| Year |
Citation |
Score |
| 2023 |
Odelin G, Faucherre A, Marchese D, Pinard A, Jaouadi H, Le Scouarnec S, Chiarelli R, Achouri Y, Faure E, Herbane M, Théron A, Avierinos JF, Jopling C, Collod-Béroud G, Rezsohazy R, et al. Variations in the poly-histidine repeat motif of HOXA1 contribute to bicuspid aortic valve in mouse and zebrafish. Nature Communications. 14: 1543. PMID 36941270 DOI: 10.1038/s41467-023-37110-x |
0.574 |
|
| 2022 |
Boerio ML, Engelhardt N, Cuddapah S, Gold JI, Marin IC, Pinard A, Guo D, Prakash SK, Milewicz DM. Further Evidence That Rare Variants Predispose to Thoracic Aortic Disease. Circulation. Genomic and Precision Medicine. e003707. PMID 36350761 DOI: 10.1161/CIRCGEN.122.003707 |
0.406 |
|
| 2020 |
Musfee FI, Guo D, Pinard AC, Hostetler EM, Blue EE, Nickerson DA, Bamshad MJ, Milewicz DM, Prakash SK. Rare deleterious variants of NOTCH1, GATA4, SMAD6, and ROBO4 are enriched in BAV with early onset complications but not in BAV with heritable thoracic aortic disease. Molecular Genetics & Genomic Medicine. e1406. PMID 32748548 DOI: 10.1002/Mgg3.1406 |
0.502 |
|
| 2020 |
Faucherre A, Maati HMO, Nasr N, Pinard A, Theron A, Odelin G, Desvignes JP, Salgado D, Collod-Béroud G, Avierinos JF, Lebon G, Zaffran S, Jopling C. Piezo1 and outflow tract and aortic valve development. Journal of Molecular and Cellular Cardiology. PMID 32251670 DOI: 10.1016/J.Yjmcc.2020.03.013 |
0.558 |
|
| 2019 |
Pinard A, Jones GT, Milewicz DM. Genetics of Thoracic and Abdominal Aortic Diseases. Circulation Research. 124: 588-606. PMID 30763214 DOI: 10.1161/Circresaha.118.312436 |
0.43 |
|
| 2018 |
Pinard A, Eudes N, Mitchell J, Bajolle F, Grelet M, Okoronkwo J, Bonnet D, Collod-Béroud G, Zaffran S. Analysis of HOXB1 gene in a cohort of patients with sporadic ventricular septal defect. Molecular Biology Reports. PMID 29923154 DOI: 10.1007/S11033-018-4212-X |
0.571 |
|
| 2018 |
Guo DC, Regalado ES, Pinard A, Chen J, Lee K, Rigelsky C, Zilberberg L, Hostetler EM, Aldred M, Wallace SE, Prakash SK, Leal SM, Bamshad MJ, Nickerson DA, et al. LTBP3 Pathogenic Variants Predispose Individuals to Thoracic Aortic Aneurysms and Dissections. American Journal of Human Genetics. 102: 706-712. PMID 29625025 DOI: 10.1016/J.Ajhg.2018.03.002 |
0.435 |
|
| 2016 |
Pinard A, Salgado D, Desvignes JP, Rai G, Hanna N, Arnaud P, Guien C, Martinez M, Faivre L, Jondeau G, Boileau C, Zaffran S, Béroud C, Collod-Béroud G. WES/WGS Reporting of Mutations from Cardiovascular "Actionable" Genes in Clinical Practice: A Key Role for UMD Knowledgebases in the era of Big Databases. Human Mutation. PMID 27647783 DOI: 10.1002/Humu.23119 |
0.558 |
|
| 2016 |
Pinard A, Miltgen M, Blanchard A, Mathieu H, Desvignes JP, Fabre A, Arnaud P, Barré L, Krahn M, Grandval P, Olschwang S, Zaffran S, Boileau C, Béroud C, Collod-Béroud G. Actionable Genes, Core Databases and LOCUS Specific Databases (LSDBs). Human Mutation. PMID 27600092 DOI: 10.1002/Humu.23112 |
0.544 |
|
| 2016 |
Theron A, Pinard A, Riberi A, Zaffran S. An uncommon cause of tricuspid regurgitation: three-dimensional echocardiographic incremental value, surgical and genetic insights. European Journal of Cardio-Thoracic Surgery : Official Journal of the European Association For Cardio-Thoracic Surgery. 50: 180-2. PMID 26670804 DOI: 10.1093/Ejcts/Ezv423 |
0.666 |
|
| Show low-probability matches. |