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Browsing by Author Cichon, S.

Full Text	Issue Date	Title	Author(s)
	2012	Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.	Jostins, L.; Ripke, S.; Weersma, R.K.; Duerr, R.H.; McGovern, D.P., et al
	2012	Identification of common variants associated with human hippocampal and intracranial volumes.	Stein, J.L.; Medland, S.E.; Arias Vasquez, A.; Hibar, D.P.; Senstad, R.E., et al
	2012	Replication study and meta-analysis in European samples supports association of the 3p21.1 locus with bipolar disorder	Vassos, E.; Steinberg, S.; Cichon, S.; Breen, G.; Sigurdsson, E., et al
	2011	Common variants at VRK2 and TCF4 conferring risk of schizophrenia	Steinberg, S.; Jong, S. de; Andreassen, O.A.; Werge, T.; Borglum, A.D., et al
	2011	Dual association of a trka polymorphism with schizophrenia	Schijndel, J.E. van; Zweeden, M. van; Loo, K.M.J. van; Djurovic, S.; Andreassen, O.A., et al
	2011	Maternally derived microduplications at 15q11-q13: implication of imprinted genes in psychotic illness	Ingason, A.; Kirov, G.; Giegling, I.; Hansen, T.; Isles, A.R., et al
	2011	Genome-wide association study in German patients with attention deficit/hyperactivity disorder	Hinney, A.; Scherag, A.; Jarick, I.; Albayrak, O.; Putter, C. de, et al
	2011	Expanding the range of ZNF804A variants conferring risk of psychosis	Steinberg, S.; Mors, O.; Borglum, A.D.; Gustafsson, O.; Werge, T., et al
	2011	Copy number variations of chromosome 16p13.1 region associated with schizophrenia	Ingason, A.; Rujescu, D.; Cichon, S.; Sigurdsson, E.; Sigmundsson, T., et al
	2009	Key susceptibility locus for nonsyndromic cleft lip with or without cleft palate on chromosome 8q24.	Birnbaum, S.; Ludwig, K.U.; Reutter, H.; Herms, S.; Steffens, M., et al
	2009	Genomewide association studies: history, rationale, and prospects for psychiatric disorders.	Franke, B.; Buitelaar, J.K.; Cichon, S.; Craddock, N.; Daly, M., et al
	2009	Disruption of the neurexin 1 gene is associated with schizophrenia.	Rujescu, D.; Ingason, A.; Cichon, S.; Pietilainen, O.P.H.; Barnes, M.R., et al
	2009	Common variants conferring risk of schizophrenia.	Stefansson, H.; Ophoff, R.A.; Steinberg, S.; Andreassen, O.A.; Cichon, S., et al
	2009	Genome-wide association study identifies 19p13.3 (UNC13A) and 9p21.2 as susceptibility loci for sporadic amyotrophic lateral sclerosis.	Es, M.A. van; Veldink, J.H.; Saris, C.G.; Blauw, H.M.; Vught, P.W. van, et al
	2008	Large recurrent microdeletions associated with schizophrenia.	Stefansson, H.; Rujescu, D.; Cichon, S.; Pietilainen, O.P.H.; Ingason, A., et al