Catia Andreassi

2.3k citations

23 papers · 1.8k indexed · 1 hit paper · h-index 15

Impact in

Genetics top 1%
- Neurogenetic and Muscular Disorders Research
Molecular Biology top 5%
- RNA modifications and cancer
- RNA Research and Splicing
- RNA and protein synthesis mechanisms
- Cancer-related gene regulation
- Muscle Physiology and Disorders
- RNA regulation and disease

Papers in ⓘ

Genetics 9
- Neurogenetic and Muscular Disorders Research 9
Molecular Biology 18
- RNA modifications and cancer 12
- RNA Research and Splicing 9
- RNA regulation and disease 2
- RNA and protein synthesis mechanisms 2

Co-authors: Sibylle Jablonka (5 shared papers)Michael Sendtner (5 shared papers)Umrao R. Monani (3 shared papers)Kathrin N. Karle (2 shared papers)Wilfried Rossoll (3 shared papers)Adolfo Saiardi (3 shared papers)Christina Brahe (4 shared papers)Serena De Vita (1 shared paper)
Journals: Human Molecular Genetics (3 papers)The Journal of Cell Biology (2 papers)Current Biology (1 paper)European Journal of Human Genetics (1 paper)Cell Reports (1 paper)
Partner nations: United Kingdom Italy United States

In The Last Decade

Catia Andreassi

22 papers receiving 1.8k citations

Hit Papers

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Smn, the spinal muscular atrophy–determining gene product, modulates axon growth and localization of β-actin mRNA in growth cones of motoneurons 2003 · 523 citations

Peers

Countries citing papers authored by Catia Andreassi

Since Specialization

Citations

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

Fields of papers citing papers by Catia Andreassi

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside Catia Andreassi, 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 Catia Andreassi Line = papers co-authored together Catia Andreassi 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 23 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	Smn, the spinal muscular atrophy–determining gene product, modulates axon growth and localization of β-actin mRNA in growth cones of motoneurons The Journal of Cell Biology ·Wilfried Rossoll, Sibylle Jablonka, Catia Andreassi, Ann-Kathrin Kröning, Kathrin N. Karle, Umrao R. Monani, Michael Sendtner Hit paper breakdown →	2003	523
2	To localize or not to localize: mRNA fate is in 3′UTR ends Trends in Cell Biology ·Catia Andreassi, (unknown)	2009	263
3	Phenylbutyrate increases SMN expression in vitro: relevance for treatment of spinal muscular atrophy European Journal of Human Genetics ·Catia Andreassi, Carla Angelozzi, Francesco Danilo Tiziano, Tiziana Vitali, Eleonora De Vincenzi, Alma Boninsegna, Marcello Villanova, Enrico Bertini, Antonella Pini, Giovanni Neri, Christina Brahe	2003	203
4	Aclarubicin treatment restores SMN levels to cells derived from type I spinal muscular atrophy patients Human Molecular Genetics ·Catia Andreassi	2001	183
5	An NGF-responsive element targets myo-inositol monophosphatase-1 mRNA to sympathetic neuron axons Nature Neuroscience ·Catia Andreassi, Carola Zimmermann, Richard Mitter, Salvatore Fusco, Serena De Vita, Adolfo Saiardi, (unknown)	2010	149
6	A transgene carrying an A2G missense mutation in the SMN gene modulates phenotypic severity in mice with severe (type I) spinal muscular atrophy The Journal of Cell Biology ·Umrao R. Monani, Matthew Pastore, Tatiana Gavrilina, Sibylle Jablonka, Thanh T. Le, Catia Andreassi, Jennifer M. DiCocco, Christian L. Lorson, Elliot J. Androphy, Michael Sendtner, Michael Podell, Arthur H.M. Burghes	2003	117
7	Electrophysiological and molecular evidence of L‐(Ca_v1), N‐ (Ca_v2.2), and R‐ (Ca_v2.3) type Ca²⁺ channels in rat cortical astrocytes Glia ·Marcello D’Ascenzo, Mauro Vairano, Catia Andreassi, Pierluigi Navarra, Gian Battista Azzena, Claudio Grassi	2003	77
8	Distinct and overlapping alterations in motor and sensory neurons in a mouse model of spinal muscular atrophy Human Molecular Genetics ·Sibylle Jablonka, Kathrin N. Karle, Beatrice Sandner, Catia Andreassi, Katja von Au, Michael Sendtner	2006	72
9	Inositol pyrophosphates regulate JMJD2C-dependent histone demethylation Proceedings of the National Academy of Sciences ·Adam Burton, Cristina Azevedo, Catia Andreassi, (unknown), Adolfo Saiardi	2013	58
10	Regulation of NGF Signaling by an Axonal Untranslated mRNA Neuron ·Hamish Crerar, Emily Scott-Solomon, Chantal Bodkin-Clarke, Catia Andreassi, Maria Hazbon, Emilie Logie, Marifé Cano‐Jaimez, Marco Gaspari, Rejji Kuruvilla, (unknown)	2019	31
11	Cytoplasmic cleavage of IMPA1 3′ UTR is necessary for maintaining axon integrity Cell Reports ·Catia Andreassi, Raphaëlle Luisier, Hamish Crerar, Marousa Darsinou, Sasja Blokzijl-Franke, Tchern Lenn, Nicholas M. Luscombe, Giovanni Cuda, Marco Gaspari, Adolfo Saiardi, (unknown)	2021	25
12	Post-transcriptional Processing of mRNA in Neurons: The Vestiges of the RNA World Drive Transcriptome Diversity Frontiers in Molecular Neuroscience ·Catia Andreassi, Hamish Crerar, (unknown)	2018	22
13	Proteomic analysis of S-nitrosylated nuclear proteins in rat cortical neurons Science Signaling ·Jacob G. Smith, Sarah G. Aldous, Catia Andreassi, Giovanni Cuda, Marco Gaspari, (unknown)	2018	21
14	Expression of the survival of motor neuron (SMN) gene in primary neurons and increase in SMN levels by activation of the N-methyl-D-aspartate glutamate receptor Neurogenetics ·Catia Andreassi, Anna Letizia Patrizi, Umrao R. Monani, Arthur H.M. Burghes, Christina Brahe, Maria Luisa Eboli	2002	17
15	Antiphospholipid antibodies bind to rat cerebellar granule cells: the role of N-methyl-d-aspartate receptors Neuroscience Letters ·(unknown), Catia Andreassi, Maria Luisa Eboli	1998	15
16	Anticardiolipin Antibodies in Patients with Primary Antiphospholipid Syndrome: A Correlation Between IgG Titre and Antibody-Induced Cell Dysfunctions in Neuronal Cell Cultures Clinical Rheumatology ·Catia Andreassi, A. Zoli, (unknown), Flavia Scuderi, Luigi Lombardi, L. Altomonte, Maria Luisa Eboli	2001	8
17	The human centromeric survival motor neuron gene (SMN2) rescues embryonic lethality in Smn / mice and results in a mouse with spinal muscular atrophy Human Molecular Genetics ·U. R. Monani, Michael Sendtner, Daniel D. Coovert, David Parsons, Catia Andreassi, Thomas Le, Sibylle Jablonka, Bertold Schrank, Wilfried Rossoll, Thomas W. Prior, Morris Gm, Arthur H.M. Burghes	2007	8
18	Injury primes mutation-bearing astrocytes for dedifferentiation in later life Current Biology ·Holly Simpson Ragdale, Melanie Clements, Wenhao Tang, Elitza Deltcheva, Catia Andreassi, Alvina G. Lai, Wai Hoong Chang, Maria Pandrea, Ivan Andrew, Laurence Gamé, Imran Uddin, Michael J. Ellis, Tariq Enver, Antonella Riccio, Samuel Marguerat, Simona Parrinello	2023	7
19	Mitochondrial Dynamics, Biogenesis, and Function Are Coordinated with the Cell Cycle by APC/C-CDH1 (Retraction of vol 15, pg 466, 2012) UCL Discovery (University College London) ·Assegid Garedew, Catia Andreassi, Salvador Moncada	2012	5
20	The predicted RNA-binding protein regulome of axonal mRNAs Genome Research ·Raphaëlle Luisier, Catia Andreassi, Lisa Mathilde Fournier, (unknown)	2023	4

About Catia Andreassi

Catia Andreassi is a scholar working on Genetics, Molecular Biology, Developmental Neuroscience, Cancer Research and Cellular and Molecular Neuroscience, having authored 23 papers that have together received 1.8k indexed citations. Recurring topics across this work include RNA modifications and cancer (12 papers), RNA Research and Splicing (9 papers), Neurogenetic and Muscular Disorders Research (9 papers), Congenital Anomalies and Fetal Surgery (3 papers), Nerve injury and regeneration (2 papers), RNA regulation and disease (2 papers), RNA and protein synthesis mechanisms (2 papers) and Systemic Lupus Erythematosus Research (2 papers). The work is most often cited by research in Genetics (979 citations), Molecular Biology (1.5k citations), Cellular and Molecular Neuroscience (235 citations), Developmental Neuroscience (41 citations) and Cell Biology (112 citations). Catia Andreassi has collaborated with scholars based in United Kingdom, Italy and United States. Frequent co-authors include Sibylle Jablonka, Michael Sendtner, Umrao R. Monani, Kathrin N. Karle, Wilfried Rossoll, Adolfo Saiardi, Christina Brahe, Serena De Vita, Salvatore Fusco and Richard Mitter. Their work appears in journals such as Human Molecular Genetics, The Journal of Cell Biology, Current Biology, European Journal of Human Genetics and Cell Reports.

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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