Publications of Andreas W. Kuss
All genres
Journal Article (32)
21.
Journal Article
2 (3), p. 2 - 2 (2010)
A distinctive gene expression fingerprint in mentally retarded male patients reflects disease-causing defects in the histone demethylose KDM5C. Pathogenetics 22.
Journal Article
85 (6), pp. 909 - 915 (2009)
Identification of Mutations in TRAPPC9, which Encodes the NIK- and IKK-β-Binding Protein, in Nonsyndromic Autosomal-Recessive Mental Retardation. American Journal of Human Genetics 23.
Journal Article
5, p. e1000487 - e1000487 (2009)
CA8 Mutations Cause a Novel Syndrome Characterized by Ataxia and Mild Mental Retardation with Predisposition to Quadrupedal Gait. PLoS Genetics 24.
Journal Article
159 (3), pp. 748 - 751 (2008)
Alopecia-mental retardation syndrome: clinical and molecular characterization of four patients. British Journal of Dermatology 25.
Journal Article
146 (3), pp. 337 - 342 (2008)
Chromosome deletions in 13q33-34: Report of four patients and review of the literature. American Journal of Medical Genetics Part A 26.
Journal Article
15 (3), pp. 375 - 378 (2007)
Mutation screening of brain-expressed X-chromosomal miRNA genes in 464 patients with nonsyndromic X-linked mental retardation. European Journal of Human Genetics: EJHG ; the Official Journal of the European Society of Human Genetics 27.
Journal Article
15 (3), pp. 375 - 378 (2007)
Mutation screening of brain-expressed X-chromosomal miRNA genes in 464 patients with nonsyndromic X-linked mental retardation. European Journal of Human Genetics: EJHG ; the Official Journal of the European Society of Human Genetics 28.
Journal Article
121 (1), pp. 43 - 48 (2007)
Homozygosity mapping in consanguineous families reveals extreme heterogeneity of non-syndromic autosomal recessive mental retardation and identifies 8 novel gene loci. Human Genetics 29.
Journal Article
28 (2), pp. 207 - 208 (2007)
Mutation frequencies of X-linked mental retardation genes in families from the EuroMRX consortium. Human Mutation 30.
Journal Article
27 (4), p. 389 - 389 (2006)
Novel JARID1C/SMCX mutations in patients with X-linked mental retardation. Human Mutation 31.
Journal Article
27 (4), p. 389 - 389 (2006)
Novel JARID1C/SMCX mutations in patients with X-linked mental retardation. Human Mutation 32.
Journal Article
118 (6), pp. 708 - 715 (2006)
SNP array-based homozygosity mapping reveals MCPH1 deletion in family with autosomal recessive mental retardation and mild microcephaly. Human Genetics