Daniel Amsallem

713 total citations
21 papers, 335 citations indexed

About

Daniel Amsallem is a scholar working on Genetics, Molecular Biology and Surgery. According to data from OpenAlex, Daniel Amsallem has authored 21 papers receiving a total of 335 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Genetics, 6 papers in Molecular Biology and 3 papers in Surgery. Recurrent topics in Daniel Amsallem's work include Genetics and Neurodevelopmental Disorders (7 papers), Genomic variations and chromosomal abnormalities (4 papers) and Epigenetics and DNA Methylation (2 papers). Daniel Amsallem is often cited by papers focused on Genetics and Neurodevelopmental Disorders (7 papers), Genomic variations and chromosomal abnormalities (4 papers) and Epigenetics and DNA Methylation (2 papers). Daniel Amsallem collaborates with scholars based in France, United States and Switzerland. Daniel Amsallem's co-authors include Philippe Jonveaux, Christophe Philippe, Laëtitia Lambert, Violaine Bourdon, Cécile Arnould, Christine Francannet, Lila Allou, David J. Amor, François Rivier and Anne Destrèe and has published in prestigious journals such as Blood, Movement Disorders and Journal of Medical Genetics.

In The Last Decade

Daniel Amsallem

21 papers receiving 319 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Daniel Amsallem France 10 222 173 81 29 25 21 335
Christalena Sofocleous Greece 14 261 1.2× 218 1.3× 67 0.8× 81 2.8× 41 1.6× 45 459
Syed K. Rafi United States 8 137 0.6× 107 0.6× 52 0.6× 25 0.9× 18 0.7× 14 264
Frédérique Sloan‐Béna Switzerland 9 87 0.4× 123 0.7× 24 0.3× 30 1.0× 16 0.6× 23 263
Dima El‐Khechen United States 8 208 0.9× 125 0.7× 49 0.6× 26 0.9× 25 1.0× 10 294
Louise Christie Australia 10 294 1.3× 197 1.1× 68 0.8× 73 2.5× 16 0.6× 14 409
Wout H. Deelen Netherlands 11 256 1.2× 232 1.3× 87 1.1× 69 2.4× 41 1.6× 16 413
Naghmeh Dorrani United States 12 367 1.7× 314 1.8× 132 1.6× 37 1.3× 11 0.4× 20 518
Anne Chun‐Hui Tsai United States 10 117 0.5× 126 0.7× 27 0.3× 47 1.6× 11 0.4× 22 295
M. A. Mori Spain 10 216 1.0× 156 0.9× 22 0.3× 82 2.8× 63 2.5× 15 378
Claudia Ciaccio Italy 11 221 1.0× 184 1.1× 66 0.8× 25 0.9× 22 0.9× 30 347

Countries citing papers authored by Daniel Amsallem

Since Specialization
Citations

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

Fields of papers citing papers by Daniel Amsallem

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Daniel Amsallem

This figure shows the co-authorship network connecting the top 25 collaborators of Daniel Amsallem. A scholar is included among the top collaborators of Daniel Amsallem 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 Daniel Amsallem. Daniel Amsallem 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.
Amsallem, Daniel, et al.. (2022). Impact of pharmacist medication review for paediatric patients: an observational study. International Journal of Pharmacy Practice. 30(5). 420–426. 3 indexed citations
2.
Delplancq, Geoffroy, et al.. (2021). The Largest Germline Heterozygous Deletion Encompassing Potocki–Shaffer and WAGR Syndromes Loci to Date: A Case Report. Neuropediatrics. 53(4). 274–278. 1 indexed citations
3.
Piard, Juliette, Matthieu Béreau, Wenshu XiangWei, et al.. (2020). The GRIA3 c.2477G > A Variant Causes an Exaggerated Startle Reflex, Chorea, and Multifocal Myoclonus. Movement Disorders. 35(7). 1224–1232. 10 indexed citations
4.
Brassier, Anaïs, Thierry Billette de Villemeur, Daniel Amsallem, et al.. (2017). Type 3 Gaucher disease, diagnostic in adulthood. Molecular Genetics and Metabolism Reports. 13. 1–2. 3 indexed citations
5.
Kuster, Alice, Jean‐Baptiste Arnoux, Magalie Barth, et al.. (2017). Diagnostic approach to neurotransmitter monoamine disorders: experience from clinical, biochemical, and genetic profiles. Journal of Inherited Metabolic Disease. 41(1). 129–139. 11 indexed citations
6.
Allou, Lila, Sophie Julia, Daniel Amsallem, et al.. (2016). Rett‐like phenotypes: expanding the genetic heterogeneity to the KCNA2 gene and first familial case of CDKL5‐related disease. Clinical Genetics. 91(3). 431–440. 33 indexed citations
7.
Valence, Stéphanie, Cathérine Garel, Annick Toutain, et al.. (2016). RELN and VLDLR mutations underlie two distinguishable clinico‐radiological phenotypes. Clinical Genetics. 90(6). 545–549. 22 indexed citations
8.
Mignot, Cyril, Agnès Guët, Caroline Nava, et al.. (2015). DYRK1A mutations in two unrelated patients. European Journal of Medical Genetics. 58(3). 168–174. 24 indexed citations
9.
Allou, Lila, Laëtitia Lambert, Daniel Amsallem, et al.. (2012). 14q12 and severe Rett-like phenotypes: new clinical insights and physical mapping of FOXG1-regulatory elements. European Journal of Human Genetics. 20(12). 1216–1223. 50 indexed citations
10.
Philippe, Christophe, et al.. (2009). Phenotypic variability in Rett syndrome associated with FOXG1 mutations in females. Journal of Medical Genetics. 47(1). 59–65. 64 indexed citations
11.
Bourdon, Violaine, et al.. (2001). A detailed analysis of the MECP2 gene: prevalence of recurrent mutations and gross DNA rearrangements in Rett syndrome patients. Human Genetics. 108(1). 43–50. 63 indexed citations
12.
Cometta, Alain, et al.. (1996). Empirical treatment of fever in neutropenic children: the role of the carbapenems. The Pediatric Infectious Disease Journal. 15(8). 744–748. 9 indexed citations
13.
Vallat, J.M., et al.. (1995). [Total permanent auricular paralysis. Review of the literature apropos of 109 cases].. PubMed. 44(3). 139–45. 12 indexed citations
14.
15.
Cahn, J, M. Flesch, A. Brion, et al.. (1992). Prevention of veno-occlusive disease of the liver after bone marrow transplantation: heparin or no heparin? [letter; comment]. Blood. 80(8). 2149–2150. 14 indexed citations
16.
Plouvier, Emmanuel, Daniel Amsallem, E Racadot, et al.. (1992). Transplantation of umbilical cord blood in neuroblastoma.. PubMed. 34(3). 243–6. 7 indexed citations
17.
Amsallem, Daniel, et al.. (1991). [Chronic intestinal pseudo-obstruction syndrome in infants and associated anomalies].. PubMed. 48(2). 119–22. 2 indexed citations
18.
Amsallem, Daniel, et al.. (1990). [Rubinstein-Taybi syndrome in 4 cases].. PubMed. 45(7-8). 471–5. 2 indexed citations
19.
Amsallem, Daniel, et al.. (1990). [Capnocytophaga septicemia during bone marrow transplantation. Apropos of 2 cases].. PubMed. 37(10). 665–7. 1 indexed citations
20.
Burguet, A., et al.. (1988). [Neurologic effects of acyclovir after an allogenic marrow graft].. PubMed. 45(5). 343–5. 2 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.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by Christalena Sofocleous Breakdown of academic impact, for papers by Syed K. Rafi Breakdown of academic impact, for papers by Frédérique Sloan‐Béna Breakdown of academic impact, for papers by Dima El‐Khechen Breakdown of academic impact, for papers by Louise Christie Breakdown of academic impact, for papers by Wout H. Deelen Breakdown of academic impact, for papers by Naghmeh Dorrani Breakdown of academic impact, for papers by Anne Chun‐Hui Tsai Breakdown of academic impact, for papers by M. A. Mori Breakdown of academic impact, for papers by Claudia Ciaccio
Rankless by CCL
2026