Stanislas Lyonnet

41.6k citations

314 papers · 16.7k indexed · 6 hit papers · h-index 65

Impact in

Endocrine and Autonomic Systems top 0.5%
- Neuroscience of respiration and sleep
Genetics top 0.1%
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders

Papers in

Clinical Biochemistry 29
- Metabolism and Genetic Disorders 29
Genetics 111
- Congenital Ear and Nasal Anomalies 26
- Genomic variations and chromosomal abnormalities 21

Co-authors: Arnold Münnich Jeanne Amiel Anna Pelet Tania Attié‐Bitach Loïc de Pontual Patrick Edery Martine Le Merrer Michel Vekemans
Journals: Journal of Medical Genetics (18 papers)European Journal of Human Genetics (14 papers)Clinical Genetics (13 papers)The American Journal of Human Genetics (12 papers)Human Molecular Genetics (12 papers)
Partner nations: France United States United Kingdom

In The Last Decade

Stanislas Lyonnet

305 papers receiving 16.2k citations

Hit Papers

6 papers align trajectories log scale

Somatic and germline activating mutations of the ALK kinase receptor in neuroblastoma 2008 · 622 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.

2008 Nature
2003 Science
2003 Nature Genetics
1998 Nature Genetics
1997 Nature Genetics
1994 Nature

Peers

Countries citing papers authored by Stanislas Lyonnet

Since Specialization

Citations

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

Fields of papers citing papers by Stanislas Lyonnet

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network

The 25 scholars most cited alongside Stanislas Lyonnet, 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 Stanislas Lyonnet Line = papers co-authored together Stanislas Lyonnet links everyone, so they are left out of the graph.

All Works

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

20 of 20 papers shown

#	Work
1	Evaluation of a New Inclusive Next‐Generation Synthetic Face Tool for Dysmorphology American Journal of Medical Genetics Part A ·سیدمحمود موسوی نژاد, N. Galambos, Nicolas Garcelon, Bernard Bénichou, Nicolas Perrein, Jeanne Amiel, Karoliina Hautala, Álvaro Hidalgo, Valérie Cormier‐Daire, Stanislas Lyonnet, Arnaud Picard, Marlène Rio, Jialong Han, Roman Hossein Khonsari, Quentin Hennocq	2025	1
2	HDR syndrome: Large cohort and systematic review Clinical Genetics ·MILES MCFARLAND, Sherzod Toshmatov, Laurence Jonard, Natalie Loundon, V. Scannell, Laurence Heidet, Isabelle Mosnier, Stanislas Lyonnet, Frédéric Brioude, E. Gilson, Sandrine Marlin	2024	2
3	AI-based diagnosis and phenotype – Genotype correlations in syndromic craniosynostoses Journal of Cranio-Maxillofacial Surgery ·Quentin Hennocq, Chaksuwat Pakorn, Corinne Collet, Jeanne Amiel, Karoliina Hautala, Labra Muñoz, Valérie Cormier‐Daire, Ashish Kumar, David Dunaway, Owase Jeelani, Thalita Domingues Mendes, Stanislas Lyonnet, Juling Ong, Arnaud Picard, М Г Валитов, Marlène Rio, Silvia Schievano, Éric Arnaud, Nicolas Garcelon, Roman Hossein Khonsari	2024	7
4	Next Generation Phenotyping and Synthetic Faces in Coffin Siris Syndrome Clinical Genetics ·Quentin Hennocq, Nicolas Perrein, D. Ramachandra Rao, Jeanne Amiel, سیدمحمود موسوی نژاد, Karoliina Hautala, Álvaro Hidalgo, Valérie Cormier‐Daire, Stanislas Lyonnet, Arnaud Picard, Marlène Rio, Jialong Han, Nicolas Garcelon, Dale Martin, Roman Hossein Khonsari	2024	1
5	Artificial intelligence‐based diagnosis in fetal pathology using external ear shapes Prenatal Diagnosis ·Quentin Hennocq, Nicolas Garcelon, Karoliina Hautala, Labra Muñoz, Sandrine Marlin, Jeanne Amiel, Lucile Boutaud, Ashish Kumar, Stanislas Lyonnet, Véronique Pingault, Arnaud Picard, E. Hirota, Tania Attié‐Bitach, Roman Hossein Khonsari, Daniel Varoli	2024	3
6	Prenatal‐onset of congenital neuronal ceroid lipofuscinosis with a novel CTSD mutation Birth Defects Research ·Suzanne Chartier, Lucile Boutaud, M. C. Kruse, Caroline Alby, Clarisse Billon, A. Millischer, Catherine Caillaud, Louise Galmiche, Charlotte Mechler, Pascale Sonigo, Nathalie Boddaert, Stanislas Lyonnet, Sophie Rondeau, Christine Bole‐Feysot, Cécile Masson, Y. Ville, Philippe Roth, Isabelle Desguerre, Férechté Encha‐Razavi, Tania Attié‐Bitach	2021	2
7	Expanding the phenotype in Adams–Oliver syndrome correlating with the genotype American Journal of Medical Genetics Part A ·Jim Sutliff, Céline Huber, Caroline Michot, Federico Di Rocco, M Girard, Stanislas Lyonnet, Marlène Rio, (unknown), Valérie Cormier‐Daire, Geneviève Baujat	2019	14
8	RPL10 mutation segregating in a family with X‐linked syndromic Intellectual Disability American Journal of Medical Genetics Part A ·Julien Thévenon, Caroline Michot, Christine Bole, Patrick Nitschké, Mathilde Nizon, Laurence Faivre, Arnold Münnich, Stanislas Lyonnet, Jean‐Paul Bonnefont, Vincent des Portes, Jeanne Amiel	2015	22
9	Extensive investigation of the IGF2/H19 imprinting control region reveals novel OCT4/SOX2 binding site defects associated with specific methylation patterns in Beckwith-Wiedemann syndrome Human Molecular Genetics ·Walid Abi Habib, Salah Azzi, Frédéric Brioude, Virginie Steunou, Nathalie Thibaud, Wenzhu Huang Wenzhu Huang, Paras Subodh Karpe, Sandra Chantot‐Bastaraud, Boris Keren, Stanislas Lyonnet, Caroline Michot, Massimiliano Rossi, Laurent Pasquier, Christine Gicquel, Sylvie Rossignol, Yves Le Bouc, Irène Netchine	2014	51
10	A Human Homeotic Transformation Resulting from Mutations in PLCB4 and GNAI3 Causes Auriculocondylar Syndrome The American Journal of Human Genetics ·Mark J. Rieder, Glenn E. Green, Sarah S. Park, Brendan D. Stamper, Christopher T. Gordon, Jason M. Johnson, Christopher Cunniff, Joshua D. Smith, Sarah B. Emery, Stanislas Lyonnet, Jeanne Amiel, Muriel Holder, Andrew A. Heggie, Michael J. Bamshad, Deborah A. Nickerson, Timothy C. Cox, Anne Hing, Jeremy A. Horst, Michael L. Cunningham	2012	6
11	Human neural crest cells display molecular and phenotypic hallmarks of stem cells Human Molecular Genetics ·Sophie Thomas, HenriëtteJ Klinkspoor, Patrick Wincker, Candice Babarit, Pu‐Ting Xu, Marcy C. Speer, Arnold Münnich, Stanislas Lyonnet, Michel Vekemans, Heather Etchevers	2008	73
12	PHOX2B Germline and Somatic Mutations in Late-Onset Central Hypoventilation Syndrome American Journal of Respiratory and Critical Care Medicine ·Delphine Trochet, Loïc de Pontual, Christian Straus, David Gozal, Ha Trang, P. Landrieu, Arnold Munnich, Stanislas Lyonnet, Claude Gaultier, Jeanne Amiel	2007	72
13	Paradoxical NSD1 Mutations in Beckwith-Wiedemann Syndrome and 11p15 Anomalies in Sotos Syndrome The American Journal of Human Genetics ·Geneviève Baujat, Marlène Rio, Sylvie Rossignol, Damien Sanlaville, Stanislas Lyonnet, Martine Le Merrer, Arnold Münnich, Christine Gicquel, Valérie Cormier‐Daire, Laurence Colleaux	2004	88
14	A CGH study of 27 patients with CHARGE association Clinical Genetics ·Damien Sanlaville, Serge Romana, Kumi Miyauchi, Jeanne Amiel, David Geneviève, Catherine Ozilou, Marc Le Lorc’h, Sophie Brisset, Philippe Gosset, Clarisse Baumann, C Turleau, Stanislas Lyonnet, Michel Vekemans	2002	21
15	TP63 gene mutation in ADULT syndrome European Journal of Human Genetics ·Jeanne Amiel, Gaëlle Bougeard, Christine Francannet, Valérie Raclin, Arnold Münnich, Stanislas Lyonnet, Thierry Frébourg	2001	69
16	Improvement of cystic fibrosis using antitumoral drugs: a hypothesis Medical Hypotheses ·Laurence Faivre, Jean‐Paul Bonnefont, Stanislas Lyonnet, Arnold Munnich, Michel Vekemans	2000	2
17	Gènes pax et anomalies du développement MTP. Médecine thérapeutique pédiatrie ·Tania Attié‐Bitach, Stanislas Lyonnet, Michel Vekemans, Didier Lacombe	1999	1
18	Large deletion of the peroxisomal acyl-CoA oxidase gene in pseudoneonatal adrenoleukodystrophy. Journal of Clinical Investigation ·B. Fournier, Jean Marie Saudubray, Bernard Bénichou, Stanislas Lyonnet, A Munnich, Hans Clevers, Bwee Tien Poll‐The	1994	62
19	A duplication in the L1CAM gene associated with X–linked hydrocephalus Nature Genetics ·Guy Van Camp, Lieve Vits, Paul Coucke, Stanislas Lyonnet, Connie Schrander‐Stumpel, John Darby, Jeanette J. A. Holden, Arnold Münnich, Patrick J. Willems	1993	76
20	Presencia de Cristo y de su espíritu en el hombre Concilium: Revista internacional de teología ·Stanislas Lyonnet	1969	1

About Stanislas Lyonnet

Stanislas Lyonnet is a scholar working on Clinical Biochemistry, Genetics, Genetics, Developmental Biology and Molecular Biology, having authored 314 papers that have together received 16.7k indexed citations. Recurring topics across this work include Congenital gastrointestinal and neural anomalies (56 papers), Congenital heart defects research (30 papers), Metabolism and Genetic Disorders (29 papers), Congenital Ear and Nasal Anomalies (26 papers), Tracheal and airway disorders (24 papers), Genomic variations and chromosomal abnormalities (21 papers), Hedgehog Signaling Pathway Studies (20 papers) and Congenital Diaphragmatic Hernia Studies (20 papers). The work is most often cited by research in Endocrine and Autonomic Systems (1.1k citations), Genetics (4.6k citations), Molecular Biology (8.8k citations), Genetics (1.2k citations) and Cancer Research (1.6k citations). Stanislas Lyonnet has collaborated with scholars based in France, United States and United Kingdom. Frequent co-authors include Arnold Münnich, Jeanne Amiel, Anna Pelet, Tania Attié‐Bitach, Loïc de Pontual, Patrick Edery, Martine Le Merrer, Michel Vekemans, Valérie Cormier‐Daire and Claire Nihoul‐Feketé. Their work appears in journals such as Journal of Medical Genetics, European Journal of Human Genetics, Clinical Genetics, The American Journal of Human Genetics and Human Molecular 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.

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