Jean‐Louis Blouin

5.3k total citations
75 papers, 2.4k citations indexed

About

Jean‐Louis Blouin is a scholar working on Genetics, Molecular Biology and Surgery. According to data from OpenAlex, Jean‐Louis Blouin has authored 75 papers receiving a total of 2.4k indexed citations (citations by other indexed papers that have themselves been cited), including 41 papers in Genetics, 32 papers in Molecular Biology and 14 papers in Surgery. Recurrent topics in Jean‐Louis Blouin's work include Genomic variations and chromosomal abnormalities (20 papers), Genetics and Neurodevelopmental Disorders (12 papers) and Prenatal Screening and Diagnostics (10 papers). Jean‐Louis Blouin is often cited by papers focused on Genomic variations and chromosomal abnormalities (20 papers), Genetics and Neurodevelopmental Disorders (12 papers) and Prenatal Screening and Diagnostics (10 papers). Jean‐Louis Blouin collaborates with scholars based in Switzerland, United States and France. Jean‐Louis Blouin's co-authors include Stylianos E. Antonarakis, Colette Rossier, Corinne Gehrig, Annie Nicole, Lucia Bartoloni, Zoubida Chettouh, M Prieur, C.D. DeLozier-Blanchet, Zohra Rahmani and Alain Aurias and has published in prestigious journals such as Proceedings of the National Academy of Sciences, The Journal of Clinical Endocrinology & Metabolism and Diabetes.

In The Last Decade

Jean‐Louis Blouin

72 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
Jean‐Louis Blouin Switzerland 27 1.1k 1.0k 376 309 280 75 2.4k
Paul Renbaum Israel 28 976 0.9× 1.6k 1.5× 413 1.1× 256 0.8× 816 2.9× 87 3.2k
Sabrina Giglio Italy 29 1.3k 1.2× 1.5k 1.4× 158 0.4× 111 0.4× 422 1.5× 116 2.6k
Ann Nordgren Sweden 29 997 0.9× 1.1k 1.1× 91 0.2× 644 2.1× 391 1.4× 134 2.6k
Annie Laquerrière France 32 584 0.5× 1.4k 1.3× 241 0.6× 153 0.5× 564 2.0× 109 3.3k
Marwan Shinawi United States 32 1.5k 1.4× 2.4k 2.3× 226 0.6× 113 0.4× 375 1.3× 137 4.3k
Bassem A. Bejjani United States 36 2.6k 2.4× 1.8k 1.7× 143 0.4× 142 0.5× 1.0k 3.6× 83 4.1k
Andrew D. Darnel Japan 26 482 0.4× 568 0.5× 311 0.8× 64 0.2× 82 0.3× 33 1.8k
Katrina Rack United Kingdom 23 390 0.4× 721 0.7× 86 0.2× 151 0.5× 106 0.4× 58 1.6k
Martin J. Somerville Canada 23 640 0.6× 767 0.7× 79 0.2× 80 0.3× 208 0.7× 45 1.8k
Mirja Somer Finland 25 816 0.8× 1.5k 1.4× 135 0.4× 42 0.1× 240 0.9× 49 2.4k

Countries citing papers authored by Jean‐Louis Blouin

Since Specialization
Citations

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

Fields of papers citing papers by Jean‐Louis Blouin

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Jean‐Louis Blouin. 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 Jean‐Louis Blouin. The network helps show where Jean‐Louis Blouin may publish in the future.

Co-authorship network of co-authors of Jean‐Louis Blouin

This figure shows the co-authorship network connecting the top 25 collaborators of Jean‐Louis Blouin. A scholar is included among the top collaborators of Jean‐Louis Blouin 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 Jean‐Louis Blouin. Jean‐Louis Blouin 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
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Pievani, Michela, Federica Ribaldi, João Jorge, et al.. (2024). Resting-state functional connectivity abnormalities in subjective cognitive decline: A 7T MRI study. Neurobiology of Aging. 144. 104–113. 1 indexed citations
3.
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Fokstuen, Siv, Lina Quteineh, Valérie Schwitzgebel, et al.. (2023). Noninvasive prenatal diagnosis of Mendelian disorders for consanguineous couples by relative genotype dosage. Clinical Genetics. 104(5). 505–515. 3 indexed citations
5.
Lang‐Muritano, Mariarosaria, et al.. (2022). Atypical familial diabetes associated with a novel NEUROD1 nonsense variant. Journal of Pediatric Endocrinology and Metabolism. 36(1). 101–104.
6.
Marconi, Caterina, Laure Lemmens, Frédéric G. Masclaux, et al.. (2021). Bi‐allelic loss of ERGIC1 causes relatively mild arthrogryposis. Clinical Genetics. 100(3). 329–333. 4 indexed citations
7.
Nouspikel, Thierry, et al.. (2021). Precision medicine in diabetes: A non‐invasive prenatal diagnostic test for the determination of fetal glucokinase mutations. Journal of Diabetes Investigation. 13(2). 256–261. 8 indexed citations
8.
Verkauskienė, Rasa, Jean‐Louis Blouin, Philippe Klee, et al.. (2020). Systematic Genetic Study of Youth With Diabetes in a Single Country Reveals the Prevalence of Diabetes Subtypes, Novel Candidate Genes, and Response to Precision Therapy. Diabetes. 69(5). 1065–1071. 19 indexed citations
9.
Lambert, Nelle, Emmanuelle Ranza, Periklis Makrythanasis, et al.. (2018). Novel NEXMIF pathogenic variant in a boy with severe autistic features, intellectual disability, and epilepsy, and his mildly affected mother. Journal of Human Genetics. 63(7). 847–850. 17 indexed citations
10.
Klee, Philippe, Mirjam Dirlewanger, Vanessa Lavallard, et al.. (2018). Combined Pancreatic Islet-Lung-Liver Transplantation in a Pediatric Patient with Cystic Fibrosis-Related Diabetes. Hormone Research in Paediatrics. 90(4). 270–274. 5 indexed citations
11.
Soravia, Claudio, Celia D. Delozier, Zuzana Dobbie, et al.. (2005). Double frameshift mutations in APC and MSH2 in the same individual. International Journal of Colorectal Disease. 20(5). 466–470. 16 indexed citations
12.
Dauvilliers, Yves, Jean‐Louis Blouin, Elisabeth Neidhart, et al.. (2004). A narcolepsy susceptibility locus maps to a 5Mb region of chromosome 21q. Annals of Neurology. 56(3). 382–388. 31 indexed citations
13.
Bartoloni, Lucia, Jean‐Louis Blouin, Amit K. Maiti, et al.. (2001). Axonemal Beta Heavy Chain Dynein DNAH9: cDNA Sequence, Genomic Structure, and Investigation of Its Role in Primary Ciliary Dyskinesia. Genomics. 72(1). 21–33. 39 indexed citations
14.
Stratakis, Constantine A., Lawrence S. Kirschner, Susan E. Taymans, et al.. (1998). Carney Complex, Peutz-Jeghers Syndrome, Cowden Disease, and Bannayan-Zonana Syndrome Share Cutaneous and Endocrine Manifestations, But Not Genetic Loci. The Journal of Clinical Endocrinology & Metabolism. 83(8). 2972–2976. 39 indexed citations
15.
Neerman‐Arbez, Marguerite, Stylianos E. Antonarakis, Jean‐Louis Blouin, et al.. (1997). The Locus for Combined Factor V-Factor VIII Deficiency (F5F8D) Maps to 18q21, between D18S849 and D18S1103. The American Journal of Human Genetics. 61(1). 143–150. 34 indexed citations
16.
Antonarakis, Stylianos E., Jean‐Louis Blouin, H H Kazazian, et al.. (1996). Linkage and sib-pair analysis reveal a potential schizophrenia susceptibility gene on chromosome 13q32. Psychiatric Genetics. 6(3). 136–136. 16 indexed citations
17.
Nadal, Marga, Montserrat Milà, Melanie Pritchard, et al.. (1996). YAC and cosmid FISH mapping of an unbalanced chromosomal translocation causing partial trisomy 21 and Down syndrome. Human Genetics. 98(4). 460–466. 14 indexed citations
18.
Morris, Michael A., et al.. (1995). Cloning of the cDNA for the Human ATP Synthase OSCP Subunit (ATP50) by Exon Trapping and Mapping to Chromosome 21q22.1-q22.2. Genomics. 28(3). 470–476. 21 indexed citations
19.
Ceballos, I., Annie Nicole, Pascale Briand, et al.. (1991). Expression of Human Cu-Zn Superoxide Dismutase Gene in Transgenic Mice: Model for Gene Dosage Effect in Down Syndrome. Free Radical Research Communications. 13(1). 581–589. 32 indexed citations
20.
Blouin, Jean‐Louis, Zohra Rahmani, Zoubida Chettouh, et al.. (1990). Slot blot method for the quantification of DNA sequences and mapping of chromosome rearrangements: application to chromosome 21.. PubMed. 46(3). 518–26. 17 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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