de Grouchy J
- Genetics top 5%
- Molecular Biology
- Pediatrics, Perinatology and Child Health top 5%
- Plant Science top 10%
- Epidemiology
- Co-authors
- C TurleauMaurice LamyO SchweisguthI EmeritC. FinazM PlachotJacqueline MandelbaumCatherine Léonard
- Topics
- Genomic variations and chromosomal abnormalities (20 papers)Prenatal Screening and Diagnostics (10 papers)Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (8 papers)
- Journals
- PubMedPubMed CentralMunich Personal RePEc Archive (Ludwig Maximilian University of Munich)
- Partner nations
- France
In The Last Decade
de Grouchy J
99 papers receiving 743 citations
Peers
Comparison fields: 5 of 77
- Genetics 467
- Molecular Biology 375
- Pediatrics, Perinatology and Child Health 191
- Plant Science 182
- Epidemiology 96
Countries citing papers authored by de Grouchy J
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).
Fields of papers citing papers by de Grouchy J
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
| # | Work | Indexed citations |
|---|---|---|
| 1 | From oocyte to embryo: a model, deduced from in vitro fertilization, for natural selection against chromosome abnormalities. | 65 |
| 2 | [Trisomy 21 by mirror duplication 46,XX,psu dic(21)ter rea (21q21q) (author's transl)]. | 4 |
| 3 | [Trisomy 13qter by tandem duplication 46, XX, dir dup 13 (q21 qter), 9qh+]. | 8 |
| 4 | [Anomaly of the nuclear maturation in vitro of golden hamster oocytes]. | 2 |
| 5 | [Dicentric Y chromosome in a male pseudohermaphrodite 45,X/46,X, dic (Y)/47, XYY]. | 8 |
| 6 | [Natural history of chromosome 1 in primates]. | 2 |
| 7 | [45,X-46,XY-47,XYY mosaicism in a patient with Turner's syndrome]. | 1 |
| 8 | [F fing chromosome (46, XY, Fr) in a boy with multiple abnormalities]. | 7 |
| 9 | [The human karyotype after treatment with alpha-chymotrypsin]. | 14 |
| 10 | [Hemorrhagic Turner's syndrome (without mosaicism)]. | 1 |
| 11 | [Clinical, biological, histological and genetic studies of De Morsier's syndrome (hypogonadotrophic hypogonadism with anosmia). 7 cases]. | 3 |
| 12 | [XXY karyotype, cardiovascular anomalies and facial dysmorphia in a 12-year-old boy]. | 2 |
| 13 | [46, XX, 1q-, 2q-, Dq+, 16q+ karyotype in a polymalformed child]. | 12 |
| 14 | Aneusomie de recombinaison: three further examples. | 25 |
| 15 | [A case of pure gonadal agenesis of female phenotype and XY karyotype]. | 2 |
| 16 | [The chromosome anomaly of Waldenström's disease]. | 1 |
| 17 | [KLINEFELTER'S SYNDROME IN CHILDREN]. | 2 |
| 18 | [CHROMOSOME ABERRATIONS AND CARCINOGENESIS]. | 1 |
| 19 | [TURNER'S SYNDROME AND 47 CHROMOSOME KARYOTYPE]. | 5 |
| 20 | [Results of an investigation of the heredity of diabetes mellitus]. | 1 |
About de Grouchy J
de Grouchy J is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Molecular Biology, having authored 103 papers that have together received 854 indexed citations. Recurring topics across this 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). The work is most often cited by research in Developmental Biology (51 citations), Genetics (467 citations) and Pediatrics, Perinatology and Child Health (191 citations) de Grouchy J has collaborated with scholars based in France. Frequent 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. Their work appears in journals such as PubMed, PubMed Central and Munich Personal RePEc Archive (Ludwig Maximilian University of Munich).
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.