Andreas J. Forstner

27.1k total citations
54 papers, 412 citations indexed

About

Andreas J. Forstner is a scholar working on Genetics, Experimental and Cognitive Psychology and Clinical Psychology. According to data from OpenAlex, Andreas J. Forstner has authored 54 papers receiving a total of 412 indexed citations (citations by other indexed papers that have themselves been cited), including 23 papers in Genetics, 16 papers in Experimental and Cognitive Psychology and 15 papers in Clinical Psychology. Recurrent topics in Andreas J. Forstner's work include Genetic Associations and Epidemiology (16 papers), Child and Adolescent Psychosocial and Emotional Development (12 papers) and Genetics and Neurodevelopmental Disorders (11 papers). Andreas J. Forstner is often cited by papers focused on Genetic Associations and Epidemiology (16 papers), Child and Adolescent Psychosocial and Emotional Development (12 papers) and Genetics and Neurodevelopmental Disorders (11 papers). Andreas J. Forstner collaborates with scholars based in Germany, Switzerland and United States. Andreas J. Forstner's co-authors include Markus M. Nöthen, Franziska Degenhardt, Marcella Rietschel, Gerhard Schratt, Stephanie H. Witt, Johannes Schumacher, Franziska Geiser, Rupert Conrad, Josef Frank and Fabian Streit and has published in prestigious journals such as PLoS ONE, NeuroImage and Neuropsychopharmacology.

In The Last Decade

Andreas J. Forstner

45 papers receiving 406 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Andreas J. Forstner Germany	13	97	92	79	75	69	54	412
Laura M. Huckins United States	13	126 1.3×	169 1.8×	107 1.4×	61 0.8×	35 0.5×	41	511
Dubravka Jancic United States	9	91 0.9×	141 1.5×	102 1.3×	127 1.7×	40 0.6×	11	447
Maria Tropeano United Kingdom	11	98 1.0×	150 1.6×	96 1.2×	55 0.7×	64 0.9×	13	372
Kathrin Schwarte Germany	12	163 1.7×	56 0.6×	207 2.6×	80 1.1×	69 1.0×	25	639
Ümit Işık Türkiye	12	91 0.9×	39 0.4×	81 1.0×	131 1.7×	22 0.3×	43	431
Justin D. Tubbs Hong Kong	11	50 0.5×	86 0.9×	75 0.9×	27 0.4×	51 0.7×	23	312
Julia Perry United Kingdom	7	71 0.7×	85 0.9×	40 0.5×	81 1.1×	26 0.4×	9	266
Lucas Kempf United States	7	47 0.5×	90 1.0×	107 1.4×	78 1.0×	67 1.0×	14	463
I. Másala Italy	14	136 1.4×	34 0.4×	59 0.7×	88 1.2×	64 0.9×	31	374
Diana M. Ciuculete Sweden	15	83 0.9×	55 0.6×	155 2.0×	34 0.5×	26 0.4×	18	368

Countries citing papers authored by Andreas J. Forstner

Since Specialization

Citations

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

Fields of papers citing papers by Andreas J. Forstner

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Andreas J. Forstner. 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 Andreas J. Forstner. The network helps show where Andreas J. Forstner may publish in the future.

Co-authorship network of co-authors of Andreas J. Forstner

This figure shows the co-authorship network connecting the top 25 collaborators of Andreas J. Forstner. A scholar is included among the top collaborators of Andreas J. Forstner 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 Andreas J. Forstner. Andreas J. Forstner 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

Forstner, Andreas J., et al.. (2025). Recalled parental behavior of women and men with social anxiety disorder – The importance of the father-child relationship. Journal of Psychiatric Research. 190. 540–546. 1 indexed citations

Sindermann, Lisa, Federico Raimondo, Konrad Oexle, et al.. (2025). Neurobiological correlates of schizophrenia-specific and highly pleiotropic genetic risk scores for neuropsychiatric disorders. Translational Psychiatry. 15(1). 230–230.

Willoughby, Emily A., Carlo Maj, Rafael Ahlskog, et al.. (2025). Within- and between-family genetic effects on educational achievement vary across countries and ages. Molecular Psychiatry. 31(4). 2029–2037.

Meller, Tina, Catarina Lundberg, Carlo Maj, et al.. (2025). Schizotypy, Psychosis Proneness, and the Polygenic Risk for Schizophrenia and Resilience. Schizophrenia Bulletin. 51(Supplement_2). S85–S94. 2 indexed citations

Kandler, Christian, et al.. (2024). A Multidisciplinary Perspective on Person-Environment Fit: Relevance, Measurement, and Future Directions. Current Directions in Psychological Science. 33(3). 198–205. 6 indexed citations

Meisenzahl, Eva, Natalia Wege, Gerd Schulte‐Körne, et al.. (2024). Clinical high risk state of major depressive episodes: Assessment of prodromal phase, its occurrence, duration and symptom patterns by the instrument the DEpression Early Prediction-INventory (DEEP-IN). Journal of Affective Disorders. 351. 403–413. 3 indexed citations

Zhao, Ling, Thomas W. Mühleisen, Bettina Burger, et al.. (2023). Relationships between neurotransmitter receptor densities and expression levels of their corresponding genes in the human hippocampus. NeuroImage. 273. 120095–120095. 5 indexed citations

Foo, Jerome C., Silke Redler, Andreas J. Forstner, et al.. (2023). Exploring the overlap between alopecia areata and major depressive disorder: Epidemiological and genetic perspectives. Journal of the European Academy of Dermatology and Venereology. 37(8). 1547–1555. 4 indexed citations

Sirignano, Lea, Fabian Streit, Jerome C. Foo, et al.. (2023). Impulsivity, decision‐making, and risk behavior in bipolar disorder and major depression from bipolar multiplex families. Brain and Behavior. 14(2). e3337–e3337. 4 indexed citations

10.

Spier, Isabel, Hannah Klinkhammer, Friederike S. David, et al.. (2023). Clinically relevant combined effect of polygenic background, rare pathogenic germline variants, and family history on colorectal cancer incidence. BMC Medical Genomics. 16(1). 42–42. 12 indexed citations

11.

Beins, Eva C., Kathrin Schwarte, Carlo Maj, et al.. (2022). Chemokine receptor 4 expression on blood T lymphocytes predicts severity of major depressive disorder. Journal of Affective Disorders. 310. 343–353. 3 indexed citations

12.

Heilbronner, Urs, Sergi Papiol, Monika Budde, et al.. (2021). “The Heidelberg Five” personality dimensions: Genome‐wide associations, polygenic risk for neuroticism, and psychopathology 20 years after assessment. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 186(2). 77–89. 4 indexed citations

13.

Frank, Mirjam, Nico Dragano, Marina Arendt, et al.. (2019). A genetic sum score of risk alleles associated with body mass index interacts with socioeconomic position in the Heinz Nixdorf Recall Study. PLoS ONE. 14(8). e0221252–e0221252. 10 indexed citations

14.

Grigoroiu‐Serbânescu, Maria, Giovanni Giaroli, Johan H. Thygesen, et al.. (2019). Predictive power of the ADHD GWAS 2019 polygenic risk scores in independent samples of bipolar patients with childhood ADHD. Journal of Affective Disorders. 265. 651–659. 13 indexed citations

15.

Martin, Jessica, Fabian Streit, Jens Treutlein, et al.. (2017). Expert and self-assessment of lifetime symptoms and diagnosis of major depressive disorder in large-scale genetic studies in the general population. Psychiatric Genetics. 27(5). 187–196. 12 indexed citations

16.

Yüksel, Dilara, Bruno Dietsche, Andreas J. Forstner, et al.. (2017). Polygenic risk for depression and the neural correlates of working memory in healthy subjects. Progress in Neuro-Psychopharmacology and Biological Psychiatry. 79(Pt B). 67–76. 17 indexed citations

17.

Forstner, Andreas J., Kerstin U. Ludwig, Anne C. Böhmer, et al.. (2017). Further evidence for genetic variation at the serotonin transporter gene SLC6A4 contributing toward anxiety. Psychiatric Genetics. 27(3). 96–102. 24 indexed citations

18.

Budde, Monika, Andreas J. Forstner, Kristina Adorjan, et al.. (2017). Genetische Grundlagen der bipolaren Störung. Der Nervenarzt. 88(7). 755–759. 9 indexed citations

19.

Heilbronner, Urs, Dörthe Malzahn, Jana Strohmaier, et al.. (2015). A common risk variant in CACNA1C supports a sex-dependent effect on longitudinal functioning and functional recovery from episodes of schizophrenia-spectrum but not bipolar disorder. European Neuropsychopharmacology. 25(12). 2262–2270. 11 indexed citations

20.

Forstner, Andreas J., Franziska Degenhardt, Gerhard Schratt, & Markus M. Nöthen. (2013). MicroRNAs as the cause of schizophrenia in 22q11.2 deletion carriers, and possible implications for idiopathic disease: a mini-review. Frontiers in Molecular Neuroscience. 6. 47–47. 41 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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