Torthaí cuardaigh - DePalma, Steven

Locus for Familial Migrainous Vertigo Disease Maps to Chromosome 5q35 de réir Bahmad, Fayez, DePalma, Steven R., Merchant, Saumil N., Bezerra, Roberta L., Oliveira, Carlos A., Seidman, Christine E., Seidman, Jonathan G.

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Phenotype-genotype association grid: a convenient method for summarizing multiple association analyses de réir Levy, Daniel, DePalma, Steven R, Benjamin, Emelia J, O'Donnell, Christopher J, Parise, Helen, Hirschhorn, Joel N, Vasan, Ramachandran S, Izumo, Seigo, Larson, Martin G

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Cardiomyocyte Proliferative Capacity Is Restricted in Mice With Lmna Mutation de réir Onoue, Kenji, Wakimoto, Hiroko, Jiang, Jiangming, Parfenov, Michael, DePalma, Steven, Conner, David, Gorham, Joshua, McKean, David, Seidman, Jonathan G., Seidman, Christine E., Saito, Yoshihiko

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A Nonsense Mutation in MSX1 Causes Witkop Syndrome de réir Jumlongras, Dolrudee, Bei, Marianna, Stimson, Jean M., Wang, Wen-Fang, DePalma, Steven R., Seidman, Christine E., Felbor, Ute, Maas, Richard, Seidman, Jonathan G., Olsen, Bjorn R.

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Spectrum of somatic mitochondrial mutations in five cancers de réir Larman, Tatianna C., DePalma, Steven R., Hadjipanayis, Angela G., Protopopov, Alexei, Zhang, Jianhua, Gabriel, Stacey B., Chin, Lynda, Seidman, Christine E., Kucherlapati, Raju, Seidman, J. G.

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NKX2-5 Mutations in an Inbred Consanguineous Population: Genetic and Phenotypic Diversity de réir Abou Hassan, Ossama K., Fahed, Akl C., Batrawi, Manal, Arabi, Mariam, Refaat, Marwan M., DePalma, Steven R., Seidman, J. G., Seidman, Christine E., Bitar, Fadi F., Nemer, Georges M.

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A novel COL1A1 mutation in infantile cortical hyperostosis (Caffey disease) expands the spectrum of collagen-related disorders de réir Gensure, Robert C., Mäkitie, Outi, Barclay, Catherine, Chan, Catherine, DePalma, Steven R., Bastepe, Murat, Abuzahra, Hilal, Couper, Richard, Mundlos, Stefan, Sillence, David, Ala Kokko, Leena, Seidman, Jonathan G., Cole, William G., Jüppner, Harald

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Filamin C cardiomyopathy variants cause protein and lysosome accumulation de réir Agarwal, Radhika, Paulo, Joao A., Toepfer, Christopher N., Ewoldt, Jourdan K., Sundaram, Subramanian, Chopra, Anant, Zhang, Qi, Gorham, Joshua, DePalma, Steven R., Chen, Christopher S., Gygi, Steven P., Seidman, Christine E., Seidman, J. G.

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HOXA2 Haploinsufficiency in Dominant Bilateral Microtia and Hearing Loss de réir Brown, Kerry K., Viana, Lucas M., Helwig, Cecilia C., Artunduaga, Maria A., Quintanilla-Dieck, Lourdes, Jarrin, Patricia, Osorno, Gabriel, McDonough, Barbara, DePalma, Steven R., Eavey, Roland D., Seidman, Jonathan G., Seidman, Christine E.

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Identification of pathogenic gene mutations in LMNA and MYBPC3 that alter RNA splicing de réir Ito, Kaoru, Patel, Parth N., Gorham, Joshua M., McDonough, Barbara, DePalma, Steven R., Adler, Emily E., Lam, Lien, MacRae, Calum A., Mohiuddin, Syed M., Fatkin, Diane, Seidman, Christine E., Seidman, J. G.

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Founder Mutation in N Terminus of Cardiac Troponin I Causes Malignant Hypertrophic Cardiomyopathy de réir Fahed, Akl C., Nemer, Georges, Bitar, Fadi F., Arnaout, Samir, Abchee, Antoine B., Batrawi, Manal, Khalil, Athar, Abou Hassan, Ossama K., DePalma, Steven R., McDonough, Barbara, Arabi, Mariam T., Ware, James S., Seidman, Jonathan G., Seidman, Christine E.

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Using Next-generation RNA Sequencing to Examine Ischemic Changes Induced by Cold Blood Cardioplegia on the Human Left Ventricular Myocardium Transcriptome de réir Muehlschlegel, Jochen D., Christodoulou, Danos C., McKean, David, Gorham, Joshua, Mazaika, Erica, Heydarpour, Mahyar, Lee, Grace, DePalma, Steven R., Perry, Tjorvi E., Fox, Amanda F., Shernan, Stanton, Seidman, Christine E., Aranki, Sary F., Seidman, Jon G., Body, Simon C.

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Discordant clinical features of identical hypertrophic cardiomyopathy twins de réir Repetti, Giuliana G., Kim, Yuri, Pereira, Alexandre C., Ingles, Jodie, Russell, Mark W., Lakdawala, Neal K., Ho, Carolyn Y., Day, Sharlene, Semsarian, Christopher, McDonough, Barbara, DePalma, Steven R., Quiat, Daniel, Green, Eric M., Seidman, Christine E., Seidman, J. G.

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BET bromodomain proteins regulate transcriptional reprogramming in genetic dilated cardiomyopathy de réir Antolic, Andrew, Wakimoto, Hiroko, Jiao, Zhe, Gorham, Joshua M., DePalma, Steven R., Lemieux, Madeleine E., Conner, David A., Lee, Da Young, Qi, Jun, Seidman, Jonathan G., Bradner, James E., Brown, Jonathan D., Haldar, Saptarsi M., Seidman, Christine E., Burke, Michael A.

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Genome-Wide Assessment for Genetic Variants Associated with Ventricular Dysfunction after Primary Coronary Artery Bypass Graft Surgery de réir Fox, Amanda A., Pretorius, Mias, Liu, Kuang-Yu, Collard, Charles D., Perry, Tjorvi E., Shernan, Stanton K., De Jager, Philip L., Hafler, David A., Herman, Daniel S., DePalma, Steven R., Roden, Dan M., Muehlschlegel, Jochen D., Donahue, Brian S., Darbar, Dawood, Seidman, J. G., Body, Simon C., Seidman, Christine E.

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Contribution of Non-Canonical Splice Variants to TTNtv Cardiomyopathy de réir Patel, Parth N., Ito, Kaoru, Willcox, Jon A.L., Haghighi, Alireza, Jang, Min Young, Gorham, Joshua M., DePalma, Steven R., Lam, Lien, McDonough, Barbara, Johnson, Renee, Lakdawala, Neal K., Roberts, Amy, Barton, Paul J.R., Cook, Stuart A., Fatkin, Diane, Seidman, Christine E., Seidman, J.G.

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Loss of RNA expression and allele-specific expression associated with congenital heart disease de réir McKean, David M., Homsy, Jason, Wakimoto, Hiroko, Patel, Neil, Gorham, Joshua, DePalma, Steven R., Ware, James S., Zaidi, Samir, Ma, Wenji, Patel, Nihir, Lifton, Richard P., Chung, Wendy K., Kim, Richard, Shen, Yufeng, Brueckner, Martina, Goldmuntz, Elizabeth, Sharp, Andrew J., Seidman, Christine E., Gelb, Bruce D., Seidman, J. G.

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Increased Burden of Cardiovascular Disease in Carriers of APOL1 Genetic Variants de réir Ito, Kaoru, Bick, Alexander G., Flannick, Jason, Friedman, David J., Genovese, Giulio, Parfenov, Michael G., DePalma, Steven R., Gupta, Namrata, Gabriel, Stacey B., Taylor, Herman A., Fox, Ervin R., Newton-Cheh, Christopher, Kathiresan, Sekar, Hirschhorn, Joel N., Altshuler, David M., Pollak, Martin R., Wilson, James G., Seidman, J. G., Seidman, Christine

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A Gene-Centric Strategy for Identifying Disease-Causing Rare Variants in Dilated Cardiomyopathy de réir Horvat, Claire, Johnson, Renee, Lam, Lien, Munro, Jacob, Mazzarotto, Francesco, Roberts, Angharad M., Herman, Daniel S., Parfenov, Michael, Haghighi, Alireza, McDonough, Barbara, DePalma, Steven R., Keogh, Anne M., Macdonald, Peter S., Hayward, Christopher S., Roberts, Amy, Barton, Paul J.R., Felkin, Leanne E., Giannoulatou, Eleni, Cook, Stuart A., Seidman, J.G., Seidman, Christine E., Fatkin, Diane

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THSD1 Mutation in the Pathogenesis of Intracranial Aneurysm and Subarachnoid Hemorrhage de réir Santiago-Sim, Teresa, Fang, Xiaoqian, Hennessy, Morgan L., Nalbach, Stephen V., DePalma, Steven R., Lee, Ming Sum, Greenway, Steven C., McDonough, Barbara, Hergenroeder, Georgene W., Patek, Kyla J., Colosimo, Sarah M., Qualmann, Krista J., Hagan, John P., Milewicz, Dianna M., MacRae, Calum A., Dymecki, Susan M., Seidman, Christine E., Seidman, J.G., Kim, Dong H.

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