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

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

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

#	Work	Indexed citations
1	Development of a Genetic Test Indicating Increased AVP/V1b Signalling in Patients with Acute Depression 2025 ·Pharmacopsychiatry ·Marcus Ising, F Holsboer, (unknown), Bertram Müller‐Myhsok	1
2	Multimodal workflows optimally predict response to repetitive transcranial magnetic stimulation in patients with schizophrenia: a multisite machine learning analysis 2024 ·Translational Psychiatry ·(unknown), Jaroslav Rokicki, Dominic Dwyer, Sergi Papiol, Fabian Streit, Marcella Rietschel, Thomas Wobrock, Bertram Müller‐Myhsok, (unknown), Lars T. Westlye, Ole A. Andreassen, Lena Palaniyappan, Neil Thomas, Alkomiet Hasan, Emanuel Schwarz, Nikolaos Koutsouleris	7
3	Sex-specific fear acquisition following early life stress is linked to amygdala and hippocampal purine and glutamate metabolism 2024 ·Communications Biology ·Joeri Bordes, Thomas Bajaj, (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), Margherita Springer, Karin Kleigrewe, Bertram Müller‐Myhsok, Nils C. Gassen, Mathias V. Schmidt	2
4	Integration of a polygenic score into guideline-recommended prediction of cardiovascular disease 2024 ·European Heart Journal ·Ling Li, Shichao Pang, (unknown), Bertram Müller‐Myhsok, Heribert Schunkert	23
5	DeepOF: a Python package for supervised andunsupervised pattern recognition in mice motion tracking data 2023 ·The Journal of Open Source Software ·(unknown), Joeri Bordes, Benno Pütz, Mathias V. Schmidt, Bertram Müller‐Myhsok	6
6	Chromosomal Region 11p14.1 is Associated with Pharmacokinetics and Pharmacodynamics of Bisoprolol 2022 ·Pharmacogenomics and Personalized Medicine ·Vanessa Fontana, Richard M. Turner, Ben Francis, Peng Yin, Benno Pütz, Timo P. Hiltunen, Sanni Ruotsalainen, Kimmo Kontula, Bertram Müller‐Myhsok, Munir Pirmohamed	6
7	DNA-methylation dynamics across short-term, exposure-containing CBT in patients with panic disorder 2022 ·Translational Psychiatry ·Sylvain Moser, Jade Martins, Darina Czamara, Jennifer Lange, Bertram Müller‐Myhsok, Angelika Erhardt	10
8	Maternal selenium levels and whole genome screen in recurrent spontaneous preterm birth population: A nested case control study 2021 ·European Journal of Obstetrics & Gynecology and Reproductive Biology ·Angharad Care, Juhi Gupta, Laura Goodfellow, Ge Zhang, (unknown), (unknown), Julio A. Landero Figueroa, (unknown), Andrew Sharp, Ana Alfirevic, Bertram Müller‐Myhsok, Louis J. Muglia, Žarko Alfirević	2
9	“The Heidelberg Five” personality dimensions: Genome‐wide associations, polygenic risk for neuroticism, and psychopathology 20 years after assessment 2021 ·American Journal of Medical Genetics Part B Neuropsychiatric Genetics ·Urs Heilbronner, Sergi Papiol, Monika Budde, Till F. M. Andlauer, Jana Strohmaier, Fabian Streit, Josef Frank, Franziska Degenhardt, Stefanie Heilmann‐Heimbach, Stephanie H. Witt, Andreas J. Forstner, Adrian Loerbroks, Manfred Amelang, Til Stürmer‎, Bertram Müller‐Myhsok, Markus M. Nöthen, Marcella Rietschel, Thomas G. Schulze	4
10	A different view on fine-scale population structure in Western African populations 2019 ·Human Genetics ·Kridsadakorn Chaichoompu, Fentaw Abegaz, Bruno Cavadas, Verónica Fernandes, Bertram Müller‐Myhsok, Luı́sa Pereira, Kristel Van Steen	12
11	Childhood maltreatment is associated with distinct genomic and epigenetic profiles in posttraumatic stress disorder 2013 ·Proceedings of the National Academy of Sciences ·Divya Mehta, Torsten Klengel, Karen N. Conneely, Alicia K. Smith, André Altmann, Thaddeus W. W. Pace, Monika Rex‐Haffner, (unknown), Mariya Gonik, Kristina B. Mercer, Bekh Bradley, Bertram Müller‐Myhsok, Kerry J. Ressler, Elisabeth B. Binder	365
12	A common variant in Myosin-18B contributes to mathematical abilities in children with dyslexia and intraparietal sulcus variability in adults 2013 ·Translational Psychiatry ·Kerstin U. Ludwig, Philipp G. Sämann, Michael P. Alexander, Jessica Becker, Jennifer Bruder, Kristina Moll, Derek Spieler, Michael Czisch, Andreas Warnke, Sophia Docherty, Oliver S. P. Davis, Robert Plomin, Markus M. Nöthen, Karin Landerl, Bertram Müller‐Myhsok, Per Hoffmann, J Schumacher, Gerd Schulte‐Körne, Darina Czamara	24
13	Genetic markers for PTSD risk and resilience among survivors of the World Trade Center attacks. 2011 ·SHILAP Revista de lepidopterología ·Casey Sarapas, Guiqing Cai, Linda M. Bierer, Julia A. Golier, Sandro Galea, Marcus Ising, Theo Rein, James Schmeidler, Bertram Müller‐Myhsok, Manfred Uhr, (unknown), Joseph D. Buxbaum, Rachel Yehuda	100
14	Imaging genetics of FOXP2 in dyslexia 2011 ·European Journal of Human Genetics ·Arndt Wilcke, Carolin Ligges, Jana Burkhardt, Michael P. Alexander, Christiane Wolf, (unknown), Peter Ahnert, Per Hoffmann, Albert J. Becker, Bertram Müller‐Myhsok, Sven Cichon, Johannes Boltze, Holger Kirsten	40
15	Somatization in major depression - clinical features and genetic associations 2011 ·Acta Psychiatrica Scandinavica ·Torsten Klengel, Angela Heck, Hildegard Pfister, Tanja Brückl, Johannes M. Hennings, Andreas Menke, Darina Czamara, Bertram Müller‐Myhsok, Marcus Ising	23
16	Genome-Wide Association Study of Antidepressant Treatment-Emergent Suicidal Ideation 2011 ·Neuropsychopharmacology ·Andreas Menke, Katharina Domschke, Darina Czamara, Torsten Klengel, Johannes M. Hennings, Susanne Lucae, Bernhard T. Baune, Volker Arolt, Bertram Müller‐Myhsok, (unknown), Elisabeth B. Binder	51
17	EPIBLASTER-fast exhaustive two-locus epistasis detection strategy using graphical processing units 2010 ·European Journal of Human Genetics ·Tony Kam-Thong, Darina Czamara, Koji Tsuda, Karsten Borgwardt, Cathryn M. Lewis, Angelika Erhardt, Bernhard Hemmer, Peter Rieckmann, (unknown), Frank Weber, Christiane Wolf, Andreas Ziegler, Benno Pütz, (unknown), Bernhard Schölkopf, Bertram Müller‐Myhsok	67
18	Gender-Specific Association of Galanin Polymorphisms with HPA-Axis Dysregulation, Symptom Severity, and Antidepressant Treatment Response 2010 ·Neuropsychopharmacology ·Paul G. Unschuld, Marcus Ising, Darina Roeske, Angelika Erhardt, Michael Specht, Stefan Kloiber, Manfred Uhr, Bertram Müller‐Myhsok, (unknown), Elisabeth B. Binder	48
19	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 2009 ·The American Journal of Gastroenterology ·Jürgen Glas, Johannes Stallhofer, Stephan Ripke, Martin Wetzke, Simone Pfennig, Wolfram Klein, Jörg T. Epplen, Thomas Griga, U Schiemann, Martin Lacher, Sibylle Koletzko, Matthias Folwaczny, Peter Lohse, Burkhard Göke, Thomas Ochsenkühn, Bertram Müller‐Myhsok, Stephan Brand	63
20	Results from a Genome-wide Search for Predisposing Genes in Sarcoidosis 2001 ·American Journal of Respiratory and Critical Care Medicine ·Manfred Schürmann, (unknown), Bertram Müller‐Myhsok, Max Schlaak, Joachim Müller‐Quernheim, E. Schwinger	141

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.

Explore authors with similar magnitude of impact