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

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

#	Title	Journal	Authors	Indexed citations
1	Contributions of common and rare genetic variation to different measures of mood and anxiety disorder in the UK Biobank	BJPsych Open	Inês Barroso, Andrés Ingason et al.	0
2	The Use of Single-Cell and Spatial Omics to Study Copy Number Variants	Biological Psychiatry	Andrés Ingason, Konstantin Khodosevich et al.	1
3	T56. NEONATAL BLOOD TRANSCRIPTOMICS REVEAL EXPRESSION SIGNATURES OF ADHD RISK	European Neuropsychopharmacology	Andrés Ingason, Christine Søholm Hansen et al.	1
4	Accuracy of haplotype estimation and whole genome imputation affects complex trait analyses in complex biobanks	Communications Biology	Vivek Appadurai, Jonas Bybjerg‐Grauholm et al.	8
5	Multi-PGS enhances polygenic prediction by combining 937 polygenic scores	Nature Communications	Clara Albiñana, Zhihong Zhu et al.	25
6	Metabolic signature of the pathogenic 22q11.2 deletion identifies carriers and provides insight into systemic dysregulation	Translational Psychiatry	Julie Courraud, Francesco Russo et al.	0
7	Associations of psychiatric disorders with sex chromosome aneuploidies in the Danish iPSYCH2015 dataset: a case-cohort study	The Lancet Psychiatry	Morten Dybdahl Krebs, Preben Bo Mortensen et al.	13
8	Infection Polygenic Factors Account for a Small Proportion of the Relationship Between Infections and Mental Disorders	Biological Psychiatry	John Shorter, Joeri Meijsen et al.	7
9	Migraine polygenic risk score associates with efficacy of migraine-specific drugs	Neurology Genetics	Lisette J. A. Kogelman, Ann-Louise Esserlind et al.	30
10	Human Disease Variation in the Light of Population Genomics	Cell	Ana Prohaska, Fernando Racimo et al.	52
11	Reproductive fitness and genetic risk of psychiatric disorders in the general population	Nature Communications	Niamh Mullins, Andrés Ingason et al.	23
12	Expression analysis in a rat psychosis model identifies novel candidate genes validated in a large case–control sample of schizophrenia	Translational Psychiatry	Andrés Ingason, Ina Giegling et al.	25
13	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	Linh T. Duong, Louise K. Hoeffding et al.	7
14	Linkage and whole genome sequencing identify a locus on 6q25–26 for formal thought disorder and implicate MEF2A regulation	Schizophrenia Research	Johan H. Thygesen, Andrés Ingason et al.	9
15	COMT val158met genotype and smooth pursuit eye movements in schizophrenia	Psychiatry Research	Ulrich Ettinger, Brynja B. Magnúsdóttir et al.	14
16	Detection of sharing by descent, long-range phasing and haplotype imputation	Nature Genetics	Augustine Kong, Gísli Másson et al.	231
17	Catechol-O-Methyltransferase Val158Met Polymorphism and Antisaccade Eye Movements in Schizophrenia	Schizophrenia Bulletin	Ulrich Ettinger, Brynja B. Magnúsdóttir et al.	30
18	Support for involvement of the AHI1 locus in schizophrenia	European Journal of Human Genetics	Andrés Ingason, Thordur Sigmundsson et al.	35
19	No significant association of the 5′ end of neuregulin 1 and schizophrenia in a large Danish sample	Schizophrenia Research	Andrés Ingason, Karen Søeby et al.	18
20	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	Tao Li, Hreinn Stefánsson et al.	124

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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