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American Journal of Human Genetics
|
November 20, 2025
Training competencies and recommendations for the next generation of public health genetics: Reflections from current leaders in the field
Diane Xue, Elizabeth E Blue, Stephanie M Fullerton, et al.
Clinical Obesity
|
October 7, 2021
Metabolically healthy obesity in children enrolled in the CANadian Pediatric Weight management Registry (CANPWR): An exploratory secondary analysis of baseline data
Samah Damanhoury, Katherine M Morrison, Rajibul Mian, et al.
HGG Advances
|
January 20, 2022
Variants in <i>LSM7</i> impair LSM complexes assembly, neurodevelopment in zebrafish and may be associated with an ultra-rare neurological disease
Alexa Derksen, Hung-Yu Shih, Diane Forget, et al.
Journal of Child Neurology
|
May 24, 2023
The Experience of Parents of Children With Genetically Determined Leukoencephalopathies With the Health Care System: A Qualitative Study
Pouneh Amir Yazdani, Marie-Lou St-Jean, Sara Matovic, et al.
Journal of Inherited Metabolic Disease
|
July 26, 2015
Child and family experiences with inborn errors of metabolism: a qualitative interview study with representatives of patient groups
Sara D Khangura, Kylie Tingley, Pranesh Chakraborty, et al.
Journal of Child Neurology
|
January 5, 2022
Experience of Parents of Children with Genetically Determined Leukoencephalopathies Regarding the Adapted Health Care Services During the COVID-19 Pandemic
Pouneh Amir Yazdani, Marie-Lou St-Jean, Sara Matovic, et al.
Journal of Medical Genetics
|
January 2, 2025
Sexual dimorphism in <i>SMAD3</i> pathogenic variant-harbouring individuals
Julie Richer, Joe Davis Velchev, Sharan Goobie, et al.
BMC Pediatrics
|
April 18, 2015
Scoping review of patient- and family-oriented outcomes and measures for chronic pediatric disease
Sara D Khangura, Maria D Karaceper, Yannis Trakadis, et al.
Orphanet Journal of Rare Diseases
|
February 5, 2016
The health system impact of false positive newborn screening results for medium-chain acyl-CoA dehydrogenase deficiency: a cohort study
Maria D Karaceper, Pranesh Chakraborty, Doug Coyle, et al.
The Patient
|
July 20, 2021
Family Experiences with Care for Children with Inherited Metabolic Diseases in Canada: A Cross-Sectional Survey
Andrea J Chow, Michael Pugliese, Laure A Tessier, et al.
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of 10
Search research articles
Search
Showing results (71-80 of 93) with videos related to
Sort By:
Page
of 10
American Journal of Human Genetics
|
November 20, 2025
Training competencies and recommendations for the next generation of public health genetics: Reflections from current leaders in the field
Diane Xue, Elizabeth E Blue, Stephanie M Fullerton, et al.
Clinical Obesity
|
October 7, 2021
Metabolically healthy obesity in children enrolled in the CANadian Pediatric Weight management Registry (CANPWR): An exploratory secondary analysis of baseline data
Samah Damanhoury, Katherine M Morrison, Rajibul Mian, et al.
HGG Advances
|
January 20, 2022
Variants in <i>LSM7</i> impair LSM complexes assembly, neurodevelopment in zebrafish and may be associated with an ultra-rare neurological disease
Alexa Derksen, Hung-Yu Shih, Diane Forget, et al.
Journal of Child Neurology
|
May 24, 2023
The Experience of Parents of Children With Genetically Determined Leukoencephalopathies With the Health Care System: A Qualitative Study
Pouneh Amir Yazdani, Marie-Lou St-Jean, Sara Matovic, et al.
Journal of Inherited Metabolic Disease
|
July 26, 2015
Child and family experiences with inborn errors of metabolism: a qualitative interview study with representatives of patient groups
Sara D Khangura, Kylie Tingley, Pranesh Chakraborty, et al.
Journal of Child Neurology
|
January 5, 2022
Experience of Parents of Children with Genetically Determined Leukoencephalopathies Regarding the Adapted Health Care Services During the COVID-19 Pandemic
Pouneh Amir Yazdani, Marie-Lou St-Jean, Sara Matovic, et al.
Journal of Medical Genetics
|
January 2, 2025
Sexual dimorphism in <i>SMAD3</i> pathogenic variant-harbouring individuals
Julie Richer, Joe Davis Velchev, Sharan Goobie, et al.
BMC Pediatrics
|
April 18, 2015
Scoping review of patient- and family-oriented outcomes and measures for chronic pediatric disease
Sara D Khangura, Maria D Karaceper, Yannis Trakadis, et al.
Orphanet Journal of Rare Diseases
|
February 5, 2016
The health system impact of false positive newborn screening results for medium-chain acyl-CoA dehydrogenase deficiency: a cohort study
Maria D Karaceper, Pranesh Chakraborty, Doug Coyle, et al.
The Patient
|
July 20, 2021
Family Experiences with Care for Children with Inherited Metabolic Diseases in Canada: A Cross-Sectional Survey
Andrea J Chow, Michael Pugliese, Laure A Tessier, et al.
Page
of 10