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 — A (Enhanced Table)

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

Name	h						Papers	Cites
Roberto Colombo Italy	16	315	253	154	121	121	35	981
Nancy Contel United States	12	463 1.5×	183 0.7×	289 1.9×	123 1.0×	79 0.7×	13	1.6k
Henrik Ryberg Sweden	16	444 1.4×	80 0.3×	223 1.4×	27 0.2×	18 0.1×	37	1.1k
Ramesh C. Juyal India	23	470 1.5×	151 0.6×	499 3.2×	201 1.7×	71 0.6×	51	1.5k
Lida Kimmel United States	8	474 1.5×	55 0.2×	85 0.6×	39 0.3×	342 2.8×	10	1.3k
Eduardo T. Cánepa Argentina	22	824 2.6×	41 0.2×	115 0.7×	48 0.4×	47 0.4×	58	1.4k
Marvin Peters Germany	21	690 2.2×	47 0.2×	87 0.6×	197 1.6×	90 0.7×	51	1.4k
D.J.A. Eckland United Kingdom	18	435 1.4×	142 0.6×	120 0.8×	14 0.1×	25 0.2×	37	1.5k
Junko Matsuda Japan	26	678 2.2×	35 0.1×	99 0.6×	50 0.4×	18 0.1×	71	1.9k
Qinghe Xing China	24	931 3.0×	37 0.1×	246 1.6×	24 0.2×	161 1.3×	82	1.8k
Takayo Sasagawa Japan	18	591 1.9×	49 0.2×	54 0.4×	20 0.2×	17 0.1×	31	1.3k

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

Youssefian, Leila, Hassan Vahidnezhad, Amir Hossein Saeidian, et al.. (2019). Inherited non-alcoholic fatty liver disease and dyslipidemia due to monoallelic ABHD5 mutations. Journal of Hepatology. 71(2). 366–370. 41 indexed citations

Colombo, Roberto, et al.. (2017). Two Novel <b><i>TEX15</i></b> Mutations in a Family with Nonobstructive Azoospermia. Gynecologic and Obstetric Investigation. 82(3). 283–286. 40 indexed citations

Dai, Zunyan, et al.. (2017). Caution in interpretation of disease causality for heterozygous loss-of-function variants in the MYH8 gene associated with autosomal dominant disorder. European Journal of Medical Genetics. 60(6). 312–316. 5 indexed citations

Tawamie, Hasan, Igor Martianov, Rebecca Buchert, et al.. (2017). Hypomorphic Pathogenic Variants in TAF13 Are Associated with Autosomal-Recessive Intellectual Disability and Microcephaly. The American Journal of Human Genetics. 100(3). 555–561. 18 indexed citations

Mandelli, Laura, Marianna Mazza, Marco Di Nicola, et al.. (2011). Serotoninergic and dopaminergic genes in bipolar disorder and response to treatments in bipolar depression. Investigation on a well-characterized naturalistic sample. 21(6 Suppl). 295–300. 1 indexed citations

Mazza, Marianna, Laura Mandelli, Leonardo Zaninotto, et al.. (2011). Factors associated with the course of symptoms in bipolar disorder during a 1-year follow-up: Depression vs. sub-threshold mixed state. Nordic Journal of Psychiatry. 65(6). 419–426. 13 indexed citations

Coleman, Rosalind, Laura Moro, Catherine Dacou‐Voutetakis, et al.. (2010). Clinical and genetic characterization of chanarin-dorfman syndrome patients: first report of large deletions in the ABHD5 gene. Orphanet Journal of Rare Diseases. 5(1). 33–33. 40 indexed citations

Tzialla, Chryssoula, Lidia Decembrino, A. Di Comite, et al.. (2010). Colonic stricture and retinitis due to cytomegalovirus infection in an immunocompetent infant. Pediatrics International. 52(4). 659–660. 10 indexed citations

Mazza, Marianna, Laura Mandelli, Giovanni Martinotti, et al.. (2010). Further evidence supporting the association between 5HTR2C gene and bipolar disorder. Psychiatry Research. 180(2-3). 151–152. 7 indexed citations

10.

Mandelli, Laura, Marianna Mazza, Giovanni Martinotti, et al.. (2009). Harm avoidance moderates the influence of serotonin transporter gene variants on treatment outcome in bipolar patients. Journal of Affective Disorders. 119(1-3). 205–209. 30 indexed citations

11.

Mazza, Marianna, Laura Mandelli, Marco Di Nicola, et al.. (2008). Clinical features, response to treatment and functional outcome of bipolar disorder patients with and without co-occurring substance use disorder: 1-year follow-up. Journal of Affective Disorders. 115(1-2). 27–35. 74 indexed citations

12.

Cichon, Sven, Ludovic Martin, Hans Christian Hennies, et al.. (2006). Increased Activity of Coagulation Factor XII (Hageman Factor) Causes Hereditary Angioedema Type III. The American Journal of Human Genetics. 79(6). 1098–1104. 250 indexed citations

13.

Musio, Antonio, Veronica Marrella, Cristina Sobacchi, et al.. (2005). Damaging‐agent sensitivity of Artemis‐deficient cell lines. European Journal of Immunology. 35(4). 1250–1256. 31 indexed citations

14.

Frisch, Amos, et al.. (2004). Origin and spread of the 1278insTATC mutation causing Tay-Sachs disease in Ashkenazi Jews: genetic drift as a robust and parsimonious hypothesis. Human Genetics. 114(4). 366–376. 20 indexed citations

15.

Magni, Fulvio, Flavio Curnis, Roberto Colombo, et al.. (2001). Biotinylation Sites of Tumor Necrosis Factor-α Determined by Liquid Chromatography–Mass Spectrometry. Analytical Biochemistry. 298(2). 181–188. 7 indexed citations

16.

Colombo, Roberto & Anna Carobene. (2000). Age of the intronic GAA triplet repeat expansion mutation in Friedreich ataxia. Human Genetics. 106(4). 455–458. 11 indexed citations

17.

Colombo, Roberto. (2000). Age Estimate of the N370S Mutation Causing Gaucher Disease in Ashkenazi Jews and European Populations: A Reappraisal of Haplotype Data. The American Journal of Human Genetics. 66(2). 692–697. 30 indexed citations

18.

Colombo, Roberto, A Bignamini, Anna Carobene, et al.. (2000). Age and origin of the FCMD 3′-untranslated-region retrotransposal insertion mutation causing Fukuyama-type congenital muscular dystrophy in the Japanese population. Human Genetics. 107(6). 559–567. 27 indexed citations

19.

Marangoni, Roberto, et al.. (1992). Plasma Lipids and Fatty Acid Levels in Chronically Uremic Patients Undergoing Blood Purification with Different Methods. Artificial Organs. 16(6). 625–629. 5 indexed citations

20.

Cusi, Daniele, Grazia Tripodi, Cristina Barlassina, et al.. (1989). Pathogenetic mechanisms in essential hypertension. Analogies between a rat model and the human disease. International Journal of Cardiology. 25. S29–S36. 3 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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