Patrice Eydoux

3.1k total citations
67 papers, 1.2k citations indexed

About

Patrice Eydoux is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Patrice Eydoux has authored 67 papers receiving a total of 1.2k indexed citations (citations by other indexed papers that have themselves been cited), including 35 papers in Molecular Biology, 34 papers in Genetics and 15 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Patrice Eydoux's work include Genomic variations and chromosomal abnormalities (21 papers), Prenatal Screening and Diagnostics (11 papers) and Congenital heart defects research (7 papers). Patrice Eydoux is often cited by papers focused on Genomic variations and chromosomal abnormalities (21 papers), Prenatal Screening and Diagnostics (11 papers) and Congenital heart defects research (7 papers). Patrice Eydoux collaborates with scholars based in Canada, United States and France. Patrice Eydoux's co-authors include Marco A. Marra, William T. Gibson, Jan M. Friedman, David Chitayat, Sylvie Langlois, Steven J.M. Jones, Rebecca L. Hood, Dennis E. Bulman, Shing H. Zhan and Richard A. Moore and has published in prestigious journals such as SHILAP Revista de lepidopterología, Blood and The American Journal of Human Genetics.

In The Last Decade

Patrice Eydoux

67 papers receiving 1.1k citations

Peers

Countries citing papers authored by Patrice Eydoux

Since Specialization

Citations

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

Fields of papers citing papers by Patrice Eydoux

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Patrice Eydoux

This figure shows the co-authorship network connecting the top 25 collaborators of Patrice Eydoux. A scholar is included among the top collaborators of Patrice Eydoux 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 Patrice Eydoux. Patrice Eydoux 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	The Eμ-Ret mouse is a novel model of hyperdiploid B-cell acute lymphoblastic leukemia 2024 ·Leukemia ·Ali Farrokhi, (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), Sumin Jo, (unknown), (unknown), (unknown), Franziska Auer, Julia Hauer, Stephan A. Grupp, Patrice Eydoux, Philipp F. Lange, Alix E. Seif, Christopher A. Maxwell, Gregor S. D. Reid	2
2	An approach to rapid characterization of DMD copy number variants for prenatal risk assessment 2021 ·American Journal of Medical Genetics Part A ·(unknown), Kieran O’Neill, (unknown), Lindsay Brown, Kamilla Schlade‐Bartusiak, Patrice Eydoux, Rosemarie Rupps, (unknown), Cornelius F. Boerkoel, Steven J.M. Jones	7
3	BMPER variants associated with a novel, attenuated subtype of diaphanospondylodysostosis 2015 ·Journal of Human Genetics ·(unknown), (unknown), Firoz Miyanji, (unknown), Christopher W. Reilly, Elena Lopez‐Rangel, Stephen J. Tredwell, (unknown), Allen Delaney, Patrice Eydoux, Margot Van Allen, Anna Lehman	11
4	Single exon-resolution targeted chromosomal microarray analysis of known and candidate intellectual disability genes 2013 ·European Journal of Human Genetics ·Tracy Tucker, Farah Zahir, Malachi Griffith, Allen Delaney, David Chai, Erica S. Tsang, Emmanuelle Lemyre, Sylvia Dobrzeniecka, Marco A. Marra, Patrice Eydoux, Sylvie Langlois, Fadi F. Hamdan, Jacques L. Michaud, Jan M. Friedman	30
5	Independent post-zygotic breaks of a dicentric chromosome result in mosaicism for an inverted duplication deletion 9p and terminal deletion 9p 2013 ·European Journal of Medical Genetics ·Kamilla Schlade‐Bartusiak, Tracy Tucker, (unknown), (unknown), Margot I. Van Allen, Patrice Eydoux, Linlea Armstrong	6
6	Uniparental disomy: can SNP array data be used for diagnosis? 2012 ·Genetics in Medicine ·Tracy Tucker, Kamilla Schlade‐Bartusiak, Patrice Eydoux, Tanya N. Nelson, Lindsay Brown	24
7	BPES with atypical premature ovarian insufficiency, and evidence of mitotic recombination, in a woman with trisomy X and a translocation t(3;11)(q22.3;q14.1) 2012 ·American Journal of Medical Genetics Part A ·Kamilla Schlade‐Bartusiak, Lindsay Brown, Brenda Lomax, Hélène Bruyèrè, (unknown), Sara Hamilton, Barbara McGillivray, Patrice Eydoux	19
8	Co‐occurrence of Joubert syndrome and Jeune asphyxiating thoracic dystrophy 2010 ·American Journal of Medical Genetics Part A ·Anna Lehman, Patrice Eydoux, D Doherty, Ian A. Glass, David Chitayat, Brian Y. Chung, Sylvie Langlois, Siu Li Yong, R. Brian Lowry, Friedhelm Hildebrandt, Peter Trnka	27
9	Molecular breakpoint mapping of 6q11‐q14 interstitial deletions in seven patients 2009 ·American Journal of Medical Genetics Part A ·Jia‐Chi Wang, (unknown), Brenda Lomax, Lesley Turner, Mary Shago, Ahmad S. Teebi, Regan Klatt, Patrick MacLeod, Siu‐Li Yong, Małgorzata J.M. Nowaczyk, Patrice Eydoux	6
10	A characteristic syndrome associated with microduplication of 8q12, inclusive of CHD7 2009 ·European Journal of Medical Genetics ·Anna Lehman, Jan M. Friedman, David Chai, Farah Zahir, Marco A. Marra, (unknown), Erica S. Tsang, Patrice Eydoux, Linlea Armstrong	17
11	A novel de novo 1.1 Mb duplication of 17q21.33 associated with cognitive impairment and other anomalies 2009 ·American Journal of Medical Genetics Part A ·Farah Zahir, Sylvie Langlois, (unknown), Patrice Eydoux, Marco A. Marra, Jan M. Friedman	11
12	Craniosynostosis associated with distal 5q‐trisomy: Further evidence that extra copy of MSX2 gene leads to craniosynostosis 2007 ·American Journal of Medical Genetics Part A ·Jia‐Chi Wang, Michelle Steinraths, (unknown), Brenda Lomax, Patrice Eydoux, Tracy Stockley, Siu‐Li Yong, Margot I. Van Allen	15
13	Translocation (Y;22) resulting in the loss of SHOX and isolated short stature 2003 ·American Journal of Medical Genetics Part A ·(unknown), Juliane Léger, Olivier Dupuy, Mohammed Hassan, (unknown), Aziza Lebbar, P Czernichow, Patrice Eydoux	17
14	Isolated non-compaction of the myocardium diagnosed in the fetus: two sporadic and two familial cases 2002 ·Cardiology in the Young ·Cláudia Moura, Y. Hillion, Farida Daïkha-Dahmane, Patrice Eydoux, C. Fallet, Jean Oury, (unknown)	29
15	Trisomy of Chromosome 10 in Two Cases of Ovarian Carcinoma 2000 ·Cancer Genetics and Cytogenetics ·Jia‐Chi Wang, Anne‐Marie Mes‐Masson, Patricia N. Tonin, Diane Provencher, Patrice Eydoux	3
16	Spastic paraplegia, optic atrophy, microcephaly with normal intelligence, and XY sex reversal: a new autosomal recessive syndrome? 1998 ·Journal of Medical Genetics ·Ahmad S. Teebi, Steven P. Miller, Harry Ostrer, Patrice Eydoux, (unknown), Kamaldine Oudjhane, Gordon V. Watters	4
17	Assignment of renal specific Na<sup>+</sup>-Phosphate cotransporter gene <i>Slc17a</i><i>1</i> to mouse chromosome bands 13A3→A4 by in situ hybridization 1997 ·Cytogenetic and Genome Research ·(unknown), Harriet S. Tenenhouse, A.S. Hewson, Patrice Eydoux	3
18	Assignment of the Gene for Cystinuria (SLC3A1) to Human Chromosome 2p21 by Fluorescence in Situ Hybridization 1994 ·Genomics ·Xiaoxiang Zhang, Rima Rozen, Matthias A. Hediger, Paul Goodyer, Patrice Eydoux	29
19	Chorionic villus sampling after first trimester diagnosis of fetal cystic hygroma colli 1989 ·European Journal of Obstetrics & Gynecology and Reproductive Biology ·J C Pons, (unknown), Patrice Eydoux, (unknown), S. Doumerc, R. Frydman, E Papiernik	17
20	Chorionic villus sampling (CVS). Randomized study of efficacy of two transcervical biopsy methods: aspiration canulas and small forceps 1989 ·European Journal of Obstetrics & Gynecology and Reproductive Biology ·J C Pons, H. Fernández, Patrice Eydoux, (unknown), S. Doumerc, R. Frydman, E Papiernik	4

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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