Thomas Werge

12.3k total citations
11 papers, 741 citations indexed

About

Thomas Werge is a scholar working on Genetics, Molecular Biology and Psychiatry and Mental health. According to data from OpenAlex, Thomas Werge has authored 11 papers receiving a total of 741 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Genetics, 3 papers in Molecular Biology and 2 papers in Psychiatry and Mental health. Recurrent topics in Thomas Werge's work include Genetic Associations and Epidemiology (6 papers), Genomics and Rare Diseases (3 papers) and Genetic Mapping and Diversity in Plants and Animals (3 papers). Thomas Werge is often cited by papers focused on Genetic Associations and Epidemiology (6 papers), Genomics and Rare Diseases (3 papers) and Genetic Mapping and Diversity in Plants and Animals (3 papers). Thomas Werge collaborates with scholars based in Denmark, United States and Norway. Thomas Werge's co-authors include Ole A. Andreassen, Andrew J. Schork, Anders M. Dale, Wesley K. Thompson, Srdjan Djurovic, Michael O’Donovan, Linda K. McEvoy, J. Cooper Roddey, Dan Rujescu and Andrew P. Morris and has published in prestigious journals such as PLoS ONE, Biological Psychiatry and The American Journal of Human Genetics.

In The Last Decade

Thomas Werge

11 papers receiving 732 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Thomas Werge Denmark	7	439	225	160	70	68	11	741
Kathleen Hodgkinson Canada	15	505 1.2×	428 1.9×	97 0.6×	68 1.0×	128 1.9×	23	1.0k
Sally L. Ricketts United Kingdom	11	272 0.6×	228 1.0×	350 2.2×	40 0.6×	202 3.0×	29	1.0k
Kimberley Kendall United Kingdom	14	589 1.3×	344 1.5×	136 0.8×	31 0.4×	138 2.0×	28	883
Po‐Chang Hsiao Taiwan	14	159 0.4×	206 0.9×	99 0.6×	55 0.8×	88 1.3×	33	603
Nicholas Craddock United Kingdom	10	331 0.8×	204 0.9×	163 1.0×	25 0.4×	53 0.8×	21	707
Matthew Bracher‐Smith United Kingdom	13	346 0.8×	190 0.8×	139 0.9×	53 0.8×	122 1.8×	23	667
L. Giuffra United States	12	393 0.9×	201 0.9×	149 0.9×	29 0.4×	110 1.6×	23	797
Derek Spieler Germany	14	151 0.3×	302 1.3×	57 0.4×	22 0.3×	38 0.6×	22	763
Christina M. Hultman Sweden	11	220 0.5×	296 1.3×	104 0.7×	34 0.5×	65 1.0×	12	539
Martina Durner United States	15	507 1.2×	288 1.3×	402 2.5×	38 0.5×	70 1.0×	29	960

Countries citing papers authored by Thomas Werge

Since Specialization

Citations

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

Fields of papers citing papers by Thomas Werge

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Thomas Werge

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

All Works

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11 of 11 papers shown

Nielsen, Trine Tollerup, Jakob Grove, Christina Mohr Jensen, et al.. (2025). Genetic Architecture and Risk of Childhood Maltreatment Across 5 Psychiatric Diagnoses. JAMA Psychiatry. 82(8). 790–790. 1 indexed citations

Borbye‐Lorenzen, Nis, Filip Ottosson, Ron Nudel, et al.. (2024). High level of immunoglobulin G targeting mycoplasma or cytomegalovirus in the newborn increases risk of ADHD. Brain Behavior and Immunity. 123. 99–107. 2 indexed citations

Nielsen, Trine Tollerup, Jinjie Duan, Daniel F. Levey, et al.. (2024). Shared genetics of ADHD, cannabis use disorder and cannabis use and prediction of cannabis use disorder in ADHD. Nature Mental Health. 2(9). 1071–1083. 1 indexed citations

Krebs, Morten Dybdahl, Preben Bo Mortensen, Anders D. Børglum, et al.. (2022). Sex Chromosome Aneuploidies are Underdiagnosed and Associated with Increased Risk of Mental Disorders. SSRN Electronic Journal. 1 indexed citations

Holland, Dominic, Yunpeng Wang, Wesley K. Thompson, et al.. (2016). Estimating Effect Sizes and Expected Replication Probabilities from GWAS Summary Statistics. Frontiers in Genetics. 7. 15–15. 27 indexed citations

Thompson, Wesley K., Yunpeng Wang, Andrew J. Schork, et al.. (2015). An Empirical Bayes Mixture Model for Effect Size Distributions in Genome-Wide Association Studies. PLoS Genetics. 11(12). e1005717–e1005717. 14 indexed citations

Bettella, Francesco, Morten Mattingsdal, Yunpeng Wang, et al.. (2015). Genetic Markers of Human Evolution Are Enriched in Schizophrenia. Biological Psychiatry. 80(4). 284–292. 77 indexed citations

Andreassen, Ole A., Wesley K. Thompson, Andrew J. Schork, et al.. (2013). Improved Detection of Common Variants Associated with Schizophrenia and Bipolar Disorder Using Pleiotropy-Informed Conditional False Discovery Rate. PLoS Genetics. 9(4). e1003455–e1003455. 233 indexed citations

Christoforou, Andrea, Sudheer Giddaluru, Kari M. Ersland, et al.. (2013). A Genetic Deconstruction of Neurocognitive Traits in Schizophrenia and Bipolar Disorder. PLoS ONE. 8(12). e81052–e81052. 16 indexed citations

10.

Andreassen, Ole A., Srdjan Djurovic, Wesley K. Thompson, et al.. (2013). Improved Detection of Common Variants Associated with Schizophrenia by Leveraging Pleiotropy with Cardiovascular-Disease Risk Factors. The American Journal of Human Genetics. 92(2). 197–209. 339 indexed citations

11.

Kähler, Anna K., Thomas Folkmann Hansen, Erik G. Jönsson, et al.. (2009). Association study of PDE4B gene variants in scandinavian schizophrenia and bipolar disorder multicenter case–control samples. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 153B(1). 86–96. 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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