Jacopo Celli

4.0k total citations · 3 hit papers
16 papers, 2.5k citations indexed

About

Jacopo Celli is a scholar working on Molecular Biology, Genetics and Surgery. According to data from OpenAlex, Jacopo Celli has authored 16 papers receiving a total of 2.5k indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Molecular Biology, 8 papers in Genetics and 6 papers in Surgery. Recurrent topics in Jacopo Celli's work include Esophageal and GI Pathology (4 papers), Genomics and Rare Diseases (3 papers) and Hedgehog Signaling Pathway Studies (3 papers). Jacopo Celli is often cited by papers focused on Esophageal and GI Pathology (4 papers), Genomics and Rare Diseases (3 papers) and Hedgehog Signaling Pathway Studies (3 papers). Jacopo Celli collaborates with scholars based in Netherlands, United Kingdom and United States. Jacopo Celli's co-authors include Johan T. den Dunnen, Peter E.M. Taschner, Jeroen F. J. Laros, Gerard C. P. Schaafsma, Ivo F.A.C. Fokkema, Hans van Bokhoven, Han G. Brunner, Ellen van Beusekom, Hülya Kayserili and Ruth Newbury‐Ecob and has published in prestigious journals such as Cell, Nature Genetics and The American Journal of Human Genetics.

In The Last Decade

Jacopo Celli

16 papers receiving 2.4k citations

Hit Papers

LOVD v.2.0: the next generation in gene variant ... 1999 2026 2008 2017 2011 1999 2002 200 400 600
What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

  1. LOVD v.2.0: the next generation in gene variant databases
    2011 694 citations Ivo F.A.C. Fokkema, Peter E.M. Taschner et al. Human Mutation profile →
  2. Heterozygous Germline Mutations in the p53 Homolog p63 Are the Cause of EEC Syndrome
    1999 536 citations Jacopo Celli, Pascal H. G. Duijf et al. Cell profile →
  3. Mutations in the O-Mannosyltransferase Gene POMT1 Give Rise to the Severe Neuronal Migration Disorder Walker-Warburg Syndrome
    2002 519 citations Sophie Currier, Alice Steinbrecher et al. The American Journal of Human Genetics profile →

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Jacopo Celli Netherlands 13 1.6k 816 408 375 247 16 2.5k
Mary Shago Canada 21 1.4k 0.9× 613 0.8× 397 1.0× 250 0.7× 183 0.7× 57 2.3k
Tetsuya Niihori Japan 27 1.8k 1.2× 495 0.6× 420 1.0× 189 0.5× 139 0.6× 78 2.9k
Gwenaëlle Collod‐Béroud France 21 1.7k 1.1× 1.6k 2.0× 274 0.7× 317 0.8× 452 1.8× 38 3.6k
Daniel C. Chung United States 24 2.5k 1.6× 805 1.0× 351 0.9× 244 0.7× 417 1.7× 73 3.4k
Ludwine Messiaen United States 39 2.2k 1.4× 932 1.1× 491 1.2× 375 1.0× 397 1.6× 145 5.0k
Ann Kuo United States 13 2.9k 1.8× 705 0.9× 397 1.0× 185 0.5× 357 1.4× 14 3.4k
Douglas J. Wilkin United States 22 1.4k 0.9× 1.1k 1.4× 265 0.6× 260 0.7× 210 0.9× 29 2.7k
Michelina Iacovino United States 28 2.4k 1.5× 398 0.5× 228 0.6× 382 1.0× 311 1.3× 57 3.1k
Anita Morén Sweden 25 2.6k 1.7× 421 0.5× 716 1.8× 232 0.6× 450 1.8× 33 3.3k
Ivan B. Lobov United States 13 2.3k 1.5× 314 0.4× 435 1.1× 190 0.5× 362 1.5× 25 3.0k

Countries citing papers authored by Jacopo Celli

Since Specialization
Citations

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

Fields of papers citing papers by Jacopo Celli

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Jacopo Celli

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

All Works

16 of 16 papers shown
1.
Monti, Matilde, Jacopo Celli, Francesco Missale, et al.. (2022). Clinical Significance and Regulation of ERK5 Expression and Function in Cancer. Cancers. 14(2). 348–348. 20 indexed citations
2.
Celli, Jacopo, Gudrun Rappold, & Beate Niesler. (2016). The Human Serotonin Type 3 Receptor Gene (HTR3A-E) Allelic Variant Database. Human Mutation. 38(2). 137–147. 14 indexed citations
3.
Celli, Jacopo. (2014). Genetics of gastrointestinal atresias. European Journal of Medical Genetics. 57(8). 424–439. 10 indexed citations
4.
Leigh, S. E. A., Ros Whittall, Nicholas Lench, et al.. (2012). Low‐Density Lipoprotein Receptor Gene Familial Hypercholesterolemia Variant Database: Update and Pathological Assessment. Annals of Human Genetics. 76(5). 387–401. 152 indexed citations
5.
Fokkema, Ivo F.A.C., Peter E.M. Taschner, Gerard C. P. Schaafsma, et al.. (2011). LOVD v.2.0: the next generation in gene variant databases. Human Mutation. 32(5). 557–563. 694 indexed citations breakdown →
6.
Lombardi, Maria, Saskia Bulk, Jacopo Celli, et al.. (2011). Mutation update for the PORCN gene. Human Mutation. 32(7). 723–728. 44 indexed citations
7.
Celli, Jacopo, Raymond Dalgleish, Mauno Vihinen, Peter E.M. Taschner, & Johan T. den Dunnen. (2011). Curating gene variant databases (LSDBs): Toward a universal standard. Human Mutation. 33(2). 291–297. 35 indexed citations
8.
Sun, Yu, Rowida Almomani, Emmelien Aten, et al.. (2010). Terminal Osseous Dysplasia Is Caused by a Single Recurrent Mutation in the FLNA Gene. The American Journal of Human Genetics. 87(1). 146–153. 45 indexed citations
9.
Bokhoven, Hans van, Jacopo Celli, Jeroen van Reeuwijk, et al.. (2005). MYCN haploinsufficiency is associated with reduced brain size and intestinal atresias in Feingold syndrome. Nature Genetics. 37(5). 465–467. 110 indexed citations
10.
Celli, Jacopo, Hans van Bokhoven, & Han G. Brunner. (2003). Feingold syndrome: Clinical review and genetic mapping. American Journal of Medical Genetics Part A. 122A(4). 294–300. 57 indexed citations
11.
Currier, Sophie, Alice Steinbrecher, Jacopo Celli, et al.. (2002). Mutations in the O-Mannosyltransferase Gene POMT1 Give Rise to the Severe Neuronal Migration Disorder Walker-Warburg Syndrome. The American Journal of Human Genetics. 71(5). 1033–1043. 519 indexed citations breakdown →
12.
Bokhoven, Hans van, John A. McGrath, Jacopo Celli, et al.. (2000). P63 mutations in the EEC, Hay-Wells, ADULT syndromes and in split hand/foot malformation reveals a genotype-phenotype correlation.. The American Journal of Human Genetics. 67(4). 41–41. 6 indexed citations
13.
Bokhoven, Hans van, Jacopo Celli, Hülya Kayserili, et al.. (2000). Mutation of the gene encoding the ROR2 tyrosine kinase causes autosomal recessive Robinow syndrome. Nature Genetics. 25(4). 423–426. 195 indexed citations
14.
Celli, Jacopo, Ellen van Beusekom, Raoul C. M. Hennekam, et al.. (2000). Familial Syndromic Esophageal Atresia Maps to 2p23-p24. The American Journal of Human Genetics. 66(2). 436–444. 25 indexed citations
15.
Steensel, Maurice A. M. Van, et al.. (1999). Probing the Gene eXpression Database for candidate genes. European Journal of Human Genetics. 7(8). 910–919. 12 indexed citations
16.
Celli, Jacopo, Pascal H. G. Duijf, Ben C.J. Hamel, et al.. (1999). Heterozygous Germline Mutations in the p53 Homolog p63 Are the Cause of EEC Syndrome. Cell. 99(2). 143–153. 536 indexed citations breakdown →

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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