Joris Andrieux

8.5k total citations
97 papers, 2.0k citations indexed

About

Joris Andrieux is a scholar working on Genetics, Molecular Biology and Genetics. According to data from OpenAlex, Joris Andrieux has authored 97 papers receiving a total of 2.0k indexed citations (citations by other indexed papers that have themselves been cited), including 66 papers in Genetics, 45 papers in Molecular Biology and 21 papers in Genetics. Recurrent topics in Joris Andrieux's work include Genomic variations and chromosomal abnormalities (48 papers), Genetics and Neurodevelopmental Disorders (25 papers) and Congenital heart defects research (16 papers). Joris Andrieux is often cited by papers focused on Genomic variations and chromosomal abnormalities (48 papers), Genetics and Neurodevelopmental Disorders (25 papers) and Congenital heart defects research (16 papers). Joris Andrieux collaborates with scholars based in France, United Kingdom and United States. Joris Andrieux's co-authors include Muriel Holder‐Espinasse, Cédric Le Caignec, Florence Petit, Bruno Delobel, F Bauters, Sylvie Manouvrier‐Hanu, Maria Tropeano, David Collier, Frenny Sheth and Jean Luc Laı̈ and has published in prestigious journals such as SHILAP Revista de lepidopterología, Blood and PLoS ONE.

In The Last Decade

Joris Andrieux

94 papers receiving 1.9k citations

Peers

Joris Andrieux
Christophe Philippe France
Palma Finelli Italy
Francisco Martı́nez Spain
David Geneviève France
Bruno Leheup France
Desirée du Sart Australia
Mitsuo Masuno Japan
W. Roy Breg United States
Willy M. Nillesen Netherlands
Israela Lerer Israel
Christophe Philippe France
Joris Andrieux
Citations per year, relative to Joris Andrieux Joris Andrieux (= 1×) peers Christophe Philippe

Countries citing papers authored by Joris Andrieux

Since Specialization
Citations

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

Fields of papers citing papers by Joris Andrieux

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Joris Andrieux

This figure shows the co-authorship network connecting the top 25 collaborators of Joris Andrieux. A scholar is included among the top collaborators of Joris Andrieux 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 Joris Andrieux. Joris Andrieux 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.
Leppä, Virpi, Stephanie N. Kravitz, Alastair J. Martin, et al.. (2016). Rare Inherited and De Novo CNVs Reveal Complex Contributions to ASD Risk in Multiplex Families. The American Journal of Human Genetics. 99(3). 540–554. 121 indexed citations
2.
Sheth, Frenny, et al.. (2015). Pure interstitial dup(6)(q22.31q22.31) – a case report. ˜The œItalian Journal of Pediatrics/Italian journal of pediatrics. 41(1). 5–5. 3 indexed citations
3.
Dharmadhikari, Avinash V., Tomasz Gambin, Przemysław Szafrański, et al.. (2014). Molecular and clinical analyses of 16q24.1 duplications involving FOXF1 identify an evolutionarily unstable large minisatellite. BMC Medical Genetics. 15(1). 128–128. 21 indexed citations
4.
Andrieux, Joris, Florence Petit, Sonia Bouquillon, et al.. (2014). ELNgene triplication responsible for familial supravalvular aortic aneurysm. Cardiology in the Young. 25(4). 712–717. 17 indexed citations
5.
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
6.
Tropeano, Maria, Joris Andrieux, & David Collier. (2013). Clinical utility gene card for: 16p13.11 microdeletion syndrome. European Journal of Human Genetics. 22(5). 713–713. 18 indexed citations
7.
Sheth, Frenny, et al.. (2013). Chromosomal imbalance letter: Phenotypic consequences of combined deletion 8pter and duplication 15qter. Molecular Cytogenetics. 6(1). 24–24. 1 indexed citations
8.
Bonnet, Céline, Asma Ali Khan, Emmanuel Bresso, et al.. (2013). Extended spectrum of MBD5 mutations in neurodevelopmental disorders. European Journal of Human Genetics. 21(12). 1457–1461. 30 indexed citations
9.
Petit, Florence, Joris Andrieux, Muriel Holder‐Espinasse, et al.. (2011). Xq12q13.1 microduplication encompassing the EFNB1 gene in a boy with congenital diaphragmatic hernia. European Journal of Medical Genetics. 54(5). e525–e527. 8 indexed citations
10.
Sheth, Frenny, Joris Andrieux, Elisabeth Ewers, et al.. (2011). Characterization of sSMC by FISH and molecular techniques. European Journal of Medical Genetics. 54(3). 247–255. 14 indexed citations
11.
Becker, Jutta, Raoul Heller, Odile Boute, et al.. (2011). 7 Mb de novo deletion within 8q21 in a patient with distal arthrogryposis type 2B (DA2B). European Journal of Medical Genetics. 54(5). e495–e500. 7 indexed citations
12.
Sheth, Frenny, Joris Andrieux, & Jayesh Sheth. (2010). Supernumerary marker chromosome in a child with microcephaly and mental retardation. Indian Pediatrics. 47(3). 277–279. 7 indexed citations
13.
Katzaki, Eleni, Gilles Morin, Marzia Pollazzon, et al.. (2010). Syndromic mental retardation with thrombocytopenia due to 21q22.11q22.12 deletion: Report of three patients. American Journal of Medical Genetics Part A. 152A(7). 1711–1717. 19 indexed citations
14.
Andrieux, Joris, Christèle Dubourg, Marlène Rio, et al.. (2009). Genotype–phenotype correlation in four 15q24 deleted patients identified by array‐CGH. American Journal of Medical Genetics Part A. 149A(12). 2813–2819. 27 indexed citations
15.
Sheth, Frenny, Elisabeth Ewers, Nadezda Kosyakova, et al.. (2009). A small supernumerary marker chromosome present in a Turner syndrome patient not derived from X- or Y-chromosome: a case report. Molecular Cytogenetics. 2(1). 22–22. 13 indexed citations
16.
Meur, Nathalie Le, Muriel Holder‐Espinasse, Sylvie Jaillard, et al.. (2009). MEF2C haploinsufficiency caused by either microdeletion of the 5q14.3 region or mutation is responsible for severe mental retardation with stereotypic movements, epilepsy and/or cerebral malformations. Journal of Medical Genetics. 47(1). 22–29. 150 indexed citations
17.
Doco‐Fenzy, Martine, Emilie Landais, Joris Andrieux, et al.. (2008). Deletion 2q36.2q36.3 with multiple renal cysts and severe mental retardation. European Journal of Medical Genetics. 51(6). 598–607. 8 indexed citations
18.
Andrieux, Joris, Catherine Roche‐Lestienne, Sandrine Geffroy, et al.. (2007). Bone morphogenetic protein antagonist gene NOG is involved in myeloproliferative disease associated with myelofibrosis. Cancer Genetics and Cytogenetics. 178(1). 11–16. 8 indexed citations
19.
Andrieux, Joris, Sandra Fert‐Ferrer, Marie‐Christine Copin, et al.. (2003). Three new cases of non-Hodgkin lymphoma with t(9;14)(p13;q32). Cancer Genetics and Cytogenetics. 145(1). 65–69. 9 indexed citations
20.
Andrieux, Joris, I. Frachon, Christophe Leroyer, et al.. (2002). Quantification of CFTR splice variants in adults with disseminated bronchiectasis, using the TaqMan fluorogenic detection system. Clinical Genetics. 62(1). 60–67. 11 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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