M. Chery
Impact in
- Genetics top 10%
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
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- Prenatal Screening and Diagnostics
Papers in
- Genetics 16
- Genetics and Neurodevelopmental Disorders 10
- Genomic variations and chromosomal abnormalities 6
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 4
- Genetic Syndromes and Imprinting 2
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- Congenital heart defects research 2
- Co-authors
- S Gilgenkrantz (20 shared papers)M Prieur (2 shared papers)Christophe Philippe (6 shared papers)Catherine Léonard (2 shared papers)Michel Fardeau (2 shared papers)André Hanauer (2 shared papers)P. Droullé (1 shared paper)Jean‐Louis Mandel (1 shared paper)
- Journals
- Genomics (4 papers)Clinical Genetics (2 papers)Journal of Medical Genetics (1 paper)British Journal of Haematology (1 paper)Prenatal Diagnosis (1 paper)
- Partner nations
- FranceSwitzerlandNetherlands
In The Last Decade
M. Chery
24 papers receiving 473 citations
Peers
Comparison fields: 5 of 46
- Genetics 290
- Pediatrics, Perinatology and Child Health 82
- Molecular Biology 268
- Genetics 35
- Cell Biology 54
Countries citing papers authored by M. Chery
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
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-authors
The 25 scholars most cited alongside M. Chery, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
Showing the 20 most-cited of 26 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Myotubular myopathy in a girl with a deletion at Xq27-q28 and unbalanced X inactivation assigns the MTM1 gene to a 600-kb region. | 1995 | 73 |
| 2 | Molecular mapping of 21 features associated with partial monosomy 21: involvement of the APP-SOD1 region. | 1995 | 66 |
| 3 | 1985 | 62 | |
| 4 | 1995 | 53 | |
| 5 | The Friedreich ataxia gene is assigned to chromosome 9q13-q21 by mapping of tightly linked markers and shows linkage disequilibrium with D9S15. | 1990 | 46 |
| 6 | 1994 | 33 | |
| 7 | 1993 | 25 | |
| 8 | 1996 | 22 | |
| 9 | 1992 | 21 | |
| 10 | 1995 | 19 | |
| 11 | Sublocalisation of the X breakpoint in the translocation (X; 18)(p11.2; q11.2) primary change in synovial sarcomas. | 1990 | 12 |
| 12 | The Noonan syndrome. The Nancy experience revisited. | 1993 | 12 |
| 13 | 1997 | 11 | |
| 14 | 1998 | 9 | |
| 15 | 1993 | 7 | |
| 16 | Interstitial deletion of the long arm of chromosome 6. | 1989 | 7 |
| 17 | [Fragile site on chromosome 2 (q11) in a case of familial lymphohistiocytosis]. | 1984 | 6 |
| 18 | [Balanced X-autosomal translocation and mental retardation. Mapping mental retardation linked to X (excluding fragile X)]. | 1989 | 5 |
| 19 | 1996 | 3 | |
| 20 | [Union of 2 carriers of a balanced translocation. Familial study of 3 generations]. | 1985 | 2 |
About M. Chery
M. Chery is a scholar working on Genetics, Molecular Biology, Pulmonary and Respiratory Medicine, Plant Science and Oncology, having authored 26 papers that have together received 498 indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (10 papers), Genomic variations and chromosomal abnormalities (6 papers), Sarcoma Diagnosis and Treatment (4 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (4 papers), Chromosomal and Genetic Variations (4 papers), Congenital heart defects research (2 papers), Autoimmune and Inflammatory Disorders Research (2 papers) and Genetic Syndromes and Imprinting (2 papers). The work is most often cited by research in Genetics (290 citations), Pediatrics, Perinatology and Child Health (82 citations), Molecular Biology (268 citations), Genetics (35 citations) and Cell Biology (54 citations). M. Chery has collaborated with scholars based in France, Switzerland and Netherlands. Frequent co-authors include S Gilgenkrantz, M Prieur, Christophe Philippe, Catherine Léonard, Michel Fardeau, André Hanauer, P. Droullé, Jean‐Louis Mandel, Morton D. Schweitzer and B. Chadefaux. Their work appears in journals such as Genomics, Clinical Genetics, Journal of Medical Genetics, British Journal of Haematology and Prenatal Diagnosis.
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.