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One or more keywords matched the following items that are connected to Daly, Mark
Item TypeName
Academic Article A common mutation in BRCA2 that predisposes to a variety of cancers is found in both Jewish Ashkenazi and non-Jewish individuals.
Academic Article Genomewide linkage analysis of bipolar disorder by use of a high-density single-nucleotide-polymorphism (SNP) genotyping assay: a comparison with microsatellite marker assays and finding of significant linkage to chromosome 6q22.
Academic Article Acheiropodia is caused by a genomic deletion in C7orf2, the human orthologue of the Lmbr1 gene.
Academic Article An integrated haplotype map of the human major histocompatibility complex.
Academic Article Haplotype structure of TNFRSF5-TNFSF5 (CD40-CD40L) and association analysis in systemic lupus erythematosus.
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 Segmental phylogenetic relationships of inbred mouse strains revealed by fine-scale analysis of sequence variation across 4.6 mb of mouse genome.
Academic Article High-density haplotype structure and association testing of the insulin-degrading enzyme (IDE) gene with type 2 diabetes in 4,206 people.
Academic Article Genetic control of serum IgE levels and asthma: linkage and linkage disequilibrium studies in an isolated population.
Academic Article Efficient multipoint linkage analysis through reduction of inheritance space.
Academic Article Mutations causing medullary cystic kidney disease type 1 lie in a large VNTR in MUC1 missed by massively parallel sequencing.
Academic Article Genome-wide association analysis identifies loci for type 2 diabetes and triglyceride levels.
Academic Article Glycerol as a correlate of impaired glucose tolerance: dissection of a complex system by use of a simple genetic trait.
Academic Article Genetic investigation of chromosome 5q GABAA receptor subunit genes in schizophrenia.
Academic Article Efficiency and power in genetic association studies.
Academic Article Myosin IXB variant increases the risk of celiac disease and points toward a primary intestinal barrier defect.
Academic Article Genome-wide detection and characterization of positive selection in human populations.
Academic Article A sequence-based variation map of 8.27 million SNPs in inbred mouse strains.
Academic Article Haplotype structure and genotype-phenotype correlations of the sulfonylurea receptor and the islet ATP-sensitive potassium channel gene region.
Academic Article WHAP: haplotype-based association analysis.
Academic Article IBD5 is associated with an extensive complicated Crohn's disease feature: implications from genotype-phenotype analysis.
Academic Article CARD15 genetic variation in a Quebec population: prevalence, genotype-phenotype relationship, and haplotype structure.
Academic Article Haplotype-based association analysis of 56 functional candidate genes in the IBD6 locus on chromosome 19.
Academic Article A second generation human haplotype map of over 3.1 million SNPs.
Academic Article Common genetic variants and modification of penetrance of BRCA2-associated breast cancer.
Academic Article Evaluating potential for whole-genome studies in Kosrae, an isolated population in Micronesia.
Academic Article Do multiple data sets provide support for a bipolar illness susceptibility locus on chromosome 18?
Academic Article Direct or indirect association in a complex disease: the role of SLC22A4 and SLC22A5 functional variants in Crohn disease.
Academic Article Three functional variants of IFN regulatory factor 5 (IRF5) define risk and protective haplotypes for human lupus.
Academic Article Haploview: analysis and visualization of LD and haplotype maps.
Academic Article IDDM17: polymorphisms in the AMACO gene are associated with dominant protection against type 1A diabetes in a Bedouin Arab family.
Academic Article A high-resolution HLA and SNP haplotype map for disease association studies in the extended human MHC.
Academic Article Whole population, genome-wide mapping of hidden relatedness.
Academic Article Use of a genetic isolate to identify rare disease variants: C7 on 5p associated with MS.
Academic Article Integrated genotype calling and association analysis of SNPs, common copy number polymorphisms and rare CNVs.
Academic Article Susceptibility to amoxicillin-clavulanate-induced liver injury is influenced by multiple HLA class I and II alleles.
Academic Article Haplotype structure in Ashkenazi Jewish BRCA1 and BRCA2 mutation carriers.
Academic Article Haplotype analysis of tumour necrosis factor receptor genes in 1p36: no evidence for association with systemic lupus erythematosus.
Academic Article A genomewide linkage-disequilibrium scan localizes the Saguenay-Lac-Saint-Jean cytochrome oxidase deficiency to 2p16.
Academic Article A common haplotype of interferon regulatory factor 5 (IRF5) regulates splicing and expression and is associated with increased risk of systemic lupus erythematosus.
Academic Article Fine mapping in 94 inbred mouse strains using a high-density haplotype resource.
Academic Article Genome-wide association study identifies five new schizophrenia loci.
Academic Article Comparing strategies to fine-map the association of common SNPs at chromosome 9p21 with type 2 diabetes and myocardial infarction.
Academic Article Haplotype-based identification of a microsomal transfer protein marker associated with the human lifespan.
Academic Article Genome-wide association study in a high-risk isolate for multiple sclerosis reveals associated variants in STAT3 gene.
Academic Article Genome-wide association scan of the time to onset of attention deficit hyperactivity disorder.
Academic Article Refined genomic localization and ethnic differences observed for the IBD5 association with Crohn's disease.
Academic Article Genome sequence, comparative analysis and haplotype structure of the domestic dog.
Academic Article Analysis of high-resolution HapMap of DTNBP1 (Dysbindin) suggests no consistency between reported common variant associations and schizophrenia.
Academic Article Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.
Academic Article A rare penetrant mutation in CFH confers high risk of age-related macular degeneration.
Academic Article Replicating genotype-phenotype associations.
Academic Article Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations.
Academic Article Common variants at CD40 and other loci confer risk of rheumatoid arthritis.
Academic Article Association of common variation in the HNF1alpha gene region with risk of type 2 diabetes.
Academic Article Parametric and nonparametric linkage analysis: a unified multipoint approach.
Academic Article Haplotype structures and large-scale association testing of the 5' AMP-activated protein kinase genes PRKAA2, PRKAB1, and PRKAB2 [corrected] with type 2 diabetes.
Academic Article Integrated detection and population-genetic analysis of SNPs and copy number variation.
Academic Article Systematic haplotype analysis resolves a complex plasma plant sterol locus on the Micronesian Island of Kosrae.
Academic Article Associations of CFHR1-CFHR3 deletion and a CFH SNP to age-related macular degeneration are not independent.
Academic Article Genetic adaptation of fatty-acid metabolism: a human-specific haplotype increasing the biosynthesis of long-chain omega-3 and omega-6 fatty acids.
Academic Article Genomewide scan of multiple sclerosis in Finnish multiplex families.
Academic Article Evidence for linkage of familial Diamond-Blackfan anemia to chromosome 8p23.3-p22 and for non-19q non-8p disease.
Academic Article High-resolution haplotype structure in the human genome.
Academic Article Support for involvement of neuregulin 1 in schizophrenia pathophysiology.
Academic Article A genome-wide association study identifies IL23R as an inflammatory bowel disease gene.
Academic Article The role of the Toll receptor pathway in susceptibility to inflammatory bowel diseases.
Concept Haplotypes
Academic Article Schizophrenia risk from complex variation of complement component 4.
Grant The Haplotype Map of the Laboratory Mouse Genome
Grant Molecular Genetics of HLA and Disease
Academic Article Human Demographic History Impacts Genetic Risk Prediction across Diverse Populations.
Academic Article Fine-Scale Genetic Structure in Finland.
Academic Article Haplotype Sharing Provides Insights into Fine-Scale Population History and Disease in Finland.
Academic Article Insights into the genetic epidemiology of Crohn's and rare diseases in the Ashkenazi Jewish population.
Academic Article Whole exome sequencing study identifies novel rare and common Alzheimer's-Associated variants involved in immune response and transcriptional regulation.
Academic Article Association of Genetic Variants in NUDT15 With Thiopurine-Induced Myelosuppression in Patients With Inflammatory Bowel Disease.
Academic Article Population Histories of the United States Revealed through Fine-Scale Migration and Haplotype Analysis.
Academic Article Tractor uses local ancestry to enable the inclusion of admixed individuals in GWAS and to boost power.
Search Criteria
  • Haplotypes
Funded by the NIH National Center for Advancing Translational Sciences through its Clinical and Translational Science Awards Program, grant number UL1TR002541.