Publications of Wei Chen
All genres
Journal Article (39)
21.
Journal Article
8 (3), pp. 190 - 197 (2008)
MicroRNAs in brain function and disease. Current Neurology and Neuroscience Reports 22.
Journal Article
26 (4), pp. 407 - 415 (2008)
Discovering microRNAs from deep sequencing data using miRDeep. Nature Biotechnology 23.
Journal Article
18 (7), pp. 1143 - 1149 (2008)
Mapping translocation breakpoints by next-generation sequencing. Genome Research 24.
Journal Article
17 (3), pp. 458 - 465 (2008)
Comparative genome hybridization suggests a role for NRXN1 and APBA2 in schizophrenia. Human Molecular Genetics 25.
Journal Article
131 (4), pp. 918 - 927 (2008)
Epilepsy and mental retardation limited to females: an under-recognized disorder. Brain 26.
Journal Article
146A (2), pp. 197 - 203 (2008)
Characterization of Interstitial Xp duplications in two families by tiling path array CGH. American Journal of Medical Genetics. American Journal of Medical Genetics Part A 27.
Journal Article
28 (7), pp. 674 - 682 (2007)
Array CGH identifies reciprocal 16p13.1 duplications and deletions that predispose to autism and/or mental retardation. Human Mutation: Variation, Databases, and Disease 28.
Journal Article
28 (7) (2007)
Array CGH identifies reciprocal 16p13.1 duplications and deletions that predispose to autism and/or mental retardation. Human Mutation: Variation, Databases, and Disease 29.
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 30.
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 31.
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 32.
Journal Article
143 (2), pp. 172 - 178 (2007)
Characterization of a 5.3 Mb deletion in 15q14 by Comparative Genomic Hybridization using a whole genome ”tiling path” BAC array in a girl with heart defect, cleft palate and developmental delay. American Journal of Medical Genetics Part A 33.
Journal Article
143 (2), pp. 172 - 178 (2007)
Characterization of a 5.3 Mb deletion in 15q14 by Comparative Genomic Hybridization using a whole genome ”tiling path” BAC array in a girl with heart defect, cleft palate and developmental delay. American Journal of Medical Genetics Part A 34.
Journal Article
15 (1), pp. 68 - 75 (2007)
X-linked mental retardation: a comprehensive molecular screen of 47 candidate genes from a 7.4 Mb interval in Xp11. European Journal of Human Genetics: EJHG ; the Official Journal of the European Society of Human Genetics 35.
Journal Article
15 (1), pp. 68 - 75 (2007)
X-linked mental retardation: a comprehensive molecular screen of 47 candidate genes from a 7.4 Mb interval in Xp11. European Journal of Human Genetics: EJHG ; the Official Journal of the European Society of Human Genetics 36.
Journal Article
115 (3-4), pp. 247 - 253 (2006)
Impact of low copy repeats on the generation of balanced and unbalanced chromosomal aberrations in mental retardation. Cytogenetic and Genome Research 37.
Journal Article
115 (3-4), pp. 247 - 253 (2006)
Impact of low copy repeats on the generation of balanced and unbalanced chromosomal aberrations in mental retardation. Cytogenetic and Genome Research 38.
Journal Article
120 (2), pp. 171 - 178 (2006)
A novel X-linked recessive mental retardation syndrome comprising macrocephaly and ciliary dysfunction is allelic to oral-facial-digital type I syndrome. Human Genetics 39.
Journal Article
6 (1), pp. 1471 - 2105 (2005)
: CGHPRO – a comprehensive data analysis tool for array CGH. BMC Bioinformatics Thesis - PhD (1)
40.
Thesis - PhD
Development and application of CGHPRO, a novel software package for retrieving, handling and analysing array CGH data. Dissertation, Freie Universität, Berlin (2006)