Αποτελέσματα αναζήτησης - F. Kyle Satterstrom

Περιορισμός αποτελεσμάτων
  1. 1
    From Sirtuin Biology to Human Diseases: An Update

    From Sirtuin Biology to Human Diseases: An Update από Carlos Sebastián, F. Kyle Satterstrom, Marcia C. Haigis, Raúl Mostoslavsky

    Έκδοση 2012
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    Revisão
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    Αποθηκεύτηκε σε:
  2. 2
    Contribution of autosomal rare and de novo variants to sex differences in autism

    Contribution of autosomal rare and de novo variants to sex differences in autism από Mahmoud Koko, F. Kyle Satterstrom, Varun Warrier, Hilary C. Martin

    Έκδοση 2025
    Λήψη πλήρους κειμένου
    Artigo
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  3. 3
    Nuclear respiratory factor 2 induces <scp>SIRT</scp>3 expression

    Nuclear respiratory factor 2 induces <scp>SIRT</scp>3 expression από F. Kyle Satterstrom, William R. Swindell, Gaëlle Laurent, Sejal Vyas, Martha L. Bulyk, Marcia C. Haigis

    Έκδοση 2015
    Λήψη πλήρους κειμένου
    Artigo
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  4. 4
    Landscape of mSWI/SNF chromatin remodeling complex perturbations in neurodevelopmental disorders

    Landscape of mSWI/SNF chromatin remodeling complex perturbations in neurodevelopmental disorders από Alfredo M. Valencia, Akshay Sankar, Pleuntje J. van der Sluijs, F. Kyle Satterstrom, Jack Fu, Michael E. Talkowski, Samantha A. Schrier Vergano, Gijs W.E. Santen, Cigall Kadoch

    Έκδοση 2023
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    Artigo
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    Αποθηκεύτηκε σε:
  5. 5
    Defective respiration and one-carbon metabolism contribute to impaired naïve T cell activation in aged mice

    Defective respiration and one-carbon metabolism contribute to impaired naïve T cell activation in aged mice από Noga Ron‐Harel, Giulia Notarangelo, Jonathan M. Ghergurovich, João A. Paulo, Peter T. Sage, Daniel Santos, F. Kyle Satterstrom, Steven P. Gygi, Joshua D. Rabinowitz, Arlene H. Sharpe, Marcia C. Haigis

    Έκδοση 2018
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    Artigo
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    Αποθηκεύτηκε σε:
  6. 6
    Mitochondrial Biogenesis and Proteome Remodeling Promote One-Carbon Metabolism for T Cell Activation

    Mitochondrial Biogenesis and Proteome Remodeling Promote One-Carbon Metabolism for T Cell Activation από Noga Ron‐Harel, Daniel Santos, Jonathan M. Ghergurovich, Peter T. Sage, Anita Reddy, Scott B. Lovitch, Noah Dephoure, F. Kyle Satterstrom, Michal Sheffer, Jessica B. Spinelli, Steven P. Gygi, Joshua D. Rabinowitz, Arlene H. Sharpe, Marcia C. Haigis

    Έκδοση 2016
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    Artigo
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    Αποθηκεύτηκε σε:
  7. 7
    Mitochondrial Sirtuin Network Reveals Dynamic SIRT3-Dependent Deacetylation in Response to Membrane Depolarization

    Mitochondrial Sirtuin Network Reveals Dynamic SIRT3-Dependent Deacetylation in Response to Membrane Depolarization από Wen Yang, Koji Nagasawa, Christian Münch, Yingjie Xu, F. Kyle Satterstrom, Seung–Min Jeong, Sebastian Hayes, Mark P. Jedrychowski, Foram Vyas, Elma Zaganjor, Virgínia Guarani, Alison E. Ringel, Steven P. Gygi, J. Wade Harper, Marcia C. Haigis

    Έκδοση 2016
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    Artigo
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    Αποθηκεύτηκε σε:
  8. 8
    PHD3 Loss in Cancer Enables Metabolic Reliance on Fatty Acid Oxidation via Deactivation of ACC2

    PHD3 Loss in Cancer Enables Metabolic Reliance on Fatty Acid Oxidation via Deactivation of ACC2 από Natalie J. German, Haejin Yoon, Rushdia Z. Yusuf, J. Patrick Murphy, Lydia W.S. Finley, Gaëlle Laurent, Wilhelm Haas, F. Kyle Satterstrom, Jlenia Guarnerio, Elma Zaganjor, Daniel Santos, Pier Paolo Pandolfi, Andrew H. Beck, Steven P. Gygi, David T. Scadden, William G. Kaelin, Marcia C. Haigis

    Έκδοση 2016
    Λήψη πλήρους κειμένου
    Artigo
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    Αποθηκεύτηκε σε:
  9. 9
    Autism spectrum disorder and attention deficit hyperactivity disorder have a similar burden of rare protein-truncating variants

    Autism spectrum disorder and attention deficit hyperactivity disorder have a similar burden of rare protein-truncating variants από F. Kyle Satterstrom, Raymond K. Walters, Tarjinder Singh, Emilie M. Wigdor, Francesco Lescai, Ditte Demontis, Jack A. Kosmicki, Jakob Grove, Christine Stevens, Jonas Bybjerg‐Grauholm, Marie Bækvad‐Hansen, Duncan S. Palmer, Julian Maller, Merete Nordentoft, Ole Mors, Elise Robinson, David M. Hougaard, Thomas Werge, Preben Bo Mortensen, Benjamin M. Neale, Anders D. Børglum, Mark J. Daly

    Έκδοση 2019
    Λήψη πλήρους κειμένου
    Artigo
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    Αποθηκεύτηκε σε:
  10. 10
    The female protective effect against autism spectrum disorder

    The female protective effect against autism spectrum disorder από Emilie M. Wigdor, Daniel J. Weiner, Jakob Grove, Jack Fu, Wesley K. Thompson, Caitlin E. Carey, Nikolas Baya, Celia van der Merwe, Raymond K. Walters, F. Kyle Satterstrom, Duncan S. Palmer, Anders Rosengren, Jonas Bybjerg‐Grauholm, David M. Hougaard, Preben Bo Mortensen, Mark J. Daly, Michael E. Talkowski, Stephan Sanders, Somer Bishop, Anders D. Børglum, Elise Robinson

    Έκδοση 2022
    Λήψη πλήρους κειμένου
    Artigo
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    Αποθηκεύτηκε σε:
  11. 11
    Differences in the genetic architecture of common and rare variants in childhood, persistent and late-diagnosed attention-deficit hyperactivity disorder

    Differences in the genetic architecture of common and rare variants in childhood, persistent and late-diagnosed attention-deficit hyperactivity disorder από Veera M. Rajagopal, Jinjie Duan, Laura Vilar‐Ribó, Jakob Grove, Tetyana Zayats, Josep Antoni Ramos‐Quiroga, F. Kyle Satterstrom, María Soler Artigas, Jonas Bybjerg‐Grauholm, Marie Bækvad‐Hansen, Thomas D. Als, Anders Rosengren, Mark J. Daly, Benjamin M. Neale, Merete Nordentoft, Thomas Werge, Ole Mors, David M. Hougaard, Preben Bo Mortensen, Marta Ribasés, Anders D. Børglum, Ditte Demontis

    Έκδοση 2022
    Λήψη πλήρους κειμένου
    Artigo
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    Αποθηκεύτηκε σε:
  12. 12
    Whole genome sequencing analysis identifies sex differences of familial pattern contributing to phenotypic diversity in autism

    Whole genome sequencing analysis identifies sex differences of familial pattern contributing to phenotypic diversity in autism από Soo-Whee Kim, Hyeji Lee, Da Yea Song, Gang‐Hee Lee, Jungeun Ji, Jung Woo Park, Jae Hyun Han, Jeewon Lee, Hee Jung Byun, Ji Son, Ye Rim Kim, Yoojeong Lee, Jae-Won Kim, Ashish Jung, Junehawk Lee, Eun-Ha Kim, So Hyun Kim, Jeong Ho Lee, F. Kyle Satterstrom, Santhosh Girirajan, Anders D. Børglum, Jakob Grove, Eunjoon Kim, Donna M. Werling, Hee Jeong Yoo, Joon‐Yong An

    Έκδοση 2024
    Λήψη πλήρους κειμένου
    Artigo
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  13. 13
    Quantifying the Impact of Rare and Ultra-rare Coding Variation across the Phenotypic Spectrum

    Quantifying the Impact of Rare and Ultra-rare Coding Variation across the Phenotypic Spectrum από Andrea Ganna, F. Kyle Satterstrom, Seyedeh M. Zekavat, Indraniel Das, Mitja Kurki, Tracy Air, Jessica Alföldi, Alicia R. Martin, Aki S. Havulinna, Andrea Byrnes, Wesley K. Thompson, Philip Nielsen, Konrad J. Karczewski, Elmo Saarentaus, Manuel A. Rivas, Namrata Gupta, Olli Pietiläinen, Connor A. Emdin, Francesco Lescai, Jonas Bybjerg‐Grauholm, Jason Flannick, Josep M. Mercader, Miriam S. Udler, Markku Laakso, Veikko Salomaa, Christina M. Hultman, Samuli Ripatti, Eija Hämäläinen, Jukka S. Moilanen, Jarmo Körkkö, Outi Kuismin, Merete Nordentoft, David M. Hougaard, Ole Mors, Thomas Werge, Preben Bo Mortensen, Daniel G. MacArthur, Mark J. Daly, Patrick F. Sullivan, Adam E. Locke, Aarno Palotie, Anders D. Børglum, Sekar Kathiresan, Benjamin M. Neale

    Έκδοση 2018
    Λήψη πλήρους κειμένου Λήψη πλήρους κειμένου
    Artigo
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    Αποθηκεύτηκε σε:
  14. 14
    Genome-wide analyses of ADHD identify 27 risk loci, refine the genetic architecture and implicate several cognitive domains

    Genome-wide analyses of ADHD identify 27 risk loci, refine the genetic architecture and implicate several cognitive domains από Ditte Demontis, G. Bragi Walters, Georgios Athanasiadis, Raymond K. Walters, Karen Therrien, Leila Farajzadeh, Georgios Voloudakis, Jaroslav Bendl, Biao Zeng, Wen Zhang, Jakob Grove, Thomas D. Als, Jinjie Duan, F. Kyle Satterstrom, Jonas Bybjerg‐Grauholm, Marie Bækved-Hansen, Ólafur Ó. Guðmundsson, Sigurður H. Magnússon, Gísli Baldursson, Katrín Davíðsdóttir, Gyða S. Haraldsdóttir, Trine Tollerup Nielsen, Esben Agerbo, Gabriel E. Hoffman, Søren Dalsgaard, Joanna Martin, Marta Ribasés, Dorret I. Boomsma, María Soler Artigas, Nina Roth Mota, Daniel P. Howrigan, Sarah E. Medland, Tetyana Zayats, Veera Manikandan, Merete Nordentoft, Ole Mors, David M. Hougaard, Preben Bo Mortensen, Mark J. Daly, Stephen V. Faraone, Hreinn Stefánsson, Panos Roussos, Barbara Franke, Thomas Werge, Benjamin M. Neale, Kāri Stefánsson, Anders D. Børglum

    Έκδοση 2022
    Λήψη πλήρους κειμένου Λήψη πλήρους κειμένου
    Pré-impressão
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    Αποθηκεύτηκε σε:
  15. 15
    Genome-wide association study of school grades identifies genetic overlap between language ability, psychopathology and creativity

    Genome-wide association study of school grades identifies genetic overlap between language ability, psychopathology and creativity από Veera M. Rajagopal, Andrea Ganna, Jonathan R. I. Coleman, Andrea G. Allegrini, Georgios Voloudakis, Jakob Grove, Thomas D. Als, Henriette Thisted Horsdal, Liselotte Petersen, Vivek Appadurai, Andrew J. Schork, Alfonso Buil, Cynthia M. Bulik, Jonas Bybjerg‐Grauholm, Marie Bækvad‐Hansen, David M. Hougaard, Ole Mors, Merete Nordentoft, Thomas Werge, Rich Belliveau, Caitlin E. Carey, Felecia Cerrato, Kimberly Chambert, Tracy Air, Mark J. Daly, Ashley Dumont, Jacqueline I. Goldstein, Christine Søholm Hansen, Daniel P. Howrigan, Hailiang Huang, Julian Maller, Alicia R. Martin, Joanna Martin, Manuel Mattheisen, Jennifer L. Moran, Benjamin M. Neale, Jonatan Pallesen, Duncan S. Palmer, Carsten Bcker Pedersen, Marianne Giørtz Pedersen, Timothy Poterba, Stephan Ripke, F. Kyle Satterstrom, Wesley K. Thompson, Patrick Turley, Raymond K. Walters, Preben Bo Mortensen, Gerome Breen, Panos Roussos, Robert Plomin, Esben Agerbo, Anders D. Børglum, Ditte Demontis

    Έκδοση 2023
    Λήψη πλήρους κειμένου Λήψη πλήρους κειμένου
    Artigo
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    Αποθηκεύτηκε σε:
  16. 16
    Deleterious coding variation associated with autism is consistent across populations, as exemplified by admixed Latin American populations

    Deleterious coding variation associated with autism is consistent across populations, as exemplified by admixed Latin American populations από Marina Natividad Avila, Seulgi Jung, F. Kyle Satterstrom, Jack Fu, Tess Levy, Laura Sloofman, Lambertus Klei, Thariana Pichardo, Christine Stevens, Caroline Cusick, Jennifer Ames, Gabriele da Silva Campos, Hilda J Cerros, Roberto Chaskel, Claudia Ismania Samogy Costa, Michael L. Cuccaro, Andrea López, Magdalena Fernández, Eugenio Ferro, Liliana Galeano, Ana Cristina De Sanctis Girardi, Anthony J. Griswold, Luis C. Hernandez, Naila Cristina Vilaça Lourenço, Yunin Ludeña, Diana Núñez, Ryan K. Oyama, Katherine Peña, Isaac N. Pessah, Rebecca J. Schmidt, Holly Morsbach Sweeney, Lizbeth Tolentino, Jaqueline Y. T. Wang, Lilia Albores‐Gallo, Lisa Croen, Carlos Cruz-Fuentes, Irva Hertz‐Picciotto, Alexander Kolevzon, María Claudia Lattig, Liliana Mayo, Maria Rita Passos-Bueno, Margaret A. Pericak‐Vance, Paige M. Siper, Flora Tassone, M. Pilar Trelles, Michael E. Talkowski, Mark J. Daly, Behrang Mahjani, Silvia De Rubeis, Edwin H. Cook, Kathryn Roeder, Catalina Betancur, Bernie Devlin, Joseph D. Buxbaum

    Έκδοση 2025
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    Αποθηκεύτηκε σε:
  17. 17
    Rare coding variation illuminates the allelic architecture, risk genes, cellular expression patterns, and phenotypic context of autism

    Rare coding variation illuminates the allelic architecture, risk genes, cellular expression patterns, and phenotypic context of autism από Jack Fu, F. Kyle Satterstrom, Minshi Peng, Harrison Brand, Ryan L. Collins, Shan Dong, Lambertus Klei, Christine Stevens, Caroline Cusick, Mehrtash Babadi, Eric Banks, Brett Collins, Sheila Dodge, Stacey B. Gabriel, Laura D. Gauthier, Samuel K. Lee, Lindsay Liang, Alicia Ljungdahl, Behrang Mahjani, Laura Sloofman, Andrey N. Smirnov, Mafalda Barbosa, Alfredo Brusco, Brian Hon‐Yin Chung, Michael L. Cuccaro, Enrico Domenici, Giovanni Battista Ferrero, J. Jay Gargus, Gail E. Herman, Irva Hertz‐Picciotto, Patrı́cia Maciel, Dara S. Manoach, Maria Rita Passos‐Bueno, Antonio M. Persico, Alessandra Renieri, Flora Tassone, Elisabetta Trabetti, Gabriele da Silva Campos, Marcus C.Y. Chan, Chiara Fallerini, Elisa Giorgio, Ana Cristina Girard, Emily Hansen‐Kiss, So Lun Lee, Carla Lintas, Yunin Ludeña, Rachel Nguyen, Lisa Pavinato, Margaret A. Pericak‐Vance, Isaac N. Pessah, Evelise Riberi, Rebecca J. Schmidt, Moyra Smith, Claudia I.C. Souza, Slavica Trajkova, Jaqueline Y. T. Wang, Mullin H.C. Yu, David J. Cutler, Silvia De Rubeis, Joseph D. Buxbaum, Mark J. Daly, Bernie Devlin, Kathryn Roeder, Stephan Sanders, Michael E. Talkowski

    Έκδοση 2021
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  18. 18
    Common risk variants identified in autism spectrum disorder

    Common risk variants identified in autism spectrum disorder από Jakob Grove, Stephan Ripke, Thomas D. Als, Manuel Mattheisen, Raymond K. Walters, Hyejung Won, Jonatan Pallesen, Esben Agerbo, Ole A. Andreassen, Richard Anney, Rich Belliveau, Francesco Bettella, Joseph D. Buxbaum, Jonas Bybjerg‐Grauholm, Marie Bækved-Hansen, Felecia Cerrato, Kimberly Chambert, Jane Christensen, Tracy Air, Karin Dellenvall, Ditte Demontis, Silvia De Rubeis, Bernie Devlin, Srdjan Djurovic, Ashle Dumont, Jacqueline I. Goldstein, Christine Søholm Hansen, Mads E. Hauberg, Mads V. Hollegaard, Sigrun Hope, Daniel P. Howrigan, Hailiang Huang, Christina M. Hultman, Lambertus Klei, Julian Maller, Joanna Martin, Alicia R. Martin, Jennifer L. Moran, Mette Nyegaard, Terje Nærland, Duncan S. Palmer, Aarno Palotie, Carsten Bøcker Pedersen, Marianne Giørtz Pedersen, Timothy Poterba, Jesper Buchhave Poulsen, Beaté St Pourcain, Per Qvist, Karola Rehnström, Avi Reichenberg, Jennifer Reichert, Elise Robinson, Kathryn Roeder, Panos Roussos, Evald Sæmundsen, Sven Sandin, F. Kyle Satterstrom, George Davey Smith, Hreinn Stefánsson, Kāri Stefánsson, Stacy Steinberg, Christine Stevens, Patrick F. Sullivan, Patrick Turley, G. Bragi Walters, Xinyi Xu, Daniel H. Geschwind, Merete Nordentoft, David M. Hougaard, Thomas Werge, Ole Mors, Preben Bo Mortensen, Benjamin M. Neale, Mark J. Daly, Anders D. Børglum

    Έκδοση 2017
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  19. 19
    Identification of common genetic risk variants for autism spectrum disorder

    Identification of common genetic risk variants for autism spectrum disorder από Jakob Grove, Stephan Ripke, Thomas D. Als, Manuel Mattheisen, Raymond K. Walters, Hyejung Won, Jonatan Pallesen, Esben Agerbo, Ole A. Andreassen, Richard Anney, Swapnil Awashti, Rich Belliveau, Francesco Bettella, Joseph D. Buxbaum, Jonas Bybjerg‐Grauholm, Marie Bækvad‐Hansen, Felecia Cerrato, Kimberly Chambert, Jane Christensen, Tracy Air, Karin Dellenvall, Ditte Demontis, Silvia De Rubeis, Bernie Devlin, Srdjan Djurovic, Ashley Dumont, Jacqueline I. Goldstein, Christine Søholm Hansen, Mads E. Hauberg, Mads V. Hollegaard, Sigrun Hope, Daniel P. Howrigan, Hailiang Huang, Christina M. Hultman, Lambertus Klei, Julian Maller, Joanna Martin, Alicia R. Martin, Jennifer L. Moran, Mette Nyegaard, Terje Nærland, Duncan S. Palmer, Aarno Palotie, Carsten Bøcker Pedersen, Marianne Giørtz Pedersen, Timothy dPoterba, Jesper Buchhave Poulsen, Beaté St Pourcain, Per Qvist, Karola Rehnström, Abraham Reichenberg, Jennifer Reichert, Elise Robinson, Kathryn Roeder, Panos Roussos, Evald Sæmundsen, Sven Sandin, F. Kyle Satterstrom, George Davey Smith, Hreinn Stefánsson, Stacy Steinberg, Christine Stevens, Patrick F. Sullivan, Patrick Turley, G. Bragi Walters, Xinyi Xu, Kāri Stefánsson, Daniel H. Geschwind, Merete Nordentoft, David M. Hougaard, Thomas Werge, Ole Mors, Preben Bo Mortensen, Benjamin M. Neale, Mark J. Daly, Anders D. Børglum

    Έκδοση 2019
    Λήψη πλήρους κειμένου
    Artigo
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  20. 20
    Discovery of the first genome-wide significant risk loci for attention deficit/hyperactivity disorder

    Discovery of the first genome-wide significant risk loci for attention deficit/hyperactivity disorder από Ditte Demontis, Raymond K. Walters, Joanna Martin, Manuel Mattheisen, Thomas D. Als, Esben Agerbo, Gísli Baldursson, Rich Belliveau, Jonas Bybjerg‐Grauholm, Marie Bækvad‐Hansen, Felecia Cerrato, Kimberly Chambert, Tracy Air, Ashley Dumont, Nicholas Eriksson, Michael J. Gandal, Jacqueline I. Goldstein, Katrina L. Grasby, Jakob Grove, Ólafur Ó. Guðmundsson, Christine Søholm Hansen, Mads E. Hauberg, Mads V. Hollegaard, Daniel P. Howrigan, Hailiang Huang, Julian Maller, Alicia R. Martin, Nicholas G. Martin, Jennifer L. Moran, Jonatan Pallesen, Duncan S. Palmer, Carsten Bøcker Pedersen, Marianne Giørtz Pedersen, Timothy Poterba, Jesper Buchhave Poulsen, Stephan Ripke, Elise Robinson, F. Kyle Satterstrom, Hreinn Stefánsson, Christine Stevens, Patrick Turley, G. Bragi Walters, Hyejung Won, Margaret J. Wright, Ole A. Andreassen, Philip Asherson, Christie L. Burton, Dorret I. Boomsma, Bru Cormand, Søren Dalsgaard, Barbara Franke, Joel Gelernter, Daniel H. Geschwind, Hákon Hákonarson, Jan Haavik, Henry R. Kranzler, Jonna Kuntsi, K. Langley, Klaus‐Peter Lesch, Christel M. Middeldorp, Andreas Reif, Luís Augusto Rohde, Panos Roussos, Russell Schachar, Pamela Sklar, Edmund Sonuga‐Barke, Patrick F. Sullivan, Anita Thapar, Joyce Y. Tung, Irwin D. Waldman, Sarah E. Medland, Kāri Stefánsson, Merete Nordentoft, David M. Hougaard, Thomas Werge, Ole Mors, Preben Bo Mortensen, Mark J. Daly, Stephen V. Faraone, Anders D. Børglum, Benjamin M. Neale

    Έκδοση 2018
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