Andrés Ingason

23.5k total citations
35 papers, 1.6k citations indexed

About

Andrés Ingason is a scholar working on Genetics, Molecular Biology and Psychiatry and Mental health. According to data from OpenAlex, Andrés Ingason has authored 35 papers receiving a total of 1.6k indexed citations (citations by other indexed papers that have themselves been cited), including 24 papers in Genetics, 19 papers in Molecular Biology and 5 papers in Psychiatry and Mental health. Recurrent topics in Andrés Ingason's work include Genetic Associations and Epidemiology (12 papers), Genomic variations and chromosomal abnormalities (10 papers) and Genetics and Neurodevelopmental Disorders (6 papers). Andrés Ingason is often cited by papers focused on Genetic Associations and Epidemiology (12 papers), Genomic variations and chromosomal abnormalities (10 papers) and Genetics and Neurodevelopmental Disorders (6 papers). Andrés Ingason collaborates with scholars based in Denmark, Iceland and United Kingdom. Andrés Ingason's co-authors include Hreinn Stefánsson, Kāri Stefánsson, Hannes Pétursson, Augustine Kong, Jeffrey R. Gulcher, Thomas Werge, David Collier, Valgerður Steinthórsdóttir, David St Clair and Phil Yates and has published in prestigious journals such as Cell, Proceedings of the National Academy of Sciences and Nature Communications.

In The Last Decade

Andrés Ingason

32 papers receiving 1.6k citations

Peers

Andrés Ingason

GENET

CMN

ONCOL

Detelina Grozeva United Kingdom

Guiqing Cai United States

Janice M. Fullerton Australia

Virginia K. Lasseter United States

Radhakrishna Vakkalanka United States

Samuel A. Rose United States

Michael Escamilla United States

Katherine Tooley United States

Dawn L. Thiselton United States

Martin Begemann Germany

Detelina Grozeva United Kingdom

Andrés Ingason

1.2k ×1.4

GENET

857 ×1.4

264 ×1.2

CMN

305 ×1.6

126 ×0.7

ONCOL

Citations per year, relative to Andrés Ingason Andrés Ingason (= 1×) peers Detelina Grozeva

Countries citing papers authored by Andrés Ingason

Since Specialization

Citations

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

Fields of papers citing papers by Andrés Ingason

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Andrés Ingason

This figure shows the co-authorship network connecting the top 25 collaborators of Andrés Ingason. A scholar is included among the top collaborators of Andrés Ingason 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 Andrés Ingason. Andrés Ingason 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

Barroso, Inês, Andrés Ingason, Daniel Stow, et al.. (2025). Contributions of common and rare genetic variation to different measures of mood and anxiety disorder in the UK Biobank. BJPsych Open. 11(3). e97–e97.

Ingason, Andrés, et al.. (2025). The Use of Single-Cell and Spatial Omics to Study Copy Number Variants. Biological Psychiatry. 99(5). 375–386. 1 indexed citations

Ingason, Andrés, Christine Søholm Hansen, Marie Bækvad‐Hansen, et al.. (2023). T56. NEONATAL BLOOD TRANSCRIPTOMICS REVEAL EXPRESSION SIGNATURES OF ADHD RISK. European Neuropsychopharmacology. 75. S191–S192. 1 indexed citations

Appadurai, Vivek, Jonas Bybjerg‐Grauholm, Morten Dybdahl Krebs, et al.. (2023). Accuracy of haplotype estimation and whole genome imputation affects complex trait analyses in complex biobanks. Communications Biology. 6(1). 101–101. 8 indexed citations

Albiñana, Clara, Zhihong Zhu, Andrew J. Schork, et al.. (2023). Multi-PGS enhances polygenic prediction by combining 937 polygenic scores. Nature Communications. 14(1). 4702–4702. 25 indexed citations

Courraud, Julie, Francesco Russo, Gonçalo Espregueira Themudo, et al.. (2023). Metabolic signature of the pathogenic 22q11.2 deletion identifies carriers and provides insight into systemic dysregulation. Translational Psychiatry. 13(1). 391–391.

Krebs, Morten Dybdahl, Preben Bo Mortensen, Anders D. Børglum, et al.. (2023). Associations of psychiatric disorders with sex chromosome aneuploidies in the Danish iPSYCH2015 dataset: a case-cohort study. The Lancet Psychiatry. 10(2). 129–138. 13 indexed citations

Shorter, John, Joeri Meijsen, Ron Nudel, et al.. (2022). Infection Polygenic Factors Account for a Small Proportion of the Relationship Between Infections and Mental Disorders. Biological Psychiatry. 92(4). 283–290. 7 indexed citations

Kogelman, Lisette J. A., Ann-Louise Esserlind, Anne Francke Christensen, et al.. (2019). Migraine polygenic risk score associates with efficacy of migraine-specific drugs. Neurology Genetics. 5(6). e364–e364. 30 indexed citations

10.

Prohaska, Ana, Fernando Racimo, Andrew J. Schork, et al.. (2019). Human Disease Variation in the Light of Population Genomics. Cell. 177(1). 115–131. 52 indexed citations

11.

Mullins, Niamh, Andrés Ingason, Jack Euesden, et al.. (2017). Reproductive fitness and genetic risk of psychiatric disorders in the general population. Nature Communications. 8(1). 15833–15833. 23 indexed citations

12.

Ingason, Andrés, Ina Giegling, Annette M. Hartmann, et al.. (2015). Expression analysis in a rat psychosis model identifies novel candidate genes validated in a large case–control sample of schizophrenia. Translational Psychiatry. 5(10). e656–e656. 25 indexed citations

13.

Duong, Linh T., Louise K. Hoeffding, Kirsten Bruun Petersen, et al.. (2015). Two rare deletions upstream of the NRXN1 gene (2p16.3) affecting the non-coding mRNA AK127244 segregate with diverse psychopathological phenotypes in a family. European Journal of Medical Genetics. 58(12). 650–653. 7 indexed citations

14.

Thygesen, Johan H., Andrés Ingason, Pär Lundin, et al.. (2015). Linkage and whole genome sequencing identify a locus on 6q25–26 for formal thought disorder and implicate MEF2A regulation. Schizophrenia Research. 169(1-3). 441–446. 9 indexed citations

15.

Ettinger, Ulrich, Brynja B. Magnúsdóttir, Thordur Sigmundsson, et al.. (2009). COMT val158met genotype and smooth pursuit eye movements in schizophrenia. Psychiatry Research. 169(2). 173–175. 14 indexed citations

16.

Kong, Augustine, Gísli Másson, Michael L. Frigge, et al.. (2008). Detection of sharing by descent, long-range phasing and haplotype imputation. Nature Genetics. 40(9). 1068–1075. 231 indexed citations

17.

Ettinger, Ulrich, Brynja B. Magnúsdóttir, Thordur Sigmundsson, et al.. (2008). Catechol-O-Methyltransferase Val158Met Polymorphism and Antisaccade Eye Movements in Schizophrenia. Schizophrenia Bulletin. 36(1). 157–164. 30 indexed citations

18.

Ingason, Andrés, Thordur Sigmundsson, Stacy Steinberg, et al.. (2007). Support for involvement of the AHI1 locus in schizophrenia. European Journal of Human Genetics. 15(9). 988–991. 35 indexed citations

19.

Ingason, Andrés, Karen Søeby, Sally Timm, et al.. (2006). No significant association of the 5′ end of neuregulin 1 and schizophrenia in a large Danish sample. Schizophrenia Research. 83(1). 1–5. 18 indexed citations

20.

Li, Tao, Hreinn Stefánsson, Guiqing Cai, et al.. (2004). Identification of a novel neuregulin 1 at-risk haplotype in Han schizophrenia Chinese patients, but no association with the Icelandic/Scottish risk haplotype. Molecular Psychiatry. 9(7). 698–704. 124 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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