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  1. 1
    Using population isolates in genetic association studies

    Using population isolates in genetic association studies por Konstantinos Hatzikotoulas, Arthur Gilly, Eleftheria Zeggini

    Publicado em 2014
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  2. 2
    Whole genome sequencing and imputation in isolated populations identify genetic associations with medically-relevant complex traits

    Whole genome sequencing and imputation in isolated populations identify genetic associations with medically-relevant complex traits por Lorraine Southam, Arthur Gilly, Dániel Süveges, Aliki‐Eleni Farmaki, Jeremy Schwartzentruber, Ioanna Tachmazidou, Angela Matchan, Nigel W. Rayner, Emmanouil Tsafantakis, Maria Karaleftheri, Yali Xue, George Dedoussis, Eleftheria Zeggini

    Publicado em 2017
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  3. 3
    Whole-genome sequencing analysis of the cardiometabolic proteome

    Whole-genome sequencing analysis of the cardiometabolic proteome por Arthur Gilly, Young‐Chan Park, Grace Png, Andrei Barysenka, Iris Fischer, Thea Bjørnland, Lorraine Southam, Dániel Süveges, Sonja Neumeyer, Nigel W. Rayner, Emmanouil Tsafantakis, Maria Karaleftheri, George Dedoussis, Eleftheria Zeggini

    Publicado em 2020
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  4. 4
    HIV Prevention in Care and Treatment Settings: Baseline Risk Behaviors among HIV Patients in Kenya, Namibia, and Tanzania

    HIV Prevention in Care and Treatment Settings: Baseline Risk Behaviors among HIV Patients in Kenya, Namibia, and Tanzania por Kidder, Daniel P., Bachanas, Pam, Medley, Amy, Pals, Sherri, Nuwagaba-Biribonwoha, Harriet, Ackers, Marta, Howard, Andrea, DeLuca, Nick, Mbatia, Redempta, Sheriff, Muhsin, Arthur, Gilly, Katuta, Frieda, Cherutich, Peter, Somi, Geoffrey

    Publicado em 2013
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  5. 5
    Mapping the serum proteome to neurological diseases using whole genome sequencing

    Mapping the serum proteome to neurological diseases using whole genome sequencing por Grace Png, Andrei Barysenka, L. Repetto, Pau Navarro, Xia Shen, Maik Pietzner, Eleanor Wheeler, Nicholas J. Wareham, Claudia Langenberg, Emmanouil Tsafantakis, Maria Karaleftheri, George Dedoussis, Anders Mälarstig, James F. Wilson, Arthur Gilly, Eleftheria Zeggini

    Publicado em 2021
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  6. 6
    Very low-depth whole-genome sequencing in complex trait association studies

    Very low-depth whole-genome sequencing in complex trait association studies por Arthur Gilly, Lorraine Southam, Dániel Süveges, Karoline Kuchenbaecker, Rachel Moore, Giorgio Melloni, Konstantinos Hatzikotoulas, Aliki‐Eleni Farmaki, Graham R. S. Ritchie, Jeremy Schwartzentruber, Petr Danecek, Britt Kilian, Martin Pollard, Xiangyu Ge, Emmanouil Tsafantakis, George Dedoussis, Eleftheria Zeggini

    Publicado em 2018
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  7. 7
    Loss-of-function variants in ADCY3 increase risk of obesity and type 2 diabetes

    Loss-of-function variants in ADCY3 increase risk of obesity and type 2 diabetes por Niels Grarup, Ida Moltke, Mette K. Andersen, Maria Dalby, Kristoffer Vitting‐Seerup, Martine Desrois, Yuvaraj Mahendran, Emil Jørsboe, Christina Viskum Lytken Larsen, Inger Katrine Dahl‐Petersen, Arthur Gilly, Dániel Süveges, George Dedoussis, Eleftheria Zeggini, Oluf Pedersen, Robin Andersson, Peter Bjerregaard, Marit E. Jørgensen, Anders Albrechtsen, Torben Hansen

    Publicado em 2018
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  8. 8
    Evaluation of shared genetic aetiology between osteoarthritis and bone mineral density identifies SMAD3 as a novel osteoarthritis risk locus

    Evaluation of shared genetic aetiology between osteoarthritis and bone mineral density identifies SMAD3 as a novel osteoarthritis risk locus por Sophie Hackinger, Katerina Trajanoska, Unnur Styrkársdóttir, Eleni Zengini, Julia Steinberg, Graham R. S. Ritchie, Konstantinos Hatzikotoulas, Arthur Gilly, Εvangelos Εvangelou, John P. Kemp, David M. Evans, Þorvaldur Ingvarsson, Helgi Jónsson, Unnur Þorsteinsdóttir, Kāri Stefánsson, Andrew W. McCaskie, Roger A. Brooks, J. Mark Wilkinson, Fernando Rivadeneira, Eleftheria Zeggini

    Publicado em 2017
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  9. 9
    Enrichment of low-frequency functional variants revealed by whole-genome sequencing of multiple isolated European populations

    Enrichment of low-frequency functional variants revealed by whole-genome sequencing of multiple isolated European populations por Yali Xue, Massimo Mezzavilla, Marc Haber, Shane McCarthy, Yuan Chen, Vagheesh M. Narasimhan, Arthur Gilly, Qasim Ayub, Vincenza Colonna, Lorraine Southam, Chris Finan, Andrea Massaia, Himanshu Chheda, Priit Palta, Graham R. S. Ritchie, Jennifer L. Asimit, George Dedoussis, Paolo Gasparini, Aarno Palotie, Samuli Ripatti, Nicole Soranzo, Daniela Toniolo, James F. Wilson, Richard Durbin, Chris Tyler‐Smith, Eleftheria Zeggini

    Publicado em 2017
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  10. 10
    The genetic architecture of osteoarthritis: insights from UK Biobank

    The genetic architecture of osteoarthritis: insights from UK Biobank por Eleni Zengini, Konstantinos Hatzikotoulas, Ioanna Tachmazidou, Julia Steinberg, Fernando Pires Hartwig, Lorraine Southam, Sophie Hackinger, Cindy G. Boer, Unnur Styrkársdóttir, Dániel Süveges, Britt Killian, Arthur Gilly, Þorvaldur Ingvarsson, Helgi Jónsson, George C. Babis, Andrew W. McCaskie, André G. Uitterlinden, Joyce B. J. van Meurs, Unnur Þorsteinsdóttir, Kāri Stefánsson, George Davey Smith, Mark Wilkinson, Eleftheria Zeggini

    Publicado em 2017
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  11. 11
    Genome-wide analyses using UK Biobank data provide insights into the genetic architecture of osteoarthritis

    Genome-wide analyses using UK Biobank data provide insights into the genetic architecture of osteoarthritis por Eleni Zengini, Konstantinos Hatzikotoulas, Ioanna Tachmazidou, Julia Steinberg, Fernando Pires Hartwig, Lorraine Southam, Sophie Hackinger, Cindy G. Boer, Unnur Styrkársdóttir, Arthur Gilly, Dániel Süveges, Britt Killian, Þorvaldur Ingvarsson, Helgi Jónsson, George C. Babis, Andrew W. McCaskie, André G. Uitterlinden, Joyce B. J. van Meurs, Unnur Þorsteinsdóttir, Kāri Stefánsson, George Davey Smith, J. Mark Wilkinson, Eleftheria Zeggini

    Publicado em 2018
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  12. 12
    Genetic characterization of Greek population isolates reveals strong genetic drift at missense and trait-associated variants

    Genetic characterization of Greek population isolates reveals strong genetic drift at missense and trait-associated variants por Kalliope Panoutsopoulou, Konstantinos Hatzikotoulas, Dionysia K. Xifara, Vincenza Colonna, Aliki‐Eleni Farmaki, Graham R. S. Ritchie, Lorraine Southam, Arthur Gilly, Ioanna Tachmazidou, Segun Fatumo, Angela Matchan, Nigel W. Rayner, Ιωάννα Ντάλλα, Massimo Mezzavilla, Yuan Chen, Chrysoula Kiagiadaki, Eleni Zengini, Vasiliki Mamakou, Antonis Athanasiadis, Μαργαρίτα Γιαννακοπούλου, Vassiliki-Eirini Kariakli, Rebecca N. Nsubuga, Alex Karabarinde, Manjinder S. Sandhu, Gil McVean, Chris Tyler‐Smith, Emmanouil Tsafantakis, Maria Karaleftheri, Yali Xue, George Dedoussis, Eleftheria Zeggini

    Publicado em 2014
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  13. 13
    The transferability of lipid loci across African, Asian and European cohorts

    The transferability of lipid loci across African, Asian and European cohorts por Karoline Kuchenbaecker, Nikita Telkar, Theresa Reiker, Robin Walters, Kuang Lin, Anders Eriksson, Deepti Gurdasani, Arthur Gilly, Lorraine Southam, Emmanouil Tsafantakis, Maria Karaleftheri, Janet Seeley, Anatoli Kamali, Gershim Asiki, Iona Y. Millwood, Michael V. Holmes, Huaidong Du, Yu Guo, Meena Kumari, George Dedoussis, Liming Li, Zhengming Chen, Manjinder S. Sandhu, Eleftheria Zeggini, Michaela Benzeval, Jonathan W. Burton, Nicholas Buck, Annette Jäckle, Heather Laurie, Peter Lynn, Stephen Pudney, Birgitta Rabe, Dieter Wolke

    Publicado em 2019
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  14. 14
    Using multivariable Mendelian randomization to estimate the causal effect of bone mineral density on osteoarthritis risk, independently of body mass index

    Using multivariable Mendelian randomization to estimate the causal effect of bone mineral density on osteoarthritis risk, independently of body mass index por April Hartley, Eleanor Sanderson, Raquel Granell, Lavinia Paternoster, Jie Zheng, George Davey Smith, Lorraine Southam, Konstantinos Hatzikotoulas, Cindy G. Boer, Joyce B. J. van Meurs, Eleftheria Zeggini, Lilja Stefánsdóttir, Yanfei Zhang, Rodrigo Coutinho de Almeida, Tian Wu, Jie Zheng, Maris Teder‐Laving, Anne Heidi Skogholt, Chikashi Terao, Eleni Zengini, George Alexiadis, Andrei Barysenka, Gyða Björnsdóttir, Maiken E. Gabrielsen, Arthur Gilly, Þorvaldur Ingvarsson, Marianne Bakke Johnsen, Helgi Jónsson, M. Kloppenburg, Almut Luetge, Reedik Mägi, Massimo Mangino, Rob G. H. H. Nelissen, Manu Shivakumar, Julia Steinberg, Hiroshi Takuwa, Laurent F. Thomas, Margo Tuerlings, George C. Babis, Jason Pui Yin Cheung, Dino Samartzis, Steve A Lietman, P. Eline Slagboom, Hreinn Stefánsson, André G. Uitterlinden, Bendik S. Winsvold, John‐Anker Zwart, Pak C. Sham, Guðmar Þorleifsson, Tom R. Gaunt, Andrew P. Morris, Ana M. Valdes, Aspasia Tsezou, Kathryn S.E. Cheah, Shiro Ikegawa, Kristian Hveem, Tõnu Esko, J. Mark Wilkinson, Ingrid Meulenbelt, Ming Ta Michael Lee, Unnur Styrkársdóttir, Celia L. Gregson, Jonathan H. Tobias

    Publicado em 2021
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  15. 15
    Deciphering osteoarthritis genetics across 826,690 individuals from 9 populations

    Deciphering osteoarthritis genetics across 826,690 individuals from 9 populations por Cindy G. Boer, Konstantinos Hatzikotoulas, Lorraine Southam, Lilja Stefánsdóttir, Yanfei Zhang, Rodrigo Coutinho de Almeida, Tian Wu, Jie Zheng, April Hartley, Maris Teder‐Laving, Anne Heidi Skogholt, Chikashi Terao, Eleni Zengini, George Alexiadis, Andrei Barysenka, Gyða Björnsdóttir, Maiken E. Gabrielsen, Arthur Gilly, Þorvaldur Ingvarsson, Marianne Bakke Johnsen, Helgi Jónsson, M. Kloppenburg, Almut Luetge, Sigrún H. Lund, Reedik Mägi, Massimo Mangino, Rob G. H. H. Nelissen, Manu Shivakumar, Julia Steinberg, Hiroshi Takuwa, Laurent F. Thomas, Margo Tuerlings, George C. Babis, Jason Pui Yin Cheung, Jae Hee Kang, Peter Kraft, Steven A. Lietman, Dino Samartzis, P. Eline Slagboom, Kāri Stefánsson, Unnur Þorsteinsdóttir, Jonathan H. Tobias, André G. Uitterlinden, Bendik S Winsvold, John‐Anker Zwart, George Davey Smith, Pak C. Sham, Guðmar Þorleifsson, Tom R. Gaunt, Andrew P. Morris, Ana M. Valdes, Aspasia Tsezou, Kathryn S.E. Cheah, Shiro Ikegawa, Kristian Hveem, Tõnu Esko, J. Mark Wilkinson, Ingrid Meulenbelt, Ming Ta Michael Lee, Joyce B. J. van Meurs, Unnur Styrkársdóttir, Eleftheria Zeggini

    Publicado em 2021
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  16. 16
    Genetic Landscape of the ACE2 Coronavirus Receptor

    Genetic Landscape of the ACE2 Coronavirus Receptor por Zhijian Yang, Erin Macdonald-Dunlop, Jiantao Chen, Ranran Zhai, Ting Li, Anne Richmond, Lucija Klarić, Nicola Pirastu, Ning Zheng, Chenqing Zheng, Yipeng Wang, Tingting Huang, Yazhou He, Huiming Guo, Kejun Ying, Stefan Gustafsson, Bram P. Prins, Anna Ramisch, Emmanouil T. Dermitzakis, Grace Png, Niclas Eriksson, Jeffrey Haessler, Xiaowei Hu, Daniela Zanetti, Thibaud Boutin, Shih‐Jen Hwang, Eleanor Wheeler, Maik Pietzner, Laura M. Raffield, Anette Kalnapenkis, James E. Peters, Ana Viñuela, Arthur Gilly, Sölve Elmståhl, George Dedoussis, John R. Petrie, Ozren Polašek, Lasse Folkersen, Yan Chen, Chen Yao, Urmo Võsa, Erola Pairo‐Castineira, Sara Clohisey, Andrew D. Bretherick, Konrad Rawlik, Tõnu Esko, Stefan Enroth, Åsa Johansson, Ulf Gyllensten, Claudia Langenberg, Daniel Levy, Caroline Hayward, Themistocles L. Assimes, Charles Kooperberg, Ani Manichaikul, Agneta Siegbahn, Lars Wallentin, Lars Lind, Eleftheria Zeggini, Jochen M. Schwenk, Adam S. Butterworth, Karl Michaëlsson, Yudi Pawitan, Peter K. Joshi, J. Kenneth Baillie, Anders Mälarstig, Alexander P. Reiner, James F. Wilson, Xia Shen

    Publicado em 2022
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  17. 17
    A reference panel of 64,976 haplotypes for genotype imputation

    A reference panel of 64,976 haplotypes for genotype imputation por Shane McCarthy, Sayantan Das, Warren W. Kretzschmar, Olivier Delaneau, Andrew R. Wood, Alexander Teumer, Hyun Min Kang, Christian Fuchsberger, Petr Danecek, Kevin Sharp, Yang Luo, Carlo Sidore, Alan Kwong, Nicholas J. Timpson, Seppo Koskinen, Scott Vrieze, Laura J. Scott, He Zhang, Anubha Mahajan, Jan H. Veldink, Ulrike Peters, Carlos N. Pato, Cornelia M. van Duijn, Christopher E. Gillies, Ilaria Gandin, Massimo Mezzavilla, Arthur Gilly, Massimiliano Cocca, Michela Traglia, Andrea Angius, Jeffrey C. Barrett, Dorrett Boomsma, Kari Branham, Gerome Breen, Chad M. Brummett, Fabio Busonero, Harry Campbell, Andrew T. Chan, Sai Chen, Emily Y. Chew, Francis S. Collins, Laura J. Corbin, George Davey Smith, George Dedoussis, Marcus Dörr, Aliki-Eleni Farmaki, Luigi Ferrucci, Lukas Forer, Ross M. Fraser, Stacey Gabriel, Shawn Levy, Leif Groop, Tabitha A. Harrison, Andrew T. Hattersley, Oddgeir L. Holmen, Kristian Hveem, Matthias Kretzler, James Lee, Matt McGue, Thomas Meitinger, David Melzer, Josine L. Min, Karen L. Mohlke, John B. Vincent, Matthias Nauck, Deborah A. Nickerson, Aarno Palotie, Michele T. Pato, Nicola Pirastu, Melvin G. McInnis, J. Brent Richards, Cinzia Sala, Veikko Salomaa, David Schlessinger, Sebastian Schoenherr, P. Eline Slagboom, Kerrin S. Small, Timothy D. Spector, Dwight Stambolian, Marcus A. Tuke, Jaakko Tuomilehto, Leonard H. van den Berg, Wouter van Rheenen, Uwe Völker, Cisca Wijmenga, Daniela Toniolo, Eleftheria Zeggini, Paolo Gasparini, Matthew G. Sampson, James F. Wilson, Timothy M. Frayling, Paul I. W. de Bakker, Morris A. Swertz, Steven A. McCarroll, Charles Kooperberg, Annelot M. Dekker, David Altshuler, Cristen J. Willer, William G. Iacono, Samuli Ripatti

    Publicado em 2016
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  18. 18
    A reference panel of 64,976 haplotypes for genotype imputation

    A reference panel of 64,976 haplotypes for genotype imputation por Shane McCarthy, Sayantan Das, Warren W. Kretzschmar, Olivier Delaneau, Andrew R. Wood, Alexander Teumer, Hyun Min Kang, Christian Fuchsberger, Petr Danecek, Kevin Sharp, Yang Luo, Carlo Sidore, Alan Kwong, Nicholas J. Timpson, Seppo Koskinen, Scott Vrieze, Laura J. Scott, He Zhang, Anubha Mahajan, Jan H. Veldink, Ulrike Peters, Carlos N. Pato, Cornelia M. van Duijn, Christopher E. Gillies, Ilaria Gandin, Massimo Mezzavilla, Arthur Gilly, Massimiliano Cocca, Michela Traglia, Andrea Angius, Jeffrey C. Barrett, Dorret I. Boomsma, Kari Branham, Gerome Breen, Chad Brummet, Fabio Busonero, Hariy Campbell, Andrew T. Chan, Sai Chen, Emily Y. Chew, Francis S. Collins, Laura J. Corbin, George Davey Smith, George Dedoussis, Marcus Dörr, Aliki‐Eleni Farmaki, Luigi Ferrucci, Lukas Forer, Ross M. Fraser, Stacey Gabriel, Shawn Levy, Leif Groop, Tabitha A. Harrison, Andrew T. Hattersley, Oddgeir L. Holmen, Kristian Hveem, Matthias Kretzler, James Lee, Matt McGue, Thomas Meitinger, David Melzer, Josine L. Min, Karen L. Mohlke, John B. Vincent, Matthias Nauck, Deborah A. Nickerson, Aarno Palotie, Michele T. Pato, Nicola Pirastu, Melvin G. Mclnnis, J. Brent Richards, Cinzia Sala, Veikko Salomaa, David Schlessinger, Sebastian Schoenheer, P. Eline Slagboom, Kerrin S. Small, Timothy D. Spector, Dwight Stambolian, Marcus A. Tuke, Jaakko Tuomilehto, Leonard van den Berg, Wouter van Rheenen, Uwe Völker, Cisca Wijmenga, Daniela Toniolo, Eleftheria Zeggini, Paolo Gasparini, Matthew G. Sampson, James F. Wilson, Timothy M. Frayling, Paul I. W. de Bakker, Morris A. Swertz, Steven A. McCarroll, Charles Kooperberg, Annelot M. Dekker, David Altshuler, Cristen Wilier, William G. Iacono, Samuli Ripatti

    Publicado em 2015
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  19. 19
    Extensive identification of genes involved in congenital and structural heart disorders and cardiomyopathy

    Extensive identification of genes involved in congenital and structural heart disorders and cardiomyopathy por Nadine Spielmann, Gregor Miller, Tudor I. Oprea, Chih‐Wei Hsu, Gisela Fobo, Goar Frishman, Corinna Montrone, Hamed Haseli Mashhadi, Jeremy Mason, Violeta Muñoz‐Fuentes, Stefanie Leuchtenberger, Andreas Ruepp, Matias Wagner, Dominik S. Westphal, Cordula M. Wolf, Agnes Görlach, Adrián Sanz‐Moreno, Yi-Li Cho, Raffaele Teperino, Stefan Brandmaier, Sapna Sharma, Isabella Galter, Manuela A. Östereicher, Lilly Zapf, Philipp Mayer‐Kuckuk, Jan Rozman, Lydia Teboul, Rosie Bunton-Stasyshyn, Heather Cater, Michelle Stewart, Skevoulla Christou, Henrik Westerberg, Amelia Willett, Janine M. Wotton, Willson Roper, Audrey E. Christiansen, Christopher Ward, Jason D. Heaney, Corey L. Reynolds, Jan Procházka, Lynette Bower, David Clary, Mohammed Selloum, Ghina Bou About, Olivia Wendling, Hugues Jacobs, Sophie Leblanc, Hamid Méziane, Tania Sorg, Enrique Audain, Arthur Gilly, Nigel W. Rayner, Juan Antonio Aguilar‐Pimentel, Lore Becker, Lillian Garrett, Sabine M. Hölter, Oana V. Amarie, Julia Calzada‐Wack, Tanja Klein‐Rodewald, Patricia da Silva‐Buttkus, Christoph Lengger, Claudia Stoeger, Raffaele Gerlini, Birgit Rathkolb, Daniela Mayr, John R. Seavitt, Angelina Gaspero, Jennie R. Green, Arturo Garza, Ritu Bohat, Leeyean Wong, Melissa L. McElwee, Sowmya Kalaga, Tara L. Rasmussen, Isabel Lorenzo, Denise G. Lanza, Rodney C. Samaco, Surabi Veeraragaven, Juan Gallegos, Petr Kašpárek, Silvia Petrezsélyová, Ruairidh King, Sara Johnson, James Cleak, Zsombor Szkoe-Kovacs, Gemma Codner, Matthew Mackenzie, Adam Caulder, Janet Kenyon, Wendy Gardiner, Hayley Phelps, Rhys Hancock, Claire Norris, Michayla Moore, Audrie Seluke, Rachel Urban, Coleen Kane, Leslie O. Goodwin, Kevin A. Peterson, Matthew Mckay

    Publicado em 2022
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  20. 20
    Translational genomics of osteoarthritis in 1,962,069 individuals

    Translational genomics of osteoarthritis in 1,962,069 individuals por Konstantinos Hatzikotoulas, Lorraine Southam, Lilja Stefánsdóttir, Cindy G. Boer, Merry‐Lynn McDonald, J. Patrick Pett, Young‐Chan Park, Margo Tuerlings, Rick Mulders, Andrei Barysenka, Ana Luiza Arruda, Vinicius Tragante, Alison Rocco, Norbert Bittner, Shibo Chen, Susanne Horn, Vinodh Srinivasasainagendra, Ken To, Georgia Katsoula, Peter Kreitmaier, Amabel Tenghe, Arthur Gilly, Liubov Arbeeva, Lane G. Chen, Agathe de Pins, Daniel Dochtermann, Cecilie Henkel, Jonas Höijer, Shuji Ito, Penelope A. Lind, Bitota Lukusa-Sawalena, Aye Ko Ko Minn, Marina Mola-Caminal, Akira Narita, Chelsea Nguyen, Ene Reimann, Micah Silberstein, Anne Heidi Skogholt, Hemant K. Tiwari, Michelle S. Yau, Ming Yue, Wei Zhao, Jin Zhou, George Alexiadis, Karina Banasik, Søren Brunak, Archie Campbell, Jackson T S Cheung, Joseph Dowsett, Tariq Faquih, Jessica D. Faul, Lijiang Fei, Anne Marie Fenstad, Takamitsu Funayama, Maiken E. Gabrielsen, Chinatsu Gocho, Kirill Gromov, Thomas Hansen, Georgi Hudjashov, Þorvaldur Ingvarsson, Jessica Johnson, Helgi Jónsson, Saori Kakehi, Juha Karjalainen, Elisa Kasbohm, Susanna Lemmelä, Kuang Lin, Xiaoxi Liu, M. Loef, Massimo Mangino, Daniel L. McCartney, Iona Y. Millwood, Joshua Richman, Mary B. Roberts, Kathleen A. Ryan, Dino Samartzis, Manu Shivakumar, Søren Thorgaard Skou, Sachiyo Sugimoto, Ken Suzuki, Hiroshi Takuwa, Maris Teder‐Laving, Laurent F. Thomas, Kohei Tomizuka, Constance Turman, Stefan Weiß, Tian Wu, Eleni Zengini, Yanfei Zhang, Manuel A. R. Ferreira, George C. Babis, Aris Baras, Tyler Barker, David J. Carey, Kathryn S.E. Cheah, Zhengming Chen, Jason Pui Yin Cheung, Mark Daly, Renée de Mutsert, Charles B. Eaton

    Publicado em 2025
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