Annie Nivelon
Impact in
- Reproductive Medicine top 5%
- Sperm and Testicular Function
- Ovarian function and disorders
- Genetics top 5%
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
- Animal Genetics and Reproduction
- Genomic variations and chromosomal abnormalities
Papers in
- Genetics 9
- Genomic variations and chromosomal abnormalities 3
- Craniofacial Disorders and Treatments 2
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 2
- Co-authors
- Didier Lacombe (2 shared papers)Alain Verloès (1 shared paper)Jacqueline Vigneron (1 shared paper)Pierre Bitoun (1 shared paper)C Laurent (3 shared papers)Valérie Cormier‐Daire (2 shared papers)Martine Le Merrer (2 shared papers)Dominique Bonneau (2 shared papers)
- Journals
- Nature Genetics (1 paper)European Journal of Pediatrics (1 paper)Journal of Medical Genetics (1 paper)Clinical Genetics (1 paper)Human Molecular Genetics (1 paper)
- Partner nations
- FranceUnited StatesAustralia
In The Last Decade
Annie Nivelon
14 papers receiving 1.1k citations
Annie Nivelon's Hit Papers
Peers
Comparison fields: 5 of 68
- Reproductive Medicine 205
- Genetics 643
- Public Health, Environmental and Occupational Health 270
- Urology 51
- Developmental Biology 19
Countries citing papers authored by Annie Nivelon
This map shows the geographic impact of Annie Nivelon'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 Annie Nivelon with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Annie Nivelon more than expected).
Fields of papers citing papers by Annie Nivelon
This network shows the impact of papers produced by Annie Nivelon. 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 Annie Nivelon. The network helps show where Annie Nivelon may publish in the future.
Co-authors
The 25 scholars most cited alongside Annie Nivelon, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
| # | Work | ||
|---|---|---|---|
| 1 | The putative forkhead transcription factor FOXL2 is mutated in blepharophimosis/ptosis/epicanthus inversus syndrome Hit paper breakdown → | 2001 | 836 |
| 2 | 1994 | 104 | |
| 3 | 1999 | 92 | |
| 4 | 1996 | 34 | |
| 5 | [Familial cases of intracranial aneurysms. Review of the literature and case report]. | 1973 | 13 |
| 6 | [Partial deletion of the long arm of a group D (13-15) chromosome :Dq-]. | 1967 | 12 |
| 7 | 1992 | 12 | |
| 8 | 2002 | 12 | |
| 9 | 1996 | 11 | |
| 10 | [Partial monosomy of a C group chromosome (Cp-)]. | 1968 | 6 |
| 11 | [Neurological manifestations of oculodentodigital dysplasia: a case report (author's transl)]. | 1982 | 4 |
| 12 | [A case of gonadal dysgenesis with a gonocytoma of XY karyotype]. | 1968 | 2 |
| 13 | [Late manifestation of homocystinuria by aphasia and spasm of 2 external iliac arteries]. | 1989 | 1 |
| 14 | [Apert's syndrome with polymetatarsia]. | 1991 | 1 |
| 15 | 2016 | 0 |
About Annie Nivelon
Annie Nivelon is a scholar working on Genetics, Genetics, Neurology, Pathology and Forensic Medicine and Molecular Biology, having authored 15 papers that have together received 1.1k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (3 papers), Prenatal Screening and Diagnostics (2 papers), Hedgehog Signaling Pathway Studies (2 papers), Craniofacial Disorders and Treatments (2 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (2 papers), Chromosomal and Genetic Variations (2 papers), Sexual Differentiation and Disorders (2 papers) and Congenital Diaphragmatic Hernia Studies (1 paper). The work is most often cited by research in Reproductive Medicine (205 citations), Genetics (643 citations), Public Health, Environmental and Occupational Health (270 citations), Urology (51 citations) and Developmental Biology (19 citations). Annie Nivelon has collaborated with scholars based in France, United States and Australia. Frequent co-authors include Didier Lacombe, Alain Verloès, Jacqueline Vigneron, Pierre Bitoun, C Laurent, Valérie Cormier‐Daire, Martine Le Merrer, Dominique Bonneau, Arnold Münnich and Gilles Guerrier. Their work appears in journals such as Nature Genetics, European Journal of Pediatrics, Journal of Medical Genetics, Clinical Genetics and Human Molecular Genetics.
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.