نتائج البحث - John D. Overton
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Molecular chaperone Hsp110 rescues a vesicle transport defect produced by an ALS-associated mutant SOD1 protein in squid axoplasm حسب Yuyu Song, Mária Nagy, Weiming Ni, Navneet K. Tyagi, Wayne A. Fenton, Francesc López‐Giráldez, John D. Overton, Arthur L. Horwich, Scott T. Brady
منشور في 2013Artigo -
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CLAMMS: a scalable algorithm for calling common and rare copy number variants from exome sequencing data حسب Jonathan S. Packer, Evan K. Maxwell, Colm O’Dushlaine, Alexander Lopez, Frederick E. Dewey, Rostislav Chernomorsky, Aris Baras, John D. Overton, Lukas Habegger, Jeffrey G. Reid
منشور في 2015Artigo -
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Whole-Exome Sequencing Reveals Somatic Mutations in HRAS and KRAS , which Cause Nevus Sebaceus حسب Jonathan Levinsohn, Li C. Tian, Lynn M. Boyden, Jennifer M. McNiff, Deepak Narayan, Erin S. Loring, Duri Yun, Jeremy Sugarman, John D. Overton, Shrikant Mane, Richard P. Lifton, Amy S. Paller, Annette Wagner, Richard J. Antaya, Keith A. Choate
منشور في 2012Carta -
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Mutation of NLRC4 causes a syndrome of enterocolitis and autoinflammation حسب Neil Romberg, Khatoun Al Moussawi, Carol Nelson‐Williams, Amy L. Stiegler, Erin Loring, Murim Choi, John D. Overton, Eric Meffre, Mustafa K. Khokha, Anita Hüttner, Brian L. West, Nikolai A. Podoltsev, Titus J. Boggon, Barbara I. Kazmierczak, Richard P. Lifton
منشور في 2014Artigo -
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Neomorphic effects of recurrent somatic mutations in <i>Yin Yang 1</i> in insulin-producing adenomas حسب M. Kyle Cromer, Murim Choi, Carol Nelson‐Williams, Annabelle L. Fonseca, John W. Kunstman, Reju Korah, John D. Overton, Shrikant Mane, Barton Kenney, Carl D. Malchoff, Peter Stålberg, Göran Åkerström, Gunnar Westin, Per Hellman, Tobias Carling, Peyman Björklund, Richard P. Lifton
منشور في 2015Artigo -
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Langerhans Cells Facilitate Epithelial DNA Damage and Squamous Cell Carcinoma حسب Badri Modi, Jason H. Neustadter, Elisa Binda, Julia M. Lewis, Renata B. Filler, Scott Roberts, Bernice Y. Kwong, Swapna Reddy, John D. Overton, Anjela Galan, Robert E. Tigelaar, Lining Cai, Peter P. Fu, Mark J. Shlomchik, Daniel H. Kaplan, Adrian Hayday, Michael Girardi
منشور في 2012Artigo -
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Use of whole genome sequencing to estimate the contribution of immune evasion and waning immunity to decreasing COVID-19 vaccine effectiveness during alpha and delta variant waves حسب Margaret L. Lind, Richard Copin, Shane McCarthy, Andreas Coppi, Fred Warner, David Ferguson, Chelsea Duckwall, Ryan Borg, M. Catherine Muenker, John D. Overton, Sara Hamon, Anbo Zhou, Derek A. T. Cummings, Albert I. Ko, Jennifer D. Hamilton, Wade L. Schulz, Matt T. Hitchings
منشور في 2022Pré-impressão -
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Use of Whole-Genome Sequencing to Estimate the Contribution of Immune Evasion and Waning Immunity on Decreasing COVID-19 Vaccine Effectiveness حسب Margaret L. Lind, Richard Copin, Shane McCarthy, Andreas Coppi, Fred Warner, David Ferguson, Chelsea Duckwall, Ryan Borg, M. Catherine Muenker, John D. Overton, Sara Hamon, Anbo Zhou, Derek A. T. Cummings, Albert I. Ko, Jennifer D. Hamilton, Wade L. Schulz, Matt D. T. Hitchings
منشور في 2022Artigo -
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Mutation spectrum of NOD2 reveals recessive inheritance as a main driver of Early Onset Crohn’s Disease حسب Julie Horowitz, Neil Warner, Jeffrey Staples, Eileen Crowley, Nehal Gosalia, Ryan Murchie, Cristopher V. Van Hout, Karoline Fiedler, Gabriel Welch, Alejandra King, Jeffrey G. Reid, John D. Overton, Aris Baras, Alan R. Shuldiner, Anne M. Griffiths, Omri Gottesman, Aleixo M. Muise, Claudia Gonzaga‐Jauregui
منشور في 2021Artigo -
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Clinical and Molecular Prevalence of Lipodystrophy in an Unascertained Large Clinical Care Cohort حسب Claudia Gonzaga‐Jauregui, Wenzhen Ge, Jeffrey Staples, Cristopher V. Van Hout, Ashish Yadav, Ryan Colonie, Joseph B. Leader, H. Lester Kirchner, Michael F. Murray, Jeffrey G. Reid, David J. Carey, John D. Overton, Alan R. Shuldiner, Omri Gottesman, Steve Gao, Jesper Gromada, Aris Baras, Judith Y. Altarejos
منشور في 2019Artigo -
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Positional Cloning of “Lisch-like”, a Candidate Modifier of Susceptibility to Type 2 Diabetes in Mice حسب Marija Dokmanovic-Chouinard, Wendy K. Chung, Jean-Claude Chèvre, Elizabeth Watson, J. Yonan, Beebe Wiegand, Yana Bromberg, Nao Wakae, Chris Wright, John D. Overton, Sujoy Ghosh, Ganesh M. Sathe, Carina Ämmälä, Kathleen K. Brown, Rokuro Ito, Charles A. LeDuc, Keely S. Solomon, Stuart G. Fischer, Rudolph L. Leibel
منشور في 2008Artigo -
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Patients With High Genome-Wide Polygenic Risk Scores for Coronary Artery Disease May Receive Greater Clinical Benefit From Alirocumab Treatment in the ODYSSEY OUTCOMES Trial حسب Amy Damask, Philippe Gabríel Steg, Gregory G. Schwartz, Michael Szarek, Emil Hagström, Lina Badimón, M. John Chapman, Cathérine Boileau, Sotirios Tsimikas, Henry N. Ginsberg, Poulabi Banerjee, Garen Manvelian, Robert Pordy, Sibylle Hess, John D. Overton, Luca A. Lotta, George D. Yancopoulos, Gonçalo R. Abecasis, Aris Baras, Charles Paulding
منشور في 2019Artigo -
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Genome-wide association study of alcohol consumption and use disorder in 274,424 individuals from multiple populations حسب Henry R. Kranzler, Hang Zhou, Rachel L. Kember, Rachel Vickers‐Smith, Amy C. Justice, Scott M. Damrauer, Philip S. Tsao, Derek Klarin, Aris Baras, Jeffrey G. Reid, John D. Overton, Daniel J. Rader, Zhongshan Cheng, Janet P. Tate, William C. Becker, John Concato, Ke Xu, Renato Polimanti, Hongyu Zhao, Joel Gelernter
منشور في 2019Artigo -
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Author Correction: Genome-wide association study of alcohol consumption and use disorder in 274,424 individuals from multiple populations حسب Henry R. Kranzler, Hang Zhou, Rachel L. Kember, Rachel Vickers‐Smith, Amy C. Justice, Scott M. Damrauer, Philip S. Tsao, Derek Klarin, Aris Baras, Jeffrey G. Reid, John D. Overton, Daniel J. Rader, Zhongshan Cheng, Janet P. Tate, William C. Becker, John Concato, Ke Xu, Renato Polimanti, Hongyu Zhao, Joel Gelernter
منشور في 2019Errata/Corrigenda -
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Polygenic Risk of Psychiatric Disorders Exhibits Cross-trait Associations in Electronic Health Record Data From European Ancestry Individuals حسب Rachel L. Kember, Alison Merikangas, Shefali S. Verma, Anurag Verma, Renae Judy, Scott M. Damrauer, Marylyn D. Ritchie, Daniel J. Rader, Maja Bućan, Gonçalo R. Abecasis, Aris Baras, Michael Cantor, Giovanni Coppola, Aris N. Economides, Luca A. Lotta, John D. Overton, Jeffrey G. Reid, Alan R. Shuldiner, Christina Beechert, Caitlin Forsythe, Erin D. Fuller, Zhenhua Gu, Michael Lattari, Alexander Lopez, John D. Overton, Thomas D. Schleicher, Maria Sotiropoulos Padilla, Karina Toledo, Louis Widom, Sarah E. Wolf, Manasi Pradhan, Kia Manoochehri, Ricardo H. Ulloa, Xiaodong Bai, Suganthi Balasubramanian, Leland Barnard, Andrew Blumenfeld, Gisu Eom, Lukas Habegger, Young S. Hahn, Alicia Hawes, Shareef Khalid, Jeffrey G. Reid, Evan K. Maxwell, William Salerno, Jeffrey Staples, Ashish Yadav, Marcus B. Jones, Lyndon J. Mitnaul
منشور في 2020Artigo -
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Genomic diagnostics within a medically underserved population: efficacy and implications حسب Kevin A. Strauss, Claudia Gonzaga‐Jauregui, Karlla W. Brigatti, Katie B. Williams, Alejandra King, Cristopher V. Van Hout, Donna L. Robinson, Millie Young, Kavita Praveen, Adam D. Heaps, Mindy Kuebler, Aris Baras, Jeffrey G. Reid, John D. Overton, Frederick E. Dewey, Robert N. Jinks, Ian Finnegan, Scott Mellis, Alan R. Shuldiner, Erik G. Puffenberger
منشور في 2017Artigo -
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Exome Sequencing in Children With Pulmonary Arterial Hypertension Demonstrates Differences Compared With Adults حسب Na Zhu, Claudia Gonzaga‐Jauregui, Carrie L. Welch, Lijiang Ma, Hongjian Qi, Alejandra King, Usha Krishnan, Erika B. Rosenzweig, D. Dunbar Ivy, Eric D. Austin, Rizwan Hamid, William C. Nichols, Michael W. Pauciulo, Katie A. Lutz, Ashley Sawle, Jeffrey G. Reid, John D. Overton, Aris Baras, Frederick E. Dewey, Yufeng Shen, Wendy K. Chung
منشور في 2018Artigo
أدوات البحث:
موضوعات ذات صلة
Biology
Genetics
Gene
Medicine
Internal medicine
Mutation
Exome sequencing
Exome
Genotype
Disease
Phenotype
Single-nucleotide polymorphism
Computational biology
Bioinformatics
Endocrinology
Population
Genome-wide association study
Genome
Biobank
Cardiology
Environmental health
Genetic association
Pathology
Cohort
Immunology
Sociology
Somatic cell
Demography
Germline mutation
Odds ratio