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

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

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20 of 20 papers shown

#	Work	Indexed citations
1	Rare Inherited and De Novo CNVs Reveal Complex Contributions to ASD Risk in Multiplex Families 2016 ·The American Journal of Human Genetics ·Virpi Leppä, Stephanie N. Kravitz, Alastair J. Martin, Joris Andrieux, Cédric Le Caignec, Dominique Martin‐Coignard, (unknown), Stephan Sanders, Jennifer K. Lowe, Rita M. Cantor, Daniel H. Geschwind	121
2	Pure interstitial dup(6)(q22.31q22.31) – a case report 2015 ·The Italian Journal of Pediatrics/Italian journal of pediatrics ·Frenny Sheth, (unknown), Joris Andrieux, Jean-Louis Blouin, Jayesh Sheth	3
3	Molecular and clinical analyses of 16q24.1 duplications involving FOXF1 identify an evolutionarily unstable large minisatellite 2014 ·BMC Medical Genetics ·Avinash V. Dharmadhikari, Tomasz Gambin, Przemysław Szafrański, Wenjian Cao, Frank J. Probst, Weihong Jin, Ping Fang, Krzysztof Gogolewski, Anna Gambin, (unknown), Sailaja Golla, (unknown), Bénédicte Duban‐Bedu, Bruno Delobel, Joris Andrieux, Kerstin Becker, Elke Holinski‐Feder, Sau Wai Cheung, Paweł Stankiewicz	21
4	ELNgene triplication responsible for familial supravalvular aortic aneurysm 2014 ·Cardiology in the Young ·(unknown), Joris Andrieux, Florence Petit, (unknown), Sonia Bouquillon, Sylvie Manouvrier‐Hanu, Jiddeke van de Kamp, Cathérine Boileau, Nadine Hanna, Guillaume Jondeau, Guy Vaksmann, V. Houfflin‐Debarge, Muriel Holder‐Espinasse	17
5	Split hand/foot malformation with long‐bone deficiency and BHLHA9 duplication: report of 13 new families 2013 ·Clinical Genetics ·Florence Petit, (unknown), 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	17
6	Clinical utility gene card for: 16p13.11 microdeletion syndrome 2013 ·European Journal of Human Genetics ·Maria Tropeano, Joris Andrieux, David Collier	18
7	Chromosomal imbalance letter: Phenotypic consequences of combined deletion 8pter and duplication 15qter 2013 ·Molecular Cytogenetics ·Frenny Sheth, Joris Andrieux, (unknown), Harsh Sheth, Manisha Desai, (unknown), (unknown), Jayesh Sheth	1
8	Extended spectrum of MBD5 mutations in neurodevelopmental disorders 2013 ·European Journal of Human Genetics ·Céline Bonnet, Asma Ali Khan, Emmanuel Bresso, (unknown), Mylène Béri, (unknown), (unknown), Joris Andrieux, Christophe Philippe, Anne Moncla, Irina Giurgea, Marie‐Dominique Devignes, Bruno Leheup, Philippe Jonveaux	30
9	Xq12q13.1 microduplication encompassing the EFNB1 gene in a boy with congenital diaphragmatic hernia 2011 ·European Journal of Medical Genetics ·Florence Petit, Joris Andrieux, Muriel Holder‐Espinasse, Sonia Bouquillon, Thomas Pennaforte, Laurent Storme, Sylvie Manouvrier‐Hanu	8
10	Characterization of sSMC by FISH and molecular techniques 2011 ·European Journal of Medical Genetics ·Frenny Sheth, Joris Andrieux, Elisabeth Ewers, Nadezda Kosyakova, Anja Weise, Harsh Sheth, Serge Romana, (unknown), Bruno Delobel, Olivier Theisen, Thomas Liehr, Sheela Nampoothiri, Jayesh Sheth	14
11	7 Mb de novo deletion within 8q21 in a patient with distal arthrogryposis type 2B (DA2B) 2011 ·European Journal of Medical Genetics ·(unknown), Jutta Becker, Raoul Heller, Odile Boute, Joris Andrieux, Juliane Hoyer, Arif B. Ekici, André Reis, Anita Rauch	7
12	Supernumerary marker chromosome in a child with microcephaly and mental retardation 2010 ·Indian Pediatrics ·Frenny Sheth, Joris Andrieux, Jayesh Sheth	7
13	Syndromic mental retardation with thrombocytopenia due to 21q22.11q22.12 deletion: Report of three patients 2010 ·American Journal of Medical Genetics Part A ·Eleni Katzaki, Gilles Morin, Marzia Pollazzon, Filomena Tiziana Papa, Sabrina Buoni, Joussef Hayek, Joris Andrieux, Laure Lecerf, Cornel Popovici, Aline Receveur, Michèle Mathieu‐Dramard, Alessandra Renieri, Francesca Mari, Nicole Philip	19
14	Genotype–phenotype correlation in four 15q24 deleted patients identified by array‐CGH 2009 ·American Journal of Medical Genetics Part A ·Joris Andrieux, Christèle Dubourg, Marlène Rio, Tania Attié‐Bitach, Elsa Delaby, Michèle Mathieu, Hubert Journel, Henri Copin, (unknown), Martine Doco‐Fenzy, Emilie Landais, Bruno Delobel, Sylvie Odent, Sylvie Manouvrier‐Hanu, Muriel Holder‐Espinasse	27
15	A small supernumerary marker chromosome present in a Turner syndrome patient not derived from X- or Y-chromosome: a case report 2009 ·Molecular Cytogenetics ·Frenny Sheth, Elisabeth Ewers, Nadezda Kosyakova, Anja Weise, Jayesh Sheth, Manisha Desai, Joris Andrieux, Joris Vermeesch, Ahmed B. Hamid, Monika Ziegler, Thomas Liehr	13
16	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 2009 ·Journal of Medical Genetics ·Nathalie Le Meur, Muriel Holder‐Espinasse, Sylvie Jaillard, Alice Goldenberg, Sylvie Joriot, Patrizia Amati‐Bonneau, Agnès Guichet, M. Barth, Aude Charollais, Hubert Journel, Stéphane Auvin, (unknown), Jean Pierre Kerckaert, Véronique David, Sylvie Manouvrier‐Hanu, Pascale Saugier-Véber, Thierry Frébourg, (unknown), Joris Andrieux, Dominique Bonneau	150
17	Deletion 2q36.2q36.3 with multiple renal cysts and severe mental retardation 2008 ·European Journal of Medical Genetics ·Martine Doco‐Fenzy, Emilie Landais, Joris Andrieux, Anouck Schneider, Brigitte Delemer, V. Sulmont, (unknown), Dominique Ploton, (unknown), Jean‐Claude Monboisse, M. Belouadah, (unknown), A. Durlach, Michel Goossens, Juliette Albuisson, Jacques Motté, Dominique Gaillard	8
18	Bone morphogenetic protein antagonist gene NOG is involved in myeloproliferative disease associated with myelofibrosis 2007 ·Cancer Genetics and Cytogenetics ·Joris Andrieux, Catherine Roche‐Lestienne, Sandrine Geffroy, Christophe Desterke, Nathalie Grardel, Isabelle Plantier, Dominik Selleslag, Jean‐Loup Demory, Jean-Luc Laı̈, Xavier Leleu, Marie‐Caroline Le Bousse‐Kerdilès, Peter Vandenberghe	8
19	Three new cases of non-Hodgkin lymphoma with t(9;14)(p13;q32) 2003 ·Cancer Genetics and Cytogenetics ·Joris Andrieux, Sandra Fert‐Ferrer, Marie‐Christine Copin, Pauline Huyghe, (unknown), James Lespinasse, F Bauters, Jean Luc Laı̈, Bruno Quesnel	9
20	Quantification of CFTR splice variants in adults with disseminated bronchiectasis, using the TaqMan fluorogenic detection system 2002 ·Clinical Genetics ·Joris Andrieux, (unknown), I. Frachon, Christophe Leroyer, C. Rogé, Virginie Scotet, Claude Férec	11

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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