Elisabetta Flex

4.1k citations

39 papers · 1.3k · h-index 21

Impact in

Immunology top 10%
- Galectins and Cancer Biology
Molecular Biology top 10%
- Protein Tyrosine Phosphatases
- RNA modifications and cancer
- Congenital heart defects research

Papers in

Molecular Biology 27
- Protein Tyrosine Phosphatases 14
- RNA modifications and cancer 10
- Ubiquitin and proteasome pathways 3
Genetics 8
- Myeloproliferative Neoplasms: Diagnosis and Treatment 3

Co-authors: Marco Tartaglia (25 shared papers)Bruno Dallapiccola (12 shared papers)Antonio Pizzuti (5 shared papers)Simone Martinelli (8 shared papers)Gianfranco Bocchinfuso (6 shared papers)Lorenzo Stella (5 shared papers)Antonio Palleschi (4 shared papers)Giuseppe Zampino (8 shared papers)
Journals: Human Mutation (6 papers)Journal of Biological Chemistry (3 papers)European Journal of Medical Genetics (2 papers)Human Molecular Genetics (2 papers)Clinical Genetics (2 papers)
Partner nations: Italy United States Belgium

In The Last Decade

Elisabetta Flex

39 papers receiving 1.3k citations

Peers

Countries citing papers authored by Elisabetta Flex

Since Specialization

Citations

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

Fields of papers citing papers by Elisabetta Flex

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside Elisabetta Flex, 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 Elisabetta Flex Line = papers co-authored together Elisabetta Flex links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

Showing the 20 most-cited of 39 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	Diversity and Functional Consequences of Germline and Somatic PTPN11 Mutations in Human Disease The American Journal of Human Genetics ·Marco Tartaglia, Simone Martinelli, Lorenzo Stella, Gianfranco Bocchinfuso, Elisabetta Flex, Viviana Cordeddu, Giuseppe Zampino, Ineke van der Burgt, Antonio Palleschi, Tamara C. Petrucci, M Sorcini, Claudia Schoch, Robin Foà, Peter D. Emanuel, Bruce D. Gelb	2006	284
2	Mutations ofZFPM2/FOG2 gene in sporadic cases of tetralogy of Fallot Human Mutation ·Antonio Pizzuti, Anna Sárközy, Anthea Newton, Emanuela Conti, Elisabetta Flex, M. Cristina Digilio, Francesca Amati, Debora Gianni, Caterina Tandoi, Bruno Marino, Merlin Crossley, Bruno Dallapiccola	2003	99
3	A Functional Variant of the Adipocyte Glycerol Channel Aquaporin 7 Gene Is Associated With Obesity and Related Metabolic Abnormalities Diabetes ·Sabrina Prudente, Elisabetta Flex, Eleonora Morini, Federica Turchi, Daria Capponi, Salvatore De Cosmo, Vittorio Tassi, Valentina Guida, Angelo Avogaro, Franco Folli, Francesca Maiani, Lucia Frittitta, Bruno Dallapiccola, Vincenzo Trischitta	2007	98
4	The Functional Q84R Polymorphism of Mammalian Tribbles Homolog TRB3 Is Associated With Insulin Resistance and Related Cardiovascular Risk in Caucasians From Italy Diabetes ·Sabrina Prudente, Marta Letizia Hribal, Elisabetta Flex, Federica Turchi, Eleonora Morini, Salvatore De Cosmo, Simonetta Bacci, Vittorio Tassi, Marina Cardellini, Renato Lauro, Giorgio Sesti, Bruno Dallapiccola, Vincenzo Trischitta	2005	89
5	A homozygousGJA1 gene mutation causes a Hallermann-Streiff/ODDD spectrum phenotype Human Mutation ·Antonio Pizzuti, Elisabetta Flex, Rita Mingarelli, Carmelo Salpietro, Leopoldo Zelante, Bruno Dallapiccola	2004	81
6	Diverse driving forces underlie the invariant occurrence of the T42A, E139D, I282V and T468M SHP2 amino acid substitutions causing Noonan and LEOPARD syndromes Human Molecular Genetics ·Simone Martinelli, Paola Torreri, Michele Tinti, Lorenzo Stella, Gianfranco Bocchinfuso, Elisabetta Flex, Alessandro Grottesi, Marina Ceccarini, Antonio Palleschi, Gianni Cesareni, Luisa Castagnoli, Tamara C. Petrucci, Bruce D. Gelb, Marco Tartaglia	2008	63
7	Acute Lymphoblastic Leukemia-associated JAK1 Mutants Activate the Janus Kinase/STAT Pathway via Interleukin-9 Receptor α Homodimers Journal of Biological Chemistry ·Tekla Hornakova, Judith Staerk, Yohan Royer, Elisabetta Flex, Marco Tartaglia, Stefan N. Constantinescu, Laurent Knoops, Jean‐Christophe Renauld	2009	55
8	Epilepsy with auditory features: A LGI1 gene mutation suggests a loss‐of‐function mechanism Annals of Neurology ·Antonio Pizzuti, Elisabetta Flex, Carlo Di Bonaventura, Tania Dottorini, Gabriella Egeo, M. Manfredi, Bruno Dallapiccola, Anna Teresa Giallonardo	2003	43
9	Loss of function of the E3 ubiquitin-protein ligase UBE3B causes Kaufman oculocerebrofacial syndrome Journal of Medical Genetics ·Elisabetta Flex, Andrea Ciolfi, Viviana Caputo, Valentina Fodale, Chiara Leoni, Daniela Melis, Maria Francesca Bedeschi, Laura Mazzanti, Antonio Pizzuti, Marco Tartaglia, Giuseppe Zampino	2013	40
10	Activating PTPN11 mutations play a minor role in pediatric and adult solid tumors Cancer Genetics and Cytogenetics ·Simone Martinelli, Claudio Carta, Elisabetta Flex, Francesco Binni, Emanuela Lucci‐Cordisco, Sonia Moretti, Efisio Puxeddu, Massimo Tonacchera, Aldo Pinchera, Heather P. McDowell, Carlo Dominici, Angelo Rosolen, Concezio Di Rocco, Riccardo Riccardi, Paolo Celli, Mauro Picardo, Maurizio Genuardi, Paola Grammatico, M Sorcini, Marco Tartaglia	2006	38
11	Distinct Acute Lymphoblastic Leukemia (ALL)-associated Janus Kinase 3 (JAK3) Mutants Exhibit Different Cytokine-Receptor Requirements and JAK Inhibitor Specificities Journal of Biological Chemistry ·Elisabeth Losdyck, Tekla Hornakova, Lorraine Springuel, Sandrine Degryse, Olga Gielen, Jan Cools, Stefan N. Constantinescu, Elisabetta Flex, Marco Tartaglia, Jean‐Christophe Renauld, Laurent Knoops	2015	37
12	Cooperating JAK1 and JAK3 mutants increase resistance to JAK inhibitors Blood ·Lorraine Springuel, Tekla Hornakova, Elisabeth Losdyck, Fanny Lambert, Emilie Leroy, Stefan N. Constantinescu, Elisabetta Flex, Marco Tartaglia, Laurent Knoops, Jean‐Christophe Renauld	2014	34
13	Identification of a novel NOG gene mutation (P35S) in an Italian family with symphalangism Human Mutation ·Massimo Mangino, Elisabetta Flex, M. Cristina Digilio, Aldo Giannotti, Bruno Dallapiccola	2002	30
14	Frameshift mutations at the C-terminus of HIST1H1E result in a specific DNA hypomethylation signature Clinical Epigenetics ·Andrea Ciolfi, Erfan Aref‐Eshghi, Simone Pizzi, Lucia Pedace, Evelina Miele, Jennifer Kerkhof, Elisabetta Flex, Simone Martinelli, Francesca Clementina Radio, Claudia Ruivenkamp, Gijs W.E. Santen, Emilia Bijlsma, Daniela Q.C.M. Barge‐Schaapveld, Katrin Õunap, Victoria Mok Siu, R. Frank Kooy, Bruno Dallapiccola, Bekim Sadiković, Marco Tartaglia	2020	29
15	Defective kinesin binding of TUBB2A causes progressive spastic ataxia syndrome resembling sacsinopathy Human Molecular Genetics ·Antonella Sferra, Fabiana Fattori, Teresa Rizza, Elisabetta Flex, Emanuele Bellacchio, Alessandro Bruselles, Stefania Petrini, Serena Cecchetti, Massimo Teson, Fabrizia Restaldi, Andrea Ciolfi, Filippo M. Santorelli, Ginevra Zanni, Sabina Barresi, Claudia Castiglioni, Marco Tartaglia, Enrico Bertini	2018	29
16	Counteracting Effects Operating on Src Homology 2 Domain-containing Protein-tyrosine Phosphatase 2 (SHP2) Function Drive Selection of the Recurrent Y62D and Y63C Substitutions in Noonan Syndrome* Journal of Biological Chemistry ·Simone Martinelli, Aurelio Pio Nardozza, Silvia Delle Vigne, G Sabetta, Paola Torreri, Gianfranco Bocchinfuso, Elisabetta Flex, Serenella Venanzi, Antonio Palleschi, Bruce D. Gelb, Gianni Cesareni, Lorenzo Stella, Luisa Castagnoli, Marco Tartaglia	2012	26
17	DNMT3A and DNMT3B Targeting as an Effective Radiosensitizing Strategy in Embryonal Rhabdomyosarcoma Cells ·Simona Camero, Giulia Vitali, Paola Pontecorvi, Simona Ceccarelli, Eleni Anastasiadou, Francesca Cicchetti, Elisabetta Flex, Silvia Pomella, Matteo Cassandri, Rossella Rota, Francesco Marampon, Cinzia Marchese, Amalia Schiavetti, Francesca Megiorni	2021	22
18	Interaction of DIO2 T92A and PPARγ2 P12A Polymorphisms in the Modulation of Metabolic Syndrome Obesity ·Mirella Fiorito, Isabella Torrente, Salvatore De Cosmo, Valentina Guida, Alessia Colosimo, Sabrina Prudente, Elisabetta Flex, Rossella Menghini, Roberto Miccoli, Giuseppe Penno, Fabio Pellegrini, Vittorio Tassi, Massimo Federici, Vincenzo Trischitta, Bruno Dallapiccola	2007	22
19	Musculo-skeletal phenotype of Costello syndrome and cardio-facio-cutaneous syndrome: insights on the functional assessment status Orphanet Journal of Rare Diseases ·Chiara Leoni, Domenico M. Romeo, Michele Pelliccioni, Mariangela Di Già, Roberta Onesimo, Valentina Giorgio, Elisabetta Flex, Marta Tedesco, Marco Tartaglia, Donato Rigante, Antonio Valassina, Giuseppe Zampino	2021	22
20	Structural and functional effects of disease‐causing amino acid substitutions affecting residues Ala72 and Glu76 of the protein tyrosine phosphatase SHP‐2 Proteins Structure Function and Bioinformatics ·Gianfranco Bocchinfuso, Lorenzo Stella, Simone Martinelli, Elisabetta Flex, Claudio Carta, Francesca Pantaleoni, B. Pispisa, Mariano Venanzi, Marco Tartaglia, Antonio Palleschi	2006	22

About Elisabetta Flex

Elisabetta Flex is a scholar working on Molecular Biology, Genetics, Immunology, Cell Biology and Oncology, having authored 39 papers that have together received 1.3k indexed citations. Recurring topics across this work include Protein Tyrosine Phosphatases (14 papers), RNA modifications and cancer (10 papers), Galectins and Cancer Biology (8 papers), Cellular transport and secretion (5 papers), Ubiquitin and proteasome pathways (3 papers), Myeloproliferative Neoplasms: Diagnosis and Treatment (3 papers), Cytokine Signaling Pathways and Interactions (3 papers) and Microtubule and mitosis dynamics (2 papers). The work is most often cited by research in Immunology (339 citations), Molecular Biology (890 citations), Cell Biology (135 citations), Genetics (78 citations) and Genetics (205 citations). Elisabetta Flex has collaborated with scholars based in Italy, United States and Belgium. Frequent co-authors include Marco Tartaglia, Bruno Dallapiccola, Antonio Pizzuti, Simone Martinelli, Gianfranco Bocchinfuso, Lorenzo Stella, Antonio Palleschi, Giuseppe Zampino, Bruce D. Gelb and Tamara C. Petrucci. Their work appears in journals such as Human Mutation, Journal of Biological Chemistry, European Journal of Medical Genetics, Human Molecular Genetics and Clinical 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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