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The SickKids Genome Clinic: developing and evaluating a pediatric model for individualized genomic medicine

Clinical genetics, 2016-01, Vol.89 (1), p.10-19

2016

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Predictive genetic testing for adult-onset disorders in minors: a critical analysis of the arguments for and against the 2013 ACMG guidelines

Clinical genetics, 2015-04, Vol.87 (4), p.301-310

2015

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Ataxia-telangiectasia and cellular responses to DNA damage

Cancer research (Chicago, Ill.), 1995-12, Vol.55 (24), p.5991-6001

MEYN, M. S

1995

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Targeted disruption of ATM leads to growth retardation, chromosomal fragmentation during meiosis, immune defects, and thymic lymphoma

Genes & development, 1996-10, Vol.10 (19), p.2411-2422

1996

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Ataxia-telangiectasia, cancer and the pathobiology of the ATM gene

Clinical genetics, 1999-05, Vol.55 (5), p.289-304

Meyn, M. Stephen

1999

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The development of the Clinician-reported Genetic testing Utility InDEx (C-GUIDE): a novel strategy for measuring the clinical utility of genetic testing

Genetics in medicine, 2020-01, Vol.22 (1), p.95-101

2020

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Parents perspectives on whole genome sequencing for their children: qualified enthusiasm?

Journal of medical ethics, 2017-08, Vol.43 (8), p.535-539

2017

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High Spontaneous Intrachromosomal Recombination Rates in Ataxia-Telangiectasia

Science (American Association for the Advancement of Science), 1993-05, Vol.260 (5112), p.1327-1330

Meyn, M. Stephen

1993

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Response to Rubanovich et al

Genetics in medicine, 2020-03, Vol.22 (3), p.667-668

2020

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Chromosome instability syndromes: lessons for carcinogenesis

Current topics in microbiology and immunology, 1997, Vol.221, p.71

Meyn, M S

1997

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Views from the clinic: Healthcare provider perspectives on whole genome sequencing in paediatrics

European journal of medical genetics, 2019-05, Vol.62 (5), p.350-356

2019

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Interaction of the Fanconi Anemia Proteins and BRCA1 in a Common Pathway

Molecular cell, 2001-02, Vol.7 (2), p.249-262

2001

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WRN or telomerase constructs reverse 4-nitroquinoline 1-oxide sensitivity in transformed Werner syndrome fibroblasts

Cancer research (Chicago, Ill.), 2000-05, Vol.60 (9), p.2372-2376

2000

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Testing the Role of p53 in the Expression of Genetic Instability and Apoptosis in Ataxia-telangiectasia

International journal of radiation biology, 1994, Vol.66 (6), p.S141-S149

1994

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The yeast TEL1 gene partially substitutes for human ATM in suppressing hyperrecombination, radiation-induced apoptosis and telomere shortening in A-T cells

Molecular biology of the cell, 2000-08, Vol.11 (8), p.2605-2616

2000

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Molecular definition of the smallest region of deletion overlap in the Wolf-Hirschhorn syndrome

American journal of human genetics, 1992-09, Vol.51 (3), p.571-578

1992

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The Atr and Atm protein kinases associate with different sites along meiotically pairing chromosomes

Genes & development, 1996-10, Vol.10 (19), p.2423-2437

1996

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Adenovirus-mediated expression of hepatic lipase in LCAT transgenic mice

Journal of lipid research, 1997-09, Vol.38 (9), p.1822-1832

1997

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The biochemical effect of Ser167 phosphorylation on Chlamydomonas reinhardtii centrin

Biochemical and biophysical research communications, 2006-03, Vol.342 (1), p.342-348

2006

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Combined hereditary and somatic mutations of replication error repair genes result in rapid onset of ultra-hypermutated cancers

Nature genetics, 2015-03, Vol.47 (3), p.257-262

2015

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Novel lacZ-based recombination vectors for mammalian cells

Gene, 1993-12, Vol.137 (2), p.163-169

1993

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TEL1 from Saccharomyces cerevisiae suppresses chromosome aberrations induced by ionizing radiation in ataxia-telangiectasia cells without affecting cell cycle checkpoints

Radiation and environmental biophysics, 2001-12, Vol.40 (4), p.309-315

2001

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Partial purification and characterization of a recombinase from human cells

Cell, 1986-03, Vol.44 (6), p.885-894

1986

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Short-term response to dietary therapy in molybdenum cofactor deficiency

Annals of neurology, 1993-11, Vol.34 (5), p.742-744

1993

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Targeted disruption of the mouse lecithin:cholesterol acyltransferase (LCAT) gene. Generation of a new animal model for human LCAT deficiency

The Journal of biological chemistry, 1997-03, Vol.272 (11), p.7506-7510

1997

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The SickKids Genome Clinic: developing and evaluating a pediatric model for individualized genomic medicine

Predictive genetic testing for adult-onset disorders in minors: a critical analysis of the arguments for and against the 2013 ACMG guidelines

Ataxia-telangiectasia and cellular responses to DNA damage

Targeted disruption of ATM leads to growth retardation, chromosomal fragmentation during meiosis, immune defects, and thymic lymphoma

Ataxia-telangiectasia, cancer and the pathobiology of the ATM gene

The development of the Clinician-reported Genetic testing Utility InDEx (C-GUIDE): a novel strategy for measuring the clinical utility of genetic testing

Parents perspectives on whole genome sequencing for their children: qualified enthusiasm?

High Spontaneous Intrachromosomal Recombination Rates in Ataxia-Telangiectasia

Response to Rubanovich et al

Chromosome instability syndromes: lessons for carcinogenesis

Views from the clinic: Healthcare provider perspectives on whole genome sequencing in paediatrics

Interaction of the Fanconi Anemia Proteins and BRCA1 in a Common Pathway

WRN or telomerase constructs reverse 4-nitroquinoline 1-oxide sensitivity in transformed Werner syndrome fibroblasts

Testing the Role of p53 in the Expression of Genetic Instability and Apoptosis in Ataxia-telangiectasia

The yeast TEL1 gene partially substitutes for human ATM in suppressing hyperrecombination, radiation-induced apoptosis and telomere shortening in A-T cells

Molecular definition of the smallest region of deletion overlap in the Wolf-Hirschhorn syndrome

The Atr and Atm protein kinases associate with different sites along meiotically pairing chromosomes

Adenovirus-mediated expression of hepatic lipase in LCAT transgenic mice

The biochemical effect of Ser167 phosphorylation on Chlamydomonas reinhardtii centrin

Combined hereditary and somatic mutations of replication error repair genes result in rapid onset of ultra-hypermutated cancers

Novel lacZ-based recombination vectors for mammalian cells

TEL1 from Saccharomyces cerevisiae suppresses chromosome aberrations induced by ionizing radiation in ataxia-telangiectasia cells without affecting cell cycle checkpoints

Partial purification and characterization of a recombinase from human cells

Short-term response to dietary therapy in molybdenum cofactor deficiency

Targeted disruption of the mouse lecithin:cholesterol acyltransferase (LCAT) gene. Generation of a new animal model for human LCAT deficiency

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