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A. Weise
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Journal Articles

Inverted Segment Size and the Presence of Recombination Hot Spot Clusters Matter in Sperm Segregation Analysis

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Subject Area:
Genetics
S.S. Bhatt, M. Manvelyan, K. Moradkhani, F. Hunstig, K. Mrasek, J. Puechberty, G. Lefort, P. Sarda, A. Weise, T. Liehr, F. Pellestor
Journal: Cytogenetic and Genome Research
Cytogenet Genome Res (2014) 142 (2): 145–149.
https://doi.org/10.1159/000356142
Published Online: 06 November 2013
View articletitled, Inverted Segment Size and the Presence of Recombination Hot Spot Clusters Matter in Sperm Segregation Analysis
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Journal Articles

Clinical Impact of Somatic Mosaicism in Cases with Small Supernumerary Marker Chromosomes

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Subject Area:
Genetics
T. Liehr, E. Klein, K. Mrasek, N. Kosyakova, R.S. Guilherme, N. Aust, C. Venner, A. Weise, A.B. Hamid
Journal: Cytogenetic and Genome Research
Cytogenet Genome Res (2013) 139 (3): 158–163.
https://doi.org/10.1159/000346026
Published Online: 29 December 2012
View articletitled, Clinical Impact of Somatic Mosaicism in Cases with Small Supernumerary Marker Chromosomes
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Journal Articles

Five Novel Locations of Neocentromeres in Human: 18q22.1, Xq27.1∼27.2, Acro p13, Acro p12, and Heterochromatin of Unknown Origin

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Subject Area:
Genetics
E. Klein, M. Rocchi, A. Ovens-Raeder, N. Kosyakova, A. Weise, M. Ziegler, M. Meins, S. Morlot, W. Fischer, M. Volleth, A. Polityko, C. Mackie Ogilvie, C. Kraus, T. Liehr
Journal: Cytogenetic and Genome Research
Cytogenet Genome Res (2012) 136 (3): 163–166.
https://doi.org/10.1159/000336648
Published Online: 01 March 2012
View articletitled, Five Novel Locations of Neocentromeres in Human: 18q22.1, Xq27.1∼27.2, Acro p13, Acro p12, and Heterochromatin of Unknown Origin
Open the PDF for Five Novel Locations of Neocentromeres in Human: 18q22.1, Xq27.1∼27.2, Acro p13, Acro p12, and Heterochromatin of Unknown Origin in another window
Journal Articles

Is There a Yet Unreported Unbalanced Chromosomal Abnormality without Phenotypic Consequences in Proximal 4p?

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Subject Area:
Genetics
T. Liehr, I. Bartels, B. Zoll, E. Ewers, K. Mrasek, N. Kosyakova, M. Merkas, A.B. Hamid, F. von Eggeling, N. Posorski, A. Weise
Journal: Cytogenetic and Genome Research
Cytogenet Genome Res (2011) 132 (1-2): 121–123.
https://doi.org/10.1159/000316393
Published Online: 20 July 2010
View articletitled, Is There a Yet Unreported Unbalanced Chromosomal Abnormality without Phenotypic Consequences in Proximal 4p?
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Journal Articles

First Case of a Neocentromere Formation in an Otherwise Normal Chromosome 7

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Subject Area:
Genetics
T. Liehr, N. Kosyakova, A. Weise, M. Ziegler, G. Raabe-Meyer
Journal: Cytogenetic and Genome Research
Cytogenet Genome Res (2010) 128 (4): 189–191.
https://doi.org/10.1159/000271471
Published Online: 23 December 2009
View articletitled, First Case of a Neocentromere Formation in an Otherwise Normal Chromosome 7
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Journal Articles

A Neocentric Isochromosome Yp Present as Additional Small Supernumerary Marker Chromosome – Evidence against U-Type Exchange Mechanism?

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Subject Area:
Genetics
F. Sheth, E. Ewers, N. Kosyakova, A. Weise, J. Sheth, S. Patil, M. Ziegler, T. Liehr
Journal: Cytogenetic and Genome Research
Cytogenet Genome Res (2009) 125 (2): 115–116.
https://doi.org/10.1159/000227835
Published Online: 31 August 2009
View articletitled, A Neocentric Isochromosome Yp Present as Additional Small Supernumerary Marker Chromosome – Evidence against U-Type Exchange Mechanism?
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Journal Articles

10p11.2 to 10q11.2 is a yet unreported region leading to unbalanced chromosomal abnormalities without phenotypic consequences

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Subject Area:
Genetics
T. Liehr, M. Stumm, R.D. Wegner, S. Bhatt, P. Hickmann, P.C. Patsalis, M. Meins, S. Morlot, V. Klaschka, E. Ewers, S. Hinreiner, K. Mrasek, N. Kosyakova, W.W. Cai, S.W. Cheung, A. Weise
Journal: Cytogenetic and Genome Research
Cytogenet Genome Res (2009) 124 (1): 102–105.
https://doi.org/10.1159/000200094
Published Online: 15 April 2009
View articletitled, 10p11.2 to 10q11.2 is a yet unreported region leading to unbalanced chromosomal abnormalities without phenotypic consequences
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Journal Articles

A new unbalanced chromosomal abnormality in 1q31.1 to 1q32 without phenotypic consequences

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Subject Area:
Genetics
K. Mrasek, G. Krüger, I. Bauer, J. Müller-Navia, T. Liehr, A. Weise
Journal: Cytogenetic and Genome Research
Cytogenet Genome Res (2008) 121 (3-4): 286–287.
https://doi.org/10.1159/000138899
Published Online: 29 August 2008
View articletitled, A new unbalanced chromosomal abnormality in 1q31.1 to 1q32 without phenotypic consequences
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Journal Articles

Neocentric small supernumerary marker chromosomes (sSMC) – three more cases and review of the literature

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Subject Area:
Genetics
T. Liehr, G.E. Utine, U. Trautmann, A. Rauch, A. Kuechler, J. Pietracz, E. Bocian, N. Kosyakova, K. Mrasek, K. Boduroglu, A. Weise, D. Aktas
Journal: Cytogenetic and Genome Research
Cytogenet Genome Res (2007) 118 (1): 31–37.
https://doi.org/10.1159/000106438
Published Online: 27 September 2007
View articletitled, Neocentric small supernumerary marker chromosomes (sSMC) – three more cases and review of the literature
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Journal Articles

Supernumerary marker chromosome 5 diagnosed by M-FISH in a child with congenital heart defect and unusual face

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Subject Area:
Genetics
C. Sarri, Y. Gyftodimou, M. Grigoriadou, E. Pandelia, S. Kalogirou, H. Kokotas, K. Mrasek, A. Weise, M.B. Petersen
Journal: Cytogenetic and Genome Research
Cytogenet Genome Res (2006) 114 (3-4): 330–337.
https://doi.org/10.1159/000094222
Published Online: 01 September 2006
View articletitled, Supernumerary marker chromosome 5 diagnosed by M-FISH in a child with congenital heart defect and unusual face
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Journal Articles

Multicolor fluorescence in situ hybridization (FISH) applied to FISH-banding

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Subject Area:
Genetics
T. Liehr, H. Starke, A. Heller, N. Kosyakova, K. Mrasek, M. Gross, C. Karst, U. Steinhaeuser, F. Hunstig, I. Fickelscher, A. Kuechler, V. Trifonov, S.A. Romanenko, A. Weise
Journal: Cytogenetic and Genome Research
Cytogenet Genome Res (2006) 114 (3-4): 240–244.
https://doi.org/10.1159/000094207
Published Online: 01 September 2006
View articletitled, Multicolor fluorescence in situ hybridization (FISH) applied to FISH-banding
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Journal Articles

Multicolor FISH used for the characterization of small supernumerary marker chromosomes (sSMC) in commercially available immortalized cell lines

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Subject Area:
Genetics
L. Brecevic, S. Michel, H. Starke, K. Müller, N. Kosyakova, K. Mrasek, A. Weise, T. Liehr
Journal: Cytogenetic and Genome Research
Cytogenet Genome Res (2006) 114 (3-4): 319–324.
https://doi.org/10.1159/000094220
Published Online: 01 September 2006
View articletitled, Multicolor FISH used for the characterization of small supernumerary marker chromosomes (sSMC) in commercially available immortalized cell lines
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Journal Articles

Small supernumerary marker chromosomes – progress towards a genotype-phenotype correlation

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Subject Area:
Genetics
T. Liehr, K. Mrasek, A. Weise, A. Dufke, L. Rodríguez, N. Martínez Guardia, A. Sanchís, J.R. Vermeesch, C. Ramel, A. Polityko, O.A. Haas, J. Anderson, U. Claussen, F. von Eggeling, H. Starke
Journal: Cytogenetic and Genome Research
Cytogenet Genome Res (2006) 112 (1-2): 23–34.
https://doi.org/10.1159/000087510
Published Online: 03 November 2005
View articletitled, Small supernumerary marker chromosomes – progress towards a genotype-phenotype correlation
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Journal Articles

A molecular cytogenetic study of chromosome evolution in chimpanzee

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Subject Area:
Genetics
M. Gross, H. Starke, V. Trifonov, U. Claussen, T. Liehr, A. Weise
Journal: Cytogenetic and Genome Research
Cytogenet Genome Res (2006) 112 (1-2): 67–75.
https://doi.org/10.1159/000087515
Published Online: 03 November 2005
View articletitled, A molecular cytogenetic study of chromosome evolution in chimpanzee
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Journal Articles

New insights into the evolution of chromosome 1

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Subject Area:
Genetics
A. Weise, H. Starke, K. Mrasek, U. Claussen, T. Liehr
Journal: Cytogenetic and Genome Research
Cytogenet Genome Res (2005) 108 (1-3): 217–222.
https://doi.org/10.1159/000080819
Published Online: 12 November 2004
View articletitled, New insights into the evolution of chromosome 1
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Journal Articles

The hierarchically organized splitting of chromosome bands into sub-bands analyzed by multicolor banding (MCB)

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Subject Area:
Genetics
H. Lehrer, A. Weise, S. Michel, H. Starke, K. Mrasek, A. Heller, A. Kuechler, U. Claussen, T. Liehr
Journal: Cytogenetic and Genome Research
Cytogenet Genome Res (2004) 105 (1): 25–28.
https://doi.org/10.1159/000078005
Published Online: 15 June 2004
View articletitled, The hierarchically organized splitting of chromosome bands into sub-bands analyzed by multicolor banding (MCB)
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Journal Articles

De novo 9-break-event in one chromosome 21 combined with a microdeletion in 21q22.11 in a mentally retarded boy with short stature

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Subject Area:
Genetics
A. Weise, O. Rittinger, H. Starke, M. Ziegler, U. Claussen, T. Liehr
Journal: Cytogenetic and Genome Research
Cytogenet Genome Res (2003) 103 (1-2): 14–16.
https://doi.org/10.1159/000076284
Published Online: 30 March 2004
View articletitled, De novo 9-break-event in one chromosome 21 combined with a microdeletion in 21q22.11 in a mentally retarded boy with short stature
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Journal Articles

Multitude multicolor chromosome banding (mMCB) – a comprehensive one-step multicolor FISH banding method

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Subject Area:
Genetics
A. Weise, A. Heller, H. Starke, K. Mrasek, A. Kuechler, B.L. Pool-Zobel, U. Claussen, T. Liehr
Journal: Cytogenetic and Genome Research
Cytogenet Genome Res (2003) 103 (1-2): 34–39.
https://doi.org/10.1159/000076286
Published Online: 30 March 2004
View articletitled, Multitude multicolor chromosome banding (mMCB) – a comprehensive one-step multicolor FISH banding method
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Journal Articles

Comparative M-FISH and CGH analyses in sensitive and drug-resistant human T-cell acute leukemia cell lines

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Subject Area:
Genetics
A. Weise, T. Liehr, T. Efferth, A. Kuechler, E. Gebhart
Journal: Cytogenetic and Genome Research
Cytogenetics and Cell Genetics (2002) 98 (2-3): 118–125.
https://doi.org/10.1159/000069808
Published Online: 14 April 2003
View articletitled, Comparative M-FISH and CGH analyses in sensitive and drug-resistant human T-cell acute leukemia cell lines
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Journal Articles

A novel family-specific translocation t(2;20)(p24.1;q13.1) associated with recurrent abortions: molecular characterization and segregation analysis in male meiosis

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Subject Area:
Genetics
R. Trappe, D. Böhm, J. Kohlhase, A. Weise, T. Liehr, G. Essers, M. Meins,, B. Zoll, I. Bartels, P. Burfeind
Journal: Cytogenetic and Genome Research
Cytogenetics and Cell Genetics (2002) 98 (1): 1–8.
https://doi.org/10.1159/000068533
Published Online: 13 February 2003
View articletitled, A novel family-specific translocation t(2;20)(p24.1;q13.1) associated with recurrent abortions: molecular characterization and segregation analysis in male meiosis
Open the PDF for A novel family-specific translocation t(2;20)(p24.1;q13.1) associated with recurrent abortions: molecular characterization and segregation analysis in male meiosis in another window