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Academic Journal

Genetic variant effects on gene expression in human pancreatic islets and their implications for T2D.

  • Authors : Viñuela A; Department of Genetic Medicine and Development, University of Geneva Medical School, 1211, Geneva, Switzerland. .; Institute for Genetics and Genomics in Geneva (iGE3), University of Geneva, 1211, Geneva, Switzerland. .

Subjects: Genetic Predisposition to Disease* ; Quantitative Trait Loci*; Blood Glucose/Blood Glucose/Blood Glucose/*genetics

  • Source: Nature communications [Nat Commun] 2020 Sep 30; Vol. 11 (1), pp. 4912. Date of Electronic Publication: 2020 Sep 30.Publisher: Nature Pub. Group Country of Publication: England NLM ID: 101528555 Publication Model: Electronic Cited Medium: Internet ISSN:

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Academic Journal

Association of gBRCA1/2 mutation locations with ovarian cancer risk in Japanese patients from the CHARLOTTE study.

  • Authors : Yoshihara K; Department of Obstetrics and Gynecology, Niigata University Graduate School of Medical and Dental Sciences, Niigata, Japan.; Enomoto T

Subjects: Genetic Predisposition to Disease* ; Mutation*; BRCA1 Protein/BRCA1 Protein/BRCA1 Protein/*genetics

  • Source: Cancer science [Cancer Sci] 2020 Sep; Vol. 111 (9), pp. 3350-3358. Date of Electronic Publication: 2020 Aug 02.Publisher: Wiley Publishing on behalf of the Japanese Cancer Association Country of Publication: England NLM ID: 101168776 Publication Model: Print-Electronic

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Academic Journal

Clinical utility of target capture-based panel sequencing in hematological malignancies: A multicenter feasibility study.

  • Authors : Yasuda T; Clinical Research Center, National Hospital Organization Nagoya Medical Center, Nagoya, Japan.; Sanada M

Subjects: Biomarkers, Tumor* ; Genetic Association Studies*/Genetic Association Studies*/Genetic Association Studies*/methods ; Genetic Predisposition to Disease*

  • Source: Cancer science [Cancer Sci] 2020 Sep; Vol. 111 (9), pp. 3367-3378. Date of Electronic Publication: 2020 Jul 17.Publisher: Wiley Publishing on behalf of the Japanese Cancer Association Country of Publication: England NLM ID: 101168776 Publication Model: Print-Electronic

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Academic Journal

Impact of DPYD, DPYS, and UPB1 gene variations on severe drug-related toxicity in patients with cancer.

  • Authors : Yokoi K; Department of Pediatrics, Fujita Health University School of Medicine, Toyoake, Japan.; Division of Molecular Genetics, Institute for Comprehensive Medical Science, Fujita Health University, Toyoake, Japan.

Subjects: Genetic Predisposition to Disease* ; Genetic Variation*; Amidohydrolases/Amidohydrolases/Amidohydrolases/*genetics

  • Source: Cancer science [Cancer Sci] 2020 Sep; Vol. 111 (9), pp. 3359-3366. Date of Electronic Publication: 2020 Jul 20.Publisher: Wiley Publishing on behalf of the Japanese Cancer Association Country of Publication: England NLM ID: 101168776 Publication Model: Print-Electronic

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Academic Journal

Vitamin D receptor polymorphisms in spontaneous preterm birth: a case-control study.

Subjects: Genetic Predisposition to Disease* ; Polymorphism, Single Nucleotide*; Premature Birth/Premature Birth/Premature Birth/*genetics

  • Source: Croatian medical journal [Croat Med J] 2020 Aug 31; Vol. 61 (4), pp. 338-345.Publisher: Medicinska Naklada Country of Publication: Croatia NLM ID: 9424324 Publication Model: Print Cited Medium: Internet ISSN: 1332-8166

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Academic Journal

A general framework for functionally informed set-based analysis: Application to a large-scale colorectal cancer study.

  • Authors : Dong X; Division of Public Health Sciences, Fred Hutchinson Cancer Research Center, Seattle, WA, USA.; Department of Biostatistics, University of Washington, Seattle, WA, USA.

Subjects: Genetic Predisposition to Disease* ; Genome-Wide Association Study*; Colorectal Neoplasms/Colorectal Neoplasms/Colorectal Neoplasms/*genetics

  • Source: PLoS genetics [PLoS Genet] 2020 Aug 24; Vol. 16 (8), pp. e1008947. Date of Electronic Publication: 2020 Aug 24 (Print Publication: 2020).Publisher: Public Library of Science Country of Publication: United States NLM ID: 101239074 Publication Model: eCollection Cited Medium: Internet

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Academic Journal

Polygenic background modifies penetrance of monogenic variants for tier 1 genomic conditions.

  • Authors : Fahed AC; Center for Genomic Medicine, Department of Medicine, Massachusetts General Hospital, Boston, MA, USA.; Division of Cardiology, Department of Medicine, Massachusetts General Hospital, Boston, MA, USA.

Subjects: Genetic Predisposition to Disease* ; Penetrance*; Multifactorial Inheritance/Multifactorial Inheritance/Multifactorial Inheritance/*genetics

  • Source: Nature communications [Nat Commun] 2020 Aug 20; Vol. 11 (1), pp. 3635. Date of Electronic Publication: 2020 Aug 20.Publisher: Nature Pub. Group Country of Publication: England NLM ID: 101528555 Publication Model: Electronic Cited Medium: Internet ISSN:

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Academic Journal

ADAMTS12, a new candidate gene for pediatric stroke.

  • Authors : Witten A; Institute of Human Genetics, Genetic Epidemiology, University of Münster, Münster, Germany.; Rühle F

Subjects: Genetic Predisposition to Disease*; ADAMTS Proteins/ADAMTS Proteins/ADAMTS Proteins/*genetics ; Stroke/Stroke/Stroke/*genetics

  • Source: PloS one [PLoS One] 2020 Aug 20; Vol. 15 (8), pp. e0237928. Date of Electronic Publication: 2020 Aug 20 (Print Publication: 2020).Publisher: Public Library of Science Country of Publication: United States NLM ID: 101285081 Publication Model: eCollection Cited Medium: Internet

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Academic Journal

Highs and lows: Genetic susceptibility to daily events.

  • Authors : Sicorello M; Department of Genetic Psychology, Faculty of Psychology, Ruhr-University Bochum, Germany.; Department of Psychosomatic Medicine and Psychotherapy, Central Institute of Mental Health, Medical Faculty Mannheim, Heidelberg University, Heidelberg, Germany.

Subjects: Genetic Predisposition to Disease* ; Life Change Events*; Serotonin Plasma Membrane Transport Proteins/Serotonin Plasma Membrane Transport Proteins/Serotonin Plasma Membrane Transport Proteins/*genetics

  • Source: PloS one [PLoS One] 2020 Aug 13; Vol. 15 (8), pp. e0237001. Date of Electronic Publication: 2020 Aug 13 (Print Publication: 2020).Publisher: Public Library of Science Country of Publication: United States NLM ID: 101285081 Publication Model: eCollection Cited Medium: Internet

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  • 1-10 of  154,752 results for ""Genetic Predisposition to Disease""