C Schluth
Impact in
-
- Genomic variations and chromosomal abnormalities
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
- Genetic Syndromes and Imprinting
- Genetics and Neurodevelopmental Disorders
-
- Prenatal Screening and Diagnostics
Papers in
- Genetics 6
- Genomic variations and chromosomal abnormalities 3
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 2
-
- Nuclear Structure and Function 1
- Co-authors
- Françoise Girard‐Lemaire (5 shared papers)Elisabeth Flori (5 shared papers)Bérénice Doray (4 shared papers)Éric Jeandidier (2 shared papers)Emmanuelle Girodon (1 shared paper)R. Favre (2 shared papers)Hélène Dollfus (1 shared paper)Bernard Gasser (1 shared paper)
- Journals
- European Journal of Human Genetics (1 paper)Prenatal Diagnosis (1 paper)Haematologica (1 paper)American Journal of Medical Genetics Part A (2 papers)PubMed (2 papers)
- Partner nations
- FranceUnited KingdomUnited States
In The Last Decade
C Schluth
8 papers receiving 101 citations
Peers
Comparison fields: 5 of 27
- Genetics 79
- Pediatrics, Perinatology and Child Health 38
- Developmental Biology 2
- Molecular Biology 48
- Genetics 6
Countries citing papers authored by C Schluth
This map shows the geographic impact of C Schluth'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 Schluth with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites C Schluth more than expected).
Fields of papers citing papers by C Schluth
This network shows the impact of papers produced by C Schluth. 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 Schluth. The network helps show where C Schluth may publish in the future.
Co-authors
The 25 scholars most cited alongside C Schluth, 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 | 2005 | 26 | |
| 2 | 2006 | 16 | |
| 3 | 2011 | 14 | |
| 4 | 2007 | 13 | |
| 5 | 2005 | 13 | |
| 6 | 2002 | 12 | |
| 7 | Recurrent neural tube defects associated with partial trisomy 2p22-pter: report of two siblings and review of the literature. | 2003 | 7 |
| 8 | Prenatal diagnosis of a true fetal tetraploidy in direct and cultured chorionic villi. | 2004 | 3 |
About C Schluth
C Schluth is a scholar working on Genetics, Molecular Biology, Pediatrics, Perinatology and Child Health, Surgery and Infectious Diseases, having authored 8 papers that have together received 104 indexed citations. Recurring topics across this work include Prenatal Screening and Diagnostics (3 papers), Genomic variations and chromosomal abnormalities (3 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (2 papers), Congenital Anomalies and Fetal Surgery (2 papers), Intestinal Malrotation and Obstruction Disorders (1 paper), Cancer Genomics and Diagnostics (1 paper), Parvovirus B19 Infection Studies (1 paper) and Nuclear Structure and Function (1 paper). The work is most often cited by research in Genetics (79 citations), Pediatrics, Perinatology and Child Health (38 citations), Developmental Biology (2 citations), Molecular Biology (48 citations) and Genetics (6 citations). C Schluth has collaborated with scholars based in France, United Kingdom and United States. Frequent co-authors include Françoise Girard‐Lemaire, Elisabeth Flori, Bérénice Doray, Éric Jeandidier, Emmanuelle Girodon, R. Favre, Hélène Dollfus, Bernard Gasser, Cécile Mignon‐Ravix and B. Langer. Their work appears in journals such as European Journal of Human Genetics, Prenatal Diagnosis, Haematologica, American Journal of Medical Genetics Part A and PubMed.
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.