C Lambotte
Impact in
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- Genetic and Kidney Cyst Diseases
- Genetics and Neurodevelopmental Disorders
- Hemoglobinopathies and Related Disorders
- Genomic variations and chromosomal abnormalities
- Ocular Disorders and Treatments
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- Fetal and Pediatric Neurological Disorders
- Neonatal Health and Biochemistry
Papers in
- Genetics 12
- Genomic variations and chromosomal abnormalities 4
- Hemoglobinopathies and Related Disorders 4
- Craniofacial Disorders and Treatments 3
- Genetics and Neurodevelopmental Disorders 2
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- Erythrocyte Function and Pathophysiology 6
- Co-authors
- Alain Verloès (7 shared papers)James F. Reynolds (2 shared papers)Giovanni Neri (1 shared paper)Roland Schoos (4 shared papers)Jacquelyn Bertrand (1 shared paper)Luc Lambotte (1 shared paper)L Koulischer (2 shared papers)F. Clarke Fraser (1 shared paper)
In The Last Decade
C Lambotte
39 papers receiving 278 citations
Peers
Comparison fields: 5 of 73
- Genetics 139
- Pediatrics, Perinatology and Child Health 63
- Genetics 29
- Clinical Biochemistry 17
- Developmental Biology 5
Countries citing papers authored by C Lambotte
This map shows the geographic impact of C Lambotte'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 C Lambotte with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites C Lambotte more than expected).
Fields of papers citing papers by C Lambotte
This network shows the impact of papers produced by C Lambotte. 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 C Lambotte. The network helps show where C Lambotte may publish in the future.
Co-authors
The 25 scholars most cited alongside C Lambotte, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
Showing the 20 most-cited of 40 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 1989 | 61 | |
| 2 | [Genetics and mental disorders]. | 1976 | 34 |
| 3 | 1988 | 29 | |
| 4 | 1978 | 26 | |
| 5 | THE EFFECT OF INSULIN ON THE UPTAKE OF POTASSIUM AND PHOSPHATE BY THE ISOLATED PERFUSED CANINE LIVER. | 1963 | 20 |
| 6 | 1990 | 14 | |
| 7 | [Association of VACTERL and hydrocephalus: a new familial entity]. | 1984 | 14 |
| 8 | 1989 | 11 | |
| 9 | 1991 | 10 | |
| 10 | 1986 | 8 | |
| 11 | 1962 | 8 | |
| 12 | Seckel syndrome: bird-headed dwarfism. | 1977 | 6 |
| 13 | 1976 | 6 | |
| 14 | 1977 | 5 | |
| 15 | [Hereditary methemoglobinemia with mental retardation. Study of 3 further cases]. | 1972 | 3 |
| 16 | Chromosome 22 mosaic monosomy (46,XY/45,XY,-22). | 1987 | 3 |
| 17 | [The HLA system and diseases]. | 1977 | 3 |
| 18 | Severe neonatal deficiency of carbamylphosphate synthetase. | 1978 | 3 |
| 19 | [The Hallermann-Streiff-François syndrome or "bird head" dyscephaly]. | 1972 | 3 |
| 20 | [Prenatal diagnosis of malformations]. | 1980 | 3 |
About C Lambotte
C Lambotte is a scholar working on Genetics, Physiology, Pediatrics, Perinatology and Child Health, Molecular Biology and Genetics, having authored 40 papers that have together received 298 indexed citations. Recurring topics across this work include Erythrocyte Function and Pathophysiology (6 papers), Genomic variations and chromosomal abnormalities (4 papers), Hemoglobinopathies and Related Disorders (4 papers), Metabolism and Genetic Disorders (3 papers), Neonatal Health and Biochemistry (3 papers), Craniofacial Disorders and Treatments (3 papers), Fetal and Pediatric Neurological Disorders (3 papers) and Genetics and Neurodevelopmental Disorders (2 papers). The work is most often cited by research in Genetics (139 citations), Pediatrics, Perinatology and Child Health (63 citations), Genetics (29 citations), Clinical Biochemistry (17 citations) and Developmental Biology (5 citations). C Lambotte has collaborated with scholars based in Belgium, France and Germany. Frequent co-authors include Alain Verloès, James F. Reynolds, Giovanni Neri, Roland Schoos, Jacquelyn Bertrand, Luc Lambotte, L Koulischer, F. Clarke Fraser, A Nivelon‐Chevallier and F Serville. Their work appears in journals such as Clinica Chimica Acta, Clinical Genetics, Clinical Chemistry, American Journal of Clinical Nutrition and Journal of Inherited Metabolic Disease.
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.