| Year |
Citation |
Score |
| 2016 |
Wang M, Sips P, Khin E, Rotival M, Sun X, Ahmed R, Widjaja AA, Schafer S, Yusoff P, Choksi PK, Ko NS, Singh MK, Epstein D, Guan Y, Houštěk J, ... ... MacRae C, et al. Wars2 is a determinant of angiogenesis. Nature Communications. 7: 12061. PMID 27389904 DOI: 10.1038/Ncomms12061 |
0.344 |
|
| 2016 |
Kapur S, Beik SP, Prem S, MacRae C. Beside Tools For Stratification Of The Etiology Of Cardiac Hypertrophy Journal of the American College of Cardiology. 67: 1305. DOI: 10.1016/S0735-1097(16)31306-7 |
0.333 |
|
| 2014 |
Triedman JK, MacRae C. Searching for a Rosetta Stone: genetic data and clinical patient management. Heart Rhythm : the Official Journal of the Heart Rhythm Society. 11: 1714-5. PMID 25046859 DOI: 10.1016/J.Hrthm.2014.07.023 |
0.35 |
|
| 2010 |
Sogah VM, Serluca FC, Fishman MC, Yelon DL, Macrae CA, Mably JD. Distinct troponin C isoform requirements in cardiac and skeletal muscle. Developmental Dynamics : An Official Publication of the American Association of Anatomists. 239: 3115-23. PMID 20925115 DOI: 10.1002/Dvdy.22445 |
0.454 |
|
| 2010 |
Kikuchi K, Holdway JE, Werdich AA, Anderson RM, Fang Y, Egnaczyk GF, Evans T, Macrae CA, Stainier DY, Poss KD. Primary contribution to zebrafish heart regeneration by gata4(+) cardiomyocytes. Nature. 464: 601-5. PMID 20336144 DOI: 10.1038/Nature08804 |
0.451 |
|
| 2005 |
Burns CG, Milan DJ, Grande EJ, Rottbauer W, MacRae CA, Fishman MC. High-throughput assay for small molecules that modulate zebrafish embryonic heart rate. Nature Chemical Biology. 1: 263-4. PMID 16408054 DOI: 10.1038/nchembio732 |
0.401 |
|
| 2004 |
Peterson RT, Shaw SY, Peterson TA, Milan DJ, Zhong TP, Schreiber SL, MacRae CA, Fishman MC. Chemical suppression of a genetic mutation in a zebrafish model of aortic coarctation. Nature Biotechnology. 22: 595-9. PMID 15097998 DOI: 10.1038/Nbt963 |
0.418 |
|
| 2004 |
MacRae CA, Fishman MC. Model Organisms for Cardiac Disease Gene Discovery Molecular Basis of Cardiovascular Disease: a Companion to Braunwald's Heart Disease. 39-48. DOI: 10.1016/B978-0-7216-9428-3.50008-1 |
0.438 |
|
| 2002 |
MacRae CA, Fishman MC. Zebrafish: the complete cardiovascular compendium. Cold Spring Harbor Symposia On Quantitative Biology. 67: 301-7. PMID 12858553 |
0.39 |
|
| 1999 |
Fatkin D, MacRae C, Sasaki T, Wolff MR, Porcu M, Frenneaux M, Atherton J, Vidaillet HJ, Spudich S, De Girolami U, Seidman JG, Seidman C, Muntoni F, Müehle G, Johnson W, et al. Missense mutations in the rod domain of the lamin A/C gene as causes of dilated cardiomyopathy and conduction-system disease. The New England Journal of Medicine. 341: 1715-24. PMID 10580070 DOI: 10.1056/Nejm199912023412302 |
0.345 |
|
| 1999 |
Siu BL, Niimura H, Osborne JA, Fatkin D, MacRae C, Solomon S, Benson DW, Seidman JG, Seidman CE. Familial dilated cardiomyopathy locus maps to chromosome 2q31. Circulation. 99: 1022-6. PMID 10051295 DOI: 10.1161/01.Cir.99.8.1022 |
0.332 |
|
| 1996 |
Benson D, Basson C, MacRae C. New understandings in the genetics of congenital heart disease. Current Opinion in Pediatrics. 8: 505-515. PMID 8946132 DOI: 10.1097/00008480-199610000-00015 |
0.367 |
|
| 1995 |
Watkins H, Conner D, Thierfelder L, Jarcho JA, MacRae C, McKenna WJ, Maron BJ, Seidman JG, Seidman CE. Mutations in the cardiac myosin binding protein-C gene on chromosome 11 cause familial hypertrophic cardiomyopathy. Nature Genetics. 11: 434-7. PMID 7493025 DOI: 10.1038/Ng1295-434 |
0.371 |
|
| 1994 |
Thierfelder L, Watkins H, MacRae C, Lamas R, McKenna W, Vosberg HP, Seldman JG, Seidman CE. α-tropomyosin and cardiac troponin T mutations cause familial hypertrophic cardiomyopathy: A disease of the sarcomere Cell. 77: 701-712. PMID 8205619 DOI: 10.1016/0092-8674(94)90054-X |
0.358 |
|
| 1994 |
Kass S, MacRae C, Graber HL, Sparks EA, McNamara D, Boudoulas H, Basson CT, Baker PB, Cody RJ, Fishman MC. A gene defect that causes conduction system disease and dilated cardiomyopathy maps to chromosome 1p1-1q1. Nature Genetics. 7: 546-51. PMID 7951328 DOI: 10.1038/Ng0894-546 |
0.506 |
|
| 1993 |
Thierfelder L, MacRae C, Watkins H, Tomfohrde J, Williams M, McKenna W, Bohm K, Noeske G, Schlepper M, Bowcock A. A familial hypertrophic cardiomyopathy locus maps to chromosome 15q2. Proceedings of the National Academy of Sciences of the United States of America. 90: 6270-4. PMID 8327508 DOI: 10.1073/Pnas.90.13.6270 |
0.32 |
|
| 1993 |
Watkins H, MacRae C, Thierfelder L, Chou Y, Frenneaux M, McKenna W, Seidman JG, Seidman CE. A disease locus for familial hypertrophic cardiomyopathy maps to chromosome 1q3. Nature Genetics. 3: 333-337. PMID 7981753 DOI: 10.1038/Ng0493-333 |
0.336 |
|
| 1991 |
Marber M, MacRae C, Joy M. Delay to invasive investigation and revascularisation for coronary heart disease in south west Thames region: a two tier system? Bmj. 302: 1189-1191. PMID 2043817 DOI: 10.1136/Bmj.302.6786.1189 |
0.306 |
|
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