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Rapid single-cell copy-number aberration analysis using high-throughput sequencing

European journal of cancer (1990), 2017-02, Vol.72, p.S24-S24

2017

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Whole-genome sequencing of circulating tumor DNA reveals relevance of focal amplifications for the management of metastatic prostate cancer

European journal of cancer (1990), 2016-07, Vol.61, p.S12-S12

2016

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Behaviour of human heterochromatic regions during the synapsis of homologous chromosomes

Human reproduction (Oxford), 2006-06, Vol.21 (6), p.1490-1497

2006

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400: Changes in colorectal carcinoma genomes under anti-EGFR therapy identified by whole-genome plasma DNA sequencing

European journal of cancer (1990), 2014-07, Vol.50, p.S96-S96

2014

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641: Whole-genome sequencing of plasma DNA reveals frequently occurring copy number changes in patients with metastatic breast cancer

European journal of cancer (1990), 2014-07, Vol.50, p.S153-S153

2014

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Towards many colors in FISH on 3D-preserved interphase nuclei

Cytogenetic and genome research, 2006-01, Vol.114 (3-4), p.367-378

2006

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Classifying by colors: FISH-based genome analysis

Cytogenetics and cell genetics, 2001, Vol.93 (1-2), p.1

2001

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Role of chromosome territories in the functional compartmentalization of the cell nucleus

Cold Spring Harbor Symposia on Quantitative Biology, 1993, Vol.58, p.777

1993

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207 - Rapid single-cell copy-number aberration analysis using high-throughput sequencing

European journal of cancer (1990), 2017-02, Vol.72, p.S24-S24

2017

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112 - Whole-genome sequencing of circulating tumor DNA reveals relevance of focal amplifications for the management of metastatic prostate cancer

European journal of cancer (1990), 2016-07, Vol.61, p.S12-S12

2016

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Zukunft der Zytogenetik

Medizinische Genetik, 2008-12, Vol.20 (4), p.349-352

Speicher, M.R.

2008

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Nichtinvasive molekulargenetische Methoden in der pränatalen Diagnostik

Medizinische Genetik, 2011-12, Vol.23 (4), p.485-490

2011

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367 Genomic profiles of single tumour cells in metastatic breast cancer patients

European journal of cancer supplements, 2010, Vol.8 (5), p.93-94

2010

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Nichtinvasive molekulargenetische Methoden in der pränatalen Diagnostik

Medizinische Genetik, 2011-12, Vol.23 (4), p.485-490

2011

Volltextzugriff (PDF)

Zukunft der Zytogenetik

Medizinische Genetik, 2008-12, Vol.20 (4), p.349-352

Speicher, M.R.

2008

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1096 Molecular signatures of disseminated tumour cells in metastatic breast cancer patients

European journal of cancer supplements, 2009, Vol.7 (2), p.113-114

2009

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Monosomy 1p36--a recently delineated, clinically recognizable syndrome

Clinical dysmorphology, 2002-01, Vol.11 (1), p.43-48

2002

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Crossover frequency and synaptonemal complex length: their variability and effects on human male meiosis

Molecular human reproduction, 2006-02, Vol.12 (2), p.123-133

2006

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An optimized, fully automated system for fast and accurate identification of chromosomal rearrangements by multiplex-FISH (M-FISH)

Cytogenetics and cell genetics, 1998, Vol.82 (3-4), p.160

1998

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Seven-fluorochrome mouse M-FISH for high-resolution analysis of interchromosomal rearrangements

Cytogenetic and genome research, 2003, Vol.103 (1-2), p.84-88

2003

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Induction of chromosomal aberrations by dacarbazine in somatic and germinal cells of mice

Mutagenesis, 2002-09, Vol.17 (5), p.383-389

2002

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Characterization of all human male synaptonemal complexes by subtelomere multiplex-FISH

Cytogenetic and genome research, 2004-01, Vol.107 (1-2), p.18-21

2004

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Heritable translocations induced by dermal exposure of male mice to acrylamide

Cytogenetic and Genome Research, 2004-01, Vol.104 (1-4), p.271-276

2004

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First non‐mosaic case of isopseudodicentric chromosome 18 (psu idic(18)(pter → q22.1::q22.1 → pter) Is associated with multiple congenital anomalies reminiscent of trisomy 18 and 18q− syndrome

American journal of medical genetics, 2004-05, Vol.127A (1), p.58-64

2004

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Facilitating haplotype analysis by fully automated analysis of all chromosomes in human-mouse hybrid cell lines

Cytogenetics and cell genetics, 2001, Vol.93 (1-2), p.11

2001

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Rapid single-cell copy-number aberration analysis using high-throughput sequencing

Whole-genome sequencing of circulating tumor DNA reveals relevance of focal amplifications for the management of metastatic prostate cancer

Behaviour of human heterochromatic regions during the synapsis of homologous chromosomes

400: Changes in colorectal carcinoma genomes under anti-EGFR therapy identified by whole-genome plasma DNA sequencing

641: Whole-genome sequencing of plasma DNA reveals frequently occurring copy number changes in patients with metastatic breast cancer

Towards many colors in FISH on 3D-preserved interphase nuclei

Classifying by colors: FISH-based genome analysis

Role of chromosome territories in the functional compartmentalization of the cell nucleus

207 - Rapid single-cell copy-number aberration analysis using high-throughput sequencing

112 - Whole-genome sequencing of circulating tumor DNA reveals relevance of focal amplifications for the management of metastatic prostate cancer

Zukunft der Zytogenetik

Nichtinvasive molekulargenetische Methoden in der pränatalen Diagnostik

367 Genomic profiles of single tumour cells in metastatic breast cancer patients

Nichtinvasive molekulargenetische Methoden in der pränatalen Diagnostik

Zukunft der Zytogenetik

1096 Molecular signatures of disseminated tumour cells in metastatic breast cancer patients

Monosomy 1p36--a recently delineated, clinically recognizable syndrome

Crossover frequency and synaptonemal complex length: their variability and effects on human male meiosis

An optimized, fully automated system for fast and accurate identification of chromosomal rearrangements by multiplex-FISH (M-FISH)

Seven-fluorochrome mouse M-FISH for high-resolution analysis of interchromosomal rearrangements

Induction of chromosomal aberrations by dacarbazine in somatic and germinal cells of mice

Characterization of all human male synaptonemal complexes by subtelomere multiplex-FISH

Heritable translocations induced by dermal exposure of male mice to acrylamide

First non‐mosaic case of isopseudodicentric chromosome 18 (psu idic(18)(pter → q22.1::q22.1 → pter) Is associated with multiple congenital anomalies reminiscent of trisomy 18 and 18q− syndrome

Facilitating haplotype analysis by fully automated analysis of all chromosomes in human-mouse hybrid cell lines

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