Publications by authors named "Andrea Shugar"

17Publications

A novel ENPP1 mutation identified in a multigenerational family affected by Cole disease.

Pediatr Dermatol 2020 Sep 29;37(5):868-871. Epub 2020 Jun 29.

Section of Dermatology, Division of Paediatric Medicine, The Hospital for Sick Children, University of Toronto, Toronto, ON, Canada.

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September 2020

Mosaic Neurofibromatosis Type 1 in Children: A Single-Institution Experience.

J Cutan Med Surg 2017 Sep/Oct;21(5):379-382. Epub 2017 Apr 27.

3 Division of Clinical and Metabolic Genetics Hospital for Sick Children, Department of Molecular Genetics, University of Toronto, Toronto, Ontario, Canada.

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June 2018

Homozygous mutation in PRUNE1 in an Oji-Cree male with a complex neurological phenotype.

Am J Med Genet A 2017 Mar;173(3):740-743

Division of Clinical and Metabolic Genetics, The Hospital for Sick Children, Ontario, Canada.

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March 2017

Teaching Genetic Counseling Skills: Incorporating a Genetic Counseling Adaptation Continuum Model to Address Psychosocial Complexity.

Authors:
Andrea Shugar

J Genet Couns 2017 Apr 28;26(2):215-223. Epub 2016 Nov 28.

Division of Clinical & Metabolic Genetics, The Hospital for Sick Children, 555 University Avenue, Toronto, ON, M5G 1X8, Canada.

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April 2017

Internet Safety Issues for Adolescents and Adults with Intellectual Disabilities.

J Appl Res Intellect Disabil 2017 Mar 23;30(2):416-418. Epub 2016 Feb 23.

The Dalglish Family 22q Clinic, Toronto General Hospital, University Health Network, Toronto, ON, Canada.

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March 2017

An increased prevalence of thyroid disease in children with 22q11.2 deletion syndrome.

Am J Med Genet A 2015 Jul 5;167(7):1560-4. Epub 2015 May 5.

Division of Clinical & Metabolic Genetics, The Hospital for Sick Children, Toronto, ON, Canada.

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July 2015

Practical guidelines for managing adults with 22q11.2 deletion syndrome.

Genet Med 2015 Aug 8;17(8):599-609. Epub 2015 Jan 8.

1] The Dalglish Family Hearts and Minds Clinic for 22q11.2 Deletion Syndrome, Toronto General Hospital, University Health Network, Toronto, Ontario, Canada [2] Clinical Genetics Research Program, Centre for Addiction and Mental Health, Toronto, Ontario, Canada [3] Department of Psychiatry and Toronto General Research Institute, University Health Network, Toronto, Ontario, Canada [4] Department of Psychiatry, University of Toronto, Toronto, Ontario, Canada [5] Institute of Medical Science, University of Toronto, Toronto, Ontario, Canada [6] Campbell Family Mental Health Research Institute, Centre for Addiction and Mental Health, Toronto, Ontario, Canada [7] Division of Cardiology, Department of Medicine, University Health Network, Toronto, Ontario, Canada.

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August 2015

Personality traits associated with genetic counselor compassion fatigue: the roles of dispositional optimism and locus of control.

J Genet Couns 2011 Oct 24;20(5):526-40. Epub 2011 Jun 24.

Department of Obstetrics and Gynecology, Prenatal Diagnosis and Medical Genetics Program, Mount Sinai Hospital, Joseph and Wolf Lebovic Health Complex, 600 University Avenue, Toronto, Ontario, M5G 1X5, Canada.

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October 2011

The co-occurrence of early onset Parkinson disease and 22q11.2 deletion syndrome.

Am J Med Genet A 2009 Mar;149A(3):525-8

Department of Medical Genetic Services, Marshfield Clinic, Marshfield, Wisconsin 54449, USA.

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March 2009

The family history: An integral component of paediatric health assessment.

Authors:
Andrea L Shugar

Paediatr Child Health 2003 Jan;8(1):33-5

North York General Hospital, Toronto, Ontario.

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January 2003