Stefan Herms

60.6k total citations
65 papers, 1.6k citations indexed

About

Stefan Herms is a scholar working on Genetics, Molecular Biology and Psychiatry and Mental health. According to data from OpenAlex, Stefan Herms has authored 65 papers receiving a total of 1.6k indexed citations (citations by other indexed papers that have themselves been cited), including 31 papers in Genetics, 28 papers in Molecular Biology and 13 papers in Psychiatry and Mental health. Recurrent topics in Stefan Herms's work include Genetic Associations and Epidemiology (11 papers), Genetics and Neurodevelopmental Disorders (9 papers) and CRISPR and Genetic Engineering (8 papers). Stefan Herms is often cited by papers focused on Genetic Associations and Epidemiology (11 papers), Genetics and Neurodevelopmental Disorders (9 papers) and CRISPR and Genetic Engineering (8 papers). Stefan Herms collaborates with scholars based in Germany, Switzerland and United States. Stefan Herms's co-authors include Per Hoffmann, Markus M. Nöthen, Oliver Brüstle, Thoralf Opitz, Marc Thier, Frank Edenhofer, Philipp Wörsdörfer, Sven Cichon, Uwe Conrath and Philipp Koch and has published in prestigious journals such as Proceedings of the National Academy of Sciences, PLoS ONE and NeuroImage.

In The Last Decade

Stefan Herms

64 papers receiving 1.6k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Stefan Herms Germany 19 909 385 315 209 156 65 1.6k
Kimberly A. Aldinger United States 25 1.3k 1.4× 613 1.6× 344 1.1× 195 0.9× 120 0.8× 48 2.3k
Priscilla D. Negraes Brazil 19 910 1.0× 255 0.7× 409 1.3× 246 1.2× 46 0.3× 34 1.5k
Cleber A. Trujillo United States 25 1.3k 1.5× 375 1.0× 581 1.8× 355 1.7× 59 0.4× 47 2.1k
Nobuko Hagiwara United States 20 1.2k 1.3× 373 1.0× 337 1.1× 94 0.4× 44 0.3× 46 1.9k
Anna Szekely United States 14 1.8k 1.9× 470 1.2× 326 1.0× 293 1.4× 33 0.2× 22 2.3k
Romeo Carrozzo Italy 20 743 0.8× 828 2.2× 313 1.0× 68 0.3× 174 1.1× 37 1.8k
Matthew S. Lawrence United States 27 2.3k 2.5× 401 1.0× 526 1.7× 132 0.6× 122 0.8× 53 3.6k
Naoko Narita Japan 24 1.4k 1.6× 768 2.0× 328 1.0× 99 0.5× 180 1.2× 50 2.6k
Cassiano Carromeu United States 16 1.4k 1.6× 562 1.5× 488 1.5× 275 1.3× 40 0.3× 28 2.0k
Aswin Sekar United States 7 706 0.8× 515 1.3× 270 0.9× 81 0.4× 239 1.5× 11 2.0k

Countries citing papers authored by Stefan Herms

Since Specialization
Citations

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

Fields of papers citing papers by Stefan Herms

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Stefan Herms

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

All Works

20 of 20 papers shown
1.
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
2.
Geiger, Lena S., Torsten Wüstenberg, Zhenxiang Zang, et al.. (2024). Longitudinal markers of cognitive procedural learning in fronto-striatal circuits and putative effects of a BDNF plasticity-related variant. npj Science of Learning. 9(1). 72–72. 1 indexed citations
3.
Czerski, Piotr M., Beata Narożna, Monika Dmitrzak‐Węglarz, et al.. (2023). Abelson Helper Integration Site 1 haplotypes and peripheral blood expression associates with lithium response and immunomodulation in bipolar patients. Psychopharmacology. 241(4). 727–738. 2 indexed citations
4.
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
5.
Hoffmann, Per, et al.. (2023). Generation of induced pluripotent stem cells from two ADHD patients and two healthy controls. Stem Cell Research. 69. 103084–103084. 4 indexed citations
6.
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
7.
Herms, Stefan, Sugirthan Sivalingam, Heiko Reutter, et al.. (2021). Genome-Wide Survey for Microdeletions or -Duplications in 155 Patients with Lower Urinary Tract Obstructions (LUTO). Genes. 12(9). 1449–1449. 4 indexed citations
8.
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
9.
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
10.
Thomsen, Hauke, Bowang Chen, Gisella Figlioli, et al.. (2016). Runs of homozygosity and inbreeding in thyroid cancer. BMC Cancer. 16(1). 227–227. 17 indexed citations
11.
Fatima, Azra, Dina Ivanyuk, Stefan Herms, et al.. (2016). Generation of human induced pluripotent stem cell line from a patient with a long QT syndrome type 2. Stem Cell Research. 16(2). 304–307. 11 indexed citations
12.
Thomsen, Hauke, Miguel Inácio da Silva Filho, Robert Johansson, et al.. (2015). Inbreeding and homozygosity in breast cancer survival. Scientific Reports. 5(1). 16467–16467. 5 indexed citations
13.
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
14.
Haenisch, Britta, Stefan Herms, & Gerhard J. Molderings. (2013). The transcriptome of the human mast cell leukemia cells HMC-1.2: an approach to identify specific changes in the gene expression profile in KitD816V systemic mastocytosis. Immunologic Research. 56(1). 155–162. 6 indexed citations
15.
Redler, Silke, F.F. Brockschmidt, Rachid Tazi‐Ahnini, et al.. (2012). Investigation of the male pattern baldness major genetic susceptibility loci AR/EDA2R and 20p11 in female pattern hair loss. British Journal of Dermatology. 166(6). 1314–1318. 36 indexed citations
16.
Thier, Marc, Philipp Wörsdörfer, Stefan Herms, et al.. (2012). Direct Conversion of Fibroblasts into Stably Expandable Neural Stem Cells. Cell stem cell. 10(4). 473–479. 402 indexed citations
17.
Nieratschker, Vanessa, Josef Frank, Thomas W. Mühleisen, et al.. (2010). The catechol-O-methyl transferase (COMT) gene and its potential association with schizophrenia: Findings from a large German case-control and family-based sample. Schizophrenia Research. 122(1-3). 24–30. 20 indexed citations
18.
Steffens, Michael, Tim Becker, Thomas Sander, et al.. (2010). Feasible and Successful: Genome-Wide Interaction Analysis Involving All 1.9 × 10<sup>11</sup> Pair-Wise Interaction Tests. Human Heredity. 69(4). 268–284. 19 indexed citations
19.
Strohmaier, Jana, Josef Frank, Jens R. Wendland, et al.. (2010). A reappraisal of the association between Dysbindin (DTNBP1) and schizophrenia in a large combined case–control and family-based sample of German ancestry. Schizophrenia Research. 118(1-3). 98–105. 16 indexed citations
20.
Nikopensius, Tiit, Laima Ambrozaitytė, Kerstin U. Ludwig, et al.. (2009). Replication of novel susceptibility locus for nonsyndromic cleft lip with or without cleft palate on chromosome 8q24 in Estonian and Lithuanian patients. American Journal of Medical Genetics Part A. 149A(11). 2551–2553. 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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