Eleonora Porcu
Active 1987–2025
- 67
- Papers
- 24,009
- Citations
- 49
- h-index
- 64
- i10-index
Citations
Citation sources
Countries
Institutions
- Harvard University1.2%
- Broad Institute0.9%
- University of Cambridge0.6%
- Massachusetts General Hospital0.6%
- University of Oxford0.6%
- Brigham and Women's Hospital0.6%
- Other95.5%
Fields
- Biochemistry, Genetics and Molecular Biology54.2%
- Medicine34.4%
- Immunology and Microbiology3.3%
- Neuroscience2.7%
- Computer Science1.1%
- Agricultural and Biological Sciences0.8%
- Other3.5%
Topics
- Genetic Associations and Epidemiology10.1%
- Genomics and Rare Diseases3.4%
- Reproductive Biology and Fertility2.5%
- Genomics and Phylogenetic Studies2.4%
- Epigenetics and DNA Methylation2.3%
- Genetic Mapping and Diversity in Plants and Animals2.3%
- Other77%
Coauthors
- Zoltán Kutalik16
- Fabio Busonero9
- Stefano Venturoli9
- Tõnu Esko9
- Alexander Teumer8
- Andrea Maschio8
- Maristella Pitzalis8
- Alexandre Reymond7
- Antonella Mulas7
- C Flamigni7
- Carlo Sidore7
- Giuseppe Damiano7
- Maristella Steri7
- Raffaella Fabbri7
- Daniel I. Chasman6
- Giorgio Pistis6
- Ilja M. Nolte6
- Leonardo Notarangelo6
- Magdalena Żołędziewska6
- Sandra Lai6
- Deborah J. Thompson5
- Felix R. Day5
- Francesca Deidda5
- Kaido Lepik5
All papers
- Large-scale cis- and trans-eQTL analyses identify thousands of genetic loci and polygenic scores that regulate blood gene expression
Authors: Urmo Võsa, Annique Claringbould, Harm-Jan Westra, Marc Jan Bonder, Patrick Deelen, Biao Zeng, Holger Kirsten, Ashis Saha, Roman Kreuzhuber, Seyhan Yazar, Harm Brugge, Roy Oelen, Dylan H. de Vries, Monique G.P. van der Wijst, Silva Kasela, Natalia Pervjakova, Isabel Alves, Marie-Julie Favé, Mawussé Agbessi, Mark Christiansen, Rick Jansen, Ilkka Seppälä, Tong Lin, Alexander Teumer, Katharina Schramm, Gibran Hemani, Joost Verlouw, Hanieh Yaghootkar, Reyhan Sönmez Flitman, Andrew Brown, Viktorija Kukushkina, Anette Kalnapenkis, Sina Rüeger, Eleonora Porcu, Jaanika Kronberg, Johannes Kettunen, Bernett Lee, Futao Zhang, Ting Qi, José Alquicira-Hernández, Wibowo Arindrarto, Frank Beutner, Peter A.C. ’t Hoen, Joyce B. J. van Meurs, Jenny van Dongen, Maarten van Iterson, Morris A. Swertz, Marc Jan Bonder, Julia Dmitrieva, Mahmoud Elansary, Benjamin P. Fairfax, Michel Georges, Bastiaan T. Heijmans, Alex W. Hewitt, Mika Kähönen, Yungil Kim, Julian C. Knight, Péter Kovács, Knut Krohn, Shuang� Li, Markus Loeffler, Urko M. Marigorta, Hailang Mei, Yukihide Momozawa, Martina Müller‐Nurasyid, Matthias Nauck, Michel G. Nivard, Brenda W.J.H. Penninx, Jonathan K. Pritchard, Olli T. Raitakari, Olaf Rötzschke, P. Eline Slagboom, Coen D.A. Stehouwer, Michael Stümvoll, Patrick Sullivan, Peter A.C. ’t Hoen, Joachim Thiery, Anke Tönjes, Jenny van Dongen, Maarten van Iterson, Jan H. Veldink, Uwe Völker, Robert Warmerdam, Cisca Wijmenga, Morris A. Swertz, Anand Kumar Andiappan, Grant W. Montgomery, Samuli Ripatti, Markus Perola, Zoltán Kutalik, Emmanouil T. Dermitzakis, Sven Bergmann, Timothy M. Frayling, Joyce B. J. van Meurs, Holger Prokisch, Habibul Ahsan, Brandon L. Pierce, Terho Lehtimäki, Dorret I. Boomsma, Bruce M. Psaty and 14 more - Nature Genetics 2021 cited by 2,182
- An integrated map of genetic variation from 1,092 human genomes
Authors: Gil A. McVean, Peter Donnelly, Anjali Gupta-Hinch, Zamin Iqbal, Iain Mathieson, Andy Rimmer, Dionysia K. Xifara, Angeliki Kerasidou, Claire Churchhouse, Olivier Delaneau, Stacey B. Gabriel, Gil McVean, David M. Altshuler, Namrata Gupta, Eric Banks, Gaurav Bhatia, Mauricio O. Carneiro, Guillermo del Angel, Giulio Genovese, Robert E. Handsaker, Robert E. Handsaker, Steven A. McCarroll, James C. Nemesh, Ryan E. Poplin, Stephen F. Schaffner, Khalid Shakir, Sharon R. Grossman, Mark A. DePristo, Ridhi Tariyal, Heng Li, Mark A. DePristo, David Reich, Matthew E. Hurles, Senduran Balasubramaniam, John Burton, Petr Danecek, Thomas M. Keane, Mark A. DePristo, Shane McCarthy, James Stalker, Michael Quail, Robert E. Handsaker, Yuan Chen, Alison J. Coffey, Vincenza Colonna, Ni Huang, Luke Jostins, Aylwyn Scally, Klaudia Walter, Yali Xue, Yujun Zhang, Ben Blackburne, Sarah J. Lindsay, Zemin Ning, Adam Frankish, Jennifer Harrow, Richard M. Durbin, Chris Tyler-Smith, Gonçalo R. Abecasis, Richard Durbin, Tom Blackwell, Fabio Busonero, Christian Fuchsberger, Goo Jun, Andrea Maschio, Eleonora Porcu, Carlo Sidore, Adrian Tan, Mary Kate Trost, Hyun Min Kang, David R. Bentley, Russell Grocock, Gonçalo R. Abecasis, Jin Yu, Zoya Kingsbury, Jin Yu, R. Keira Cheetham, Tony Cox, Michael Eberle, Lisa Murray, Richard Shaw, Aravinda Chakravarti, Andrew G. Clark, Alon Keinan, Juan L. Rodriguez-Flores, Francisco M. De La Vega, Jeremiah Degenhardt, Evan E. Eichler, Paul Flicek, Laura Clarke, Rasko Leinonen, Richard E. Smith, Xiangqun Zheng-Bradley, Kathryn Beal, Fiona Cunningham, Javier Herrero, William M. McLaren, Graham R. S. Ritchie, Jonathan Barker, Gavin Kelman and 263 more - Nature 2012 cited by 8,269
- Participation bias in the UK Biobank distorts genetic associations and downstream analyses
Authors: Tabea Schoeler, Doug Speed, Eleonora Porcu, Nicola Pirastu, Jean‐Baptiste Pingault, Zoltán Kutalik - Nature Human Behaviour 2023 cited by 389
- A cross-disorder dosage sensitivity map of the human genome
Authors: Ryan L. Collins, Joseph Glessner, Eleonora Porcu, Maarja Lepamets, Rhonda Brandon, Christopher Lauricella, Lide Han, Theodore Morley, Lisa‐Marie Niestroj, Jacob C. Ulirsch, Selin Everett, Daniel P. Howrigan, Philip M. Boone, Jack Fu, Konrad J. Karczewski, Georgios Kellaris, Chelsea Lowther, Diane Lucente, Kiana Mohajeri, Margit Nõukas, Xander Nuttle, Kaitlin E. Samocha, Mi K. Trinh, Farid Ullah, Urmo Võsa, Andres Metspalu, Reedik Mägi, Mari Nelis, Lili Milani, Tõnu Esko, Matthew E. Hurles, Swaroop Aradhya, Erica E. Davis, Hilary K. Finucane, James F. Gusella, Aura Janze, Nicholas Katsanis, Ludmila Matyakhina, Benjamin M. Neale, D. B. Sanders, Stephanie Warren, Jennelle C. Hodge, Dennis Lal, Douglas M. Ruderfer, Jeanne Meck, Reedik Mägi, Tõnu Esko, Alexandre Reymond, Zoltán Kutalik, Håkon Håkonarson, Shamil Sunyaev, Harrison Brand, Michael E. Talkowski - Cell 2022 cited by 371
- Genome sequencing elucidates Sardinian genetic architecture and augments association analyses for lipid and blood inflammatory markers
Authors: Carlo Sidore, Fabio Busonero, Andrea Maschio, Eleonora Porcu, Silvia Naitza, Magdalena Żołędziewska, Antonella Mulas, Giorgio Pistis, Maristella Steri, Fabrice Danjou, Alan Kwong, Vicente Diego Ortega del Vecchyo, Charleston W. K. Chiang, Jennifer L. Bragg‐Gresham, Maristella Pitzalis, Ramaiah Nagaraja, Brendan Tarrier, Christine Brennan, Sergio Uzzau, Christian Fuchsberger, Rossano Atzeni, Frédéric Reinier, Riccardo Berutti, Jie Huang, Nicholas J. Timpson, Daniela Toniolo, Paolo Gasparini, Giovanni Malerba, George Dedoussis, Eleftheria Zeggini, Nicole Soranzo, Chris Jones, Robert Lyons, Andrea Angius, Hyun Min Kang, John Novembre, Serena Sanna, David Schlessinger, Francesco Cucca, Gonçalo R. Abecasis - Nature Genetics 2015 cited by 413
- Genome-wide analyses identify a role for SLC17A4 and AADAT in thyroid hormone regulation
Authors: Alexander Teumer, Layal Chaker, Stefan Groeneweg, Yong Li, Celia Di Munno, Caterina Barbieri, Ulla T. Schultheiß, Michela Traglia, Tarunveer S. Ahluwalia, Masato Akiyama, Emil V. R. Appel, Dan E. Arking, Alice M. Arnold, Arne Astrup, Marian Beekman, John Beilby, Sofie Bekaert, Eric Boerwinkle, Suzanne J. Brown, Marc De Buyzere, Purdey J. Campbell, Graziano Ceresini, Charlotte Cerqueira, Francesco Cucca, Ian J. Deary, Joris Deelen, Kai‐Uwe Eckardt, Arif B. Ekici, Johan G. Eriksson, Luigi Ferrrucci, Tom Fiers, Edoardo Fiorillo, Ian Ford, Caroline S. Fox, Christian Fuchsberger, Tessel E. Galesloot, Christian Gieger, Martin Gögele, Alessandro De Grandi, Niels Grarup, Karin Halina Greiser, Kadri Haljas, Torben Hansen, Sarah E. Harris, Diana van Heemst, Martin den Heijer, Andrew A. Hicks, Wouter den Hollander, Georg Homuth, Jennie Hui, M. Arfan Ikram, Till Ittermann, Richard A. Jensen, Jiaojiao Jing, J. Wouter Jukema, Eero Kajantie, Yoichiro Kamatani, Elisa Kasbohm, Jean‐Marc Kaufman, Lambertus A. Kiemeney, M. Kloppenburg, Florian Kronenberg, Michiaki Kubo, Jari Lahti, Bruno Lapauw, Shuo Li, David C. Liewald, Lifelines Cohort Study, Behrooz Z. Alizadeh, H. Marike Boezen, Lude Franke, Pim van der Harst, Gerjan Navis, Marianne G. Rots, Harold Snieder, Morris A. Swertz, Cisca Wijmenga, Ee Mun Lim, Allan Linneberg, Michela Marina, Deborah Mascalzoni, Koichi Matsuda, Daniel Medenwald, Christa Meisinger, Ingrid Meulenbelt, Tim De Meyer, Henriette E. Meyer zu Schwabedissen, Rafael Mikolajczyk, Matthijs Moed, Romana T. Netea‐Maier, Ilja M. Nolte, Yukinori Okada, Mauro Pala, Cristian Pattaro, Oluf Pedersen, Astrid Petersmann, Eleonora Porcu, Iris Postmus, Peter P. Pramstaller, Bruce M. Psaty and 38 more - Nature Communications 2018 cited by 289
- Mendelian randomization integrating GWAS and eQTL data reveals genetic determinants of complex and clinical traits
Authors: Eleonora Porcu, Sina Rüeger, Kaido Lepik, Mawussé Agbessi, Habibul Ahsan, Isabel Alves, Anand Kumar Andiappan, Wibowo Arindrarto, Philip Awadalla, Alexis Battle, Frank Beutner, Marc Jan Bonder, Dorret I. Boomsma, Mark Christiansen, Annique Claringbould, Patrick Deelen, Tõnu Esko, Marie-Julie Favé, Lude Franke, Timothy M. Frayling, Sina A. Gharib, Gregory Gibson, Bastiaan T. Heijmans, Gibran Hemani, Rick Jansen, Mika Kähönen, Anette Kalnapenkis, Silva Kasela, Johannes Kettunen, Yungil Kim, Holger Kirsten, Péter Kovács, Knut Krohn, Jaanika Kronberg-Guzman, Viktorija Kukushkina, Bernett Lee, Terho Lehtimäki, Markus Loeffler, Urko M. Marigorta, Hailang Mei, Lili Milani, Grant W. Montgomery, Martina Müller‐Nurasyid, Matthias Nauck, Michel G. Nivard, Brenda W.J.H. Penninx, Markus Perola, Natalia Pervjakova, Brandon L. Pierce, Joseph E. Powell, Holger Prokisch, Bruce M. Psaty, Olli T. Raitakari, Samuli Ripatti, Olaf Rötzschke, Ashis Saha, Markus Scholz, Katharina Schramm, Ilkka Seppälä, P. Eline Slagboom, Coen D.A. Stehouwer, Michael Stümvoll, Patrick Sullivan, Peter A.C. ’t Hoen, Alexander Teumer, Joachim Thiery, Tong Lin, Anke Tönjes, Jenny van Dongen, Maarten van Iterson, Joyce B. J. van Meurs, Jan H. Veldink, Joost Verlouw, Peter M. Visscher, Uwe Völker, Urmo Võsa, Harm-Jan Westra, Cisca Wijmenga, Hanieh Yaghootkar, Jian Yang, Biao Zeng, Futao Zhang, Wibowo Arindrarto, Marian Beekman, Dorret I. Boomsma, Jan Bot, Joris Deelen, Patrick Deelen, Lude Franke, Bastiaan T. Heijmans, Peter A.C. ’t Hoen, Bert A. Hofman, Jouke J. Hottenga, Aaron Isaacs, Marc Jan Bonder, P. Mila Jhamai, Rick Jansen, Szymon M. Kiełbasa, Nico Lakenberg, René Luijk and 35 more - Nature Communications 2019 cited by 347
- Genomic analyses identify hundreds of variants associated with age at menarche and support a role for puberty timing in cancer risk
Authors: The LifeLines Cohort Study, Felix R. Day, kConFab/AOCS Investigators, Deborah J. Thompson, Hannes Helgason, Daniel I. Chasman, Hilary K. Finucane, Patrick Sulem, Katherine S. Ruth, Sean Whalen, Abhishek Sarkar, Eva Albrecht, Elisabeth Altmaier, Marzyeh Amini, Caterina Barbieri, Thibaud Boutin, Archie Campbell, Ellen W. Demerath, Ayush Giri, Chunyan He, Jouke‐Jan Hottenga, Robert Karlsson, Ivana Kolčić, Po‐Ru Loh, Kathryn L. Lunetta, Massimo Mangino, Marco Brumat, George McMahon, Sarah E. Medland, Ilja M. Nolte, Raymond Noordam, Teresa Nutile, Lavinia Paternoster, Natalia Perjakova, Eleonora Porcu, Lynda M. Rose, Katharina E. Schraut, Ayellet V. Segrè, Albert V. Smith, Lisette Stolk, Alexander Teumer, Irene L. Andrulis, Stefania Bandinelli, Matthias W. Beckmann, Javier Benı́tez, Sven Bergmann, Murielle Bochud, Eric Boerwinkle, Stig E. Bojesen, Manjeet K. Bolla, Judith S. Brand, Hiltrud Brauch, Hermann Brenner, Linda Broer, Thomas Brüning, Julie E. Buring, Harry Campbell, Eulalia Catamo, Stephen J. Chanock, Georgia Chenevix‐Trench, Tanguy Corre, Fergus J. Couch, Diana L. Cousminer, Angela Cox, Laura Crisponi, Kamila Czene, George Davey Smith, Eco J. C. de Geus, Renée de Mutsert, Immaculata De Vivo, Joe Dennis, Peter Devilee, Isabel dos‐Santos‐Silva, Alison M. Dunning, Johan G. Eriksson, Peter A. Fasching, Lindsay Fernández‐Rhodes, Luigi Ferrucci, Dieter Flesch‐Janys, Lude Franke, Marike Gabrielson, Ilaria Gandin, Graham G. Giles, Harald Grallert, Daníel F. Guðbjartsson, Pascal Guénel, Per Hall, Emily Hallberg, Ute Hamann, Tamara B. Harris, Catharina A. Hartman, Gerardo Heiss, Maartje J. Hooning, John L. Hopper, Frank B. Hu, David J. Hunter, M. Arfan Ikram, Hae Kyung Im, Marjo‐Riitta Järvelin, Peter K. Joshi and 118 more - Nature Genetics 2017 cited by 646
- Large-scale genomic analyses link reproductive aging to hypothalamic signaling, breast cancer susceptibility and BRCA1-mediated DNA repair
Authors: Felix R. Day, kConFab Investigators, AOCS Investigators, Generation Scotland, LifeLines Cohort Study, Katherine S. Ruth, Deborah J. Thompson, Kathryn L. Lunetta, Natalia Pervjakova, Daniel I. Chasman, Lisette Stolk, Hilary K. Finucane, Patrick Sulem, Brendan Bulik‐Sullivan, Tõnu Esko, Andrew D. Johnson, Cathy E. Elks, Nora Franceschini, Chunyan He, Elisabeth Altmaier, Jennifer A. Brody, Lude L Franke, Jennifer E. Huffman, Margaux F. Keller, Patrick F. McArdle, Teresa Nutile, Eleonora Porcu, Antonietta Robino, Lynda M. Rose, Ursula M. Schick, Jennifer A. Smith, Alexander Teumer, Michela Traglia, Dragana Vuckovic, Jie Yao, Wei Zhao, Eva Albrecht, Najaf Amin, Tanguy Corre, Jouke‐Jan Hottenga, Massimo Mangino, Albert V. Smith, Toshiko Tanaka, Gonçalo R. Abecasis, Irene L. Andrulis, Hoda Anton‐Culver, Antonis C. Antoniou, Volker Arndt, Alice M. Arnold, Caterina Barbieri, Matthias W. Beckmann, Alicia Beeghly‐Fadiel, Javier Benı́tez, Leslie Bernstein, Suzette J. Bielinski, Carl Blomqvist, Eric Boerwinkle, Natalia Bogdanova, Stig E. Bojesen, Manjeet K. Bolla, Anne‐Lise Børresen‐Dale, Thibaud Boutin, Hiltrud Brauch, Hermann Brenner, Thomas Brüning, Barbara Burwinkel, Archie Campbell, Harry Campbell, Stephen J. Chanock, J. Ross Chapman, Yii-Der Ida Chen, Georgia Chenevix‐Trench, Fergus J. Couch, Andrea D. Coviello, Angela Cox, Kamila Czene, Hatef Darabi, Immaculata De Vivo, Ellen W. Demerath, Joe Dennis, Peter Devilee, Thilo Dörk, Isabel dos‐Santos‐Silva, Alison M. Dunning, John D. Eicher, Peter A. Fasching, Jessica D. Faul, Jonine D. Figueroa, Dieter Flesch‐Janys, Ilaria Gandin, Melissa E. Garcia, Montserrat García‐Closas, Graham G. Giles, Giorgia Girotto, Mark S. Goldberg, Anna González‐Neira, Mark O. Goodarzi, Megan L. Grove, Daníel F. Guðbjartsson, Pascal Guénel and 145 more - Nature Genetics 2015 cited by 451
- Parent-of-origin-specific allelic associations among 106 genomic loci for age at menarche
Authors: Australian Ovarian Cancer Study, John R. B. Perry, The GENICA Network, kConFab, The LifeLines Cohort Study, Felix R. Day, Cathy E. Elks, Patrick Sulem, Deborah J. Thompson, Teresa Ferreira, Chunyan He, Daniel I. Chasman, Tōnu Esko, Guðmar Þorleifsson, Eva Albrecht, Wei Ang, Tanguy Corre, Diana L. Cousminer, Bjarke Feenstra, Nora Franceschini, Andrea Ganna, Andrew D. Johnson, Sanela Kjellqvist, Kathryn L. Lunetta, George McMahon, Ilja M. Nolte, Lavinia Paternoster, Eleonora Porcu, Albert V. Smith, Lisette Stolk, Alexander Teumer, Natalia Tšernikova, Emmi Tikkanen, Sheila Ulivi, Erin K. Wagner, Najaf Amin, Laura J. Bierut, Enda M. Byrne, Jouke‐Jan Hottenga, Daniel L. Koller, Massimo Mangino, Tune H. Pers, Laura M. Yerges-Armstrong, Jing Hua Zhao, Irene L. Andrulis, Hoda Anton‐Culver, Femke Atsma, Stefania Bandinelli, Matthias W. Beckmann, Javier Benı́tez, Carl Blomqvist, Stig E. Bojesen, Manjeet K. Bolla, Bernardo Bonanni, Hiltrud Brauch, Hermann Brenner, Julie E. Buring, Jenny Chang‐Claude, Stephen J. Chanock, Jinhui Chen, Georgia Chenevix‐Trench, J. Margriet Collée, Fergus J. Couch, David Couper, Andrea D. Coviello, Angela Cox, Kamila Czene, Pio D’Adamo, George Davey Smith, Immaculata De Vivo, Ellen W. Demerath, Joe Dennis, Peter Devilee, Aida Karina Dieffenbach, Alison M. Dunning, Guðný Eiríksdóttir, Johan G. Eriksson, Peter A. Fasching, Luigi Ferrucci, Dieter Flesch‐Janys, Henrik Flyger, Tatiana Foroud, Lude Franke, Melissa E. Garcia, Montserrat García‐Closas, Frank Geller, Eco J. C. de Geus, Graham G. Giles, Daníel F. Guðbjartsson, Vilmundur Guðnason, Pascal Guénel, Suiqun Guo, Per Hall, Ute Hamann, Robin Haring, Catharina A. Hartman, Andrew C. Heath, Albert Hofman, Maartje J. Hooning, John L. Hopper and 102 more - Nature 2014 cited by 666
- Genetic Variants Regulating Immune Cell Levels in Health and Disease
Authors: Valeria Orrù, Maristella Steri, Gabriella Sole, Carlo Sidore, Francesca Virdis, Mariano Dei, Sandra Lai, Magdalena Żołędziewska, Fabio Busonero, Antonella Mulas, Matteo Floris, Wieslawa I. Mentzen, Silvana Anna Maria Urru, Stefania Olla, Michele Marongiu, Maria Grazia Piras, Monia Lobina, Andrea Maschio, Maristella Pitzalis, Maria Francesca Urru, Marco Marcelli, Roberto Cusano, Francesca Deidda, Valentina Serra, Manuela Oppo, Rosella Pilu, Frédéric Reinier, Riccardo Berutti, Luca Pireddu, Ilenia Zara, Eleonora Porcu, Alan Kwong, Christine Brennan, Brendan Tarrier, Robert Lyons, Hyun Min Kang, Sergio Uzzau, Rossano Atzeni, Maria Consuelo Valentini, Davide Firinu, Lidia Leoni, Gianluca Rotta, Silvia Naitza, Andrea Angius, Mauro Congia, Michael B. Whalen, Chris M. Jones, David Schlessinger, Gonçalo R. Abecasis, Edoardo Fiorillo, Serena Sanna, Francesco Cucca - Cell 2013 cited by 371
- Overexpression of the Cytokine BAFF and Autoimmunity Risk
Authors: Maristella Steri, Valeria Orrù, Maria Laura Idda, Maristella Pitzalis, Mauro Pala, Ilenia Zara, Carlo Sidore, V. Faà, Matteo Floris, Manila Deiana, Isadora Asunis, Eleonora Porcu, Antonella Mulas, Maria Grazia Piras, Monia Lobina, Sandra Lai, Mara Marongiu, Valentina Serra, Michele Marongiu, Gabriella Sole, Fabio Busonero, Andrea Maschio, Roberto Cusano, Gianmauro Cuccuru, Francesca Deidda, Fausto Poddie, Gabriele Farina, Mariano Dei, Francesca Virdis, Stefania Olla, Maria Anna Satta, Mario Pani, Alessandro Delitala, Eleonora Cocco, Jessica Frau, Giancarlo Coghe, Lorena Lorefice, Giuseppe Fenu, Paola Ferrigno, Maria Ban, Nadia Barizzone, Maurizio Leone, Franca Rosa Guerini, Matteo Piga, Davide Firinu, Ingrid Kockum, Izaura Lima Bomfim, Tomas Olsson, Lars Alfredsson, Ana Suárez, Patrícia Carreira, María Jesús Castillo‐Palma, Joseph Marcus, Mauro Congia, Andrea Angius, Maurizio Melis, Antonio González, Marta E. Alarcón‐Riquelme, Berta Martins da Silva, Maurizio Marchini, Maria Giovanna Danieli, Stefano Del Giacco, Alessandro Mathieu, Antonello Pani, Stephen B. Montgomery, Giulio Rosati, Jan Hillert, Stephen Sawcer, Sandra D’Alfonso, John A. Todd, John Novembre, Gonçalo R. Abecasis, Michael B. Whalen, Maria Giovanna Marrosu, Alessandra Meloni, Serena Sanna, Myriam Gorospe, David Schlessinger, Edoardo Fiorillo, Magdalena Żołędziewska, Francesco Cucca - New England Journal of Medicine 2017 cited by 392
- Integrating sequence and array data to create an improved 1000 Genomes Project haplotype reference panel
Authors: Olivier Delaneau, Jonathan Marchini, Gil McVean, Peter Donnelly, Gerton Lunter, Jonathan Marchini, Simon Myers, Anjali Gupta Hinch, Zamin Iqbal, Iain Mathieson, Andy Rimmer, Dionysia K. Xifara, Angeliki Kerasidou, Claire Churchhouse, Olivier Delaneau, David Altshuler, Stacey Gabriel, Eric S. Lander, Namrata Gupta, Mark J. Daly, Mark A. DePristo, Eric Banks, Gaurav Bhatia, Mauricio O. Carneiro, Guillermo del Angel, Giulio Genovese, Robert E. Handsaker, Chris Hart, Steven A. McCarroll, James Nemesh, Ryan Poplin, S. F. Schaffner, Khalid Shakir, Pardis C. Sabeti, Sharon R. Grossman, Shervin Tabrizi, Ridhi Tariya, Heng Li, David Reich, Richard Durbin, Matthew E. Hurles, Senduran Balasubramaniam, John H. Burton, Petr Danecek, Thomas Keane, Anja Kolb-Kokocinski, Shane McCarthy, James Stalker, Michael A. Quail, Qasim Ayub, Yuan Chen, Alison J. Coffey, Vincenza Colonna, Ni Huang, Luke Jostins, Aylwyn Scally, Klaudia Walter, Yali Xue, Yujun Zhang, Ben Blackburne, Sarah Lindsay, Zemin Ning, Adam Frankish, Jennifer Harrow, Chris Tyler‐Smith, Gonalo R. Abecasis, Hyun Min Kang, Paul Anderson, Tom Blackwell, Fabio Busonero, Christian Fuchsberger, Goo Jun, Andrea Maschio, Eleonora Porcu, Carlo Sidore, Adrian Tan, Mary Kate Trost, David Bentley, Russell Grocock, Sean Humphray, Terena James, Zoya Kingsbury, Markus Bauer, R. Keira Cheetham, Tony Cox, Michael A. Eberle, Lisa Murray, Richard J. Shaw, Aravinda Chakravarti, Andrew G. Clark, Alon Keinan, Juan L. Rodríguez-Flores, Francisco M. De La Vega, Jeremiah D. Degenhardt, Evan E. Eichler, Paul Flicek, Laura Clarke, Rasko Leinonen, Richard E. Smith, Xiangqun Zheng-Bradley and 285 more - Nature Communications 2014 cited by 457
- The individual and global impact of copy-number variants on complex human traits
Authors: Chiara Auwerx, Maarja Lepamets, Marie C. Sadler, Marion Patxot, Miloš Stojanov, David Baud, Reedik Mägi, Tõnu Esko, Andres Metspalu, Lili Milani, Reedik Mägi, Mari Nelis, Eleonora Porcu, Alexandre Reymond, Zoltán Kutalik - The American Journal of Human Genetics 2022 cited by 92
- Differentially expressed genes reflect disease-induced rather than disease-causing changes in the transcriptome
Authors: Eleonora Porcu, Marie C. Sadler, Kaido Lepik, Chiara Auwerx, Andrew R. Wood, Antoine Weihs, Maroun Bou Sleiman, Diogo M. Ribeiro, Stefania Bandinelli, Toshiko Tanaka, Matthias Nauck, Uwe Völker, Olivier Delaneau, Andres Metspalu, Alexander Teumer, Timothy M. Frayling, Federico Santoni, Alexandre Reymond, Zoltán Kutalik - Nature Communications 2021 cited by 139
- Unraveling the polygenic architecture of complex traits using blood eQTL metaanalysis
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