C. Menzel

发表

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 .

MicroRNA, mRNA, and protein expression link development and aging in human and macaque brain.

M. Lachmann, P. Khaitovich, Hao Hu, 2010, Genome research.

Mutations in autism susceptibility candidate 2 (AUTS2) in patients with mental retardation

N. Tommerup, H. Ropers, E. Niebuhr, 2007, Human Genetics.

Disruption of the serine/threonine kinase 9 gene causes severe X-linked infantile spasms and mental retardation.

E. Haan, J. Gécz, N. Tommerup, 2003, American journal of human genetics.

Mutations in the ZNF41 gene are associated with cognitive deficits: identification of a new candidate for X-linked mental retardation.

H. Ropers, B. Echenne, M. Partington, 2003, American journal of human genetics.

MicroRNA Expression and Regulation in Human, Chimpanzee, and Macaque Brains

S. Pääbo, P. Khaitovich, C. Menzel, 2011, PLoS genetics.

Molecular cytogenetic analysis of a de novo interstitial deletion of 5q23.3q31.2 and its phenotypic consequences

H. Scherthan, H. Ropers, V. Kalscheuer, 2006, American journal of medical genetics. Part A.

Molecular cloning of Xp11 breakpoints in two unrelated mentally retarded females with X;autosome translocations

A. Rosenthal, N. Tommerup, H. Ropers, 2000, Cytogenetic and Genome Research.

Characterization of a 16 Mb interstitial chromosome 7q21 deletion by tiling path array CGH

H. Ropers, V. Kalscheuer, A. Tzschach, 2007, American journal of medical genetics. Part A.

Characterization of an interstitial 4q32 deletion in a patient with mental retardation and a complex chromosome rearrangement

H. Ropers, V. Kalscheuer, A. Tzschach, 2010, 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.

Impact of low copy repeats on the generation of balanced and unbalanced chromosomal aberrations in mental retardation

V. Kalscheuer, C. Menzel, R. Ullmann, 2006, Cytogenetic and Genome Research.

Sequence features associated with microRNA strand selection in humans and flies

P. Khaitovich, Wei Chen, C. Menzel, 2009, BMC Genomics.

Disruption of Netrin G1 by a balanced chromosome translocation in a girl with Rett syndrome

H. Firth, N. Tommerup, M. Ferguson-Smith, 2005, European Journal of Human Genetics.

Truncation of the Down syndrome candidate gene DYRK1A in two unrelated patients with microcephaly.

Reinhard Ullmann, Zeynep Tümer, Niels Tommerup, 2008, American journal of human genetics.

aging in human and macaque brain MicroRNA , mRNA , and protein expression link development and Material

M. Lachmann, P. Khaitovich, Hao Hu, 2010 .

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.

Disruption of the TCF4 gene in a girl with mental retardation but without the classical Pitt–Hopkins syndrome

H. Ropers, C. V. van Ravenswaaij-Arts, D. Smeets, 2008, American journal of medical genetics. Part A.

Intergenic and Repeat Transcription in Human, Chimpanzee and Macaque Brains Measured by RNA-Seq

Na Li, Hao Hu, Zheng Yan, 2010, PLoS Comput. Biol..

A balanced chromosomal translocation disrupting ARHGEF9 is associated with epilepsy, anxiety, aggression, and mental retardation

Reinhard Ullmann, Cheng Fang, Kirsten Harvey, 2009, Human mutation.

A cryptic deletion of 2q35 including part of the PAX3 gene detected by breakpoint mapping in a child with autism and a de novo 2;8 translocation

L. Willatt, N. Tommerup, M. Ferguson-Smith, 2002, Journal of medical genetics.

Systematic characterisation of disease associated balanced chromosome rearrangements by FISH: cytogenetically and genetically anchored YACs identify microdeletions and candidate regions for mental retardation genes

N. Tommerup, T. Haaf, C. Menzel, 1999, Journal of medical genetics.

Hypergonadotropic hypogonadism in a patient with inv ins (2;4).

V. Kalscheuer, A. Tzschach, C. Menzel, 2009, International journal of andrology.

Blepharophimosis-Ptosis-Epicanthus Inversus Syndrome in a Girl with Chromosome Translocation t(2;3)(q33;q23)

H. Ropers, V. Kalscheuer, A. Tzschach, 2008, Ophthalmic genetics.

A translocation breakpoint cluster disrupts the newly defined 3' end of the SNURF-SNRPN transcription unit on chromosome 15.

A. Hüttenhofer, N. Tommerup, H. Ropers, 2001, Human molecular genetics.

Breakpoints around the HOXD cluster result in various limb malformations

S. Mundlos, A. Silahtaroglu, Z. Tümer, 2005, Journal of Medical Genetics.

Truncation of the CNS-expressed JNK3 in a patient with a severe developmental epileptic encephalopathy

B. Dan, H. Ropers, V. Kalscheuer, 2005, Human Genetics.

Heterotaxy and cardiac defect in a girl with chromosome translocation t(X;1)(q26;p13.1) and involvement of ZIC3

H. Ropers, V. Kalscheuer, A. Tzschach, 2006, European Journal of Human Genetics.

Molecular cytogenetic analysis of a de novo interstitial chromosome 10q22 deletion

H. Ropers, V. Kalscheuer, A. Tzschach, 2006, American Journal of Medical Genetics. Part A.

Estimating accuracy of RNA-Seq and microarrays with proteomics

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