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Donor germ‐line variants associate with outcomes of allogeneic hematopoietic stem cell transplantation in patients with myelodysplastic syndromes.
- Published in:
- American Journal of Hematology, 2024, v. 99, n. 4, p. 770, doi. 10.1002/ajh.27243
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- Publication type:
- Article
Correction to: Genetic variant predictors of gene expression provide new insight into risk of colorectal cancer.
- Published in:
- 2019
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- Publication type:
- Correction Notice
Genetic variant predictors of gene expression provide new insight into risk of colorectal cancer.
- Published in:
- Human Genetics, 2019, v. 138, n. 4, p. 307, doi. 10.1007/s00439-019-01989-8
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- Publication type:
- Article
Enrichment of colorectal cancer associations in functional regions: Insight for using epigenomics data in the analysis of whole genome sequence-imputed GWAS data.
- Published in:
- PLoS ONE, 2017, v. 12, n. 11, p. 1, doi. 10.1371/journal.pone.0186518
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- Publication type:
- Article
On asymptotic distributions of several test statistics for familial relatedness in linear mixed models.
- Published in:
- Statistics in Medicine, 2023, v. 42, n. 17, p. 2962, doi. 10.1002/sim.9762
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- Publication type:
- Article
Exome sequencing identifies rare LDLR and APOA5 alleles conferring risk for myocardial infarction.
- Published in:
- Nature, 2015, v. 518, n. 7537, p. 102, doi. 10.1038/nature13917
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- Publication type:
- Article
Genetic analyses of gynecological disease identify genetic relationships between uterine fibroids and endometrial cancer, and a novel endometrial cancer genetic risk region at the WNT4 1p36.12 locus.
- Published in:
- Human Genetics, 2021, v. 140, n. 9, p. 1353, doi. 10.1007/s00439-021-02312-0
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- Publication type:
- Article
Statistical Design and Analysis of RNA Sequencing Data.
- Published in:
- Genetics, 2010, v. 185, n. 2, p. 405, doi. 10.1534/genetics.110.114983
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- Publication type:
- Article
Rare and Coding Region Genetic Variants Associated With Risk of Ischemic Stroke.
- Published in:
- JAMA Neurology, 2015, v. 72, n. 7, p. 781, doi. 10.1001/jamaneurol.2015.0582
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- Publication type:
- Article
A network analysis to identify mediators of germline-driven differences in breast cancer prognosis.
- Published in:
- Nature Communications, 2020, v. 11, n. 1, p. 1, doi. 10.1038/s41467-019-14100-6
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- Publication type:
- Article
A Two-Stage Poisson Model for Testing RNA-Seq Data.
- Published in:
- Statistical Applications in Genetics & Molecular Biology, 2011, v. 10, n. 1, p. 1, doi. 10.2202/1544-6115.1627
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- Publication type:
- Article
Exploring drivers of gene expression in the Cancer Genome Atlas.
- Published in:
- Bioinformatics, 2019, v. 35, n. 1, p. 62, doi. 10.1093/bioinformatics/bty551
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- Publication type:
- Article
Cellular reprogramming for successful CNS axon regeneration is driven by a temporally changing cast of transcription factors.
- Published in:
- Scientific Reports, 2019, v. 9, n. 1, p. N.PAG, doi. 10.1038/s41598-019-50485-6
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- Publication type:
- Article
Genome-wide association study of germline variants and breast cancer-specific mortality.
- Published in:
- 2019
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- Publication type:
- journal article
A unified linear mixed model for familial relatedness and population structure in genetic association studies.
- Published in:
- Genetic Epidemiology, 2021, v. 45, n. 3, p. 305, doi. 10.1002/gepi.22371
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- Publication type:
- Article
Mendelian randomization analysis with survival outcomes.
- Published in:
- Genetic Epidemiology, 2021, v. 45, n. 1, p. 16, doi. 10.1002/gepi.22354
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- Publication type:
- Article
Transcriptome‐wide association study of breast cancer risk by estrogen‐receptor status.
- Published in:
- Genetic Epidemiology, 2020, v. 44, n. 5, p. 442, doi. 10.1002/gepi.22288
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- Publication type:
- Article
A Variational Bayes Discrete Mixture Test for Rare Variant Association.
- Published in:
- Genetic Epidemiology, 2014, v. 38, n. 1, p. 21, doi. 10.1002/gepi.21772
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- Publication type:
- Article
Testing for Rare Variant Associations in the Presence of Missing Data.
- Published in:
- Genetic Epidemiology, 2013, v. 37, n. 6, p. 529, doi. 10.1002/gepi.21736
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- Publication type:
- Article
Imputation of coding variants in African Americans: better performance using data from the exome sequencing project.
- Published in:
- Bioinformatics, 2013, v. 29, n. 21, p. 2744, doi. 10.1093/bioinformatics/btt477
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- Publication type:
- Article
Genome-wide association of white blood cell counts in Hispanic/Latino Americans: the Hispanic Community Health Study/Study of Latinos.
- Published in:
- Human Molecular Genetics, 2017, v. 26, n. 6, p. 1193, doi. 10.1093/hmg/ddx024
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- Publication type:
- Article
Testing the role of predicted gene knockouts in human anthropometric trait variation.
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- Human Molecular Genetics, 2016, v. 25, n. 10, p. 2082, doi. 10.1093/hmg/ddw055
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- Publication type:
- Article
A meta-analysis of 120 246 individuals identifies 18 new loci for fibrinogen concentration.
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- Human Molecular Genetics, 2016, v. 25, n. 2, p. 358, doi. 10.1093/hmg/ddv454
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- Publication type:
- Article
Association of exome sequences with plasma C-reactive protein levels in >9000 participants.
- Published in:
- Human Molecular Genetics, 2015, v. 24, n. 2, p. 559, doi. 10.1093/hmg/ddu450
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- Publication type:
- Article
Whole-exome imputation of sequence variants identified two novel alleles associated with adult body height in African Americans.
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- Human Molecular Genetics, 2014, v. 23, n. 24, p. 6607, doi. 10.1093/hmg/ddu361
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- Publication type:
- Article
Post-GWAS gene–environment interplay in breast cancer: results from the Breast and Prostate Cancer Cohort Consortium and a meta-analysis on 79 000 women.
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- Human Molecular Genetics, 2014, v. 23, n. 19, p. 5260, doi. 10.1093/hmg/ddu223
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- Publication type:
- Article
Quantifying rare, deleterious variation in 12 human cytochrome P450 drug-metabolism genes in a large-scale exome dataset.
- Published in:
- Human Molecular Genetics, 2014, v. 23, n. 8, p. 1957
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- Publication type:
- Article
Genome-wide interaction analysis of menopausal hormone therapy use and breast cancer risk among 62,370 women.
- Published in:
- Scientific Reports, 2022, v. 12, n. 1, p. 1, doi. 10.1038/s41598-022-10121-2
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- Publication type:
- Article
The fate of duplicated genes in a polyploid plant genome.
- Published in:
- Plant Journal, 2013, v. 73, n. 1, p. 143, doi. 10.1111/tpj.12026
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- Publication type:
- Article
Deleterious heteroplasmic mitochondrial mutations are associated with an increased risk of overall and cancer-specific mortality.
- Published in:
- Nature Communications, 2023, v. 14, n. 1, p. 1, doi. 10.1038/s41467-023-41785-7
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- Publication type:
- Article
Rare and low-frequency coding variants in CXCR2 and other genes are associated with hematological traits.
- Published in:
- Nature Genetics, 2014, v. 46, n. 6, p. 629, doi. 10.1038/ng.2962
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- Publication type:
- Article
Meta-analysis of gene-level tests for rare variant association.
- Published in:
- Nature Genetics, 2014, v. 46, n. 2, p. 200, doi. 10.1038/ng.2852
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- Publication type:
- Article
Contemporary evaluation of estrogen receptor and progesterone receptor expression in breast cancer-associated stroma.
- Published in:
- Breast Cancer Research & Treatment, 2022, v. 196, n. 3, p. 453, doi. 10.1007/s10549-022-06754-6
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- Publication type:
- Article
Combined Associations of a Polygenic Risk Score and Classical Risk Factors With Breast Cancer Risk.
- Published in:
- 2021
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- Publication type:
- journal article
Regeneration Rosetta: An Interactive Web Application To Explore Regeneration-Associated Gene Expression and Chromatin Accessibility.
- Published in:
- G3: Genes | Genomes | Genetics, 2019, v. 9, n. 12, p. 3953, doi. 10.1534/g3.119.400729
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- Publication type:
- Article
Association of Sickle Cell Trait With Chronic Kidney Disease and Albuminuria in African Americans.
- Published in:
- JAMA: Journal of the American Medical Association, 2014, v. 312, n. 20, p. 2115, doi. 10.1001/jama.2014.15063
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- Publication type:
- Article
Common variants in breast cancer risk loci predispose to distinct tumor subtypes.
- Published in:
- 2022
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- Publication type:
- journal article
Association of germline genetic variants with breast cancer-specific survival in patient subgroups defined by clinic-pathological variables related to tumor biology and type of systemic treatment.
- Published in:
- 2021
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- Publication type:
- journal article
Common α-globin variants modify hematologic and other clinical phenotypes in sickle cell trait and disease.
- Published in:
- PLoS Genetics, 2018, v. 14, n. 3, p. 1, doi. 10.1371/journal.pgen.1007293
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- Publication type:
- Article
Individualized multi-omic pathway deviation scores using multiple factor analysis.
- Published in:
- 2022
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- Publication type:
- journal article
Validation of human telomere length multi-ancestry meta-analysis association signals identifies POP5 and KBTBD6 as human telomere length regulation genes.
- Published in:
- Nature Communications, 2024, v. 15, n. 1, p. 1, doi. 10.1038/s41467-024-48394-y
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- Publication type:
- Article
Improving polygenic risk prediction in admixed populations by explicitly modeling ancestral-differential effects via GAUDI.
- Published in:
- Nature Communications, 2024, v. 15, n. 1, p. 1, doi. 10.1038/s41467-024-45135-z
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- Publication type:
- Article
Differential expression—the next generation and beyond.
- Published in:
- Briefings in Functional Genomics, 2012, v. 11, n. 1, p. 57, doi. 10.1093/bfgp/elr041
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- Publication type:
- Article
Rare variant association studies: considerations, challenges and opportunities.
- Published in:
- Genome Medicine, 2015, v. 7, n. 1, p. 1, doi. 10.1186/s13073-015-0138-2
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- Publication type:
- Article
A genome-wide gene-environment interaction study of breast cancer risk for women of European ancestry.
- Published in:
- Breast Cancer Research, 2023, v. 25, n. 1, p. 1, doi. 10.1186/s13058-023-01691-8
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- Publication type:
- Article
Correction to: Multi-ethnic genome-wide association analyses of white blood cell and platelet traits in the Population Architecture using Genomics and Epidemiology (PAGE) Study.
- Published in:
- BMC Genomics, 2021, p. 1, doi. 10.1186/s12864-021-07919-1
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- Publication type:
- Article
Multi-ethnic genome-wide association analyses of white blood cell and platelet traits in the Population Architecture using Genomics and Epidemiology (PAGE) study.
- Published in:
- BMC Genomics, 2021, v. 22, n. 1, p. 1, doi. 10.1186/s12864-021-07745-5
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- Publication type:
- Article
Whole-exome sequencing of 14 389 individuals from the ESP and CHARGE consortia identifies novel rare variation associated with hemostatic factors.
- Published in:
- Human Molecular Genetics, 2022, v. 31, n. 18, p. 3120, doi. 10.1093/hmg/ddac100
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- Publication type:
- Article
Mendelian randomization analyses suggest a role for cholesterol in the development of endometrial cancer.
- Published in:
- International Journal of Cancer, 2021, v. 148, n. 2, p. 307, doi. 10.1002/ijc.33206
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- Publication type:
- Article
Identification of nine new susceptibility loci for endometrial cancer.
- Published in:
- Nature Communications, 2018, v. 9, n. 1, p. 1, doi. 10.1038/s41467-018-05427-7
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- Publication type:
- Article