Rasika A Mathias


Ontology type: schema:Person     


Person Info

NAME

Rasika A

SURNAME

Mathias

Publications in SciGraph latest 50 shown

  • 2019-02 Leveraging linkage evidence to identify low-frequency and rare variants on 16p13 associated with blood pressure using TOPMed whole genome sequencing data in HUMAN GENETICS
  • 2019-01-15 Author Correction: Assembly of a pan-genome from deep sequencing of 910 humans of African descent in NATURE GENETICS
  • 2018-12 The genetics of smoking in individuals with chronic obstructive pulmonary disease in RESPIRATORY RESEARCH
  • 2018-11-19 Assembly of a pan-genome from deep sequencing of 910 humans of African descent in NATURE GENETICS
  • 2018-01 Multiancestry association study identifies new asthma risk loci that colocalize with immune-cell enhancer marks in NATURE GENETICS
  • 2017-12 Identifying tagging SNPs for African specific genetic variation from the African Diaspora Genome in SCIENTIFIC REPORTS
  • 2017-03 Genome-wide association analyses for lung function and chronic obstructive pulmonary disease identify new loci and potential druggable targets in NATURE GENETICS
  • 2016-10-11 A continuum of admixture in the Western Hemisphere revealed by the African Diaspora genome in NATURE COMMUNICATIONS
  • 2016-10-11 Challenges and disparities in the application of personalized genomic medicine to populations with African ancestry in NATURE COMMUNICATIONS
  • 2015-12 Genome-wide association study of platelet aggregation in African Americans in BMC GENETICS
  • 2015-12 Low-frequency and rare exome chip variants associate with fasting glucose and type 2 diabetes susceptibility in NATURE COMMUNICATIONS
  • 2015-12 Ethnic-specific associations of rare and low-frequency DNA sequence variants with asthma in NATURE COMMUNICATIONS
  • 2015-10 A global reference for human genetic variation in NATURE
  • 2015-07-01 Directional dominance on stature and cognition in diverse human populations in NATURE
  • 2014-12 Integrating sequence and array data to create an improved 1000 Genomes Project haplotype reference panel in NATURE COMMUNICATIONS
  • 2014-12 Integrated genome-wide association, coexpression network, and expression single nucleotide polymorphism analysis identifies novel pathway in allergic rhinitis in BMC MEDICAL GENOMICS
  • 2014-06 Genetic Variants in the FADS Gene: Implications for Dietary Recommendations for Fatty Acid Intake in CURRENT NUTRITION REPORTS
  • 2014 Introduction to Genetics and Genomics in Asthma: Genetics of Asthma in HETEROGENEITY IN ASTHMA
  • 2013-01 Genome-wide study identifies two loci associated with lung function decline in mild to moderate COPD in HUMAN GENETICS
  • 2012-08 Exome sequencing of extreme phenotypes identifies DCTN4 as a modifier of chronic Pseudomonas aeruginosa infection in cystic fibrosis in NATURE GENETICS
  • 2012-06 Detectable clonal mosaicism from birth to old age and its relationship to cancer in NATURE GENETICS
  • 2011-12 The impact of FADS genetic variants on ω6 polyunsaturated fatty acid metabolism in African Americans in BMC GENETICS
  • 2011-09 Recombination rates in admixed individuals identified by ancestry-based inference in NATURE GENETICS
  • 2011-09 Meta-analysis of genome-wide association studies of asthma in ethnically diverse North American populations in NATURE GENETICS
  • 2011-06 Genome partitioning of genetic variation for complex traits using common SNPs in NATURE GENETICS
  • 2011-03 A common variant in the CDKN2B gene on chromosome 9p21 protects against coronary artery disease in Americans of African ancestry in JOURNAL OF HUMAN GENETICS
  • 2010-12 A combined genome-wide linkage and association approach to find susceptibility loci for platelet function phenotypes in European American and African American families with coronary artery disease in BMC MEDICAL GENOMICS
  • 2010-06 Polymorphisms in the sialic acid-binding immunoglobulin-like lectin-8 (Siglec-8) gene are associated with susceptibility to asthma in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 2009-12 Evaluation of random forests performance for genome-wide association studies in the presence of interaction effects in BMC PROCEEDINGS
  • 2007-03 Rage gene promoter polymorphisms and diabetic retinopathy in a clinic-based population from South India in EYE
  • 2006-12 A graphical assessment of p-values from sliding window haplotype tests of association to identify asthma susceptibility loci on chromosome 11q in BMC GENETICS
  • 2006-01 Variants in the gene encoding C3 are associated with asthma and related phenotypes among African Caribbean families in GENES & IMMUNITY
  • 2005-12 Application of the regression of offspring on mid-parent method to detect associations between single-nucleotide polymorphisms and the beta 2 electroencephalogram phenotype in the COGA data in BMC GENETICS
  • 2005-12 Investigation of altering single-nucleotide polymorphism density on the power to detect trait loci and frequency of false positive in nonparametric linkage analyses of qualitative traits in BMC GENETICS
  • 2005-12 Identification of tag single-nucleotide polymorphisms in regions with varying linkage disequilibrium in BMC GENETICS
  • 2004-05 Genome scan for loci linked to mite sensitivity: the Collaborative Study on the Genetics of Asthma (CSGA) in GENES & IMMUNITY
  • 2003-12 Comparison of year-of-exam- and age-matched estimates of heritability in the Framingham Heart Study data in BMC GENETICS
  • 2003-07 Evidence for asthma susceptibility genes on chromosome 11 in an African-American population in HUMAN GENETICS
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