Pierre‐Simon Jouk

4.9k total citations
90 papers, 2.4k citations indexed

About

Pierre‐Simon Jouk is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Pierre‐Simon Jouk has authored 90 papers receiving a total of 2.4k indexed citations (citations by other indexed papers that have themselves been cited), including 35 papers in Molecular Biology, 30 papers in Genetics and 20 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Pierre‐Simon Jouk's work include Genomic variations and chromosomal abnormalities (10 papers), Prenatal Screening and Diagnostics (9 papers) and Congenital heart defects research (8 papers). Pierre‐Simon Jouk is often cited by papers focused on Genomic variations and chromosomal abnormalities (10 papers), Prenatal Screening and Diagnostics (9 papers) and Congenital heart defects research (8 papers). Pierre‐Simon Jouk collaborates with scholars based in France, United States and United Kingdom. Pierre‐Simon Jouk's co-authors include Yves Usson, Pierre F. Ray, Klaus Dieterich, Joël Lunardi, Sylviane Hennebicq, Charles Coutton, Christine Cans, S N Jarvis, Mary‐Jane Platt and Karla Hemming and has published in prestigious journals such as Science, The Lancet and Nature Genetics.

In The Last Decade

Pierre‐Simon Jouk

87 papers receiving 2.3k citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Pierre‐Simon Jouk France 24 872 616 543 364 362 90 2.4k
Luca Fusi United Kingdom 33 1.2k 1.4× 276 0.4× 630 1.2× 1.2k 3.2× 475 1.3× 73 3.8k
Frederick R. Bieber United States 25 795 0.9× 931 1.5× 564 1.0× 105 0.3× 268 0.7× 56 2.6k
Mana M. Parast United States 37 2.0k 2.3× 230 0.4× 1.5k 2.8× 372 1.0× 638 1.8× 92 4.8k
Lucia Bartoloni Italy 19 724 0.8× 834 1.4× 191 0.4× 212 0.6× 176 0.5× 38 1.9k
Christian J. Thaler Germany 32 432 0.5× 153 0.2× 450 0.8× 821 2.3× 767 2.1× 148 2.9k
Yuval Yaron Israel 35 1.2k 1.4× 1.2k 2.0× 2.6k 4.9× 553 1.5× 877 2.4× 182 4.8k
W. Colin Duncan United Kingdom 37 1.0k 1.1× 312 0.5× 432 0.8× 1.4k 4.0× 1.5k 4.1× 132 4.0k
Éric Bieth France 24 1.1k 1.3× 690 1.1× 348 0.6× 119 0.3× 67 0.2× 72 2.1k
Karen Helene Ørstavik Norway 26 1.5k 1.7× 1.4k 2.2× 517 1.0× 97 0.3× 115 0.3× 71 2.9k
Cynthia M. Powell United States 28 953 1.1× 1.2k 1.9× 536 1.0× 41 0.1× 185 0.5× 79 2.5k

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 of co-authors of Pierre‐Simon Jouk

This figure shows the co-authorship network connecting the top 25 collaborators of Pierre‐Simon Jouk. A scholar is included among the top collaborators of Pierre‐Simon Jouk based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Pierre‐Simon Jouk. Pierre‐Simon Jouk is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Auriau, Johanne, Yves Usson, & Pierre‐Simon Jouk. (2022). The Nematic Chiral Liquid Crystal Structure of the Cardiac Myoarchitecture: Disclinations and Topological Singularities. Journal of Cardiovascular Development and Disease. 9(11). 371–371. 2 indexed citations
2.
Niranjan, Tejasvi, Melanie May, Patrick Tarpey, et al.. (2019). Dysregulations of sonic hedgehog signaling in MED12‐related X‐linked intellectual disability disorders. Molecular Genetics & Genomic Medicine. 7(4). e00569–e00569. 10 indexed citations
3.
Deloison, B., P. Sonigo, A. Millischer, et al.. (2018). Prenatally diagnosed periventricular nodular heterotopia: Further delineation of the imaging phenotype and outcome. European Journal of Medical Genetics. 61(12). 773–782. 12 indexed citations
4.
Lorès, Patrick, Hervé Sartelet, Brice Poreau, et al.. (2018). Genomic duplication in the 19q13.42 imprinted region identified as a new genetic cause of intrauterine growth restriction. Clinical Genetics. 94(6). 575–580. 5 indexed citations
5.
Yang, Feng, Yuemin Zhu, Pierre‐Simon Jouk, et al.. (2018). Quantitative comparison of human myocardial fiber orientations derived from DTI and polarized light imaging. Physics in Medicine and Biology. 63(21). 215003–215003. 10 indexed citations
6.
Hashimoto, Satoru, Melanie May, Alexey Epanchintsev, et al.. (2017). MED12-related XLID disorders are dose-dependent of immediate early genes (IEGs) expression. Human Molecular Genetics. 26(11). 2062–2075. 17 indexed citations
7.
Jouk, Pierre‐Simon, et al.. (2017). Postnatal myocardium remodelling generates inhomogeneity in the architecture of the ventricular mass. Surgical and Radiologic Anatomy. 40(1). 75–83. 5 indexed citations
8.
Tanno, Pauline Le, Brice Poreau, Françoise Devillard, et al.. (2014). Maternal complex chromosomal rearrangement leads to TCF12 microdeletion in a patient presenting with coronal craniosynostosis and intellectual disability. American Journal of Medical Genetics Part A. 164(6). 1530–1536. 13 indexed citations
9.
Petit, Florence, Joris Andrieux, Geneviève Baujat, et al.. (2013). Split hand/foot malformation with long‐bone deficiency and BHLHA9 duplication: report of 13 new families. Clinical Genetics. 85(5). 464–469. 17 indexed citations
10.
Ego, Anne, et al.. (2013). Stillbirth classification in population-based data and role of fetal growth restriction: the example of RECODE. BMC Pregnancy and Childbirth. 13(1). 182–182. 13 indexed citations
11.
Coutton, Charles, Raoudha Zouari, Mariem Ben Khelifa, et al.. (2012). MLPA and sequence analysis of DPY19L2 reveals point mutations causing globozoospermia. Human Reproduction. 27(8). 2549–2558. 52 indexed citations
12.
Edery, Patrick, Charles Marcaillou, Mourad Sahbatou, et al.. (2011). Association of TALS Developmental Disorder with Defect in Minor Splicing Component U4atac snRNA. Science. 332(6026). 240–243. 159 indexed citations
13.
Millat, Gilles, Patrice Bouvagnet, Philippe Chevalier, et al.. (2011). Clinical and mutational spectrum in a cohort of 105 unrelated patients with dilated cardiomyopathy. European Journal of Medical Genetics. 54(6). e570–e575. 75 indexed citations
14.
Jouk, Pierre‐Simon, Jean-Jacques Roux, Ariane Paoloni‐Giacobino, et al.. (2008). Prenatal manifestation in a family affected by nevoid basal cell carcinoma syndrome. European Journal of Medical Genetics. 51(5). 472–478. 7 indexed citations
15.
Guillem, Pascale, Christine Cans, Elisabeth Robert‐Gnansia, Ségolène Aymé, & Pierre‐Simon Jouk. (2007). Rare diseases in disabled children: an epidemiological survey. Archives of Disease in Childhood. 93(2). 115–118. 26 indexed citations
16.
Jouk, Pierre‐Simon, Annick Labarre‐Vila, Paulette Mezin, et al.. (2007). C.P.1.13 A homozygous null mutation in TPM2 gene causes autosomal recessive nemaline myopathy associated with multiple pterygia. Neuromuscular Disorders. 17(9-10). 837–838. 2 indexed citations
17.
18.
Mallaret, Michel, et al.. (2003). Carbimazole-Related Gastroschisis. Annals of Pharmacotherapy. 37(6). 829–831. 11 indexed citations
19.
Jouk, Pierre‐Simon, et al.. (2001). Diastrophic dwarfism and pregnancy. The Lancet. 358(9295). 1778–1778. 8 indexed citations
20.
Satre, Véronique, Nicole Monnier, Carmen Ayuso, et al.. (1999). 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. 65(1). 68–76. 42 indexed citations

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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