Philippe Parent

2.6k citations

35 papers · 518 indexed · h-index 14

Impact in

Genetics top 10%
- Genomic variations and chromosomal abnormalities
- Genetic and Kidney Cyst Diseases
- Genomics and Rare Diseases
Pulmonary and Respiratory Medicine top 10%
- Cystic Fibrosis Research Advances
- Neonatal Respiratory Health Research
- Tracheal and airway disorders

Papers in ⓘ

Genetics 15
- Genomic variations and chromosomal abnormalities 9
- Genetic and Kidney Cyst Diseases 2
Pulmonary and Respiratory Medicine 13
- Cystic Fibrosis Research Advances 9
- Neonatal Respiratory Health Research 4

Co-authors: Marc De Braekeleer (11 shared papers)Claude Férec (12 shared papers)I. Duguépéroux (8 shared papers)Virginie Scotet (8 shared papers)Nathalie Douet‐Guilbert (6 shared papers)Fréderic Morel (7 shared papers)Marie‐Pierre Audrézet (8 shared papers)Bernard Mercier (4 shared papers)
Journals: Journal of Cystic Fibrosis (3 papers)Human Genetics (2 papers)Pediatric Surgery International (2 papers)Orphanet Journal of Rare Diseases (1 paper)European Journal of Human Genetics (1 paper)
Partner nations: France United Kingdom Italy

In The Last Decade

Philippe Parent

34 papers receiving 482 citations

Peers

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-authors

The 25 scholars most cited alongside Philippe Parent, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Philippe Parent Line = papers co-authored together Philippe Parent links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

Showing the 20 most-cited of 35 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	Neonatal screening for cystic fibrosis in Brittany, France: assessment of 10 years' experience and impact on prenatal diagnosis The Lancet ·Virginie Scotet, Marc De Braekeleer, Michel Roussey, G. Rault, Philippe Parent, M. Dagorne, Hubert Journel, A. Lemoigne, Jean-Pierre Codet, Michel Catheline, Véronique David, André Chaventré, I. Duguépéroux, C. Verlingue, I. Quéré, Bernard Mercier, Marie‐Pierre Audrézet, Claude Férec	2000	85
2	A deep intronic mutation in the RB1 gene leads to intronic sequence exonisation European Journal of Human Genetics ·Catherine Dehainault, Dorothée Michaux, Sabine Pagès-Berhouet, Virginie Caux‐Moncoutier, François Doz, Laurence Desjardins, Jérôme Couturier, Philippe Parent, Dominique Stoppa‐Lyonnet, Marion Gauthier‐Villars, Claude Houdayer	2007	52
3	Detection of an unexpected subtelomeric 15q26.2 → qter deletion in a little girl: Clinical and cytogenetic studies American Journal of Medical Genetics Part A ·L Pinson, Aurore Perrin, C. Plouzennec, Philippe Parent, Charles Metz, M Collet, M.‐J. Le Bris, Nathalie Douet‐Guilbert, Fréderic Morel, Marc De Braekeleer	2005	46
4	Neonatal screening for cystic fibrosis: result of a pilot study using both immunoreactive trypsinogen and cystic fibrosis gene mutation analyses Human Genetics ·Claude Férec, C. Verlingue, Philippe Parent, Julie Morin, Jean-Pierre Codet, G. Rault, M. Dagorne, A. Lemoigne, Hubert Journel, M. Roussey, B. Le Marec, Michel Catheline, M.‐P. Audrézet, Bernard Mercier	1995	32
5	CNS involvement in OFD1 syndrome: a clinical, molecular, and neuroimaging study Orphanet Journal of Rare Diseases ·Ennio Del Giudice, Marina Macca, Floriana Imperati, Alessandra D’Amico, Philippe Parent, Laurent Pasquier, Valérie Layet, Stanislas Lyonnet, Veronique Stamboul-Darmency, Christel Thauvin‐Robinet, Brunella Franco, (unknown)	2014	29
6	Prevalence of CFTR mutations in hypertrypsinaemia detected through neonatal screening for cystic fibrosis Clinical Genetics ·Virginie Scotet, Marc De Braekeleer, M.‐P. Audrézet, Laurence Lodé, C. Verlingue, I. Quéré, Bernard Mercier, I. Duguépéroux, Jean-Pierre Codet, Marie‐Pierre Moineau, Philippe Parent, Claude Férec	2001	28
7	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 ·Audrey Basinko, Nathalie Douet‐Guilbert, Philippe Parent, G Blondin, M. Mingam, Françoise Monot, Fréderic Morel, Marie‐Josée Le Bris, Marc De Braekeleer	2008	25
8	Patients homozygous for the 17p 11.2 duplication in charcot‐marie‐tooth type 1A Disease Annals of Neurology ·Éric Leguern, Riadh Gouider, Dominique Mabin, Sanjeev Bs, Nazha Birouk, Philippe Parent, P. Bouché, Alexis Brice	1997	25
9	Spatial and temporal distribution of cystic fibrosis and of its mutations in Brittany, France: a retrospective study from 1960 Human Genetics ·Virginie Scotet, Dominique Gillet, I. Duguépéroux, Marie‐Pierre Audrézet, Gil Bellis, Bénédicte Garnier, Michel Roussey, G. Rault, Philippe Parent, Marc De Braekeleer, Claude Férec, Rishi Prajwal H L	2002	23
10	Prenatal diagnosis of cystic fibrosis: the 18‐year experience of Brittany (western France) Prenatal Diagnosis ·Virginie Scotet, I. Duguépéroux, Marie‐Pierre Audrézet, Martine Blayau, Pierre Boisseau, Hubert Journel, Philippe Parent, Claude Férec	2008	17
11	Acral dysostosis dyserythropoiesis syndrome European Journal of Pediatrics ·M. Le Merrer, Robert Girot, Philippe Parent, Valérie Cormier‐Daire, P Maroteaux	1995	17
12	A small de novo 16q24.1 duplication in a woman with severe clinical features European Journal of Medical Genetics ·Sylvia Redon, Caroline Bénech, Séverine Audebert‐Bellanger, Gaëlle Friocourt, Marc Planes, Philippe Parent, Claude Férec	2013	16
13	Oral-facial-digital syndrome type I cells exhibit impaired DNA repair; unanticipated consequences of defective OFD1 outside of the cilia network Human Molecular Genetics ·I Abramowiçz, Gillian Carpenter, Mariaevelina Alfieri, Rita Colnaghi, Emily Outwin, Philippe Parent, Christel Thauvin‐Robinet, Daniela Iaconis, Brunella Franco, Mark O’Driscoll	2016	14
14	Prenatal Sonographic Patterns in Six Cases of Wolf-Hirschhorn (4p–) Syndrome Fetal Diagnosis and Therapy ·G. Boog, Claudine Le Vaillant, Michel Collet, Pierre‐François Dupré, Philippe Parent, A. Bongain, Bernard Benoît, C. Trastour	2004	14
15	Balanced complex chromosome rearrangement in male infertility: case report and literature review Andrologia ·Huong Minh Nguyen, Fréderic Morel, Perrine Pennamen, Philippe Parent, Nathalie Douet‐Guilbert, M.‐J. Le Bris, Audrey Basinko, Sylvie Roche, Marc De Braekeleer, Aurore Perrin	2014	12
16	Highlighting the impact of cascade carrier testing in cystic fibrosis families Journal of Cystic Fibrosis ·I. Duguépéroux, C. L’Hostis, Marie‐Pierre Audrézet, G. Rault, I. Frachon, R Bernard, Philippe Parent, Martine Blayau, Sébastien Schmitt, Emmanuelle Génin, Claude Férec, Virginie Scotet	2016	10
17	Balanced transmission of a paternal complex chromosomal rearrangement involving chromosomes 2, 3, and 18 American Journal of Medical Genetics Part A ·Audrey Basinko, Aurore Perrin, Huyen Anh Nguyen, Fréderic Morel, Marie‐Josée Le Bris, A.‐H. Saliou, Michel Collet, Philippe Parent, Caroline Bénech, Sylvia Quéméner, Claude Férec, Nathalie Douet‐Guilbert, Marc De Braekeleer	2010	8
18	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 ·Audrey Basinko, Séverine Audebert‐Bellanger, Nathalie Douet‐Guilbert, Jérémie Le Franc, Philippe Parent, Sylvia Quéméner, Philippe La Selve, Clément Bovo, Fréderic Morel, Marie‐Josée Le Bris, Marc De Braekeleer	2011	8
19	Neonatal ovarian cysts Pediatric Surgery International ·J. Gaudin, C. Le Treguilly, Philippe Parent, Hélène Le Guern, Jean‐Jacques Chabaud, G. Boog, B Jéhannin	1988	8
20	L'association CHARGE Archives de Pédiatrie ·E Finel, Philippe Parent, JD Giroux, L de Parscau	1996	7

About Philippe Parent

Philippe Parent is a scholar working on Genetics, Pulmonary and Respiratory Medicine, Molecular Biology, Pediatrics, Perinatology and Child Health and Surgery, having authored 35 papers that have together received 518 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (9 papers), Cystic Fibrosis Research Advances (9 papers), Prenatal Screening and Diagnostics (4 papers), Chromosomal and Genetic Variations (4 papers), Neonatal Respiratory Health Research (4 papers), Genomics and Chromatin Dynamics (3 papers), Child Nutrition and Feeding Issues (2 papers) and Genetic and Kidney Cyst Diseases (2 papers). The work is most often cited by research in Genetics (208 citations), Pulmonary and Respiratory Medicine (210 citations), Pediatrics, Perinatology and Child Health (118 citations), Genetics (48 citations) and Ophthalmology (21 citations). Philippe Parent has collaborated with scholars based in France, United Kingdom and Italy. Frequent co-authors include Marc De Braekeleer, Claude Férec, I. Duguépéroux, Virginie Scotet, Nathalie Douet‐Guilbert, Fréderic Morel, Marie‐Pierre Audrézet, Bernard Mercier, C. Verlingue and G. Rault. Their work appears in journals such as Journal of Cystic Fibrosis, Human Genetics, Pediatric Surgery International, Orphanet Journal of Rare Diseases and European Journal of Human Genetics.

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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