de Grouchy J
- Genetics top 10%
- Molecular Biology
- Plant Science
- Pediatrics, Perinatology and Child Health
- Physiology
- Co-authors
- C TurleauF Chavin-ColinClaudine JunienRomano TenconiB. DutrillauxC. FinazJ.P. LejeuneMaurice Lamy
- Topics
- Genomic variations and chromosomal abnormalities (12 papers)Prenatal Screening and Diagnostics (5 papers)Chromosomal and Genetic Variations (5 papers)
- Journals
- PubMedMunich Personal RePEc Archive (Ludwig Maximilian University of Munich)Annales de Génétique
- Partner nations
- France
In The Last Decade
de Grouchy J
36 papers receiving 312 citations
Peers
Comparison fields: 5 of 60
- Genetics 221
- Molecular Biology 195
- Plant Science 101
- Pediatrics, Perinatology and Child Health 66
- Physiology 26
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 | The decrease of catalase or esterase D activity in patients with microdeletions of 11p or 13q does not increase their radiosensitivity. | 2 |
| 2 | The beta amyloid protein (AD-AP) cDNA hybridizes in normal and Alzheimer individuals near the interface of 21q21 and q22.1. | 23 |
| 3 | Two patients with interstitial del (14q), one with features of Holt-Oram syndrome. Exclusion mapping of PI (alpha-1-antitrypsin). | 34 |
| 4 | The human gene map: a review. | 4 |
| 5 | [Ocular anomalies in phenotype 46,XY,r(14) (ring chromosome 14)]. | 2 |
| 6 | [46,XX/46,XX,del (10) (p13)/47,XX,+r/47,XX,del (10) (p13), + r mosaicism and partial trisomy 10p phenotype (author's transl)]. | 5 |
| 7 | Chromosome Y avec satellite (Yqs) et organisateur nucléolaire survenu de novo. | 15 |
| 8 | [Satellited Y chromosome (Yqs) and nucleolar organizer occurring de novo]. | 12 |
| 9 | [Ring of the chromosome 4. II. Without facial dysmorphism]. | 8 |
| 10 | [Pure trisomy 9p 47,XX,+ del(9) (q11). Discovery of one cell 46,XX, del(9) (q11) in the father]. | 5 |
| 11 | [De novo interstitial deletion Del (1) (q24 q32.1) in a malformed child]. | 6 |
| 12 | [Chromosomal breakage in incontinentia pigmenti. Study of a family]. | 4 |
| 13 | [21 p-maternal in duplicate in a case of trisomy 21]. | 11 |
| 14 | [Chromosomal asynchrony in a case of xeroderma pigmentosum]. | 2 |
| 15 | [Selective endoreduplication of a supernumerary chromosome in a case of multiple myeloma (Kahler's disease)]. | 4 |
| 16 | [ Chromosome analysis of a clonal development in a case of myeloid leykemia]. | 3 |
| 17 | [Ph-1 chromosome and loss of small acrocentrics in a chronic myeloid leukemia of prolonged development in a man]. | 5 |
| 18 | A complex familial chromosome translocation. | 7 |
| 19 | [17-18 RING-CHROMOSOMES AND CONGENITAL MALFORMATIONS IN A YOUNG GIRL]. | 21 |
| 20 | [FAMILIAL ANECEPHALY AND REARRANGEMENT OF 2 13-15 CHROMOSOMES]. | 5 |
About de Grouchy J
de Grouchy J is a scholar working on Genetics, Hematology and Pediatrics, Perinatology and Child Health, having authored 37 papers that have together received 353 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (12 papers), Prenatal Screening and Diagnostics (5 papers) and Chromosomal and Genetic Variations (5 papers). The work is most often cited by research in Genetics (221 citations), Developmental Biology (9 citations) and Pediatrics, Perinatology and Child Health (66 citations) de Grouchy J has collaborated with scholars based in France. Frequent co-authors include C Turleau, F Chavin-Colin, Claudine Junien, Romano Tenconi, B. Dutrillaux, C. Finaz, J.P. Lejeune, Maurice Lamy, A Betz and François Doré. Their work appears in journals such as PubMed, Munich Personal RePEc Archive (Ludwig Maximilian University of Munich) and Annales de Génétique.
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.