Marco Tartaglia

26.7k total citations · 4 hit papers
322 papers, 10.8k citations indexed

About

Marco Tartaglia is a scholar working on Molecular Biology, Immunology and Genetics. According to data from OpenAlex, Marco Tartaglia has authored 322 papers receiving a total of 10.8k indexed citations (citations by other indexed papers that have themselves been cited), including 234 papers in Molecular Biology, 93 papers in Immunology and 89 papers in Genetics. Recurrent topics in Marco Tartaglia's work include Protein Tyrosine Phosphatases (127 papers), Galectins and Cancer Biology (79 papers) and RNA modifications and cancer (45 papers). Marco Tartaglia is often cited by papers focused on Protein Tyrosine Phosphatases (127 papers), Galectins and Cancer Biology (79 papers) and RNA modifications and cancer (45 papers). Marco Tartaglia collaborates with scholars based in Italy, United States and Germany. Marco Tartaglia's co-authors include Bruce D. Gelb, Giuseppe Zampino, Amy E. Roberts, Michael A. Patton, Andrew H. Crosby, Steve Jeffery, Kamini Kalidas, Han G. Brunner, Judith Allanson and Alessandra Fragale and has published in prestigious journals such as The Lancet, Journal of Biological Chemistry and Journal of Clinical Investigation.

In The Last Decade

Marco Tartaglia

311 papers receiving 10.7k 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.

Mutations in PTPN11, encoding the protein tyrosine phosphatase SHP-2, cause Noonan syndrome

2001 1.2k citations Marco Tartaglia, Giuseppe Zampino et al. profile →
Somatic mutations in PTPN11 in juvenile myelomonocytic leukemia, myelodysplastic syndromes and acute myeloid leukemia

2003 723 citations Marco Tartaglia, Charlotte M. Niemeyer et al. profile →
PTPN11 Mutations in Noonan Syndrome: Molecular Spectrum, Genotype-Phenotype Correlation, and Phenotypic Heterogeneity

2002 522 citations Marco Tartaglia et al. profile →
Noonan syndrome

2013 498 citations Marco Tartaglia et al. profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Marco Tartaglia Italy	49	8.5k	4.0k	1.9k	1.8k	647	322	10.8k
Han‐Woong Lee South Korea	37	6.5k 0.8×	2.1k 0.5×	2.9k 1.5×	887 0.5×	518 0.8×	112	11.5k
Carol B. Ware United States	41	6.1k 0.7×	1.8k 0.5×	1.0k 0.5×	994 0.5×	538 0.8×	73	9.6k
Kay‐Uwe Wagner United States	55	5.5k 0.6×	1.5k 0.4×	5.1k 2.6×	1.9k 1.0×	655 1.0×	161	10.8k
Akiko Hata United States	51	9.9k 1.2×	1.2k 0.3×	1.8k 1.0×	840 0.5×	583 0.9×	109	13.2k
Tarik Möröy Germany	54	4.6k 0.5×	2.5k 0.6×	2.2k 1.1×	1.6k 0.9×	552 0.9×	166	8.7k
Vittorio Sartorelli United States	55	9.9k 1.2×	1.1k 0.3×	1.6k 0.8×	1.3k 0.7×	496 0.8×	102	12.5k
Minetaro Ogawa Japan	52	6.5k 0.8×	3.1k 0.8×	2.1k 1.1×	860 0.5×	887 1.4×	155	11.5k
Denise Sheer United Kingdom	51	6.0k 0.7×	1.4k 0.3×	2.1k 1.1×	1.9k 1.1×	701 1.1×	178	10.9k
Katia Manova United States	47	7.4k 0.9×	1000 0.2×	1.9k 1.0×	1.7k 1.0×	636 1.0×	79	10.7k
Rami I. Aqeilan United States	48	8.4k 1.0×	1.1k 0.3×	1.5k 0.8×	2.5k 1.4×	753 1.2×	121	11.2k

Countries citing papers authored by Marco Tartaglia

Since Specialization

Citations

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

Fields of papers citing papers by Marco Tartaglia

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Marco Tartaglia

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

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

Onesimo, Roberta, Valentina Giorgio, Donato Rigante, et al.. (2023). Predicting the clinical trajectory of feeding and swallowing abilities in CHARGE syndrome. European Journal of Pediatrics. 182(4). 1869–1877. 5 indexed citations

Onesimo, Roberta, Valentina Trevisan, Chiara Leoni, et al.. (2023). From Feeding Challenges to Oral-Motor Dyspraxia: A Comprehensive Description of 10 New Cases with CTNNB1 Syndrome. Genes. 14(10). 1843–1843. 6 indexed citations

Compagnucci, Claudia, et al.. (2022). Teleost Fish and Organoids: Alternative Windows Into the Development of Healthy and Diseased Brains. Frontiers in Molecular Neuroscience. 15. 855786–855786.

Liu, Yingzi, Christian F. Guerrero‐Juarez, Fei Xiao, et al.. (2022). Hedgehog signaling reprograms hair follicle niche fibroblasts to a hyper-activated state. Developmental Cell. 57(14). 1758–1775.e7. 49 indexed citations

Leoni, Chiara, Francesca Clementina Radio, Giovanni Chillemi, et al.. (2021). Broadening the phenotypic spectrum of Beta3GalT6 ‐associated phenotypes. American Journal of Medical Genetics Part A. 185(10). 3153–3160. 4 indexed citations

Alfieri, Paolo, Maria Lisa Dentici, M. Cristina Digilio, et al.. (2021). Cognitive and Adaptive Characterization of Children and Adolescents with KBG Syndrome: An Explorative Study. Journal of Clinical Medicine. 10(7). 1523–1523. 2 indexed citations

Anselmi, Massimiliano, Paolo Calligari, Jochen S. Hub, et al.. (2020). Structural Determinants of Phosphopeptide Binding to the N-Terminal Src Homology 2 Domain of the SHP2 Phosphatase. Journal of Chemical Information and Modeling. 60(6). 3157–3171. 17 indexed citations

Lorca, Rebeca, Luca Pannone, Elías Cuesta‐Llavona, et al.. (2020). Compound heterozygosity for PTPN11 variants in a subject with Noonan syndrome provides insights into the mechanism of SHP2 ‐related disorders. Clinical Genetics. 99(3). 457–461. 3 indexed citations

Martinelli, Simone, Luca Pannone, Christina Lißewski, et al.. (2020). Pathogenic PTPN11 variants involving the poly‐glutamine Gln ²⁵⁵ ‐Gln ²⁵⁶ ‐Gln ²⁵⁷ stretch highlight the relevance of helix B in SHP2's functional regulation. Human Mutation. 41(6). 1171–1182. 1 indexed citations

10.

Alfieri, Paolo, Lorenzo Sinibaldi, Giovanni Valeri, et al.. (2020). Further insight into the neurobehavioral pattern of children carrying the 2p16.3 heterozygous deletion involving NRXN1: Report of five new cases. Genes Brain & Behavior. 19(7). e12687–e12687. 5 indexed citations

11.

Niceta, Marcello, Domenico Barbuti, Neerja Gupta, et al.. (2019). Skeletal abnormalities are common features in Aymé‐Gripp syndrome. Clinical Genetics. 97(2). 362–369. 10 indexed citations

12.

Dentici, Maria Lisa, Sabina Barresi, Marcello Niceta, et al.. (2019). Expanding the clinical spectrum associated with PACS2 mutations. Clinical Genetics. 95(4). 525–531. 17 indexed citations

13.

Servidei, Tiziana, Daniela Meco, Valentina Muto, et al.. (2017). Novel SEC61G – EGFR Fusion Gene in Pediatric Ependymomas Discovered by Clonal Expansion of Stem Cells in Absence of Exogenous Mitogens. Cancer Research. 77(21). 5860–5872. 20 indexed citations

14.

Hornakova, Tekla, Sandrine Degryse, Olga Gielen, et al.. (2015). Distinct Acute Lymphoblastic Leukemia (ALL)-associated Janus Kinase 3 (JAK3) Mutants Exhibit Different Cytokine-Receptor Requirements and JAK Inhibitor Specificities. Journal of Biological Chemistry. 290(48). 29022–29034. 37 indexed citations

15.

Alfieri, Paolo, Giorgia Piccini, Maria Luigia Gambardella, et al.. (2014). Behavioral Profile in RASopathies. American Journal of Medical Genetics Part A. 164(4). 934–942. 64 indexed citations

16.

Motta, Marialetizia, Massimo Tatti, Simone Martinelli, et al.. (2011). Efficient one-step chromatographic purification and functional characterization of recombinant human Saposin C. Protein Expression and Purification. 78(2). 209–215. 1 indexed citations

17.

Maccalli, Cristina, Veronica Di Cristanziano, Valentina Fodale, et al.. (2008). Induction of Both CD8+ and CD4+ T-Cell–Mediated Responses in Colorectal Cancer Patients by Colon Antigen-1. Clinical Cancer Research. 14(22). 7292–7303. 8 indexed citations

18.

Sárközy, Anna, et al.. (2006). Noonan's syndrome and related disorders: Clinical-molecular update and guidelines. The Italian Journal of Pediatrics/Italian journal of pediatrics. 32(3). 145–155. 3 indexed citations

19.

Loh, Mignon L., Simone Martinelli, Viviana Cordeddu, et al.. (2004). Acquired PTPN11 mutations occur rarely in adult patients with myelodysplastic syndromes and chronic myelomonocytic leukemia. Leukemia Research. 29(4). 459–462. 49 indexed citations

20.

Tartaglia, Marco, Alessandra Fragale, & Piero A. Battaglia. (2001). A Competitive PCR-Based Method to Measure Human Fibroblast Growth Factor Receptor 1–4 (FGFR1–4) Gene Expression. DNA and Cell Biology. 20(6). 367–379. 14 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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