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| Lessons on the pathogenesis of aneurysm from heritable conditions ME Lindsay, HC Dietz Nature 473 (7347), 308-316, 2011 | 566 | 2011 |
| Noncanonical TGFβ signaling contributes to aortic aneurysm progression in Marfan syndrome mice TM Holm, JP Habashi, JJ Doyle, D Bedja, YC Chen, C Van Erp, ... Science 332 (6027), 358-361, 2011 | 548 | 2011 |
| American heart association council on E, prevention statistics c, stroke statistics s. heart disease and stroke statistics-2019 update: a report from the American heart association EJ Benjamin, P Muntner, A Alonso, MS Bittencourt, CW Callaway, ... Circulation 139 (10), e56-e528, 2019 | 510 | 2019 |
| Loss-of-function mutations in TGFB2 cause a syndromic presentation of thoracic aortic aneurysm ME Lindsay, D Schepers, NA Bolar, JJ Doyle, E Gallo, J Fert-Bober, ... Nature genetics 44 (8), 922-927, 2012 | 492 | 2012 |
| Mutations in the TGF-β repressor SKI cause Shprintzen-Goldberg syndrome with aortic aneurysm AJ Doyle, JJ Doyle, SL Bessling, S Maragh, ME Lindsay, D Schepers, ... Nature genetics 44 (11), 1249-1254, 2012 | 304 | 2012 |
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| Regeneration next: toward heart stem cell therapeutics EM Hansson, ME Lindsay, KR Chien Cell stem cell 5 (4), 364-377, 2009 | 218 | 2009 |
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| Ran-binding protein 3 is a cofactor for Crm1-mediated nuclear protein export ME Lindsay, JM Holaska, K Welch, BM Paschal, IG Macara The Journal of cell biology 153 (7), 1391-1402, 2001 | 180 | 2001 |
| Npap60/Nup50 is a tri-stable switch that stimulates importin-α: β-mediated nuclear protein import ME Lindsay, K Plafker, AE Smith, BE Clurman, IG Macara Cell 110 (3), 349-360, 2002 | 149 | 2002 |
| A mutation update on the LDS‐associated genes TGFB2/3 and SMAD2/3 D Schepers, G Tortora, H Morisaki, G MacCarrick, M Lindsay, D Liang, ... Human mutation 39 (5), 621-634, 2018 | 144 | 2018 |
| Risk of aortic dissection in the moderately dilated ascending aorta JB Kim, M Spotnitz, ME Lindsay, TE MacGillivray, EM Isselbacher, ... Journal of the American College of Cardiology 68 (11), 1209-1219, 2016 | 143 | 2016 |
| Phenotypic refinement of heart failure in a national biobank facilitates genetic discovery KG Aragam, M Chaffin, RT Levinson, G McDermott, SH Choi, ... Circulation 139 (4), 489-501, 2019 | 140 | 2019 |
| An HDAC9-MALAT1-BRG1 complex mediates smooth muscle dysfunction in thoracic aortic aneurysm CL Lino Cardenas, CW Kessinger, Y Cheng, C MacDonald, ... Nature communications 9 (1), 1009, 2018 | 140 | 2018 |
| ROBO4 variants predispose individuals to bicuspid aortic valve and thoracic aortic aneurysm RA Gould, H Aziz, CE Woods, MA Seman-Senderos, E Sparks, C Preuss, ... Nature genetics 51 (1), 42-50, 2019 | 133 | 2019 |
| Deep learning enables genetic analysis of the human thoracic aorta JP Pirruccello, MD Chaffin, EL Chou, SJ Fleming, H Lin, M Nekoui, ... Nature genetics 54 (1), 40-51, 2022 | 121 | 2022 |
| A deleterious gene-by-environment interaction imposed by calcium channel blockers in Marfan syndrome JJ Doyle, AJ Doyle, NK Wilson, JP Habashi, D Bedja, RE Whitworth, ... Elife 4, e08648, 2015 | 114 | 2015 |
Eric IsselbacherMassachusetts General Hospital在 partners.org 的电子邮件经过验证
Eric IsselbacherMassachusetts General Hospital在 partners.org 的电子邮件经过验证