Found: 34
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Oxido-reductive regulation of vascular remodeling by receptor tyrosine kinase ROS1.
- Published in:
- Journal of Clinical Investigation, 2014, v. 124, n. 12, p. 5159, doi. 10.1172/JCI77484
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- Publication type:
- Article
Letter to the Editor Regarding Lavanya et al. A patient with a novel pathogenic variant in COL5A1 exhibiting prominent vascular and cardiac features.
- Published in:
- American Journal of Medical Genetics. Part A, 2022, v. 188, n. 9, p. 2832, doi. 10.1002/ajmg.a.62875
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- Publication type:
- Article
Spontaneous coronary artery dissection is infrequent in individuals with heritable thoracic aortic disease despite partially shared genetic susceptibility.
- Published in:
- American Journal of Medical Genetics. Part A, 2022, v. 188, n. 5, p. 1448, doi. 10.1002/ajmg.a.62661
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- Publication type:
- Article
Systematic evaluation of coding variation identifies a candidate causal variant in TM6SF2 influencing total cholesterol and myocardial infarction risk.
- Published in:
- Nature Genetics, 2014, v. 46, n. 4, p. 345, doi. 10.1038/ng.2926
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- Publication type:
- Article
Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium.
- Published in:
- Nature Genetics, 2009, v. 41, n. 11, p. 1191, doi. 10.1038/ng.466
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- Publication type:
- Article
From Atherosclerosis to Spontaneous Coronary Artery Dissection: Defining a Clinical and Genetic Risk Spectrum for Myocardial Infarction.
- Published in:
- Current Atherosclerosis Reports, 2024, v. 26, n. 7, p. 331, doi. 10.1007/s11883-024-01208-4
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- Publication type:
- Article
Genetic association analysis highlights new loci that modulate hematological trait variation in Caucasians and African Americans.
- Published in:
- Human Genetics, 2011, v. 129, n. 3, p. 307, doi. 10.1007/s00439-010-0925-1
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- Publication type:
- Article
4097 Transcriptome and molecular analysis of erythropoietin-induced hypertension.
- Published in:
- 2020
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- Publication type:
- Abstract
Time course analysis of gene expression identifies multiple genes with differential expression in patients with in-stent restenosis.
- Published in:
- BMC Medical Genomics, 2011, v. 4, n. 1, p. 20, doi. 10.1186/1755-8794-4-20
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- Publication type:
- Article
Advancements in the Genetics of Spontaneous Coronary Artery Dissection.
- Published in:
- Current Cardiology Reports, 2023, v. 25, n. 12, p. 1735, doi. 10.1007/s11886-023-01989-1
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- Publication type:
- Article
Current progress in clinical, molecular, and genetic aspects of adult fibromuscular dysplasia.
- Published in:
- Cardiovascular Research, 2022, v. 118, n. 1, p. 65, doi. 10.1093/cvr/cvab086
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- Publication type:
- Article
Lysyl oxidase interactions with transforming growth factor‐β during angiogenesis are mediated by endothelin 1.
- Published in:
- FASEB Journal, 2021, v. 35, n. 9, p. 1, doi. 10.1096/fj.202001860RR
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- Publication type:
- Article
Clinical and biochemical profiles suggest fibromuscular dysplasia is a systemic disease with altered TGF-β expression and connective tissue features.
- Published in:
- FASEB Journal, 2014, v. 28, n. 8, p. 3313, doi. 10.1096/fj.14-251207
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- Publication type:
- Article
Genetic variation in CCDC93 is associated with elevated central systolic blood pressure, impaired arterial relaxation, and mitochondrial dysfunction.
- Published in:
- PLoS Genetics, 2024, v. 20, n. 9, p. 1, doi. 10.1371/journal.pgen.1011151
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- Publication type:
- Article
Placental transcriptome analysis of hypertensive pregnancies identifies distinct gene expression profiles of preeclampsia superimposed on chronic hypertension.
- Published in:
- BMC Medical Genomics, 2023, v. 16, n. 1, p. 1, doi. 10.1186/s12920-023-01522-x
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- Publication type:
- Article
Genetic and clinical determinants of abdominal aortic diameter: genome-wide association studies, exome array data and Mendelian randomization study.
- Published in:
- Human Molecular Genetics, 2022, v. 31, n. 20, p. 3566, doi. 10.1093/hmg/ddac051
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- Publication type:
- Article
Molecular genetic evaluation of pediatric renovascular hypertension due to renal artery stenosis and abdominal aortic coarctation in neurofibromatosis type 1.
- Published in:
- Human Molecular Genetics, 2022, v. 31, n. 3, p. 334, doi. 10.1093/hmg/ddab241
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- Publication type:
- Article
An Asian-specific MPL genetic variant alters JAK–STAT signaling and influences platelet count in the population.
- Published in:
- Human Molecular Genetics, 2021, v. 30, n. 9, p. 836, doi. 10.1093/hmg/ddab062
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- Publication type:
- Article
No large-effect low-frequency coding variation found for myocardial infarction.
- Published in:
- Human Molecular Genetics, 2014, v. 23, n. 17, p. 4721, doi. 10.1093/hmg/ddu175
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- Publication type:
- Article
Genetic associations with expression for genes implicated in GWAS studies for atherosclerotic cardiovascular disease and blood phenotypes.
- Published in:
- Human Molecular Genetics, 2014, v. 23, n. 3, p. 782, doi. 10.1093/hmg/ddt461
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- Publication type:
- Article
Loci influencing blood pressure identified using a cardiovascular gene-centric array.
- Published in:
- Human Molecular Genetics, 2013, v. 22, n. 16, p. 3394
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- Publication type:
- Article
Loci influencing blood pressure identified using a cardiovascular gene-centric array.
- Published in:
- Human Molecular Genetics, 2013, v. 22, n. 8, p. 1663
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- Publication type:
- Article
A genome-wide association study identifies a region at chromosome 12 as a potential susceptibility locus for restenosis after percutaneous coronary intervention.
- Published in:
- Human Molecular Genetics, 2011, v. 20, n. 23, p. 4748, doi. 10.1093/hmg/ddr389
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- Publication type:
- Article
Positional identification of variants of Adamts16 linked to inherited hypertension.
- Published in:
- Human Molecular Genetics, 2011, v. 20, n. 21, p. 4297, doi. 10.1093/hmg/ddr286
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- Publication type:
- Article
Combined admixture mapping and association analysis identifies a novel blood pressure genetic locus on 5p13: contributions from the CARe consortium.
- Published in:
- Human Molecular Genetics, 2011, v. 20, n. 11, p. 2285, doi. 10.1093/hmg/ddr113
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- Publication type:
- Article
Generalization and fine mapping of red blood cell trait genetic associations to multi‐ethnic populations: The PAGE study.
- Published in:
- American Journal of Hematology, 2018, v. 93, n. 8, p. 1061, doi. 10.1002/ajh.25161
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- Publication type:
- Article
Genome-Wide Association Study of White Blood Cell Count in 16,388 African Americans: the Continental Origins and Genetic Epidemiology Network (COGENT).
- Published in:
- PLoS Genetics, 2011, v. 7, n. 6, p. 1, doi. 10.1371/journal.pgen.1002108
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- Publication type:
- Article
Positional identification of variants of Adamts16 linked to inherited hypertension.
- Published in:
- Human Molecular Genetics, 2009, v. 18, n. 15, p. 2825, doi. 10.1093/hmg/ddp218
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- Publication type:
- Article
First International Consensus on the diagnosis and management of fibromuscular dysplasia.
- Published in:
- Vascular Medicine, 2019, v. 24, n. 2, p. 164, doi. 10.1177/1358863X18821816
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- Publication type:
- Article
Bilateral internal mammary artery fibromuscular dysplasia discovered upon evaluation for reconstructive breast surgery.
- Published in:
- 2015
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- Publication type:
- Case Study
Association Between Absolute Neutrophil Count and Variation at TCIRG1: The NHLBI Exome Sequencing Project.
- Published in:
- Genetic Epidemiology, 2016, v. 40, n. 6, p. 470, doi. 10.1002/gepi.21976
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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
On Averaging Power for Genetic Association and Linkage Studies.
- Published in:
- Human Heredity, 2005, v. 59, n. 1, p. 14, doi. 10.1159/000084732
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- Publication type:
- Article
Genetics of coronary artery calcification among African Americans, a meta-analysis.
- Published in:
- BMC Medical Genetics, 2013, v. 14, n. 1, p. 1, doi. 10.1186/1471-2350-14-75
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- Publication type:
- Article