| P50 | author | Lakshmanan K Iyer | Q59149689 |
| | Eric C Wooten | Q59193990 |
| | Gordon S. Huggins | Q114427846 |
| P2093 | author name string | David E Housman | |
| | Maria Claudia Montefusco | |
| | Navin K Kapur | |
| | Michael E Mendelsohn | |
| | Douglas D Payne | |
| | Alyson Kelley Hedgepeth | |
| P2860 | cites work | INK4/ARF transcript expression is associated with chromosome 9p21 variants linked to atherosclerosis | Q21562488 |
| | Are rare variants responsible for susceptibility to complex diseases? | Q22337172 |
| | Mutations in NOTCH1 cause aortic valve disease | Q24307999 |
| | Novel NOTCH1 mutations in patients with bicuspid aortic valve disease and thoracic aortic aneurysms | Q24323103 |
| | Cytoscape: a software environment for integrated models of biomolecular interaction networks | Q24515682 |
| | A second generation human haplotype map of over 3.1 million SNPs | Q24651939 |
| | The links between axin and carcinogenesis | Q24672469 |
| | STRING 7--recent developments in the integration and prediction of protein interactions | Q24675384 |
| | PLINK: a tool set for whole-genome association and population-based linkage analyses | Q24677407 |
| | Screening large-scale association study data: exploiting interactions using random forests | Q24809535 |
| | Linear models and empirical bayes methods for assessing differential expression in microarray experiments | Q27860758 |
| | Fate of the mammalian cardiac neural crest | Q28139176 |
| | Defective angiogenesis in mice lacking endoglin | Q28144833 |
| | Efficiency and power in genetic association studies | Q28278645 |
| | Defective ALK5 signaling in the neural crest leads to increased postmigratory neural crest cell apoptosis and severe outflow tract defects | Q28506220 |
| | Endoglin is required for myogenic differentiation potential of neural crest stem cells | Q28510584 |
| | Genetic Power Calculator: design of linkage and association genetic mapping studies of complex traits | Q29614876 |
| | Complement factor H polymorphism and age-related macular degeneration | Q29614931 |
| | Endoglin (CD105) expression in the human heart throughout gestation: an immunohistochemical study. | Q51944540 |
| | Clinical and pathophysiological implications of a bicuspid aortic valve. | Q53783947 |
| | Familial thoracic aortic dilation and bicommissural aortic valve: A prospective analysis of natural history and inheritance | Q57150549 |
| | Novel missense mutations (p.T596M and p.P1797H) in NOTCH1 in patients with bicuspid aortic valve | Q57315168 |
| | Identifying SNPs predictive of phenotype using random forests | Q57363161 |
| | Evidence in favor of linkage to human chromosomal regions 18q, 5q and 13q for bicuspid aortic valve and associated cardiovascular malformations | Q60696745 |
| | Distribution of endoglin in early human development reveals high levels on endocardial cushion tissue mesenchyme during valve formation | Q74482103 |
| | Elevated expressions of osteopontin and tenascin C in ascending aortic aneurysms are associated with trileaflet aortic valves as compared with bicuspid aortic valves | Q80335640 |
| | Evidence of genetic locus heterogeneity for familial bicuspid aortic valve | Q80837194 |
| | Inference of population structure using multilocus genotype data: dominant markers and null alleles | Q29615942 |
| | ENDEAVOUR update: a web resource for gene prioritization in multiple species | Q30482616 |
| | Gene prioritization through genomic data fusion | Q33242612 |
| | Gene expression signature in peripheral blood detects thoracic aortic aneurysm | Q33302909 |
| | Loss of Notch signalling induced by Dll4 causes arterial calibre reduction by increasing endothelial cell response to angiogenic stimuli | Q33393502 |
| | Coding-sequence determinants of gene expression in Escherichia coli | Q33428917 |
| | How many genetic variants remain to be discovered? | Q33517108 |
| | On safari to Random Jungle: a fast implementation of Random Forests for high-dimensional data | Q33588377 |
| | Heart valve development: endothelial cell signaling and differentiation | Q33607338 |
| | Prioritized subset analysis: improving power in genome-wide association studies | Q33805649 |
| | Bicuspid aortic valve is heritable | Q34331122 |
| | Alleles in the HtrA serine peptidase 1 gene alter the risk of neovascular age-related macular degeneration | Q34565579 |
| | Notch signaling in cardiac development | Q34780720 |
| | CANDID: a flexible method for prioritizing candidate genes for complex human traits. | Q35571604 |
| | FitSNPs: highly differentially expressed genes are more likely to have variants associated with disease | Q37105918 |
| | Notch signaling in cardiac development and disease. | Q37382226 |
| | Aortopathy is prevalent in relatives of bicuspid aortic valve patients | Q37387539 |
| | Surgical pathology of aortic valve disease. A study based on 602 specimens | Q40767031 |
| | The neural crest as a possible pathogenetic factor in coarctation of the aorta and bicuspid aortic valve | Q43457386 |
| | The Wnt/beta-catenin pathway regulates cardiac valve formation | Q47073676 |
| P275 | copyright license | Creative Commons Attribution 4.0 International | Q20007257 |
| P6216 | copyright status | copyrighted | Q50423863 |
| P4510 | describes a project that uses | Cytoscape | Q3699942 |
| | limma | Q112236343 |
| P433 | issue | 1 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | aorta | Q101004 |
| P304 | page(s) | e8830 | |
| P577 | publication date | 2010-01-21 | |
| P1433 | published in | PLOS One | Q564954 |
| P1476 | title | Application of gene network analysis techniques identifies AXIN1/PDIA2 and endoglin haplotypes associated with bicuspid aortic valve | |
| P478 | volume | 5 | |