Alexey Shadrin

9.1k total citations
102 papers, 1.9k citations indexed

About

Alexey Shadrin is a scholar working on Genetics, Molecular Biology and Psychiatry and Mental health. According to data from OpenAlex, Alexey Shadrin has authored 102 papers receiving a total of 1.9k indexed citations (citations by other indexed papers that have themselves been cited), including 70 papers in Genetics, 32 papers in Molecular Biology and 13 papers in Psychiatry and Mental health. Recurrent topics in Alexey Shadrin's work include Genetic Associations and Epidemiology (66 papers), Genetic Mapping and Diversity in Plants and Animals (15 papers) and Bioinformatics and Genomic Networks (13 papers). Alexey Shadrin is often cited by papers focused on Genetic Associations and Epidemiology (66 papers), Genetic Mapping and Diversity in Plants and Animals (15 papers) and Bioinformatics and Genomic Networks (13 papers). Alexey Shadrin collaborates with scholars based in Norway, United States and United Kingdom. Alexey Shadrin's co-authors include Oleksandr Frei, Ole A. Andreassen, Olav B. Smeland, Anders M. Dale, Srdjan Djurovic, Kevin S. O’Connell, Shahram Bahrami, Chun Chieh Fan, Dominic Holland and Wesley K. Thompson and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nature Communications and Nature Genetics.

In The Last Decade

Alexey Shadrin

92 papers receiving 1.9k citations

Peers

Alexey Shadrin
Sophie E. Legge United Kingdom
Chun Chieh Fan United States
Elliott Rees United Kingdom
Tiffany A. Greenwood United States
Ann E. Pulver United States
Alexey Shadrin
Citations per year, relative to Alexey Shadrin Alexey Shadrin (= 1×) peers Kevin S. O’Connell

Countries citing papers authored by Alexey Shadrin

Since Specialization
Citations

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

Fields of papers citing papers by Alexey Shadrin

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Alexey Shadrin

This figure shows the co-authorship network connecting the top 25 collaborators of Alexey Shadrin. A scholar is included among the top collaborators of Alexey Shadrin 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 Alexey Shadrin. Alexey Shadrin 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.
Meer, Dennis van der, Alexey Shadrin, Ole A. Andreassen, et al.. (2025). No causal links between estradiol and female’s brain and mental health using Mendelian randomization. Nature Communications. 16(1). 10915–10915.
2.
Karadag, Naz, Espen Hagen, Alexey Shadrin, et al.. (2024). Dissecting the Shared Genetic Architecture of Common Epilepsies With Cortical Brain Morphology. Neurology Genetics. 10(3). e200143–e200143. 2 indexed citations
3.
Jahołkowski, Piotr, Alexey Shadrin, Svend Andersen, et al.. (2024). Incidence and Genetic Risk of Juvenile Idiopathic Arthritis in Norway by Latitude. Arthritis & Rheumatology. 77(4). 458–467. 2 indexed citations
4.
Wortinger, Laura A., Anne-Kristin Stavrum, Alexey Shadrin, et al.. (2024). Divergent epigenetic responses to perinatal asphyxia in severe mental disorders. Translational Psychiatry. 14(1). 16–16. 5 indexed citations
5.
Bahrami, Shahram, Kaja Nordengen, Jaroslav Rokicki, et al.. (2024). The genetic landscape of basal ganglia and implications for common brain disorders. Nature Communications. 15(1). 8476–8476. 2 indexed citations
6.
Tesfaye, Markos, Letícia Spíndola, Anne-Kristin Stavrum, et al.. (2024). Sex effects on DNA methylation affect discovery in epigenome-wide association study of schizophrenia. Molecular Psychiatry. 29(8). 2467–2477. 4 indexed citations
7.
Rokicki, Jaroslav, Siri Birkeland, Francesco Bettella, et al.. (2024). An evolutionary timeline of the oxytocin signaling pathway. Communications Biology. 7(1). 471–471. 6 indexed citations
8.
Parker, Nadine, Weiqiu Cheng, Guy Hindley, et al.. (2023). Genetic Overlap Between Global Cortical Brain Structure, C-Reactive Protein, and White Blood Cell Counts. Biological Psychiatry. 95(1). 62–71. 10 indexed citations
9.
Leonardsen, Esten H., Didac Vidal‐Piñeiro, James M. Roe, et al.. (2023). Genetic architecture of brain age and its causal relations with brain and mental disorders. Molecular Psychiatry. 28(7). 3111–3120. 19 indexed citations
10.
Dalvie, Shareefa, Alexey Shadrin, Dennis van der Meer, et al.. (2023). Distributed genetic effects of the corpus callosum subregions suggest links to neuropsychiatric disorders and related traits. Acta Neuropsychiatrica. 37. e23–e23. 1 indexed citations
11.
Jahołkowski, Piotr, Guy Hindley, Alexey Shadrin, et al.. (2023). Genome-wide Association Analysis of Schizophrenia and Vitamin D Levels Shows Shared Genetic Architecture and Identifies Novel Risk Loci. Schizophrenia Bulletin. 49(6). 1654–1664. 5 indexed citations
12.
Werner, Maren Caroline Frogner, Alexey Shadrin, Synve Hoffart Lunding, et al.. (2022). Immune marker levels in severe mental disorders: associations with polygenic risk scores of related mental phenotypes and psoriasis. Translational Psychiatry. 12(1). 38–38. 23 indexed citations
13.
Rahman, Zillur, Shahram Bahrami, Guy Hindley, et al.. (2022). Shared genetic loci between depression and cardiometabolic traits. PLoS Genetics. 18(5). e1010161–e1010161. 29 indexed citations
14.
Bahrami, Shahram, Kaja Nordengen, Alexey Shadrin, et al.. (2022). Distributed genetic architecture across the hippocampal formation implies common neuropathology across brain disorders. Nature Communications. 13(1). 3436–3436. 12 indexed citations
15.
Bahrami, Shahram, Alexey Shadrin, Oleksandr Frei, et al.. (2021). Genetic loci shared between major depression and intelligence with mixed directions of effect. Nature Human Behaviour. 5(6). 795–801. 29 indexed citations
16.
Rødevand, Linn, Shahram Bahrami, Oleksandr Frei, et al.. (2021). Polygenic overlap and shared genetic loci between loneliness, severe mental disorders, and cardiovascular disease risk factors suggest shared molecular mechanisms. Translational Psychiatry. 11(1). 3–3. 38 indexed citations
17.
Maximov, Ivan I., Dennis van der Meer, Ann‐Marie G. de Lange, et al.. (2021). Fast qualitY conTrol meThod foR derIved diffUsion Metrics (YTTRIUM) in big data analysis: U.K. Biobank 18,608 example. Human Brain Mapping. 42(10). 3141–3155. 21 indexed citations
18.
Meer, Dennis van der, Oleksandr Frei, Tobias Kaufmann, et al.. (2020). Understanding the genetic determinants of the brain with MOSTest. Nature Communications. 11(1). 3512–3512. 86 indexed citations
19.
Holland, Dominic, Oleksandr Frei, Rahul S. Desikan, et al.. (2020). Beyond SNP heritability: Polygenicity and discoverability of phenotypes estimated with a univariate Gaussian mixture model. PLoS Genetics. 16(5). e1008612–e1008612. 104 indexed citations
20.
O’Connell, Kevin S., Alexey Shadrin, Shahram Bahrami, et al.. (2019). Identification of genetic overlap and novel risk loci for attention-deficit/hyperactivity disorder and bipolar disorder. Molecular Psychiatry. 26(8). 4055–4065. 30 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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