Publications
-
Castilla-Vallmanya L, Centeno-Pla M, Serrano M, Franco-Valls, H, Martinez-Cabrera, R, Prat-Planas, A, Rojano, E, Ranea, JAG, Seoane, P, Oliva-Mussara C, Paredes-Fuentes, AJ, Marfany G, Artuch-Iriberri R, Grinberg-Vaisman DR, Rabionet-Janssen R, Balcells S and Urreizti R.
Advancing in Schaaf-Yang syndrome pathophysiology: from bedside to subcellular analyses of truncated MAGEL2
JOURNAL OF MEDICAL GENETICS . 60(4): 406-415. Number of citations: 2
-
Weiner DJ, Ling E, Erdin S, Tai DJC, Yadav R, Grove J, Fu JM, Nadig A, Carey CE, Baya N, Bybjerg-Grauholm J, Berretta S, Macosko EZ, Sebat J, O'Connor LJ, Hougaard DM, Børglum AD, Talkowski ME, McCarroll SA and Robinson EB.
Statistical and functional convergence of common and rare genetic influences on autism at chromosome 16p.
NATURE GENETICS . 54(11): 1630-1639. Number of citations: 3
-
O'Leary, A, Fernandez-Castillo N, Gan, G, Yang, YB, Yotova, AY, Kranz, TM, Grunewald, L, Freudenberg, F, Anton-Galindo, E, Cabana-Domínguez J, Harneit, A, Schweiger, JI, Schwarz, K, Ma, R, Chen, JF, Schwarz, E, Rietschel, M, Tost, H, Meyer-Lindenberg, A, Pane-Farre, CA, Kircher, T, Hamm, AO, Burguera, D, Mota, NR, Franke, B, Schweiger, S, Winter, J, Heinz, A, Erk, S, Romanczuk-Seiferth, N, Walter, H, Ströhle A, Fehm, L, Fydrich, T, Lueken, U, Weber, H, Lang, T, Gerlach, AL, Nöthen MM, Alpers, GW, Arolt, V, Witt, S, Richter, J, Straube, B, Cormand B, Slattery, DA and Reif, A.
Behavioural and functional evidence revealing the role of RBFOX1 variation in multiple psychiatric disorders and traits
MOLECULAR PSYCHIATRY . 27(11): 4464-4473. Number of citations: 11
-
Fritz N, Berens S, Dong Y, Martínez C, Schmitteckert S, Houghton LA, Goebel-Stengel M, Wahl V, Kabisch M, Götze D, D'Amato M, Zheng T, Röth R, Mönnikes H, Tesarz J, Engel F, Gauss A, Raithel M, Andresen V, Keller J, Frieling T, Pehl C, Stein-Thöringer C, Clarke G, Kennedy PJ, Cryan JF, Dinan TG, Quigley EMM, Spiller R, Beltrán C, Madrid AM, Torres V, Mayer EA, Sayuk G, Gazouli M, Karamanolis G, Bustamante M, Estivil X, Rabionet-Janssen R, Hoffmann P, Nöthen MM, Heilmann-Heimbach S, Schmidt B, Franke A, Lieb W, Herzog W, Boeckxstaens G, Wouters MM, Simrén M, Rappold GA, Vicario M, Santos J, Schaefert R, Lorenzo-Bermejo J and Niesler B.
The serotonin receptor 3E variant is a risk factor for female IBS-D
JOURNAL OF MOLECULAR MEDICINE-JMM . 100(11): 1617-1627. Number of citations: 2
-
Jaworek, T, Xu, HC, Gaynor, BJ, Cole, JW, Rannikmae, K, Stanne, TM, Tomppo, L, Abedi, V, Amouyel, P, Armstrong, ND, Attia, J, Bell, S, Benavente, OR, Boncoraglio, GB, Butterworth, A, Carcel-Marquez, J, Chen, ZM, Chong, M, Cruchaga, C, Cushman, M, Danesh, J, Debette, S, Duggan, DJ, Durda, JP, Engstrom, G, Enzinger, C, Faul, JD, Fecteau, NS, Fernandez-Cadenas, I, Gieger, C, Giese, AK, Grewal, RP, Grittner, U, Havulinna, AS, Heitsch, L, Hochberg, MC, Holliday, E, Hu, J, Ilinca, A, Irvin, MR, Jackson, RD, Jacob, MA, Rabionet-Janssen R, Jimenez-Conde, J, Johnson, JA, Kamatani, Y, Kardia, SLR, Koido, M, Kubo, M, Lange, L, Lee, JM, Lemmens, R, Levi, CR, Li, J, Li, LM, Lin, K, Lopez, H, Luke, S, Maguire, J, McArdle, PF, McDonough, CW, Meschia, JF, Metso, T, Muller-Nurasyid, M, O'Connor, TD, O'Donnell, M, Peddareddygari, LR, Pera, J, Perry, JA, Peters, A, Putaala, J, Ray, D, Rexrode, K, Ribases, M, Rosand, J, Rothwell, PM, Rundek, T, Ryan, KA, Sacco, RL, Salomaa, V, Sanchez-Mora, C, Schmidt, R, Sharma, P, Slowik, A, Smith, JA, Smith, NL, Wassertheil-Smoller, S, Soderholm, M, Stine, OC, Strbian, D, Sudlow, CLM, Tatlisumak, T, Terao, C, Thijs, V, Torres-Aguila, NP, Tregouet, DA, Tuladhar, AM, Veldink, JH, Walters, RG, Weir, DR, Woo, D, Worrall, BB, Hong, CC, Ross, OA, Zand, R, de Leeuw, FE, Lindgren, AG, Pare, G, Anderson, CD, Markus, HS, Jern, C, Malik, R, Dichgans, M, Mitchell, BD and Kittner, SJ.
Contribution of Common Genetic Variants to Risk of Early-Onset Ischemic Stroke
Neurology . 99(16): 1738-1754. Number of citations: 6
-
Mattheisen, M, Grove, J, Als, TD, Martin, J, Voloudakis, G, Meier, S, Demontis, D, Bendl, J, Walters, R, Carey, CE, Rosengren, A, Strom, NI, Hauberg, ME, Zeng, B, Hoffman, G, Zhang, W, Bybjerg-Grauholm, J, Bækvad-Hansen M, Agerbo, E, Cormand B, Nordentoft, M, Werge, T, Mors, O, Hougaard, DM, Buxbaum, JD, Faraone, SV, Franke, B, Dalsgaard, S, Mortensen, PB, Robinson, EB, Roussos, P, Neale, BM, Daly, MJ and Børglum AD.
Identification of shared and differentiating genetic architecture for autism spectrum disorder, attention-deficit hyperactivity disorder and case subgroups
NATURE GENETICS . 54(10): 1470-1478. Number of citations: 5
-
Vainieri I, Martin J, Rommel AS, Asherson P, Banaschewski T, Buitelaar J, Cormand B, Crosbie J, Faraone SV, Franke B, Loo SK, Miranda A, Manor I, Oades RD, Purves KL, Ramos-Quiroga JA, Ribasés M, Roeyers H, Rothenberger A, Schachar R, Sergeant J, Steinhausen HC, Vuijk PJ, Doyle AE and Kuntsi J.
Polygenic association between attention-deficit/hyperactivity disorder liability and cognitive impairments.
PSYCHOLOGICAL MEDICINE . 52(14): 3150-3158. Number of citations: 7
-
Mitchell BL, Diaz-Torres S, Bivol S, Cuellar-Partida G, Gerring ZF, Martin NG, Medland SE, Grasby KL, Nyholt DR and Rentería ME.
Elucidating the relationship between migraine risk and brain structure using genetic data.
BRAIN . 145(9): 3214-3224. Number of citations: 10
-
Domingo-Rodriguez, L, Cabana-Domínguez J, Fernandez-Castillo N, Cormand B, Martin-Garcia, E and Maldonado, R.
Differential expression of miR-1249-3p and miR-34b-5p between vulnerable and resilient phenotypes of cocaine addiction
ADDICTION BIOLOGY . 27(5): . Number of citations: 8
-
Antón-Galindo E, Dalla Vecchia E, Orlandi JG, Castro G, Gualda EJ, Young AMJ, Guasch-Piqueras M, Arenas C, Herrera-Úbeda C, Garcia-Fernàndez J, Aguado F, Loza-Alvarez P, Cormand B, Norton WHJ and Fernandez-Castillo N.
Deficiency of the ywhaz gene, involved in neurodevelopmental disorders, alters brain activity and behaviour in zebrafish.
MOLECULAR PSYCHIATRY . 27(9): 3739-3748. Number of citations: 6