Eugenio Sangiorgi

4.2k citations

28 papers · 2.9k indexed · 3 hit papers · h-index 15

Oncology top 2%
- Cancer Cells and Metastasis 3
Developmental Biology top 5%
- Congenital limb and hand anomalies 4
Genetics top 2%
- Genomic variations and chromosomal abnormalities 4
Molecular Biology top 5%
- Congenital heart defects research 4
- Epigenetics and DNA Methylation 4
- Inflammasome and immune disorders 3
Cancer Research top 10%
Pulmonary and Respiratory Medicine
- Kidney Stones and Urolithiasis Treatments 2
Pathology and Forensic Medicine
- Autoimmune Bullous Skin Diseases 2

Co-authors: Mario R. Capecchi Akifumi Ootani Calvin J. Kuo Xingnan Li Shuji Toda Hajime Sugihara Irving L. Weissman Hiroo Ueno
Cited by: Oncology Developmental Biology Genetics
Partner nations: Italy United States Switzerland

In The Last Decade

Eugenio Sangiorgi

27 papers receiving 2.8k citations

Hit Papers

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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.

2011 The intestinal stem cell markers Bmi1 and Lgr5 identify two functionally distinct populations
2009 Sustained in vitro intestinal epithelial culture within a Wnt-dependent stem cell niche
2008 Bmi1 is expressed in vivo in intestinal stem cells

Peers

Countries citing papers authored by Eugenio Sangiorgi

Since Specialization

Citations

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

Fields of papers citing papers by Eugenio Sangiorgi

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network

The 25 scholars most cited alongside Eugenio Sangiorgi, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Eugenio Sangiorgi Line = papers co-authored together Eugenio Sangiorgi links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	Base-Excision Repair Mutational Signature in Two Sebaceous Carcinomas of the Eyelid Eugenio Sangiorgi,Federico Giannuzzi,Clelia Molinario,Giulia Rapari,Melania Riccio,Giovanni Cuffaro,Federica Castri,Roberta Benvenuto,Maurizio Genuardi,Daniela Massi,Gustavo Savino	2023	2
2	Identification by Exome Sequencing of Predisposing Variants in Familial Cases of Autoinflammatory Recurrent Fevers Eugenio Sangiorgi,Alessia Azzarà,Roberto Rumore,Ilaria Cassano,Elena Verrecchia,Luciano Giacò,Maria Alessandra Tullio,Fiorella Gurrieri,Raffaele Manna	2023	0
3	Results of a Gene Panel Approach in a Cohort of Patients with Incomplete Distal Renal Tubular Acidosis and Nephrolithiasis Viola D’Ambrosio,Alessia Azzarà,Eugenio Sangiorgi,Fiorella Gurrieri,Bernhard Hess,Giovanni Gambaro,Pietro Manuel Ferraro	2021	10
4	Identification of new candidate genes for spina bifida through exome sequencing Alessia Azzarà,Claudia Rendeli,Anna Maria Crivello,Fulvia Brugnoletti,Roberto Rumore,E. Ausili,Eugenio Sangiorgi,Fiorella Gurrieri	2021	10
5	Rare missense variants in the ALPK1 gene may predispose to periodic fever, aphthous stomatitis, pharyngitis and adenitis (PFAPA) syndrome Eugenio Sangiorgi,Alessia Azzarà,Clelia Molinario,Roberta Pietrobono,Donato Rigante,Elena Verrecchia,Ludovico Luca Sicignano,Maurizio Genuardi,Fiorella Gurrieri,Raffaele Manna	2019	23
6	In Silico Design of E3 Ubiquitin-Protein Ligase NEDD4-1 Inhibitors: An Alternative Approach for Targeting the MAPK Pathway in Cancer Therapy Davide Pirolli,Benedetta Righino,Beatrice Tropea,Fiorella Gurrieri,Eugenio Sangiorgi,Maria Cristina De Rosa	2019	1
7	Defective activation of the MAPK/ERK pathway, leading to PARP1 and DNMT1 dysregulation, is a common defect in IgA nephropathy and Henoch-Schönlein purpura Annamaria Milillo,Clelia Molinario,Stefano Costanzi,Gisella Vischini,Francesca La Carpia,Francesco La Greca,Donato Rigante,Giovanni Gambaro,Fiorella Gurrieri,Eugenio Sangiorgi	2018	8
8	Phenotypic effects of chronic and acute use of methiopropamine in a mouse model Federica Foti,Matteo Marti,Andrea Ossato,Sabrine Bilel,Eugenio Sangiorgi,Francesco Botrè,Bruna Cerbelli,Alfonso Baldi,Fabio De‐Giorgio	2018	16
9	Variants in TNIP1, a regulator of the NF-kB pathway, found in two patients with neural tube defects Francesca La Carpia,Claudia Rendeli,Clelia Molinario,Annamaria Milillo,Chiara Farroni,Natalia Cannelli,E. Ausili,V. Paolucci,Giovanni Neri,Costantino Romagnoli,Eugenio Sangiorgi,Fiorella Gurrieri	2016	3
10	A SPRY2 mutation leading to MAPK/ERK pathway inhibition is associated with an autosomal dominant form of IgA nephropathy Annamaria Milillo,Francesca La Carpia,Stefano Costanzi,Vanessa D’Urbano,Maurizio Martini,Paola Lanuti,Gisella Vischini,Luigi Maria Larocca,Marco Marchisio,Sebastianó Miscia,Antonio Amoroso,Fiorella Gurrieri,Eugenio Sangiorgi	2015	13
11	BMI1 represses Ink4a/Arf and Hox genes to regulate stem cells in the rodent incisor Brian Biehs,Jimmy K. Hu,Nicolas Strauli,Eugenio Sangiorgi,Heekyung Jung,Ralf-Peter Heber,Sunita P. Ho,Alice F. Goodwin,Jeremy S. Dasen,Mario R. Capecchi,Ophir D. Klein	2013	119
12	The intestinal stem cell markers Bmi1 and Lgr5 identify two functionally distinct populationsbreakdown → Kelley S. Yan,Luis A. Chia,Xingnan Li,Akifumi Ootani,James Su,Josephine Y. Lee,Nan Su,Yuling Luo,Sarah C. Heilshorn,Manuel R. Amieva,Eugenio Sangiorgi,Mario R. Capecchi,Calvin J. Kuo	2011	634
13	Morphology and Immunophenotyping of a Monolateral Ovotestis in a 46,XderY/45,X Mosaic Individual With Ambiguous Genitalia Gian Franco Zannoni,Valerio Gaetano Vellone,Emanuela Lucci‐Cordisco,Eugenio Sangiorgi,Maria Eufemia Grimaldi,Caterina Neri,Lorenzo Nanni,Giovanni Neri	2009	2
14	Sustained in vitro intestinal epithelial culture within a Wnt-dependent stem cell nichebreakdown → Akifumi Ootani,Xingnan Li,Eugenio Sangiorgi,Quoc T. Ho,Hiroo Ueno,Shuji Toda,Hajime Sugihara,Kazuma Fujimoto,Irving L. Weissman,Mario R. Capecchi,Calvin J. Kuo	2009	684
15	In vivo evaluation of PhiC31 recombinase activity using a self-excision cassette Eugenio Sangiorgi,Zhang Shu-hua,Mario R. Capecchi	2008	20
16	A New Susceptibility Locus for Migraine with Aura in the 15q11-q13 Genomic Region Containing Three GABA-A Receptor Genes Luisa Russo,Paolo Mariotti,Eugenio Sangiorgi,Tiziana Giordano,Iolanda Ricci,Francesca R. Lupi,Rossella Chiera,Andrea Guzzetta,Giovanni Neri,Fiorella Gurrieri	2005	64
17	Limb anomalies: Developmental and evolutionary aspects Fiorella Gurrieri,Klaus Kjaer,Eugenio Sangiorgi,Giovanni Neri	2002	23
18	Split hand/split foot malformation with hearing loss: first report of families linked to the SHFM1 locus in 7q21 Darci Tackels‐Horne,A. Toburen,Eugenio Sangiorgi,Fiorella Gurrieri,Xavier de Mollerat,Rita Fischetto,F Causio,Katie Clarkson,RE Stevenson,CE Schwartz	2001	36
19	Genomic organization and embryonic expression ofSuppressor of Fused, a candidate gene for the split‐hand/split‐foot malformation type 3 Thomas W. Grimm,Stephan Teglund,Darci Tackels,Eugenio Sangiorgi,Fiorella Gurrieri,Charles E. Schwartz,Rune Toftgård	2001	12
20	A split hand-split foot (SHFM3) gene is located at 10Q24→25 Petros Tsipouras,Fiorella Gurrieri,Panagiotis Prinos,Darci Tackels,Michael W. Kilpatrick,Judith Allanson,Maurizio Genuardi,Ana Vuckov,Luigia Nanni,Eugenio Sangiorgi,Giovanna Garofalo,Mark E. Nuñes,Giovanni Neri,Charles E. Schwartz	1996	46

About Eugenio Sangiorgi

Eugenio Sangiorgi is a scholar working on Developmental Biology, Nephrology and Genetics, having authored 28 papers that have together received 2.9k indexed citations. Recurring topics across this work include Congenital heart defects research (4 papers), Congenital limb and hand anomalies (4 papers), Epigenetics and DNA Methylation (4 papers), Genomic variations and chromosomal abnormalities (4 papers), Cancer Cells and Metastasis (3 papers), Inflammasome and immune disorders (3 papers), Kidney Stones and Urolithiasis Treatments (2 papers) and Autoimmune Bullous Skin Diseases (2 papers). The work is most often cited by research in Oncology (1.5k citations), Developmental Biology (63 citations) and Genetics (807 citations). Eugenio Sangiorgi has collaborated with scholars based in Italy, United States and Switzerland. Frequent co-authors include Mario R. Capecchi, Akifumi Ootani, Calvin J. Kuo, Xingnan Li, Shuji Toda, Hajime Sugihara, Irving L. Weissman, Hiroo Ueno, Kazuma Fujimoto and Nan Su.

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