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Gabriele Senger

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Gene Amplification

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Thomas Liehr; Heike Starke; Gabriele Senger; Cindy Melotte; Anja Weise; Joris R Vermeesch
Overrepresentation of small supernumerary marker chromosomes (sSMC) from chromosome 6 origin in cases with multiple sSMC.
Ilse Chudoba; Gabriele Hickmann; T Friedrich; A Jauch; Peter Kozlowski; Gabriele Senger
mBAND: a high resolution multicolor banding technique for the detection of complex intrachromosomal aberrations.
Jörg Seidel; Anita Heller; Gabriele Senger; Heike Starke; Ilse Chudoba; Christine Kelbova; Holger Tönnies; Heidemarie Neitzel; Claudia Haase; Volkmar Beensen; Felix Zintl; Uwe Claussen; Thomas Liehr
A multiple translocation event in a patient with hexadactyly, facial dysmorphism, mental retardation and behaviour disorder characterised comprehensively by molecular cytogenetics. Case report and review of the literature.

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All Publications

2006: Thomas Liehr; Heike Starke; Gabriele Senger; Cindy Melotte; Anja Weise; Joris R Vermeesch
Overrepresentation of small supernumerary marker chromosomes (sSMC) from chromosome 6 origin in cases with multiple sSMC.
American journal of medical genetics. Part A 2006;140(1):46-51.
2004: Ilse Chudoba; Gabriele Hickmann; T Friedrich; A Jauch; Peter Kozlowski; Gabriele Senger
mBAND: a high resolution multicolor banding technique for the detection of complex intrachromosomal aberrations.
Cytogenetic and genome research 2004;104(1-4):390-3.
2003: Jörg Seidel; Anita Heller; Gabriele Senger; Heike Starke; Ilse Chudoba; Christine Kelbova; Holger Tönnies; Heidemarie Neitzel; Claudia Haase; Volkmar Beensen; Felix Zintl; Uwe Claussen; Thomas Liehr
A multiple translocation event in a patient with hexadactyly, facial dysmorphism, mental retardation and behaviour disorder characterised comprehensively by molecular cytogenetics. Case report and review of the literature.
European journal of pediatrics 2003;162(9):582-8.
2003: Thomas Liehr; Heike Starke; Anita Heller; Anja Weise; Volkmar Beensen; Gabriele Senger; Gabriele Kittner; M Prechtel; Uwe Claussen; Jörg Seidel
Evidence for a new microdeletion syndrome in 15q21.
International journal of molecular medicine 2003;11(5):575-7.
2003: Miriam Spiegel; Gabriele Hickmann; Gabriele Senger; Peter Kozlowski; Oliver Bartsch
Two new cases of analphoid marker chromosomes.
American journal of medical genetics. Part A 2003;116A(3):284-9.
2002: Heike Starke; Jörg Seidel; Wolfram Henn; Sylvia Reichardt; Marianne Volleth; Markus Stumm; Christine Behrend; Klaus R Sandig; Christine Kelbova; Gabriele Senger; Beate Albrecht; Ingo Hansmann; Anita Heller; Uwe Claussen; Thomas Liehr
Homologous sequences at human chromosome 9 bands p12 and q13-21.1 are involved in different patterns of pericentric rearrangements.
European journal of human genetics : EJHG 2002;10(12):790-800.
2001: Heike Starke; Gabriele Senger; M Kossakiewicz; H Tittelbach; D Rau; Nikolai Rubtsov; Vladimir Trifonov; Anita Heller; Isabell Hartmann; Uwe Claussen; Thomas Liehr
Maternal insertion of 18q11.2-q12.2 in 18p11.3 of the same chromosome analysed by microdissection and multicolour banding (MCB).
Prenatal diagnosis 2001;21(12):1049-52.
2001: Johannes Lemke; Ilse Chudoba; Gabriele Senger; Markus Stumm; I F Loncarevic; C Henry; B Zabel; Uwe Claussen
Improved definition of chromosomal breakpoints using high-resolution multicolour banding.
Human genetics 2001;108(6):478-83.
2000: Anita Heller; Jörg Seidel; Axel Hübler; Heike Starke; Volkmar Beensen; Gabriele Senger; M Rocchi; Jutta Wirth; Ilse Chudoba; Uwe Claussen; Thomas Liehr
Molecular cytogenetic characterisation of partial trisomy 9q in a case with pyloric stenosis and a review.
Journal of medical genetics 2000;37(7):529-32.
2000: Anita Heller; Ilse Chudoba; C Bleck; Gabriele Senger; Uwe Claussen; Thomas Liehr
Microdissection based comparative genomic hybridization analysis (micro-CGH) of secondary acute myelogenous leukemias.
International journal of oncology 2000;16(3):461-8.
2000: Susanne Röttger; Katrin Schiebel; Gabriele Senger; S Ebner; Werner Schempp; Gerd Scherer
An SRY-negative 47,XXY mother and daughter.
Cytogenetics and cell genetics 2000;91(1-4):204-7.
1999: Ilse Chudoba; Y Franke; Gabriele Senger; G Sauerbrei; S Demuth; Volkmar Beensen; Annett Neumann; Ingo Hansmann; Uwe Claussen
Maternal UPD 20 in a hyperactive child with severe growth retardation.
European journal of human genetics : EJHG 1999;7(5):533-40.
1999: Ilse Chudoba; A Plesch; T Lörch; Johannes Lemke; Uwe Claussen; Gabriele Senger
High resolution multicolor-banding: a new technique for refined FISH analysis of human chromosomes.
Cytogenetics and cell genetics 1999;84(3-4):156-60.
1997: Gabriele Senger; Ilse Chudoba; UK Friedrich; Niels Tommerup; Uwe Claussen; Karen Brøndum-Nielsen
Prenatal diagnosis of a half-cryptic translocation using chromosome microdissection.
Prenatal diagnosis 1997;17(4):369-74.
1996: N Rubtsov; Gabriele Senger; H Kuzcera; A Neumann; C Kelbova; Kerstin Junker; Volkmar Beensen; Uwe Claussen
Interstitial deletion of chromosome 6q: precise definition of the breakpoints by microdissection, DNA amplification, and reverse painting.
Human genetics 1996;97(6):705-9.
1996: Gabriele Senger
YAC localization by fluorescence in situ hybridization.
Methods in molecular biology (Clifton, N.J.) 1996;54():87-96.
1994: Johannes Wienberg; Anna Jauch; Hermann-Josef Lüdecke; Gabriele Senger; Bernhard Horsthemke; Uwe Claussen; Thomas Cremer; Norbert Arnold; Christoph Lengauer
The origin of human chromosome 2 analyzed by comparative chromosome mapping with a DNA microlibrary.
Chromosome research : an international journal on the molecular, supramolecular and evolutionary aspects of chromosome biology 1994;2(5):405-10.
1994: Walter Bardenheuer; S Szymanski; A Lux; Hermann-Josef Lüdecke; Bernhard Horsthemke; Uwe Claussen; Gabriele Senger; David I Smith; N D Wang; D LePaslier
Characterization of a microdissection library from human chromosome region 3p14.
Genomics 1994;19(2):291-7.
1992: A Puech; L Ahnine; Hermann-Josef Lüdecke; Gabriele Senger; Alasdair Ivens; Cécile Jeanpierre; P Little; Bernhard Horsthemke; Uwe Claussen; C Jones
11p15.5-specific libraries for identification of potential gene sequences involved in Beckwith-Wiedemann syndrome and tumorigenesis.
Genomics 1992;13(4):1274-80.
1991: G Hampton; G Leuteritz; Hermann-Josef Lüdecke; Gabriele Senger; U Trautmann; H Thomas; E Solomon; W F Bodmer; Bernhard Horsthemke; Uwe Claussen
Characterization and mapping of microdissected genomic clones from the adenomatous polyposis coli (APC) region.
Genomics 1991;11(2):247-51.
1991: U Trautmann; G Leuteritz; Gabriele Senger; Uwe Claussen; Wolfgang G Ballhausen
Detection of APC region-specific signals by nonisotopic chromosomal in situ suppression (CISS)-hybridization using a microdissection library as a probe.
Human genetics 1991;87(4):495-7.
1991: W Fiedler; Uwe Claussen; Hermann-Josef Lüdecke; Gabriele Senger; Bernhard Horsthemke; A Geurts Van Kessel; W Goertzen; R Fahsold
New markers for the neurofibromatosis-2 region generated by microdissection of chromosome 22.
Genomics 1991;10(3):786-91.
1991: L M Davis; Bernhard Zabel; Gabriele Senger; Hermann-Josef Lüdecke; B Metzroth; K Call; D Housman; Uwe Claussen; Bernhard Horsthemke; TB Shows
A tumor chromosome rearrangement further defines the 11p13 Wilms tumor locus.
Genomics 1991;10(3):588-92.
1991: Uwe Claussen; H J Ludecke; Gabriele Senger; Bernhard Horsthemke
Construction of band-specific DNA-libraries by microdissection of GTG-banded human chromosomes and universal enzymatic DNA amplification.
Bulletin de l'Association des anatomistes 1991;75(229):133-6.
1991: Irene Newsham; Uwe Claussen; Hermann-Josef Lüdecke; M Mason; Gabriele Senger; Bernhard Horsthemke; Webster K Cavenee
Microdissection of chromosome band 11p15.5: characterization of probes mapping distal to the HBBC locus.
Genes, chromosomes & cancer 1991;3(2):108-16.
1990: L M Davis; Gabriele Senger; Hermann-Josef Lüdecke; Uwe Claussen; Bernhard Horsthemke; S S Zhang; B Metzroth; K Hohenfellner; Bernhard Zabel; TB Shows
Somatic cell hybrid and long-range physical mapping of 11p13 microdissected genomic clones.
Proceedings of the National Academy of Sciences of the United States of America 1990;87(18):7005-9.
1990: R N MacKinnon; Mark Hirst; M V Bell; J E Watson; Uwe Claussen; H J Ludecke; Gabriele Senger; Bernhard Horsthemke; Kay E Davies
Microdissection of the fragile X region.
American journal of human genetics 1990;47(2):181-6.
1990: Gabriele Senger; Hermann-Josef Lüdecke; Bernhard Horsthemke; Uwe Claussen
Microdissection of banded human chromosomes.
Human genetics 1990;84(6):507-11.
1990: Hermann-Josef Lüdecke; Gabriele Senger; Uwe Claussen; Bernhard Horsthemke
Construction and characterization of band-specific DNA libraries.
Human genetics 1990;84(6):512-6.
1990: Karin Buiting; M Neumann; Hermann-Josef Lüdecke; Gabriele Senger; Uwe Claussen; J Antich; Eberhard Passarge; Bernhard Horsthemke
Microdissection of the Prader-Willi syndrome chromosome region and identification of potential gene sequences.
Genomics 1990;6(3):521-7.
1989: Hermann-Josef Lüdecke; R Burdiek; Gabriele Senger; Uwe Claussen; Eberhard Passarge; Bernhard Horsthemke
Maternal origin of a de novo chromosome 8 deletion in a patient with Langer-Giedion syndrome.
Human genetics 1989;82(4):327-9.
1989: Hermann-Josef Lüdecke; Gabriele Senger; Uwe Claussen; Bernhard Horsthemke
Cloning defined regions of the human genome by microdissection of banded chromosomes and enzymatic amplification.
Nature 1989;338(6213):348-50.