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Genetic identification of cell types underlying brain complex traits yields insights into the etiology of Parkinson's disease
Genetic identification of cell types underlying brain complex traits yields insights into the etiology of Parkinson's disease
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Genetic identification of cell types underlying brain complex traits yields insights into the etiology of Parkinson's disease

Bryois, Julien ; Skene, Nathan G ; Hansen, Thomas Folkmann ; Kogelman, Lisette J A ; Watson, Hunna J ; Liu, Zijing ; Brueggeman, Leo ; Breen, Gerome ; Bulik, Cynthia M ; Arenas, Ernest ; Hjerling-Leffler, Jens ; Sullivan, Patrick F

Nature genetics, 2020-05, Vol.52 (5), p.482-493 [Periódico revisado por pares]

United States: Nature Publishing Group

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2
Shared polygenic risk and causal inferences in amyotrophic lateral sclerosis
Shared polygenic risk and causal inferences in amyotrophic lateral sclerosis
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Shared polygenic risk and causal inferences in amyotrophic lateral sclerosis

Noyce, Alastair J. ; Hemani, Gibran ; Mora, Gabriele ; Bartolomei, Ilaria ; Benigni, Michele ; Borghero, Giuseppe ; Brunetti, Maura ; Calvo, Andrea ; Cammarosano, Stefania ; Cannas, Antonino ; Caponnetto, Claudia ; Casale, Federico ; Cavallaro, Sebastiano ; Chiò, Adriano ; Colletti, Tiziana ; Conforti, Francesca L. ; Conte, Amelia ; Corrado, Lucia ; Costantino, Emanuela ; D'Alfonso, Sandra ; Femiano, Cinzia ; Ferrarese, Carlo ; Fini, Nicola ; Floris, Gianluca ; Grassano, Maurizio ; Lattante, Serena ; Logroscino, Giancarlo ; Loi, Daniela ; Mancardi, Gianluigi ; Mandich, Paola ; Manera, Umberto ; Marinou, Kalliopi ; Marrali, Giuseppe ; Marrosu, Maria Giovanna ; Mazzini, Letizia ; Melis, Maurizio ; Messina, Sonia ; Mora, Gabriele ; Occhineri, Patrizia ; Origone, Paola ; Pani, Carla ; Petrucci, Antonio ; Pirisi, Angelo ; Restagno, Gabriella ; Ricci, Claudia ; Riva, Nilo ; Sabatelli, Mario ; Santarelli, Marialuisa ; Spataro, Rossella ; Tanel, Raffaella ; Tremolizzo, Lucio ; Volanti, Paolo ; Zollino, Marcella ; Arepalli, Sampath ; Bowser, Robert ; Broach, James ; Camu, William ; Chia, Ruth ; Chiò, Adriano ; Ding, Jinhui ; Dunckley, Travis L. ; Eicher, John D. ; Faghri, Faraz ; Feldman, Eva ; Fratta, Pietro ; Geiger, Joshua T. ; Gerhard, Glenn ; Hardy, John ; Harms, Matthew B. ; Heiman‐Patterson, Terry D. ; Kamel, Freya ; MacGowan, Daniel J.L. ; Maragakis, Nicholas J. ; Murphy, Natalie A. ; Myllykangas, Liisa ; Nalls, Mike A. ; Nicolas, Aude ; Orrell, Richard W. ; Pamphlett, Roger ; Pickering‐Brown, Stuart ; Pioro, Erik ; Pliner, Hannah A. ; Pulst, Stefan M. ; Ravits, John M. ; Rothstein, Jeffrey D. ; Salvi, Erika ; Sendtner, Michael ; Simmons, Zachary ; Stone, David C. ; Sulkava, Raimo ; Troncoso, Juan C. ; Van Damme, Philip ; Van Deerlin, Vivianna M. ; Van Den Bosch, Ludo ; Zinman, Lorne ; Tienari, Pentti J. ; Stone, David J. ; Nalls, Mike A. ; Singleton, Andrew B. ; Traynor, Bryan J.

Annals of neurology, 2019-04, Vol.85 (4), p.470-481 [Periódico revisado por pares]

Hoboken, USA: John Wiley & Sons, Inc

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3
Genetic association analysis of 77,539 genomes reveals rare disease etiologies
Genetic association analysis of 77,539 genomes reveals rare disease etiologies
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Genetic association analysis of 77,539 genomes reveals rare disease etiologies

Greene, Daniel ; Pirri, Daniela ; Frudd, Karen ; Sackey, Ege ; Al-Owain, Mohammed ; Giese, Arnaud P J ; Ramzan, Khushnooda ; Riaz, Sehar ; Yamanaka, Itaru ; Boeckx, Nele ; Thys, Chantal ; Gelb, Bruce D ; Brennan, Paul ; Hartill, Verity ; Harvengt, Julie ; Kosho, Tomoki ; Mansour, Sahar ; Masuno, Mitsuo ; Ohata, Takako ; Stewart, Helen ; Taibah, Khalid ; Turner, Claire L S ; Imtiaz, Faiqa ; Riazuddin, Saima ; Morisaki, Takayuki ; Ostergaard, Pia ; Loeys, Bart L ; Morisaki, Hiroko ; Ahmed, Zubair M ; Birdsey, Graeme M ; Freson, Kathleen ; Mumford, Andrew ; Turro, Ernest

Nature medicine, 2023-03, Vol.29 (3), p.679-688 [Periódico revisado por pares]

United States: Nature Publishing Group

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4
The ENIGMA Consortium: large-scale collaborative analyses of neuroimaging and genetic data
The ENIGMA Consortium: large-scale collaborative analyses of neuroimaging and genetic data
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The ENIGMA Consortium: large-scale collaborative analyses of neuroimaging and genetic data

Vasquez, Alejandro Arias ; Renteria, Miguel E. ; Agartz, Ingrid ; Apostolova, Liana G. ; Bastin, Mark E. ; Bauer, Michael ; Bearden, Carrie E. ; Binder, Elisabeth B. ; Bøen, Erlend ; Bowman, Ian J. ; Brohawn, David G. ; Buitelaar, Jan ; Carless, Melanie A. ; Ching, Christopher R. K. ; Conrod, Patricia ; Depondt, Chantal ; de Zubicaray, Greig I. ; Djurovic, Srdjan ; Duggirala, Ravindranath ; Dyer, Thomas D. ; Ekman, Carl Johan ; Emsell, Louise ; Fears, Scott ; Fedko, Iryna ; Fox, Peter T. ; Francks, Clyde ; Frodl, Thomas ; Frouin, Vincent ; Godlewska, Beata ; Haukvik, Unn K. ; Hickie, Ian B. ; Hoekstra, Pieter J. ; Homuth, Georg ; Hulshoff Pol, Hilleke E. ; Hwang, Kristy S. ; Kim, Sungeun ; Kochunov, Peter ; Krämer, Bernd ; Kwok, John B. J. ; Laje, Gonzalo ; Landman, Bennett A. ; Lauriello, John ; Li, Chiang-shan ; Liberg, Benny ; Liu, Xinmin ; Macciardi, Fabio ; Malt, Ulrik F. ; Mattheisen, Manuel ; Meyer-Lindenberg, Andreas ; Melle, Ingrid ; Mohnke, Sebastian ; Morris, Derek W. ; Mueller, Bryon A. ; Mühleisen, Thomas W. ; Müller-Myhsok, Bertram ; Nichols, Thomas E. ; Oosterlaan, Jaap ; Pandolfo, Massimo ; Papmeyer, Martina ; Pausova, Zdenka ; Penninx, Brenda W. ; Peterson, Charles P. ; Potkin, Steven G. ; Rasmussen, Jerod ; Rijpkema, Mark ; Risacher, Shannon L. ; Roiz-Santiañez, Roberto ; Romanczuk-Seiferth, Nina ; Rujescu, Dan ; Salami, Alireza ; Scanlon, Cathy ; Schmaal, Lianne ; Schnack, Hugo G. ; Schork, Andrew J. ; Seidman, Larry ; Shen, Li ; Smoller, Jordan W. ; Sponheim, Scott R. ; Starr, John M. ; Sussmann, Jessika ; Sämann, Philipp G. ; Teumer, Alexander ; Toga, Arthur W. ; Trabzuni, Daniah ; Turner, Jessica ; Van den Heuvel, Martijn ; van Eijk, Kristel ; van Erp, Theo G. M. ; van Haren, Neeltje E. M. ; van ‘t Ent, Dennis ; van Tol, Marie-Jose ; Valdés Hernández, Maria C. ; Versace, Amelia ; Weale, Michael E. ; Westlye, Lars T. ; Whelan, Christopher D. ; Wittfeld, Katharina ; Zilles, David ; Freimer, Nelson B. ; Lawrence, Natalia S.

Brain imaging and behavior, 2014, Vol.8 (2), p.153-182 [Periódico revisado por pares]

Boston: Springer US

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5
A genome-wide association study for survival from a multi-centre European study identified variants associated with COVID-19 risk of death
A genome-wide association study for survival from a multi-centre European study identified variants associated with COVID-19 risk of death
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A genome-wide association study for survival from a multi-centre European study identified variants associated with COVID-19 risk of death

Minnai, Francesca ; Biscarini, Filippo ; Esposito, Martina ; Dragani, Tommaso A ; Bujanda, Luis ; Rahmouni, Souad ; Alarcón-Riquelme, Marta E ; Bernardo, David ; Carnero-Montoro, Elena ; Buti, Maria ; Zeberg, Hugo ; Asselta, Rosanna ; Romero-Gómez, Manuel ; Fernandez-Cadenas, Israel ; Fallerini, Chiara ; Zguro, Kristina ; Croci, Susanna ; Baldassarri, Margherita ; Bruttini, Mirella ; Furini, Simone ; Renieri, Alessandra ; Colombo, Francesca

Scientific reports, 2024-02, Vol.14 (1), p.3000-3000, Article 3000 [Periódico revisado por pares]

England: Nature Publishing Group

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6
Multivariate genome-wide analysis of immunoglobulin G N-glycosylation identifies new loci pleiotropic with immune function
Multivariate genome-wide analysis of immunoglobulin G N-glycosylation identifies new loci pleiotropic with immune function
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Multivariate genome-wide analysis of immunoglobulin G N-glycosylation identifies new loci pleiotropic with immune function

Shadrina, Alexandra S ; Zlobin, Alexander S ; Zaytseva, Olga O ; Klarić, Lucija ; Sharapov, Sodbo Z ; D Pakhomov, Eugene ; Perola, Marcus ; Esko, Tonu ; Hayward, Caroline ; Wilson, James F ; Lauc, Gordan ; Aulchenko, Yurii S ; Tsepilov, Yakov A

Human molecular genetics, 2021-06, Vol.30 (13), p.1259-1270 [Periódico revisado por pares]

England: Oxford University Press

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7
SARS-CoV-2 susceptibility and COVID-19 disease severity are associated with genetic variants affecting gene expression in a variety of tissues
SARS-CoV-2 susceptibility and COVID-19 disease severity are associated with genetic variants affecting gene expression in a variety of tissues
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SARS-CoV-2 susceptibility and COVID-19 disease severity are associated with genetic variants affecting gene expression in a variety of tissues

D’Antonio, Matteo ; Chwialkowska, Karolina ; Tenesa, Albert ; D’Mellow, Kenton ; Aprile von Hohenstaufen, Kathrin ; Eltoukhy, Madonna M. ; Yassen, Amr M. ; Moahmed, Hanteera S. ; Tobin, Martin D. ; Guyatt, Anna L. ; Hollox, Edward J. ; Sharififard, Bahareh ; Abdollahi, Hamed ; Puthanakit, Thanyawee ; Suchartlikitwong, Pintip ; Sodsai, Pimpayao ; Alaamery, Manal ; Aljawini, Nora ; Albesher, Nour ; Alahmadey, Ziab Z. ; Suliman, Bandar A. ; Al-Afghani, Hani ; Massadeh, Salam ; Muiño, Elena ; Coto, Eliecer ; Albaiceta, Guillermo M. ; Dietl, Beatriz ; Martí-Fàbregas, Joan ; Villalonga, Joan Montaner ; Menéndez-Valladares, Paloma ; Glessner, Joseph R. ; Forgetta, Vincenzo ; Ghosh, Biswarup ; Guiot, Julien ; Guntz, Julien ; Beguin, Yves ; Claassen, Sabine ; Malaise, Olivier ; Daya, Michelle ; Chavan, Sameer ; Laisk, Triin ; Alavere, Helene ; Metsalu, Kristjan ; Peterson, Pärt ; Cortés, Beatriz ; Torrents, David ; Fallerini, Chiara ; Doddato, Gabriella ; Bruttini, Mirella ; Pinto, Anna Maria ; Bruno, Raffaele ; Picchiotti, Nicola ; Mantovani, Stefania ; Bargagli, Elena ; D’Alessandro, Miriana ; Franchi, Federico ; Cantarini, Luca ; Tacconi, Danilo ; Desanctis, Elena ; Antinori, Andrea ; Vergori, Alessandra ; Baratti, Stefano ; Menatti, Elisabetta ; Trotta, Tullio ; Martinelli, Enrico ; Bachetti, Tiziana ; Ceri, Stefano ; Parati, Gianfranco ; Ravaglia, Sabrina ; Catena, Emanuele ; Pessina, Gloria ; Tumbarello, Mario ; Guarnaccia, Alessandra ; Boughton, Andrew P. ; Annis, Aubrey ; Carey, Dave J. ; Gass, Matthew C. ; Abecasis, Goncalo R. ; Butterworth, Adam S. ; Nivard, Michel (M.G.) ; de geus, Eco (E.J.C.) ; Verma, Anurag ; Ritchie, Marylyn D. ; Verma, Shefali S. ; Lucas, Anastasia ; Karczewski, Konrad J. ; Walters, Raymond K. ; Palmer, Duncan S. ; Sarma, Gopal ; Crook, Derrick W. ; Koelling, Nils ; Moutsianas, Loukas ; Rhodes, Daniel ; Ball, Catherine A. ; Baltzell, Asher Haug ; Gaddis, Michael ; Noto, Keith ; Tang, Lara ; Nadkarni, Girish N. ; Choi, Sam

Cell reports (Cambridge), 2021-11, Vol.37 (7), p.110020-110020, Article 110020 [Periódico revisado por pares]

United States: Elsevier Inc

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8
Epilepsy, hippocampal sclerosis and febrile seizures linked by common genetic variation around SCN1A
Epilepsy, hippocampal sclerosis and febrile seizures linked by common genetic variation around SCN1A
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Epilepsy, hippocampal sclerosis and febrile seizures linked by common genetic variation around SCN1A

Kasperavičiūtė, Dalia ; Catarino, Claudia B ; Matarin, Mar ; Leu, Costin ; Novy, Jan ; Tostevin, Anna ; Leal, Bárbara ; Hessel, Ellen V. S ; Hallmann, Kerstin ; Hildebrand, Michael S ; Dahl, Hans-Henrik M ; Ryten, Mina ; Trabzuni, Daniah ; Ramasamy, Adaikalavan ; Alhusaini, Saud ; Doherty, Colin P ; Dorn, Thomas ; Hansen, Jörg ; Krämer, Günter ; Steinhoff, Bernhard J ; Zumsteg, Dominik ; Duncan, Susan ; Kälviäinen, Reetta K ; Eriksson, Kai J ; Kantanen, Anne-Mari ; Pandolfo, Massimo ; Gruber-Sedlmayr, Ursula ; Schlachter, Kurt ; Reinthaler, Eva M ; Stogmann, Elisabeth ; Zimprich, Fritz ; Théâtre, Emilie ; Smith, Colin ; O’Brien, Terence J ; Meng Tan, K ; Petrovski, Slave ; Robbiano, Angela ; Paravidino, Roberta ; Zara, Federico ; Striano, Pasquale ; Sperling, Michael R ; Buono, Russell J ; Hakonarson, Hakon ; Chaves, João ; Costa, Paulo P ; Silva, Berta M ; da Silva, António M ; de Graan, Pierre N. E ; Koeleman, Bobby P. C ; Becker, Albert ; Schoch, Susanne ; von Lehe, Marec ; Reif, Philipp S ; Rosenow, Felix ; Becker, Felicitas ; Weber, Yvonne ; Lerche, Holger ; Rössler, Karl ; Buchfelder, Michael ; Hamer, Hajo M ; Kobow, Katja ; Coras, Roland ; Blumcke, Ingmar ; Scheffer, Ingrid E ; Berkovic, Samuel F ; Weale, Michael E ; Delanty, Norman ; Depondt, Chantal ; Cavalleri, Gianpiero L ; Kunz, Wolfram S ; Sisodiya, Sanjay M

Brain (London, England : 1878), 2013-10, Vol.136 (10), p.3140-3150 [Periódico revisado por pares]

Oxford: Oxford University Press

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9
SLITRK2, an X-linked modifier of the age at onset in C9orf72 frontotemporal lobar degeneration
SLITRK2, an X-linked modifier of the age at onset in C9orf72 frontotemporal lobar degeneration
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SLITRK2, an X-linked modifier of the age at onset in C9orf72 frontotemporal lobar degeneration

Barbier, Mathieu ; Camuzat, Agnès ; Hachimi, Khalid El ; Guegan, Justine ; Rinaldi, Daisy ; Lattante, Serena ; Houot, Marion ; Sánchez-Valle, Raquel ; Sabatelli, Mario ; Antonell, Anna ; Molina-Porcel, Laura ; Clot, Fabienne ; Couratier, Philippe ; van der Ende, Emma ; van der Zee, Julie ; Manzoni, Claudia ; Camu, William ; Cazeneuve, Cécile ; Sellal, François ; Didic, Mira ; Golfier, Véronique ; Pasquier, Florence ; Duyckaerts, Charles ; Rossi, Giacomina ; Bruni, Amalia C ; Alvarez, Victoria ; Gómez-Tortosa, Estrella ; de Mendonça, Alexandre ; Graff, Caroline ; Masellis, Mario ; Nacmias, Benedetta ; Oumoussa, Badreddine Mohand ; Jornea, Ludmila ; Forlani, Sylvie ; Van Deerlin, Viviana ; Rohrer, Jonathan D ; Gelpi, Ellen ; Rademakers, Rosa ; Van Swieten, John ; Le Guern, Eric ; Van Broeckhoven, Christine ; Ferrari, Raffaele ; Génin, Emmanuelle ; Brice, Alexis ; Le Ber, Isabelle

Brain (London, England : 1878), 2021-10, Vol.144 (9), p.2798-2811 [Periódico revisado por pares]

England: Oxford University Press

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10
Marker imputation with low-density marker panels in Dutch Holstein cattle
Marker imputation with low-density marker panels in Dutch Holstein cattle
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Marker imputation with low-density marker panels in Dutch Holstein cattle

Zhang, Z. ; Druet, T.

Journal of dairy science, 2010-11, Vol.93 (11), p.5487-5494 [Periódico revisado por pares]

New York, NY: Elsevier Inc

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