Found: 35
Select item for more details and to access through your institution.
Insights into the genetic architecture of haematological traits from deep phenotyping and whole-genome sequencing for two Mediterranean isolated populations.
- Published in:
- Scientific Reports, 2022, v. 12, n. 1, p. 1, doi. 10.1038/s41598-021-04436-9
- By:
- Publication type:
- Article
Transferability of genetic loci and polygenic scores for cardiometabolic traits in British Pakistani and Bangladeshi individuals.
- Published in:
- Nature Communications, 2022, v. 13, n. 1, p. 1, doi. 10.1038/s41467-022-32095-5
- By:
- Publication type:
- Article
Widespread genomic influences on phenotype in Dravet syndrome, a 'monogenic' condition.
- Published in:
- Brain: A Journal of Neurology, 2023, v. 146, n. 9, p. 3885, doi. 10.1093/brain/awad111
- By:
- Publication type:
- Article
Type 2 diabetes risks and determinants in second-generation migrants and mixed ethnicity people of South Asian and African Caribbean descent in the UK.
- Published in:
- Diabetologia, 2022, v. 65, n. 1, p. 113, doi. 10.1007/s00125-021-05580-7
- By:
- Publication type:
- Article
Genome-wide association studies and cross-population meta-analyses investigating short and long sleep duration.
- Published in:
- Nature Communications, 2023, v. 14, n. 1, p. 1, doi. 10.1038/s41467-023-41249-y
- By:
- Publication type:
- Article
Assessing Associations between the AURKA-HMMR-TPX2-TUBG1 Functional Module and Breast Cancer Risk in BRCA1/2 Mutation Carriers.
- Published in:
- PLoS ONE, 2015, v. 10, n. 4, p. 1, doi. 10.1371/journal.pone.0120020
- By:
- Publication type:
- Article
The transferability of lipid loci across African, Asian and European cohorts.
- Published in:
- Nature Communications, 2019, v. 10, n. 1, p. N.PAG, doi. 10.1038/s41467-019-12026-7
- By:
- Publication type:
- Article
Publisher Correction: Shared heritability and functional enrichment across six solid cancers.
- Published in:
- 2019
- By:
- Publication type:
- Correction Notice
Shared heritability and functional enrichment across six solid cancers.
- Published in:
- Nature Communications, 2019, v. 10, n. 1, p. 1, doi. 10.1038/s41467-018-08054-4
- By:
- Publication type:
- Article
Author Correction: Cohort-wide deep whole genome sequencing and the allelic architecture of complex traits.
- Published in:
- Nature Communications, 2018, v. 9, n. 1, p. 1, doi. 10.1038/s41467-018-07730-9
- By:
- Publication type:
- Article
Cohort-wide deep whole genome sequencing and the allelic architecture of complex traits.
- Published in:
- Nature Communications, 2018, v. 9, n. 1, p. 1, doi. 10.1038/s41467-018-07070-8
- By:
- Publication type:
- Article
The KL-VS sequence variant of Klotho and cancer risk in BRCA1 and BRCA2 mutation carriers.
- Published in:
- Breast Cancer Research & Treatment, 2012, v. 132, n. 3, p. 1119, doi. 10.1007/s10549-011-1938-8
- By:
- Publication type:
- Article
An original phylogenetic approach identified mitochondrial haplogroup T1a1 as inversely associated with breast cancer risk in BRCA2 mutation carriers.
- Published in:
- Breast Cancer Research, 2015, v. 17, n. 1, p. 1, doi. 10.1186/s13058-015-0567-2
- By:
- Publication type:
- Article
Associations of common breast cancer susceptibility alleles with risk of breast cancer subtypes in BRCA1 and BRCA2 mutation carriers.
- Published in:
- 2014
- By:
- Publication type:
- journal article
An original phylogenetic approach identified mitochondrial haplogroup T1a1 as inversely associated with breast cancer risk in BRCA2 mutation carriers.
- Published in:
- 2015
- By:
- Publication type:
- journal article
Common variants at 12p11, 12q24, 9p21, 9q31.2 and in ZNF365 are associated with breast cancer risk for BRCA1 and/or BRCA2 mutation carriers.
- Published in:
- 2012
- By:
- Publication type:
- journal article
Integrating polygenic risk scores in the prediction of type 2 diabetes risk and subtypes in British Pakistanis and Bangladeshis: A population-based cohort study.
- Published in:
- PLoS Medicine, 2022, v. 19, n. 5, p. 1, doi. 10.1371/journal.pmed.1003981
- By:
- Publication type:
- Article
Identification of four novel susceptibility loci for oestrogen receptor negative breast cancer.
- Published in:
- Nature Communications, 2016, v. 7, n. 4, p. 11375, doi. 10.1038/ncomms11375
- By:
- Publication type:
- Article
Cell-type-specific enrichment of risk-associated regulatory elements at ovarian cancer susceptibility loci.
- Published in:
- Human Molecular Genetics, 2015, v. 24, n. 13, p. 3595, doi. 10.1093/hmg/ddv101
- By:
- Publication type:
- Article
Risks of Breast, Ovarian, and Contralateral Breast Cancer for BRCA1 and BRCA2 Mutation Carriers.
- Published in:
- 2017
- By:
- Publication type:
- journal article
Fine-Scale Mapping at 9p22.2 Identifies Candidate Causal Variants That Modify Ovarian Cancer Risk in BRCA1 and BRCA2 Mutation Carriers.
- Published in:
- PLoS ONE, 2016, v. 11, n. 7, p. 1, doi. 10.1371/journal.pone.0158801
- By:
- Publication type:
- Article
Editorial: Genetics of Complex Traits and Diseases From Under-Represented Populations.
- Published in:
- Frontiers in Genetics, 2022, v. 12, p. 1, doi. 10.3389/fgene.2021.817683
- By:
- Publication type:
- Article
Genetic risk scores and dementia risk across different ethnic groups in UK Biobank.
- Published in:
- PLoS ONE, 2022, v. 17, n. 12, p. 1, doi. 10.1371/journal.pone.0277378
- By:
- Publication type:
- Article
Polygenic risk scores indicate extreme ages at onset of breast cancer in female BRCA1/2 pathogenic variant carriers.
- Published in:
- 2022
- By:
- Publication type:
- journal article
DNA Glycosylases Involved in Base Excision Repair May Be Associated with Cancer Risk in <i>BRCA1</i> and <i>BRCA2</i> Mutation Carriers.
- Published in:
- PLoS Genetics, 2014, v. 10, n. 4, p. 1, doi. 10.1371/journal.pgen.1004256
- By:
- Publication type:
- Article
Genome-Wide Association Study in BRCA1 Mutation Carriers Identifies Novel Loci Associated with Breast and Ovarian Cancer Risk.
- Published in:
- PLoS Genetics, 2013, v. 9, n. 3, p. 1, doi. 10.1371/journal.pgen.1003212
- By:
- Publication type:
- Article
Identification of a BRCA2-Specific Modifier Locus at 6p24 Related to Breast Cancer Risk.
- Published in:
- PLoS Genetics, 2013, v. 9, n. 3, p. 1, doi. 10.1371/journal.pgen.1003173
- By:
- Publication type:
- Article
Ovarian cancer susceptibility alleles and risk of ovarian cancer in BRCA1 and BRCA2 mutation carriers.
- Published in:
- Human Mutation, 2012, v. 33, n. 4, p. 690, doi. 10.1002/humu.22025
- By:
- Publication type:
- Article
Selecting instruments for Mendelian randomization in the wake of genome-wide association studies.
- Published in:
- 2016
- By:
- Publication type:
- journal article
Comparing the effects of CETP in East Asian and European ancestries: a Mendelian randomization study.
- Published in:
- Nature Communications, 2024, v. 15, n. 1, p. 1, doi. 10.1038/s41467-024-49109-z
- By:
- Publication type:
- Article
Adolescent Verbal Memory as a Psychosis Endophenotype: A Genome-Wide Association Study in an Ancestrally Diverse Sample.
- Published in:
- Genes, 2022, v. 13, n. 1, p. 106, doi. 10.3390/genes13010106
- By:
- Publication type:
- Article
The Influence of CYP2D6 and CYP2C19 Genetic Variation on Diabetes Mellitus Risk in People Taking Antidepressants and Antipsychotics.
- Published in:
- Genes, 2021, v. 12, n. 11, p. 1758, doi. 10.3390/genes12111758
- By:
- Publication type:
- Article
Combination therapy as a potential risk factor for the development of type 2 diabetes in patients with schizophrenia: the GOMAP study.
- Published in:
- BMC Psychiatry, 2018, v. 18, n. 1, p. N.PAG, doi. 10.1186/s12888-018-1826-4
- By:
- Publication type:
- Article
Very low-depth whole-genome sequencing in complex trait association studies.
- Published in:
- Bioinformatics, 2019, v. 35, n. 15, p. 2555, doi. 10.1093/bioinformatics/bty1032
- By:
- Publication type:
- Article
Evaluation of Polygenic Risk Scores for Breast and Ovarian Cancer Risk Prediction in BRCA1 and BRCA2 Mutation Carriers.
- Published in:
- 2017
- By:
- Publication type:
- journal article