Caroline Schluth‐Bolard

3.4k total citations
43 papers, 786 citations indexed

About

Caroline Schluth‐Bolard is a scholar working on Genetics, Molecular Biology and Plant Science. According to data from OpenAlex, Caroline Schluth‐Bolard has authored 43 papers receiving a total of 786 indexed citations (citations by other indexed papers that have themselves been cited), including 32 papers in Genetics, 20 papers in Molecular Biology and 11 papers in Plant Science. Recurrent topics in Caroline Schluth‐Bolard's work include Genomic variations and chromosomal abnormalities (23 papers), Genetics and Neurodevelopmental Disorders (11 papers) and Chromosomal and Genetic Variations (11 papers). Caroline Schluth‐Bolard is often cited by papers focused on Genomic variations and chromosomal abnormalities (23 papers), Genetics and Neurodevelopmental Disorders (11 papers) and Chromosomal and Genetic Variations (11 papers). Caroline Schluth‐Bolard collaborates with scholars based in France, United States and Switzerland. Caroline Schluth‐Bolard's co-authors include Damien Sanlaville, Patrick Edery, Audrey Labalme, C Turleau, Marianne Till, Frédérique Magdinier, Éric Gilson, Alexandre Ottaviani, Gaëtan Lesca and Amina Boussouar and has published in prestigious journals such as The EMBO Journal, PLoS ONE and Molecular Biology and Evolution.

In The Last Decade

Caroline Schluth‐Bolard

38 papers receiving 712 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Caroline Schluth‐Bolard France 15 434 375 125 124 90 43 786
Ilia V. Soloviev Russia 14 356 0.8× 579 1.5× 160 1.3× 28 0.2× 152 1.7× 26 788
Sylvie Jaillard France 16 435 1.0× 397 1.1× 44 0.4× 22 0.2× 148 1.6× 54 802
Birgit Schechinger Germany 6 246 0.6× 218 0.6× 55 0.4× 79 0.6× 22 0.2× 8 519
Carolina Sismani Cyprus 19 515 1.2× 735 2.0× 184 1.5× 14 0.1× 266 3.0× 75 984
María‐Isabel Tejada Spain 16 389 0.9× 581 1.5× 50 0.4× 28 0.2× 63 0.7× 46 758
Julien Thévenon France 15 450 1.0× 474 1.3× 18 0.1× 25 0.2× 54 0.6× 51 798
Buffy S. Ellsworth United States 14 571 1.3× 345 0.9× 26 0.2× 36 0.3× 34 0.4× 29 937
Claude‐Lise Richer Canada 15 458 1.1× 397 1.1× 194 1.6× 18 0.1× 95 1.1× 35 759
B Delobel France 11 170 0.4× 313 0.8× 85 0.7× 19 0.2× 117 1.3× 18 451
Buhe Nashun China 11 788 1.8× 125 0.3× 46 0.4× 28 0.2× 46 0.5× 19 913

Countries citing papers authored by Caroline Schluth‐Bolard

Since Specialization
Citations

This map shows the geographic impact of Caroline Schluth‐Bolard'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 Caroline Schluth‐Bolard with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Caroline Schluth‐Bolard more than expected).

Fields of papers citing papers by Caroline Schluth‐Bolard

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Caroline Schluth‐Bolard. 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 Caroline Schluth‐Bolard. The network helps show where Caroline Schluth‐Bolard may publish in the future.

Co-authorship network of co-authors of Caroline Schluth‐Bolard

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

All Works

20 of 20 papers shown
1.
2.
Pons, Linda, et al.. (2023). Chromosomal rearrangement in the 22q11.2 region: a critical locus for sociability and attentional skills. Psychiatric Genetics. 33(5). 202–205.
3.
Labrune, Elsa, Sandrine Giscard d’Estaing, B. Cuzin, et al.. (2022). Delaying testicular sperm extraction in 47,XXY Klinefelter patients does not impair the sperm retrieval rate, and AMH levels are higher when TESE is positive. Human Reproduction. 37(11). 2518–2531. 8 indexed citations
4.
Pons, Linda, Tiffany Busa, Chantal Missirian, et al.. (2022). Disruption and deletion of the proximal part of TCF4 are associated with mild intellectual disability: About three new patients. European Journal of Medical Genetics. 65(4). 104458–104458. 3 indexed citations
5.
Hanna, Nadine, Sophie Dupuis‐Girod, Marianne Till, et al.. (2020). A Case of Trisomy 13 Mosaicism Presenting with a Severe Aortic Root Dilatation and Marfanoid Habitus due to an Unpredictable Cytogenetic Mechanism. Cytogenetic and Genome Research. 160(2). 72–79.
6.
Chatron, Nicolas, Michel Pugeat, Marianne Till, et al.. (2020). Follow-up of two adult brothers with homozygous CEP57 pathogenic variants expands the phenotype of Mosaic Variegated Aneuploidy Syndrome. European Journal of Medical Genetics. 63(11). 104044–104044. 8 indexed citations
7.
Caignec, Cédric Le, Olivier Pichon, C. Bonnard, et al.. (2019). Fryns type mesomelic dysplasia of the upper limbs caused by inverted duplications of the HOXD gene cluster. European Journal of Human Genetics. 28(3). 324–332. 10 indexed citations
8.
Poulat, Anne‐Lise, Nicolas Chatron, Audrey Labalme, et al.. (2019). Asparagine synthetase deficiency: A novel case with an unusual molecular mechanism. Molecular Genetics and Metabolism Reports. 21. 100509–100509. 6 indexed citations
9.
Alix, Eudéline, et al.. (2017). Prenatal Diagnosis of Trisomy 2p due to Terminal 2p Duplication including Interstitial Telomeric Sequences. Cytogenetic and Genome Research. 153(3). 117–124. 2 indexed citations
10.
Chatron, Nicolas, James Lespinasse, Audrey Labalme, et al.. (2017). Genetic Counselling Pitfall: Co-Occurrence of an 11.8-Mb Xp22 Duplication and an Xp21.2 Duplication Disrupting IL1RAPL1. Molecular Syndromology. 8(6). 325–330. 4 indexed citations
11.
Perrard, Marie‐Hélène, Caroline Schluth‐Bolard, Sandrine Giscard d’Estaing, et al.. (2016). Complete Human and Rat Ex Vivo Spermatogenesis from Fresh or Frozen Testicular Tissue. Biology of Reproduction. 95(4). 89–89. 85 indexed citations
12.
Hestand, Matthew S., Hilde Van Esch, Pascale Kleinfinger, et al.. (2016). A Distinct Class of Chromoanagenesis Events Characterized by Focal Copy Number Gains. Human Mutation. 37(7). 661–668. 24 indexed citations
13.
Louvrier, Camille, Audrey Labalme, Vincent des Portes, et al.. (2015). Characterization of a de novo Supernumerary Neocentric Ring Chromosome Derived from Chromosome 7. Cytogenetic and Genome Research. 147(2-3). 111–117. 14 indexed citations
14.
Pons, Linda, Audrey Labalme, Marianne Till, et al.. (2014). A new syndrome of intellectual disability with dysmorphism due to TBL1XR1 deletion. American Journal of Medical Genetics Part A. 167(1). 164–168. 35 indexed citations
15.
Putoux, Audrey, Audrey Labalme, Jean‐Marie André, et al.. (2013). Jacobsen and Beckwith–Wiedemann syndromes in a child with mosaicism for partial 11pter trisomy and partial 11qter monosomy. American Journal of Medical Genetics Part A. 161(2). 331–337. 13 indexed citations
16.
Boutry‐Kryza, Nadia, Audrey Labalme, Marianne Till, et al.. (2011). An 800 kb deletion at 17q23.2 including the MED13 (THRAP1) gene, revealed by aCGH in a patient with a SMC 17p. American Journal of Medical Genetics Part A. 158A(2). 400–405. 16 indexed citations
17.
Ottaviani, Alexandre, Caroline Schluth‐Bolard, Éric Gilson, & Frédérique Magdinier. (2010). D4Z4as a prototype of CTCF and lamins-dependent insulator in human cells. Nucleus. 1(1). 30–36. 25 indexed citations
18.
Schluth‐Bolard, Caroline, Damien Sanlaville, Audrey Labalme, et al.. (2010). 17p13.1 microdeletion involving the TP53 gene in a boy presenting with mental retardation but no tumor. American Journal of Medical Genetics Part A. 152A(5). 1278–1282. 29 indexed citations
19.
Ottaviani, Alexandre, Caroline Schluth‐Bolard, Sylvie Rival‐Gervier, et al.. (2009). Identification of a perinuclear positioning element in human subtelomeres that requires A‐type lamins and CTCF. The EMBO Journal. 28(16). 2428–2436. 68 indexed citations
20.
Schluth‐Bolard, Caroline, Marianne Till, Patrick Edery, & Damien Sanlaville. (2008). Syndromes chromosomiques émergents. Pathologie Biologie. 56(6). 380–387. 3 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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