Jacopo Celli

4.0k citations

16 papers · 2.5k indexed · 3 hit papers · h-index 13

Molecular Biology top 5%
Genetics top 2%
Oncology top 10%
Surgery top 10%
Cancer Research top 10%

Co-authors: 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
Topics: Esophageal and GI Pathology (4 papers)Genomics and Rare Diseases (3 papers)Hedgehog Signaling Pathway Studies (3 papers)
Cited by: Developmental Biology Genetics Molecular Biology
Journals: Cell Nature Genetics The American Journal of Human Genetics
Partner nations: Netherlands United Kingdom United States

In The Last Decade

Jacopo Celli

16 papers receiving 2.4k citations

Hit Papers

align trajectories

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.

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 →
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 →
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

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

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16 of 16 papers shown

#	Work	Indexed citations
1	Clinical Significance and Regulation of ERK5 Expression and Function in Cancer 2022 ·Cancers ·Matilde Monti,Jacopo Celli,Francesco Missale,(unknown),(unknown),Elisa Belloni,Anna Di Matteo,Silvia Lonardi,William Vermi,Claudia Ghigna,Emanuele Giurisato	20
2	The Human Serotonin Type 3 Receptor Gene (HTR3A-E) Allelic Variant Database 2016 ·Human Mutation ·Jacopo Celli,Gudrun Rappold,Beate Niesler	14
3	Genetics of gastrointestinal atresias 2014 ·European Journal of Medical Genetics ·Jacopo Celli	10
4	Low‐Density Lipoprotein Receptor Gene Familial Hypercholesterolemia Variant Database: Update and Pathological Assessment 2012 ·Annals of Human Genetics ·(unknown),S. E. A. Leigh,Ros Whittall,Nicholas Lench,Alison Taylor,Corin Yeats,Christine Orengo,Andrew C.R. Martin,Jacopo Celli,Steve E. Humphries	152
5	LOVD v.2.0: the next generation in gene variant databasesbreakdown → 2011 ·Human Mutation ·Ivo F.A.C. Fokkema,Peter E.M. Taschner,Gerard C. P. Schaafsma,Jacopo Celli,Jeroen F. J. Laros,Johan T. den Dunnen	694
6	Mutation update for the PORCN gene 2011 ·Human Mutation ·Maria Lombardi,Saskia Bulk,Jacopo Celli,(unknown),Michael T. Gabbett,Lilian Bomme Ousager,(unknown),Maria Soller,Eva‐Lena Stattin,(unknown),Robert Śmigiel,(unknown)	44
7	Curating gene variant databases (LSDBs): Toward a universal standard 2011 ·Human Mutation ·Jacopo Celli,Raymond Dalgleish,Mauno Vihinen,Peter E.M. Taschner,Johan T. den Dunnen	35
8	Terminal Osseous Dysplasia Is Caused by a Single Recurrent Mutation in the FLNA Gene 2010 ·The American Journal of Human Genetics ·Yu Sun,Rowida Almomani,Emmelien Aten,Jacopo Celli,(unknown),Hanka Venselaar,Stephen P. Robertson,Anna Baroncini,Brunella Franco,Lina Basel‐Vanagaite,Emiko Horii,Ricardo Drut,Yavuz Ariyürek,Johan T. den Dunnen,Martijn H. Breuning	45
9	MYCN haploinsufficiency is associated with reduced brain size and intestinal atresias in Feingold syndrome 2005 ·Nature Genetics ·Hans van Bokhoven,Jacopo Celli,Jeroen van Reeuwijk,Tuula Rinne,Bob Glaudemans,Ellen van Beusekom,Paul N.M.A. Rieu,Ruth Newbury‐Ecob,Chin Chiang,Han G. Brunner	110
10	Feingold syndrome: Clinical review and genetic mapping 2003 ·American Journal of Medical Genetics Part A ·Jacopo Celli,Hans van Bokhoven,Han G. Brunner	57
11	Mutations in the O-Mannosyltransferase Gene POMT1 Give Rise to the Severe Neuronal Migration Disorder Walker-Warburg Syndromebreakdown → 2002 ·The American Journal of Human Genetics ·(unknown),Sophie Currier,Alice Steinbrecher,Jacopo Celli,Ellen van Beusekom,Bert van der Zwaag,Hülya Kayserili,Luciano Merlini,David Chitayat,William B. Dobyns,Bru Cormand,(unknown),Jesús Cruces,Thomas Voït,Christopher A. Walsh,Hans van Bokhoven,Han G. Brunner	519
12	P63 mutations in the EEC, Hay-Wells, ADULT syndromes and in split hand/foot malformation reveals a genotype-phenotype correlation. 2000 ·The American Journal of Human Genetics ·Hans van Bokhoven,John A. McGrath,(unknown),Jacopo Celli,Ben C.J. Hamel,Rob de Waal,Amy Yang,Frank McKeon,Volker Doetsch,Kaate R. J. Vanmolkot,Peter Propping,Fiorella Gurrieri,Giovanni Neri,(unknown),HG Brunner	6
13	Mutation of the gene encoding the ROR2 tyrosine kinase causes autosomal recessive Robinow syndrome 2000 ·Nature Genetics ·Hans van Bokhoven,Jacopo Celli,Hülya Kayserili,Ellen van Beusekom,Sevim Balcı,Wim Brussel,F Skovby,(unknown),E. Ferda Perçin,Nurten Akarsu,Han G. Brunner	195
14	Familial Syndromic Esophageal Atresia Maps to 2p23-p24 2000 ·The American Journal of Human Genetics ·Jacopo Celli,Ellen van Beusekom,Raoul C. M. Hennekam,M. Esther Gallardo,(unknown),Santiago Rodrı́guez de Córdoba,Jeffrey W. Innis,(unknown),Rainer König,Helen Kingston,John Tolmie,(unknown),Hans van Bokhoven,Han G. Brunner	25
15	Probing the Gene eXpression Database for candidate genes 1999 ·European Journal of Human Genetics ·Maurice A. M. Van Steensel,Jacopo Celli,(unknown),HG Brunner	12
16	Heterozygous Germline Mutations in the p53 Homolog p63 Are the Cause of EEC Syndromebreakdown → 1999 ·Cell ·Jacopo Celli,Pascal H. G. Duijf,Ben C.J. Hamel,Michael J. Bamshad,Bridget Kramer,(unknown),Ruth Newbury‐Ecob,Raoul C. M. Hennekam,Griet Van Buggenhout,Arie van Haeringen,C. Geoffrey Woods,Anthonie J. van Essen,Rob de Waal,Gert Vriend,Daniel A. Haber,Annie Yang,Frank McKeon,Han G. Brunner,Hans van Bokhoven	536

About Jacopo Celli

Jacopo Celli is a scholar working on Genetics, Gastroenterology and Molecular Biology, having authored 16 papers that have together received 2.5k indexed citations. Recurring topics across this work include Esophageal and GI Pathology (4 papers), Genomics and Rare Diseases (3 papers) and Hedgehog Signaling Pathway Studies (3 papers). The work is most often cited by research in Developmental Biology (74 citations), Genetics (816 citations) and Molecular Biology (1.6k citations). Jacopo Celli has collaborated with scholars based in Netherlands, United Kingdom and United States. Frequent 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. Their work appears in journals such as Cell, Nature Genetics and The American Journal of Human Genetics.

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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