Resultados da busca - Douglas M. Ruderfer
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Telomere Length as a Quantitative Trait: Genome-Wide Survey and Genetic Mapping of Telomere Length-Control Genes in Yeast por Tonibelle Gatbonton, Maria Imbesi, Melisa Nelson, Joshua M. Akey, Douglas M. Ruderfer, Leonid Kruglyak, Julian A. Simon, Antonio Bedalov
Publicado em 2006Artigo -
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Significant shared heritability underlies suicide attempt and clinically predicted probability of attempting suicide por Douglas M. Ruderfer, Colin G. Walsh, Matthew Aguirre, Yosuke Tanigawa, Jessica D. Ribeiro, Joseph C. Franklin, Manuel A. Rivas
Publicado em 2019Artigo -
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Improving ascertainment of suicidal ideation and suicide attempt with natural language processing por Cosmin A. Bejan, Michael Ripperger, Drew Wilimitis, Ryan Ahmed, Jooeun Kang, Katelyn Robinson, Theodore Morley, Douglas M. Ruderfer, Colin G. Walsh
Publicado em 2022Artigo -
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Characterizing trends in clinical genetic testing: A single-center analysis of EHR data from 1.8 million patients over two decades por Lisa Bastarache, Rory J. Tinker, Bryce Schuler, Lucas Richter, John A. Phillips, William W. Stead, Gillian W. Hooker, Josh F. Peterson, Douglas M. Ruderfer
Publicado em 2025Artigo -
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Transcriptional signatures of schizophrenia in hiPSC-derived NPCs and neurons are concordant with post-mortem adult brains por Gabriel E. Hoffman, Brigham J. Hartley, Erin Flaherty, Ian Ladran, Peter Gochman, Douglas M. Ruderfer, Eli A. Stahl, Judith L. Rapoport, Pamela Sklar, Kristen Brennand
Publicado em 2017Artigo -
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Patterns of genic intolerance of rare copy number variation in 59,898 human exomes por Douglas M. Ruderfer, Tymor Hamamsy, Monkol Lek, Konrad J. Karczewski, David Kavanagh, Kaitlin E. Samocha, Mark J. Daly, Daniel G. MacArthur, Menachem Fromer, Shaun Purcell
Publicado em 2016Artigo -
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Genetic modifiers and subtypes in schizophrenia: Investigations of age at onset, severity, sex and family history por Sarah E. Bergen, Colm O’Dushlaine, Phil H. Lee, Ayman H. Fanous, Douglas M. Ruderfer, Stephan Ripke, Patrick F. Sullivan, Jordan W. Smoller, Shaun Purcell, Aiden Corvin
Publicado em 2014Artigo -
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Improving genetic prediction by leveraging genetic correlations among human diseases and traits por Robert Maier, Zhihong Zhu, Sang Lee, Maciej Trzaskowski, Douglas M. Ruderfer, Eli A. Stahl, Stephan Ripke, Naomi R. Wray, Jian Yang, Peter M. Visscher, Matthew R. Robinson
Publicado em 2018Artigo -
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Sleep patterns and risk of chronic disease as measured by long-term monitoring with commercial wearable devices in the All of Us Research Program por Neil S. Zheng, Jeffrey Annis, Hiral Master, Lide Han, Karla Gleichauf, Jack Ching, Melody Nasser, Peyton L. Coleman, Stacy Desine, Douglas M. Ruderfer, John Hernandez, Logan Schneider, Evan L. Brittain
Publicado em 2024Artigo -
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Increased burden of ultra-rare protein-altering variants among 4,877 individuals with schizophrenia por Giulio Genovese, Menachem Fromer, Eli A. Stahl, Douglas M. Ruderfer, Kimberly Chambert, Mikael Landén, Jennifer L. Moran, Shaun Purcell, Pamela Sklar, Patrick F. Sullivan, Christina M. Hultman, Steven A. McCarroll
Publicado em 2016Artigo -
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The ExAC browser: displaying reference data information from over 60 000 exomes por Konrad J. Karczewski, Ben Weisburd, Brett Thomas, Matthew Solomonson, Douglas M. Ruderfer, David Kavanagh, Tymor Hamamsy, Monkol Lek, Kaitlin E. Samocha, Beryl B. Cummings, Daniel Birnbaum, Mark J. Daly, Daniel G. MacArthur
Publicado em 2016Artigo -
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Polygenic overlap between schizophrenia risk and antipsychotic response: a genomic medicine approach por Douglas M. Ruderfer, Alexander W. Charney, Ben Readhead, Brian Kidd, Anna K. Kähler, Paul J. Kenny, Michael J. Keiser, Jennifer L. Moran, Christina M. Hultman, Stuart A. Scott, Patrick F. Sullivan, Shaun Purcell, Joel T. Dudley, Pamela Sklar
Publicado em 2016Artigo -
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Rare Copy Number Variation in Treatment-Resistant Major Depressive Disorder por Colm Ó'Dúshláine, Stephan Ripke, Douglas M. Ruderfer, Steven P. Hamilton, Maurizio Fava, Dan V. Iosifescu, Isaac S. Kohane, Susanne Churchill, Víctor M. Castro, Caitlin C. Clements, Sarah R. Blumenthal, Shawn N. Murphy, Jordan W. Smoller, Roy H. Perlis
Publicado em 2014Artigo -
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Cis-acting regulation of brain-specific ANK3 gene expression by a genetic variant associated with bipolar disorder por Erroll H. Rueckert, Douglas Barker, Douglas M. Ruderfer, Sarah E. Bergen, Colm O’Dushlaine, Catherine J. Luce, Steven D. Sheridan, Kraig M. Theriault, Kimberly Chambert, Jennifer L. Moran, Shaun Purcell, Jon M. Madison, Stephen J. Haggarty, Pamela Sklar
Publicado em 2012Artigo -
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Discovery and Statistical Genotyping of Copy-Number Variation from Whole-Exome Sequencing Depth por Menachem Fromer, Jennifer L. Moran, Kimberly Chambert, Eric Banks, Sarah E. Bergen, Douglas M. Ruderfer, Robert E. Handsaker, Steven A. McCarroll, Michael O’Donovan, Michael J. Owen, George Kirov, Patrick F. Sullivan, Christina M. Hultman, Pamela Sklar, Shaun Purcell
Publicado em 2012Artigo -
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Clinical laboratory test-wide association scan of polygenic scores identifies biomarkers of complex disease por Jessica Dennis, Julia Sealock, Péter Straub, Young A Lee, Donald Hucks, Ky’Era V. Actkins, Annika Faucon, Yen‐Chen Anne Feng, Tian Ge, Slavina Goleva, Maria Niarchou, Kritika Singh, Theodore Morley, Jordan W. Smoller, Douglas M. Ruderfer, Jonathan D. Mosley, Guanhua Chen, Lea K. Davis
Publicado em 2021Artigo -
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Multi-omic characterization of brain changes in the vascular endothelial growth factor family during aging and Alzheimer's disease por Mabel Seto, Logan Dumitrescu, Emily R. Mahoney, Annah M. Sclafani, Philip L. De Jager, Vilas Menon, Mary Ellen I. Koran, Renã A. S. Robinson, Douglas M. Ruderfer, Nancy J. Cox, Nicholas T. Seyfried, Angela L. Jefferson, Julie A. Schneider, David A. Bennett, Vladislav Petyuk, Timothy J. Hohman
Publicado em 2023Artigo
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Assuntos relacionados
Biology
Genetics
Gene
Medicine
Psychiatry
Genotype
Single-nucleotide polymorphism
Schizophrenia (object-oriented programming)
Computational biology
Genome
Genome-wide association study
Genetic association
Psychology
Internal medicine
Computer science
Mutation
Phenotype
Population
Copy-number variation
Disease
Environmental health
Neuroscience
Bioinformatics
Bipolar disorder
Exome sequencing
Cognition
Exome
Gene expression
Expression quantitative trait loci
Pathology