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Conference Papers

Hesam-Shariati S; Overs B; Toma C; Watkeys O; Green M; Roberts G; Leung V; Stuart A; Schofield PR; Mitchell PB; Fullerton J, 2019, 'EPIGENOME-WIDE ASSOCIATION STUDY (EWAS) OF YOUNG PEOPLE WITH FAMILIAL RISK OF BIPOLAR DISORDER', in EUROPEAN NEUROPSYCHOPHARMACOLOGY, ELSEVIER, CA, Los Angeles, pp. S192 - S192, presented at 27th World Congress of Psychiatric Genetics (WCPG), CA, Los Angeles, 26 October 2019 - 31 October 2019, http://dx.doi.org/10.1016/j.euroneuro.2019.08.149

Fullerton J; toma C; shaw A; allcock R; mitchell P; schofield P; Schofield P, 2015, 'Addressing Rare Variant Contributions to the Genetic Architecture of Bipolar Disorder, Utilizing Extended Families with Highly Penetrant Forms of Illness', in European Neuropsychopharmacology, ELSEVIER SCIENCE BV, Toronto, Canada, pp. S293 - S293, presented at XXIII World Congress of Psychiatric Genetics, Toronto, Canada, 28 October 2015 - 30 October 2015, http://dx.doi.org/10.1016/j.euroneuro.2015.09.009

Sintas C; Carreno O; Corominas R; Serra SA; Vila M; Fernandez-Castillo N; Toma C; Pons R; Llaneza M; Sobrido MJ; Grinberg D; Valverde MA; Fernandez-Fernandez JM; Macaya A; Cormand B, 2013, 'Screening of cacna1a and ATP1A2 genes in hemiplegic migraine: clinical, genetic and functional studies', in JOURNAL OF HEADACHE AND PAIN, SPRINGER-VERLAG ITALIA SRL, http://dx.doi.org/10.1186/1129-2377-14-S1-P26

Perez-Duenas B; Ormazabal A; Toma C; Torrico B; Cormand B; Serrano M; Sierra C; De Grandis E; Pineda M; Campistol J; Garcia-Cazorla A; Artuch R, 2010, 'CEREBRAL FOLATE DEFICIENCY AND DISEASES OF THE CENTRAL NERVOUS SYSTEM IN CHILDHOOD', in JOURNAL OF INHERITED METABOLIC DISEASE, SPRINGER, pp. S159 - S159, https://www.webofscience.com/api/gateway?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000281735000510&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=891bb5ab6ba270e68a29b250adbe88d1

Bacchelli E; Blasi F; Carone S; Toma C; Lamb J; Sykes N; Barnby G; Morris A; Winchester L; Butler H; Bailey AJ; Monaco AP; Maestrini E, 2006, 'A gene centric association study of 1500 SNPs in the chromosome 2q autism susceptibility locus', in AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS, WILEY-LISS, ITALY, Cagliari, pp. 767 - 768, presented at 14th World Congress on Psychiatric Genetics, ITALY, Cagliari, 28 October 2006 - 01 November 2006, https://www.webofscience.com/api/gateway?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000240877700370&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=891bb5ab6ba270e68a29b250adbe88d1


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