M. Chery

684 total citations
26 papers, 466 citations indexed

About

M. Chery is a scholar working on Genetics, Molecular Biology and Pulmonary and Respiratory Medicine. According to data from OpenAlex, M. Chery has authored 26 papers receiving a total of 466 indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Genetics, 11 papers in Molecular Biology and 5 papers in Pulmonary and Respiratory Medicine. Recurrent topics in M. Chery's work include Genetics and Neurodevelopmental Disorders (10 papers), Genomic variations and chromosomal abnormalities (6 papers) and Sarcoma Diagnosis and Treatment (4 papers). M. Chery is often cited by papers focused on Genetics and Neurodevelopmental Disorders (10 papers), Genomic variations and chromosomal abnormalities (6 papers) and Sarcoma Diagnosis and Treatment (4 papers). M. Chery collaborates with scholars based in France, Switzerland and Netherlands. M. Chery's co-authors include S Gilgenkrantz, M Prieur, Christophe Philippe, Catherine Léonard, Michel Fardeau, André Hanauer, B. Foliguet, P. Droullé, A.J. Driesel and Jean‐Louis Mandel and has published in prestigious journals such as British Journal of Haematology, Genomics and Journal of Medical Genetics.

In The Last Decade

M. Chery

24 papers receiving 461 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
M. Chery France	12	284	281	82	58	56	26	466
Rudolf A. Pfeiffer Germany	13	383 1.3×	438 1.6×	75 0.9×	97 1.7×	38 0.7×	18	672
F. Prieto Spain	13	203 0.7×	297 1.1×	67 0.8×	69 1.2×	28 0.5×	35	503
Chantal Missirian France	16	418 1.5×	404 1.4×	100 1.2×	36 0.6×	41 0.7×	39	720
Tiina Alitalo Finland	20	332 1.2×	604 2.1×	48 0.6×	61 1.1×	88 1.6×	30	964
C E de Die-Smulders Netherlands	13	266 0.9×	272 1.0×	90 1.1×	19 0.3×	29 0.5×	21	516
Giulia Arrigo Italy	12	240 0.8×	339 1.2×	48 0.6×	43 0.7×	70 1.3×	21	594
Ada Rosenmann Israel	16	252 0.9×	347 1.2×	91 1.1×	108 1.9×	146 2.6×	36	650
Heidi A. Heilstedt United States	9	415 1.5×	307 1.1×	70 0.9×	81 1.4×	25 0.4×	9	568
Marsha Speevak Canada	17	420 1.5×	302 1.1×	141 1.7×	96 1.7×	32 0.6×	37	636
Maria Luisa Giovannucci Uzielli Italy	13	316 1.1×	287 1.0×	49 0.6×	60 1.0×	54 1.0×	26	546

Countries citing papers authored by M. Chery

Since Specialization

Citations

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

Fields of papers citing papers by M. Chery

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of M. Chery

This figure shows the co-authorship network connecting the top 25 collaborators of M. Chery. A scholar is included among the top collaborators of M. Chery 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 M. Chery. M. Chery 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

Sloan‐Béna, Frédérique, Christophe Philippe, Bruno Leheup, et al.. (1998). Characterisation of an inverted X chromosome (p11.2q21.3) associated with mental retardation using FISH.. Journal of Medical Genetics. 35(2). 146–150. 6 indexed citations

Martel, Véronique, Agnès Guerci, Marie‐José Gregoire, et al.. (1997). De novo methylation of tumour suppressor genes CDKN2A and CDKN2B is a rare finding in B‐cell chronic lymphocytic leukaemia. British Journal of Haematology. 99(2). 320–324. 11 indexed citations

Marçon, F, et al.. (1997). [Familial supravalvular aortic stenosis. Investigation in a family and review of the literature].. PubMed. 90(5). 719–24.

Fauré, S., M. Chery, Luísa Mota‐Vieira, et al.. (1996). Physical Mapping of 49 Microsatellite Markers on Chromosome 19 and Correlation with the Genetic Linkage Map. Genomics. 32(3). 458–461. 3 indexed citations

Camus, Philippe, et al.. (1996). X chromosome inactivation in 30 girls with Rett syndrome: Analysis using the probe. Human Genetics. 97(2). 247–250. 22 indexed citations

Huret, J. L., et al.. (1995). Monosomy 21q: two cases of del(21q) and review of the literature. Clinical Genetics. 48(3). 140–147. 38 indexed citations

Chettouh, Zoubida, M. F. Croquette, B Delobel, et al.. (1995). Molecular mapping of 21 features associated with partial monosomy 21: involvement of the APP-SOD1 region.. PubMed. 57(1). 62–71. 66 indexed citations

Philippe, Christophe, M. Chery, Hélène Gilgenkrantz, et al.. (1994). Additional case of female monozygotic twins discordant for the clinical manifestations of Duchenne muscular dystrophy due to opposite X‐chromosome inactivation. American Journal of Medical Genetics. 52(2). 198–206. 32 indexed citations

Gilgenkrantz, S, Christophe Philippe, & M. Chery. (1994). Chromosome rearrangements and human gene mapping. Biomedicine & Pharmacotherapy. 48(5-6). 225–230. 1 indexed citations

10.

Serville, F, Paule Bénit, Pascale Saugier-Véber, et al.. (1993). Prenatal exclusion of X‐linked hydrocephalus‐stenosis of the aqueduct of sylvius sequence using closely linked DNA markers. Prenatal Diagnosis. 13(6). 435–439. 4 indexed citations

11.

Philippe, Christophe, et al.. (1993). Physical Mapping of DNA Markers in the q13-q22 Region of the Human X Chromosome. Genomics. 17(1). 147–152. 23 indexed citations

12.

Chery, M., et al.. (1993). The Noonan syndrome. The Nancy experience revisited.. PubMed. 4(2). 113–8. 12 indexed citations

13.

Blackshear, Perry J., Jane S. Tuttle, Rebecca J. Oakey, et al.. (1992). Chromosomal mapping of the human (MACS) and mouse (Macs) genes encoding the MARCKS protein. Genomics. 14(1). 168–174. 21 indexed citations

14.

Grégoire, M. J., et al.. (1991). A new case of myxoid liposarcoma with complex rearrangement including the t(12;16)(q13;p11). Cancer Genetics and Cytogenetics. 52(2). 269–269. 1 indexed citations

15.

Hanauer, André, M. Chery, Ricardo Fujita, et al.. (1990). The Friedreich ataxia gene is assigned to chromosome 9q13-q21 by mapping of tightly linked markers and shows linkage disequilibrium with D9S15.. PubMed. 46(1). 133–7. 45 indexed citations

16.

Gilgenkrantz, S, et al.. (1990). Sublocalisation of the X breakpoint in the translocation (X; 18)(p11.2; q11.2) primary change in synovial sarcomas.. PubMed. 5(7). 1063–6. 12 indexed citations

17.

Chery, M., et al.. (1989). Interstitial deletion of the long arm of chromosome 6.. PubMed. 32(2). 82–6. 7 indexed citations

18.

Grégoire, M. J., et al.. (1989). Translocation (X;18) and loss of the other X in synovial sarcoma with rearrangement of the timp oncogene. Cancer Genetics and Cytogenetics. 38(2). 160–160. 1 indexed citations

19.

Gilgenkrantz, S, et al.. (1985). [Union of 2 carriers of a balanced translocation. Familial study of 3 generations].. PubMed. 28(3). 164–6. 2 indexed citations

20.

Gilgenkrantz, S, M. J. Grégoire, M. Chery, Pierre Bordigoni, & D Olive. (1984). Site fragile sur le chromosome 2 (q11) dans un cas de lymphohistiocytose familiale.. 32(3).

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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