P. De Mas

2.2k total citations
9 papers, 367 citations indexed

About

P. De Mas is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, P. De Mas has authored 9 papers receiving a total of 367 indexed citations (citations by other indexed papers that have themselves been cited), including 3 papers in Genetics, 2 papers in Molecular Biology and 2 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in P. De Mas's work include Chromosomal and Genetic Variations (2 papers), Prenatal Screening and Diagnostics (2 papers) and Genomic variations and chromosomal abnormalities (2 papers). P. De Mas is often cited by papers focused on Chromosomal and Genetic Variations (2 papers), Prenatal Screening and Diagnostics (2 papers) and Genomic variations and chromosomal abnormalities (2 papers). P. De Mas collaborates with scholars based in France and Switzerland. P. De Mas's co-authors include Marie‐Claire Vincent, Patrick Calvas, Louis Bujan, Roger Mieusset, F Pontonnier, Myriam Daudin, G. Bourrouillou, Jean‐Michel Vallat, Albert David and Marie‐Christine Arné‐Bes and has published in prestigious journals such as Human Reproduction, Journal of Andrology and American Journal of Medical Genetics Part A.

In The Last Decade

P. De Mas

9 papers receiving 343 citations

Peers

Countries citing papers authored by P. De Mas

Since Specialization

Citations

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

Fields of papers citing papers by P. De Mas

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by P. De Mas. 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 P. De Mas. The network helps show where P. De Mas may publish in the future.

Co-authorship network of co-authors of P. De Mas

This figure shows the co-authorship network connecting the top 25 collaborators of P. De Mas. A scholar is included among the top collaborators of P. De Mas 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 P. De Mas. P. De Mas is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

Sort: Min cites: Since: Top N: Style:

9 of 9 papers shown

#	Work	Indexed citations
1	Double deletion of a chromosome 21 inserted in a chromosome 22 in an azoospermic patient 2015 ·Clinical Case Reports ·(unknown), (unknown), P. De Mas, Laurence Bouneau, (unknown), (unknown), Patrick Calvas	2
2	Genotype-Phenotype Correlations in Charcot-Marie-Tooth Disease Type 2 Caused by Mitofusin 2 Mutations 2009 ·Archives of Neurology ·(unknown), Benoît Funalot, Robert Ouvrier, Leïla Lazaro, Annick Toutain, P. De Mas, P. Bouché, Brigitte Gilbert‐Dussardier, Marie‐Christine Arné‐Bes, (unknown), Hubert Journel, Marie-Christine Minot-Myhié, Claire Le Guillou, Karima Ghorab, Laurent Magy, Franck Sturtz, Jean‐Michel Vallat, Corinne Magdelaine	92
3	Molecular characterization of a cryptic 2q37 deletion in a patient with Albright hereditary osteodystrophy‐like phenotype 2004 ·American Journal of Medical Genetics Part A ·Nicolas Chassaing, P. De Mas, (unknown), (unknown), Sophie Julia, G. Bourrouillou, Patrick Calvas, Éric Bieth	21
4	Subtelomeric 6p deletion: Clinical, FISH, and array CGH characterization of two cases 2004 ·American Journal of Medical Genetics Part A ·Cédric Le Caignec, P. De Mas, Marie‐Claire Vincent, (unknown), G. Bourrouillou, Jean‐Marie Rival, Albert David	32
5	Cytogenetic Investigations of Infertile Men With Low Sperm Counts: A 25‐Year Experience 2002 ·Journal of Andrology ·Marie‐Claire Vincent, Myriam Daudin, P. De Mas, (unknown), Roger Mieusset, F Pontonnier, Patrick Calvas, Louis Bujan, (unknown)	89
6	Increased aneuploidy in spermatozoa from testicular tumour patients after chemotherapy with cisplatin, etoposide and bleomycin 2001 ·Human Reproduction ·P. De Mas	122
7	Regroupement familial marocain aux Pays-Bas 1968- 1987: un aperçu quantitatif 1990 ·UvA-DARE (University of Amsterdam) ·P. De Mas	1
8	De gezinshereniging van Marokkanen in Nederland, 1968-1984 : een onderzoek naar de omvang, de aard en de gebieden van herkomst en vestiging 1985 ·UvA-DARE (University of Amsterdam) ·P. De Mas, (unknown)	3
9	Marges marocaines : limites de la cooperation au développement dans une région périphérique : le cas du Rif 1978 ·UvA-DARE (University of Amsterdam) ·P. De Mas	5

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.

Explore authors with similar magnitude of impact