Bertram Müller‐Myhsok

59.2k total citations · 1 hit paper
197 papers, 8.7k citations indexed

About

Bertram Müller‐Myhsok is a scholar working on Genetics, Molecular Biology and Epidemiology. According to data from OpenAlex, Bertram Müller‐Myhsok has authored 197 papers receiving a total of 8.7k indexed citations (citations by other indexed papers that have themselves been cited), including 56 papers in Genetics, 44 papers in Molecular Biology and 24 papers in Epidemiology. Recurrent topics in Bertram Müller‐Myhsok's work include Genetic Associations and Epidemiology (24 papers), Stress Responses and Cortisol (22 papers) and Reading and Literacy Development (17 papers). Bertram Müller‐Myhsok is often cited by papers focused on Genetic Associations and Epidemiology (24 papers), Stress Responses and Cortisol (22 papers) and Reading and Literacy Development (17 papers). Bertram Müller‐Myhsok collaborates with scholars based in Germany, United Kingdom and United States. Bertram Müller‐Myhsok's co-authors include Marcus Ising, Manfred Uhr, Susanne Lucae, Elisabeth B. Binder, Thomas Gasser, Benno Pütz, Stefan Kloiber, Darina Czamara, Gerd Schulte‐Körne and Juliane Winkelmann and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nature Communications and Neuron.

In The Last Decade

Bertram Müller‐Myhsok

192 papers receiving 8.5k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

SKP2 attenuates autophagy through Beclin1-ubiquitination and its inhibition reduces MERS-Coronavirus infection

2019 272 citations Nils C. Gassen, Bertram Müller‐Myhsok et al. profile →

Peers

Bertram Müller‐Myhsok

GENET

NEURO

CMN

Günter K. Stalla Germany

Robert H. Lipsky United States

Ian Everall United Kingdom

A. Dessa Sadovnick Canada

Jacob Raber United States

Dan Rujescu Germany

Taishiro Kishimoto Japan

Kazuhiko Nakamura Japan

Andreas Papassotiropoulos Switzerland

Ke Xu United States

Günter K. Stalla Germany

Bertram Müller‐Myhsok

2.5k ×1.3

840 ×0.5

GENET

948 ×0.7

NEURO

1.7k ×1.5

1.2k ×1.2

CMN

Citations per year, relative to Bertram Müller‐Myhsok Bertram Müller‐Myhsok (= 1×) peers Günter K. Stalla

Countries citing papers authored by Bertram Müller‐Myhsok

Since Specialization

Citations

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

Fields of papers citing papers by Bertram Müller‐Myhsok

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Bertram Müller‐Myhsok. 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 Bertram Müller‐Myhsok. The network helps show where Bertram Müller‐Myhsok may publish in the future.

Co-authorship network of co-authors of Bertram Müller‐Myhsok

This figure shows the co-authorship network connecting the top 25 collaborators of Bertram Müller‐Myhsok. A scholar is included among the top collaborators of Bertram Müller‐Myhsok 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 Bertram Müller‐Myhsok. Bertram Müller‐Myhsok 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

Ising, Marcus, et al.. (2025). Development of a Genetic Test Indicating Increased AVP/V1b Signalling in Patients with Acute Depression. Pharmacopsychiatry. 58(3). 132–138. 1 indexed citations

Rokicki, Jaroslav, Dominic Dwyer, Sergi Papiol, et al.. (2024). Multimodal workflows optimally predict response to repetitive transcranial magnetic stimulation in patients with schizophrenia: a multisite machine learning analysis. Translational Psychiatry. 14(1). 196–196. 7 indexed citations

Bordes, Joeri, Thomas Bajaj, Margherita Springer, et al.. (2024). Sex-specific fear acquisition following early life stress is linked to amygdala and hippocampal purine and glutamate metabolism. Communications Biology. 7(1). 1684–1684. 2 indexed citations

Li, Ling, et al.. (2024). Integration of a polygenic score into guideline-recommended prediction of cardiovascular disease. European Heart Journal. 45(20). 1843–1852. 23 indexed citations

Bordes, Joeri, et al.. (2023). DeepOF: a Python package for supervised andunsupervised pattern recognition in mice motion tracking data. The Journal of Open Source Software. 8(86). 5394–5394. 6 indexed citations

Fontana, Vanessa, Richard M. Turner, Ben Francis, et al.. (2022). Chromosomal Region 11p14.1 is Associated with Pharmacokinetics and Pharmacodynamics of Bisoprolol. Pharmacogenomics and Personalized Medicine. Volume 15. 249–260. 6 indexed citations

Moser, Sylvain, Jade Martins, Darina Czamara, et al.. (2022). DNA-methylation dynamics across short-term, exposure-containing CBT in patients with panic disorder. Translational Psychiatry. 12(1). 46–46. 10 indexed citations

Care, Angharad, Juhi Gupta, Laura Goodfellow, et al.. (2021). Maternal selenium levels and whole genome screen in recurrent spontaneous preterm birth population: A nested case control study. European Journal of Obstetrics & Gynecology and Reproductive Biology. 265. 203–211. 2 indexed citations

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

10.

Chaichoompu, Kridsadakorn, Fentaw Abegaz, Bruno Cavadas, et al.. (2019). A different view on fine-scale population structure in Western African populations. Human Genetics. 139(1). 45–59. 12 indexed citations

11.

Mehta, Divya, Torsten Klengel, Karen N. Conneely, et al.. (2013). Childhood maltreatment is associated with distinct genomic and epigenetic profiles in posttraumatic stress disorder. Proceedings of the National Academy of Sciences. 110(20). 8302–8307. 365 indexed citations

12.

Ludwig, Kerstin U., Philipp G. Sämann, Michael P. Alexander, et al.. (2013). A common variant in Myosin-18B contributes to mathematical abilities in children with dyslexia and intraparietal sulcus variability in adults. Translational Psychiatry. 3(2). e229–e229. 24 indexed citations

13.

Sarapas, Casey, Guiqing Cai, Linda M. Bierer, et al.. (2011). Genetic markers for PTSD risk and resilience among survivors of the World Trade Center attacks.. SHILAP Revista de lepidopterología. 30(2-3). 101–10. 100 indexed citations

14.

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

15.

Klengel, Torsten, Angela Heck, Hildegard Pfister, et al.. (2011). Somatization in major depression - clinical features and genetic associations. Acta Psychiatrica Scandinavica. 124(4). 317–328. 23 indexed citations

16.

Menke, Andreas, Katharina Domschke, Darina Czamara, et al.. (2011). Genome-Wide Association Study of Antidepressant Treatment-Emergent Suicidal Ideation. Neuropsychopharmacology. 37(3). 797–807. 51 indexed citations

17.

Kam-Thong, Tony, Darina Czamara, Koji Tsuda, et al.. (2010). EPIBLASTER-fast exhaustive two-locus epistasis detection strategy using graphical processing units. European Journal of Human Genetics. 19(4). 465–471. 67 indexed citations

18.

Unschuld, Paul G., Marcus Ising, Darina Roeske, et al.. (2010). Gender-Specific Association of Galanin Polymorphisms with HPA-Axis Dysregulation, Symptom Severity, and Antidepressant Treatment Response. Neuropsychopharmacology. 35(7). 1583–1592. 48 indexed citations

19.

Glas, Jürgen, Johannes Stallhofer, Stephan Ripke, et al.. (2009). Novel Genetic Risk Markers for Ulcerative Colitis in the IL2/IL21 Region Are in Epistasis With IL23R and Suggest a Common Genetic Background for Ulcerative Colitis and Celiac Disease. The American Journal of Gastroenterology. 104(7). 1737–1744. 63 indexed citations

20.

Schürmann, Manfred, et al.. (2001). Results from a Genome-wide Search for Predisposing Genes in Sarcoidosis. American Journal of Respiratory and Critical Care Medicine. 164(5). 840–846. 141 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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