Organizing Committee
- Anne Bassett, Director, Clinical Genetics Research Program, Centre for Addiction and Mental Health, Toronto, Canada; Medical Advisory Board, The International 22q11.2 Foundation, Inc.; Program Chair, The Eighth Biennial International 22q11.2 Deletion Syndrome Meeting
- Carol Cavana, President and Founding Board Member, The International 22q11.2 Foundation, Inc., Matawan, NJ, USA
- Christina Mannices, Manager Medical Staff Affairs, CME, The Children’s Hospital of Philadelphia, PA, USA
- Donna M. McDonald-McGinn, Associate Director, Clinical Genetics Center; Program Director, The “22q and You” Center, The Children’s Hospital of Philadelphia and The University of Pennsylvania School of Medicine, Philadelphia, PA; Founding Board Member, The International 22q11.2 Foundation, Inc.; Secretary General, The Eighth Biennial International 22q11.2 Deletion Syndrome Meeting; Conference Chair, The 2nd Biennial 22q11.2 Deletion Syndrome Meeting, Philadelphia, PA, USA
- Swati Patel, Undergraduate Student, Drexel University; Intern, The International 22q11.2 Foundation, Inc., Philadelphia, PA, USA
- Wendy Rose, Secretary and Founding Board Member, The International 22q11.2 Foundation, Inc., Moorestown, NJ, USA
- Elizabeth Utsch-George, CME Conference Planner, The Children’s Hospital of Philadelphia, PA
- Fred Weiner, Executive Director, Dragonfly Forest, Conshohocken, PA; Board Member, The International 22q11.2 Foundation, Inc.
Family Program Committee
- Anne Bassett, Director, Clinical Genetics Research Program, Centre for Addiction and Mental Health, Toronto, Canada; Medical Advisory Board, The International 22q11.2 Foundation, Inc.; Program Chair, The Eighth Biennial International 22q11.2 Deletion Syndrome Meeting
- Michelle Breedlove Sells, Director of Development and Community Outreach, “The Ryan and Jenny Dempster Family Foundation”, Atlanta, GA, USA
- Carol Cavana, President and Founding Board Member, The International 22q11.2 Foundation, Inc., Matawan, NJ, USA
- Karlene Coleman, RN, MN, Certified Genetic Counselor, Children’s Healthcare of Atlanta, GA, USA
- Ryan and Jenny Dempster, President and Vice President of “The Ryan and Jenny Dempster Family Foundation”, Atlanta, GA, USA
- Mindy Dodge, PRA, Clinic Coordinator, Chromosome 22q11.2 Deletion Syndrome Specialty Clinic, Children’s Hospital Colorado, Aurora, CO, USA
- Barb Hass-Givler, MEd, BCBA, Board Certified Behavior Analyst, Education Specialist, Genetic Services at Elwyn, PA, USA
- Shelia Kambin, Attending Physician, Center for Fetal Diagnosis and Therapy, The Children’s Hospital of Philadelphia, PA; Board Member, The International 22q11.2 Foundation, Inc.
- Maria Kamper, President, VCFS 22q11 Foundation, Charlton, Australia
- Daniella Krijger, Founder and President, Hoezo Anders Foundation; Author of Anders; Former Member,22q11.2 Support Network, Utrecht, The Netherlands
- Anne Lawlor, 22q Ireland Support Group, Dublin, Republic of Ireland
- Donna M. McDonald-McGinn, Associate Director, Clinical Genetics Center; Program Director, The “22q and You” Center, The Children’s Hospital of Philadelphia and The University of Pennsylvania School of Medicine, Philadelphia, PA; Founding Board Member, The International 22q11.2 Foundation, Inc.; Secretary General, The Eighth Biennial International 22q11.2 Deletion Syndrome Meeting; Conference Chair, The 2nd Biennial 22q11.2 Deletion Syndrome Meeting, Philadelphia, PA, USA
- Melissa K. Maisenbacher, MS, CGC, Natera, Inc., Redwood City, CA, USA
- Silvia Riccio, Italian Aide 22 Support Group, Rome, Italy
- Wendy Rose, Secretary and Founding Board Member, The International 22q11.2 Foundation, Inc., Moorestown, NJ
- Stephan Schmid, Founder and President, Kids-22q11 e.v., Kempten, Germany
- Jill Stein, Paradise Valley, AZ, USA
- Stephanie St-Pierre, Founder, Chromosome 22 Central, Timmins, Ontario, Canada
- Fred Weiner, Executive Director, Dragonfly Forest, Conshohocken, PA; Board Member, The International 22q11.2 Foundation, Inc.
- Julie Wooton, Founder and President, Max Appeal, Wollaston Stourbridge, England; Conference Chair, The 7th Biennial 22q11.2 Deletion Syndrome Meeting, Coventry, England
Professional Program Committee
- Anne Bassett, Director, Clinical Genetics Research Program, Centre for Addiction and Mental Health, Toronto, Canada; Medical Advisory Board, The International 22q11.2 Foundation, Inc.; Program Chair, The Eighth Biennial International 22q11.2 Deletion Syndrome Meeting
- Koenraad Devriendt, Center for Human Genetics, University Hospital Gasthuisberg, Leuven, Belgium
- Maria Cristina Digilio, Medical Genetics, Department of Pediatric Medicine, Pediatric Cardiology, and Cytogenetics, Bambino Gesù Children’s Hospital, Rome, Italy
- Alex Forsyth, Specialist Speech and Language Therapist, Great Ormond Street Children’s Hospital, London, UK
- Sixto García-Miñaúr, Department of Clinical Genetics, Institute of Medical and Molecular Genetics, La Paz University Hospital, Madrid, Spain
- Alex Habel, Great Ormond Street Children’s Hospital, London, UK
- Hiroshi Kawame, Medical Director, Master’s Program in Genetic Counseling Professor; Department of Genetic Counseling, Ochanomizu University, Tokyo, Japan
- Bruno Marino, Professor of Pediatrics; Chief Division of Pediatric Cardiology; Director of Department of Pediatrics, “La Sapienza” University of Rome, Rome, Italy; Conference Chair, The 3rd Biennial 22q11.2 Deletion Syndrome Meeting, Rome, Italy
- Donna M. McDonald-McGinn, Associate Director, Clinical Genetics Center; Program Director, The “22q and You” Center, The Children’s Hospital of Philadelphia and The University of Pennsylvania School of Medicine, Philadelphia, PA; Founding Board Member, The International 22q11.2 Foundation, Inc.; Secretary General, The Eighth Biennial International 22q11.2 Deletion Syndrome Meeting; Conference Chair, The 2nd Biennial 22q11.2 Deletion Syndrome Meeting, Philadelphia, PA, USA
- Bernice Morrow, Professor, Director of Division of Human Genetics, Albert Einstein College of Medicine, Bronx, NY
- Sólveig Óskarsdóttir, Consultant in Pediatrics, The Queen Silvia Children’s Hospital, Gothenburg, Sweden
- Christina Persson, Department of LogoPedics & Phoniatrics, The Sahlgrenska Academy at Goteborg University, Gothenburg, Sweden
- Nicole Philip, Department of Medical Genetics, The Children’s Hospital of la Timone, Marseille, France; Conference Chair, The 5th Biennial 22q11.2 Deletion Syndrome Meeting, Marseilles, France
- Peter Scambler, Molecular Medicine Unit, UCL Institute of Child Health, London, UK
- Kathleen Sullivan, Professor of Pediatrics; University of Pennsylvania, Medical School; Chief, Division of Allergy Immunology and Infectious Diseases, The Children’s Hospital of Philadelphia, PA, USA
- Damian Heine Suñer, Molecular Genetics Laboratory, Department of Genetics, Hospital Son Espases, Palma, Spain
- Ann Swillen, Professor, Center of Human Genetics, University Hospital of Gasthuisberg; Department of Human Genetics, Department of Rehabilitation Sciences, University of Leuven, Leuven, Belgium
- Nancy Unanue, Endocrinology and Genetics Unit, Children’s, Hospital Clinico San Borja Arriarán; Maternal and Child Health Research Institute, University of Chile, Clinica Las Condes, Santiago, Chile
- Jacob Vorstman, Assistant Professor Child and Adolescent Psychiatry & Psychiatry Genetics, Rudolf Magnus Institute of Neuroscience, University of Medical Center Utrecht; Conference Chair, The 6th Biennial 22q11.2 Deletion Syndrome Meeting, Utrecht, The Netherlands
2012 Auction Committee
- Anne Bassett, Toronto, Canada
- Carol Cavana, Matawan, NJ, USA
- Colleen Ciak, Delran, NJ, USA
- Sheila Kambin, Philadelphia, PA, USA
- Melissa K. Maisenbacher, Redwood City, CA, USA
- Donna M. McDonald-McGinn, Philadelphia, PA, USA
- Swati Patel, Philadelphia, PA, USA
- Wendy Rose, Moorestown, NJ, USA
- Kathleen Sullivan, Philadelphia, PA, USA
- Joe Uccello, Colchester, CT, USA
- Paula Uccello, Colchester, CT, USA
