| Year |
Citation |
Score |
| 2021 |
Onoue K, Wakimoto H, Jiang J, Parfenov M, DePalma S, Conner D, Gorham J, McKean D, Seidman JG, Seidman CE, Saito Y. Cardiomyocyte Proliferative Capacity Is Restricted in Mice With Mutation. Frontiers in Cardiovascular Medicine. 8: 639148. PMID 34250035 DOI: 10.3389/fcvm.2021.639148 |
0.309 |
|
| 2020 |
Hsieh A, Morton SU, Willcox JAL, Gorham JM, Tai AC, Qi H, DePalma S, McKean D, Griffin E, Manheimer KB, Bernstein D, Kim RW, Newburger JW, Porter GA, Srivastava D, et al. EM-mosaic detects mosaic point mutations that contribute to congenital heart disease. Genome Medicine. 12: 42. PMID 32349777 DOI: 10.1186/S13073-020-00738-1 |
0.345 |
|
| 2019 |
Jang MY, Tai AC, Patel PN, Ito K, Gorham J, Pereira AC, McKean DM, Seidman CE, Seidman JG. Abstract 467: Identification of Novel Pathogenic Mutations in Non-Canonical RNA Splice Sites in Congenital Heart Disease Circulation Research. 125. DOI: 10.1161/Res.125.Suppl_1.467 |
0.325 |
|
| 2016 |
DeLaughter DM, Bick AG, Wakimoto H, McKean D, Gorham JM, Kathiriya IS, Hinson JT, Homsy J, Gray J, Pu W, Bruneau BG, Seidman JG, Seidman CE. Single-Cell Resolution of Temporal Gene Expression during Heart Development. Developmental Cell. PMID 27840107 DOI: 10.1016/J.Devcel.2016.10.001 |
0.353 |
|
| 2016 |
McKean DM, Homsy J, Wakimoto H, Patel N, Gorham J, DePalma SR, Ware JS, Zaidi S, Ma W, Patel N, Lifton RP, Chung WK, Kim R, Shen Y, Brueckner M, et al. Loss of RNA expression and allele-specific expression associated with congenital heart disease. Nature Communications. 7: 12824. PMID 27670201 DOI: 10.1038/Ncomms12824 |
0.383 |
|
| 2015 |
Homsy J, Zaidi S, Shen Y, Ware JS, Samocha KE, Karczewski KJ, DePalma SR, McKean D, Wakimoto H, Gorham J, Jin SC, Deanfield J, Giardini A, Porter GA, Kim R, et al. De novo mutations in congenital heart disease with neurodevelopmental and other congenital anomalies. Science (New York, N.Y.). 350: 1262-6. PMID 26785492 DOI: 10.1126/Science.Aac9396 |
0.376 |
|
| 2014 |
van den Boogaard M, Smemo S, Burnicka-Turek O, Arnolds DE, van de Werken HJ, Klous P, McKean D, Muehlschlegel JD, Moosmann J, Toka O, Yang XH, Koopmann TT, Adriaens ME, Bezzina CR, de Laat W, et al. A common genetic variant within SCN10A modulates cardiac SCN5A expression. The Journal of Clinical Investigation. 124: 1844-52. PMID 24642470 DOI: 10.1172/Jci73140 |
0.329 |
|
| 2014 |
Christodoulou DC, Wakimoto H, Onoue K, Eminaga S, Gorham JM, DePalma SR, Herman DS, Teekakirikul P, Conner DA, McKean DM, Domenighetti AA, Aboukhalil A, Chang S, Srivastava G, McDonough B, et al. 5'RNA-Seq identifies Fhl1 as a genetic modifier in cardiomyopathy. The Journal of Clinical Investigation. 124: 1364-70. PMID 24509080 DOI: 10.1172/Jci70108 |
0.326 |
|
| 2012 |
McKean DM, Niswander L. Defects in GPI biosynthesis perturb Cripto signaling during forebrain development in two new mouse models of holoprosencephaly. Biology Open. 1: 874-83. PMID 23213481 DOI: 10.1242/Bio.20121982 |
0.515 |
|
| 2010 |
Mao J, McKean DM, Warrier S, Corbin JG, Niswander L, Zohn IE. The iron exporter ferroportin 1 is essential for development of the mouse embryo, forebrain patterning and neural tube closure. Development (Cambridge, England). 137: 3079-88. PMID 20702562 DOI: 10.1242/Dev.048744 |
0.501 |
|
| 2005 |
Ihida-Stansbury K, McKean DM, Gebb SA, Martin JF, Stevens T, Nemenoff R, Vaughn J, Lane K, Loyd J, Wheeler L, Morrell NW, Ivy D, Jones PL. Regulation and functions of the paired-related homeobox gene PRX1 in pulmonary vascular development and disease. Chest. 128: 591S. PMID 16373852 DOI: 10.1378/Chest.128.6_Suppl.591S |
0.307 |
|
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