Martin Kircher

Molecular Biology · 2010–2024

A researcher in the Science corpus: 17 papers; trusts 27 researchers and is trusted by 13 researchers here, as inferred from the citation graph.

Subfields

Molecular Biology — 383 citations into it; #3,301 of 17,773 by trust here, #1,575 by citations
Genetics — 259 citations into it; #3,399 of 6,854 by trust here, #182 by citations
Computational Biology & Bioinformatics — 35 citations into it
Ecology — 27 citations into it; #4,313 of 10,717 by trust here, #4,784 by citations
Artificial Intelligence — 18 citations into it; #25,188 of 35,345 by trust here, #23,731 by citations
Spectroscopy — 11 citations into it
Electrical and Electronic Engineering — 5 citations into it

Whom Martin Kircher trusts overall

Their strongest outbound trust, strongest first, inferred from their citations.

Who trusts Martin Kircher overall

Papers from Martin Kircher's perspective

Ordered by how strongly the researchers Martin Kircher trusts endorse each paper. Same corpus, a different order for every researcher.

Potential etiologic and functional implications of genome-wide association loci for human diseases and traits (Proceedings of the National Academy of Sciences of the United States of America)
Mapping and quantifying mammalian transcriptomes by RNA-Seq (Nature Methods)
The Human Gene Mutation Database: 2008 update
Genome sequencing in microfabricated high-density picolitre reactors (Nature)
Substantial biases in ultra-short read data sets from high-throughput DNA sequencing (Nucleic Acids Research)
Bioinformatics Applications Note Databases and Ontologies Deriving the Consequences of Genomic Variants with the Ensembl Api and Snp Effect Predictor
Genome-Wide Mapping of in Vivo Protein-DNA Interactions (Science)
A Draft Sequence of the Neandertal Genome (Science)
Personalized Copy-Number and Segmental Duplication Maps using Next-Generation Sequencing (Nature Genetics)
Analysis of protein-coding genetic variation in 60,706 humans

Their papers

A general framework for estimating the relative pathogenicity of human genetic variants (2014) — 5,961 citations
The evolution of gene expression levels in mammalian organs (2011) — 1,209 citations
Deep proteome and transcriptome mapping of a human cancer cell line (2011) — 991 citations
CADD: predicting the deleteriousness of variants throughout the human genome (2018) — 3,218 citations
Double indexing overcomes inaccuracies in multiplex sequencing on the Illumina platform (2011) — 1,091 citations
High‐throughput DNA sequencing – concepts and limitations (2010) — 644 citations
Illumina sequencing library preparation for highly multiplexed target capture and sequencing. (2010) — 2,252 citations
Characterization of ancient and modern genomes by SNP detection and phylogenomic and metagenomic analysis using PALEOMIX (2014) — 515 citations
CADD-Splice—improving genome-wide variant effect prediction using deep learning-derived splice scores (2021) — 563 citations
Multiplex Assessment of Protein Variant Abundance by Massively Parallel Sequencing (2018) — 402 citations
CADD v1.7: using protein language models, regulatory CNNs and other nucleotide-level scores to improve genome-wide variant predictions (2024) — 369 citations
Cell-free DNA comprises an in vivo nucleosome footprint that informs its tissues-of-origin (2016) — 1,291 citations
The Genetic Basis of Mendelian Phenotypes: Discoveries, Challenges, and Opportunities. (2015) — 611 citations
The complete genome sequence of a Neandertal from the Altai Mountains (2013) — 1,650 citations
A HIGH COVERAGE GENOME SEQUENCE FROM AN ARCHAIC DENISOVAN INDIVIDUAL (2012) — 1,845 citations
Genetic history of an archaic hominin group from Denisova Cave in Siberia (2010) — 1,704 citations
A Draft Sequence of the Neandertal Genome (2010) — 3,888 citations