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| Issue Date | Title | Author(s) |
|---|---|---|
| 25-Jan-2021 | Risk variants and polygenic architecture of disruptive behavior disorders in the context of attention-deficit/hyperactivity disorder | Demontis, Ditte; Walters, Raymond; Rajagopal, Veera M.; Waldman, Irwin D.; Grove, Jakob; Als, Thomas D.; Dalsgaard, Soren; Ribasés Haro, Marta; Grauholm, Jonas; Bækvad-Hansen, Maria; Werge, Thomas; Nordentoft, Merete; Mors, Ole; Mortensen, Preben Bo; Psychiatric Genomics Consortium (PGC); Cormand Rifà, Bru; Hougaard, David M.; Neale, Benjamin M.; Franke, Barbara; Faraone, Stephen V.; Børglum, Anders D. |
| 2020 | Genomic analysis of the natural history of attention-deficit/hyperactivity disorder using Neanderthal and ancient Homo sapiens samples | Esteller-Cucala, Paula; Maceda, Iago; Børglum, Anders D.; Demontis, Ditte; Faraone, Stephen V.; Cormand Rifà, Bru; Lao, Oscar |
| 24-Nov-2020 | Variants of the aggression-related RBFOX1 gene in a population representative birth cohort study: aggressiveness, personality and alcohol use disorder | Vaht, Mariliis; Laas, Kariina; Fernàndez Castillo, Noèlia; Kurrikoff, Triin; Kanarik, Margus; Faraone, Stephen V.; Tooding, Liina-Mai; Veidebaum, Toomas; Franke, Barbara; Reif, Andreas; Cormand Rifà, Bru; Harro, Jaanus |
| 2-Jan-2020 | Cross-disorder genetic analyses implicate dopaminergic signaling as a biological link between Attention-Deficit/Hyperactivity Disorder and obesity measures | Roth Mota, Nina; Poelmans, Geert; Klein, Marieke; Torrico, Bàrbara; Fernàndez Castillo, Noèlia; Cormand Rifà, Bru; Reif, Andreas; Franke, Barbara; Arias Vasquez, Alejandro |
| 26-Sep-2022 | Identification of shared and differentiating genetic risk for autism spectrum disorder, attention deficit hyperactivity disorder and case subgroups | Mattheisen, Manuel; Grove, Jakob; Als, Thomas D.; Martin, Joanna; Voloudakis, Georgios; Meier, Sandra; Demontis, Ditte; Bendl, Jaroslav; Walters, Raymond; Carrey, Caitlin E.; Rosengren, Anders; Strom, Nora I.; Hauberg, Mads Engel; Zeng, Biao; Hoffman, Gabriel; Bybjerg-Grauholm, J.; Bækvad-Hansen, M.; Agerbo, Esben; Cormand Rifà, Bru; Nordentoft, Merete; Werge, Thomas; Mors, Ole; Hougaard, David M.; Buxbaum, Joseph D.; Faraone, Stephen V.; Franke, Barbara; Dalsgaard, Søren; Mortensen, Preben B.; Robinson, Elise B.; Roussos, Panos; Neale, Benjamin M.; Daly, Mark J.; Børglum, Anders D. |
| 23-Jul-2020 | Early-infantile onset epilepsy and developmental delay caused by bi-allelic GAD1 variants | Neuray, Caroline; Maroofian, Reza; Scala, Marcello; Sultan, Tipu; Pai, Gurpur S.; Mojarrad, Majid; El Khashab, Heba; deHoll, Leigh; Yue, Wyatt; Alsaif, Hessa S.; Zanetti, Maria N.; Bello, Oscar; Person, Richard; Eslahi, Atieh; Khazaei, Zaynab; Feizabadi, Masoumeh H; Efthymiou, Stephanie; SYNaPS Study Group; El Bassyouni, Hala T.; Soliman, Doaa R.; Tekes, Selahattin; Ozer, Leyla; Baltaci, Volkan; Khan, Suliman; Beetz, Christian; Amr, Khalda S.; Salpietro, Vicenzo; Jamshidi, Yalda; Alkuraya, Fowzan S.; Houlden, Henry; Cormand Rifà, Bru |
| 5-Mar-2020 | Bi-allelic JAM2 Variants Lead to Early-Onset Recessive Primary Familial Brain Calcification | Schottlaender, Lucia V.; Abeti, Rosella; Jaunmuktane, Zane; Macmillan, Carol; Chelban, Viorica; O'Callaghan, Benjamin; McKinley, John; Maroofian, Reza; Efthymiou, Stepanie; Athanasiou Fragkouli, Alkyoni; Forbes, Raeburn; Soutar, Marc P.M.; Livingston, John H.; Kalmar, Bernadett; Swayne, Orlando; Hotton, Gary; SYNAPS Study Group; Pittman, Alan; Mendes de Oliveira, João Ricardo; de Grandis, Maria; Richard Loendt, Angela; Launchbury, Francesca; Althonayan, Juri; McDonnell, Gavin; Carr, Aisling S.; Khan, Suliman; Beetz, Christian; Bisgin, Atil; Tug Bozdogan, Sevcan; Begtrup, Amber; Torti, Erin; Greensmith, Linda; Giunti, Paola; Morrison, Patrick J.; Brandner, Sebastian; Aurrand Lions, Michael; Houlden, Henry; Cormand Rifà, Bru |
| 10-Nov-2020 | Inhibition of G-protein signalling in cardiac dysfunction of intellectual developmental disorder with cardiac arrhythmia (IDDCA) syndrome | De Nittis, Pasquelena; Efthymiou. Sephanie; Sarre, Alexandre; Guex, Nicolas; Chrast, Jacqueline; Putoux, Audrey; Sultan, Tipu; Raza Alvi, Javeria; Ur Rahman, Zia; Zafar, Faisal; Rana, Nuzhat; Rahman, Fatima; Anwar, Najwa; Maqbool, Shazia; Zaki, Maha S.; Gleeson, Joseph G; Murphy, David; Galehdari, Hamid; Shariati, Gholamreza; Mazaheri, Neda; Sedaghat, Alireza; Lesca, Gaetan; Chatron, Nicolas; Salpietro, Vincenzo; Christoforou, Marilena; Houlden, Henry; Simonds, William F; Pedrazzini, Thierry; Maroofian, Reza; Reymond, Alexandre; Cormand Rifà, Bru; SYNAPS Study Group |
| 1-Sep-2020 | Improved diagnosis of rare disease patients through systematic detection of runs of homozygosity | Matalonga Borrel, Lesley; Laurie, Steven; Papakonstantinou, Anastasios; Piscia, Davide; Mereu, Elisabetta; Bullich, Gemma; Thompson, Rachel; Horvath, Rita; Pérez Jurado, Luis; Riess, Olaf; Gut, Ivo; van Ommen, Gert Jan; Lochmüller, Hanns; Beltrán, Sergi; RD-Connect Genome-Phenome Analysis Platform and UR; Cormand Rifà, Bru; Balcells Comas, Susana; Grinberg Vaisman, Daniel Raúl; Urreizti, Roser; Garrabou Tornos, Glòria |
| 9-Feb-2023 | Genome-wide DNA methylation analysis in an antimigraine-treated preclinical model of cortical spreading depolarization | Vila-Pueyo, Marta; Cuenca León, Ester; Queirós, Ana C.; Kulis, Marta; Sintas Vives, Cèlia; Cormand Rifà, Bru; Martín-Subero, José Ignacio; Pozo-Rosich, Patricia; Fernàndez Castillo, Noèlia; Macaya Ruiz, Alfons |
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