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Microarray based comparative genomic hybridisation (array-CGH) detects submicroscopic chromosomal deletions and duplications in patients with learning disability/mental retardation and dysmorphic features

Journal of medical genetics, 2004-04, Vol.41 (4), p.241-248

2004

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Array-CGH detection of micro rearrangements in mentally retarded individuals: clinical significance of imbalances present both in affected children and normal parents

Journal of medical genetics, 2006-02, Vol.43 (2), p.180-186

2006

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Prenatal detection of unbalanced chromosomal rearrangements by array CGH

Journal of medical genetics, 2006-04, Vol.43 (4), p.353-361

2006

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The complex nature of constitutional de novo apparently balanced translocations in patients presenting with abnormal phenotypes

Journal of medical genetics, 2005-01, Vol.42 (1), p.8-16

2005

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Small regions of overlapping deletions on 6q26 in human astrocytic tumours identified using chromosome 6 tile path array-CGH

Oncogene, 2006-02, Vol.25 (8), p.1261-1271

2006

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A comprehensive study of chromosome 16q in invasive ductal and lobular breast carcinoma using array CGH

Oncogene, 2006-10, Vol.25 (49), p.6544-6553

2006

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Multiple sub-microscopic genomic lesions are a universal feature of chronic myeloid leukaemia at diagnosis

Leukemia, 2008-09, Vol.22 (9), p.1806-1807

2008

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Array painting: a method for the rapid analysis of aberrant chromosomes using DNA microarrays

Journal of medical genetics, 2003-09, Vol.40 (9), p.664-670

2003

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Prenatal Diagnosis by Array-CGH

European journal of medical genetics, 2005-07, Vol.48 (3), p.232-240

2005

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Chromatin Architecture of the Human Genome: Gene-Rich Domains Are Enriched in Open Chromatin Fibers

Cell, 2004-09, Vol.118 (5), p.555-566

2004

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Tiling path resolution mapping of constitutional 1p36 deletions by array-CGH: contiguous gene deletion or “deletion with positional effect” syndrome?

Journal of medical genetics, 2005-02, Vol.42 (2), p.166-171

2005

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A DNA damage checkpoint response in telomere-initiated senescence

Nature, 2003-11, Vol.426 (6963), p.194-198

2003

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Sites of Differential DNA Methylation between Placenta and Peripheral Blood: Molecular Markers for Noninvasive Prenatal Diagnosis of Aneuploidies

The American journal of pathology, 2009-05, Vol.174 (5), p.1609-1618

2009

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Genomic and Protein Expression Profiling Identifies CDK6 As Novel Independent Prognostic Marker in Medulloblastoma

Journal of clinical oncology, 2005-12, Vol.23 (34), p.8853-8862

2005

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DNA microarrays for comparative genomic hybridization based on DOP-PCR amplification of BAC and PAC clones

Genes chromosomes & cancer, 2003-04, Vol.36 (4), p.361-374

2003

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High-resolution analysis of genomic copy number alterations in bladder cancer by microarray-based comparative genomic hybridization

Oncogene, 2004-03, Vol.23 (12), p.2250-2263

2004

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Guidelines for molecular karyotyping in constitutional genetic diagnosis

European journal of human genetics : EJHG, 2007-11, Vol.15 (11), p.1105-1114

2007

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Replication timing of the human genome

Human molecular genetics, 2004-01, Vol.13 (2), p.191-202

2004

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A canine cancer-gene microarray for CGH analysis of tumors

Cytogenetic and Genome Research, 2003-01, Vol.102 (1-4), p.254-260

2003

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Array comparative genomic hybridization analysis of colorectal cancer cell lines and primary carcinomas

Cancer research (Chicago, Ill.), 2004-07, Vol.64 (14), p.4817-4825

2004

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Tetrasomy 21pter→q21.2 in a male infant without typical Down’s syndrome dysmorphic features but moderate mental retardation

Journal of medical genetics, 2004-03, Vol.41 (3), p.e26-26

2004

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Combined array-comparative genomic hybridization and single-nucleotide polymorphism-loss of heterozygosity analysis reveals complex changes and multiple forms of chromosomal instability in colorectal cancers

Cancer research (Chicago, Ill.), 2006-04, Vol.66 (7), p.3471-3479

2006

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Applications of combined DNA microarray and chromosome sorting technologies

Chromosome research, 2004, Vol.12 (1), p.35-43

2004

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Identification of the serine acetyltransferase gene of Staphylococcus xylosus

FEMS microbiology letters, 1997, Vol.148 (2), p.181-187

1997

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Genome-Wide Screening of Genomic Alterations and Their Clinicopathologic Implications in Non–Small Cell Lung Cancers

Clinical cancer research, 2005-12, Vol.11 (23), p.8235-8242

2005

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Microarray based comparative genomic hybridisation (array-CGH) detects submicroscopic chromosomal deletions and duplications in patients with learning disability/mental retardation and dysmorphic features

Array-CGH detection of micro rearrangements in mentally retarded individuals: clinical significance of imbalances present both in affected children and normal parents

Prenatal detection of unbalanced chromosomal rearrangements by array CGH

The complex nature of constitutional de novo apparently balanced translocations in patients presenting with abnormal phenotypes

Small regions of overlapping deletions on 6q26 in human astrocytic tumours identified using chromosome 6 tile path array-CGH

A comprehensive study of chromosome 16q in invasive ductal and lobular breast carcinoma using array CGH

Multiple sub-microscopic genomic lesions are a universal feature of chronic myeloid leukaemia at diagnosis

Array painting: a method for the rapid analysis of aberrant chromosomes using DNA microarrays

Prenatal Diagnosis by Array-CGH

Chromatin Architecture of the Human Genome: Gene-Rich Domains Are Enriched in Open Chromatin Fibers

Tiling path resolution mapping of constitutional 1p36 deletions by array-CGH: contiguous gene deletion or “deletion with positional effect” syndrome?

A DNA damage checkpoint response in telomere-initiated senescence

Sites of Differential DNA Methylation between Placenta and Peripheral Blood: Molecular Markers for Noninvasive Prenatal Diagnosis of Aneuploidies

Genomic and Protein Expression Profiling Identifies CDK6 As Novel Independent Prognostic Marker in Medulloblastoma

DNA microarrays for comparative genomic hybridization based on DOP-PCR amplification of BAC and PAC clones

High-resolution analysis of genomic copy number alterations in bladder cancer by microarray-based comparative genomic hybridization

Guidelines for molecular karyotyping in constitutional genetic diagnosis

Replication timing of the human genome

A canine cancer-gene microarray for CGH analysis of tumors

Array comparative genomic hybridization analysis of colorectal cancer cell lines and primary carcinomas

Tetrasomy 21pter→q21.2 in a male infant without typical Down’s syndrome dysmorphic features but moderate mental retardation

Combined array-comparative genomic hybridization and single-nucleotide polymorphism-loss of heterozygosity analysis reveals complex changes and multiple forms of chromosomal instability in colorectal cancers

Applications of combined DNA microarray and chromosome sorting technologies

Identification of the serine acetyltransferase gene of Staphylococcus xylosus

Genome-Wide Screening of Genomic Alterations and Their Clinicopathologic Implications in Non–Small Cell Lung Cancers

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