Publicaciones
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Zhao L, Zhao W, Cao J and Tu Y.
Causal relationships between migraine and microstructural white matter: a Mendelian randomization study.
JOURNAL OF HEADACHE AND PAIN . 24(1): 10-10. Nº de citas: 13
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Demontis D, Walters GB, Athanasiadis G, Walters R, Therrien K, Nielsen TT, Farajzadeh L, Voloudakis G, Bendl J, Zeng B, Zhang W, Grove J, Als TD, Duan J, Satterstrom FK, Bybjerg-Grauholm J, Bækved-Hansen M, Gudmundsson OO, Magnusson SH, Baldursson G, Davidsdottir K, Haraldsdottir GS, Agerbo E, Hoffman GE, Dalsgaard S, Martin J, Ribasés M, Boomsma DI, Soler Artigas M, Roth Mota N, Howrigan D, Medland SE, Zayats T, Rajagopal VM, Nordentoft M, Mors O, Hougaard DM, Mortensen PB, Daly MJ, Faraone SV, Stefansson H, Roussos P, Franke B, Werge T, Neale BM, Stefansson K and Børglum AD.
Genome-wide analyses of ADHD identify 27 risk loci, refine the genetic architecture and implicate several cognitive domains.
NATURE GENETICS . 55(2): 198-208. Nº de citas: 165
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Vila-Pueyo M, Cuenca-León E, Queirós AC, Kulis M, Sintas C, Cormand B, Martín-Subero JI, Pozo-Rosich P, Fernandez-Castillo N and Macaya A.
Genome-wide DNA methylation analysis in an antimigraine-treated preclinical model of cortical spreading depolarization
Cephalalgia . 43(2): . Nº de citas: 6
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Martinez-Gil N, Patino-Salazar JD, Rabionet-Janssen R, Grinberg-Vaisman DR and Balcells S.
Genome-wide association studies (GWAS) vs functional validation: the challenge of the post-GWAS era
Revista de Osteoporosis y Metabolismo Mineral . 15(1): 29-39. Nº de citas: 1
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Cabana-Domínguez J, Anton-Galindo E, Fernandez-Castillo N, Singgih EL, O'Leary A, Norton WH, Strekalova T, Schenck A, Reif A, Lesch KP, Slattery D and Cormand B.
The translational genetics of ADHD and related phenotypes in model organisms
NEUROSCIENCE AND BIOBEHAVIORAL REVIEWS . 144: 104949-104949. Nº de citas: 4
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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. Nº de citas: 15
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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. Nº de citas: 2
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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. Nº de citas: 18
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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. Nº de citas: 7
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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. Nº de citas: 27