Canlyniadau Chwilio - DePalma, Steven

Locus for Familial Migrainous Vertigo Disease Maps to Chromosome 5q35 gan 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 gan 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 gan 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 gan 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 gan 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 gan 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 gan 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 gan 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 gan 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 gan 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 gan 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 gan 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 gan 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 gan 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 gan 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 gan 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 gan 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 gan 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 gan 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 gan 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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