20170501 CCMG-CCGM - Symposium 1 CNV and New Pathogenic Models in Neurodevelopmental Disorders Question Title * 1. Please assess the Sessions overrall Strongly Disagree Disagree Neutral Agree Strongly Agree Sufficient time was allowed for audience participation/active learning Sufficient time was allowed for audience participation/active learning Strongly Disagree Sufficient time was allowed for audience participation/active learning Disagree Sufficient time was allowed for audience participation/active learning Neutral Sufficient time was allowed for audience participation/active learning Agree Sufficient time was allowed for audience participation/active learning Strongly Agree The facilities were satisfactory The facilities were satisfactory Strongly Disagree The facilities were satisfactory Disagree The facilities were satisfactory Neutral The facilities were satisfactory Agree The facilities were satisfactory Strongly Agree The session was free from commercial bias The session was free from commercial bias Strongly Disagree The session was free from commercial bias Disagree The session was free from commercial bias Neutral The session was free from commercial bias Agree The session was free from commercial bias Strongly Agree Overall, I would rate this Symposium as excellent Overall, I would rate this Symposium as excellent Strongly Disagree Overall, I would rate this Symposium as excellent Disagree Overall, I would rate this Symposium as excellent Neutral Overall, I would rate this Symposium as excellent Agree Overall, I would rate this Symposium as excellent Strongly Agree Please assess each Speaker by their Session: Question Title * 2. Pathogenic CNVs, the adult phenotype, and counselling about long term outcomeSpeaker: Anne Bassett Department of Psychiatry, University of Toronto, Toronto ONObjectives: At the end of this session, participants will be able to:1. Appreciate the important role of counselling about the adult phenotype of pathogenic copy number variations for individuals at different life stages 2. List three treatable conditions usually arising in adulthood associated with at least two different pathogenic CNVs 3. Describe potential benefits of genetic diagnosis for patients with schizophrenia, their families, and their clinicians Poor Fair Good Very Good Outstanding Clarity of Voice Clarity of Voice Poor Clarity of Voice Fair Clarity of Voice Good Clarity of Voice Very Good Clarity of Voice Outstanding Met Stated Objectives Met Stated Objectives Poor Met Stated Objectives Fair Met Stated Objectives Good Met Stated Objectives Very Good Met Stated Objectives Outstanding Balanced & Unbiased Balanced & Unbiased Poor Balanced & Unbiased Fair Balanced & Unbiased Good Balanced & Unbiased Very Good Balanced & Unbiased Outstanding Relevant to Practice Overall Relevant to Practice Overall Poor Relevant to Practice Overall Fair Relevant to Practice Overall Good Relevant to Practice Overall Very Good Relevant to Practice Overall Outstanding Time for Active Learning Time for Active Learning Poor Time for Active Learning Fair Time for Active Learning Good Time for Active Learning Very Good Time for Active Learning Outstanding Comments Question Title * 3. The joy and pain of genetic counselling for recurrent CNVs implicated in neurodevelopmental disordersSpeaker: Melissa Carter Children’s Hospital of Eastern Ontario, Ottawa ONObjectives: At the end of this session, participants will be able to:1. Discuss the differences between a "syndrome" and a "susceptibility variant" with respect to recurrent CNVs 2. Understand one's own biases, and those in the case report literature, regarding these CNVs 3. Identify the gaps in the current evidence base for the pathogenic nature of these CNVs 4. Share ideas about how to counsel our patients in the absence of certainty Poor Fair Good Very Good Outstanding Clarity of Voice Clarity of Voice Poor Clarity of Voice Fair Clarity of Voice Good Clarity of Voice Very Good Clarity of Voice Outstanding Met Stated Objectives Met Stated Objectives Poor Met Stated Objectives Fair Met Stated Objectives Good Met Stated Objectives Very Good Met Stated Objectives Outstanding Balanced & Unbiased Balanced & Unbiased Poor Balanced & Unbiased Fair Balanced & Unbiased Good Balanced & Unbiased Very Good Balanced & Unbiased Outstanding Relevant to Practice Overall Relevant to Practice Overall Poor Relevant to Practice Overall Fair Relevant to Practice Overall Good Relevant to Practice Overall Very Good Relevant to Practice Overall Outstanding Time for Active Learning Time for Active Learning Poor Time for Active Learning Fair Time for Active Learning Good Time for Active Learning Very Good Time for Active Learning Outstanding Comments Question Title * 4. Gene Dosage effects on cognition and additive/oligogenic models in the neurodevelopmental clinicSpeaker: Sebastien JacquemontHôpital Ste-Justine, Montréal QC Objectives: At the end of this session, participants will be able to:1. Understand the heritability of cognitive and behavioral traits 2. Understand the quantitative effects of genomic variants on cognitive and behavioral traits 3. Use available data to understand the contribution of genomic variants to the symptoms present in patients referred for a neurodevelopmental disorder. 4. Understand the implication of these studies on genetic counselling Poor Fair Good Very Good Outstanding Clarity of Voice Clarity of Voice Poor Clarity of Voice Fair Clarity of Voice Good Clarity of Voice Very Good Clarity of Voice Outstanding Met Stated Objectives Met Stated Objectives Poor Met Stated Objectives Fair Met Stated Objectives Good Met Stated Objectives Very Good Met Stated Objectives Outstanding Balanced & Unbiased Balanced & Unbiased Poor Balanced & Unbiased Fair Balanced & Unbiased Good Balanced & Unbiased Very Good Balanced & Unbiased Outstanding Relevant to Practice Overall Relevant to Practice Overall Poor Relevant to Practice Overall Fair Relevant to Practice Overall Good Relevant to Practice Overall Very Good Relevant to Practice Overall Outstanding Time for Active Learning Time for Active Learning Poor Time for Active Learning Fair Time for Active Learning Good Time for Active Learning Very Good Time for Active Learning Outstanding Comments Question Title * 5. Gene Dosage effects on cognition and additive/oligogenic models in the neurodevelopmental clinicSpeaker: Melissa Carter Children’s Hospital of Eastern Ontario, Ottawa ON Objectives: At the end of this session, participants will be able to:1. Understand the heritability of cognitive and behavioral traits 2. Understand the quantitative effects of genomic variants on cognitive and behavioral traits 3. Use available data to understand the contribution of genomic variants to the symptoms present in patients referred for a neurodevelopmental disorder. 4. Understand the implication of these studies on genetic counselling Poor Fair Good Very Good Outstanding Clarity of Voice Clarity of Voice Poor Clarity of Voice Fair Clarity of Voice Good Clarity of Voice Very Good Clarity of Voice Outstanding Met Stated Objectives Met Stated Objectives Poor Met Stated Objectives Fair Met Stated Objectives Good Met Stated Objectives Very Good Met Stated Objectives Outstanding Balanced & Unbiased Balanced & Unbiased Poor Balanced & Unbiased Fair Balanced & Unbiased Good Balanced & Unbiased Very Good Balanced & Unbiased Outstanding Relevant to Practice Overall Relevant to Practice Overall Poor Relevant to Practice Overall Fair Relevant to Practice Overall Good Relevant to Practice Overall Very Good Relevant to Practice Overall Outstanding Time for Active Learning Time for Active Learning Poor Time for Active Learning Fair Time for Active Learning Good Time for Active Learning Very Good Time for Active Learning Outstanding Comments Question Title * 6. Copy Number Variants in Neurodevelopmental DisordersSpeaker: Christian Marshall The Hospital for Sick Children, Toronto ON Objectives: At the end of this session, participants will be able to:1. Differentiate between recurrent and non-recurrent copy number variants and identify the mechanisms that lead to their formation.2. Describe the strategies used for interpretation of copy number variants including the criteria used to establish clinical significance.3. Identify the most common CNVs associated with neurodevelopmental disorders. Poor Fair Good Very Good Outstanding Clarity of Voice Clarity of Voice Poor Clarity of Voice Fair Clarity of Voice Good Clarity of Voice Very Good Clarity of Voice Outstanding Met Stated Objectives Met Stated Objectives Poor Met Stated Objectives Fair Met Stated Objectives Good Met Stated Objectives Very Good Met Stated Objectives Outstanding Balanced & Unbiased Balanced & Unbiased Poor Balanced & Unbiased Fair Balanced & Unbiased Good Balanced & Unbiased Very Good Balanced & Unbiased Outstanding Relevant to Practice Overall Relevant to Practice Overall Poor Relevant to Practice Overall Fair Relevant to Practice Overall Good Relevant to Practice Overall Very Good Relevant to Practice Overall Outstanding Time for Active Learning Time for Active Learning Poor Time for Active Learning Fair Time for Active Learning Good Time for Active Learning Very Good Time for Active Learning Outstanding Comments Question Title * 7. As a result of attending this session, I am planning to: a) Discuss the session with my colleagues b) Pursue additional learning activities. c) Complete a Personal Learning Project. d) Not change my practice. e) Change my practice. Question Title * 8. Please explain any changes you plan to make or personal learning projects you will pursue as a result of this session: Question Title * 9. Please indicate which CanMEDS roles you felt were addressed during this educational activity. (Select all that apply) Medical Expert Communicator Collaborator Manager Health Advocate Scholar Professional Question Title * 10. General comments about individual speaker: Question Title * 11. What topics would you like to be addressed at future conferences to keep you up to date in your profession? Done