Publications by authors named "Corinna Menzel"

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MicroRNA expression and regulation in human, chimpanzee, and macaque brains.
Hai Yang Hu, Song Guo, Jiang Xi, Zheng Yan, Ning Fu, Corinna Menzel

PLoS Genet· October 2011

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Genomic analysis of miRNAs in an extreme mammalian hibernator, the Arctic ground squirrel.
Yuting Liu, Wenchao Hu, Haifang Wang, Minghua Lu, Chunxuan Shao, Corinna Menzel

Physiol Genomics· September 2010

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MicroRNA, mRNA, and protein expression link development and aging in human and macaque brain.
Mehmet Somel, Song Guo, Ning Fu, Zheng Yan, Hai Yang Hu, Corinna Menzel

Genome Res· September 2010

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Intergenic and repeat transcription in human, chimpanzee and macaque brains measured by RNA-Seq.
Augix Guohua Xu, Liu He, Zhongshan Li, Ying Xu, Mingfeng Li, Corinna Menzel

PLoS Comput Biol· July 2010

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Comprehensive survey of human brain microRNA by deep sequencing.
Ning-Yi Shao, Hai Yang Hu, Zheng Yan, Ying Xu, Hao Hu, Corinna Menzel

BMC Genomics· June 2010

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Breakpoint analysis of balanced chromosome rearrangements by next-generation paired-end sequencing.
Wei Chen, Reinhard Ullmann, Claudia Langnick, Corinna Menzel, Zofia Wotschofsky

Eur J Hum Genet· May 2010

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Characterization of an interstitial 4q32 deletion in a patient with mental retardation and a complex chromosome rearrangement.
Andreas Tzschach, Corinna Menzel, Fikret Erdogan, Erman Salih Istifli, Martin Rieger

Am J Med Genet A· April 2010

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Mutation screening in 86 known X-linked mental retardation genes by droplet-based multiplex PCR and massive parallel sequencing.
Hao Hu, Klaus Wrogemann, Vera Kalscheuer, Andreas Tzschach, Hugues Richard, Corinna Menzel

Hugo J· December 2009

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Erratum to: Mutation screening in 86 known X-linked mental retardation genes by droplet-based multiplex PCR and massive parallel sequencing.
Hao Hu, Klaus Wrogemann, Vera Kalscheuer, Andreas Tzschach, Hugues Richard, Corinna Menzel

Hugo J· December 2009

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Sequence features associated with microRNA strand selection in humans and flies.
Hai Yang Hu, Zheng Yan, Ying Xu, Hao Hu, Corinna Menzel

BMC Genomics· September 2009

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Estimating accuracy of RNA-Seq and microarrays with proteomics.
Xing Fu, Ning Fu, Song Guo, Zheng Yan, Ying Xu, Corinna Menzel

BMC Genomics· April 2009

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A balanced chromosomal translocation disrupting ARHGEF9 is associated with epilepsy, anxiety, aggression, and mental retardation.
Vera M Kalscheuer, Luciana Musante, Cheng Fang, Kirsten Hoffmann, Celine Fuchs, Corinna Menzel

Hum Mutat· January 2009

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Disruption of the TCF4 gene in a girl with mental retardation but without the classical Pitt-Hopkins syndrome.
Vera M Kalscheuer, Ilse Feenstra, Conny M A Van Ravenswaaij-Arts, Dominique F C M Smeets, Corinna Menzel

Am J Med Genet A· August 2008

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Mapping translocation breakpoints by next-generation sequencing.
Wei Chen, Vera Kalscheuer, Andreas Tzschach, Corinna Menzel, Reinhard Ullmann

Genome Res· July 2008

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Truncation of the Down syndrome candidate gene DYRK1A in two unrelated patients with microcephaly.
Rikke S Møller, Sabine Kübart, Maria Hoeltzenbein, Babett Heye, Ida Vogel, Corinna Menzel

Am J Hum Genet· May 2008

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Blepharophimosis-ptosis-epicanthus inversus syndrome in a girl with chromosome translocation t(2;3)(q33;q23).
Andreas Tzschach, Christina Kelbova, Sabine Weidensee, Hartmut Peters, Hans-Hilger Ropers, Corinna Menzel

Ophthalmic Genet· March 2008

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Mutations in autism susceptibility candidate 2 (AUTS2) in patients with mental retardation.
Vera M Kalscheuer, David FitzPatrick, Niels Tommerup, Merete Bugge, Erik Niebuhr, Corinna Menzel

Hum Genet· May 2007

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Characterization of a 16 Mb interstitial chromosome 7q21 deletion by tiling path array CGH.
Andreas Tzschach, Corinna Menzel, Fikret Erdogan, Marei Schubert, Maria Hoeltzenbein

Am J Med Genet A· February 2007

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Heterotaxy and cardiac defect in a girl with chromosome translocation t(X;1)(q26;p13.1) and involvement of ZIC3.
Andreas Tzschach, Maria Hoeltzenbein, Kirsten Hoffmann, Corinna Menzel, Alexander Beyer

Eur J Hum Genet· December 2006

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Molecular cytogenetic analysis of a de novo interstitial chromosome 10q22 deletion.
Andreas Tzschach, Ines Krause-Plonka, Corinna Menzel, Andreas Knoblauch, Holger Toennies

Am J Med Genet A· May 2006

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Molecular cytogenetic analysis of a de novo interstitial deletion of 5q23.3q31.2 and its phenotypic consequences.
Andreas Tzschach, Ines Krause-Plonka, Corinna Menzel, Vera Kalscheuer, Holger Toennies

Am J Med Genet A· March 2006

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Truncation of the CNS-expressed JNK3 in a patient with a severe developmental epileptic encephalopathy.
Sarah A Shoichet, Laurence Duprez, Olivier Hagens, Vicki Waetzig, Corinna Menzel

Hum Genet· January 2006

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Disruption of Netrin G1 by a balanced chromosome translocation in a girl with Rett syndrome.
Isabella Borg, Kristine Freude, Sabine Kübart, Kirsten Hoffmann, Corinna Menzel

Eur J Hum Genet· August 2005

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Mutations in the ZNF41 gene are associated with cognitive deficits: identification of a new candidate for X-linked mental retardation.
Sarah A Shoichet, Kirsten Hoffmann, Corinna Menzel, Udo Trautmann, Bettina Moser

Am J Hum Genet· December 2003

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Disruption of the serine/threonine kinase 9 gene causes severe X-linked infantile spasms and mental retardation.
Vera M Kalscheuer, Jiong Tao, Andrew Donnelly, Georgina Hollway, Eberhard Schwinger, Corinna Menzel

Am J Hum Genet· June 2003

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