Ivo G. Gut
Molecular Biology · 2007–2020
A researcher in the Science corpus: 22 papers; trusts 3 researchers and is trusted by 0 researchers here, as inferred from the citation graph.
Subfields
- Molecular Biology — 271 citations into it
- Genetics — 152 citations into it
Whom Ivo G. Gut trusts overall
Their strongest outbound trust, strongest first, inferred from their citations.
Papers from Ivo G. Gut's perspective
Ordered by how strongly the researchers Ivo G. Gut trusts endorse each paper. Same corpus, a different order for every researcher.
- Genome-wide methylation analysis of human colon cancer reveals similar hypo- and hypermethylation at conserved tissue-specific CpG island shores (Nature Genetics)
- DNA methylation patterns and epigenetic memory.
- Quantitative high-throughput analysis of DNA methylation patterns by base-specific cleavage and mass spectrometry. (Proceedings of the National Academy of Sciences of the United States of America)
- A comparison of normalization methods for high density oligonucleotide array data based on variance and bias (Bioinform.)
- A new multipoint method for genome-wide association studies by imputation of genotypes (Nature Genetics)
- Genetic analysis of genome-wide variation in human gene expression (Nature)
- A simple method for estimating global DNA methylation using bisulfite PCR of repetitive DNA elements. (Nucleic Acids Research)
- Highly parallel genome-wide expression profiling of individual cells using nanoliter droplets
- Association of NOD2 leucine-rich repeat variants with susceptibility to Crohn's disease (Nature)
- Droplet barcoding for single cell transcriptomics applied to embryonic stem cells (Cell)
Their papers
- Transcriptome and genome sequencing uncovers functional variation in humans (2013) — 2,017 citations
- A genome-wide association study of global gene expression (2007) — 1,046 citations
- bigSCale: an analytical framework for big-scale single-cell data (2017) — 73 citations
- DNA methylation analysis by pyrosequencing (2007) — 693 citations
- International network of cancer genome projects (2010) — 2,229 citations
- Distinct DNA methylomes of newborns and centenarians (2012) — 802 citations
- Benchmarking single-cell RNA-sequencing protocols for cell atlas projects (2020) — 413 citations
- Epigenomic analysis detects widespread gene-body DNA hypomethylation in chronic lymphocytic leukemia (2012) — 601 citations
- Whole-genome sequencing identifies recurrent mutations in chronic lymphocytic leukaemia (2011) — 1,652 citations
- Genome-wide association study identifies variants at CLU and CR1 associated with Alzheimer's disease (2009) — 1,386 citations
- Exome sequencing identifies recurrent mutations of the splicing factor SF3B1 gene in chronic lymphocytic leukemia (2011) — 1,154 citations
- A susceptibility locus for lung cancer maps to nicotinic acetylcholine receptor subunit genes on 15q25 (2008) — 1,289 citations
- Analyses of non-coding somatic drivers in 2,658 cancer whole genomes (2020) — 508 citations
- β-Glucan Reverses the Epigenetic State of LPS-Induced Immunological Tolerance (2016) — 600 citations
- Non-coding recurrent mutations in chronic lymphocytic leukaemia (2015) — 918 citations
- Great ape genetic diversity and population history (2013) — 858 citations
- A Large-Scale, Consortium-Based Genomewide Association Study of Asthma (2010) — 1,842 citations
- Faculty Opinions recommendation of Genome-wide association study identifies eight loci associated with blood pressure. (2009) — 1,206 citations
- SLCO1B1 variants and statin-induced myopathy--a genomewide study. (2008) — 2,015 citations
- Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease (2008) — 2,710 citations