M Prieur

4.7k citations

75 papers · 2.6k indexed · h-index 26

Impact in

Genetics top 1%
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
Pediatrics, Perinatology and Child Health top 2%
- Prenatal Screening and Diagnostics

Papers in

Genetics 44
- Genomic variations and chromosomal abnormalities 33
- Genetics and Neurodevelopmental Disorders 10
- Genomics and Rare Diseases 7
- Genetic Syndromes and Imprinting 5
Cancer Research 8

Co-authors: Alain Aurias Bernard Dutrillaux J Lejeune Zoubida Chettouh C Turleau F Ledeist Jean‐Louis Blouin E. Viégas-Pèquignot
Journals: Human Genetics (8 papers)Journal of Medical Genetics (5 papers)Clinical Genetics (4 papers)Chromosoma (2 papers)Breast Cancer Research and Treatment (2 papers)
Partner nations: France Lebanon United Kingdom

In The Last Decade

M Prieur

75 papers receiving 2.5k citations

Peers

Countries citing papers authored by M Prieur

Since Specialization

Citations

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

Fields of papers citing papers by M Prieur

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside M Prieur, 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 M Prieur Line = papers co-authored together M Prieur links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	Classification of Human Chromosome 21 Gene-Expression Variations in Down Syndrome: Impact on Disease Phenotypes The American Journal of Human Genetics ·Emilie Ait‐Yahya, Julie Aubert, Luce Dauphinot, Isabelle Rivals, M Prieur, علی رضا الأمینی, Jean Rossier, L. Personnaz, Nicole Créau, Henri Bléhaut, Stéphane Robin, Jean‐Maurice Delabar, Marie‐Claude Potier	2007	210
2	Genome‐wide screening using automated fluorescent genotyping to detect cryptic cytogenetic abnormalities in children with idiopathic syndromic mental retardation Clinical Genetics ·Guntram Borck, Marlène Rio, Damien Sanlaville, Richard Redon, Florence Molinari, Delphine Bacq, O Raoul, Valérie Cormier‐Daire, Stanislas Lyonnet, Jeanne Amiel, M. Le Merrer, Vahdat Heidary, M Prieur, Michel Vekemans, M S de Assumpção, A Munnich, Laurence Colleaux	2004	6
3	[A preliminary study to assess the value of the DNA chips SpectralChip to detect subtle constitutional chromosome imbalances]. PubMed ·Kumi Miyauchi, Damien Sanlaville, Erwin Edyansyah, Eze Blessing Ebere, Marc Le Lorc’h, Magda Juliana Rodríguez, M Prieur, Laurence Colleaux, Arnold Münnich, C Turleau, Moncef Benkhalifa, Md Jafor Sadek, Marcel Vekemans, Serge Romana	2004	9
4	Automated fluorescent genotyping detects 10% of cryptic subtelomeric rearrangements in idiopathic syndromic mental retardation Journal of Medical Genetics ·Marlène Rio, Florence Molinari, S. Heuertz, Catherine Ozilou, Philippe Gosset, O Raoul, Valérie Cormier‐Daire, Aliza Amiel, Stanislas Lyonnet, Vera Judith Blanco Miranda, C Turleau, Marie‐Christine de Blois, M Prieur, Serge Romana, Michel Vekemans, Arnold Münnich, Laurence Colleaux	2002	54
5	Comparative genomic hybridisation in mentally retarded patients with dysmorphic features and a normal karyotype Clinical Genetics ·Fernando Glenadel Braga, Head Lr, Catherine Ozilou, Philippe Gosset, Alain Aurias, Henrique Santiago Alberto Carlos, M Prieur, O Raoul, Laurence Colleaux, Arnold Münnich, Serge Romana, Michel Vekemans, C Turleau	2001	33
6	Chromosome 7q22-q31 duplication: Report of a new case and review American Journal of Medical Genetics ·EKA EKA NURSETIANI, Philippe Gosset, Erik van Zwet, Kumi Miyauchi, C Turleau, Michel Vekemans, Jacques Loiselet, M Prieur	2000	9
7	New Natural Inactivating Mutations of the Follicle-Stimulating Hormone Receptor: Correlations between Receptor Function and Phenotype Molecular Endocrinology ·Philippe Touraine, Isabelle Beau, A. Gougeon, Geri Méduri, Keizo Shigenobu, C. Pichard, Yu. N. Gorbunov, Bernard‐Jean Paniel, M Prieur, J.R. Zorn, Edwin Milgröm, F Kuttenn, Micheline Misrahi	1999	187
8	Wilms' tumor and gonadal dysgenesis in a child with the 2q37.1 deletion syndrome Clinical Genetics ·Krystal L Detweiler, Jeanne Amiel, François Doz, M Prieur, J Couturier, L.S.S. Barretto, Isabelle Henry, Arnold Munnich, Michel Vekemans, Stanislas Lyonnet	1998	24
9	An embryonic-like methylation pattern of classical satellite DNA is observed in ICF syndrome Human Molecular Genetics ·Marc Jeanpierre, C Turleau, Alain Aurias, M Prieur, F Ledeist, Alain Fischer, E. Viégas-Pèquignot	1993	219
10	Genetic evolution of breast cancer: II. relationship with estrogen and progesterone receptor expression Breast Cancer Research and Treatment ·H Magdelénat, Michèle Gerbault‐Seureau, Peyman Nejat Dehkordi, M Prieur, Bernard Dutrillaux	1992	16
11	Prolonged G2 phase of breast cancer cells and chromosome damage European Journal of Cancer and Clinical Oncology ·Bernard Dutrillaux, Michèle Gerbault‐Seureau, B Zafrani, M Prieur	1991	8
12	Chromosomal aberrations induced by low-dose γ-irradiation study of R-banded chromosomes of human lymphocytes Mutation research. Fundamental and molecular mechanisms of mutagenesis ·D. Lefrançois, Walid Al Achkar, Alain Aurias, J Couturier, A.M. Dutrillaux, Bernard Dutrillaux, Jinchun Peng, Michèle Gerbault‐Seureau, Françoise Hoffschir, Valeria Guerra-Espinosa, M. Lombard, Martine Muleris, M Prieur, Michelle Ricoul, Laure Sabatier, E. Viégas-Pèquignot	1989	12
13	Acquired chromosome rearrangements in human lymphocytes: effect of aging Human Genetics ·M Prieur, Walid Al Achkar, Alain Aurias, J. Couturier, A.M. Dutrillaux, Bernard Dutrillaux, Jinchun Peng, M. Gerbault-Seureau, Françoise Hoffschir, Valeria Guerra-Espinosa, D. Lefrançois, M. Lombard, Martine Muleris, Michelle Ricoul, Laure Sabatier, E. Viégas-Pèquignot	1988	50
14	[Mosaic tetrasomy 12p. Identical nature of the Pallister syndrome, the Teschler-Nicola/Killian syndrome and mosaic tetrasomy 21]. PubMed ·S Gilgenkrantz, Fryns Jp, P. Droullé, Morton D. Schweitzer, B. Chadefaux, M Prieur	1987	3
15	Diagrammatic representation for chromosomal mutagenesis studies III. Radiation-induced rearrangements in Pan troglodytes (chimpanzee) Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis ·Maike Falk, Nem-Yun Boo, M Prieur, Bernard Dutrillaux	1985	11
16	[Exact localization of several fragile sites remains uncertain. The example of fra(10) sensitive to folate]. PubMed ·B. Dutrillaux, Martine Muleris, M Prieur	1985	3
17	[Partial trisomy for the long arm of chromosome 2 due to malsegregation of a maternal insertion : ins(6;2)(p22;q24q34)]. Munich Personal RePEc Archive (Ludwig Maximilian University of Munich) ·J Couturier, Alain Aurias, M Prieur, A Barois	1977	12
18	[Chromosome 8 : complete trisomy and segmental trisomies]. PubMed ·Rethoré Mo, Alain Aurias, J Couturier, Bernard Dutrillaux, M Prieur, J Lejeune	1977	33
19	Analyse des changes de chromatides dans les cellules somatiques humaines: Traitement au BUDR (5 bromodoxyuridine) et fluorescence bicolore par l'acridine orange Chromosoma ·Bernard Dutrillaux, Sylvia Haight, M Prieur, J Lejeune	1974	32
20	[Free 21 trisomy in mother and daughter]. PubMed ·Rethoré Mo, J Lafourcade, M Prieur, TAGARAM KONDALA RAO, 国彦中島, Ahmand Najafi, J Lejeune	1970	2

About M Prieur

M Prieur is a scholar working on Genetics, Genetics, Cancer Research, Developmental Biology and Molecular Biology, having authored 75 papers that have together received 2.6k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (33 papers), Genetics and Neurodevelopmental Disorders (10 papers), Chromosomal and Genetic Variations (8 papers), Genomics and Rare Diseases (7 papers), DNA Repair Mechanisms (7 papers), Congenital heart defects research (6 papers), Prenatal Screening and Diagnostics (6 papers) and Genetic Syndromes and Imprinting (5 papers). The work is most often cited by research in Genetics (1.5k citations), Pediatrics, Perinatology and Child Health (449 citations), Molecular Biology (1.4k citations), Developmental Biology (37 citations) and Reproductive Medicine (140 citations). M Prieur has collaborated with scholars based in France, Lebanon and United Kingdom. Frequent co-authors include Alain Aurias, Bernard Dutrillaux, J Lejeune, Zoubida Chettouh, C Turleau, F Ledeist, Jean‐Louis Blouin, E. Viégas-Pèquignot, O Raoul and Alain Fischer. Their work appears in journals such as Human Genetics, Journal of Medical Genetics, Clinical Genetics, Chromosoma and Breast Cancer Research and Treatment.

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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