J Battin
- Genetics top 10%
- Molecular Biology
- Pediatrics, Perinatology and Child Health
- Surgery
- Endocrinology, Diabetes and Metabolism
- Topics
- Sexual Differentiation and Disorders (7 papers)Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (5 papers)Congenital limb and hand anomalies (5 papers)
- Journals
- Archives of Disease in ChildhoodJournal of the Neurological SciencesJournal of Medical Genetics
- Partner nations
- FranceUnited KingdomUnited States
In The Last Decade
J Battin
45 papers receiving 405 citations
Peers
Comparison fields: 5 of 68
- Genetics 228
- Molecular Biology 154
- Pediatrics, Perinatology and Child Health 87
- Surgery 84
- Endocrinology, Diabetes and Metabolism 55
Countries citing papers authored by J Battin
This map shows the geographic impact of J Battin'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 J Battin with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites J Battin more than expected).
Fields of papers citing papers by J Battin
This network shows the impact of papers produced by J Battin. 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 J Battin. The network helps show where J Battin may publish in the future.
Co-authorship network of co-authors of J Battin
This figure shows the co-authorship network connecting the top 25 collaborators of J Battin. A scholar is included among the top collaborators of J Battin 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 J Battin. J Battin is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
| # | Work | Indexed citations |
|---|---|---|
| 1 | 0 | |
| 2 | 53 | |
| 3 | Early pubertal development in children adopted from abroad. | 1 |
| 4 | 37 | |
| 5 | 1 | |
| 6 | 1 | |
| 7 | 2 | |
| 8 | 18p monosomy with midline defects and a de novo satellite identified by FISH. | 15 |
| 9 | 0 | |
| 10 | 33 | |
| 11 | 40 | |
| 12 | 63 | |
| 13 | Congenital marked hypertrichosis and Laband syndrome in a child: overlap between the gingival fibromatosis-hypertrichosis and Laband syndromes. | 17 |
| 14 | 15 | |
| 15 | 2 | |
| 16 | Acanthosis nigricans, hirsutisme et diabète insulino-résistant. | 2 |
| 17 | [Heterogenity of the cryptorchid syndrome. Study of the pituitary gonadotropin reserve in 50 prepuberal bodys]. | 1 |
| 18 | [Extra-hepatic biliary lithiasis in children. Results of a multicentre enquiry (100 cases) (author's transl)]. | 1 |
| 19 | [A rare neurolipidosis with subcutaneous and articular node lesions: disseminated Farber's lipogranulomatosis]. | 5 |
| 20 | [Idiopathic diffuse pulmonary interstitial fibrosis in children. (Hamman-Rich syndrome)]. | 1 |
About J Battin
J Battin is a scholar working on Developmental Biology, Anatomy and Pharmacy, having authored 51 papers that have together received 429 indexed citations. Recurring topics across this work include Sexual Differentiation and Disorders (7 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (5 papers) and Congenital limb and hand anomalies (5 papers). The work is most often cited by research in Developmental Biology (54 citations), Genetics (228 citations) and Reproductive Medicine (39 citations). J Battin has collaborated with scholars based in France, United Kingdom and United States. Frequent co-authors include Didier Lacombe, J.M. Limal, M Colle, P Rochiccioli, S. Baron, Antonio David, M A Patton, M Bost, A.-M. Bertrand and G Malpuech. Their work appears in journals such as Archives of Disease in Childhood, Journal of the Neurological Sciences and Journal of Medical 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.