Valère Cacheux

1.3k total citations
12 papers, 847 citations indexed

About

Valère Cacheux is a scholar working on Molecular Biology, Genetics and Surgery. According to data from OpenAlex, Valère Cacheux has authored 12 papers receiving a total of 847 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Molecular Biology, 6 papers in Genetics and 2 papers in Surgery. Recurrent topics in Valère Cacheux's work include Genomic variations and chromosomal abnormalities (3 papers), Congenital heart defects research (2 papers) and Congenital gastrointestinal and neural anomalies (2 papers). Valère Cacheux is often cited by papers focused on Genomic variations and chromosomal abnormalities (3 papers), Congenital heart defects research (2 papers) and Congenital gastrointestinal and neural anomalies (2 papers). Valère Cacheux collaborates with scholars based in France, Singapore and Germany. Valère Cacheux's co-authors include Michel Goossens, Serge Amselem, Bénédicte Duriez, Estelle Escudier, Anne-Marie Bridoux, Gaëlle Pennarun, Catherine Chapelin, Irène Netchine, Gilles Roger and Annick Clément and has published in prestigious journals such as Nature Genetics, FEBS Letters and The American Journal of Human Genetics.

In The Last Decade

Valère Cacheux

11 papers receiving 820 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Valère Cacheux France 10 417 415 244 166 128 12 847
Rodger Palmer United Kingdom 13 494 1.2× 397 1.0× 146 0.6× 105 0.6× 76 0.6× 20 915
Bartłomiej Budny Poland 14 396 0.9× 376 0.9× 209 0.9× 70 0.4× 82 0.6× 45 706
Mark J. McCabe United Kingdom 16 259 0.6× 331 0.8× 234 1.0× 59 0.4× 82 0.6× 22 707
Paolo Fontana Italy 16 180 0.4× 224 0.5× 163 0.7× 216 1.3× 160 1.3× 47 884
Xiao Hui Liao United States 10 150 0.4× 574 1.4× 278 1.1× 189 1.1× 151 1.2× 15 1.0k
Elisabetta Lapi Italy 18 477 1.1× 534 1.3× 66 0.3× 61 0.4× 70 0.5× 48 957
A.J. Notini Australia 11 236 0.6× 399 1.0× 254 1.0× 96 0.6× 48 0.4× 14 715
Thomas A. Maher United States 13 147 0.4× 270 0.7× 46 0.2× 137 0.8× 112 0.9× 23 586
Kyriaki S. Alatzoglou United Kingdom 15 327 0.8× 334 0.8× 491 2.0× 26 0.2× 114 0.9× 23 821
Vassos Neocleous Cyprus 15 261 0.6× 444 1.1× 223 0.9× 38 0.2× 62 0.5× 61 728

Countries citing papers authored by Valère Cacheux

Since Specialization
Citations

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

Fields of papers citing papers by Valère Cacheux

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Valère Cacheux. 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 Valère Cacheux. The network helps show where Valère Cacheux may publish in the future.

Co-authorship network of co-authors of Valère Cacheux

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

All Works

12 of 12 papers shown
1.
Aksoy, Irène, Kagistia Hana Utami, Cecilia Lanny Winata, et al.. (2016). Personalized genome sequencing coupled with iPSC technology identifies GTDC1 as a gene involved in neurodevelopmental disorders. Human Molecular Genetics. 26(2). 367–382. 15 indexed citations
2.
Utami, Kagistia Hana, Cecilia Lanny Winata, Axel M. Hillmer, et al.. (2014). Impaired Development Of Neural-Crest Cell Derived Organs and Intellectual Disability Caused ByMED13LHaploinsufficiency. Human Mutation. 35(11). n/a–n/a. 38 indexed citations
3.
Perche, Olivier, Arnaud Menuet, Kagistia Hana Utami, et al.. (2013). Combined deletion of two Condensin II system genes (NCAPG2 and MCPH1) in a case of severe microcephaly and mental deficiency. European Journal of Medical Genetics. 56(11). 635–641. 21 indexed citations
4.
Bassez, Guillaume, Olivier Camand, Valère Cacheux, et al.. (2004). Pleiotropic and diverse expression of ZFHX1B gene transcripts during mouse and human development supports the various clinical manifestations of the “Mowat–Wilson” syndrome. Neurobiology of Disease. 15(2). 240–250. 40 indexed citations
5.
Wilson, Meredith, David Mowat, Florence Dastot‐Le Moal, et al.. (2003). Further delineation of the phenotype associated with heterozygous mutations in ZFHX1B. American Journal of Medical Genetics Part A. 119A(3). 257–265. 69 indexed citations
6.
Pennarun, Gaëlle, Anne-Marie Bridoux, Estelle Escudier, et al.. (2002). Isolation and Expression of the Human hPF20 Gene Orthologous to Chlamydomonas pf20. American Journal of Respiratory Cell and Molecular Biology. 26(3). 362–370. 30 indexed citations
7.
Pennarun, Gaëlle, Catherine Chapelin, Estelle Escudier, et al.. (2000). The human dynein intermediate chain 2 gene (DNAI2): cloning, mapping, expression pattern, and evaluation as a candidate for primary ciliary dyskinesia. Human Genetics. 107(6). 642–649. 31 indexed citations
8.
Netchine, Irène, Marie‐Laure Sobrier, Heiko Krude, et al.. (2000). Mutations in LHX3 result in a new syndrome revealed by combined pituitary hormone deficiency. Nature Genetics. 25(2). 182–186. 241 indexed citations
9.
Pennarun, Gaëlle, Estelle Escudier, Catherine Chapelin, et al.. (1999). Loss-of-Function Mutations in a Human Gene Related to Chlamydomonas reinhardtii Dynein IC78 Result in Primary Ciliary Dyskinesia. The American Journal of Human Genetics. 65(6). 1508–1519. 261 indexed citations
10.
Ramond, Sylvie, Valère Cacheux, M Cadiou, et al.. (1998). Pentasomy 13q in a Case of Acute Myelogenous Leukemia (M0). Cancer Genetics and Cytogenetics. 107(1). 73–75.
11.
Duquesnoy, Philippe, Anne Roy, Florence Dastot, et al.. (1998). Human Prop‐1: cloning, mapping, genomic structure. FEBS Letters. 437(3). 216–220. 98 indexed citations
12.
Martin, Emmanuel, et al.. (1995). Localization of the CDKN4/p27Kip1 gene to human chromosome 12p12.3. Human Genetics. 96(6). 668–670. 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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