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One or more keywords matched the following items that are connected to Lander, Eric
Item TypeName
Academic Article Analysis of the DNA sequence and duplication history of human chromosome 15.
Academic Article Founding father.
Academic Article Identification of the Finnish founder mutation for diastrophic dysplasia (DTD).
Academic Article An integrated haplotype map of the human major histocompatibility complex.
Academic Article The structure of haplotype blocks in the human genome.
Academic Article The mosaic structure of variation in the laboratory mouse genome.
Academic Article Genetic control of serum IgE levels and asthma: linkage and linkage disequilibrium studies in an isolated population.
Academic Article A high-resolution linkage-disequilibrium map of the human major histocompatibility complex and first generation of tag single-nucleotide polymorphisms.
Academic Article Mutations causing medullary cystic kidney disease type 1 lie in a large VNTR in MUC1 missed by massively parallel sequencing.
Academic Article Efficient mapping of mendelian traits in dogs through genome-wide association.
Academic Article Genome-wide detection and characterization of positive selection in human populations.
Academic Article Linkage disequilibrium mapping in isolated founder populations: diastrophic dysplasia in Finland.
Academic Article Haplotype-based association analysis of 56 functional candidate genes in the IBD6 locus on chromosome 19.
Academic Article A composite of multiple signals distinguishes causal variants in regions of positive selection.
Academic Article Searching for signals of evolutionary selection in 168 genes related to immune function.
Academic Article Detecting recent positive selection in the human genome from haplotype structure.
Academic Article The case for selection at CCR5-Delta32.
Academic Article A draft sequence of the Neandertal genome.
Academic Article Identification and functional validation of the novel antimalarial resistance locus PF10_0355 in Plasmodium falciparum.
Academic Article A genomewide linkage-disequilibrium scan localizes the Saguenay-Lac-Saint-Jean cytochrome oxidase deficiency to 2p16.
Academic Article Characterization of the MODY3 phenotype. Early-onset diabetes caused by an insulin secretion defect.
Academic Article Genome sequence, comparative analysis, and population genetics of the domestic horse.
Academic Article Assembly of polymorphic genomes: algorithms and application to Ciona savignyi.
Academic Article Genome sequence, comparative analysis and haplotype structure of the domestic dog.
Academic Article Family-based association study of 76 candidate genes in bipolar disorder: BDNF is a potential risk locus. Brain-derived neutrophic factor.
Academic Article Positive natural selection in the human lineage.
Academic Article Parametric and nonparametric linkage analysis: a unified multipoint approach.
Academic Article Linkage disequilibrium in the human genome.
Academic Article Localization of the EPM1 gene for progressive myoclonus epilepsy on chromosome 21: linkage disequilibrium allows high resolution mapping.
Academic Article Genomewide scan of multiple sclerosis in Finnish multiplex families.
Academic Article High-resolution haplotype structure in the human genome.
Concept Haplotypes
Academic Article Genome-wide association study identifies shared risk loci common to two malignancies in golden retrievers.
Academic Article Improved imputation accuracy of rare and low-frequency variants using population-specific high-coverage WGS-based imputation reference panel.
Academic Article Type 2 Diabetes Variants Disrupt Function of SLC16A11 through Two Distinct Mechanisms.
Academic Article Whole exome sequencing study identifies novel rare and common Alzheimer's-Associated variants involved in immune response and transcriptional regulation.
Academic Article Gain-of-Function Claims for Type-2-Diabetes-Associated Coding Variants in SLC16A11 Are Not Supported by the Experimental Data.
Academic Article Prioritizing disease and trait causal variants at the TNFAIP3 locus using functional and genomic features.
Search Criteria
  • Haplotypes
Funded by the NIH National Center for Advancing Translational Sciences through its Clinical and Translational Science Awards Program, grant number UL1TR002541.