Lars Bertram

33.3k total citations · 7 hit papers
172 papers, 13.0k citations indexed

About

Lars Bertram is a scholar working on Molecular Biology, Genetics and Physiology. According to data from OpenAlex, Lars Bertram has authored 172 papers receiving a total of 13.0k indexed citations (citations by other indexed papers that have themselves been cited), including 80 papers in Molecular Biology, 72 papers in Genetics and 71 papers in Physiology. Recurrent topics in Lars Bertram's work include Alzheimer's disease research and treatments (61 papers), Genetic Associations and Epidemiology (47 papers) and Bioinformatics and Genomic Networks (33 papers). Lars Bertram is often cited by papers focused on Alzheimer's disease research and treatments (61 papers), Genetic Associations and Epidemiology (47 papers) and Bioinformatics and Genomic Networks (33 papers). Lars Bertram collaborates with scholars based in Germany, United States and United Kingdom. Lars Bertram's co-authors include Rudolph E. Tanzi, Kristina Mullin, Deborah Blacker, Matthew B. McQueen, Christina M. Lill, John P. A. Ioannidis, Muin J. Khoury, Fotini K. Kavvoura, Marilyn Albert and Reisa A. Sperling and has published in prestigious journals such as Nature, Science and New England Journal of Medicine.

In The Last Decade

Lars Bertram

169 papers receiving 12.7k citations

Hit Papers

Twenty Years of the Alzheimer’s Disease Amyloid Hypothesi... 2005 2026 2012 2019 2005 2006 2008 2005 2010 400 800 1.2k

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Lars Bertram Germany 48 6.1k 5.3k 2.1k 2.0k 1.7k 172 13.0k
Margaret A. Pericak‐Vance United States 63 4.8k 0.8× 7.0k 1.3× 2.8k 1.3× 2.4k 1.2× 1.5k 0.9× 340 18.4k
Elizabeth H. Corder United States 28 6.7k 1.1× 3.6k 0.7× 1.5k 0.7× 1.4k 0.7× 2.9k 1.7× 59 11.3k
Gerard D. Schellenberg United States 65 9.5k 1.6× 7.7k 1.5× 2.2k 1.0× 2.6k 1.3× 2.1k 1.3× 214 16.9k
P. C. Gaskell United States 23 6.3k 1.0× 3.7k 0.7× 1.4k 0.7× 2.1k 1.0× 2.3k 1.4× 45 10.7k
Yadong Huang United States 63 6.9k 1.1× 5.3k 1.0× 712 0.3× 2.7k 1.3× 1.2k 0.7× 143 13.9k
Lindsay A. Farrer United States 71 7.2k 1.2× 7.4k 1.4× 4.4k 2.1× 3.1k 1.5× 4.3k 2.6× 425 23.6k
Jerzy Węgiel United States 44 4.5k 0.7× 3.2k 0.6× 1.2k 0.6× 1.3k 0.7× 1.2k 0.7× 122 9.1k
Simon Lovestone United Kingdom 79 9.5k 1.6× 7.7k 1.5× 1.6k 0.8× 2.7k 1.3× 5.3k 3.1× 368 21.0k
Christian J. Pike United States 62 6.8k 1.1× 4.3k 0.8× 2.0k 0.9× 2.9k 1.4× 653 0.4× 117 13.2k
Roberta Dı́az Brinton United States 78 4.4k 0.7× 4.6k 0.9× 5.5k 2.6× 3.7k 1.8× 1.2k 0.7× 278 19.3k

Countries citing papers authored by Lars Bertram

Since Specialization
Citations

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

Fields of papers citing papers by Lars Bertram

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Lars Bertram

This figure shows the co-authorship network connecting the top 25 collaborators of Lars Bertram. A scholar is included among the top collaborators of Lars Bertram 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 Lars Bertram. Lars Bertram 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
2.
Paul, Kimberly C., Susan Searles Nielsen, Valerija Dobričić, et al.. (2024). Genome-wide meta-analysis of short-tandem repeats for Parkinson’s disease risk using genotype imputation. Brain Communications. 6(3). fcae146–fcae146. 2 indexed citations
3.
Drewelies, Johanna, Valentin Max Vetter, Sandra Duezel, et al.. (2024). There Are Multiple Clocks That Time Us: Cross-Sectional and Longitudinal Associations Among 14 Alternative Indicators of Age and Aging. The Journals of Gerontology Series A. 80(6). 3 indexed citations
4.
Vetter, Valentin Max, et al.. (2023). DNA methylation age acceleration is associated with risk of diabetes complications. SHILAP Revista de lepidopterología. 3(1). 21–21. 15 indexed citations
5.
Vetter, Valentin Max, Dominik Spira, Johanna Drewelies, et al.. (2022). Relationship Between 5 Epigenetic Clocks, Telomere Length, and Functional Capacity Assessed in Older Adults: Cross-Sectional and Longitudinal Analyses. The Journals of Gerontology Series A. 77(9). 1724–1733. 30 indexed citations
6.
Prokopenko, Dmitry, Sanghun Lee, Julian Hecker, et al.. (2022). Region-based analysis of rare genomic variants in whole-genome sequencing datasets reveal two novel Alzheimer’s disease-associated genes: DTNB and DLG2. Molecular Psychiatry. 27(4). 1963–1969. 16 indexed citations
7.
Algharably, Engi, Maximilian König, Vera Regitz‐Zagrosek, et al.. (2022). Longitudinal effects of a common UMOD variant on kidney function, blood pressure, cognitive and physical function in older women and men. Journal of Human Hypertension. 37(8). 709–717. 1 indexed citations
8.
Grotzinger, Andrew D., Christina M. Lill, Lars Bertram, et al.. (2022). Genetic associations with learning over 100 days of practice. npj Science of Learning. 7(1). 7–7. 1 indexed citations
9.
Dobričić, Valerija, Marcel Schilling, Jessica Schulz, et al.. (2022). Differential microRNA expression analyses across two brain regions in Alzheimer’s disease. Translational Psychiatry. 12(1). 352–352. 33 indexed citations
10.
Dobričić, Valerija, Marcel Schilling, David Bartrés‐Faz, et al.. (2022). Epigenome-Wide Association Study in Peripheral Tissues Highlights DNA Methylation Profiles Associated with Episodic Memory Performance in Humans. Biomedicines. 10(11). 2798–2798. 4 indexed citations
11.
Lee, Sanghun, Georg Hahn, Julian Hecker, et al.. (2022). A comparison between similarity matrices for principal component analysis to assess population stratification in sequenced genetic data sets. Briefings in Bioinformatics. 24(1). 5 indexed citations
12.
Kusters, Cynthia, Kimberly C. Paul, Aline Duarte Folle, et al.. (2021). Increased Menopausal Age Reduces the Risk of Parkinson's Disease: A Mendelian Randomization Approach. Movement Disorders. 36(10). 2264–2272. 29 indexed citations
13.
Walhovd, Kristine B., Anders M. Fjell, Øystein Sørensen, et al.. (2020). Genetic risk for Alzheimer disease predicts hippocampal volume through the human lifespan. Neurology Genetics. 6(5). e506–e506. 28 indexed citations
14.
Bertram, Lars, Johannes Helmuth, Claudia Mischung, et al.. (2020). Mutation spectrum and polygenic score in German patients with familial hypercholesterolemia. Clinical Genetics. 98(5). 457–467. 11 indexed citations
15.
Fjell, Anders M., Donatas Sederevičius, Markus H. Sneve, et al.. (2019). Self-reported Sleep Problems Related to Amyloid Deposition in Cortical Regions with High HOMER1 Gene Expression. Cerebral Cortex. 30(4). 2144–2156. 13 indexed citations
16.
Wohlers, Inken, et al.. (2019). Alzheimer's disease risk SNPs show no strong effect on miRNA expression in human lymphoblastoid cell lines. Neurobiology of Aging. 86. 202.e1–202.e3. 2 indexed citations
17.
Dobričić, Valerija, et al.. (2018). Field synopsis and systematic meta-analyses of genetic association studies in isolated dystonia. Parkinsonism & Related Disorders. 57. 50–57. 6 indexed citations
18.
Chuang, Yu‐Hsuan, Christina M. Lill, Pei‐Chen Lee, et al.. (2016). Gene-Environment Interaction in Parkinson's Disease: Coffee, <b><i>ADORA2A</i></b>, and <b><i>CYP1A2</i></b>. Neuroepidemiology. 47(3-4). 192–200. 32 indexed citations
19.
Dolan, Siobhan M., Mads V. Hollegaard, Mario Merialdi, et al.. (2010). Synopsis of Preterm Birth Genetic Association Studies: The Preterm Birth Genetics Knowledge Base (PTBGene). Public Health Genomics. 13(7-8). 514–523. 52 indexed citations
20.
Farris, Wesley, Malcolm A. Leissring, Elizabeth A. Eckman, et al.. (2004). Partial Loss-of-Function Mutations in Insulin-Degrading Enzyme that Induce Diabetes also Impair Degradation of Amyloid β-Protein. American Journal Of Pathology. 164(4). 1425–1434. 202 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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