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Short telomeres result in chromosomal instability in hematopoietic cells and precede malignant evolution in human aplastic anemia

Leukemia, 2012-04, Vol.26 (4), p.700-707

2012

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Single-Cell Genetic Analysis of Ductal Carcinoma in Situ and Invasive Breast Cancer Reveals Enormous Tumor Heterogeneity yet Conserved Genomic Imbalances and Gain of MYC during Progression

The American journal of pathology, 2012-11, Vol.181 (5), p.1807-1822

2012

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Rb inactivation accelerates neoplastic growth and substitutes for recurrent amplification of cIAP1, cIAP2 and Yap1 in sporadic mammary carcinoma associated with p53 deficiency

Oncogene, 2010-10, Vol.29 (42), p.5700-5711

2010

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Genomic Amplification of the Human Telomerase Gene ( TERC) in Pap Smears Predicts the Development of Cervical Cancer

The American journal of pathology, 2005-04, Vol.166 (4), p.1229-1238

2005

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Common Genetic Variants Associate with Serum Phosphorus Concentration

Journal of the American Society of Nephrology, 2010-07, Vol.21 (7), p.1223-1232

2010

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Selective serotonin reuptake inhibitor treatment and depression are associated with poststroke mortality

The Annals of pharmacotherapy, 2011-07, Vol.45 (7-8), p.888-897

2011

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Frequent translocation t(4;14)(p16.3;q32.3) in multiple myeloma is associated with increased expression and activating mutations of fibroblast growth factor receptor 3

Nature genetics, 1997-07, Vol.16 (3), p.260-264

1997

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Chromosomal imbalances in oral squamous cell carcinoma: Examination of 31 cell lines and review of the literature

Oral oncology, 2008-04, Vol.44 (4), p.369-382

2008

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Frequent Dysregulation of the c-maf Proto-Oncogene at 16q23 by Translocation to an Ig Locus in Multiple Myeloma

Blood, 1998-06, Vol.91 (12), p.4457-4463

1998

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A 12-gene genomic instability signature predicts clinical outcomes in multiple cancer types

The International journal of biological markers, 2010-10, Vol.25 (4), p.219-228

2010

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The consequences of chromosomal aneuploidy on gene expression profiles in a cell line model for prostate carcinogenesis

Cancer research (Chicago, Ill.), 2001-11, Vol.61 (22), p.8143-8149

2001

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Ventricular assist device implantation in patients on percutaneous extracorporeal life support without switching to conventional cardiopulmonary bypass system

European journal of cardio-thoracic surgery, 2012-06, Vol.41 (6), p.1366-1370

2012

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The Septin 9 (MSF) gene is amplified and overexpressed in mouse mammary gland adenocarcinomas and human breast cancer cell lines

Cancer research (Chicago, Ill.), 2003-05, Vol.63 (9), p.2179-2187

2003

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Centrosome abnormalities, recurring deletions of chromosome 4, and genomic amplification of HER2/neu define mouse mammary gland adenocarcinomas induced by mutant HER2/neu

Oncogene, 2002-01, Vol.21 (6), p.890-898

2002

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Insertion of c-Myc into Igh induces B-cell and plasma-cell neoplasms in mice

Cancer research (Chicago, Ill.), 2005-02, Vol.65 (4), p.1306-1315

2005

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Weight change after an atypical antipsychotic switch

The Annals of pharmacotherapy, 2003-10, Vol.37 (10), p.1381-1386

2003

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Abnormal DNA content predicts the occurrence of carcinomas in non-dysplastic oral white patches

Oral oncology, 2001-10, Vol.37 (7), p.558-565

2001

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MLL-SEPTIN6 fusion recurs in novel translocation of chromosomes 3, X, and 11 in infant acute myelomonocytic leukaemia and in t(X;11) in infant acute myeloid leukaemia, and MLL genomic breakpoint in complex MLL-SEPTIN6 rearrangement is a DNA topoisomerase II cleavage site

Oncogene, 2002-07, Vol.21 (30), p.4706-4714

2002

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Spectral karyotyping and fluorescence in situ hybridization detect novel chromosomal aberrations, a recurring involvement of chromosome 21 and amplification of the MYC oncogene in acute myeloid leukaemia M2

British journal of haematology, 2001-05, Vol.113 (2), p.305-317

2001

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Safety and efficacy of vigabatrin and carbamazepine in newly diagnosed epilepsy : a multicentre randomised double-blind study

The Lancet (British edition), 1999-07, Vol.354 (9172), p.13-19

CHADWICK, D

1999

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Correlation of microscopic phenotype with genotype in a formalin-fixed, paraffin-embedded testicular germ cell tumor with universal DNA amplification, comparative genomic hybridization, and interphase cytogenetics

The American journal of pathology, 1995-06, Vol.146 (6), p.1332-1340

1995

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Spectral karyotyping demonstrates genetically unstable skin-homing T lymphocytes in cutaneous T-cell lymphoma

Experimental dermatology, 2007-02, Vol.16 (2), p.98-103

2007

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Cost Minimization Analysis of Antiepileptic Drugs in Newly Diagnosed Epilepsy in 12 European Countries

Epilepsia (Copenhagen), 2000-01, Vol.41 (S5), p.S37-S44

2000

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Color vision tests for early detection of antiepileptic drug toxicity

Neurology, 1997-05, Vol.48 (5), p.1394-1397

1997

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Short telomeres result in chromosomal instability in hematopoietic cells and precede malignant evolution in human aplastic anemia

Human metabolic individuality in biomedical and pharmaceutical research

Single-Cell Genetic Analysis of Ductal Carcinoma in Situ and Invasive Breast Cancer Reveals Enormous Tumor Heterogeneity yet Conserved Genomic Imbalances and Gain of MYC during Progression

Rb inactivation accelerates neoplastic growth and substitutes for recurrent amplification of cIAP1, cIAP2 and Yap1 in sporadic mammary carcinoma associated with p53 deficiency

Genomic Amplification of the Human Telomerase Gene ( TERC) in Pap Smears Predicts the Development of Cervical Cancer

Common Genetic Variants Associate with Serum Phosphorus Concentration

Selective serotonin reuptake inhibitor treatment and depression are associated with poststroke mortality

Frequent translocation t(4;14)(p16.3;q32.3) in multiple myeloma is associated with increased expression and activating mutations of fibroblast growth factor receptor 3

Chromosomal imbalances in oral squamous cell carcinoma: Examination of 31 cell lines and review of the literature

Frequent Dysregulation of the c-maf Proto-Oncogene at 16q23 by Translocation to an Ig Locus in Multiple Myeloma

A 12-gene genomic instability signature predicts clinical outcomes in multiple cancer types

The consequences of chromosomal aneuploidy on gene expression profiles in a cell line model for prostate carcinogenesis

Ventricular assist device implantation in patients on percutaneous extracorporeal life support without switching to conventional cardiopulmonary bypass system

The Septin 9 (MSF) gene is amplified and overexpressed in mouse mammary gland adenocarcinomas and human breast cancer cell lines

Centrosome abnormalities, recurring deletions of chromosome 4, and genomic amplification of HER2/neu define mouse mammary gland adenocarcinomas induced by mutant HER2/neu

Insertion of c-Myc into Igh induces B-cell and plasma-cell neoplasms in mice

Weight change after an atypical antipsychotic switch

Abnormal DNA content predicts the occurrence of carcinomas in non-dysplastic oral white patches

MLL-SEPTIN6 fusion recurs in novel translocation of chromosomes 3, X, and 11 in infant acute myelomonocytic leukaemia and in t(X;11) in infant acute myeloid leukaemia, and MLL genomic breakpoint in complex MLL-SEPTIN6 rearrangement is a DNA topoisomerase II cleavage site

Spectral karyotyping and fluorescence in situ hybridization detect novel chromosomal aberrations, a recurring involvement of chromosome 21 and amplification of the MYC oncogene in acute myeloid leukaemia M2

Safety and efficacy of vigabatrin and carbamazepine in newly diagnosed epilepsy : a multicentre randomised double-blind study

Correlation of microscopic phenotype with genotype in a formalin-fixed, paraffin-embedded testicular germ cell tumor with universal DNA amplification, comparative genomic hybridization, and interphase cytogenetics

Spectral karyotyping demonstrates genetically unstable skin-homing T lymphocytes in cutaneous T-cell lymphoma

Cost Minimization Analysis of Antiepileptic Drugs in Newly Diagnosed Epilepsy in 12 European Countries

Color vision tests for early detection of antiepileptic drug toxicity

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