Suchergebnisse - Veera M. Rajagopal

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  1. 1
    Kinetics of IgM and IgG antibodies after scrub typhus infection and the clinical implications

    Kinetics of IgM and IgG antibodies after scrub typhus infection and the clinical implications von George M. Varghese, Veera M. Rajagopal, Paul Trowbridge, Divya Purushothaman, Sherry Joseph Martin

    Veröffentlicht 2018
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  2. 2
    Integrative transcriptome imputation reveals tissue-specific and shared biological mechanisms mediating susceptibility to complex traits

    Integrative transcriptome imputation reveals tissue-specific and shared biological mechanisms mediating susceptibility to complex traits von Wen Zhang, Georgios Voloudakis, Veera M. Rajagopal, Ben Readhead, Joel T. Dudley, Eric E. Schadt, Johan Björkegren, Yungil Kim, John F. Fullard, Gabriel E. Hoffman, Panos Roussos

    Veröffentlicht 2019
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  3. 3
    Genome-wide association study in individuals of European and African ancestry and multi-trait analysis of opioid use disorder identifies 19 independent genome-wide significant risk loci

    Genome-wide association study in individuals of European and African ancestry and multi-trait analysis of opioid use disorder identifies 19 independent genome-wide significant risk... von Joseph D. Deak, Hang Zhou, Marco Galimberti, Daniel F. Levey, Frank R. Wendt, Sandra Sanchez‐Roige, Alexander S. Hatoum, Emma C. Johnson, Yaira Z. Nuñez, Ditte Demontis, Anders D. Børglum, Veera M. Rajagopal, Mariela Jennings, Rachel L. Kember, Amy C. Justice, Howard J. Edenberg, Arpana Agrawal, Renato Polimanti, Henry R. Kranzler, Joel Gelernter

    Veröffentlicht 2022
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  4. 4
    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 von 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

    Veröffentlicht 2022
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  5. 5
    Gene expression imputation across multiple brain regions provides insights into schizophrenia risk

    Gene expression imputation across multiple brain regions provides insights into schizophrenia risk von Laura M. Huckins, Amanda Dobbyn, Douglas M. Ruderfer, Gabriel E. Hoffman, Weiqing Wang, Antonio F. Pardiñas, Veera M. Rajagopal, Thomas D. Als, Hoang T. Nguyen, Kiran Girdhar, James Boocock, Panos Roussos, Menachem Fromer, Robin S. S. Kramer, Enrico Domenici, Eric R. Gamazon, Shaun Purcell, Ditte Demontis, Anders D. Børglum, James Walters, Michael O’Donovan, Patrick F. Sullivan, Michael J. Owen, Bernie Devlin, Solveig K. Sieberts, Nancy J. Cox, Hae Kyung Im, Pamela Sklar, Eli A. Stahl

    Veröffentlicht 2019
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  6. 6
    Genome-wide association study implicates CHRNA2 in cannabis use disorder

    Genome-wide association study implicates CHRNA2 in cannabis use disorder von Ditte Demontis, Veera M. Rajagopal, Thorgeir E. Thorgeirsson, Thomas D. Als, Jakob Grove, Kalle Leppälä, Daníel F. Guðbjartsson, Jonatan Pallesen, Carsten Hjorthøj, Gunnar W. Reginsson, Þórarinn Tyrfingsson, Valgerður Rúnarsdóttir, Per Qvist, Jane Christensen, Jonas Bybjerg‐Grauholm, Marie Bækvad‐Hansen, Laura M. Huckins, Eli A. Stahl, Allan Timmermann, Esben Agerbo, David M. Hougaard, Thomas Werge, Ole Mors, Preben Bo Mortensen, Merete Nordentoft, Mark J. Daly, Hreinn Stefánsson, Kāri Stefánsson, Mette Nyegaard, Anders D. Børglum

    Veröffentlicht 2019
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  7. 7
    Multi-ancestry genome-wide association study of cannabis use disorder yields insight into disease biology and public health implications

    Multi-ancestry genome-wide association study of cannabis use disorder yields insight into disease biology and public health implications von Daniel F. Levey, Marco Galimberti, Joseph D. Deak, Frank R. Wendt, Arjun Bhattacharya, Dóra Koller, Kelly Harrington, Rachel Quaden, Emma C. Johnson, Priya Gupta, Mahantesh I. Biradar, Max Lam, Megan E. Cooke, Veera M. Rajagopal, Stefany Lucas Lopes Empke, Hang Zhou, Yaira Z. Nuñez, Henry R. Kranzler, Howard J. Edenberg, Arpana Agrawal, Jordan W. Smoller, Todd Lencz, David M. Hougaard, Anders D. Børglum, Ditte Demontis, J. Michael Gaziano, Michael J. Gandal, Renato Polimanti, Murray B. Stein, Joel Gelernter

    Veröffentlicht 2023
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  8. 8
    Exome sequencing and analysis of 454,787 UK Biobank participants

    Exome sequencing and analysis of 454,787 UK Biobank participants von Joshua Backman, Alexander Li, Anthony Marcketta, Dylan Sun, Joelle Mbatchou, Michael D. Kessler, Christian Benner, Daren Liu, Adam E. Locke, Suganthi Balasubramanian, Ashish Yadav, Nilanjana Banerjee, Christopher E. Gillies, Amy Damask, Simon Liu, Xiaodong Bai, Alicia Hawes, Evan K. Maxwell, Lauren Gurski, Kyoko Watanabe, Jack A. Kosmicki, Veera M. Rajagopal, Jason Mighty, Marcus B. Jones, Lyndon J. Mitnaul, Eli A. Stahl, Giovanni Coppola, Eric Jorgenson, Lukas Habegger, William Salerno, Alan R. Shuldiner, Luca A. Lotta, John D. Overton, Michael Cantor, Jeffrey G. Reid, George D. Yancopoulos, Hyun Min Kang, Jonathan Marchini, Aris Baras, Gonçalo R. Abecasis, Manuel A. R. Ferreira

    Veröffentlicht 2021
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  9. 9
    Common and rare variant associations with clonal haematopoiesis phenotypes

    Common and rare variant associations with clonal haematopoiesis phenotypes von Michael D. Kessler, Amy Damask, Sean O’Keeffe, Nilanjana Banerjee, Dadong Li, Kyoko Watanabe, Anthony Marketta, Michael Van Meter, Stefan Semrau, Julie Horowitz, Jing Tang, Jack A. Kosmicki, Veera M. Rajagopal, Yuxin Zou, Yariv Houvras, Arkopravo Ghosh, Christopher E. Gillies, Joelle Mbatchou, Ryan R. White, Niek Verweij, Jonas Bovijn, Neelroop Parikshak, Michelle G. LeBlanc, Marcus B. Jones, David J. Glass, Luca A. Lotta, Michael Cantor, Gurinder S. Atwal, Adam E. Locke, Manuel A. R. Ferreira, Raquel P. Deering, Charles Paulding, Alan R. Shuldiner, Gavin Thurston, Adolfo A. Ferrando, Will Salerno, Jeffrey G. Reid, John D. Overton, Jonathan Marchini, Hyun Min Kang, Aris Baras, Gonçalo R. Abecasis, Eric Jorgenson

    Veröffentlicht 2022
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  10. 10
    A deep catalog of protein-coding variation in 985,830 individuals

    A deep catalog of protein-coding variation in 985,830 individuals von Kathie Sun, Xiaodong Bai, Siying Chen, Suying Bao, Manav Kapoor, Chuanyi Zhang, Joshua Backman, Tyler Joseph, Evan K. Maxwell, George Mitra, Alexander Gorovits, Adam J. Mansfield, Boris Boutkov, Sujit Gokhale, Lukas Habegger, Anthony Marcketta, Adam E. Locke, Michael D. Kessler, Deepika Sharma, Jeffrey Staples, Jonas Bovijn, Sahar Gelfman, Alessandro Di Gioia, Veera M. Rajagopal, Alexander Lopez, Jennifer Rico Varela, J Larracilla Alegre, Jaime Berúmen, Roberto Tapia‐Conyer, Pablo Kuri‐Morales, Jason Torres, Jonathan Emberson, Rory Collins, Michael Cantor, Timothy A. Thornton, Hyun Min Kang, John D. Overton, Alan R. Shuldiner, María Laura Cremona, Mona Nafde, Aris Baras, Gonçalo R. Abecasis, Jonathan Marchini, Jeffrey G. Reid, William Salerno, Suganthi Balasubramanian

    Veröffentlicht 2023
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  11. 11
    Depression pathophysiology, risk prediction of recurrence and comorbid psychiatric disorders using genome-wide analyses

    Depression pathophysiology, risk prediction of recurrence and comorbid psychiatric disorders using genome-wide analyses von Thomas D. Als, Mitja Kurki, Jakob Grove, Georgios Voloudakis, Karen Therrien, Elisa Tasanko, Trine Tollerup Nielsen, Joonas Naamanka, Kumar Veerapen, Daniel F. Levey, Jaroslav Bendl, Jonas Bybjerg‐Grauholm, Biao Zeng, Ditte Demontis, Anders Rosengren, Georgios Athanasiadis, Marie Bækved-Hansen, Per Qvist, G. Bragi Walters, Thorgeir E. Thorgeirsson, Hreinn Stefánsson, Katherine L. Musliner, Veera M. Rajagopal, Leila Farajzadeh, Janne Pia Thirstrup, Bjarni J. Vilhjálmsson, John J. McGrath, Manuel Mattheisen, Sandra Meier, Esben Agerbo, Kāri Stefánsson, Merete Nordentoft, Thomas Werge, David M. Hougaard, Preben Bo Mortensen, Murray B. Stein, Joel Gelernter, Iiris Hovatta, Panos Roussos, Mark J. Daly, Ole Mors, Aarno Palotie, Anders D. Børglum

    Veröffentlicht 2023
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  12. 12
    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 von 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

    Veröffentlicht 2023
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  13. 13
    Risk variants and polygenic architecture of disruptive behavior disorders in the context of attention-deficit/hyperactivity disorder

    Risk variants and polygenic architecture of disruptive behavior disorders in the context of attention-deficit/hyperactivity disorder von Ditte Demontis, Raymond K. Walters, Veera M. Rajagopal, Irwin D. Waldman, Jakob Grove, Thomas D. Als, Søren Dalsgaard, Marta Ribasés, Jonas Bybjerg‐Grauholm, Maria Bækvad-Hansen, Thomas Werge, Merete Nordentoft, Ole Mors, Preben Bo Mortensen, Ole A. Andreassen, María J. Arranz, Tobias Banaschewski, Claiton Henrique Dotto Bau, Mark A. Bellgrove, Joseph Biederman, Isabell Brikell, Jan K. Buitelaar, Christie L. Burton, Miguel Casas, Jennifer Crosbie, Alysa E. Doyle, Richard P. Ebstein, Josephine Elia, Elizabeth C. Corfield, Eugênio H. Grevet, Natalie Grizenko, Alexandra Havdahl, Ziarih Hawi, Johannes Hebebrand, Amaia Hervás, Sarah Hohmann, Jan Haavik, Ridha Joober, Lindsey Kent, Jonna Kuntsi, K. Langley, Henrik Larsson, Klaus‐Peter Lesch, Patrick W. L. Leung, Calwing Liao, Sandra K. Loo, Joanna Martin, Nicholas G. Martin, Sarah E. Medland, Ana Miranda, Nina Roth Mota, Robert D. Oades, Josep Antoni Ramos‐Quiroga, Andreas Reif, Marcella Rietschel, Herbert Roeyers, Luís Augusto Rohde, Aribert Rothenberger, Paula Rovira, Cristina Sánchez‐Mora, Russell Schachar, Sarojini M. Sengupta, María Soler Artigas, Hans‐Christoph Steinhausen, Anita Thapar, Stephanie H. Witt, Li Yang, Tetyana Zayats, Yanli Zhang‐James, Bru Cormand, David M. Hougaard, Benjamin M. Neale, Barbara Franke, Stephen V. Faraone, Anders D. Børglum

    Veröffentlicht 2021
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  14. 14
    Author Correction: Risk variants and polygenic architecture of disruptive behavior disorders in the context of attention-deficit/hyperactivity disorder

    Author Correction: Risk variants and polygenic architecture of disruptive behavior disorders in the context of attention-deficit/hyperactivity disorder von Ditte Demontis, Raymond K. Walters, Veera M. Rajagopal, Irwin D. Waldman, Jakob Grove, Thomas D. Als, Søren Dalsgaard, Marta Ribasés, Jonas Bybjerg‐Grauholm, Maria Bækvad-Hansen, Thomas Werge, Merete Nordentoft, Ole Mors, Preben Bo Mortensen, Ole A. Andreassen, María J. Arranz, Tobias Banaschewski, Claiton Henrique Dotto Bau, Mark A. Bellgrove, Joseph Biederman, Isabell Brikell, Jan K. Buitelaar, Christie L. Burton, Miguel Casas, Jennifer Crosbie, Alysa E. Doyle, Richard P. Ebstein, Josephine Elia, Elizabeth C. Corfield, Eugênio H. Grevet, Natalie Grizenko, Alexandra Havdahl, Ziarih Hawi, Johannes Hebebrand, Amaia Hervás, Sarah Hohmann, Jan Haavik, Ridha Joober, Lindsey Kent, Jonna Kuntsi, K. Langley, Henrik Larsson, Klaus‐Peter Lesch, Patrick W. L. Leung, Calwing Liao, Sandra K. Loo, Joanna Martin, Nicholas G. Martin, Sarah E. Medland, Ana Miranda, Nina Roth Mota, Robert D. Oades, Josep Antoni Ramos‐Quiroga, Andreas Reif, Marcella Rietschel, Herbert Roeyers, Luís Augusto Rohde, Aribert Rothenberger, Paula Rovira, Cristina Sánchez‐Mora, Russell Schachar, Sarojini M. Sengupta, María Soler Artigas, Hans‐Christoph Steinhausen, Anita Thapar, Stephanie H. Witt, Li Yang, Tetyana Zayats, Yanli Zhang‐James, Bru Cormand, David M. Hougaard, Benjamin M. Neale, Barbara Franke, Stephen V. Faraone, Anders D. Børglum

    Veröffentlicht 2021
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  15. 15
    Genetic analyses identify widespread sex-differential participation bias

    Genetic analyses identify widespread sex-differential participation bias von Nicola Pirastu, Mattia Cordioli, Priyanka Nandakumar, Gianmarco Mignogna, Abdel Abdellaoui, Benjamin Hollis, Masahiro Kanai, Veera M. Rajagopal, Pietro Della Briotta Parolo, Nikolas Baya, Caitlin E. Carey, Juha Karjalainen, Thomas D. Als, Matthijs D. van der Zee, Felix R. Day, Ken K. Ong, Michelle Agee, Stella Aslibekyan, Robert K. Bell, Katarzyna Bryc, Sarah Clark, Sarah L. Elson, Kipper Fletez‐Brant, Pierre Fontanillas, Nicholas A. Furlotte, Pooja Gandhi, Karl Heilbron, Barry Hicks, Karen E. Huber, Ethan M. Jewett, Yunxuan Jiang, Aaron Kleinman, Keng‐Han Lin, Nadia K. Litterman, Marie K. Luff, Matthew H. McIntyre, Kimberly F. McManus, Joanna L. Mountain, Sahar V. Mozaffari, Elizabeth S. Noblin, Carrie A. M. Northover, Jared O’Connell, Aaron A. Petrakovitz, Steven J. Pitts, G. David Poznik, J. Fah Sathirapongsasuti, Janie F. Shelton, Suyash Shringarpure, Chao Tian, Joyce Y. Tung, Robert J. Tunney, Vladimir Vacic, Xin Wang, Amir Zare, Preben Bo Mortensen, Ole Mors, Thomas Werge, Merete Nordentoft, David M. Hougaard, Jonas Bybjerg‐Grauholm, Marie Bækvad‐Hansen, Takayuki Morisaki, Eco J. C. de Geus, Rino Bellocco, Yukinori Okada, Anders D. Børglum, Peter K. Joshi, Adam Auton, David A. Hinds, Benjamin M. Neale, Raymond K. Walters, Michel G. Nivard, John R. B. Perry, Andrea Ganna

    Veröffentlicht 2021
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  16. 16
    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 von Ditte Demontis, G. Bragi Walters, Georgios Athanasiadis, Raymond K. Walters, Karen Therrien, Trine Tollerup Nielsen, Leila Farajzadeh, Georgios Voloudakis, Jaroslav Bendl, Biau 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, 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 M. Rajagopal, Alexandra Havdahl, Alysa E. Doyle, Andreas Reif, Anita Thapar, Bru Cormand, Calwing Liao, Christie L. Burton, Claiton Henrique Dotto Bau, Diego Luiz Rovaris, Edmund Sonuga‐Barke, Elizabeth C. Corfield, Eugênio H. Grevet, Henrik Larsson, Ian R. Gizer, Irwin D. Waldman, Isabell Brikell, Jan Haavik, Jennifer Crosbie, James J. McGough, Jonna Kuntsi, Joseph Glessner, K. Langley, Klaus‐Peter Lesch, Luís Augusto Rohde, Mara Helena Hutz, Marieke Klein, Mark A. Bellgrove, Martin Tesli, Michael O’Donovan, Ole A. Andreassen, Patrick W. L. Leung, Pedro Mário Pan, Ridha Joober, Russell Schachar, Sandra K. Loo, Stephanie H. Witt, Ted Reichborn‐Kjennerud, Tobias Banaschewski, Ziarih Hawi, Mark J. Daly, Ole Mors, 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

    Veröffentlicht 2023
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  17. 17
    Author Correction: Genome-wide analyses of ADHD identify 27 risk loci, refine the genetic architecture and implicate several cognitive domains

    Author Correction: Genome-wide analyses of ADHD identify 27 risk loci, refine the genetic architecture and implicate several cognitive domains von Ditte Demontis, G. Bragi Walters, Georgios Athanasiadis, Raymond K. Walters, Karen Therrien, Trine Tollerup Nielsen, Leila Farajzadeh, Georgios Voloudakis, Jaroslav Bendl, Biau 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, Esben Agerbo, Gabriel E. Hoffman, Søren Dalsgaard, Jonna Martin, Marta Ribasés, Dorret I. Boomsma, María Soler Artigas, Nina Roth Mota, Daniel P. Howrigan, Sarah E. Medland, Tetyana Zayats, Veera M. Rajagopal, Alexandra Havdahl, Alysa E. Doyle, Andreas Reif, Anita Thapar, Bru Cormand, Calwing Liao, Christie L. Burton, Claiton Henrique Dotto Bau, Diego Luiz Rovaris, Edmund Sonuga‐Barke, Elizabeth C. Corfield, Eugênio H. Grevet, Henrik Larsson, Ian R. Gizer, Irwin D. Waldman, Isabell Brikell, Jan Haavik, Jennifer Crosbie, James J. McGough, Jonna Kuntsi, Joseph Glessner, K. Langley, Klaus‐Peter Lesch, Luís Augusto Rohde, Mara Helena Hutz, Marieke Klein, Mark A. Bellgrove, Martin Tesli, Michael O’Donovan, Ole A. Andreassen, Patrick W. L. Leung, Pedro Mário Pan, Ridha Joober, Russell Schachar, Sandra K. Loo, Stephanie H. Witt, Ted Reichborn‐Kjennerud, Tobias Banaschewski, Ziarih Hawi, Mark J. Daly, Ole Mors, 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

    Veröffentlicht 2023
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  18. 18
    A deep catalogue of protein-coding variation in 983,578 individuals

    A deep catalogue of protein-coding variation in 983,578 individuals von Kathie Sun, Xiaodong Bai, Siying Chen, Suying Bao, Chuanyi Zhang, Manav Kapoor, Joshua Backman, Tyler Joseph, Evan K. Maxwell, George Mitra, Alexander Gorovits, Adam J. Mansfield, Boris Boutkov, Sujit Gokhale, Lukas Habegger, Anthony Marcketta, Adam E. Locke, Liron Ganel, Alicia Hawes, Michael D. Kessler, Deepika Sharma, Jeffrey Staples, Jonas Bovijn, Sahar Gelfman, Alessandro Di Gioia, Veera M. Rajagopal, Alexander Lopez, Jennifer Rico Varela, Jesús Alegre-Díaz, Jaime Berúmen, Roberto Tapia‐Conyer, Pablo Kuri‐Morales, Jason Torres, Jonathan Emberson, Rory Collins, Gonçalo R. Abecasis, Giovanni Coppola, Andrew Deubler, Aris Economides, Adolfo A. Ferrando, Luca A. Lotta, Alan R. Shuldiner, Katherine Siminovitch, Christina Beechert, Erin D. Brian, Laura M. Cremona, Hang Du, Caitlin Forsythe, Zhenhua Gu, Kristy Guevara, Michael Lattari, Kia Manoochehri, Prathyusha Challa, Manasi Pradhan, Raymond Reynoso, Ricardo Schiavo, Maria Sotiropoulos Padilla, Chenggu Wang, Sarah E. Wolf, Amelia Averitt, Nilanjana Banerjee, Dadong Li, Sameer Malhotra, Justin Mower, Mudasar Sarwar, Jeffrey C. Staples, Sean Yu, Aaron Zhang, Andrew Bunyea, Krishna Pawan Punuru, Sanjay Sreeram, Gisu Eom, Benjamin Sultan, Rouel Lanche, Vrushali Mahajan, Eliot Austin, Sean O’Keeffe, Razvan Panea, Tommy Polanco, Ayesha Rasool, Lance Zhang, Evan Edelstein, Ju Guan, Olga Krasheninina, Samantha Zarate, Adam J. Mansfield, Evan K. Maxwell, Kathie Sun, Manuel Allen Revez Ferreira, Kathy Burch, Adrián I. Campos, Lei Chen, Sam Choi, Amy Damask, Sheila M. Gaynor, Benjamin Geraghty, Arkopravo Ghosh, Salvador Romero Martinez, Christopher E. Gillies, Lauren Gurski

    Veröffentlicht 2024
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  19. 19
    Genome-wide analyses of individual differences in quantitatively assessed reading- and language-related skills in up to 34,000 people

    Genome-wide analyses of individual differences in quantitatively assessed reading- and language-related skills in up to 34,000 people von Else Eising, Nazanin Mirza‐Schreiber, Eveline L. de Zeeuw, Carol A. Wang, Dongnhu T. Truong, Andrea G. Allegrini, Chin Yang Shapland, Gu Zhu, Karen G. Wigg, Margot Gerritse, Barbara Molz, Gökberk Alagöz, Alessandro Gialluisi, Filippo Abbondanza, Kaili Rimfeld, Marjolein van Donkelaar, Zhijie Liao, Philip R. Jansen, Till F. M. Andlauer, Timothy C. Bates, Manon Bernard, Kirsten Blokland, Milene Bonte, Anders D. Børglum, Thomas Bourgeron, Daniel Brandeis, Fabiola Ceroni, Valéria Csépe, Philip S. Dale, Peter F. de Jong, John C. DeFries, Jean‐François Démonet, Ditte Demontis, Yu Feng, Scott D. Gordon, Sharon Guger, Marianna E. Hayiou‐Thomas, Juan Hernández, Jouke‐Jan Hottenga, Charles Hulme, Juha Kere, Elizabeth N. Kerr, Tanner Koomar, Karin Landerl, Gabriel Leonard, Maureen W. Lovett, Heikki Lyytinen, Nicholas G. Martin, Angela Martinelli, Urs Maurer, Jacob J. Michaelson, Kristina Moll, Anthony P. Monaco, Angela Morgan, Markus M. Nöthen, Zdenka Pausová, Craig E. Pennell, Bruce F. Pennington, Kaitlyn M. Price, Veera M. Rajagopal, Franck Ramus, Louis Richer, Nuala H. Simpson, Shelley D. Smith, Maggie Snowling, John Stein, Lisa J. Strug, Joel B. Talcott, Henning Tiemeier, Marc P. van der Schroeff, Ellen Verhoef, Kate E. Watkins, Margaret Wilkinson, Margaret J. Wright, Cathy L. Barr, Dorret I. Boomsma, Manuel Carreiras, Marie-Christine Franken, Jeffrey R. Gruen, Michelle Luciano, Bertram Müller‐Myhsok, Dianne F. Newbury, Richard K. Olson, Silvia Paracchini, Tomáš Paus, Robert Plomin, Sheena Reilly, Gerd Schulte‐Körne, J. Bruce Tomblin, Elsje van Bergen, Andrew J. O. Whitehouse, Erik G. Willcutt, Beaté St Pourcain, Clyde Francks, Simon E. Fisher

    Veröffentlicht 2022
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