Roberto Colombo

1.6k total citations
35 papers, 981 citations indexed

About

Roberto Colombo is a scholar working on Molecular Biology, Psychiatry and Mental health and Cellular and Molecular Neuroscience. According to data from OpenAlex, Roberto Colombo has authored 35 papers receiving a total of 981 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Molecular Biology, 11 papers in Psychiatry and Mental health and 6 papers in Cellular and Molecular Neuroscience. Recurrent topics in Roberto Colombo's work include Bipolar Disorder and Treatment (10 papers), Schizophrenia research and treatment (4 papers) and Metabolism and Genetic Disorders (3 papers). Roberto Colombo is often cited by papers focused on Bipolar Disorder and Treatment (10 papers), Schizophrenia research and treatment (4 papers) and Metabolism and Genetic Disorders (3 papers). Roberto Colombo collaborates with scholars based in Italy, Japan and United States. Roberto Colombo's co-authors include Christian Drouet, Ludovic Martin, Sven Cichon, Markus M. Nöthen, Felicitas Müller, Thomas Renné, W. J. Stevens, Konrad Bork, Hans Christian Hennies and Anna Karpushova and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Analytical Biochemistry and Journal of Agricultural and Food Chemistry.

In The Last Decade

Roberto Colombo

35 papers receiving 964 citations

Peers

Countries citing papers authored by Roberto Colombo

Since Specialization

Citations

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

Fields of papers citing papers by Roberto Colombo

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Roberto Colombo

This figure shows the co-authorship network connecting the top 25 collaborators of Roberto Colombo. A scholar is included among the top collaborators of Roberto Colombo 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 Roberto Colombo. Roberto Colombo 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	Inherited non-alcoholic fatty liver disease and dyslipidemia due to monoallelic ABHD5 mutations 2019 ·Journal of Hepatology ·Leila Youssefian, Hassan Vahidnezhad, Amir Hossein Saeidian, (unknown), Soheila Sotoudeh, Parvin Mansouri, (unknown), Sirous Zeinali, Michael A. Levine, Ketty Peris, Roberto Colombo, Jouni Uitto	41
2	Two Novel <b><i>TEX15</i></b> Mutations in a Family with Nonobstructive Azoospermia 2017 ·Gynecologic and Obstetric Investigation ·Roberto Colombo, Alessandro Pontoglio, (unknown)	40
3	Caution in interpretation of disease causality for heterozygous loss-of-function variants in the MYH8 gene associated with autosomal dominant disorder 2017 ·European Journal of Medical Genetics ·Zunyan Dai, (unknown), (unknown), Alessandro Pontoglio, Lora Jh Bean, Roberto Colombo, Madhuri Hegde	5
4	Hypomorphic Pathogenic Variants in TAF13 Are Associated with Autosomal-Recessive Intellectual Disability and Microcephaly 2017 ·The American Journal of Human Genetics ·Hasan Tawamie, Igor Martianov, (unknown), Rebecca Buchert, Gabrielle Mengus, Steffen Uebe, Luigi Janiri, W. Hirsch, Johannes Schumacher, Fulvia Ferrazzi, Heinrich Sticht, André Reis, Irwin Davidson, Roberto Colombo, Rami Abou Jamra	18
5	Serotoninergic and dopaminergic genes in bipolar disorder and response to treatments in bipolar depression. Investigation on a well-characterized naturalistic sample 2011 ·Laura Mandelli, Marianna Mazza, Marco Di Nicola, Giovanni Martinotti, Daniela Tavian, E. Colombo, Sara Missaglia, Gloria Negri, Diana De Ronchi, Roberto Colombo, Luigi Janiri, Alessandro Serretti	1
6	Factors associated with the course of symptoms in bipolar disorder during a 1-year follow-up: Depression vs. sub-threshold mixed state 2011 ·Nordic Journal of Psychiatry ·Marianna Mazza, Laura Mandelli, Leonardo Zaninotto, Marco Di Nicola, Giovanni Martinotti, Désirée Harnic, Angelo Bruschi, Valeria Catalano, D. Tedeschi, Roberto Colombo, Pietro Bria, Alessandro Serretti, Luigi Janiri	13
7	Clinical and genetic characterization of chanarin-dorfman syndrome patients: first report of large deletions in the ABHD5 gene 2010 ·Orphanet Journal of Rare Diseases ·(unknown), Rosalind Coleman, Laura Moro, Catherine Dacou‐Voutetakis, Solaf M. Elsayed, Daniele Prati, Agostino Colli, (unknown), Roberto Colombo, Daniela Tavian	40
8	Colonic stricture and retinitis due to cytomegalovirus infection in an immunocompetent infant 2010 ·Pediatrics International ·Chryssoula Tzialla, Lidia Decembrino, A. Di Comite, Lina Bollani, Roberto Colombo, Mauro Stronati	10
9	Further evidence supporting the association between 5HTR2C gene and bipolar disorder 2010 ·Psychiatry Research ·Marianna Mazza, Laura Mandelli, Giovanni Martinotti, Marco Di Nicola, Daniela Tavian, Gloria Negri, E. Colombo, Sara Missaglia, Diana De Ronchi, Roberto Colombo, Luigi Janiri, Alessandro Serretti	7
10	Harm avoidance moderates the influence of serotonin transporter gene variants on treatment outcome in bipolar patients 2009 ·Journal of Affective Disorders ·Laura Mandelli, Marianna Mazza, Giovanni Martinotti, Marco Di Nicola, Daniela Tavian, E. Colombo, Sara Missaglia, Diana De Ronchi, Roberto Colombo, Luigi Janiri, Alessandro Serretti	30
11	Clinical features, response to treatment and functional outcome of bipolar disorder patients with and without co-occurring substance use disorder: 1-year follow-up 2008 ·Journal of Affective Disorders ·Marianna Mazza, Laura Mandelli, Marco Di Nicola, Désirée Harnic, Valeria Catalano, D. Tedeschi, Giovanni Martinotti, Roberto Colombo, Pietro Bria, Alessandro Serretti, Luigi Janiri	74
12	Increased Activity of Coagulation Factor XII (Hageman Factor) Causes Hereditary Angioedema Type III 2006 ·The American Journal of Human Genetics ·Sven Cichon, Ludovic Martin, Hans Christian Hennies, Felicitas Müller, (unknown), Anna Karpushova, W. J. Stevens, Roberto Colombo, Thomas Renné, Christian Drouet, Konrad Bork, Markus M. Nöthen	250
13	Damaging‐agent sensitivity of Artemis‐deficient cell lines 2005 ·European Journal of Immunology ·Antonio Musio, Veronica Marrella, Cristina Sobacchi, Francesca Rucci, Laura Fariselli, Silvia Giliani, Gaetana Lanzi, Luigi D. Notarangelo, Domenico Delia, Roberto Colombo, Paolo Vezzoni, Anna Villa	31
14	Origin and spread of the 1278insTATC mutation causing Tay-Sachs disease in Ashkenazi Jews: genetic drift as a robust and parsimonious hypothesis 2004 ·Human Genetics ·Amos Frisch, Roberto Colombo, Elena Michaelovsky, (unknown), Boleslaw Goldman, Leah Peleg	20
15	Biotinylation Sites of Tumor Necrosis Factor-α Determined by Liquid Chromatography–Mass Spectrometry 2001 ·Analytical Biochemistry ·Fulvio Magni, Flavio Curnis, (unknown), Roberto Colombo, Angelina Sacchi, Angelo Corti, M. Galli Kienle	7
16	Age of the intronic GAA triplet repeat expansion mutation in Friedreich ataxia 2000 ·Human Genetics ·Roberto Colombo, Anna Carobene	11
17	Age Estimate of the N370S Mutation Causing Gaucher Disease in Ashkenazi Jews and European Populations: A Reappraisal of Haplotype Data 2000 ·The American Journal of Human Genetics ·Roberto Colombo	30
18	Age and origin of the FCMD 3′-untranslated-region retrotransposal insertion mutation causing Fukuyama-type congenital muscular dystrophy in the Japanese population 2000 ·Human Genetics ·Roberto Colombo, A Bignamini, Anna Carobene, Junko Sasaki, Masashi Tachikawa, Kazuhiro Kobayashi, Tatsushi Toda	27
19	Plasma Lipids and Fatty Acid Levels in Chronically Uremic Patients Undergoing Blood Purification with Different Methods 1992 ·Artificial Organs ·Roberto Marangoni, (unknown), (unknown), Roberto Colombo, Franca Marangoni, Cristina Mosconi, (unknown)	5
20	Pathogenetic mechanisms in essential hypertension. Analogies between a rat model and the human disease 1989 ·International Journal of Cardiology ·Daniele Cusi, (unknown), (unknown), Grazia Tripodi, Cristina Barlassina, Roberto Colombo, (unknown), (unknown), Giuseppe Vezzoli, Giuseppe Bianchi	3

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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