Canlyniadau Chwilio - Gerald Goh

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  1. 1
    Application of Whole Exome Sequencing to Identify Disease-Causing Variants in Inherited Human Diseases

    Application of Whole Exome Sequencing to Identify Disease-Causing Variants in Inherited Human Diseases gan Gerald Goh, Murim Choi

    Cyhoeddwyd 2012
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  2. 2
    PRKACA mutations in cortisol-producing adenomas and adrenal hyperplasia: a single-center study of 60 cases

    PRKACA mutations in cortisol-producing adenomas and adrenal hyperplasia: a single-center study of 60 cases gan Anne Thiel, Anna‐Carinna Reis, Matthias Haase, Gerald Goh, M. Schott, Holger S. Willenberg, Ute I. Scholl

    Cyhoeddwyd 2015
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  3. 3
    Mutational landscape of MCPyV-positive and MCPyV-negative Merkel cell carcinomas with implications for immunotherapy

    Mutational landscape of MCPyV-positive and MCPyV-negative Merkel cell carcinomas with implications for immunotherapy gan Gerald Goh, Trent Walradt, Vladimir Markarov, Astrid Blom, Nadeem Riaz, Ryan Doumani, K. Stafstrom, Ata S. Moshiri, Lola Yelistratova, Jonathan Levinsohn, Timothy A. Chan, Paul Nghiem, Richard P. Lifton, Jaehyuk Choi

    Cyhoeddwyd 2015
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  4. 4
    Genetic landscape of metastatic and recurrent head and neck squamous cell carcinoma

    Genetic landscape of metastatic and recurrent head and neck squamous cell carcinoma gan Matthew L. Hedberg, Gerald Goh, Simion I. Chiosea, Julie E. Bauman, Maria L. Freilino, Yan Zeng, Lin Wang, Brenda Diergaarde, William E. Gooding, Vivian Wai Yan Lui, Roy S. Herbst, Richard P. Lifton, Jennifer R. Grandis

    Cyhoeddwyd 2015
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  5. 5
    Identification of a gain-of-function STAT3 mutation (p.Y640F) in lymphocytic variant hypereosinophilic syndrome

    Identification of a gain-of-function STAT3 mutation (p.Y640F) in lymphocytic variant hypereosinophilic syndrome gan Sarah R. Walker, Chen Wang, Trent Walradt, Bok Sil Hong, Justin R. Tanner, Jonathan Levinsohn, Gerald Goh, Antonio Subtil, Stuart R. Lessin, Warren R. Heymann, Eric C. Vonderheid, Brett King, Richard P. Lifton, Jaehyuk Choi

    Cyhoeddwyd 2015
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  6. 6
    Genetic landscape of metastatic and recurrent head and neck squamous cell carcinoma

    Genetic landscape of metastatic and recurrent head and neck squamous cell carcinoma gan Matthew L. Hedberg, Gerald Goh, Simion I. Chiosea, Julie E. Bauman, Maria L. Freilino, Yan Zeng, Lin Wang, Brenda Diergaarde, William E. Gooding, Vivian Wai Yan Lui, Roy S. Herbst, Richard P. Lifton, Jennifer R. Grandis

    Cyhoeddwyd 2016
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    Errata/Corrigenda
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  7. 7
    Increased Levels of Macrophage Inflammatory Proteins Result in Resistance to R5-Tropic HIV-1 in a Subset of Elite Controllers

    Increased Levels of Macrophage Inflammatory Proteins Result in Resistance to R5-Tropic HIV-1 in a Subset of Elite Controllers gan Wendy E. Walker, Sebastian Kurscheid, Samit R. Joshi, Charlie A. Lopez, Gerald Goh, Murim Choi, Lydia Barakat, John G. Francis, Ann Fisher, Michael J. Kozal, Heidi Zapata, Albert C. Shaw, Richard P. Lifton, Richard E. Sutton, Erol Fikrig

    Cyhoeddwyd 2015
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  8. 8
    DNA replication stress mediates APOBEC3 family mutagenesis in breast cancer

    DNA replication stress mediates APOBEC3 family mutagenesis in breast cancer gan Nnennaya Kanu, Maria Antonietta Cerone, Gerald Goh, Lykourgos‐Panagiotis Zalmas, Jiřina Bártková, Michelle Dietzen, Nicholas McGranahan, Rebecca Rogers, Emily K. Law, Irina Gromova, Maik Kschischo, Michael I. Walton, Olivia W. Rossanese, Jiří Bártek, Reuben S. Harris, Subramanian Venkatesan, Charles Swanton

    Cyhoeddwyd 2016
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  9. 9
    Association and Mutation Analyses of 16p11.2 Autism Candidate Genes

    Association and Mutation Analyses of 16p11.2 Autism Candidate Genes gan Ravinesh A. Kumar, Christian R. Marshall, Judith A. Badner, Timothy D. Babatz, Zohar Mukamel, Kimberly A. Aldinger, Jyotsna Sudi, Camille W. Brune, Gerald Goh, Samer Karamohamed, James S. Sutcliffe, Edwin H. Cook, Daniel H. Geschwind, William B. Dobyns, Stephen W. Scherer, Susan L. Christian

    Cyhoeddwyd 2009
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  10. 10
    Characterization of the mutational landscape of anaplastic thyroid cancer via whole-exome sequencing

    Characterization of the mutational landscape of anaplastic thyroid cancer via whole-exome sequencing gan John W. Kunstman, C. Christofer Juhlin, Gerald Goh, T Brown, Adam Stenman, James M. Healy, Jill C. Rubinstein, Murim Choi, Nimrod Kiss, Carol Nelson‐Williams, Shrikant Mane, David L. Rimm, Manju L. Prasad, Anders Höög, Jan Zedenius, Catharina Larsson, Reju Korah, Richard P. Lifton, Tobias Carling

    Cyhoeddwyd 2015
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  11. 11
    Novel somatic mutations in primary hyperaldosteronism are related to the clinical, radiological and pathological phenotype

    Novel somatic mutations in primary hyperaldosteronism are related to the clinical, radiological and pathological phenotype gan Ute I. Scholl, James M. Healy, Anne Thiel, Annabelle L. Fonseca, T Brown, John W. Kunstman, Matthew J. Horne, Dimo Dietrich, Jasmin Riemer, S. Kücükköylü, Esther N. Reimer, Anna‐Carinna Reis, Gerald Goh, Glen Kristiansen, Amit Mahajan, Reju Korah, Richard P. Lifton, Manju L. Prasad, Tobias Carling

    Cyhoeddwyd 2015
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  12. 12
    Whole‐exome sequencing defines the mutational landscape of pheochromocytoma and identifies <i><scp>KMT</scp>2<scp>D</scp></i> as a recurrently mutated gene

    Whole‐exome sequencing defines the mutational landscape of pheochromocytoma and identifies <i><scp>KMT</scp>2<scp>D</scp></i> as a recurrently mutated gene gan C. Christofer Juhlin, Adam Stenman, Felix Haglund, Victoria Clark, T Brown, Jacob F. Baranoski, Kaya Bilgüvar, Gerald Goh, Jenny Welander, Fredrika Svahn, Jill C. Rubinstein, Stefano Caramuta, Katsuhito Yasuno, Murat Günel, Martin Bäckdahl, Oliver Gimm, Peter Söderkvist, Manju L. Prasad, Reju Korah, Richard P. Lifton, Tobias Carling

    Cyhoeddwyd 2015
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  13. 13
    Recurrent activating mutation in PRKACA in cortisol-producing adrenal tumors

    Recurrent activating mutation in PRKACA in cortisol-producing adrenal tumors gan Gerald Goh, Ute I. Scholl, James M. Healy, Murim Choi, Manju L. Prasad, Carol Nelson‐Williams, John W. Kunstman, John W. Kuntsman, Reju Korah, Anna‐Carinna Suttorp, Dimo Dietrich, Matthias Haase, Holger S. Willenberg, Peter Stålberg, Per Hellman, Göran Åkerström, Peyman Björklund, Tobias Carling, Richard P. Lifton

    Cyhoeddwyd 2014
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  14. 14
    Recurrent gain of function mutation in calcium channel CACNA1H causes early-onset hypertension with primary aldosteronism

    Recurrent gain of function mutation in calcium channel CACNA1H causes early-onset hypertension with primary aldosteronism gan Ute I. Scholl, Gabriel Stölting, Carol Nelson‐Williams, Alfred A. Vichot, Murim Choi, Erin Loring, Manju L. Prasad, Gerald Goh, Tobias Carling, C. Christofer Juhlin, Ivo Quack, Lars Christian Rump, Anne Thiel, Marc B. Lande, Britney G Frazier, Majid Rasoulpour, David L Bowlin, Christine B. Sethna, Howard Trachtman, Christoph Fahlke, Richard P. Lifton

    Cyhoeddwyd 2015
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  15. 15
    Whole-Exome Sequencing Characterizes the Landscape of Somatic Mutations and Copy Number Alterations in Adrenocortical Carcinoma

    Whole-Exome Sequencing Characterizes the Landscape of Somatic Mutations and Copy Number Alterations in Adrenocortical Carcinoma gan C. Christofer Juhlin, Gerald Goh, James M. Healy, Annabelle L. Fonseca, Ute I. Scholl, Adam Stenman, John W. Kunstman, T Brown, John D. Overton, Shrikant Mane, Carol Nelson‐Williams, Martin Bäckdahl, Anna‐Carinna Suttorp, Matthias Haase, Murim Choi, Joseph Schlessinger, David L. Rimm, Anders Höög, Manju L. Prasad, Reju Korah, Catharina Larsson, Richard P. Lifton, Tobias Carling

    Cyhoeddwyd 2014
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  16. 16
    Genomic landscape of cutaneous T cell lymphoma

    Genomic landscape of cutaneous T cell lymphoma gan Jaehyuk Choi, Gerald Goh, Trent Walradt, Bok Sil Hong, Christopher G. Bunick, Kan Chen, Robert Bjornson, Yaakov Maman, Tiffany Wang, Jesse Tordoff, Kacie R. Carlson, John D. Overton, Kristina J. Liu, Julia M. Lewis, Lesley Devine, Lisa Barbarotta, Francine M. Foss, Antonio Subtil, Eric C. Vonderheid, Richard L. Edelson, David G. Schatz, Titus J. Boggon, Michael Girardi, Richard P. Lifton

    Cyhoeddwyd 2015
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  17. 17
    Somatic and germline CACNA1D calcium channel mutations in aldosterone-producing adenomas and primary aldosteronism

    Somatic and germline CACNA1D calcium channel mutations in aldosterone-producing adenomas and primary aldosteronism gan Ute I. Scholl, Gerald Goh, Gabriel Stölting, Regina Campos de Oliveira, Murim Choi, John D. Overton, Annabelle L. Fonseca, Reju Korah, Lee F. Starker, John W. Kunstman, Manju L. Prasad, Erum A. Hartung, Nelly Mauras, Matthew Benson, Tammy M. Brady, Jay R. Shapiro, Erin Loring, Carol Nelson‐Williams, Steven K. Libutti, Shrikant Mane, Per Hellman, Gunnar Westin, Göran Åkerström, Peyman Björklund, Tobias Carling, Christoph Fahlke, Patricia Hidalgo, Richard P. Lifton

    Cyhoeddwyd 2013
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  18. 18
    Exome sequencing identifies recurrent somatic RAC1 mutations in melanoma

    Exome sequencing identifies recurrent somatic RAC1 mutations in melanoma gan Michael Krauthammer, Yong Kong, Byung Hak Ha, Perry Evans, Antonella Bacchiocchi, Jamie P. McCusker, Elaine Cheng, Matthew J. Davis, Gerald Goh, Murim Choi, Stephan Ariyan, Deepak Narayan, Ken Dutton‐Regester, Ana Capatana, Edna C. Holman, Marcus Bosenberg, Mario Sznol, Harriet M. Kluger, Douglas E. Brash, David F. Stern, Miguel A. Materin, Roger S. Lo, Shrikant Mane, Shuangge Ma, Kenneth K. Kídd, Nicholas K. Hayward, Richard P. Lifton, Joseph Schlessinger, Titus J. Boggon, Ruth Halaban

    Cyhoeddwyd 2012
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  19. 19
    Intratumoural evolutionary landscape of high-risk prostate cancer: the PROGENY study of genomic and immune parameters

    Intratumoural evolutionary landscape of high-risk prostate cancer: the PROGENY study of genomic and immune parameters gan Mark Linch, Gerald Goh, Crispin T. Hiley, Yaalini Shanmugabavan, Nicholas McGranahan, Andrew Rowan, Yunka Wong, Henry King, Andrew J.S. Furness, Alex Freeman, J. Linares, Ayse U. Akarca, Javier Herrero, Rachel Rosenthal, Nathalie Harder, G Schmidt, Gareth A. Wilson, Nicolai J. Birkbak, Richard Mitter, Stefan C. Dentro, Paul Cathcart, Manit Arya, Edward W. Johnston, Rachel Scott, Michelle Hung, Mark Emberton, Gerhardt Attard, Zoltán Szállási, Shonit Punwani, Sergio A. Quezada, Teresa Marafioti, Marco Gerlinger, Hashim U. Ahmed, Charles Swanton

    Cyhoeddwyd 2017
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  20. 20
    Multiple Recurrent De Novo CNVs, Including Duplications of the 7q11.23 Williams Syndrome Region, Are Strongly Associated with Autism

    Multiple Recurrent De Novo CNVs, Including Duplications of the 7q11.23 Williams Syndrome Region, Are Strongly Associated with Autism gan Stephan Sanders, A. Gulhan Ercan‐Sencicek, Vanessa Hus, Rui Luo, Michael T. Murtha, Daniel Moreno‐De‐Luca, Su H. Chu, Michael Moreau, Abha R. Gupta, Susanne Thomson, Christopher E. Mason, Kaya Bilgüvar, Patrícia B. S. Celestino-Soper, Murim Choi, Emily L. Crawford, Lea K. Davis, Nicole R. Davis Wright, Rahul M. Dhodapkar, Michael DiCola, Nicholas M. DiLullo, Thomas Fernandez, Vikram Fielding‐Singh, Daniel O. Fishman, Stephanie Frahm, Rouben Garagaloyan, Gerald Goh, Sindhuja Kammela, Lambertus Klei, Jennifer K. Lowe, Sabata C. Lund, Anna D. McGrew, Kyle A. Meyer, William J. Moffat, John D. Murdoch, Brian J. O’Roak, G Ober, Rebecca S. Pottenger, Melanie J. Raubeson, Youeun Song, Qi Wang, Brian L. Yaspan, Timothy W. Yu, Ilana R. Yurkiewicz, Arthur L. Beaudet, Rita M. Cantor, Martin Curland, Dorothy E. Grice, Murat Günel, Richard P. Lifton, Shrikant Mane, Donna M. Martin, Chad A. Shaw, Michael Sheldon, Jay A. Tischfield, Christopher A. Walsh, Eric M. Morrow, David H. Ledbetter, Éric Fombonne, Catherine Lord, Christa Lese Martin, Andrew I. Brooks, James S. Sutcliffe, Edwin H. Cook, Daniel H. Geschwind, Kathryn Roeder, Bernie Devlin, Matthew W. State

    Cyhoeddwyd 2011
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