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Browsing by Author Jensen, L.R.

Full Text	Issue Date	Title	Author(s)
	2011	Hybridisation-based resequencing of 17 X-linked intellectual disability genes in 135 patients reveals novel mutations in ATRX, SLC6A8 and PQBP1	Jensen, L.R.; Chen, W.; Moser, B.; Lipkowitz, B.; Schroeder, C., et al
	2010	A distinctive gene expression fingerprint in mentally retarded male patients reflects disease-causing defects in the histone demethylase KDM5C.	Jensen, L.R.; Bartenschlager, H.; Rujirabanjerd, S.; Tzschach, A.; Numann, A., et al
	2008	MCT8 mutation analysis and identification of the first female with Allan-Herndon-Dudley syndrome due to loss of MCT8 expression.	Frints, S.G.; Lenzner, S.; Bauters, M.; Jensen, L.R.; Esch, H. van, et al
	2007	X-linked mental retardation: a comprehensive molecular screen of 47 candidate genes from a 7.4 Mb interval in Xp11.	Jensen, L.R.; Lenzner, S.; Moser, B.; Freude, K.; Tzschach, A., et al
	2007	Mutation frequencies of X-linked mental retardation genes in families from the EuroMRX consortium.	Brouwer, A.P.M. de; Yntema, H.G.; Kleefstra, T.; Lugtenberg, D.; Oudakker, A.R., et al
	2007	Mutation screening of brain-expressed X-chromosomal miRNA genes in 464 patients with nonsyndromic X-linked mental retardation.	Chen, W.; Jensen, L.R.; Gecz, J.; Fryns, J.P.; Moraine, C., et al
	2006	Chromosomal copy number changes in patients with non-syndromic X linked mental retardation detected by array CGH.	Lugtenberg, D.; Brouwer, A.P.M. de; Kleefstra, T.; Oudakker, A.R.; Frints, S.G., et al
	2006	Novel JARID1C/SMCX mutations in patients with X-linked mental retardation.	Tzschach, A.; Lenzner, S.; Moser, B.; Reinhardt, R.; Chelly, J., et al
	2005	Mutations in the JARID1C gene, which is involved in transcriptional regulation and chromatin remodeling, cause X-linked mental retardation.	Jensen, L.R.; Amende, M.; Gurok, U.; Moser, B.; Gimmel, V., et al
	2004	Mutations in the FTSJ1 gene coding for a novel S-adenosylmethionine-binding protein cause nonsyndromic X-linked mental retardation.	Freude, K.; Hoffmann, K.; Jensen, L.R.; Delatycki, M.B.; Portes, V. des, et al