1.0k total citations 103 papers, 854 citations indexed
About
de Grouchy J is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health.
According to data from OpenAlex, de Grouchy J has authored 103 papers receiving a total of 854 indexed citations (citations by other indexed papers that have themselves been cited), including 35 papers in Genetics, 21 papers in Molecular Biology and 11 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in de Grouchy J's work include Genomic variations and chromosomal abnormalities (20 papers), Prenatal Screening and Diagnostics (10 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (8 papers) de Grouchy J is often cited by papers focused on Genomic variations and chromosomal abnormalities (20 papers), Prenatal Screening and Diagnostics (10 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (8 papers) de Grouchy J collaborates with scholars based in France de Grouchy J's co-authors include C Turleau, Maurice Lamy, O Schweisguth, I Emerit, C. Finaz, M Plachot, Jacqueline Mandelbaum, Catherine Léonard, P. Couillin and J Salat‐Baroux and has published in prestigious journals such as PubMed, PubMed Central and Munich Personal RePEc Archive (Ludwig Maximilian University of Munich).
Citations per year, relative to de Grouchy J de Grouchy J (= 1×)
peers
S Armendares
Countries citing papers authored by de Grouchy J
Since
Specialization
Citations
This map shows the geographic impact of de Grouchy J'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 de Grouchy J with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites de Grouchy J more than expected).
This network shows the impact of papers produced by de Grouchy J. 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 de Grouchy J. The network helps show where de Grouchy J may publish in the future.
Co-authorship network of co-authors of de Grouchy J
This figure shows the co-authorship network connecting the top 25 collaborators of de Grouchy J.
A scholar is included among the top collaborators of de Grouchy J 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 de Grouchy J. de Grouchy J is excluded from
the visualization to improve readability, since they are connected to all nodes in the network.
All Works
20 of 20 papers shown
1.
Plachot, M, de Grouchy J, Jacqueline Mandelbaum, et al.. (1987). From oocyte to embryo: a model, deduced from in vitro fertilization, for natural selection against chromosome abnormalities.. PubMed. 30(1). 22–32.65 indexed citations
2.
Turleau, C, et al.. (1980). [Trisomy 21 by mirror duplication 46,XX,psu dic(21)ter rea (21q21q) (author's transl)].. PubMed. 23(3). 187–9.4 indexed citations
3.
J, de Grouchy, et al.. (1978). [Trisomy 13qter by tandem duplication 46, XX, dir dup 13 (q21 qter), 9qh+].. Munich Personal RePEc Archive (Ludwig Maximilian University of Munich). 21(4). 247–51.8 indexed citations
4.
Plachot, M, Jacqueline Mandelbaum, & de Grouchy J. (1978). [Anomaly of the nuclear maturation in vitro of golden hamster oocytes].. Munich Personal RePEc Archive (Ludwig Maximilian University of Munich). 21(1). 33–9.2 indexed citations
5.
J, de Grouchy, et al.. (1977). [Dicentric Y chromosome in a male pseudohermaphrodite 45,X/46,X, dic (Y)/47, XYY].. PubMed. 20(3). 185–9.8 indexed citations
6.
Finaz, C., et al.. (1977). [Natural history of chromosome 1 in primates].. PubMed. 20(2). 85–92.2 indexed citations
7.
J, de Grouchy, et al.. (1973). [45,X-46,XY-47,XYY mosaicism in a patient with Turner's syndrome].. PubMed. 16(2). 123–5.1 indexed citations
8.
J, de Grouchy, et al.. (1972). [F fing chromosome (46, XY, Fr) in a boy with multiple abnormalities].. PubMed. 15(2). 121–6.7 indexed citations
9.
Finaz, C. & de Grouchy J. (1971). [The human karyotype after treatment with alpha-chymotrypsin].. PubMed. 14(4). 309–11.14 indexed citations
10.
J, de Grouchy, et al.. (1971). [Hemorrhagic Turner's syndrome (without mosaicism)].. PubMed. 22(4). 405–9.1 indexed citations
11.
Turpin, G, et al.. (1970). [Clinical, biological, histological and genetic studies of De Morsier's syndrome (hypogonadotrophic hypogonadism with anosmia). 7 cases].. PubMed. 31(2). 234–6.3 indexed citations
12.
Emerit, I, de Grouchy J, J Frézal, et al.. (1968). [XXY karyotype, cardiovascular anomalies and facial dysmorphia in a 12-year-old boy].. PubMed. 25(5). 531–9.2 indexed citations
13.
J, de Grouchy, et al.. (1968). [46, XX, 1q-, 2q-, Dq+, 16q+ karyotype in a polymalformed child].. PubMed. 11(2). 129–31.12 indexed citations
14.
J, de Grouchy, et al.. (1966). Aneusomie de recombinaison: three further examples.. PubMed Central. 18(5). 467–84.25 indexed citations
15.
Bernard, Simon de, et al.. (1966). [A case of pure gonadal agenesis of female phenotype and XY karyotype].. PubMed. 26(5). 572–82.2 indexed citations
16.
Hartmann, Lynn C., et al.. (1965). [The chromosome anomaly of Waldenström's disease].. PubMed. 8(1). 55–9.1 indexed citations
17.
Lamy, Maurice, Nathalie Josso, de Grouchy J, & C Nèzelof. (1963). [KLINEFELTER'S SYNDROME IN CHILDREN].. PubMed. 11. 1301–9.2 indexed citations
18.
J, de Grouchy. (1963). [CHROMOSOME ABERRATIONS AND CARCINOGENESIS].. PubMed. 70. 601–6.1 indexed citations
19.
J, de Grouchy, et al.. (1963). [TURNER'S SYNDROME AND 47 CHROMOSOME KARYOTYPE].. PubMed. 6. 25–8.5 indexed citations
20.
Lamy, Martine, J Frézal, & de Grouchy J. (1957). [Results of an investigation of the heredity of diabetes mellitus].. PubMed. 2(9). 907–19.1 indexed citations
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