Pierre‐Simon Jouk

4.9k citations

90 papers · 2.4k indexed · h-index 24

Reproductive Medicine top 2%
Pediatrics, Perinatology and Child Health top 2%
- Prenatal Screening and Diagnostics 9
- Fetal and Pediatric Neurological Disorders 7
Obstetrics and Gynecology top 5%
Genetics top 5%
- Genomic variations and chromosomal abnormalities 10
- Neurogenetic and Muscular Disorders Research 8
- Genetics and Neurodevelopmental Disorders 7
Genetics top 5%
- Genomic variations and chromosomal abnormalities 10
- Neurogenetic and Muscular Disorders Research 8
- Genetics and Neurodevelopmental Disorders 7
Molecular Biology
- Congenital heart defects research 8
Cardiology and Cardiovascular Medicine
- Cardiomyopathy and Myosin Studies 7
- Cardiovascular Function and Risk Factors 7

Co-authors: Yves Usson Pierre F. Ray Klaus Dieterich Joël Lunardi Sylviane Hennebicq Charles Coutton Christine Cans Mary‐Jane Platt
Cited by: Reproductive Medicine Pediatrics, Perinatology and Child Health Obstetrics and Gynecology
Journals: Science (1 paper)The Lancet (2 papers)Nature Genetics (1 paper)
Partner nations: France United States United Kingdom

In The Last Decade

Pierre‐Simon Jouk

87 papers receiving 2.3k citations

Peers

Countries citing papers authored by Pierre‐Simon Jouk

Since Specialization

Citations

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

Fields of papers citing papers by Pierre‐Simon Jouk

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Pierre‐Simon Jouk. 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 Pierre‐Simon Jouk. The network helps show where Pierre‐Simon Jouk may publish in the future.

Co-authorship network

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

All Works

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20 of 20 papers shown

#	Work
1	The Nematic Chiral Liquid Crystal Structure of the Cardiac Myoarchitecture: Disclinations and Topological Singularities Journal of Cardiovascular Development and Disease ·Johanne Auriau,Yves Usson,Pierre‐Simon Jouk	2022	2
2	Dysregulations of sonic hedgehog signaling in MED12‐related X‐linked intellectual disability disorders Molecular Genetics & Genomic Medicine ·Siddharth Srivastava,Tejasvi Niranjan,Melanie May,Patrick Tarpey,William Allen,Anna Hackett,Pierre‐Simon Jouk,Lucy Raymond,Slyvain Briault,Cindy Skinner,Annick Toutain,Jozef Gécz,William R. Heath,Roger E. Stevenson,Charles E. Schwartz,Tao Wang	2019	10
3	Quantitative comparison of human myocardial fiber orientations derived from DTI and polarized light imaging Physics in Medicine and Biology ·Feng Yang,Yuemin Zhu,Gabrielle Michalowicz,Pierre‐Simon Jouk,Laurent Fanton,Magalie Viallon,Patrick Clarysse,Pierre Croisille,Yves Usson	2018	10
4	Prenatally diagnosed periventricular nodular heterotopia: Further delineation of the imaging phenotype and outcome European Journal of Medical Genetics ·B. Deloison,P. Sonigo,A. Millischer,Thibaud Quibel,Mara Cavallin,G. Benoist,Chloé Quēlin,Pierre‐Simon Jouk,Dorit Lev,Marianne Alison,Clarisse Baumann,C. Beldjord,F. Razavi,B. Bessières,Nathalie Boddaert,Y. Ville,L. J. Salomon,Nadia Bahi‐Buisson	2018	12
5	Postnatal myocardium remodelling generates inhomogeneity in the architecture of the ventricular mass Surgical and Radiologic Anatomy ·Pierre‐Simon Jouk,Ba Luu Truong,Gabrielle Michalowicz,Yves Usson	2017	5
6	MED12-related XLID disorders are dose-dependent of immediate early genes (IEGs) expression Human Molecular Genetics ·Lise‐Marie Donnio,Baptiste Bidon,Satoru Hashimoto,Melanie May,Alexey Epanchintsev,Colm J. Ryan,William Allen,Anna Hackett,Jozef Gécz,Cindy Skinner,Roger E. Stevenson,Arjan P.M. de Brouwer,Charles Coutton,Christine Francannet,Pierre‐Simon Jouk,Charles E. Schwartz,Jean‐Marc Egly	2017	17
7	Split hand/foot malformation with long‐bone deficiency and BHLHA9 duplication: report of 13 new families Clinical Genetics ·Florence Petit,A.‐S. Jourdain,Joris Andrieux,Geneviève Baujat,Clarisse Baumann,Claire Bénéteau,A. David,Laurence Faivre,Dominique Gaillard,Brigitte Gilbert‐Dussardier,Pierre‐Simon Jouk,Cédric Le Caignec,Philippe Loget,Laurent Pasquier,Nicole Porchet,Muriel Holder‐Espinasse,Sylvie Manouvrier‐Hanu,Fabienne Escande	2013	17
8	Stillbirth classification in population-based data and role of fetal growth restriction: the example of RECODE BMC Pregnancy and Childbirth ·Anne Ego,Jennifer Zeitlin,Pierre Batailler,Séverine Cornec,Anne Fondeur,Marion Baran-Marszak,Pierre‐Simon Jouk,Thierry Debillon,Christine Cans	2013	13
9	Complete agenesis of major salivary glands International Journal of Pediatric Otorhinolaryngology ·Eszter Berta,G. Bettega,Pierre‐Simon Jouk,Gopal Billy,F. Nugues,B. Morand	2013	11
10	MLPA and sequence analysis of DPY19L2 reveals point mutations causing globozoospermia Human Reproduction ·Charles Coutton,Raoudha Zouari,Farid Abada,Mariem Ben Khelifa,Ghaya Merdassi,Chahnez Triki,Denise Escalier,Laëtitia Hesters,Valérie Mitchell,Rachel Lévy,Nathalie Sermondade,Florence Boitrelle,François Vialard,Véronique Satre,Sylviane Hennebicq,Pierre‐Simon Jouk,Christophe Arnoult,Joël Lunardi,Pierre F. Ray	2012	52
11	Association of TALS Developmental Disorder with Defect in Minor Splicing Component U4atac snRNA Science ·Patrick Edery,Charles Marcaillou,Mourad Sahbatou,Audrey Labalme,Joëlle Chastang,Renaud Touraine,Emmanuel Tubacher,Faiza Senni,Michael B. Bober,Sheela Nampoothiri,Pierre‐Simon Jouk,Elisabeth Steichen,Siren Berland,Annick Toutain,Carol A. Wise,Damien Sanlaville,Francis Rousseau,Françoise Clerget‐Darpoux,Anne‐Louise Leutenegger	2011	159
12	Clinical and mutational spectrum in a cohort of 105 unrelated patients with dilated cardiomyopathy European Journal of Medical Genetics ·Gilles Millat,Patrice Bouvagnet,Philippe Chevalier,Laurent Sebbag,Arnaud Dulac,Claire Dauphin,Pierre‐Simon Jouk,Marie‐Ange Delrue,Jean‐Benoît Thambo,Philippe Le Métayer,Marie‐France Seronde,Laurence Bonhomme‐Faivre,Jean‐Christophe Eicher,Robert Rousson	2011	75
13	Prevalence and spectrum of mutations in a cohort of 192 unrelated patients with hypertrophic cardiomyopathy European Journal of Medical Genetics ·Gilles Millat,Patrice Bouvagnet,Philippe Chevalier,Claire Dauphin,Pierre‐Simon Jouk,Antoine Da Costa,Fabienne Prieur,J. Bresson,Laurence Bonhomme‐Faivre,Jean‐Christophe Eicher,Nicolas Chassaing,Hervé Crehalet,Raphaël Porcher,Claire Rodriguez‐Lafrasse,Robert Rousson	2010	115
14	Paracentric inversion of chromosome 2 associated with cryptic duplication of 2q14 and deletion of 2q37 in a patient with autism American Journal of Medical Genetics Part A ·Françoise Devillard,Vincent Guinchat,Daniel Moreno‐De‐Luca,Anne‐Claude Tabet,Nicolas Gruchy,Pascale Guillem,Marie‐Ange Nguyen Morel,Nathalie Leporrier,Marion Leboyer,Pierre‐Simon Jouk,James Lespinasse,Catalina Betancur	2010	14
15	Prenatal manifestation in a family affected by nevoid basal cell carcinoma syndrome European Journal of Medical Genetics ·Yann Le Brun Keris,Pierre‐Simon Jouk,Géraldine Saada-Sebag,Jean-Jacques Roux,Bertrand Mattei,Laure Bagait,Ariane Paoloni‐Giacobino,Bernard Grandchamp,Nadem Soufir,James Lespinasse	2008	7
16	Rare diseases in disabled children: an epidemiological survey Archives of Disease in Childhood ·Pascale Guillem,Christine Cans,Elisabeth Robert‐Gnansia,Ségolène Aymé,Pierre‐Simon Jouk	2007	26
17	C.P.1.13 A homozygous null mutation in TPM2 gene causes autosomal recessive nemaline myopathy associated with multiple pterygia Neuromuscular Disorders ·Pierre‐Simon Jouk,Annick Labarre‐Vila,Paulette Mezin,S. Drouhin,Isabelle Marty,Joël Lunardi,Nicole Monnier	2007	2
18	Trends in elective terminations of pregnancy between 1989 and 2000 in a French county (the Isère) Prenatal Diagnosis ·Pascale Guillem,Bibiana Fabre,C. Cans,Elisabeth Robert‐Gnansia,Pierre‐Simon Jouk	2003	38
19	Diastrophic dwarfism and pregnancy The Lancet ·(unknown),Pierre‐Simon Jouk,Jean‐Claude Pons	2001	8
20	Characterization of a Germline Mosaicism in Families with Lowe Syndrome, and Identification of Seven Novel Mutations in the OCRL1 Gene The American Journal of Human Genetics ·Véronique Satre,Nicole Monnier,Florence Berthoin,Carmen Ayuso,Alain Joannard,Pierre‐Simon Jouk,Isidora López‐Pajares,André Megabarne,Henri Jean Philippe,Henri Plauchu,María Torres,Joël Lunardi	1999	42

About Pierre‐Simon Jouk

Pierre‐Simon Jouk is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Genetics, having authored 90 papers that have together received 2.4k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (10 papers), Prenatal Screening and Diagnostics (9 papers), Congenital heart defects research (8 papers), Neurogenetic and Muscular Disorders Research (8 papers), Cardiomyopathy and Myosin Studies (7 papers), Fetal and Pediatric Neurological Disorders (7 papers), Cardiovascular Function and Risk Factors (7 papers) and Genetics and Neurodevelopmental Disorders (7 papers). The work is most often cited by research in Reproductive Medicine (364 citations), Pediatrics, Perinatology and Child Health (543 citations) and Obstetrics and Gynecology (173 citations). Pierre‐Simon Jouk has collaborated with scholars based in France, United States and United Kingdom. Frequent co-authors include Yves Usson, Pierre F. Ray, Klaus Dieterich, Joël Lunardi, Sylviane Hennebicq, Charles Coutton, Christine Cans, Mary‐Jane Platt, Jane L. Hutton and Gudrun Hagberg. Their work appears in journals such as Science, The Lancet and Nature 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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