MB SNiP Screen

Knowledge that can change your life

MB SNiP Screen

  • ■  No needles, no fuss!
  • ■  A focus on clinical validity
  • ■  We can screen your DNA for over
    160 traits and conditions including
    pre-screen and post-screen
    genetic counseling session
  • Related Articles

    Listed below are links to news, reports, and discussion articles related to the science of DNA gene screening.

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    Common sequence variants in the LOXL1 gene confer susceptibility to exfoliation glaucoma
    http://www.ncbi.nlm.nih.gov/pu…

    Systematic association mapping identifies NELL1 as a novel IBD disease gene
    http://www.ncbi.nlm.nih.gov/pu…

    Genetic variations associated with diabetic nephropathy and type II diabetes in a Japanese population
    http://www.ncbi.nlm.nih.gov/pu…

    A whole genome association study of neuroticism using DNA pooling
    http://www.ncbi.nlm.nih.gov/pu…

    Risk alleles for multiple sclerosis identified by a genomewide study
    http://www.ncbi.nlm.nih.gov/pu…

    Genetic variants regulating ORMDL3 expression contribute to the risk of childhood asthma
    http://www.ncbi.nlm.nih.gov/pu…

    Genome-Wide Association Scan Shows Genetic Variants in the FTO Gene Are Associated with Obesity-Related Traits
    http://www.ncbi.nlm.nih.gov/pu…

    A genetic risk factor for periodic limb movements in sleep
    http://www.ncbi.nlm.nih.gov/pu…

    Genomewide association analysis of coronary artery disease
    http://www.ncbi.nlm.nih.gov/pu…

    Genome-wide association study of restless legs syndrome identifies common variants in three genomic regions
    http://www.ncbi.nlm.nih.gov/pu…

    A genome-wide association scan identifies the hepatic cholesterol transporter ABCG8 as a susceptibility factor for human gallstone disease
    http://www.ncbi.nlm.nih.gov/pu…

    A genome-wide association study identifies KIAA0350 as a type 1 diabetes gene
    http://www.ncbi.nlm.nih.gov/pu…

    Genome-wide association scan identifies a colorectal cancer susceptibility locus on chromosome 8q24
    http://www.ncbi.nlm.nih.gov/pu…

    A genome-wide association scan of tag SNPs identifies a susceptibility variant for colorectal cancer at 8q24.21
    http://www.ncbi.nlm.nih.gov/pu…

    Variants conferring risk of atrial fibrillation on chromosome 4q25
    http://www.ncbi.nlm.nih.gov/pu…

    Type 2 diabetes whole-genome association study in four populations: the DiaGen consortium
    http://www.ncbi.nlm.nih.gov/pu…

    A genome-wide association study for celiac disease identifies risk variants in the region harboring IL2 and IL21
    http://www.ncbi.nlm.nih.gov/pu…

    GAB2 alleles modify Alzheimer's risk in APOE epsilon4 carriers
    http://www.ncbi.nlm.nih.gov/pu…

    Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls
    http://www.ncbi.nlm.nih.gov/pu…

    Robust associations of four new chromosome regions from genome-wide analyses of type 1 diabetes
    http://www.ncbi.nlm.nih.gov/pu…

    Sequence variants in the autophagy gene IRGM and multiple other replicating loci contribute to Crohn's disease susceptibility
    http://www.ncbi.nlm.nih.gov/pu…

    Genome-wide association study identifies novel breast cancer susceptibility loci
    http://www.ncbi.nlm.nih.gov/pu…

    A genome-wide association study identifies alleles in FGFR2 associated with risk of sporadic postmenopausal breast cancer
    http://www.ncbi.nlm.nih.gov/pu…

    Common variants on chromosomes 2q35 and 16q12 confer susceptibility to estrogen receptor-positive breast cancer
    http://www.ncbi.nlm.nih.gov/pu…

    Genome-wide pharmacogenetic investigation of a hepatic adverse event without clinical signs of immunopathology suggests an underlying immune pathogenesis
    http://www.ncbi.nlm.nih.gov/pu…

    A genome-wide association study implicates diacylglycerol kinase eta (DGKH) and several other genes in the etiology of bipolar disorder
    http://www.ncbi.nlm.nih.gov/pu…

    A genome-wide genotyping study in patients with ischaemic stroke: initial analysis and data release
    http://www.ncbi.nlm.nih.gov/pu…

    A common variant on chromosome 9p21 affects the risk of myocardial infarction
    http://www.ncbi.nlm.nih.gov/pu…

    A variant in CDKAL1 influences insulin response and risk of type 2 diabetes
    http://www.ncbi.nlm.nih.gov/pu…

    Genome-wide association analysis identifies loci for type 2 diabetes and triglyceride levels
    http://www.ncbi.nlm.nih.gov/pu…

    A genome-wide association study of type 2 diabetes in Finns detects multiple susceptibility variants
    http://www.ncbi.nlm.nih.gov/pu…

    Replication of genome-wide association signals in UK samples reveals risk loci for type 2 diabetes
    http://www.ncbi.nlm.nih.gov/pu…

    Genome-wide association study identifies new susceptibility loci for Crohn disease and implicates autophagy in disease pathogenesis
    http://www.ncbi.nlm.nih.gov/pu…

    Identification of PVT1 as a candidate gene for end-stage renal disease in type 2 diabetes using a pooling-based genome-wide single nucleotide polymorphism association study
    http://www.ncbi.nlm.nih.gov/pu…

    Genome-wide association study identifies a second prostate cancer susceptibility variant at 8q24
    http://www.ncbi.nlm.nih.gov/pu…

    A high-density whole-genome association study reveals that APOE is the major susceptibility gene for sporadic late-onset Alzheimer's disease
    http://www.ncbi.nlm.nih.gov/pu…

    Converging evidence for a pseudoautosomal cytokine receptor gene locus in schizophrenia
    http://www.ncbi.nlm.nih.gov/pu…

    Novel Crohn disease locus identified by genome-wide association maps to a gene desert on 5p13.1 and modulates expression of PTGER4
    http://www.ncbi.nlm.nih.gov/pu…

    Genome-wide genotyping in amyotrophic lateral sclerosis and neurologically normal controls: first stage analysis and public release of data
    http://www.ncbi.nlm.nih.gov/pu…

    A genome-wide association study identifies novel risk loci for type 2 diabetes
    http://www.ncbi.nlm.nih.gov/pu…

    Novel genes identified in a high-density genome wide association study for nicotine dependence
    http://www.ncbi.nlm.nih.gov/pu…

    A genome-wide association study identifies IL23R as an inflammatory bowel disease gene
    http://www.ncbi.nlm.nih.gov/pu…

    HTRA1 promoter polymorphism in wet age-related macular degeneration
    http://www.ncbi.nlm.nih.gov/pu…

    Genome-wide genotyping in Parkinson's disease and neurologically normal controls: first stage analysis and public release of data
    http://www.ncbi.nlm.nih.gov/pu…

    A common genetic variant in the NOS1 regulator NOS1AP modulates cardiac repolarization
    http://www.ncbi.nlm.nih.gov/pu…

    High-resolution whole-genome association study of Parkinson disease
    http://www.ncbi.nlm.nih.gov/pu…

    Complement factor H polymorphism in age-related macular degeneration
    http://www.ncbi.nlm.nih.gov/pu…

    http://www.eurekalert.org/pub_releases/2006-05/cshl-llc053006.php
    http://www.eurekalert.org/pub_…

    International Multiple Sclerosis Genetics Consortium, Hafler DA, Compston A, Sawcer S, Lander ES, Daly MJ, De Jager PL, de Bakker PI, Gabriel SB, Mirel DB, Ivinson AJ, Pericak-Vance MA, Gregory SG, Rioux JD, McCauley JL, Haines JL, Barcellos LF, Cree B, Oksenberg JR, Hauser SL.
    http://www.ncbi.nlm.nih.gov/pu…

    Association between single-nucleotide polymorphisms in hormone metabolism and DNA repair genes and epithelial ovarian cancer: results from two Australian studies and an additional validation set.
    http://www.ncbi.nlm.nih.gov/pu…

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