Gerard Muntané

6.4k total citations
44 papers, 842 citations indexed

About

Gerard Muntané is a scholar working on Molecular Biology, Genetics and Neurology. According to data from OpenAlex, Gerard Muntané has authored 44 papers receiving a total of 842 indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Molecular Biology, 14 papers in Genetics and 9 papers in Neurology. Recurrent topics in Gerard Muntané's work include Genetic Associations and Epidemiology (8 papers), Parkinson's Disease Mechanisms and Treatments (7 papers) and Genetics and Neurodevelopmental Disorders (6 papers). Gerard Muntané is often cited by papers focused on Genetic Associations and Epidemiology (8 papers), Parkinson's Disease Mechanisms and Treatments (7 papers) and Genetics and Neurodevelopmental Disorders (6 papers). Gerard Muntané collaborates with scholars based in Spain, United States and Germany. Gerard Muntané's co-authors include Isidró Ferrer, Esther Dalfó, Marta Martínez‐Vicente, Ana Martı́nez, Elisabet Vilella, Lourdes Martorell, Arcadi Navarro, Manuel J. Bández, Alberto Boveris and Carmen Gómez and has published in prestigious journals such as Nature Communications, Bioinformatics and Scientific Reports.

In The Last Decade

Gerard Muntané

42 papers receiving 829 citations

Peers

Gerard Muntané
Andrew E. Arrant United States
Amy R. Dunn United States
Kelly M. Lohr United States
Aurélie Joly‐Amado United States
Andrew E. Arrant United States
Gerard Muntané
Citations per year, relative to Gerard Muntané Gerard Muntané (= 1×) peers Andrew E. Arrant

Countries citing papers authored by Gerard Muntané

Since Specialization
Citations

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

Fields of papers citing papers by Gerard Muntané

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Gerard Muntané

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

All Works

20 of 20 papers shown
1.
Callado, Luís F., Helena Torrell-Galceran, Elisabet Vilella, et al.. (2024). High number of mitochondrial DNA alterations in postmortem brain tissue of patients with schizophrenia compared to healthy controls. Psychiatry Research. 337. 115928–115928. 5 indexed citations
2.
Ortega, Eva González, et al.. (2024). Influence of the typology and timing of childhood trauma in psychoticism. Archives of Women s Mental Health. 27(5). 705–719. 2 indexed citations
3.
Muntané, Gerard, Javier Vázquez-Bourgón, Lourdes Martorell, et al.. (2023). Polygenic risk scores enhance prediction of body mass index increase in individuals with a first episode of psychosis. European Psychiatry. 66(1). e28–e28. 9 indexed citations
4.
Vogel-González, Marina, Gerard ILL‐Raga, Gerard Muntané, et al.. (2023). Human genetic adaptation related to cellular zinc homeostasis. PLoS Genetics. 19(9). e1010950–e1010950. 2 indexed citations
5.
Vilar‐Ribó, Laura, Judit Cabana‐Domínguez, Lourdes Martorell, et al.. (2023). Shared genetic architecture between attention-deficit/hyperactivity disorder and lifespan. Neuropsychopharmacology. 48(7). 981–990. 3 indexed citations
6.
Papiol, Sergi, Urs Heilbronner, María Dolores Moltó, et al.. (2023). Common genetic variants contribute to heritability of age at onset of schizophrenia. Translational Psychiatry. 13(1). 201–201. 8 indexed citations
7.
Valenzuela, Alejandro, Xavier Farré, David Juan, et al.. (2023). CAAStools: a toolbox to identify and test Convergent Amino Acid Substitutions. Bioinformatics. 39(10). 3 indexed citations
8.
Guardiola, Montse, Gerard Muntané, Lourdes Martorell, et al.. (2023). Metabolic Overlap between Alzheimer’s Disease and Metabolic Syndrome Identifies the PVRL2 Gene as a New Modulator of Diabetic Dyslipidemia. International Journal of Molecular Sciences. 24(8). 7415–7415. 4 indexed citations
9.
Moreno, Irene, Vanessa Sánchez‐Gistau, Laura Ortega, et al.. (2023). High blood levels of brain-derived neurotrophic factor (BDNF) mRNA in early psychosis are associated with inflammatory markers. Journal of Psychiatric Research. 164. 440–446.
10.
González‐Peñas, Javier, Covadonga M. Díaz‐Caneja, Álvaro Andreu-Bernabeu, et al.. (2023). Recent natural selection conferred protection against schizophrenia by non-antagonistic pleiotropy. Scientific Reports. 13(1). 15500–15500. 4 indexed citations
11.
Ayesa‐Arriola, Rosa, Javier Vázquez-Bourgón, Benedicto Crespo‐Facorro, et al.. (2022). Cross-sectional and longitudinal assessment of the association between DDR1 variants and processing speed in patients with early psychosis and healthy controls. Journal of Psychiatric Research. 158. 49–55. 1 indexed citations
12.
Farré, Xavier, Paul R. H. J. Timmers, Peter K. Joshi, et al.. (2021). Comparative Analysis of Mammal Genomes Unveils Key Genomic Variability for Human Life Span. Molecular Biology and Evolution. 38(11). 4948–4961. 24 indexed citations
13.
Moura, Manuel Castro de, Gerard Muntané, Lourdes Martorell, et al.. (2021). DDR1 methylation is associated with bipolar disorder and the isoform expression and methylation of myelin genes. Epigenomics. 13(11). 845–858. 3 indexed citations
14.
Labad, Javier, Susana Ochoa, Ángel Cabezas, et al.. (2021). Cognitive Biases Questionnaire for Psychosis (CBQp): Spanish Validation and Relationship With Cognitive Insight in Psychotic Patients. Frontiers in Psychiatry. 11. 596625–596625. 7 indexed citations
15.
Martorell, Lourdes, Gerard Muntané, Irene Moreno, et al.. (2019). Increased levels of serum leptin in the early stages of psychosis. Journal of Psychiatric Research. 111. 24–29. 20 indexed citations
16.
Canales‐Rodríguez, Erick J., Joaquim Raduà, María José Cortés, et al.. (2018). Discoidin domain receptor 1 gene variants are associated with decreased white matter fractional anisotropy and decreased processing speed in schizophrenia. Journal of Psychiatric Research. 110. 74–82. 16 indexed citations
17.
Muntané, Gerard, Gabriel Santpere, William W. Seeley, et al.. (2017). Interhemispheric gene expression differences in the cerebral cortex of humans and macaque monkeys. Brain Structure and Function. 222(7). 3241–3254. 15 indexed citations
18.
Muntané, Gerard, Julie E. Horvath, Patrick R. Hof, et al.. (2014). Analysis of Synaptic Gene Expression in the Neocortex of Primates Reveals Evolutionary Changes in Glutamatergic Neurotransmission. Cerebral Cortex. 25(6). 1596–1607. 23 indexed citations
19.
Muntané, Gerard, Isidró Ferrer, & Marta Martínez‐Vicente. (2011). α-synuclein phosphorylation and truncation are normal events in the adult human brain. Neuroscience. 200. 106–119. 103 indexed citations
20.
Muntané, Gerard, Esther Dalfó, M. Rey, et al.. (2006). Glial fibrillary acidic protein is a major target of glycoxidative and lipoxidative damage in Pick's disease. Journal of Neurochemistry. 99(1). 177–185. 48 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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