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Multiple Defects in Type III Collagen Synthesis Are Associated with the Pathogenesis of Abdominal Aortic Aneurysmsa.
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- Annals of the New York Academy of Sciences, 1996, v. 800, n. 1, p. 216, doi. 10.1111/j.1749-6632.1996.tb33312.x
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- Article
Candidate Genes for Abdominal Aortic Aneurysmsa.
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- Annals of the New York Academy of Sciences, 1996, v. 800, n. 1, p. 186, doi. 10.1111/j.1749-6632.1996.tb33309.x
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- Publication type:
- Article
Gene Expression Study in Positron Emission Tomography-Positive Abdominal Aortic Aneurysms Identifies CCL18 as a Potential Biomarker for Rupture Risk.
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- Molecular Medicine, 2014, v. 21, n. 2, p. 697, doi. 10.2119/molmed.2014.00065
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- Publication type:
- Article
Gene Expression Study in Positron Emission Tomography–Positive Abdominal Aortic Aneurysms Identifies CCL18 as a Potential Biomarker for Rupture Risk
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- Molecular Medicine, 2014, v. 20, n. 1, p. 697, doi. 10.2119/molmed.2014.00065
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- Publication type:
- Article
Fine mapping of the Schnyder’s crystalline corneal dystrophy locus.
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- Human Genetics, 2004, v. 114, n. 6, p. 594, doi. 10.1007/s00439-004-1110-1
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- Publication type:
- Article
SMAD3 deficiency promotes vessel wall remodeling, collagen fiber reorganization and leukocyte infiltration in an inflammatory abdominal aortic aneurysm mouse model.
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- Scientific Reports, 2015, p. 10180, doi. 10.1038/srep10180
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- Publication type:
- Article
eMERGE Phenome-Wide Association Study (PheWAS) identifies clinical associations and pleiotropy for stop-gain variants.
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- BMC Medical Genomics, 2016, v. 9, p. 19, doi. 10.1186/s12920-016-0191-8
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- Publication type:
- Article
MicroRNA expression signature in human abdominal aortic aneurysms.
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- BMC Medical Genomics, 2012, v. 5, n. 1, p. 25, doi. 10.1186/1755-8794-5-25
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- Publication type:
- Article
Genome-Wide Approach to Finding Abdominal Aortic Aneurysm Susceptibility Genes in Humans.
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- Annals of the New York Academy of Sciences, 2006, v. 1085, n. 1, p. 270, doi. 10.1196/annals.1383.022
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- Publication type:
- Article
Aneurysm Outreach Inc., a Nonprofit Organization, Offers Community-Based, Ultrasonography Screening for Abdominal Aortic Aneurysms.
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- Annals of the New York Academy of Sciences, 2006, v. 1085, n. 1, p. 291, doi. 10.1196/annals.1383.032
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- Publication type:
- Article
Global Expression Profiles in Human Normal and Aneurysmal Abdominal Aorta Based on Two Distinct Whole Genome Microarray Platforms.
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- Annals of the New York Academy of Sciences, 2006, v. 1085, n. 1, p. 360, doi. 10.1196/annals.1383.041
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- Publication type:
- Article
HLA–DQA Is Associated with Abdominal Aortic Aneurysms in the Belgian Population.
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- Annals of the New York Academy of Sciences, 2006, v. 1085, n. 1, p. 392, doi. 10.1196/annals.1383.045
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- Article
Concluding Remarks.
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- Annals of the New York Academy of Sciences, 2006, v. 1085, n. 1, p. 407, doi. 10.1196/annals.1383.051
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- Article
Editorial: FDA-Approved Drug Repositioning for P-Glycoprotein Overexpressing Resistant Cancer.
- Published in:
- 2021
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- Publication type:
- Editorial
Functionally significant SNP MMP8 promoter haplotypes and preterm premature rupture of membranes (PPROM).
- Published in:
- Human Molecular Genetics, 2004, v. 13, n. 21, p. 2659, doi. 10.1093/hmg/ddh287
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- Article
Novel Genetic Mechanisms for Aortic Aneurysms.
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- Current Atherosclerosis Reports, 2010, v. 12, n. 4, p. 259, doi. 10.1007/s11883-010-0111-x
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- Article
The Potential Role of DNA Methylation in Abdominal Aortic Aneurysms.
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- International Journal of Molecular Sciences, 2015, v. 16, n. 5, p. 11259, doi. 10.3390/ijms160511259
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- Article
Immunohistochemical Analysis of the Natural Killer Cell Cytotoxicity Pathway in Human Abdominal Aortic Aneurysms.
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- International Journal of Molecular Sciences, 2015, v. 16, n. 5, p. 11196, doi. 10.3390/ijms160511196
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- Article
Transcriptional (ChIP-Chip) Analysis of ELF1, ETS2, RUNX1 and STAT5 in Human Abdominal Aortic Aneurysm.
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- International Journal of Molecular Sciences, 2015, v. 16, n. 5, p. 11229, doi. 10.3390/ijms160511229
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- Article
Cascade Immune Mechanisms of Protection against Mycobacterium tuberculosis (IMPAc-TB): study protocol for the Household Contact Study in the Western Cape, South Africa.
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- 2022
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- Publication type:
- journal article
High-resolution physical map for chromosome 16q12.1-q13, the Blau syndrome locus.
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- BMC Genomics, 2002, v. 3, p. 24, doi. 10.1186/1471-2164-3-24
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- Publication type:
- Article
Evidence of linkage and association on chromosome 20 for late-onset Alzheimer disease.
- Published in:
- Neurogenetics, 2004, v. 5, n. 2, p. 121, doi. 10.1007/s10048-004-0174-3
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- Article
The foundation of precision medicine: integration of electronic health records with genomics through basic, clinical, and translational research.
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- Frontiers in Genetics, 2015, v. 6, p. 1, doi. 10.3389/fgene.2015.00104
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- Article
Imputation and quality control steps for combining multiple genome-wide datasets.
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- Frontiers in Genetics, 2014, v. 5, p. 1, doi. 10.3389/fgene.2014.00370
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- Publication type:
- Article
Controlling for population structure and genotyping platform bias in the eMERGE multi-institutional biobank linked to electronic health records.
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- Frontiers in Genetics, 2014, v. 5, p. 1, doi. 10.3389/fgene.2014.00352
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- Article
eMERGEing progress in genomics--the first seven years.
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- Frontiers in Genetics, 2014, v. 5, p. 1, doi. 10.3389/fgene.2014.00184
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- Publication type:
- Article
eMERGEing progress in genomics---the first seven years.
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- Frontiers in Genetics, 2014, v. 5, p. 1, doi. 10.3389/fgene.2014.00184
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- Publication type:
- Article
Fibulin-2 exhibits high degree of variability, but no structural changes concordant with abdominal aortic aneurysms.
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- European Journal of Human Genetics, 1998, v. 6, n. 6, p. 642, doi. 10.1038/sj.ejhg.5200245
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- Publication type:
- Article
Ehlers-Danlos Syndrome Type IV: A Single Base Substitution of the Last Nucleotide of Exon 34 in COL3A1 Leads to Exon Skipping.
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- Journal of Investigative Dermatology, 1995, v. 105, n. 3, p. 352, doi. 10.1111/1523-1747.ep12320704
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- Publication type:
- Article
Environmental and life-style risk factors for esophageal squamous cell carcinoma in Africa: a systematic review and meta-analysis.
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- BMC Public Health, 2023, v. 23, n. 1, p. 1, doi. 10.1186/s12889-023-16629-0
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- Publication type:
- Article
The CARD15 2936insC mutation and TLR4 896 A>G polymorphism in African Americans and risk of preterm premature rupture of membranes (PPROM).
- Published in:
- Molecular Human Reproduction, 2002, v. 8, n. 11, p. 1031, doi. 10.1093/molehr/8.11.1031
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- Article
A polymorphism in the matrix metalloproteinase-9 promoter is associated with increased risk of preterm premature rupture of membranes in African Americans.
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- Molecular Human Reproduction, 2002, v. 8, n. 5, p. 494, doi. 10.1093/molehr/8.5.494
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- Publication type:
- Article
Neutrophil degranulation, NETosis and platelet degranulation pathway genes are co-induced in whole blood up to six months before tuberculosis diagnosis.
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- PLoS ONE, 2022, v. 17, n. 12, p. 1, doi. 10.1371/journal.pone.0278295
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- Article
P1-280: Novel polymorphism in lipoprotein receptor-related protein 1 (LRP1) shows significant association with Alzheimer’s disease
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- 2006
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- Publication type:
- Abstract
P1-280: Novel polymorphism in lipoprotein receptor-related protein 1 (LRP1) shows significant association with Alzheimer’s disease
- Published in:
- 2006
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- Publication type:
- Abstract
Targeted next-generation sequencing identifies novel variants in candidate genes for Parkinson's disease in Black South African and Nigerian patients.
- Published in:
- BMC Medical Genetics, 2020, v. 21, n. 1, p. 1, doi. 10.1186/s12881-020-0953-1
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- Publication type:
- Article
Pharmacological inhibition of Notch signaling regresses pre-established abdominal aortic aneurysm.
- Published in:
- Scientific Reports, 2019, v. 9, n. 1, p. N.PAG, doi. 10.1038/s41598-019-49682-0
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- Article
Mechanistic Phenotypes: An Aggregative Phenotyping Strategy to Identify Disease Mechanisms Using GWAS Data.
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- PLoS ONE, 2013, v. 8, n. 12, p. 1, doi. 10.1371/journal.pone.0081503
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- Article
Editorial: Functional Genomics and Proteomics in Term and Preterm Parturition.
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- Journal of Clinical Endocrinology & Metabolism, 2002, v. 87, n. 6, p. 2431, doi. 10.1210/jcem.87.6.8689
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- Article
Identifying gene-gene interactions that are highly associated with four quantitative lipid traits across multiple cohorts.
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- Human Genetics, 2017, v. 136, n. 2, p. 165, doi. 10.1007/s00439-016-1738-7
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- Article
Esophageal Cancer Genomics in Africa: Recommendations for Future Research.
- Published in:
- Frontiers in Genetics, 2022, v. 13, p. 1, doi. 10.3389/fgene.2022.864575
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- Publication type:
- Article
A review of genome-wide transcriptomics studies in Parkinson's disease.
- Published in:
- European Journal of Neuroscience, 2018, v. 47, n. 1, p. 1, doi. 10.1111/ejn.13760
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- Publication type:
- Article
Risk Factor Assessment in a Greek Cohort of Patients With Large Abdominal Aortic Aneurysms.
- Published in:
- Angiology, 2019, v. 70, n. 1, p. 35, doi. 10.1177/0003319718774474
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- Publication type:
- Article
Matricellular protein CCN3 mitigates abdominal aortic aneurysm.
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- 2016
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- Publication type:
- journal article
Novel Pathways in the Pathobiology of Human Abdominal Aortic Aneurysms.
- Published in:
- Pathobiology, 2012, v. 80, n. 1, p. 1, doi. 10.1159/000339303
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- Publication type:
- Article
Smooth muscle cell-specific Notch1 haploinsufficiency restricts the progression of abdominal aortic aneurysm by modulating CTGF expression.
- Published in:
- PLoS ONE, 2017, v. 12, n. 5, p. 1, doi. 10.1371/journal.pone.0178538
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- Article
Analysis of positional candidate genes in the AAA1 susceptibility locus for abdominal aortic aneurysms on chromosome 19.
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- BMC Medical Genetics, 2011, v. 12, n. 1, p. 14, doi. 10.1186/1471-2350-12-14
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- Publication type:
- Article
Analytical approaches to detect maternal/fetal genotype incompatibilities that increase risk of pre-eclampsia.
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- BMC Medical Genetics, 2008, v. 9, p. 1, doi. 10.1186/1471-2350-9-60
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- Publication type:
- Article
Evidence for association between the HLA-DQA locus and abdominal aortic aneurysms in the Belgian population: a case control study.
- Published in:
- BMC Medical Genetics, 2006, v. 7, p. 67, doi. 10.1186/1471-2350-7-67
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- Publication type:
- Article
Identification of novel functional sequence variants in the gene for peptidase inhibitor 3.
- Published in:
- BMC Medical Genetics, 2006, v. 7, p. 49, doi. 10.1186/1471-2350-7-49
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- Publication type:
- Article