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Browsing by Author Ophoff, R.A.

Full Text	Issue Date	Title	Author(s)
	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
	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
	2011	Copy number variations of chromosome 16p13.1 region associated with schizophrenia	Ingason, A.; Rujescu, D.; Cichon, S.; Sigurdsson, E.; Sigmundsson, T., et al
	2011	No association between a common single nucleotide polymorphism, rs4141463, in the MACROD2 gene and autism spectrum disorder.	Curran, S.; Bolton, P.; Rozsnyai, K.; Chiocchetti, A.; Klauck, S.M., 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	European genome-wide association study identifies SLC14A1 as a new urinary bladder cancer susceptibility gene	Rafnar, T.; Vermeulen, H.H.M.; Sulem, P.; Thorleifsson, G.; Aben, K.K.H., et al
	2011	Paternal age and psychiatric disorders: findings from a Dutch population registry.	Buizer-Voskamp, J.E.; Laan, W.; Staal, W.G.; Hennekam, E.A.; Aukes, M.F., et al
	2011	Angiogenin variants in Parkinson disease and amyotrophic lateral sclerosis.	Es, M.A. van; Schelhaas, H.J.; Vught, P.W. van; Ticozzi, N.; Andersen, P.M., et al
	2011	Corrigendum: Genome-wide association study of systemic sclerosis identifies CD247 as a new susceptibility locus.	Radstake, T.R.D.J.; Gorlova, O.; Rueda, B.; Martin, J.E.; Alizadeh, B.Z., 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	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	Identification of novel genetic markers associated with clinical phenotypes of systemic sclerosis through a genome-wide association strategy	Gorlova, O.; Martin, J.E.; Rueda, B.; Koeleman, B.P.; Ying, J., et al
	2011	Genome-wide analysis shows increased frequency of copy number variation deletions in dutch schizophrenia patients	Buizer-Voskamp, J.E.; Muntjewerff, J.W.; Strengman, E.; Sabatti, C.; Stefansson, H., et al
	2011	Effects of season of birth and a common MTHFR gene variant on the risk of schizophrenia	Muntjewerff, J.W.; Ophoff, R.A.; Buizer-Voskamp, J.E.; Strengman, E.; Heijer, M. den
	2010	Genome-wide association study of systemic sclerosis identifies CD247 as a new susceptibility locus.	Radstake, T.R.D.J.; Gorlova, O.; Rueda, B.; Martin, J.E.; Alizadeh, B.Z., et al
	2010	A large genome scan for rare CNVs in amyotrophic lateral sclerosis.	Blauw, H.M.; Al-Chalabi, A.; Andersen, P.M.; Vught, P.W. van; Diekstra, F.P., et al
	2010	Recurrent inversion events at 17q21.31 microdeletion locus are linked to the MAPT H2 haplotype.	Rao, P.N.; Li, W.; Vissers, L.E.L.M.; Veltman, J.A.; Ophoff, R.A.
	2010	FUS mutations in familial amyotrophic lateral sclerosis in the Netherlands.	Groen, E.J.; Es, M.A. van; Vught, P.W. van; Spliet, W.G.; Engelen-Lee, J. van, et al
	2010	A sequence variant at 4p16.3 confers susceptibility to urinary bladder cancer.	Kiemeney, L.A.L.M.; Sulem, P.; Besenbacher, S.; Vermeulen, S.; Sigurdsson, A., et al
	2009	A common variant in DRD3 receptor is associated with autism spectrum disorder.	Krom, M. de; Staal, W.G.; Ophoff, R.A.; Hendriks, J.; Buitelaar, J.K., 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
	2009	Analysis of FGGY as a risk factor for sporadic amyotrophic lateral sclerosis.	Es, M.A. van; Vught, P.W. van; Veldink, J.H.; Andersen, P.M.; Birve, A., 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	A case of ALS-FTD in a large FALS pedigree with a K17I ANG mutation.	Es, M.A. van; Diekstra, F.P.; Veldink, J.H.; Baas, F.; Bourque, P.R., et al
	2008	Genetic variation in DPP6 is associated with susceptibility to amyotrophic lateral sclerosis.	Es, M.A. van; Vught, P.W. van; Blauw, H.M.; Franke, L.; Saris, C.G., et al
	2008	CNTNAP2 gene dosage variation is associated with schizophrenia and epilepsy.	Friedman, J.I.; Vrijenhoek, T.; Markx, S.; Janssen, I.M.; Vliet, W.A. van der, et al
	2008	Recurrent CNVs disrupt three candidate genes in schizophrenia patients.	Vrijenhoek, T.; Buizer-Voskamp, J.E.; Stelt, I van der; Strengman, E.; Sabatti, C., et al
	2008	Large recurrent microdeletions associated with schizophrenia.	Stefansson, H.; Rujescu, D.; Cichon, S.; Pietilainen, O.P.H.; Ingason, A., et al
	2007	ITPR2 as a susceptibility gene in sporadic amyotrophic lateral sclerosis: a genome-wide association study.	Es, M.A. van; Vught, P.W. van; Blauw, H.M.; Franke, L.; Saris, C.G., et al
	1995	Hypokalemic periodic paralysis and the dihydropyridine receptor (CACNL1A3): genotype/phenotype correlations for two predominant mutations and evidence for the absence of a founder effect in 16 caucasian families	Elbaz, A.; Vale-Santos, J.; Jurkat-Rott, K.; Lapie, P.; Ophoff, R.A., et al
	1995	Mutation in DHP receptor alpha1 subunit (CACLN1A3) gene in a Dutch family with hypokalaemic periodic paralysis	Boerman, R.H.; Ophoff, R.A.; Links, T.P.; Eijk, R. van; Sandkuijl, L.A., et al