P. D. de Bakker
Genetics · 2006–2018
A researcher in the Science corpus: 18 papers; trusts 1 researcher and is trusted by 0 researchers here, as inferred from the citation graph.
Subfields
- Genetics — 183 citations into it
Whom P. D. de Bakker trusts overall
Their strongest outbound trust, strongest first, inferred from their citations.
Who trusts P. D. de Bakker overall
Papers from P. D. de Bakker's perspective
Ordered by how strongly the researchers P. D. de Bakker trusts endorse each paper. Same corpus, a different order for every researcher.
- Methods for detecting associations with rare variants for common diseases: application to analysis of sequence data. (American Journal of Human Genetics)
- Common SNPs explain a large proportion of heritability for human height (Nature Genetics)
- The Protein Data Bank.
- Robust relationship inference in genome-wide association studies
- SFCHECK: a unified set of procedures for evaluating the quality of macromolecular structure-factor data and their agreement with the atomic model.
- Controlling the false discovery rate: a practical and powerful approach to multiple testing
- [20] Processing of X-ray diffraction data collected in oscillation mode.
- Genetic Mapping in Human Disease (Science)
- The Genome Analysis Toolkit: a MapReduce framework for analyzing next-generation DNA sequencing data. (Genome Research)
- PROCHECK: a program to check the stereochemical quality of protein structures
Their papers
- A second generation human haplotype map of over 3.1 million SNPs (2007) — 4,677 citations
- PLINK: a tool set for whole-genome association and population-based linkage analyses. (2007) — 32,716 citations
- Knowledge-based real-space explorations for low-resolution structure determination. (2006) — 28 citations
- Integrating common and rare genetic variation in diverse human populations (2010) — 3,033 citations
- Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes (2018) — 1,405 citations
- Defining the role of common variation in the genomic and biological architecture of adult human height (2014)
- Association between alcohol and cardiovascular disease: Mendelian randomisation analysis based on individual participant data (2014) — 637 citations
- Mendelian randomization of blood lipids for coronary heart disease (2014) — 726 citations
- An international effort towards developing standards for best practices in analysis, interpretation and reporting of clinical genome sequencing results in the CLARITY Challenge (2014) — 308 citations
- Imputing Amino Acid Polymorphisms in Human Leukocyte Antigens (2013) — 651 citations
- Plasma HDL cholesterol and risk of myocardial infarction: a mendelian randomisation study (2012) — 2,232 citations
- Five amino acids in three HLA proteins explain most of the association between MHC and seropositive rheumatoid arthritis (2012) — 954 citations
- High density genetic mapping identifies new susceptibility loci for rheumatoid arthritis (2012) — 656 citations
- Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis (2011) — 2,780 citations
- Pooled association tests for rare variants in exon-resequencing studies. (2010) — 651 citations
- The Major Genetic Determinants of HIV-1 Control Affect HLA Class I Peptide Presentation (2010) — 1,234 citations
- STAT4 and the risk of rheumatoid arthritis and systemic lupus erythematosus. (2007) — 1,095 citations
- Risk alleles for multiple sclerosis identified by a genomewide study. (2007) — 1,623 citations