Kristin G. Ardlie

Genetics · 2002–2020

A researcher in the Science corpus: 45 papers; trusts 1 researcher and is trusted by 4 researchers here, as inferred from the citation graph.

Subfields

• Genetics — 469 citations into it; #3,776 of 6,854 by trust here, #44 by citations

Whom Kristin G. Ardlie trusts overall

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

1. J. K. Pritchard
2. David Reich

Who trusts Kristin G. Ardlie overall

1. Pankaj Kumar Gupta
2. Reedik Mägi
3. John M. Butler
4. S. Rustgi
5. S. Chao
6. B. Singh
7. Benjamin M. Neale

Papers from Kristin G. Ardlie's perspective

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

1. Next-generation genotype imputation service and methods (Nature Genetics)
2. SNPs in KCNQ1 are associated with susceptibility to type 2 diabetes in East Asian and European populations (Nature Genetics)
3. A Draft Sequence of the Neandertal Genome (Science)
4. Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes (Nature Genetics)
5. Supporting Online Material Materials and Methods Figs. S1 to S3 Tables S1 to S5 References Worldwide Human Relationships Inferred from Genome-wide Patterns of Variation
6. Linkage disequilibrium in the human genome (Nature)
7. An expanded view of complex traits: from polygenic to omnigenic (Cell)
8. Linkage disequilibrium in humans: models and data. (American Journal of Human Genetics)
9. Partitioning heritability of regulatory and cell-type-specific variants across 11 common diseases. (American Journal of Human Genetics)
10. A global reference for human genetic variation

Their papers

• The Cancer Cell Line Encyclopedia enables predictive modeling of anticancer drug sensitivity (2012) — 7,455 citations
• Exome sequencing identifies recurrent SPOP, FOXA1 and MED12 mutations in prostate cancer (2012) — 1,524 citations
• A missense single-nucleotide polymorphism in a gene encoding a protein tyrosine phosphatase (PTPN22) is associated with rheumatoid arthritis. (2004) — 1,595 citations
• Comprehensive molecular portraits of human breast tumors (2012) — 7,518 citations
• The Mutational Landscape of Head and Neck Squamous Cell Carcinoma (2011) — 2,541 citations
• Comprehensive Molecular Characterization of Human Colon and Rectal Cancer (2012) — 7,754 citations
• Mutational heterogeneity in cancer and the search for new cancer genes (2013) — 1,147 citations
• The Genotype-Tissue Expression (GTEx) project (2013) — 8,629 citations
• Melanoma genome sequencing reveals frequent PREX2 mutations (2012) — 752 citations
• A Landscape of Driver Mutations in Melanoma (2012) — 2,528 citations
• Initial genome sequencing and analysis of multiple myeloma (2011) — 1,464 citations
• Genetic effects on gene expression across human tissues (2017) — 3,717 citations
• Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes (2008) — 1,910 citations
• The human transcriptome across tissues and individuals (2015) — 1,238 citations
• Patterns of linkage disequilibrium in the human genome (2002) — 1,052 citations
• Punctuated Evolution of Prostate Cancer Genomes (2013) — 1,269 citations
• The GTEx Consortium atlas of genetic regulatory effects across human tissues (2019) — 4,770 citations
• Massively-parallel single nucleus RNA-seq with DroNc-seq (2017) — 971 citations
• Integrated Genomic Analyses of Ovarian Carcinoma (2011) — 7,559 citations
• The Genotype-Tissue Expression (GTEx) pilot analysis: Multitissue gene regulation in humans (2015) — 4,590 citations