C. Hartl
Molecular Biology · 2011–2018
A researcher in the Science corpus: 8 papers; trusts 1 researcher and is trusted by 1 researcher here, as inferred from the citation graph.
Subfields
- Molecular Biology — 133 citations into it
Whom C. Hartl trusts
Their strongest outbound trust, strongest first, inferred from their citations.
- Steve Horvath (in Molecular Biology)
Who trusts C. Hartl
- Heng Li (in Genetics)
Papers from C. Hartl's perspective
Ordered by how strongly the researchers C. Hartl trusts endorse each paper. Same corpus, a different order for every researcher.
- Searching for SNPs with cloud computing (Genome Biology)
- Exome sequencing as a tool for Mendelian disease gene discovery
- A framework for variation discovery and genotyping using next-generation DNA sequencing data
- Variation in genome-wide mutation rates within and between human families (Nature Genetics)
- dbSNP: the NCBI database of genetic variation
- Genomic divergences between humans and other hominoids and the effective population size of the common ancestor of humans and chimpanzees. (American Journal of Human Genetics)
- The Human Gene Mutation Database: 2008 update
- An abundance of rare functional variants in 202 drug target genes sequenced in 14,002 people (Science)
- A General Framework for Weighted Gene Co-Expression Network Analysis (Statistical Applications in Genetics and Molecular Biology)
- Fast R Functions for Robust Correlations and Hierarchical Clustering (Journal of Statistical Software)
Their papers
- A framework for variation discovery and genotyping using next-generation DNA sequencing data (2011) — 11,249 citations
- A global reference for human genetic variation (2015) — 16,925 citations
- From FastQ data to high confidence variant calls: the Genome Analysis Toolkit best practices pipeline (2013) — 6,636 citations
- The genetic architecture of type 2 diabetes (2016) — 1,066 citations
- Genome-wide changes in lncRNA, splicing, and regional gene expression patterns in autism (2016) — 654 citations
- Shared molecular neuropathology across major psychiatric disorders parallels polygenic overlap (2018) — 1,009 citations
- An integrated map of genetic variation from 1,092 human genomes (2012) — 8,008 citations
- Variation in genome-wide mutation rates within and between human families (2011) — 604 citations