M Poissonnier

949 total citations
20 papers, 712 citations indexed

About

M Poissonnier is a scholar working on Molecular Biology, Genetics and Public Health, Environmental and Occupational Health. According to data from OpenAlex, M Poissonnier has authored 20 papers receiving a total of 712 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Molecular Biology, 7 papers in Genetics and 4 papers in Public Health, Environmental and Occupational Health. Recurrent topics in M Poissonnier's work include Genomic variations and chromosomal abnormalities (5 papers), Metabolism and Genetic Disorders (3 papers) and Hypothalamic control of reproductive hormones (3 papers). M Poissonnier is often cited by papers focused on Genomic variations and chromosomal abnormalities (5 papers), Metabolism and Genetic Disorders (3 papers) and Hypothalamic control of reproductive hormones (3 papers). M Poissonnier collaborates with scholars based in France, Morocco and United States. M Poissonnier's co-authors include O Raoul, Delphine Allard, M O Rethoré, Zohra Rahmani, Jean‐Louis Blouin, Zoubida Chettouh, Annie Nicole, M Prieur, J. F. Mattéi and N. Créau-Goldberg and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Biochemical and Biophysical Research Communications and FEBS Letters.

In The Last Decade

M Poissonnier

19 papers receiving 678 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
M Poissonnier France	14	324	317	221	114	58	20	712
Dian Soewarto Germany	18	615 1.9×	398 1.3×	145 0.7×	58 0.5×	16 0.3×	25	939
Marcella Ma United Kingdom	15	505 1.6×	200 0.6×	84 0.4×	72 0.6×	26 0.4×	22	895
Miriam Verhoef‐Post Netherlands	20	598 1.8×	380 1.2×	310 1.4×	59 0.5×	23 0.4×	22	1.2k
Robert Fraser Canada	13	303 0.9×	143 0.5×	48 0.2×	34 0.3×	12 0.2×	16	603
André Stutz Switzerland	6	646 2.0×	136 0.4×	171 0.8×	15 0.1×	24 0.4×	7	886
Bruno Barenton France	18	439 1.4×	227 0.7×	71 0.3×	39 0.3×	18 0.3×	46	970
Natalia Danilovich Canada	17	244 0.8×	386 1.2×	379 1.7×	115 1.0×	7 0.1×	22	1.0k
H. Nowakowski Germany	15	192 0.6×	202 0.6×	17 0.1×	41 0.4×	32 0.6×	61	645
Jason O. Rahal United States	6	256 0.8×	249 0.8×	164 0.7×	62 0.5×	6 0.1×	6	809
Marco Conti United States	14	391 1.2×	163 0.5×	171 0.8×	21 0.2×	10 0.2×	15	796

Countries citing papers authored by M Poissonnier

Since Specialization

Citations

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

Fields of papers citing papers by M Poissonnier

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of M Poissonnier

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

1.

Rahmani, Zohra, Jean‐Louis Blouin, N. Créau-Goldberg, et al.. (2005). Down syndrome critical region around D21S55 on proximal 21q22.3. American Journal of Medical Genetics. 37(S7). 98–103. 27 indexed citations

2.

Poissonnier, M, et al.. (1996). [OSTEOMALACIC DYSTROPHY IN PREMATURES].. PubMed. 11. 367–83.

3.

Stoeckel, M.E., et al.. (1994). Expression of the ?-subunit of glycoprotein hormones in the pars tuberalis-specific glandular cells in rat, mouse and guinea-pig. Cell and Tissue Research. 278(3). 617–624. 27 indexed citations

4.

Stoeckel, M.E., et al.. (1994). Expression of the ?-subunit of glycoprotein hormones in the pars tuberalis-specific glandular cells in rat, mouse and guinea-pig. Cell and Tissue Research. 278(3). 617–624. 17 indexed citations

5.

Miélot, F, et al.. (1993). Acute lymphoblastic leukemia with trisomy 21 constitutional mosaicism. Cancer Genetics and Cytogenetics. 66(1). 70–72. 2 indexed citations

6.

Hindelang, C., et al.. (1993). Early Expression of the Glycoprotein Hormone Alpha-Subunit in the Pars Tuberalis of the Rat Pituitary Gland during Ontogenesis. Neuroendocrinology. 58(6). 616–624. 39 indexed citations

7.

Poissonnier, M, C Turleau, M Olivier‐Martin, et al.. (1992). Interstitial deletion of the proximal region of the long arm of chromosome 18, del(18q12) a distinct clinical entity? A report of two new cases.. PubMed. 35(3). 146–51. 14 indexed citations

8.

Blouin, Jean‐Louis, Zohra Rahmani, Zoubida Chettouh, et al.. (1990). Slot blot method for the quantification of DNA sequences and mapping of chromosome rearrangements: application to chromosome 21.. PubMed. 46(3). 518–26. 17 indexed citations

9.

Rahmani, Zohra, Jean‐Louis Blouin, N. Créau-Goldberg, et al.. (1989). Critical role of the D21S55 region on chromosome 21 in the pathogenesis of Down syndrome.. Proceedings of the National Academy of Sciences. 86(15). 5958–5962. 209 indexed citations

10.

Poissonnier, M, et al.. (1988). [Genetic counseling in a case of neuro-ectodermosis: Vera Price trichothiodystrophy. Brittle hair with reduced sulfur content].. PubMed. 36(4). 361–5. 3 indexed citations

11.

Poissonnier, M, et al.. (1987). [True hermaphroditism in a child with a chimeric XX/XY chromosome, a double erythrocyte population and an unusual Lewis (a+ b+) phenotype].. PubMed. 35(2-3). 119–29. 3 indexed citations

12.

Chadefaux, B., M O Rethoré, O Raoul, et al.. (1985). Cystathionine beta synthase: Gene dosage effect in trisomy 21. Biochemical and Biophysical Research Communications. 128(1). 40–44. 79 indexed citations

13.

Chadefaux, B., et al.. (1984). Assignment of human phosphoribosylglycinamide synthetase locus to region 21q221. Human Genetics. 66(2-3). 190–192. 29 indexed citations

14.

Poissonnier, M, et al.. (1983). [Lethal mandibulofacial and ulnofibular dysostosis].. PubMed. 30(9). 713–7. 1 indexed citations

15.

Counis, Raymond, Maïthé Corbani, M Poissonnier, & M Jutisz. (1982). Characterization of the precursors of α and >β subunits of follitropin following cell-free translation of rat and ovine pituitary mRNAs. Biochemical and Biophysical Research Communications. 107(3). 998–1005. 19 indexed citations

16.

Counis, Raymond, et al.. (1981). Cell‐free translation of the rat pituitary messenger RNA coding for the precursors of α and β subunits of lutropin. FEBS Letters. 123(2). 151–155. 20 indexed citations

17.

Sinet, Pierre‐Marie, J Couturier, B. Dutrillaux, et al.. (1976). Trisomie 21 et superoxyde dismutase-1 (IPO-A). Experimental Cell Research. 97(1). 47–55. 146 indexed citations

18.

Poissonnier, M, et al.. (1976). [Partial trisomy 21 (21q21 - 21q22.2)].. PubMed. 19(1). 69–73. 38 indexed citations

19.

Poissonnier, M, et al.. (1976). TRISOMIE 21 PARTIELLE (21Q21->21Q22.2). 20 indexed citations

20.

Poissonnier, M, et al.. (1969). Familial Factors in a Population of Epileptic Adolescents. Epilepsia. 10(1). 47–54. 2 indexed citations

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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