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Explaining sex differences in risk of bloodstream infections using mediation analysis in the population-based HUNT study in Norway.
- Published in:
- Scientific Reports, 2022, v. 12, n. 1, p. 1, doi. 10.1038/s41598-022-12569-8
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- Publication type:
- Article
Risks of preterm birth among non-Hispanic black and non-Hispanic white women: Effect modification by maternal age.
- Published in:
- 2019
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- Publication type:
- journal article
Examining the effect of obesity-associated gene variants on breast cancer survivors in a randomized weight loss intervention.
- Published in:
- Breast Cancer Research & Treatment, 2021, v. 187, n. 2, p. 487, doi. 10.1007/s10549-021-06151-5
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- Publication type:
- Article
A pooled genome-wide association study identifies pancreatic cancer susceptibility loci on chromosome 19p12 and 19p13.3 in the full-Jewish population.
- Published in:
- Human Genetics, 2021, v. 140, n. 2, p. 309, doi. 10.1007/s00439-020-02205-8
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- Publication type:
- Article
In-Depth Analysis of Genetic Variation Associated with Severe West Nile Viral Disease.
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- Vaccines, 2020, v. 8, n. 4, p. 744, doi. 10.3390/vaccines8040744
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- Publication type:
- Article
Iron status and the risk of sepsis and severe COVID-19: a two-sample Mendelian randomization study.
- Published in:
- Scientific Reports, 2022, v. 12, n. 1, p. 1, doi. 10.1038/s41598-022-20679-6
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- Publication type:
- Article
Association between the SERPINE1 (PAI-1) 4G/5G insertion/deletion promoter polymorphism (rs1799889) and pre-eclampsia: a systematic review and meta-analysis.
- Published in:
- Molecular Human Reproduction, 2013, v. 19, n. 3, p. 136, doi. 10.1093/molehr/gas056
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- Publication type:
- Article
Identification of genetic variants associated with dengue or West Nile virus disease: a systematic review and meta-analysis.
- Published in:
- 2018
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- Publication type:
- journal article
Multiethnic genome-wide association study identifies ethnic-specific associations with body mass index in Hispanics and African Americans.
- Published in:
- BMC Immunology, 2016, v. 17, p. 1, doi. 10.1186/s12863-016-0387-0
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- Publication type:
- Article
Genome-Wide Gene by Environment Interaction Analysis Identifies Common SNPs at 17q21.2 that Are Associated with Increased Body Mass Index Only among Asthmatics.
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- PLoS ONE, 2015, v. 10, n. 12, p. 1, doi. 10.1371/journal.pone.0144114
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- Publication type:
- Article
Neural-Specific Deletion of Htra2 Causes Cerebellar Neurodegeneration and Defective Processing of Mitochondrial OPA1.
- Published in:
- PLoS ONE, 2014, v. 9, n. 12, p. 1, doi. 10.1371/journal.pone.0115789
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- Publication type:
- Article
Stage and Gene Specific Signatures Defined by Histones H3K4me2 and H3K27me3 Accompany Mammalian Retina Maturation In Vivo.
- Published in:
- PLoS ONE, 2012, v. 7, n. 10, p. 1, doi. 10.1371/journal.pone.0046867
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- Publication type:
- Article
Genetic Signatures of Exceptional Longevity in Humans.
- Published in:
- PLoS ONE, 2012, v. 7, n. 1, p. 1, doi. 10.1371/journal.pone.0029848
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- Publication type:
- Article
dbPEC: a comprehensive literature-based database for preeclampsia related genes and phenotypes.
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- Database: The Journal of Biological Databases & Curation, 2016, v. 2016, p. 1, doi. 10.1093/database/baw006
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- Publication type:
- Article
Genetic Risk Score for Essential Hypertension and Risk of Preeclampsia.
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- American Journal of Hypertension, 2016, v. 29, n. 1, p. 17, doi. 10.1093/ajh/hpv069
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- Publication type:
- Article
Genetic Predisposition to Dyslipidemia and Risk of Preeclampsia.
- Published in:
- American Journal of Hypertension, 2015, v. 28, n. 7, p. 915, doi. 10.1093/ajh/hpu242
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- Publication type:
- Article
Type 2 cytokine genes as allergic asthma risk factors after viral bronchiolitis in early childhood.
- Published in:
- Frontiers in Immunology, 2023, v. 13, p. 01, doi. 10.3389/fimmu.2022.1054119
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- Publication type:
- Article
Exhaustive Genome-Wide Search for SNP-SNP Interactions Across 10 Human Diseases.
- Published in:
- G3: Genes | Genomes | Genetics, 2016, v. 6, n. 7, p. 2043, doi. 10.1534/g3.116.028563
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- Publication type:
- Article
Genome-Wide Association Study of Pre-Eclampsia Detects Novel Maternal Single Nucleotide Polymorphisms and Copy-Number Variants in Subsets of the Hyperglycemia and Adverse Pregnancy Outcome (HAPO) Study Cohort.
- Published in:
- Annals of Human Genetics, 2013, v. 77, n. 4, p. 277, doi. 10.1111/ahg.12021
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- Publication type:
- Article
Association of iron status with the risk of bloodstream infections: results from the prospective population-based HUNT Study in Norway.
- Published in:
- 2018
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- Publication type:
- journal article
Discovery and Mediation Analysis of Cross-Phenotype Associations Between Asthma and Body Mass Index in 12q13.2.
- Published in:
- American Journal of Epidemiology, 2021, v. 190, n. 1, p. 85, doi. 10.1093/aje/kwaa144
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- Publication type:
- Article
RE: "RACIAL AND ETHNIC DIFFERENCES IN SOCIOECONOMIC POSITION AND RISK OF CHILDHOOD ACUTE LYMPHOBLASTIC LEUKEMIA".
- Published in:
- 2019
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- Publication type:
- Letter to the Editor
Statistical Analysis of Multiple Phenotypes in Genetic Epidemiologic Studies: From Cross-Phenotype Associations to Pleiotropy.
- Published in:
- American Journal of Epidemiology, 2018, v. 187, n. 4, p. 855, doi. 10.1093/aje/kwx296
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- Publication type:
- Article
Parental Age and Risk of Pediatric Cancer in the Offspring: A Population-Based Record-Linkage Study in California.
- Published in:
- American Journal of Epidemiology, 2017, v. 186, n. 7, p. 843, doi. 10.1093/aje/kwx160
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- Publication type:
- Article
Cesarean Section and Risk of Childhood Acute Lymphoblastic Leukemia in a Population-Based, Record-Linkage Study in California.
- Published in:
- American Journal of Epidemiology, 2017, v. 185, n. 2, p. 96, doi. 10.1093/aje/kww153
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- Publication type:
- Article
Systematically identifying genetic signatures including novel SNP-clusters, nonsense variants, frame-shift INDELs, and long STR expansions that potentially link to unknown phenotypes existing in dog breeds.
- Published in:
- BMC Genomics, 2023, v. 24, n. 1, p. 1, doi. 10.1186/s12864-023-09390-6
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- Publication type:
- Article
Genome-wide search identifies a gene-gene interaction between 20p13 and 2q14 in asthma.
- Published in:
- BMC Genetics, 2016, v. 17, p. 1, doi. 10.1186/s12863-016-0376-3
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- Publication type:
- Article
Multiethnic genome-wide association study identifies ethnic-specific associations with body mass index in Hispanics and African Americans.
- Published in:
- BMC Genetics, 2016, v. 17, p. 1, doi. 10.1186/s12863-016-0387-0
- By:
- Publication type:
- Article
LDER-GE estimates phenotypic variance component of gene–environment interactions in human complex traits accurately with GE interaction summary statistics and full LD information.
- Published in:
- Briefings in Bioinformatics, 2024, v. 25, n. 4, p. 1, doi. 10.1093/bib/bbae335
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- Publication type:
- Article
Genome-wide association study identifies a maternal copy-number deletion in PSG11 enriched among preeclampsia patients.
- Published in:
- BMC Pregnancy & Childbirth, 2012, v. 12, n. 1, p. 61, doi. 10.1186/1471-2393-12-61
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- Publication type:
- Article
BMI1 enhancer polymorphism underlies chromosome 10p12.31 association with childhood acute lymphoblastic leukemia.
- Published in:
- International Journal of Cancer, 2018, v. 143, n. 11, p. 2647, doi. 10.1002/ijc.31622
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- Publication type:
- Article
Body mass index and risk of dying from a bloodstream infection: A Mendelian randomization study.
- Published in:
- 2020
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- Publication type:
- journal article
GWAS in childhood acute lymphoblastic leukemia reveals novel genetic associations at chromosomes 17q12 and 8q24.21.
- Published in:
- Nature Communications, 2018, v. 9, n. 1, p. 1, doi. 10.1038/s41467-017-02596-9
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- Publication type:
- Article
Disease risk prediction with rare and common variants.
- Published in:
- BMC Proceedings, 2011, v. 5, n. Suppl 9, p. 1, doi. 10.1186/1753-6561-5-S9-S61
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- Publication type:
- Article
Variants in JAZF1 are associated with asthma, type 2 diabetes, and height in the United Kingdom biobank population.
- Published in:
- Frontiers in Genetics, 2023, p. 1, doi. 10.3389/fgene.2023.1129389
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- Publication type:
- Article
The genetic contribution of the X chromosome in age-related hearing loss.
- Published in:
- Frontiers in Genetics, 2023, v. 14, p. 01, doi. 10.3389/fgene.2023.1106328
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- Publication type:
- Article
Mutations in the Wolfram syndrome1 gene (WFS1) are a common cause of low frequencysensorineural hearing loss.
- Published in:
- Human Molecular Genetics, 2001, v. 10, n. 22, p. 2501, doi. 10.1093/hmg/10.22.2501
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- Publication type:
- Article
General, but not abdominal, overweight increases odds of asthma among Norwegian adolescents: the Young-HUNT study.
- Published in:
- 2014
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- Publication type:
- Journal Article
General, but not abdominal, overweight increases odds of asthma among Norwegian adolescents: the Young- HUNT study.
- Published in:
- Acta Paediatrica, 2014, v. 103, n. 12, p. 1270, doi. 10.1111/apa.12775
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- Publication type:
- Article
Epidemiology and outcome of sepsis in adult patients with Streptococcus pneumoniae infection in a Norwegian county 1993-2011: an observational study.
- Published in:
- 2016
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- Publication type:
- journal article
Attempted Replication of 50 Reported Asthma Risk Genes Identifies a SNP in RAD50 as Associated with Childhood Atopic Asthma.
- Published in:
- Human Heredity, 2011, v. 71, n. 2, p. 97, doi. 10.1159/000319536
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- Publication type:
- Article
Map Error Reduction: Using Genetic and Sequence-Based Physical Maps to Order Closely Linked Markers.
- Published in:
- Human Heredity, 2002, v. 54, n. 1, p. 34, doi. 10.1159/000066697
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- Publication type:
- Article
MendelProb: probability and sample size calculations for Mendelian studies of exome and whole genome sequence data.
- Published in:
- Bioinformatics, 2019, v. 35, n. 3, p. 529, doi. 10.1093/bioinformatics/bty542
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- Publication type:
- Article
Whole-exome sequencing of a pedigree segregating asthma.
- Published in:
- BMC Medical Genetics, 2012, v. 13, n. 1, p. 1, doi. 10.1186/1471-2350-13-95
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- Publication type:
- Article