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Please give me a copy of my child's raw genomic data

Npj genomic medicine, 2021-02, Vol.6 (1), p.15-15, Article 15

2021

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Author Correction: Please give me a copy of my child's raw genomic data

Npj genomic medicine, 2021-03, Vol.6 (1), p.26-26, Article 26

2021

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Update on antidepressant use during breastfeeding

Canadian family physician, 2013-06, Vol.59 (6), p.633-634

2013

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P479: The Clinician-reported Genetic testing Utility InDEx: A revised tool to quantify genome-wide sequencing utility in neonatal intensive care (C-GUIDE NICU)

Genetics in Medicine Open, 2024, Vol.2, p.101378, Article 101378

2024

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P383: The clinician-reported genetic testing utility InDEx in the NICU (C-GUIDETM-NICU): Quantifying genome-wide sequencing utility in neonatal critical care

Genetics in Medicine Open, 2023, Vol.1 (1), p.100419, Article 100419

2023

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P543: Design and early findings from a mixed-methods study exploring the genomics era role of the medical geneticist in Canada

Genetics in Medicine Open, 2024, Vol.2, p.101442, Article 101442

2024

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P516: The Genetics Navigator: The development and usability testing of a new patient-facing digital health application to support clinical genetic testing

Genetics in Medicine Open, 2024, Vol.2, p.101415, Article 101415

2024

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Free genetic testing is not free of clinical and ethical considerations

Canadian Medical Association journal (CMAJ), 2024-07, Vol.196 (26), p.E910-E911

2024

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P531: Developing the patient-reported Genetic testing Utility InDEx (P-GUIDE): Assessing value of genetic testing from patients’ perspectives in multiple clinical contexts

Genetics in Medicine Open, 2024, Vol.2, p.101430, Article 101430

2024

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Equity implications of patient-initiated recontact and follow-up in clinical genetics

European journal of human genetics : EJHG, 2023-05, Vol.31 (5), p.495-496

2023

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Bioethics at the bedside

Paediatrics & child health, 2022-07, Vol.27 (4), p.203-205

2022

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The point‐of‐care use of a facial phenotyping tool in the genetics clinic: An ethics tête‐a‐tête

American journal of medical genetics. Part A, 2021-02, Vol.185 (2), p.658-660

2021

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The point-of-care use of a facial phenotyping tool in the genetics clinic: enhancing diagnosis and education with machine learning

Molecular genetics and metabolism, 2021-04, Vol.132, p.S103

2021

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eP155 - The point-of-care use of a facial phenotyping tool in the genetics clinic: enhancing diagnosis and education with machine learning

Molecular genetics and metabolism, 2021-04, Vol.132, p.S103-S103

2021

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Germline EPHB2 receptor variants in familial colorectal cancer

PloS one, 2008-08, Vol.3 (8), p.e2885-e2885

2008

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Canadian College of Medical Geneticists (CCMG) points to consider: resuming genetic services in a pandemic—a summary

Journal of medical genetics, 2022-01, Vol.59 (1), p.101-104

2022

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Next generation of free? Points to consider when navigating sponsored genetic testing

Journal of medical genetics, 2024-03, Vol.61 (4), p.299-304

2024

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eP431: Applying the clinician-reported genetic testing utility InDEx (C-GUIDE) to genome sequencing

Genetics in medicine, 2022-03, Vol.24 (3), p.S269-S270

2022

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The point‐of‐care use of a facial phenotyping tool in the genetics clinic: Enhancing diagnosis and education with machine learning

American journal of medical genetics. Part A, 2021-04, Vol.185 (4), p.1151-1158

2021

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Assessing the Performance of the Clinician-reported Genetic Testing Utility InDEx (C-GUIDE): Further Evidence of Inter-rater Reliability

Clinical therapeutics, 2023-08, Vol.45 (8), p.729-735

2023

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DNA methylation signature associated with Bohring-Opitz syndrome: a new tool for functional classification of variants in ASXL genes

European journal of human genetics : EJHG, 2022-06, Vol.30 (6), p.695-702

2022

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Screening for facial differences worldwide: equity and ethics

The Lancet. Digital health, 2021-10, Vol.3 (10), p.e615-e616

2021

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Applying the Clinician-reported Genetic testing Utility InDEx (C-GUIDE) to genome sequencing: further evidence of validity

European journal of human genetics : EJHG, 2022-12, Vol.30 (12), p.1423-1431

2022

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Evaluation of the diagnostic accuracy of exome sequencing and its impact on diagnostic thinking for patients with rare disease in a publicly funded health care system: A prospective cohort study

Genetics in medicine, 2024-02, Vol.26 (2), p.101012, Article 101012

2024

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Please give me a copy of my child's raw genomic data

Author Correction: Please give me a copy of my child's raw genomic data

Update on antidepressant use during breastfeeding

P479: The Clinician-reported Genetic testing Utility InDEx: A revised tool to quantify genome-wide sequencing utility in neonatal intensive care (C-GUIDE NICU)

P383: The clinician-reported genetic testing utility InDEx in the NICU (C-GUIDETM-NICU): Quantifying genome-wide sequencing utility in neonatal critical care

P543: Design and early findings from a mixed-methods study exploring the genomics era role of the medical geneticist in Canada

P516: The Genetics Navigator: The development and usability testing of a new patient-facing digital health application to support clinical genetic testing

Free genetic testing is not free of clinical and ethical considerations

P531: Developing the patient-reported Genetic testing Utility InDEx (P-GUIDE): Assessing value of genetic testing from patients’ perspectives in multiple clinical contexts

Equity implications of patient-initiated recontact and follow-up in clinical genetics

Bioethics at the bedside

The point‐of‐care use of a facial phenotyping tool in the genetics clinic: An ethics tête‐a‐tête

The point-of-care use of a facial phenotyping tool in the genetics clinic: enhancing diagnosis and education with machine learning

eP155 - The point-of-care use of a facial phenotyping tool in the genetics clinic: enhancing diagnosis and education with machine learning

Germline EPHB2 receptor variants in familial colorectal cancer

Canadian College of Medical Geneticists (CCMG) points to consider: resuming genetic services in a pandemic—a summary

Next generation of free? Points to consider when navigating sponsored genetic testing

eP431: Applying the clinician-reported genetic testing utility InDEx (C-GUIDE) to genome sequencing

The point‐of‐care use of a facial phenotyping tool in the genetics clinic: Enhancing diagnosis and education with machine learning

Assessing the Performance of the Clinician-reported Genetic Testing Utility InDEx (C-GUIDE): Further Evidence of Inter-rater Reliability

Patient-facing digital tools for delivering genetic services: a systematic review

DNA methylation signature associated with Bohring-Opitz syndrome: a new tool for functional classification of variants in ASXL genes

Screening for facial differences worldwide: equity and ethics

Applying the Clinician-reported Genetic testing Utility InDEx (C-GUIDE) to genome sequencing: further evidence of validity

Evaluation of the diagnostic accuracy of exome sequencing and its impact on diagnostic thinking for patients with rare disease in a publicly funded health care system: A prospective cohort study

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