Lars Bertram
Genetics · 2005–2018
A researcher in the Science corpus: 12 papers; trusts 5 researchers and is trusted by 6 researchers here, as inferred from the citation graph.
Subfields
- Genetics — 156 citations into it
- Molecular Biology — 115 citations into it; #6,103 of 17,773 by trust here, #4,299 by citations
- Physiology — 74 citations into it; #866 of 2,276 by trust here, #743 by citations
- Neurology — 34 citations into it; #959 of 1,455 by trust here, #428 by citations
- Statistics and Probability — 21 citations into it
- Economics and Econometrics — 7 citations into it
Whom Lars Bertram trusts overall
Their strongest outbound trust, strongest first, inferred from their citations.
- J. Wakefield
- John P. A. Ioannidis
- N. Risch
- Ronald L. Hamilton
- J. Peters
- Rudolph E. Tanzi
- Samuel P. Dickson
- J. McClellan
- Mark I. McCarthy
Who trusts Lars Bertram overall
- Rudolph E. Tanzi
- D. Holtzman
- G. Bu
- Perry G. Ridge
- Berislav Zlokovic
- Martin Citron
- L. Ittner
- J. Götz
- Li Shen
- R. Bell
Papers from Lars Bertram's perspective
Ordered by how strongly the researchers Lars Bertram trusts endorse each paper. Same corpus, a different order for every researcher.
- Siglecs and their roles in the immune system (Nature reviews. Immunology)
- Finding the missing heritability of complex diseases (Nature)
- Neuropathological stageing of Alzheimer-related changes
- Why Most Published Research Findings Are False
- Rare Variants of IFIH1, a Gene Implicated in Antiviral Responses, Protect against Type 1 Diabetes (Science)
- Mutations in LRRK2 cause autosomal-dominant parkinsonism with pleomorphic pathology. (Neuron)
- Defining the role of common variation in the genomic and biological architecture of adult human height
- Rare Variants Create Synthetic Genome-Wide Associations (PLoS Biology)
- Mutations in the DJ-1 Gene Associated with Autosomal Recessive Early-Onset Parkinsonism (Science)
- Searching for genetic determinants in the new millennium (Nature)
Their papers
- The genetic epidemiology of neurodegenerative disease. (2005) — 632 citations
- Systematic meta-analyses of Alzheimer disease genetic association studies: the AlzGene database (2007) — 1,885 citations
- Thirty years of Alzheimer's disease genetics: the implications of systematic meta-analyses (2008) — 788 citations
- A comprehensive 1000 Genomes-based genome-wide association meta-analysis of coronary artery disease (2015) — 2,034 citations
- Study of 300,486 individuals identifies 148 independent genetic loci influencing general cognitive function (2018) — 630 citations
- Preclinical Alzheimer’s disease: Definition, natural history, and diagnostic criteria (2016) — 1,741 citations
- Genome-wide association study identifies 74 loci associated with educational attainment (2016) — 1,288 citations
- Genetic variants associated with subjective well-being, depressive symptoms and neuroticism identified through genome-wide analyses (2016) — 986 citations
- Large-scale meta-analysis of genome-wide association data identifies six new risk loci for Parkinson’s disease (2014) — 1,858 citations
- The genetics of Alzheimer disease: back to the future. (2010) — 866 citations
- Systematic meta-analyses and field synopsis of genetic association studies in schizophrenia: the SzGene database (2008) — 1,082 citations
- Increased hippocampal activation in mild cognitive impairment compared to normal aging and AD (2005) — 886 citations