David Schlessinger

Genetics · 2001–2020

A researcher in the Science corpus: 19 papers; trusts 1 researcher and is trusted by 0 researchers here, as inferred from the citation graph.

Subfields

• Genetics — 245 citations into it

Whom David Schlessinger trusts

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

1. Gonçalo R. Abecasis (in Genetics)

Papers from David Schlessinger's perspective

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

1. MaCH: Using Sequence and Genotype Data to Estimate Haplotypes and Unobserved Genotypes (Genetic Epidemiology)
2. A note on exact tests of Hardy-Weinberg equilibrium. (American Journal of Human Genetics)
3. PEDSTATS: descriptive statistics, graphics and quality assessment for gene mapping data (Bioinform.)
4. Heritability of Cardiovascular and Personality Traits in 6,148 Sardinians (PLoS Genetics)
5. Defining the role of common variation in the genomic and biological architecture of adult human height
6. Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes (Nature Genetics)
7. A linear complexity phasing method for thousands of genomes (Nature Methods)
8. Estimating the Dimension of a Model
9. Principal components analysis corrects for stratification in genome-wide association studies
10. Genome-Wide Association Scan Shows Genetic Variants in the FTO Gene Are Associated with Obesity-Related Traits (PLoS Genetics)

Their papers

• Next-generation genotype imputation service and methods (2016) — 3,622 citations
• Identification of ten loci associated with height highlights new biological pathways in human growth (2008) — 644 citations
• The DNA sequence of the human X chromosome (2005) — 1,099 citations
• Author Correction: An integrated multi-omics approach identifies epigenetic alterations associated with Alzheimer’s disease (2020) — 765 citations
• Genome-wide association study identifies 74 loci associated with educational attainment (2016) — 1,288 citations
• Genetic variants associated with subjective well-being, depressive symptoms and neuroticism identified through genome-wide analyses (2016) — 986 citations
• Defining the role of common variation in the genomic and biological architecture of adult human height (2014)
• Supplementary Material 7 (2014)
• GWAS of 126,559 Individuals Identifies Genetic Variants Associated with Educational Attainment (2013) — 874 citations
• Biological, Clinical, and Population Relevance of 95 Loci for Blood Lipids (2010) — 3,781 citations
• Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution (2010) — 973 citations
• Faculty Opinions recommendation of Genome-wide association study identifies eight loci associated with blood pressure. (2009) — 1,206 citations
• Common variants at 30 loci contribute to polygenic dyslipidemia (2008) — 1,471 citations
• Newly identified loci that influence lipid concentrations and risk of coronary artery disease (2008) — 1,690 citations
• Genome-wide association study shows BCL11A associated with persistent fetal hemoglobin and amelioration of the phenotype of β-thalassemia (2008) — 618 citations
• Six new loci associated with body mass index highlight a neuronal influence on body weight regulation (2008) — 1,801 citations
• Genome-Wide Association Scan Shows Genetic Variants in the FTO Gene Are Associated with Obesity-Related Traits (2007) — 1,746 citations
• Heritability of Cardiovascular and Personality Traits in 6,148 Sardinians (2006) — 594 citations
• The putative forkhead transcription factor FOXL2 is mutated in blepharophimosis/ptosis/epicanthus inversus syndrome (2001) — 952 citations