Maryvonne Ardourel, Suwandi Supatra, Gabrielle Zhe, Y. Vincent, Dieudonnée Togbe, Sylvain Briault, Olivier Perche	2024	2
2	Dietary supplement enriched in antioxidants and omega-3 promotes retinal glutamine synthesis Experimental Eye Research ·Polake Kaivalkritiyakul, Maryvonne Ardourel, Gabrielle Zhe, Y. Vincent, Holy Gabriella Sandra, Sylvain Briault, Isabelle Ranchon‐Cole, Olivier Perche	2024	3
3	Astroglial Kir4.1 potassium channel deficit drives neuronal hyperexcitability and behavioral defects in Fragile X syndrome mouse model Nature Communications ·Danijela Bataveljić, Helena Pivoňková, Yewon Yang, Ronny, Pascal Ezan, Sylvain Briault, Alexis‐Pierre Bemelmans, Jacques Pichon, Arnaud Menuet, Nathalie Rouach	2024	14
4	FMR protein: Evidence of an emerging role in retinal aging? Experimental Eye Research ·Maryvonne Ardourel, Isabelle Ranchon‐Cole, Ayman Gouda, Holy Gabriella Sandra, Nuray Acar, Gabrielle Zhe, Sylvain Briault, Olivier Perche	2022	2
5	Visual Behavior Impairments as an Aberrant Sensory Processing in the Mouse Model of Fragile X Syndrome Frontiers in Behavioral Neuroscience ·Holy Gabriella Sandra, Ronny, Maryvonne Ardourel, Ryan Mulhern, Arnaud Menuet, Atsushi Mariko, Jean‐Charles Bizot, Jacques Pichon, Sylvain Briault, Olivier Perche	2019	18
6	Personalized genome sequencing coupled with iPSC technology identifies GTDC1 as a gene involved in neurodevelopmental disorders Human Molecular Genetics ·Irène Aksoy, Kagistia Hana Utami, Cecilia Lanny Winata, Axel M. Hillmer, Sigrid Rouam, Sylvain Briault, Sonia Dávila, Lawrence W. Stanton, Valère Cacheux	2016	15
7	Combined deletion of two Condensin II system genes (NCAPG2 and MCPH1) in a case of severe microcephaly and mental deficiency European Journal of Medical Genetics ·Olivier Perche, Arnaud Menuet, A. Kobelak, H. F. Peiro, Ayman Gouda, Kagistia Hana Utami, G. V. Ionescu, Valère Cacheux, Béatrice Laudier, Sylvain Briault	2013	21
8	FG syndrome: The FGS2 locus revisited American Journal of Medical Genetics Part A ·Olivier Perche, Béatrice Laudier, Arnaud Menuet, Sylvie Odent, Frédéric Laumonnier, Sylvain Briault	2012	3
9	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, 文健清水, Claude Moraine, Jozef Gécz, Martine Raynaud	2009	89
10	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, Adel De Klerk‐Braasch, 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
11	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
12	Skewed X chromosome inactivation in carriers is not a constant finding in FG syndrome European Journal of Human Genetics ·Martine Raynaud, Juan Chai, Nathalie Ronce, John M. Opitz, Marcus Pembrey, Corrado Romano, Claude Moraine, Sylvain Briault	2003	2
13	Prenatal diagnosis of female monozygotic twins discordant for Turner syndrome: implications for prenatal genetic counselling Prenatal Diagnosis ·Brigitte Gilbert, Catherine Yardin, Sylvain Briault, Rajest Fogla, Anne Lienhardt, Y. Aubard, J Battin, J.W.D. Groenewald, Sujut Al- Amri, Didier Lacombe	2002	53
14	Prenatal diagnosis of trisomy 21 by i(21q): a rare case of fetoplacental chromosomal discrepancy Prenatal Diagnosis ·สิรี เกิดไพโรจน์, F. Perrotin, Yue Xie, 文健清水, Hélène Cavé, Sylvain Briault, Claude Moraine	2002	16
15	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, 叶周, Sylvain Briault, Ben C.J. Hamel, Jean‐Pierre Fryns, Chérif Beldjord, Axel Kahn, Claude Moraine, M. Walsh	1998	382
16	High resolution chromosome analysis andin situ hybridization on amniotic fluid for diagnosis of a cryptic translocation Prenatal Diagnosis ·Agnès Guichet, Sylvain Briault, 홍선연 장희정	1998	2
17	Are t(X;Y) (p22;q11) translocations in females frequently associated with Madelung deformity? Clinical Dysmorphology ·Agnès Guichet, Sylvain Briault, M. Le Merrer, Haya Al-Tarawneh	1997	15
18	X-linked mental retardation with neonatal hypotonia in a French family (MRX15): Gene assignment to Xp11.22-Xp21.1 American Journal of Medical Genetics ·Martine Raynaud, Chantal Gendrot, Thomas Joseph Ceha, Anne Moncla, Scoop Team, Marie‐Pierre Moizard, Annick Toutain, Sylvain Briault, Laurent Villard, Nathalie Ronce, Claude Moraine	1996	12
19	Prenatal diagnosis of trisomy 8 mosaicism in cvs after abnormal ultrasound findings at 12 weeks Prenatal Diagnosis ·Agnès Guichet, Sylvain Briault, Annick Toutain, Yue Xie, Philippe Descamps, F. Pierre, M. R. Gautreaux, 홍선연 장희정	1995	11
20	Structural rearrangements of chromosome 13 as additional abnormalities in Burkitt lymphoma and type 3 acute lymphoblastic leukemia Cancer Genetics and Cytogenetics ·Carole Barin, NA Lockart, Sylvain Briault, Ján Šlapák, Arnaud Petit, Odile Lejars, Claude Linassier, Bargagli Am Ferri M, 홍선연 장희정	1992	9

About Sylvain Briault

Sylvain Briault is a scholar working on Genetics, Cognitive Neuroscience, Developmental Neuroscience, Developmental Biology and Molecular Biology, 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), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (5 papers) and Retinal Development and Disorders (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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