Per Hoffmann

48.2k total citations
158 papers, 3.6k citations indexed

About

Per Hoffmann is a scholar working on Genetics, Molecular Biology and Psychiatry and Mental health. According to data from OpenAlex, Per Hoffmann has authored 158 papers receiving a total of 3.6k indexed citations (citations by other indexed papers that have themselves been cited), including 59 papers in Genetics, 55 papers in Molecular Biology and 13 papers in Psychiatry and Mental health. Recurrent topics in Per Hoffmann's work include Genetic Associations and Epidemiology (23 papers), Genetics and Neurodevelopmental Disorders (19 papers) and Reading and Literacy Development (12 papers). Per Hoffmann is often cited by papers focused on Genetic Associations and Epidemiology (23 papers), Genetics and Neurodevelopmental Disorders (19 papers) and Reading and Literacy Development (12 papers). Per Hoffmann collaborates with scholars based in Germany, Switzerland and United States. Per Hoffmann's co-authors include Markus M. Nöthen, Stefan Herms, Gerd Schulte‐Körne, Oliver Brüstle, Johannes Schumacher, Bertram Müller‐Myhsok, Marc Thier, Frank Edenhofer, Kerstin U. Ludwig and Philipp Wörsdörfer and has published in prestigious journals such as Nature, The Journal of Immunology and PLoS ONE.

In The Last Decade

Per Hoffmann

149 papers receiving 3.4k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Per Hoffmann Germany	34	1.6k	845	459	425	335	158	3.6k
Lisbeth Tranebjærg Denmark	43	3.6k 2.3×	2.3k 2.7×	643 1.4×	147 0.3×	415 1.2×	163	6.7k
Mark Johnson United Kingdom	30	2.7k 1.7×	469 0.6×	428 0.9×	70 0.2×	260 0.8×	55	5.0k
Maria Bitner‐Glindzicz United Kingdom	37	3.2k 2.0×	761 0.9×	319 0.7×	103 0.2×	395 1.2×	94	5.1k
Heather Gordish‐Dressman United States	40	2.6k 1.7×	1.1k 1.3×	311 0.7×	113 0.3×	436 1.3×	179	5.2k
Kimberly F. Doheny United States	28	1.8k 1.2×	1.3k 1.5×	471 1.0×	47 0.1×	240 0.7×	48	3.8k
Kevin M. Flanigan United States	45	5.6k 3.6×	1.2k 1.4×	1.2k 2.5×	238 0.6×	483 1.4×	189	7.3k
Annick Toutain France	36	2.5k 1.6×	1.5k 1.8×	469 1.0×	46 0.1×	455 1.4×	138	4.0k
Richard J. Sinke Netherlands	39	2.2k 1.4×	1.2k 1.4×	1.2k 2.6×	43 0.1×	491 1.5×	119	4.4k
Paula R. Clemens United States	38	5.9k 3.8×	1.7k 2.0×	671 1.5×	341 0.8×	558 1.7×	116	7.8k
Francesco Muntoni United Kingdom	50	5.1k 3.3×	687 0.8×	1.6k 3.5×	196 0.5×	782 2.3×	250	7.5k

Countries citing papers authored by Per Hoffmann

Since Specialization

Citations

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

Fields of papers citing papers by Per Hoffmann

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Per Hoffmann

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

Glässner, A, Michael Steffens, Gerda Wurpts, et al.. (2025). Analysis of differential gene expression of PBMC for the in vitro detection of drug sensitization. Allergology International. 74(3). 414–423.

Hench, Juergen, Stephan Frank, Per Hoffmann, et al.. (2025). DNA Methylation Array Analysis Identifies Biological Subgroups of Cutaneous Melanoma and Reveals Extensive Differences with Benign Melanocytic Nevi. Diagnostics. 15(5). 531–531. 1 indexed citations

Philipsen, Alexandra, Allan H. Young, Mário F. Juruena, et al.. (2024). A New Intervention for Implementation of Pharmacogenetics in Psychiatry: A Description of the PSY-PGx Clinical Study. Pharmaceuticals. 17(2). 151–151. 8 indexed citations

Thomsen, Hauke, Subhayan Chattopadhyay, Niels Weinhold, et al.. (2024). Haplotype analysis identifies functional elements in monoclonal gammopathy of unknown significance. Blood Cancer Journal. 14(1). 140–140. 1 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

Zillich, Lea, Josef Frank, Jerome C. Foo, et al.. (2022). Multi-omics signatures of alcohol use disorder in the dorsal and ventral striatum. Translational Psychiatry. 12(1). 190–190. 16 indexed citations

Hoffmann, Per, et al.. (2021). Generation of integration-free induced pluripotent stem cell lines from four pediatric ADHD patients. Stem Cell Research. 53. 102268–102268. 9 indexed citations

Pechlivanis, Sonali, Susanne Moebus, Nils Lehmann, et al.. (2021). Pharmacogenetic association of diabetes-associated genetic risk score with rapid progression of coronary artery calcification following treatment with HMG-CoA-reductase inhibitors —results of the Heinz Nixdorf Recall Study. Naunyn-Schmiedeberg s Archives of Pharmacology. 394(8). 1713–1725. 5 indexed citations

Zillich, Lea, Josef Frank, Fabian Streit, et al.. (2021). Epigenome-wide association study of alcohol use disorder in five brain regions. Neuropsychopharmacology. 47(4). 832–839. 20 indexed citations

10.

Nashef, Aysar, Matthias Munz, Ervin I. Weiss, et al.. (2020). Translation of mouse model to human gives insights into periodontitis etiology. Scientific Reports. 10(1). 4892–4892. 15 indexed citations

11.

Jäger, Susanne, Rafael R. C. Cuadrat, Clemens Wittenbecher, et al.. (2020). Mendelian Randomization Study on Amino Acid Metabolism Suggests Tyrosine as Causal Trait for Type 2 Diabetes. Nutrients. 12(12). 3890–3890. 8 indexed citations

12.

Jäger, Susanne, Rafael R. C. Cuadrat, Per Hoffmann, Clemens Wittenbecher, & Matthias B. Schulze. (2020). Desaturase Activity and the Risk of Type 2 Diabetes and Coronary Artery Disease: A Mendelian Randomization Study. Nutrients. 12(8). 2261–2261. 16 indexed citations

13.

Herms, Stefan, Per Hoffmann, Sven Cichon, et al.. (2020). Gene expression is stable in a complete CIB1 knockout keratinocyte model. Scientific Reports. 10(1). 14952–14952. 3 indexed citations

14.

Fickl, Stefan, Fabian Hüttig, André Heimbach, et al.. (2018). The severity of human peri‐implantitis lesions correlates with the level of submucosal microbial dysbiosis. Journal Of Clinical Periodontology. 45(12). 1498–1509. 69 indexed citations

15.

Giddaluru, Sudheer, Francesco Bettella, Thomas Espeseth, et al.. (2017). Analysis of the joint effect of SNPs to identify independent loci and allelic heterogeneity in schizophrenia GWAS data. Translational Psychiatry. 7(12). 1289–1289. 5 indexed citations

16.

Fernández‐Rebollo, Eduardo, Birgit Mentrup, Regina Ebert, et al.. (2017). Human Platelet Lysate versus Fetal Calf Serum: These Supplements Do Not Select for Different Mesenchymal Stromal Cells. Scientific Reports. 7(1). 5132–5132. 65 indexed citations

17.

Jäger, Susanne, Simone Wahl, Janine Kröger, et al.. (2017). Genetic variants including markers from the exome chip and metabolite traits of type 2 diabetes. Scientific Reports. 7(1). 6037–6037. 11 indexed citations

18.

Nokhbehsaim, Marjan, Sigrun Eick, Andressa Vilas Boas Nogueira, et al.. (2013). Stimulation of MMP-1 and CCL2 by NAMPT in PDL Cells. Mediators of Inflammation. 2013. 1–12. 42 indexed citations

19.

Stich, Benjamin, Claude Urbany, Per Hoffmann, & Christiane Gebhardt. (2013). Population structure and linkage disequilibrium in diploid and tetraploid potato revealed by genome‐wide high‐density genotyping using the SolCAP SNP array. Plant Breeding. 132(6). 718–724. 39 indexed citations

20.

Wilcke, Arndt, Carolin Ligges, Jana Burkhardt, et al.. (2011). Imaging genetics of FOXP2 in dyslexia. European Journal of Human Genetics. 20(2). 224–229. 40 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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