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The Influence of Smoking and Occupational Risk Factors on DNA Methylation in the AHRR and F2RL3 Genes

Cancer epidemiology, biomarkers & prevention, 2024-02, Vol.33 (2), p.224-233

2024

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A cross-sectional study of global DNA methylation and risk of colorectal adenoma

BMC cancer, 2014-07, Vol.14 (1), p.488-488, Article 488

2014

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Paternal transmission of fragile X syndrome

American journal of medical genetics, 2004-08, Vol.129A (2), p.184-189

2004

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A model for GFRα4 function and a potential modifying role in multiple endocrine neoplasia 2

Oncogene, 2005-02, Vol.24 (6), p.1091-1097

2005

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Data sharing to improve concordance in variant interpretation across laboratories: results from the Canadian Open Genetics Repository

Journal of medical genetics, 2022-06, Vol.59 (6), p.571-578

2022

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Biomarkers measured in buccal and blood leukocyte DNA as proxies for colon tissue global methylation

International journal of molecular epidemiology and genetics, 2014-01, Vol.5 (2), p.120-124

2014

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Boy with 47,XXY,del(15)(q11.2q13) karyotype and Prader–Willi syndrome: A new case and review of the literature

American journal of medical genetics, 2004-02, Vol.125A (1), p.73-76

2004

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Risk of venous thromboembolism associated with the common hereditary haemochromatosis Hfe gene (C282Y) mutation

British journal of haematology, 1999-04, Vol.105 (1), p.95-97

1999

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Quantitative neuropathological changes in presymptomatic Huntington's disease

Annals of neurology, 2001-01, Vol.49 (1), p.29-34

2001

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A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosomes

Cell, 1993-03, Vol.72 (6), p.971-983

1993

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A model for GFR alpha 4 function and a potential modifying role in multiple endocrine neoplasia 2

Oncogene, 2005-02, Vol.24 (6), p.1091-1097

2005

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Genetic basis of familial Meniere's disease

Journal of otolaryngology, 2002-02, Vol.31 (1), p.1

2002

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Mutation of RET codon 768 is associated with the FMTC phenotype

Clinical genetics, 1997-02, Vol.51 (2), p.81-85

1997

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Severe haemophilia A in a female resulting from two de novo factor VIII mutations

British journal of haematology, 1995-08, Vol.90 (4), p.906-909

1995

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A model for GFR 4 function and a potential modifying role in multiple endocrine neoplasia 2

Oncogene, 2005-02, Vol.24 (6), p.1091-1097

2005

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A past mutation at isoleucine 397 is now a common cause of moderate/mild haemophilia B

British journal of haematology, 1990-06, Vol.75 (2), p.212-216

1990

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Characterization of the original Christmas disease mutation (cysteine 206----serine): from clinical recognition to molecular pathogenesis

Thrombosis and haemostasis, 1992-01, Vol.67 (1), p.63-65

1992

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A past mutation at Isoleucine397 is now a common cause of moderate/mild haemophilia B

British journal of haematology, 1990-06, Vol.75 (2), p.212-216

1990

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MULTIPLE Xba I POLYMORPHISMS IN HAEMOPHILIA A

British journal of haematology, 1990-06, Vol.75 (2), p.292-295

1990

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Chronic and Episodic Interpersonal Stress as Statistically Unique Predictors of Depression in Two Samples of Emerging Adults

Journal of abnormal psychology (1965), 2015-11, Vol.124 (4), p.918-932

2015

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The Link Between Nonsuicidal Self-Injury and Acquired Capability for Suicide: A Longitudinal Study

Journal of abnormal psychology (1965), 2015-11, Vol.124 (4), p.1110-1115

2015

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A randomized controlled trial of yoga for pregnant women with symptoms of depression and anxiety

Complementary therapies in clinical practice, 2015-08, Vol.21 (3), p.166-172

2015

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Elevated Responding to Safe Conditions as a Specific Risk Factor for Anxiety Versus Depressive Disorders: Evidence From a Longitudinal Investigation

Journal of abnormal psychology (1965), 2012-05, Vol.121 (2), p.315-324

2012

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Dissecting CASK : Novel splice site variant associated with male MICPCH phenotype

Clinical genetics, 2024-08

2024

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The Influence of Smoking and Occupational Risk Factors on DNA Methylation in the AHRR and F2RL3 Genes

A cross-sectional study of global DNA methylation and risk of colorectal adenoma

Paternal transmission of fragile X syndrome

A model for GFRα4 function and a potential modifying role in multiple endocrine neoplasia 2

Data sharing to improve concordance in variant interpretation across laboratories: results from the Canadian Open Genetics Repository

Biomarkers measured in buccal and blood leukocyte DNA as proxies for colon tissue global methylation

Data sharing as a national quality improvement program: reporting on BRCA1 and BRCA2 variant-interpretation comparisons through the Canadian Open Genetics Repository (COGR)

Boy with 47,XXY,del(15)(q11.2q13) karyotype and Prader–Willi syndrome: A new case and review of the literature

Risk of venous thromboembolism associated with the common hereditary haemochromatosis Hfe gene (C282Y) mutation

Quantitative neuropathological changes in presymptomatic Huntington's disease

A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosomes

A model for GFR alpha 4 function and a potential modifying role in multiple endocrine neoplasia 2

Genetic basis of familial Meniere's disease

Mutation of RET codon 768 is associated with the FMTC phenotype

Severe haemophilia A in a female resulting from two de novo factor VIII mutations

A model for GFR 4 function and a potential modifying role in multiple endocrine neoplasia 2

A past mutation at isoleucine 397 is now a common cause of moderate/mild haemophilia B

Characterization of the original Christmas disease mutation (cysteine 206----serine): from clinical recognition to molecular pathogenesis

A past mutation at Isoleucine397 is now a common cause of moderate/mild haemophilia B

MULTIPLE Xba I POLYMORPHISMS IN HAEMOPHILIA A

Chronic and Episodic Interpersonal Stress as Statistically Unique Predictors of Depression in Two Samples of Emerging Adults

The Link Between Nonsuicidal Self-Injury and Acquired Capability for Suicide: A Longitudinal Study

A randomized controlled trial of yoga for pregnant women with symptoms of depression and anxiety

Elevated Responding to Safe Conditions as a Specific Risk Factor for Anxiety Versus Depressive Disorders: Evidence From a Longitudinal Investigation

Dissecting CASK : Novel splice site variant associated with male MICPCH phenotype

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