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47 Cross-ancestry GWAS meta-analysis of keloids discovers novel susceptibility loci in diverse populations.
- Published in:
- 2024
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- Publication type:
- Abstract
430 Genome-wide meta-analysis identifies novel risk loci for uterine fibroids across multiple ancestry groups.
- Published in:
- 2024
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- Abstract
Genetically-predicted placental gene expression is associated with birthweight and adult body mass index.
- Published in:
- Scientific Reports, 2023, v. 13, n. 1, p. 1, doi. 10.1038/s41598-022-26572-6
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- Publication type:
- Article
Genetic architecture of heart failure with preserved versus reduced ejection fraction.
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- Nature Communications, 2022, v. 13, n. 1, p. 1, doi. 10.1038/s41467-022-35323-0
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- Article
Impact of obesity on post-operative arrhythmias after congenital heart surgery in children and young adults.
- Published in:
- 2022
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- Publication type:
- journal article
Uterine fibroid polygenic risk score (PRS) associates and predicts risk for uterine fibroid.
- Published in:
- Human Genetics, 2022, v. 141, n. 11, p. 1739, doi. 10.1007/s00439-022-02442-z
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- Article
Integrating gene expression and clinical data to identify drug repurposing candidates for hyperlipidemia and hypertension.
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- Nature Communications, 2022, v. 13, n. 1, p. 1, doi. 10.1038/s41467-021-27751-1
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- Article
Large-Scale Multi-Omics Studies Provide New Insights into Blood Pressure Regulation.
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- International Journal of Molecular Sciences, 2022, v. 23, n. 14, p. 7557, doi. 10.3390/ijms23147557
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- Article
Effect of CYP3A5 and CYP3A4 Genetic Variants on Fentanyl Pharmacokinetics in a Pediatric Population.
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- Clinical Pharmacology & Therapeutics, 2022, v. 111, n. 4, p. 896, doi. 10.1002/cpt.2506
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- Publication type:
- Article
Integrating gene expression and clinical data to identify drug repurposing candidates for hyperlipidemia and hypertension.
- Published in:
- Nature Communications, 2022, v. 13, n. 1, p. 1, doi. 10.1038/s41467-021-27751-1
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- Publication type:
- Article
Evidence that geographic variation in genetic ancestry associates with uterine fibroids.
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- Human Genetics, 2021, v. 140, n. 10, p. 1433, doi. 10.1007/s00439-021-02322-y
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- Publication type:
- Article
Genetic analysis of endometriosis and depression identifies shared loci and implicates causal links with gastric mucosa abnormality.
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- Human Genetics, 2021, v. 140, n. 3, p. 529, doi. 10.1007/s00439-020-02223-6
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- Publication type:
- Article
PheMap: a multi-resource knowledge base for high-throughput phenotyping within electronic health records.
- Published in:
- 2020
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- Publication type:
- journal article
4577 Resistant hypertension potentiates the risk of End-Stage Kidney Disease among African-Americans independent of APOL1 genotype in the Million Veteran Program.
- Published in:
- 2020
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- Publication type:
- Abstract
The polygenic architecture of left ventricular mass mirrors the clinical epidemiology.
- Published in:
- Scientific Reports, 2020, v. 10, n. 1, p. 1, doi. 10.1038/s41598-020-64525-z
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- Publication type:
- Article
Calcium: magnesium intake ratio and colorectal carcinogenesis, results from the prostate, lung, colorectal, and ovarian cancer screening trial.
- Published in:
- 2019
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- Publication type:
- journal article
A Trans -Ethnic Genome-Wide Association Study of Uterine Fibroids.
- Published in:
- Frontiers in Genetics, 2019, p. N.PAG, doi. 10.3389/fgene.2019.00511
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- Publication type:
- Article
Estimating Uterine Fibroid SNP-Based Heritability in European American Women with Imaging-Confirmed Fibroids.
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- Human Heredity, 2019, v. 84, n. 2, p. 73, doi. 10.1159/000501335
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- Publication type:
- Article
A study paradigm integrating prospective epidemiologic cohorts and electronic health records to identify disease biomarkers.
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- Nature Communications, 2018, v. 9, n. 1, p. 1, doi. 10.1038/s41467-018-05624-4
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- Publication type:
- Article
Gene‐based evaluation of low‐frequency variation and genetically‐predicted gene expression impacting risk of keloid formation.
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- Annals of Human Genetics, 2018, v. 82, n. 4, p. 206, doi. 10.1111/ahg.12245
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- Publication type:
- Article
Exploring the phenotypic consequences of tissue specific gene expression variation inferred from GWAS summary statistics.
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- Nature Communications, 2018, v. 9, n. 1, p. 1, doi. 10.1038/s41467-018-03621-1
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- Publication type:
- Article
Interactions between calcium intake and polymorphisms in genes essential for calcium reabsorption and risk of colorectal neoplasia in a two-phase study.
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- Molecular Carcinogenesis, 2017, v. 56, n. 10, p. 2258, doi. 10.1002/mc.22678
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- Article
Evidence of selection as a cause for racial disparities in fibroproliferative disease.
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- PLoS ONE, 2017, v. 12, n. 8, p. 1, doi. 10.1371/journal.pone.0182791
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- Article
African genetic ancestry interacts with body mass index to modify risk for uterine fibroids.
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- PLoS Genetics, 2017, v. 13, n. 7, p. 1, doi. 10.1371/journal.pgen.1006871
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- Publication type:
- Article
Admixture mapping of pelvic organ prolapse in African Americans from the Women’s Health Initiative Hormone Therapy trial.
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- PLoS ONE, 2017, v. 12, n. 6, p. 1, doi. 10.1371/journal.pone.0178839
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- Publication type:
- Article
Meta-analysis identifies five novel loci associated with endometriosis highlighting key genes involved in hormone metabolism.
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- Nature Communications, 2017, v. 8, n. 5, p. 15539, doi. 10.1038/ncomms15539
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- Article
Evaluating the role of race and medication in protection of uterine fibroids by type 2 diabetes exposure.
- Published in:
- 2017
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- Publication type:
- journal article
Rare variants in fox-1 homolog A (RBFOX1) are associated with lower blood pressure.
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- PLoS Genetics, 2017, v. 13, n. 3, p. 1, doi. 10.1371/journal.pgen.1006678
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- Article
Evaluating electronic health record data sources and algorithmic approaches to identify hypertensive individuals.
- Published in:
- 2017
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- Publication type:
- journal article
Calcium/magnesium intake ratio, but not magnesium intake, interacts with genetic polymorphism in relation to colorectal neoplasia in a two-phase study.
- Published in:
- Molecular Carcinogenesis, 2016, v. 55, n. 10, p. 1449, doi. 10.1002/mc.22387
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- Publication type:
- Article
Renal cell cancer histological subtype distribution differs by race and sex.
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- BJU International, 2016, v. 117, n. 2, p. 260, doi. 10.1111/bju.12950
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- Publication type:
- Article
Genetic Determinants of Pelvic Organ Prolapse among African American and Hispanic Women in the Women’s Health Initiative.
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- PLoS ONE, 2015, v. 10, n. 10, p. 1, doi. 10.1371/journal.pone.0141647
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- Publication type:
- Article
Genetic Determinants of Metabolism and Benign Prostate Enlargement: Associations with Prostate Volume.
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- PLoS ONE, 2015, v. 10, n. 7, p. 1, doi. 10.1371/journal.pone.0132028
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- Publication type:
- Article
Contribution of common non-synonymous variants in PCSK1 to body mass index variation and risk of obesity: a systematic review and meta-analysis with evidence from up to 331 175 individuals.
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- Human Molecular Genetics, 2015, v. 24, n. 12, p. 3582, doi. 10.1093/hmg/ddv097
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- Article
Addressing Population-Specific Multiple Testing Burdens in Genetic Association Studies.
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- Annals of Human Genetics, 2015, v. 79, n. 2, p. 136, doi. 10.1111/ahg.12095
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- Publication type:
- Article
Enhancing Uterine Fibroid Research Through Utilization of Biorepositories Linked to Electronic Medical Record Data.
- Published in:
- 2014
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- Publication type:
- Journal Article
Phenome-wide association studies demonstrating pleiotropy of genetic variants within FTO with and without adjustment for body mass index.
- Published in:
- Frontiers in Genetics, 2014, v. 5, p. 1, doi. 10.3389/fgene.2014.00250
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- Publication type:
- Article
Subclinical Hypothyroidism and Risk for Incident Ischemic Stroke Among Postmenopausal Women.
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- Thyroid, 2014, v. 24, n. 8, p. 1210, doi. 10.1089/thy.2014.0106
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- Article
Variants in <i>BET1L</i> and <i>TNRC6B</i> associate with increasing fibroid volume and fibroid type among European Americans.
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- Human Genetics, 2013, v. 132, n. 12, p. 1361, doi. 10.1007/s00439-013-1340-1
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- Article
Subclinical hypothyroidism and risk for incident myocardial infarction among postmenopausal women.
- Published in:
- 2013
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- Publication type:
- journal article
A meta-analysis identifies new loci associated with body mass index in individuals of African ancestry.
- Published in:
- Nature Genetics, 2013, v. 45, n. 6, p. 690, doi. 10.1038/ng.2608
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- Publication type:
- Article
Incidence and Predictors of End Stage Renal Disease among Low-Income Blacks and Whites.
- Published in:
- PLoS ONE, 2012, v. 7, n. 10, p. 1, doi. 10.1371/journal.pone.0048407
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- Publication type:
- Article
Optimized Selection of Unrelated Subjects for Whole-Genome Sequencing Studies of Rare High-Penetrance Alleles.
- Published in:
- Genetic Epidemiology, 2012, v. 36, n. 5, p. 472, doi. 10.1002/gepi.21641
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- Publication type:
- Article
Network-Assisted Investigation of Combined Causal Signals from Genome-Wide Association Studies in Schizophrenia.
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- PLoS Computational Biology, 2012, v. 8, n. 7, p. 1, doi. 10.1371/journal.pcbi.1002587
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- Publication type:
- Article
MCP1 SNPs and Pulmonary Tuberculosis in Cohorts from West Africa, the USA and Argentina: Lack of Association or Epistasis with IL12B Polymorphisms.
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- PLoS ONE, 2012, v. 7, n. 2, p. 1, doi. 10.1371/journal.pone.0032275
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- Publication type:
- Article
HTR1B, ADIPOR1, PPARGC1A, and CYP19A1 and Obesity in a Cohort of Caucasians and African Americans: An Evaluation of Gene-Environment Interactions and Candidate Genes.
- Published in:
- American Journal of Epidemiology, 2012, v. 175, n. 1, p. 11, doi. 10.1093/aje/kwr272
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- Publication type:
- Article
HTR1B, ADIPOR1, PPARGC1A, and CYP19A1 and Obesity in a Cohort of Caucasians and African Americans: An Evaluation of Gene-Environment Interactions and Candidate Genes.
- Published in:
- 2012
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- Publication type:
- Journal Article
Enriching targeted sequencing experiments for rare disease alleles.
- Published in:
- Bioinformatics, 2011, v. 27, n. 15, p. 2112, doi. 10.1093/bioinformatics/btr324
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- Publication type:
- Article
Vitamin D Receptor Gene as a Candidate Gene for Parkinson Disease.
- Published in:
- Annals of Human Genetics, 2011, v. 75, n. 2, p. 201, doi. 10.1111/j.1469-1809.2010.00631.x
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- Publication type:
- Article
Interleukin 12B (IL12B) Genetic Variation and Pulmonary Tuberculosis: A Study of Cohorts from The Gambia, Guinea-Bissau, United States and Argentina.
- Published in:
- PLoS ONE, 2011, v. 6, n. 2, p. 1, doi. 10.1371/journal.pone.0016656
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- Publication type:
- Article