Blar i Norwegian Institute of Public Health Open Repository på forfatter "Bybjerg-Grauholm, Jonas"
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Discovery of the first genome-wide significant risk loci for attention deficit/hyperactivity disorder
Demontis, Ditte; Walters, Raymond K.; Martin, Joanna; Mattheisen, Manuel; Als, Thomas D.; Agerbo, Esben; Baldursson, Gisli; Belliveau, Rich; Bybjerg-Grauholm, Jonas; Bækvad-Hansen, Marie; Cerrato, Felecia; Chambert, Kimberly; Churchhouse, Claire; Dumont, Ashley; Gandal, Michael; Goldstein, Jacqueline I.; Grasby, Katrina L.; Grove, Jakob; Gudmundsson, Ólafur O.; Hansen, Christine S; Hauberg, Mads Engel; Hollegaard, Mads V; Howrigan, Daniel P.; Huang, Hailiang; Jugessur, Astanand; Myhre, Ronny; Stoltenberg, Camilla; Andreassen, Ole Andreas; Asherson, Philip; Burton, Christie L.; Boomsma, Dorret I.; Cormand, Bru; Dalsgaard, Søren; Haavik, Jan; Sonuga-Barke, Edmund J.S.; Sullivan, Patrick F.; Thapar, Anita; Tung, Joyce Y.; Waldman, Irwin; Medland, Sarah E.; Stefansson, Kari; Nordentoft, Merete; Hougaard, David M.; Werge, Thomas; Mors, Ole; Mortensen, Preben Bo; Daly, Mark J.; Faraone, Stephen V.; Børglum, Anders D.; Neale, Benjamin M (Peer reviewed; Journal article, 2018) -
Genetic correlates of phenotypic heterogeneity in autism
Warrier, Varun; Zhang, Xinhe; Reed, Patrick; Havdahl, Alexandra; Moore, Tyler M.; Cliquet, Freddy; Leblond, Claire S.; Rolland, Thomas; Rosengren, Anders; Caceres, Antonia San Jose; Hayward, Hannah; Crawley, Daisy; Faulkner, Jessica; Sabet, Jessica; Ellis, Claire; Oakley, Bethany; Loth, Eva; Charman, Tony; Murphy, Declan; Holt, Rosemary; Waldman, Jack; Upadhyay, Jessica; Gunby, Nicola; Lai, Meng-Chuan; Renouf, Gwilym; Ruigrok, Amber; Taylor, Emily; Ziauddeen, Hisham; Deakin, Julia; di Bruttopilo, Sara Ambrosino; van Dijk, Sarai; Rijks, Yvonne; Koops, Tabitha; Douma, Miriam; Spaan, Alyssia; Selten, Iris; Steffers, Maarten; van Themaat, Anna Ver Loren; Bast, Nico; Baumeister, Sarah; O’Dwyer, Larry; Bours, Carsten; Rausch, Annika; von Rhein, Daniel; Cornelissen, Ineke; de Bruin, Yvette; Graauwmans, Maartje; Kostrzewa, Elzbieta; Cauvet, Elodie; Tammimies, Kristiina; Sitnikow, Rouslan; Dumas, Guillaume; Kim, Yang-Min; Bourgeron, Thomas; Hougaard, David M.; Bybjerg-Grauholm, Jonas; Werge, Thomas; Mortensen, Preben Bo; Mors, Ole; Nordentoft, Merete; Adhya, Dwaipayan; Alamanza, Armandina; Allison, Carrie; Garvey, Isabelle; Parsons, Tracey; Smith, Paula; Tsompanidis, Alex; Burton, Graham J.; Heazell, Alexander E. P.; Gabis, Lidia V.; Biron-Shental, Tal; Lancaster, Madeline A.; Srivastava, Deepak P.; Mill, Jonathan; Rowitch, David H.; Hurles, Matthew E.; Geschwind, Daniel H.; Børglum, Anders D.; Robinson, Elise B.; Grove, Jakob; Martin, Hilary C.; Bourgeron, Thomas; Baron-Cohen, Simon (Peer reviewed; Journal article, 2022) -
Genetic predisposition to hypertension is associated with preeclampsia in European and Central Asian women
Steinthorsdottir, Valgerdur; McGinnis, Ralph; Williams, Nicholas O.; Stefánsdóttir, Lilja; Thorleifsson, Gudmar; Shooter, Scott; Fadista, João; Sigurdsson, Jon K.; Auro, Kirsi; Berezina, Galina; Borges, Maria-Carolina; Bumpstead, Suzannah; Bybjerg-Grauholm, Jonas; Colgiu, Irina; Dolby, Vivien A.; Dudbridge, Frank; Engel, Stephanie M.; Franklin, Christopher S.; Frigge, Michael L; Frisbaek, Yr; Geirsson, Reynir T.; Geller, Frank; Gretarsdottir, Solveig; Gudbjartsson, Daniel F.; Harmon, Quaker; Hougaard, David Michael; Hegay, Tatyana; Helgadottir, Anna; Hjartardóttir, Sigrún; Jääskeläinen, Tiina; Johannsdottir, Hrefna; Jonsdottir, Ingileif; Juliusdottir, Thorhildur; Kalsheker, Noor; Kasimov, Abdumadjit; Kemp, John P.; Kivinen, Katja; Klungsøyr, Kari; Lee, Wai K; Melbye, Mads; Miedzybrodska, Zosia; Moffett, Ashley; Najmutdinova, Dilbar; Nishanova, Firuza; Olafsdottir, Thorunn; Perola, Markus; Pipkin, Fiona Broughton; Poston, Lucilla; Prescott, Gordon; Saevarsdottir, Saedis; Salimbayeva, Damilya; Scaife, Paula Juliet; Skotte, Line; Staines-Urias, Eleonora; Stefansson, Olafur A.; Sørensen, Karina Meden; Thomsen, Liv Cecilie Vestrheim; Tragante, Vinicius; Trogstad, Lill; Simpson, Nigel A.B.; Aripova, Tamara; Casas, Juan P; Dominiczak, Anna F; Walker, James J.; Thorsteinsdottir, Unnur; Iversen, Ann-Charlotte; Feenstra, Bjarke; Lawlor, Deborah A.; Boyd, Heather Allison; Magnus, Per; Laivuori, Hannele; Zakhidova, Nodira; Syvatova, Gulnara; Stefansson, Kari; Morgan, Linda (Peer reviewed; Journal article, 2020) -
Statistical and functional convergence of common and rare genetic influences on autism at chromosome 16p
Weiner, Daniel J.; Ling, Emi; Erdin, Serkan; Tai, Derek J. C.; Yadav, Rachita; Grove, Jakob; Fu, Jack M.; Nadig, Ajay; Carey, Caitlin E.; Baya, Nikolas; Bybjerg-Grauholm, Jonas; Mortensen, Preben B.; Werge, Thomas; Demontis, Ditte; Mors, Ole; Nordentoft, Merete; Als, Thomas D.; Baekvad-Hansen, Marie; Rosengren, Anders; Havdahl, Alexandra Karoline Saasen; Hedemand, Anne; Palotie, Aarno; Chakravarti, Aravinda; Arking, Dan; Sulovari, Arvis; Starnawska, Anna; Thiruvahindrapuram, Bhooma; de Leeuw, Christiaan; Carey, Caitlin; Ladd-Acosta, Christine; van der Merwe, Celia; Devlin, Bernie; Cook, Edwin H.; Eichler, Evan; Corfield, Elizabeth Claire; Dieleman, Gwen; Schellenberg, Gerard; Hakonarson, Hakon; Coon, Hilary; Dziobek, Isabel; Vorstman, Jacob; Girault, Jessica; Sutcliffe, James S.; Duan, Jinjie; Nurnberger, John; Hallmayer, Joachim; Buxbaum, Joseph; Piven, Joseph; Weiss, Lauren; Davis, Lea; Janecka, Magdalena; Mattheisen, Manuel; State, Matthew W.; Gill, Michael; Daly, Mark; Uddin, Mohammed; Andreassen, Ole; Szatmari, Peter; Lee, Phil Hyoun; Anney, Richard; Ripke, Stephan; Satterstrom, Kyle; Santangelo, Susan; Kuo, Susan; van Elst, Ludger Tebartz; Rolland, Thomas; Bougeron, Thomas; Polderman, Tinca; Turner, Tychele; Underwood, Jack; Manikandan, Veera; Pillalamarri, Vamsee; Warrier, Varun; Philipsen, Alexandra; Reif, Andreas; Hinney, Anke; Cormand, Bru; Bau, Claiton H. D.; Rovaris, Diego Luiz; Sonuga-Barke, Edmund; Grevet, Eugenio Horacio; Salum, Giovanni; Larsson, Henrik Bo W.; Buitelaar, Jan; Haavik, Jan; McGough, James; Kuntsi, Jonna; Elia, Josephine; Lesch, Klaus-Peter; Klein, Marieke; Bellgrove, Mark; Tesli, Martin Steen; Leung, Patrick W. L.; Pan, Pedro M.; Dalsgaard, Søren; Loo, Sandra; Medland, Sarah; Faraone, Stephen; Reichborn-Kjennerud, Ted; Banaschewski, Tobias; Hawi, Ziarih; Berretta, Sabina; Macosko, Evan Z.; Sebat, Jonathan; O’Connor, Luke J.; Hougaard, David M.; Børglum, Anders D.; Talkowski, Michael E.; McCarroll, Steven A.; Robinson, Elise B. (Peer reviewed; Journal article, 2022) -
The genetic architecture of sporadic and multiple consecutive miscarriage
Laisk, Triin; Soares, Ana Luiza G.; Ferreira, Teresa; Painter, Jodie N.; Censin, Jenny C.; Laber, Samantha; Bacelis, Jonas; Chen, Chia-Yen; Lepamets, Maarja; Lin, Kuang; Liu, Siyang; Millwood, Iona Y.; Ramu, Avinash; Southcombe, Jennifer; Andersen, Marianne S.; Yang, Ling; Becker, Christian M.; Børglum, Anders D.; Gordon, Scott D.; Bybjerg-Grauholm, Jonas; Helgeland, Øyvind; Hougaard, David M.; Jin, Xin; Johansson, Stefan; Juodakis, Julius; Kartsonaki, Christina; Kukushkina, Viktorija; Lind, Penelope A.; Metspalu, Andres; Montgomery, Grant W.; Morris, Andrew P.; Mors, Ole; Mortensen, Preben B.; Njølstad, Pål Rasmus; Nordentoft, Merete; Nyholt, Dale R.; Lippincott, Margaret; Seminara, Stephanie; Salumets, Andres; Snieder, Harold; Zondervan, Krina; Werge, Thomas; Chen, Zhengming; Conrad, Donald F.; Jacobsson, Bo; Li, Liming; Martin, Nicholas G.; Neale, Benjamin M.; Nielsen, Rasmus; Walters, Robin G. (Peer reviewed; Journal article, 2020)