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X-WR-CALDESC:Events for CCMG | CCGM
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DTSTART;TZID=America/Toronto:20260220T110000
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DTSTAMP:20260626T130903
CREATED:20260211T215529Z
LAST-MODIFIED:20260212T203441Z
UID:10000116-1771585200-1771588800@ccmg.51-222-78-205.ygkweb.ca
SUMMARY:TeleGraf
DESCRIPTION:About this series – Telehealth for Genetics Residents and Fellows. A monthly teaching session brought to you by the members of the RCPSC Specialty Committee in Medical Genetics. \nTo register\, click the button below or go to https://us06web.zoom.us/webinar/register/WN_2LAO5jlHSQ-WA_xonc9ouA. \n \n  \n  \n  \n  \n2025-2026 TeleGraf from 11:00am – 12:00pm ET on:\nFriday\, February 20\, 2026\nHiding in Plain Sight – What we have learned about and from ReNU Syndrome in 18 Months \nOver the course of this presentation we will reflect on the remarkable progress made in the understanding of the ReNU syndrome since it was first identified about 18 months. We will also provide perspectives from clinicians\, researchers and families on some of the major priorities moving forward. \nLearning Objectives: \n\nIdentify classes of genetic variants not well detected by routine clinical testing.\nDescribe the clinical features of ReNU syndrome and related disorders.\nReflect on the importance of patients and families as partners with clinicians and scientists in identifying priorities in rare disease care and research.\n\nSpeakers: Dr. Micheil Innes & Lindsay Pearse \n \nDr. Micheil Innes is a Professor of Pediatrics and Medical Genetics\, Cumming School of Medicine\, University of Calgary. His clinical interests include dysmorphology\, neurogenetics and hereditary endocrine disorders and his academic program focuses on gene discovery\, syndrome delineation and translation of novel genetic technologies to the clinic. He is a past chair of the Specialty Committee of Medical Genetics and Genomics at the Royal College\, and was a previous (and current acting) program director of the Medical Genetics and Genomics residency training program at the University of Calgary. \n  \n \nLindsay Pearse is a co-founder of ReNU Syndrome United and serves as the Vice President of the Board. She resides in Northern Virginia with her husband and three sons\, ages 9\, 4\, and 2. Her oldest son\, Lars\, was diagnosed with ReNU syndrome in March 2024. Lindsay is a passionate disability rights advocate and has served as a gubernatorial appointee on the Virginia Developmental Disabilities Council for the past 6 years. Lindsay has 20 years of experience in the public and nonprofit sectors\, and most recently spent 10+ years overseeing strategy and operations at the United Nations Foundation. Lindsay is immensely grateful to finally have our community of ReNU warriors and is honored to be involved in advancing the mission of ReNU Syndrome United. \n\n\n\nFriday\, March 20\, 2026 – Tentative\nFriday\, April 17\, 2026\nFriday\, May 15\, 2026\nFriday\, June 19\, 2026
URL:https://ccmg.51-222-78-205.ygkweb.ca/event/telegraf-4-5/
ORGANIZER;CN="CCMG | CCGM":MAILTO:info@ccmg-ccgm.org
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DTSTART;TZID=America/Toronto:20260227T120000
DTEND;TZID=America/Toronto:20260227T130000
DTSTAMP:20260626T130903
CREATED:20260219T214605Z
LAST-MODIFIED:20260302T214932Z
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SUMMARY:Can-GARD/CCMG – The Leading Strand Series
DESCRIPTION:This series is for genetics health professionals led by the Canadian College of Medical Genetics and co-sponsored by Can-GARD. Speakers will be translation-focused researchers\, clinicians and innovators.  The series will help attendees anticipate\, access\, and apply new approaches and technologies for patient care. \nThe Can-GARD/CCMG Leading Strand Series is a self-approved group learning activity (Section 1) as defined by the Maintenance of Certification Program of the Royal College of Physicians and Surgeons of Canada. \nWe are pleased to share that as of the 2026/2027 season\, the Garrod Association will be providing two presentations per season. \nTo register\, click the button below or go to: https://us06web.zoom.us/webinar/register/WN_e2yO6xnsSK2v70BLslqwjA  \n \n  \n  \n  \n2025-2026 Leading Strand from 12:00pm – 1:00pm ET on:\nFriday February 27\, 2026\nIntegrating Genomics into Pediatric Care \nThis session will provide an overview of the development of a genomics program for the care for children at Children’s Wisconsin. \nLearning Objectives: \n\nExplain the importance of integrating genomics.\nUnderstand the challenges involved.\nDescribe the process of integrating genomic information into patient care.\nAppreciate the various nuances in overall genomic medicine.\n\nSpeaker: Dr. Donald Basel \nDr. Donald Basel is a Professor of Pediatrics and Division Chief of Genetics at MCW. He serves as the Medical Director for Genetics and the Undiagnosed Center of Excellence at Children’s Wisconsin. He has been a practicing geneticist for 25 years\, 7 years in bench research developing proof of concept therapies for targeted down regulation of collagen in a osteogenesis imperfect mouse model. He has grown the genomics program at CW/MCW and implemented an integrated genomics approach to diagnosis and care for children at CW. He is the PI on several studies for inborn errors of metabolism and has a strong track record of research collaboration. He is a keen advocate for healthy kids in Wisconsin and strives to improve quality of care and equitable access to tertiary care for all.\n \nFriday March 27\, 2026 \nFriday April 24\, 2026\nFriday May 29\, 2026\nFriday June 26\, 2026
URL:https://ccmg.51-222-78-205.ygkweb.ca/event/can-gard-ccmg-the-leading-strand-series-4-7/
ORGANIZER;CN="CCMG | CCGM":MAILTO:info@ccmg-ccgm.org
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