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فلترة بواسطة : مؤلف Subject : genome-wide association study
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Gene expression, methylation and neuropathology correlations at progressive supranuclear palsy risk loci

Subjects: Male; Risk; 0301 basic medicine

  • Source: Acta Neuropathologica. 132:197-211

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Determining the genetic basis of anthracycline-cardiotoxicity by molecular response QTL mapping in induced cardiomyocytes

Subjects: 0301 basic medicine; Anthracycline; QH301-705.5

  • Source: eLife, Vol 7 (2018)

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Replication of progressive supranuclear palsy genome-wide association study identifies SLCO1A2 and DUSP10 as new susceptibility loci

Subjects: Male; 0301 basic medicine; medicine.medical_specialty

  • Source: Molecular neurodegenerationMolecular Neurodegeneration, Vol 13, Iss 1, Pp 1-10 (2018)Molecular Neurodegeneration

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Potential genetic modifiers of disease risk and age at onset in patients with frontotemporal lobar degeneration and GRN mutations: a genome-wide association study

Subjects: 0301 basic medicine; Oncology; Male

  • Source: The lancet neurologyThe Lancet Neurology, 17(6), 548-558. Lancet Publishing GroupThe lancet / Neurology 17(6), 548-558 (2018). doi:10.1016/S1474-4422(18)30126-1Pottier, C,

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Breast Cancer Clinical Trial of Chemotherapy and Trastuzumab: Potential Tool to Identify Cardiac Modifying Variants of Dilated Cardiomyopathy

Subjects: Oncology; lcsh:Diseases of the circulatory (Cardiovascular) system; medicine.medical_specialty

  • Source: Journal of Cardiovascular Development and DiseaseJournal of Cardiovascular Development and Disease, Vol 4, Iss 2, p 6 (2017)Journal of Cardiovascular Development and Disease; Volume 4;

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Late-onset Alzheimer disease risk variants mark brain regulatory loci

Subjects: Genetics; Regulation of gene expression; 0303 health sciences

  • Source: Neurology: Genetics

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Whole Genome Sequence of Multiple Myeloma-Prone C57BL/KaLwRij Mouse Strain Suggests the Origin of Disease Involves Multiple Cell Types

Subjects: Paraproteinemia; Somatic cell; lcsh:Medicine

  • Source: PLoS ONEPLoS ONE, Vol 10, Iss 5, p e0127828 (2015)

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Genome-wide association study of corticobasal degeneration identifies risk variants shared with progressive supranuclear palsy

Subjects: Male; genetics [Basal Ganglia Diseases]; genetics [Kinesin]

  • Source: Nature Communications 6(1), 7247 (2015). doi:10.1038/ncomms8247Nature communicationsNature Communications

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African American exome sequencing identifies potential risk variants at Alzheimer disease loci

Subjects: 0301 basic medicine; Genetics; education.field_of_study

  • Source: Neurology: Genetics

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Identification of novel variants in colorectal cancer families by high-throughput exome sequencing

Subjects: Adult; Male; Epidemiology

  • Source: Cancer epidemiology, biomarkersprevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology. 22(7)

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