Canlyniadau Chwilio - Karl Heilbron

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  1. 1
    Positive epistasis between co-infecting plasmids promotes plasmid survival in bacterial populations

    Positive epistasis between co-infecting plasmids promotes plasmid survival in bacterial populations gan Álvaro San Millán, Karl Heilbron, R. Craig MacLean

    Cyhoeddwyd 2013
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  2. 2
    Fitness Is Strongly Influenced by Rare Mutations of Large Effect in a Microbial Mutation Accumulation Experiment

    Fitness Is Strongly Influenced by Rare Mutations of Large Effect in a Microbial Mutation Accumulation Experiment gan Karl Heilbron, Macarena Toll‐Riera, Mila Kojadinovic, R. Craig MacLean

    Cyhoeddwyd 2014
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  3. 3
    Gene–Environment Interactions for Parkinson's Disease

    Gene–Environment Interactions for Parkinson's Disease gan Alexandra Reynoso, Roberta Torricelli, Benjamin Meir Jacobs, Jingchunzi Shi, Stella Aslibekyan, Lucy Norcliffe–Kaufmann, Alastair Noyce, Karl Heilbron

    Cyhoeddwyd 2023
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  4. 4
    Parkinson’s disease determinants, prediction and gene–environment interactions in the UK Biobank

    Parkinson’s disease determinants, prediction and gene–environment interactions in the UK Biobank gan Benjamin Meir Jacobs, Daniel Belete, Jonathan P. Bestwick, Cornelis Blauwendraat, Sara Bandrés‐Ciga, Karl Heilbron, Ruth Dobson, Mike A. Nalls, Andrew Singleton, John Hardy, Gavin Giovannoni, Andrew J. Lees, Anette Schrag, Alastair Noyce

    Cyhoeddwyd 2020
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  5. 5
    The Parkinson's Disease Mendelian Randomization Research Portal

    The Parkinson's Disease Mendelian Randomization Research Portal gan Alastair Noyce, Sara Bandrés‐Ciga, Jonggeol Kim, Karl Heilbron, Demis A. Kia, Gibran Hemani, Angli Xue, Debbie A. Lawlor, George Davey Smith, Raquel Durán, Ziv Gan‐Or, Cornelis Blauwendraat, J. Raphael Gibbs, David A. Hinds, Jian Yang, Peter M. Visscher, Jack Cuzick, Huw R. Morris, John Hardy, Nicholas Wood, Mike A. Nalls, Andrew Singleton

    Cyhoeddwyd 2019
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  6. 6
    Avoiding dynastic, assortative mating, and population stratification biases in Mendelian randomization through within-family analyses

    Avoiding dynastic, assortative mating, and population stratification biases in Mendelian randomization through within-family analyses gan Ben Brumpton, Eleanor Sanderson, Karl Heilbron, Fernando Pires Hartwig, Sean Harrison, Gunnhild Åberge Vie, Yoonsu Cho, Laura D Howe, Amanda Hughes, Dorret I. Boomsma, Alexandra Havdahl, John L. Hopper, Michael C. Neale, Michel G. Nivard, Nancy L. Pedersen, Chandra A. Reynolds, Elliot M. Tucker‐Drob, Andrew D. Grotzinger, Laurence J Howe, Tim Morris, Shuai Li, Ben Brumpton, Eleanor Sanderson, Karl Heilbron, Fernando Pires Hartwig, Sean Harrison, Gunnhild Åberge Vie, Yoonsu Cho, Laura D Howe, Amanda Hughes, Dorret I. Boomsma, Alexandra Havdahl, John L. Hopper, Michael C. Neale, Michel G. Nivard, Nancy L. Pedersen, Chandra A. Reynolds, Elliot M. Tucker‐Drob, Andrew D. Grotzinger, Laurence J Howe, Tim Morris, Shuai Li, Adam Auton, Frank Windmeijer, Wei‐Min Chen, Johan Hå‌kon Bjø‌rngaard, Kristian Hveem, Cristen J. Willer, David M. Evans, Jaakko Kaprio, George Davey Smith, Bjørn Olav Åsvold, Gibran Hemani, Neil M Davies, Karl Heilbron, Adam Auton, Adam Auton, Frank Windmeijer, Wei‐Min Chen, Johan Hå‌kon Bjø‌rngaard, Kristian Hveem, Cristen J. Willer, David M. Evans, Jaakko Kaprio, George Davey Smith, Bjørn Olav Åsvold, Gibran Hemani, Neil M Davies

    Cyhoeddwyd 2020
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  7. 7
    Insights into Ancestral Diversity in Parkinson’s Disease Risk: A Comparative Assessment of Polygenic Risk Scores

    Insights into Ancestral Diversity in Parkinson’s Disease Risk: A Comparative Assessment of Polygenic Risk Scores gan Paula Saffie Awad, Mary B. Makarious, Inas Elsayed, Arinola O. Sanyaolu, Peter Wild Crea, Artur Francisco Schumacher Schuh, Kristin S Levine, Dan Vitale, Mathew J. Koretsky, Jeffrey Kim, Thiago Peixoto Leal, María Teresa Periñán, Sumit Dey, Alastair Noyce, Armando Reyes‐Palomares, Noela Rodríguez-Losada, Jia Nee Foo, Wael Mohamed, Karl Heilbron, Lucy Norcliffe‐Kaufmann, Mie Rizig, Njideka Okubadejo, Mike A. Nalls, Cornelis Blauwendraat, Andrew Singleton, Hampton L. Leonard, Ignácio F. Mata, Sara Bandrés‐Ciga

    Cyhoeddwyd 2023
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  8. 8
    Insights into ancestral diversity in Parkinson’s disease risk: a comparative assessment of polygenic risk scores

    Insights into ancestral diversity in Parkinson’s disease risk: a comparative assessment of polygenic risk scores gan Paula Saffie Awad, Spencer Grant, Mary B. Makarious, Inas Elsayed, Arinola O. Sanyaolu, Peter Wild Crea, Artur Francisco Schumacher Schuh, Kristin Levine, Dan Vitale, Mathew J. Koretsky, Jeffrey Kim, Thiago Peixoto Leal, María Teresa Periñán, Sumit Dey, Alastair Noyce, Armando Reyes‐Palomares, Noela Rodríguez-Losada, Jia Nee Foo, Wael Mohamed, Karl Heilbron, Lucy Norcliffe‐Kaufmann, Mie Rizig, Njideka Okubadejo, Mike A. Nalls, Cornelis Blauwendraat, Andrew B. Singleton, Hampton L. Leonard, Ignácio F. Mata, Sara Bandrés‐Ciga

    Cyhoeddwyd 2025
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  9. 9
    The Parkinson’s phenome—traits associated with Parkinson’s disease in a broadly phenotyped cohort

    The Parkinson’s phenome—traits associated with Parkinson’s disease in a broadly phenotyped cohort gan Karl Heilbron, Alastair Noyce, Pierre Fontanillas, Babak Alipanahi, Mike A. Nalls, Michelle Agee, A. Auton, R. K. Bell, Katarzyna Bryc, Sarah L. Elson, Nicholas A. Furlotte, David A. Hinds, Jey C. McCreight, Karen E. Huber, Aaron Kleinman, Nadia K. Litterman, M. H. McIntyre, Joanna L. Mountain, Elizabeth S. Noblin, Carrie A. M. Northover, Steven J. Pitts, J. Fah Sathirapongsasuti, Olga V. Sazonova, Janie F. Shelton, Suyash Shringarpure, C Tian, Joyce Y. Tung, Vladimir Vacic, Catherine H. Wilson, Paul J. Cannon

    Cyhoeddwyd 2019
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  10. 10
    Parkinson's disease age at onset genome‐wide association study: Defining heritability, genetic loci, and α‐synuclein mechanisms

    Parkinson's disease age at onset genome‐wide association study: Defining heritability, genetic loci, and α‐synuclein mechanisms gan Cornelis Blauwendraat, Karl Heilbron, Costanza L. Vallerga, Sara Bandrés‐Ciga, Rainer von Coelln, Lasse Pihlstrøm, Javier Simón‐Sánchez, Claudia Schulte, Manu Sharma, Lynne Krohn, Ari Siitonen, Hirotaka Iwaki, Hampton L. Leonard, Alastair Noyce, Manuela Tan, J. Raphael Gibbs, Dena Hernández, Sonja W. Scholz, Joseph Jankovic, Lisa M. Shulman, Suzanne Lesage, Jean‐Christophe Corvol, Alexis Brice, Jacobus J. van Hilten, Johan Marinus, Johanna Eerola‐Rautio, Pentti J. Tienari, Kari Majamaa, Mathias Toft, Donald G. Grosset, Thomas Gasser, Peter Heutink, Joshua Shulman, Nicholas Wood, John Hardy, Huw R. Morris, David A. Hinds, Jacob Gratten, Peter M. Visscher, Ziv Gan‐Or, Mike A. Nalls, Andrew B. Singleton

    Cyhoeddwyd 2019
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  11. 11
    Characterizing the Genetic Architecture of Parkinson's Disease in Latinos

    Characterizing the Genetic Architecture of Parkinson's Disease in Latinos gan Douglas P. Loesch, Andréa R. V. R. Horimoto, Karl Heilbron, Elif Irem Sarihan, Miguel Inca‐Martinez, Emily Mason, Mario Cornejo‐Olivas, Luis Torres, Pilar Mazzetti, Carlos Cosentino, Elison Sarapura‐Castro, Andrea Rivera‐Valdivia, Ángel C. Medina, Elena Diéguez, Víctor Raggio, Andrés G. Lescano, Vítor Tumas, Vanderci Borges, Henrique Ballalai Ferraz, Carlos Roberto de Mello Rieder, Artur Francisco Schumacher Schuh, Bruno Lopes Santos‐Lobato, Carlos Velez‐Pardo, Marlene Jiménez-Del-Río, Francisco Lopera, Sonia Moreno, Pedro Chaná‐Cuevas, William Fernández, Gonzálo Arboleda, Humberto Arboleda, Carlos Bustos, Dora Yearout, Cyrus P. Zabetian, Paul J. Cannon, Timothy A. Thornton, Timothy D. O’Connor, Ignácio F. Mata

    Cyhoeddwyd 2021
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  12. 12
    Characterizing the genetic architecture of Parkinson’s disease in Latinos

    Characterizing the genetic architecture of Parkinson’s disease in Latinos gan Douglas P. Loesch, Andréa R. V. R. Horimoto, Karl Heilbron, Elif Irem Sarihan, Miguel Inca‐Martinez, Emily Mason, Mario Cornejo‐Olivas, Luis Torres, Pilar Mazzetti, Carlos Cosentino, Elison Sarapura‐Castro, Andrea Rivera‐Valdivia, Ángel C. Medina, Elena Diéguez, Víctor Raggio, Andrés G. Lescano, Vítor Tumas, Vanderci Borges, Henrique Ballalai Ferraz, Carlos Roberto de Mello Rieder, Artur Francisco Schumacher Schuh, Bruno Lopes Santos‐Lobato, Carlos Velez‐Pardo, Marlene Jiménez-Del-Río, Francisco Lopera, Sonia Moreno, Pedro Chaná‐Cuevas, William Fernández, Gonzálo Arboleda, Humberto Arboleda, Carlos Bustos, Dora Yearout, Cyrus P. Zabetian, Paul J. Cannon, Timothy A. Thornton, Timothy D. O’Connor, Ignácio F. Mata

    Cyhoeddwyd 2020
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  13. 13
    Fine‐Mapping of <i>SNCA</i> in Rapid Eye Movement Sleep Behavior Disorder and Overt Synucleinopathies

    Fine‐Mapping of <i>SNCA</i> in Rapid Eye Movement Sleep Behavior Disorder and Overt Synucleinopathies gan Lynne Krohn, Richard Y. J. Wu, Karl Heilbron, Jennifer A. Ruskey, Sandra B. Laurent, Cornelis Blauwendraat, Armaghan Alam, Isabelle Arnulf, Joshua Shulman, Yves Dauvilliers, Birgit Högl, Mathias Toft, Kari Anne Bjørnarå, Ambra Stefani, Evi Holzknecht, Christelle Monaca, Beatriz Abril, Giuseppe Plazzi, Elena Antelmi, Luigi Ferini‐Strambi, Peter Young, Anna Heidbreder, Valérie Cochen De Cock, Brit Mollenhauer, Friederike Sixel‐Döring, Claudia Trenkwalder, Karel Šonka, David Kemlink, Michela Figorilli, Monica Puligheddu, Femke Dijkstra, Mineke Viaene, Wolfang Oertel, Marco Toffoli, Gian Luigi Gigli, Mariarosaria Valente, Jean‐François Gagnon, Mike A. Nalls, Andrew B. Singleton, Alex Désautels, Jacques Montplaisir, Paul J. Cannon, Owen A. Ross, Bradley F. Boeve, Nicolas Dupré, Edward A. Fon, Ronald B. Postuma, Lasse Pihlstrøm, Guy A. Rouleau, Ziv Gan‐Or

    Cyhoeddwyd 2020
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  14. 14
    Association of Essential Tremor With Novel Risk Loci

    Association of Essential Tremor With Novel Risk Loci gan Calwing Liao, Charles-Etienne Castonguay, Karl Heilbron, Veikko Vuokila, Miranda Medeiros, Gabrielle Houle, Fulya Akçimen, Jay P. Ross, Hélène Catoire, Mónica Díez-Fairén, Jooeun Kang, Stefanie H. Mueller, Simon Girard, Franziska Hopfner, Delia Lorenz, Lorraine N. Clark, Alexandra I. Soto‐Beasley, Stephan Klebe, Mark Hallett, Zbigniew K. Wszołek, Manuela Pendziwiat, Oswaldo Lorenzo‐Betancor, Klaus Seppi, Daniela Berg, Carles Vilariño‐Güell, Ronald B. Postuma, Geneviève Bernard, Nicolas Dupré, Joseph Jankovic, Claudia M. Testa, Owen A. Ross, Thomas Arzberger, Sylvain Chouinard, Elan D. Louis, Paola Mandich, Carmine Vitale, Paolo Barone, Elena García‐Martín, Hortensia Alonso‐Navarro, José A. G. Agúndez, Félix Javier Jiménez‐Jiménez, Pau Pástor, Alex Rajput, Günther Deuschl, Gregor Kuhlenbäumer, Inge A. Meijer, Patrick A. Dion, Guy A. Rouleau

    Cyhoeddwyd 2022
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  15. 15
    Parkinson’s disease genetics: identifying novel risk loci, providing causal insights and improving estimates of heritable risk

    Parkinson’s disease genetics: identifying novel risk loci, providing causal insights and improving estimates of heritable risk gan Mike A. Nalls, Cornelis Blauwendraat, Costanza L. Vallerga, Karl Heilbron, Sara Bandrés‐Ciga, Diana Chang, Manuela Tan, Demis A. Kia, Alastair Noyce, Angli Xue, José Brás, Emily Young, Ranier von Coelln, Javier Simón‐Sánchez, Claudia Schulte, Manu Sharma, Lynne Krohn, Lasse Pihlstrøm, Ari Siitonen, Hirotaka Iwaki, Hampton L. Leonard, Faraz Faghri, J. Raphael Gibbs, Dena G. Hernandez, Sonja W. Scholz, Juan A. Botía, María Martínez, Jean-Chrstophe Corvol, Suzanne Lesage, Joseph Jankovic, Lisa M. Shulman, Margaret Sutherland, Pentti J. Tienari, Kari Majamaa, Mathias Toft, Alexis Brice, Jian Yang, Ziv Gan-Orr, Thomas M Gasser, Peter M Heutink, Joshua Shulman, Nicolas A Wood, David A. Hinds, J. R. Hardy, Huw R. Morris, Jacob M Gratten, Peter M. Visscher, Robert Graham, Andrew Singleton

    Cyhoeddwyd 2018
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  16. 16
    Fox Insight collects online, longitudinal patient-reported outcomes and genetic data on Parkinson’s disease

    Fox Insight collects online, longitudinal patient-reported outcomes and genetic data on Parkinson’s disease gan Luba Smolensky, Ninad Amondikar, Karen Crawford, Scott Neu, Catherine Kopil, Margaret Daeschler, Lindsey Riley, Michelle Agee, Babak Alipanahi, Adam Auton, Robert K. Bell, Katarzyna Bryc, Paul J. Cannon, Sarah L. N. Clarke, Sarah L. Elson, Peter Fonseca, Pierre Fontanillas, Nicholas A. Furlotte, Barry Hicks, David A. Hinds, Karl Heilbron, 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, Elizabeth S. Noblin, Carrie A. M. Northover, Steven J. Pitts, G. David Poznik, Helen Rowbotham, J. Fah Sathirapongsasuti, Madeleine Schloetter, Janie F. Shelton, Suyash Shringarpure, Chao Tian, Joyce Y. Tung, Vladimir Vacic, Xin Wang, Catherine H. Wilson, Anne Wojcicki, Linda Yu, Ethan Brown, Arthur W. Toga, Caroline M. Tanner

    Cyhoeddwyd 2020
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  17. 17
    Expanding Parkinson’s disease genetics: novel risk loci, genomic context, causal insights and heritable risk

    Expanding Parkinson’s disease genetics: novel risk loci, genomic context, causal insights and heritable risk gan Mike A. Nalls, Cornelis Blauwendraat, Costanza L. Vallerga, Karl Heilbron, Sara Bandrés‐Ciga, Diana Chang, Manuela Tan, Demis A. Kia, Alastair Noyce, Angli Xue, José Brás, Emily Young, Rainer von Coelln, Javier Simón‐Sánchez, Claudia Schulte, Manu Sharma, Lynne Krohn, Lasse Pihlstrøm, Ari Siitonen, Hirotaka Iwaki, Hampton L. Leonard, Faraz Faghri, J. Raphael Gibbs, Dena G. Hernandez, Sonja W. Scholz, Juan A. Botía, María Martínez, Jean‐Christophe Corvol, Suzanne Lesage, Joseph Jankovic, Lisa M. Shulman, Margaret Sutherland, Pentti J. Tienari, Kari Majamaa, Mathias Toft, Ole A. Andreassen, Tushar Bangale, Alexis Brice, Jian Yang, Ziv Gan‐Or, Thomas Gasser, Peter Heutink, Joshua Shulman, Nicholas Wood, David A. Hinds, John Hardy, Huw R. Morris, Jacob Gratten, Peter M. Visscher, Robert Graham, Andrew Singleton

    Cyhoeddwyd 2018
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  18. 18
    Genome-wide association and multi-omic analyses reveal ACTN2 as a gene linked to heart failure

    Genome-wide association and multi-omic analyses reveal ACTN2 as a gene linked to heart failure gan Marios Arvanitis, Emmanouil Tampakakis, Yanxiao Zhang, Wei Wang, Adam Auton, 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, David A. Hinds, Karen E. Huber, Ethan M. Jewett, Yunxuan Jiang, Aaron Kleinman, Keng‐Han Lin, Nadia K. Litterman, Jennifer C. McCreight, Matthew H. McIntyre, Kimberly F. McManus, Joanna L. Mountain, Sahar V. Mozaffari, Priyanka Nandakumar, Elizabeth S. Noblin, Carrie A. M. Northover, Jared O’Connell, Steven J. Pitts, G. David Poznik, J. Fah Sathirapongsasuti, Anjali J. Shastri, Janie F. Shelton, Suyash Shringarpure, Chao Tian, Joyce Y. Tung, Robert J. Tunney, Vladimir Vacic, Xin Wang, Amir S. Zare, Diptavo Dutta, Stephanie Glavaris, Ali R. Keramati, Nilanjan Chatterjee, C. Neil, Bing Ren, Wendy S. Post, Alexis Battle

    Cyhoeddwyd 2020
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  19. 19
    A population-specific reference panel for improved genotype imputation in African Americans

    A population-specific reference panel for improved genotype imputation in African Americans gan Jared O’Connell, Taedong Yun, Meghan E. Moreno, Helen Li, Nadia K. Litterman, Alexey Kolesnikov, Elizabeth S. Noblin, Pi-Chuan Chang, Anjali J. Shastri, Elizabeth H. Dorfman, Suyash Shringarpure, Stella Aslibekyan, Elizabeth Babalola, Robert K. Bell, Jessica Bielenberg, Katarzyna Bryc, Emily Bullis, Daniella Coker, Gabriel Cuéllar-Partida, Devika Dhamija, Sayantan Das, Sarah L. Elson, Teresa Filshtein, Kipper Fletez‐Brant, Pierre Fontanillas, Will Freyman, Pooja Gandhi, Karl Heilbron, Alejandro Hernandez, Barry Hicks, David A. Hinds, Ethan M. Jewett, Yunxuan Jiang, Katelyn Kukar, Keng-Han Lin, Maya Lowe, Jey C. McCreight, Matthew H. McIntyre, Steven J. Micheletti, Joanna L. Mountain, Priyanka Nandakumar, Aaron A. Petrakovitz, G. David Poznik, Morgan Schumacher, Janie F. Shelton, Jingchunzi Shi, Christophe Toukam Tchakouté, Vinh Tran, Joyce Y. Tung, Xin Wang, Wei Wang, Catherine H. Weldon, Peter Wilton, Corinna Wong, Adam Auton, Andrew Carroll, Cory Y. McLean

    Cyhoeddwyd 2021
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  20. 20
    Genome-wide meta-analysis of insomnia prioritizes genes associated with metabolic and psychiatric pathways

    Genome-wide meta-analysis of insomnia prioritizes genes associated with metabolic and psychiatric pathways gan Kyoko Watanabe, Philip R. Jansen, Jeanne E. Savage, Priyanka Nandakumar, Xin Wang, Michelle Agee, Stella Aslibekyan, Adam Auton, 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, Jennifer C. McCreight, Matthew H. McIntyre, Kimberly F. McManus, Joanna L. Mountain, Sahar V. Mozaffari, Elizabeth S. Noblin, Carrie A. M. Northover, Jared O’Connell, Steven J. Pitts, G. David Poznik, J. Fah Sathirapongsasuti, Janie F. Shelton, Jing Shi, Suyash Shringarpure, Chao Tian, Joyce Y. Tung, Robert J. Tunney, Vladimir Vacic, Wei Wang, David A. Hinds, Joel Gelernter, Daniel F. Levey, Renato Polimanti, Murray B. Stein, Eus J.W. Van Someren, August B. Smit, Daniëlle Posthuma

    Cyhoeddwyd 2022
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