Philippe Parent

2.6k total citations
35 papers, 518 citations indexed

About

Philippe Parent is a scholar working on Genetics, Pulmonary and Respiratory Medicine and Molecular Biology. According to data from OpenAlex, Philippe Parent has authored 35 papers receiving a total of 518 indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Genetics, 13 papers in Pulmonary and Respiratory Medicine and 9 papers in Molecular Biology. Recurrent topics in Philippe Parent's work include Cystic Fibrosis Research Advances (9 papers), Genomic variations and chromosomal abnormalities (9 papers) and Neonatal Respiratory Health Research (4 papers). Philippe Parent is often cited by papers focused on Cystic Fibrosis Research Advances (9 papers), Genomic variations and chromosomal abnormalities (9 papers) and Neonatal Respiratory Health Research (4 papers). Philippe Parent collaborates with scholars based in France, United Kingdom and Italy. Philippe Parent's co-authors include Marc De Braekeleer, Claude Férec, I. Duguépéroux, Virginie Scotet, Marie‐Pierre Audrézet, Fréderic Morel, Nathalie Douet‐Guilbert, C. Verlingue, Bernard Mercier and G. Rault and has published in prestigious journals such as The Lancet, Annals of Neurology and Social Science & Medicine.

In The Last Decade

Philippe Parent

34 papers receiving 482 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Philippe Parent France 14 210 208 130 118 49 35 518
Kaplan Jc France 12 167 0.8× 67 0.3× 185 1.4× 89 0.8× 13 0.3× 50 405
G. Fekete Hungary 12 48 0.2× 173 0.8× 281 2.2× 75 0.6× 14 0.3× 32 490
Anne De Paepe Belgium 12 60 0.3× 298 1.4× 85 0.7× 73 0.6× 19 0.4× 21 434
Alexandra Efthymiadou Greece 12 179 0.9× 108 0.5× 119 0.9× 33 0.3× 7 0.1× 27 485
Peggy Modaff United States 15 150 0.7× 297 1.4× 229 1.8× 108 0.9× 7 0.1× 35 625
J. W. E. Oorthuys Netherlands 12 45 0.2× 345 1.7× 211 1.6× 87 0.7× 16 0.3× 25 558
Judith M.A. Verhagen Netherlands 11 105 0.5× 161 0.8× 184 1.4× 42 0.4× 5 0.1× 35 464
Cheryl S. Reid United States 11 101 0.5× 321 1.5× 89 0.7× 47 0.4× 12 0.2× 18 483
Julia E. Ostberg United Kingdom 10 112 0.5× 389 1.9× 188 1.4× 26 0.2× 16 0.3× 15 592
Anne Bergougnoux France 15 311 1.5× 116 0.6× 225 1.7× 33 0.3× 5 0.1× 41 685

Countries citing papers authored by Philippe Parent

Since Specialization
Citations

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

Fields of papers citing papers by Philippe Parent

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Philippe Parent

This figure shows the co-authorship network connecting the top 25 collaborators of Philippe Parent. A scholar is included among the top collaborators of Philippe Parent 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 Philippe Parent. Philippe Parent 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.
Tougeron, David, Simon Pernot, Thibault Mazard, et al.. (2024). 143P Efficacy of immunotherapy in gastro-intestinal (GI) tumors with mismatch repair deficient (MMRd) unusual phenotype. Annals of Oncology. 35. S272–S272. 1 indexed citations
2.
Duguépéroux, I., Marie‐Pierre Audrézet, G. Rault, et al.. (2016). Highlighting the impact of cascade carrier testing in cystic fibrosis families. Journal of Cystic Fibrosis. 15(4). 452–459. 10 indexed citations
3.
Carpenter, Gillian, Mariaevelina Alfieri, Rita Colnaghi, et al.. (2016). Oral-facial-digital syndrome type I cells exhibit impaired DNA repair; unanticipated consequences of defective OFD1 outside of the cilia network. Human Molecular Genetics. 26(1). ddw364–ddw364. 14 indexed citations
4.
Ruivard, M., M. Bonnin, J.-L. Pouly, et al.. (2015). Influence des anticoagulants sur la prise en charge péri-partum. Gynécologie Obstétrique & Fertilité. 43(3). 187–190. 4 indexed citations
5.
Giudice, Ennio Del, Alessandra D’Amico, Philippe Parent, et al.. (2014). CNS involvement in OFD1 syndrome: a clinical, molecular, and neuroimaging study. Orphanet Journal of Rare Diseases. 9(1). 74–74. 29 indexed citations
6.
Duguépéroux, I., Marie‐Pierre Audrézet, Philippe Parent, et al.. (2012). Cascade testing in families of carriers identified through newborn screening in Western Brittany (France). Journal of Cystic Fibrosis. 12(4). 338–344. 1 indexed citations
7.
Basinko, Audrey, Séverine Audebert‐Bellanger, Nathalie Douet‐Guilbert, et al.. (2011). Subtelomeric monosomy 11q and trisomy 16q in siblings and an unrelated child: Molecular characterization of two der(11)t(11;16). American Journal of Medical Genetics Part A. 155(9). 2281–2287. 8 indexed citations
8.
Basinko, Audrey, Aurore Perrin, Fréderic Morel, et al.. (2010). Balanced transmission of a paternal complex chromosomal rearrangement involving chromosomes 2, 3, and 18. American Journal of Medical Genetics Part A. 152A(10). 2646–2650. 8 indexed citations
9.
Parent, Philippe, et al.. (2009). Are IVC Filters Required in Combat Support Hospitals?. Journal of the Royal Army Medical Corps. 155(3). 210–212. 2 indexed citations
10.
Basinko, Audrey, Nathalie Douet‐Guilbert, Marie‐Josée Le Bris, et al.. (2008). Molecular cytogenetic characterization of an 8p22–8p23.2 duplication derived from a maternal intrachromosomal insertion in a child with congenital heart malformation, delayed puberty, and learning disabilities. American Journal of Medical Genetics Part A. 146A(22). 2950–2954. 7 indexed citations
11.
Basinko, Audrey, Nathalie Douet‐Guilbert, Philippe Parent, et al.. (2008). Familial interstitial deletion of the short arm of chromosome 4 (p15.33–p16.3) characterized by molecular cytogenetic analysis. American Journal of Medical Genetics Part A. 146A(7). 899–903. 25 indexed citations
12.
Chanet, V., et al.. (2007). Thrombophlébites nodulaires et maladies systémiques granulomateuses. La Revue de Médecine Interne. 28(6). 416–419. 1 indexed citations
13.
Dehainault, Catherine, Dorothée Michaux, Sabine Pagès-Berhouet, et al.. (2007). A deep intronic mutation in the RB1 gene leads to intronic sequence exonisation. European Journal of Human Genetics. 15(4). 473–477. 52 indexed citations
14.
Pinson, L, Aurore Perrin, Philippe Parent, et al.. (2005). Detection of an unexpected subtelomeric 15q26.2 → qter deletion in a little girl: Clinical and cytogenetic studies. American Journal of Medical Genetics Part A. 138A(2). 160–165. 46 indexed citations
15.
Scotet, Virginie, Marc De Braekeleer, M.‐P. Audrézet, et al.. (2001). Prevalence of CFTR mutations in hypertrypsinaemia detected through neonatal screening for cystic fibrosis. Clinical Genetics. 59(1). 42–47. 28 indexed citations
16.
Scotet, Virginie, Marc De Braekeleer, Michel Roussey, et al.. (2000). Neonatal screening for cystic fibrosis in Brittany, France: assessment of 10 years' experience and impact on prenatal diagnosis. The Lancet. 356(9232). 789–794. 85 indexed citations
17.
Leguern, Éric, Riadh Gouider, Dominique Mabin, et al.. (1997). Patients homozygous for the 17p 11.2 duplication in charcot‐marie‐tooth type 1A Disease. Annals of Neurology. 41(1). 104–108. 25 indexed citations
18.
Parent, Philippe, et al.. (1996). L'association CHARGE. Archives de Pédiatrie. 3(10). 1020–1025. 7 indexed citations
19.
Férec, Claude, C. Verlingue, Philippe Parent, et al.. (1995). Neonatal screening for cystic fibrosis: result of a pilot study using both immunoreactive trypsinogen and cystic fibrosis gene mutation analyses. Human Genetics. 96(5). 542–548. 32 indexed citations
20.
Merrer, M. Le, Robert Girot, Philippe Parent, Valérie Cormier‐Daire, & P Maroteaux. (1995). Acral dysostosis dyserythropoiesis syndrome. European Journal of Pediatrics. 154(5). 384–388. 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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