C Schluth

429 total citations
8 papers, 104 citations indexed

About

C Schluth is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, C Schluth has authored 8 papers receiving a total of 104 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Genetics, 4 papers in Molecular Biology and 3 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in C Schluth's work include Prenatal Screening and Diagnostics (3 papers), Genomic variations and chromosomal abnormalities (3 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (2 papers). C Schluth is often cited by papers focused on Prenatal Screening and Diagnostics (3 papers), Genomic variations and chromosomal abnormalities (3 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (2 papers). C Schluth collaborates with scholars based in France, United Kingdom and United States. C Schluth's co-authors include Françoise Girard‐Lemaire, Elisabeth Flori, Bérénice Doray, Éric Jeandidier, Bernard Gasser, Marie‐Geneviève Mattéi, Emmanuelle Girodon, F. Becmeur, Véronique Pingault and Yves Alembik and has published in prestigious journals such as Haematologica, European Journal of Human Genetics and Prenatal Diagnosis.

In The Last Decade

C Schluth

8 papers receiving 101 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
C Schluth France	7	79	48	38	9	7	8	104
Debra Rita United States	4	50 0.6×	32 0.7×	32 0.8×	6 0.7×	6 0.9×	5	78
Sharyn Stock‐Myer Australia	3	77 1.0×	43 0.9×	109 2.9×	9 1.0×	9 1.3×	5	143
Paulette Barahona Australia	6	88 1.1×	36 0.8×	74 1.9×	21 2.3×	8 1.1×	14	148
Giovanni Neri Italy	4	46 0.6×	34 0.7×	11 0.3×	14 1.6×	6 0.9×	7	80
A.L. Mosca France	6	61 0.8×	30 0.6×	18 0.5×	5 0.6×	12 1.7×	8	69
Dominique Le Tessier France	8	119 1.5×	66 1.4×	82 2.2×	6 0.7×	37 5.3×	15	167
Rosa Baldinger Switzerland	5	54 0.7×	41 0.9×	36 0.9×	7 0.8×	4 0.6×	5	90
Céline Pebrel‐Richard France	7	91 1.2×	69 1.4×	39 1.0×	26 2.9×	20 2.9×	20	138
Stacey Curry United States	4	56 0.7×	60 1.3×	41 1.1×	21 2.3×	3 0.4×	4	150
Alessandra Ferrarini Switzerland	7	74 0.9×	75 1.6×	11 0.3×	18 2.0×	19 2.7×	10	126

Countries citing papers authored by C Schluth

Since Specialization

Citations

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

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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-authorship network of co-authors of C Schluth

This figure shows the co-authorship network connecting the top 25 collaborators of C Schluth. A scholar is included among the top collaborators of C Schluth 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 C Schluth. C Schluth is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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8 of 8 papers shown

1.

Petit, Arnaud, Christine Ragu, Chris Ottolenghi, et al.. (2011). Functional analysis of the NUP98-CCDC28A fusion protein. Haematologica. 97(3). 379–387. 14 indexed citations

2.

Schluth, C, Guntram Borck, Richard Redon, et al.. (2007). New case of interstitial deletion 12(q15‐q21.2) in a girl with facial dysmorphism and mental retardation. American Journal of Medical Genetics Part A. 146A(1). 93–96. 13 indexed citations

3.

Schluth, C, Mireille Cossée, Françoise Girard‐Lemaire, et al.. (2006). Phenotype in X chromosome rearrangements: pitfalls of X inactivation study. Pathologie Biologie. 55(1). 29–36. 16 indexed citations

4.

Schluth, C, Marie‐Geneviève Mattéi, Cécile Mignon‐Ravix, et al.. (2005). Intrachromosomal triplication for the distal part of chromosome 15q. American Journal of Medical Genetics Part A. 136A(2). 179–184. 13 indexed citations

5.

Flori, Elisabeth, Emmanuelle Girodon, F. Becmeur, et al.. (2005). Trisomy 7 mosaicism, maternal uniparental heterodisomy 7 and Hirschsprung's disease in a child with Silver–Russell syndrome. European Journal of Human Genetics. 13(9). 1013–1018. 26 indexed citations

6.

Schluth, C, Bérénice Doray, Françoise Girard‐Lemaire, et al.. (2004). Prenatal diagnosis of a true fetal tetraploidy in direct and cultured chorionic villi.. PubMed. 15(4). 429–36. 3 indexed citations

7.

Doray, Bérénice, R. Favre, B. Gasser, et al.. (2003). Recurrent neural tube defects associated with partial trisomy 2p22-pter: report of two siblings and review of the literature.. PubMed. 14(2). 165–72. 7 indexed citations

8.

Schluth, C, Bérénice Doray, Françoise Girard‐Lemaire, et al.. (2002). Prenatal sonographic diagnosis of the 49,XXXXY syndrome. Prenatal Diagnosis. 22(13). 1177–1180. 12 indexed citations

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.

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