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Evaluating the impact of scoring parameters on the structure of intra-specific genetic variation using RawGeno, an R package for automating AFLP scoring

BMC bioinformatics, 2009-01, Vol.10 (1), p.33-33, Article 33

2009

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Copy number analysis of survival motor neuron genes by multiplex ligation-dependent probe amplification

Genetics in medicine, 2007-04, Vol.9 (4), p.241-248

2007

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Increased number of sex chromosomes affects height in a nonlinear fashion: A study of 305 patients with sex chromosome aneuploidy

American journal of medical genetics. Part A, 2010-05, Vol.152A (5), p.1206-1212

2010

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Maintenance of EGFR and EGFRvIII expressions in an in vivo and in vitro model of human glioblastoma multiforme

Experimental cell research, 2011-07, Vol.317 (11), p.1513-1526

2011

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MLPA analysis for a panel of syndromes with mental retardation reveals imbalances in 5.8% of patients with mental retardation and dysmorphic features, including duplications of the Sotos syndrome and Williams–Beuren syndrome regions

European journal of medical genetics, 2007-01, Vol.50 (1), p.33-42

2007

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Multiplex ligation-dependent probe amplification (MLPA) in prenatal diagnosis-experience of a large series of rapid testing for aneuploidy of chromosomes 13, 18, 21, X, and Y

Prenatal diagnosis, 2008-12, Vol.28 (12), p.1119-1125

2008

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Automatic analysis of multiplex ligation-dependent probe amplification products (exemplified by a commercial kit for prenatal aneuploidy detection)

Electrophoresis, 2005-11, Vol.26 (22), p.4327-4332

2005

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Investigation of patients with mental retardation and dysmorphic features using comparative genomic hybridization and subtelomeric multiplex ligation dependent probe amplication

American journal of medical genetics. Part A, 2005-12, Vol.139A (3), p.231-233

2005

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Computer-assisted prenatal aneuploidy screening for chromosome 13, 18, 21, X and Y based on multiplex ligation-dependent probe amplification (MLPA)

European journal of human genetics : EJHG, 2005-02, Vol.13 (2), p.171-175

2005

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Deletions below 10 megabasepairs are detected in comparative genomic hybridization by standard reference intervals

Genes chromosomes & cancer, 1999-08, Vol.25 (4), p.410-413

1999

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Comparative genomic hybridization reveals a recurrent pattern of chromosomal aberrations in severe dysplasia/carcinoma in situ of the cervix and in advanced-stage cervical carcinoma

Genes chromosomes & cancer, 1999-02, Vol.24 (2), p.144-150

1999

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Automatic assessment of the quality of G-banded metaphases. A preliminary study

Journal of radiation research, 1992, Vol.33 Suppl (SUPPLEMENT), p.152-158

1992

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Investigation of patients with mental retardation and dysmorphic features using comparative genomic hybridization and subtelomeric multiplex ligation dependent probe amplification

American journal of medical genetics. Part A, 2005-12, Vol.139 (3), p.231-233

2005

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Comparative genomic hybridization in clinical cytogenetics

American journal of human genetics, 1995-11, Vol.57 (5), p.1211-1220

1995

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High resolution comparative genomic hybridisation analysis reveals imbalances in dyschromosomal patients with normal or apparently balanced conventional karyotypes

European journal of human genetics : EJHG, 2000-09, Vol.8 (9), p.661-668

2000

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Detection of chromosomal aberrations in seminomatous germ cell tumours using comparative genomic hybridization

Genes chromosomes & cancer, 1997-12, Vol.20 (4), p.412-418

1997

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Claes Lundsteen-in Memoriam

European journal of human genetics : EJHG, 2004-08, Vol.12 (8), p.603-603

2004

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Improved sensitivity in comparative genomic hybridization analysis of DNA heteroploid cell mixtures after pre-enrichment of subpopulations by fluorescence activated cell sorting

Analytical cellular pathology, 1999, Vol.19 (3-4), p.119-124

1999

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Automation of cytogenetics: Present state and the future

Biology of the cell, 1992, Vol.76 (2), p.251-251

1992

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Automatic assessment of the quality of G-banded metaphases A preliminary study

JOURNAL OF RADIATION RESEARCH, 1992-03, Vol.33 (suppl), p.152-158

1992

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Automated multiple-cell karyotyping: a clinical feasibility study

Clinical genetics, 1991-05, Vol.39 (5), p.338-346

1991

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Detection of chromosomal gains and losses in comparative genomic hybridization analysis based on standard reference intervals

Cytometry (New York, N.Y.), 1998-03, Vol.31 (3), p.163-173

1998

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Investigation of patients with mental retardation and dysmorphic features using comparative genomic hybridization and subtelomeric multiplex ligation dependent probe amplication. Author's reply

American journal of medical genetics, 2005, Vol.139A (3), p.231-233

2005

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Comparative genomic hybridization reveals non-random chromosomal aberrations in early preinvasive cervical lesions

Cancer genetics and cytogenetics, 2001-08, Vol.129 (1), p.47-51

2001

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Automatic correction of the interfering effect of unsuppressed interspersed repetitive sequences in comparative genomic hybridization analysis

Cytometry (New York, N.Y.), 1997-06, Vol.28 (2), p.130-134

1997

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Evaluating the impact of scoring parameters on the structure of intra-specific genetic variation using RawGeno, an R package for automating AFLP scoring

Copy number analysis of survival motor neuron genes by multiplex ligation-dependent probe amplification

Increased number of sex chromosomes affects height in a nonlinear fashion: A study of 305 patients with sex chromosome aneuploidy

Maintenance of EGFR and EGFRvIII expressions in an in vivo and in vitro model of human glioblastoma multiforme

MLPA analysis for a panel of syndromes with mental retardation reveals imbalances in 5.8% of patients with mental retardation and dysmorphic features, including duplications of the Sotos syndrome and Williams–Beuren syndrome regions

Multiplex ligation-dependent probe amplification (MLPA) in prenatal diagnosis-experience of a large series of rapid testing for aneuploidy of chromosomes 13, 18, 21, X, and Y

Automatic analysis of multiplex ligation-dependent probe amplification products (exemplified by a commercial kit for prenatal aneuploidy detection)

Investigation of patients with mental retardation and dysmorphic features using comparative genomic hybridization and subtelomeric multiplex ligation dependent probe amplication

Computer-assisted prenatal aneuploidy screening for chromosome 13, 18, 21, X and Y based on multiplex ligation-dependent probe amplification (MLPA)

Deletions below 10 megabasepairs are detected in comparative genomic hybridization by standard reference intervals

Comparative genomic hybridization reveals a recurrent pattern of chromosomal aberrations in severe dysplasia/carcinoma in situ of the cervix and in advanced-stage cervical carcinoma

Automatic assessment of the quality of G-banded metaphases. A preliminary study

Investigation of patients with mental retardation and dysmorphic features using comparative genomic hybridization and subtelomeric multiplex ligation dependent probe amplification

Comparative genomic hybridization in clinical cytogenetics

High resolution comparative genomic hybridisation analysis reveals imbalances in dyschromosomal patients with normal or apparently balanced conventional karyotypes

Detection of chromosomal aberrations in seminomatous germ cell tumours using comparative genomic hybridization

Claes Lundsteen-in Memoriam

Improved sensitivity in comparative genomic hybridization analysis of DNA heteroploid cell mixtures after pre-enrichment of subpopulations by fluorescence activated cell sorting

Automation of cytogenetics: Present state and the future

Automatic assessment of the quality of G-banded metaphases A preliminary study

Automated multiple-cell karyotyping: a clinical feasibility study

Detection of chromosomal gains and losses in comparative genomic hybridization analysis based on standard reference intervals

Investigation of patients with mental retardation and dysmorphic features using comparative genomic hybridization and subtelomeric multiplex ligation dependent probe amplication. Author's reply

Comparative genomic hybridization reveals non-random chromosomal aberrations in early preinvasive cervical lesions

Automatic correction of the interfering effect of unsuppressed interspersed repetitive sequences in comparative genomic hybridization analysis

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