Ilaria Guella

2.5k total citations
45 papers, 1.3k citations indexed

About

Ilaria Guella is a scholar working on Molecular Biology, Neurology and Cellular and Molecular Neuroscience. According to data from OpenAlex, Ilaria Guella has authored 45 papers receiving a total of 1.3k indexed citations (citations by other indexed papers that have themselves been cited), including 18 papers in Molecular Biology, 18 papers in Neurology and 11 papers in Cellular and Molecular Neuroscience. Recurrent topics in Ilaria Guella's work include Parkinson's Disease Mechanisms and Treatments (17 papers), Neurological diseases and metabolism (7 papers) and Blood Coagulation and Thrombosis Mechanisms (7 papers). Ilaria Guella is often cited by papers focused on Parkinson's Disease Mechanisms and Treatments (17 papers), Neurological diseases and metabolism (7 papers) and Blood Coagulation and Thrombosis Mechanisms (7 papers). Ilaria Guella collaborates with scholars based in Canada, Italy and United States. Ilaria Guella's co-authors include Matthew J. Farrer, Marquis P. Vawter, Rosanna Asselta, Stefano Duga, Joanne Trinh, Flora Peyvandi, Tatiana Foroud, Howard J. Edenberg, John R. Kelsoe and Daniel L. Koller and has published in prestigious journals such as Blood, Annals of Neurology and Biological Psychiatry.

In The Last Decade

Ilaria Guella

45 papers receiving 1.3k citations

Peers

Countries citing papers authored by Ilaria Guella

Since Specialization

Citations

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

Fields of papers citing papers by Ilaria Guella

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ilaria Guella

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

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	The effect of rapid exome sequencing on downstream health care utilization for infants with suspected genetic disorders in an intensive care unit 2022 ·Genetics in Medicine ·(unknown), Nick Dragojlovic, (unknown), Jan M. Friedman, Horacio Osiovich, Tara Candido, Jan Christilaw, Christèle du Souich, Alison M. Elliott, Daniel M. Evans, Matthew J. Farrer, Ilaria Guella, Anna Lehman, Larry D. Lynd, Leah Tooman	4
2	Pathophysiology of and therapeutic options for a GABRA1 variant linked to epileptic encephalopathy 2019 ·Molecular Brain ·Yunfei Bai, (unknown), (unknown), Peter Axerio-Cilies, Jie Lu, Linda Huh, Mary Connolly, Ilaria Guella, Matthew J. Farrer, Qing Xu, Lidong Liu, Michelle Demos, Yu Tian Wang	14
3	Case reports: novel TUBG1 mutations with milder neurodevelopmental presentations 2019 ·BMC Medical Genetics ·(unknown), Ilaria Guella, Elke H. Roland, Michael A. Sargent, Cyrus Boelman	10
4	Pipeline to gene discovery - Analysing familial Parkinsonism in the Queensland Parkinson's Project 2018 ·Parkinsonism & Related Disorders ·Steven R. Bentley, (unknown), Ilaria Guella, Javed Fowdar, Peter A. Silburn, Stephen A. Wood, Matthew J. Farrer, George D. Mellick	12
5	An Infant With Epilepsy and Recurrent Hemiplegia due to Compound Heterozygous Variants in ATP1A2 2017 ·Pediatric Neurology ·(unknown), Sarah E. Buerki, Ilaria Guella, Eric Toyota, Daniel M. Evans, Marna B. McKenzie, Anita Datta, Aspasia Michoulas, Shelin Adam, Margot I. Van Allen, Tanya N. Nelson, Matthew J. Farrer, Mary Connolly, Michelle Demos	15
6	Dopamine receptors and BDNF -haplotypes predict dyskinesia in Parkinson's disease 2017 ·Parkinsonism & Related Disorders ·Cynthia Kusters, Kimberly C. Paul, Ilaria Guella, Jeff M. Bronstein, Janet S. Sinsheimer, Matthew J. Farrer, Beate Ritz	30
7	Conjugal parkinsonism – Clinical, pathology and genetic study. No evidence of person-to-person transmission 2016 ·Parkinsonism & Related Disorders ·Ali H. Rajput, (unknown), Leslie W. Ferguson, Christopher A. Robinson, Ilaria Guella, Matthew J. Farrer, Alexander Rajput	13
8	LRRK2-Related Parkinson Disease 2014 ·Joanne Trinh, Matthew J. Farrer, Owen A. Ross, Ilaria Guella	1
9	Parkinson's disease, genetic variability and the Faroe Islands 2014 ·Parkinsonism & Related Disorders ·Maria Skaalum Petersen, Ilaria Guella, Sára Bech, Emil K. Gustavsson, Matthew J. Farrer	9
10	Clinical and molecular characterisation of 21 patients affected by quantitative fibrinogen deficiency 2014 ·Thrombosis and Haemostasis ·Rosanna Asselta, Manuela Platé, (unknown), Munira Borhany, Ilaria Guella, Giulia Soldà, Abdolreza Afrasiabi, Marzia Menegatti, (unknown), Flora Peyvandi, Stefano Duga	33
11	Analysis of miR-137 expression and rs1625579 in dorsolateral prefrontal cortex 2013 ·Journal of Psychiatric Research ·Ilaria Guella, Adolfo Sequeira, Brandi Rollins, Linda Morgan, Federica Torri, Theo G.M. van Erp, R Myers, Jack D. Barchas, Alan F. Schatzberg, Stanley J. Watson, Huda Akil, William E. Bunney, Steven G. Potkin, Fabìo Macciardi, Marquis P. Vawter	110
12	Evidence of allelic imbalance in the schizophrenia susceptibility gene ZNF804A in human dorsolateral prefrontal cortex 2013 ·Schizophrenia Research ·Ilaria Guella, Adolfo Sequeira, Brandi Rollins, Ling Morgan, R Myers, Stanley J. Watson, Huda Akil, William E. Bunney, Lynn E. DeLisi, William Byerley, Marquis P. Vawter	28
13	SNCA and MAPT genes: Independent and joint effects in Parkinson disease in the Italian population 2011 ·Parkinsonism & Related Disorders ·Luca Trotta, Ilaria Guella, Giulia Soldà, Francesca Sironi, Silvana Tesei, Margherita Canesi, Gianni Pezzoli, Stefano Goldwurm, Stefano Duga, Rosanna Asselta	38
14	Identification of the first Alu-mediated large deletion involving the F5 gene in a compound heterozygous patient with severe factor V deficiency 2011 ·Thrombosis and Haemostasis ·Ilaria Guella, Elvezia Maria Paraboschi, (unknown), Rosanna Asselta, Stefano Duga	8
15	Common variants in the haemostatic gene pathway contribute to risk of early-onset myocardial infarction in the Italian population 2011 ·Thrombosis and Haemostasis ·Ilaria Guella, (unknown), P A Merlini, Flora Peyvandi, (unknown), Rosanna Asselta, Stefano Duga	21
16	The association of factor V Leiden with myocardial infarction is replicated in 1880 patients with premature disease 2010 ·Journal of Thrombosis and Haemostasis ·Pier Mannuccio Mannucci, Rosanna Asselta, Stefano Duga, Ilaria Guella, Marta Spreafico, Luca A. Lotta, Pier Angelica Merlini, Flora Peyvandi, Sekar Kathiresan, Diego Ardissino	40
17	Mutational screening and zebrafish functional analysis of GIGYF2 as a Parkinson-disease gene 2010 ·Neurobiology of Aging ·Ilaria Guella, Anna Pistocchi, Rosanna Asselta, Valeria Rimoldi, Anna Ghilardi, Francesca Sironi, Luca Trotta, Paola Primignani, Michela Zini, Anna Zecchinelli, Domenico Coviello, Gianni Pezzoli, Luca Del Giacco, Stefano Duga, Stefano Goldwurm	19
18	Effects of PCSK9 genetic variants on plasma LDL cholesterol levels and risk of premature myocardial infarction in the Italian population 2010 ·Journal of Lipid Research ·Ilaria Guella, Rosanna Asselta, Diego Ardissino, Pier Angelica Merlini, Flora Peyvandi, Sekar Kathiresan, Pier Mannuccio Mannucci, Marco Tubaro, Stefano Duga	40
19	Molecular characterization of two novel mutations causing factor XI deficiency: A splicing defect and a missense mutation responsible for a CRM+ defect 2008 ·Thrombosis and Haemostasis ·Ilaria Guella, Giulia Soldà, Silvia Spena, Rosanna Asselta, (unknown), Maria Luisa Tenchini, Giancarlo Castaman, Stefano Duga	17
20	Functional analysis of missense mutations in the Myocyte Enhancer Factor 2A (MEF2A) gene do not support their causal role in the pathogenesis of myocardial infarction 2008 ·European Journal of Human Genetics ·Ilaria Guella, Valeria Rimoldi, Piera Angelica Merlini, Rosanna Asselta, Elvezia Maria Paraboschi, Maura Francolini, Flora Peyvandi, Diego Ardissino, P.M. Mannucci, Stefano Duga	1

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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