Wei Chen

发表

Discovering microRNAs from deep sequencing data using miRDeep

N. Rajewsky, M. Friedländer, Wei Chen, 2008, Nature Biotechnology.

Mapping translocation breakpoints by next-generation sequencing.

Martin Vingron, Marcel H. Schulz, Fikret Erdogan, 2008, Genome research.

BMC Genomics BioMed Central Methodology article Estimating accuracy of RNA-Seq and microarrays with proteomics

P. Khaitovich, Wei Chen, Yixue Li, 2022 .

MicroRNAs in brain function and disease

Wei Chen, A. Kuss, 2008, Current neurology and neuroscience reports.

De novo truncating mutations in ASXL3 are associated with a novel clinical phenotype with similarities to Bohring-Opitz syndrome

J. Lupski, R. Gibbs, T. Wienker, 2013, Genome Medicine.

Altered Histone Acetylation Is Associated with Age-Dependent Memory Impairment in Mice

Lennart Opitz, Wei Chen, Laurent Farinelli, 2010, Science.

Array CGH identifies reciprocal 16p13.1 duplications and deletions that predispose to autism and/or mental retardation

Fikret Erdogan, Reinhard Ullmann, Wei Chen, 2007, Human mutation.

A Novel Locus and Candidate Gene for Familial Developmental Dyslexia on Chromosome 4q.

M. Nöthen, J. Ott, Wei Chen, 2020, Zeitschrift fur Kinder- und Jugendpsychiatrie und Psychotherapie.

Deep sequencing reveals 50 novel genes for recessive cognitive disorders

Wei Chen, Reinhard Ullmann, Dagmar Wieczorek, 2011, Nature.

A 3-base pair deletion, c.9711_9713del, in DMD results in intellectual disability without muscular dystrophy

Wei Chen, S. Nabuurs, J. T. Dunnen, 2013, European Journal of Human Genetics.

Hybridisation-based resequencing of 17 X-linked intellectual disability genes in 135 patients reveals novel mutations in ATRX, SLC6A8 and PQBP1

J. Gécz, Wei Chen, R. Reinhardt, 2011, European Journal of Human Genetics.

Characterization of interstitial Xp duplications in two families by tiling path array CGH

Wei Chen, H. Ropers, A. Tzschach, 2008, American journal of medical genetics. Part A.

Comprehensive survey of human brain microRNA by deep sequencing

Na Li, Philipp Khaitovich, Hai Yang Hu, 2010, BMC Genomics.

Genomic analysis of miRNAs in an extreme mammalian hibernator, the Arctic ground squirrel.

P. Khaitovich, Wei Chen, C. Menzel, 2010, Physiological genomics.

Comparative genome hybridization suggests a role for NRXN1 and APBA2 in schizophrenia.

Fikret Erdogan, Reinhard Ullmann, Wei Chen, 2007, Human molecular genetics.

Erratum to: Mutation screening in 86 known X-linked mental retardation genes by droplet-based multiplex PCR and massive parallel sequencing

S. Haas, Wei Chen, H. Richard, 2009, The HUGO Journal.

Mutation screening in 86 known X-linked mental retardation genes by droplet-based multiplex PCR and massive parallel sequencing

Hao Hu, Hugues Richard, Stefan A. Haas, 2009, The HUGO Journal.

Breakpoint analysis of balanced chromosome rearrangements by next-generation paired-end sequencing

Reinhard Ullmann, Wei Chen, Hao Hu, 2010, European Journal of Human Genetics.

ST3GAL3 mutations impair the development of higher cognitive functions.

Wei Chen, H. Ropers, A. Tzschach, 2011, American journal of human genetics.

De novo truncating mutations in ASXL3 are associated with a novel clinical phenotype with similarities to Bohring-Opitz syndrome

J. Lupski, R. Gibbs, T. Wienker, 2013, Genome Medicine.

A Novel Locus and Candidate Gene for Familial Developmental Dyslexia on Chromosome 4q.

M. Nöthen, J. Ott, Wei Chen, 2020, Zeitschrift für Kinder- und Jugendpsychiatrie und Psychotherapie.

Genetics of intellectual disability in consanguineous families

T. Wienker, Wei Chen, R. Herwig, 2019, Molecular Psychiatry.

Homozygosity mapping in consanguineous families reveals extreme heterogeneity of non-syndromic autosomal recessive mental retardation and identifies 8 novel gene loci

Wei Chen, S. Lenzner, H. Ropers, 2007, Human Genetics.

Mutation screening of brain-expressed X-chromosomal miRNA genes in 464 patients with nonsyndromic X-linked mental retardation

J. Gécz, Wei Chen, H. Ropers, 2007, European Journal of Human Genetics.

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

Wei Chen, H. Ropers, C. Spaich, 2007, American Journal of Medical Genetics. Part A.

CGHPRO – A comprehensive data analysis tool for array CGH

Wei Chen, Fikret Erdogan, H.-Hilger Ropers, 2005, BMC Bioinformatics.

A novel X-linked recessive mental retardation syndrome comprising macrocephaly and ciliary dysfunction is allelic to oral–facial–digital type I syndrome

Wei Chen, A. Latos-Bieleńska, H. Omran, 2006, Human Genetics.

Next generation sequencing in a family with autosomal recessive Kahrizi syndrome (OMIM 612713) reveals a homozygous frameshift mutation in SRD5A3

Wei Chen, A. Tzschach, R. Ullmann, 2011, European Journal of Human Genetics.

Estimating accuracy of RNA-Seq and microarrays with proteomics

P. Khaitovich, Wei Chen, Yixue Li, 2009, BMC genomics.

X-exome sequencing of 405 unresolved families identifies seven novel intellectual disability genes

K. Friend, M. Shaw, E. Haan, 2015, Molecular Psychiatry.

High frequency of submicroscopic genomic aberrations detected by tiling path array comparative genome hybridisation in patients with isolated congenital heart disease

Wei Chen, Z. Tümer, N. Tommerup, 2008, Journal of Medical Genetics.