Pierre‐Simon Jouk - Concepedia

Author

Pierre‐Simon Jouk

Centre Hospitalier Universitaire de Grenoble ORCID

Also Known As

Gipsy Lopez, Guillaume Jondeau, Jouk, P.S., Jouk, Pierre-Simon, P S Jouk, P. Jouk, P. S. JOUK, P. S. Jouk, P.-S. Jouk, P.S Jouk

155

Publications

4.8K

Citations

H-Index

134

Concepts

All Affiliations

Centre Hospitalier Universitaire de Grenoble Inserm Université Grenoble Alpes Centre National de la Recherche Scientifique Université Joseph Fourier

About

Pierre‐Simon Jouk is an author at Centre Hospitalier Universitaire de Grenoble specializing in medicine, genetics, and molecular genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	22	34	2.6K
2	Public Health	10	10	1.4K
3	Health Sciences	5	5	123
4	Engineering	4	4	123
5	Education	3	3	103

Pierre‐Simon Jouk

Publications

4.4K

Citations

H-Index

Page 1

	Year	Citations
Mutations in DNAH1, which Encodes an Inner Arm Heavy Chain Dynein, Lead to Male Infertility from Multiple Morphological Abnormalities of the Sperm Flagella Mariem Ben Khelifa, Charles Coutton, Raoudha Zouari, The American Journal of Human Genetics BiologyChromatinInfertilityGeneticsSperm Biology	2013	464
Cerebral palsy and intrauterine growth in single births: European collaborative study S N Jarvis, Svetlana V. Glinianaia, Maria-Giulia Torrioli, The Lancet European Collaborative StudyPediatricsIntrauterine GrowthMaternal HealthPreterm Birth	2003	326
Homozygous mutation of AURKC yields large-headed polyploid spermatozoa and causes male infertility Klaus Dieterich, Ricardo Soto‐Rifo, A.K. Faure, Nature Genetics SpermatogenesisInfertilityAndrologyDevelopmental BiologyFertility	2007	274
Mutations in CFAP43 and CFAP44 cause male infertility and flagellum defects in Trypanosoma and human Charles Coutton, Alexandra Vargas, Amir Amiri‐Yekta, Nature Communications	2018	233
Association of TALS Developmental Disorder with Defect in Minor Splicing Component <i>U4atac</i> snRNA Patrick Edery, Charles Marcaillou, Mourad Sahbatou, Science	2011	222
A Recurrent Deletion of DPY19L2 Causes Infertility in Man by Blocking Sperm Head Elongation and Acrosome Formation Radu Harbuz, Raoudha Zouari, Virginie Pierre, The American Journal of Human Genetics SpermatogenesisAcrosome FormationInfertilityAndrologyDevelopmental Biology	2011	195
Prevalence and spectrum of mutations in a cohort of 192 unrelated patients with hypertrophic cardiomyopathy Gilles Millat, Patrice Bouvagnet, Philippe Chevalier, European Journal of Medical Genetics CardiomyopathyUnrelated PatientsCardiovascular DiseaseGeneticsGenetic Epidemiology	2010	160
Clinical and mutational spectrum in a cohort of 105 unrelated patients with dilated cardiomyopathy Gilles Millat, Patrice Bouvagnet, Philippe Chevalier, European Journal of Medical Genetics CardiomyopathyHeart FailureUnrelated PatientsCardiovascular DiseaseGenetic Epidemiology	2011	110
Mutations in CNTNAP1 and ADCY6 are responsible for severe arthrogryposis multiplex congenita with axoglial defects Annie Laquerrière, Jérôme Maluenda, Adrien Camus, Human Molecular Genetics Pns MyelinationDevelopmental BiologyAutoimmune DiseaseMendelian DisorderGenetic Disorder	2013	109
Three-dimensional cartography of the pattern of the myofibres in the second trimester fetal human heart Pierre‐Simon Jouk, Yves Usson, Gabrielle Michalowicz, Anatomy and Embryology Obstetric ImagingFetal MedicineThree-dimensional CartographyCongenital Heart DefectAnatomy	2000	108

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