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 Welcome! Our affiliation with Arcadia University'southward Genetic Counseling Program began on October 1, 2014. Since then, under the academic directorship of Kathleen Valverde, MS, CGC, and Laura Conway, PhD, CGC, the Course has been reorganized to meliorate navigation and report organization and new lectures and tutorials have equaled over 62 contact hours. All course materials may be viewed on your iPad or tablet. Visit us on Facebook (Genetics Online Review Course) to be the first to know about upcoming additions, new materials and their post dates. Registrants volition also be able to larn near new postings on the Class site through periodic due east-blasts we ship to our registrants, only. We are grateful to Betsy Gettig, MS, CGC, for her involvement and leadership with this course and who was instrumental in taking the course from an onsite to an online format. She is at present in a corporate role and retains the title of Course Director Emeritus. As ever, additions, updates and improvements both in the academics and functionality of this grade have been largely based on your communications with usa. Please continue provide us with your thoughts and we promise to continue to exist responsive to you. Bea Leopold and Audrey Lombard, Direction Squad
Chris Huziak, IT Manager
Kathy Valverde, MS, CGC, and Laura Conway, PhD, CGC, Academic Co-directors Sponsor and Management Registration and Course Dates of Tape History Online Learning Target Course Participants Statement of Purpose Class Goals Meeting your Individualized and Grouping Report Goals Faculty Kinesthesia Biosketches Continuing Pedagogy Units (CEUs) Conflict of Interest Disclosure Argument Lectures Sessions Registration Fee Schedule Counterfoil Policy Registration Contact Information Register Now past mail service Register Online with Credit Cards Bookish Sponsorship: Arcadia Academy Genetic Counseling Program Management: Bea Leopold, BLCommunications, LLC, Wallingford, Pennsylvania Registration is ongoing and bachelor anytime. Your registration is valid for 9 total months following the date y'all receive your access information, most often within three business days of your registration. For example: If your registration date is February 20, 2018, your admission will be active until November 30, 2018. If your registration date is October 1, 2018, your access will be active until July 31, 2019. If you are in a written report group, access will exist released in one case all members are registered. Your access will begin on the mean solar day we ship your codes. The genealogy of this course traces back to Dr. Elizabeth F. Neufeld, now Professor Emerita at the Department of Biological Chemistry at the University of California at Los Angeles. In 1984, Dr. Neufeld urged Dan Camerini-Otero, MD, PhD, Alan Schechter, MD, and John Mulvihill, MD, to develop a two-24-hour interval course in medical genetics nether the sponsorship of the Interinstitute Medical Genetics Plan of the National Institutes of Health in anticipation of the pending examination past the newly-formed American Board of Medical Genetics. With directors and venues and e'er changing subject matters and emphases, courses were given in 1984, 1987, 1990 and 1993. For subsequent cycles, 1996 through 2005, Elizabeth (Betsy) Gettig, MS, CGC, joined Dr. Mulvihill as co-manager and the National Society of Genetic Counselors collaborated in a concern and managerial role under the management of Bea Leopold, NSGC's Executive Manager. In 2007, in its 10th update, the class converted to an online format, directed by Ms. Gettig and Dr. Mulvihill at the University of Pittsburgh Section of Human Genetics. Ms. Leopold connected equally business and management director through her consulting visitor, BLCommunications. With changes to the exam dates, the course was bachelor on an ongoing, open up enrollment footing. The course was granted approving in 2008 for Category I Continuing Education Units (CEUs) by the American Board of Genetic Counseling. From 2009 - 2015, it was canonical for CMEs by the Oklahoma Academy Health Sciences Heart's Part of Continuing Professional person Evolution. Due to low requests for CMEs, they were no longer offered after June 30, 2015. In 2014, in its 30th year, the bookish habitation moved to Arcadia University with Kathleen Valverde, MS, CGC, and Dr. Laura Conway, PhD, CGC, as Bookish Directors. Dr. Mulvihill continues as Medical Manager, and the grade continues nether the business organisation management of BLCommunications, LLC. Ms. Gettig retains the title Course Director Emeritus. With this leadership team, the course volition keep to expand and update its offerings to provide loftier-level, intensive and broad-reaching teaching to serve the medical genetics and genetic counseling customs and other related professionals. Online learning has many advantages. - Information technology is available 24/seven, meeting your schedule and pace preferences.
- It saves travel-related expenses and lost time from the office.
- Information technology provides a generous allotment of CEUs for practicing genetic counselors to fulfill ongoing educational requirements, all at the convenience of your office or habitation computer.
You, the registrants, win past being offered a comprehensive, well-organized programme "in existent time" that delivers the highest quality didactic and interactive learning environment. We look forward to your participation and to meeting your needs with stellar service too as fast, efficient and effective learning opportunities. This course has been developed as an advanced, intensive learning feel for the post-obit groups: - Individuals preparing to sit for the American Board of Genetic Counseling or American Board of Medical Genetics examinations and maintenance of certification (EMOC).
- Genetic professionals wishing to earn ABGC-approved Category i CEUs.
- Certified genetic counselors, geneticists and other health care professionals seeking to review or refresh their knowledge of genetics and genetic counseling to fulfill continuing pedagogy requirements by the American Board of Genetic Counseling or other genetics or genomics certifying bodies.
- Clinicians, scientists, health care providers with a desire for an in-depth survey of bones and clinical genetics and genetic counseling best practices.
- Genomic industry sales or scientific squad members wishing for an intensive, self-paced review of basic genetics.
- Individuals with a desire to explore their understanding of avant-garde and clinical genetics.
The purpose of this grade is to provide a comprehensive review of the field of medical genetics, advances in genomic medicine and issues related to genetic counseling. It may be utilized as an aid in preparation for the American Board of Genetic Counseling (ABGC) and American Board of Medical Genetics (ABMG) comprehensive examinations or as an in-depth educational experience for those seeking a knowledge base or refresher in these areas of study. Form registrants must have an understanding of basic and practical genetics, genomics, statistics and counseling theory to derive maximum benefit from this class. This course is an intensive online review of medical genetics and genetic counseling. At the conclusion of the course, participants should be able: - To identify specific areas of strengths and weaknesses in genetic cognition and counseling theory using pre- and mail service-test tools.
- To utilize basic genetic principles and case study examples in medical and genetic counseling practise.
- To apply knowledge, concepts and theories learned throughout the course to amend genetics practice skills.
Access to this class is available on a secured, password-protected website. Registrants may access the course on whatsoever computer at whatsoever time, 24/vii. All registrants will be invited to voluntarily complete an online pre-test prior to taking the course to identify specific areas of strength and weakness. Results are not graded or shared with others. The intent of the pre-test is to allow registrants to place areas of full-bodied written report. A mail service-test is too bachelor, and once again, the results are not graded or shared with others. These tests may be taken repeatedly for self-assessment purposes. Biochemical Genetics
Lewis J. Waber, MD, PhD, UT Southwestern Medical Center, Dallas TX (ret.); Colleen Muraresku, MS, CGC, Children'due south Hospital of Philadelphia, Philadelphia PA Cancer
Katherine A. Schneider, MPH, CGC, Dana-Farber Cancer Institute, Boston MA; Jill Stopfer, MS, CGC, Dana-Farber Cancer Institute, Boston MA Cardiovascular Genetics
Emily Yard. James, MS, CGC, Invitae, Pittsburgh PA
Cytogenetics
Stuart Schwartz, PhD, Laboratory Corporation of America, Enquiry Triangle Park NC Ideals
Dawn C. Allain, MS, LGC, The Ohio State University Genetic Counseling Program, Columbus OH Genetic Counseling Principles and Practice
Carrie Atzinger, MS, CGC, Academy of Cincinnati, Cincinnati OH; Kathryn Spitzer Kim, MS, CGC, Stanford, CA (former Director of Genetic Counseling Education, Arcadia University, Glenside, PA); Lisa Kessler, MS, CGC, Arcadia Academy, Glenside PA; Kathleen Valverde, MS, CGC, Arcadia University, Glenside PA Genetics and the Law
Emily M. James, MS, CGC, Invitae, Pittsburgh PA
Introduction to Course
Kathleen Valverde, MS, CGC, Arcadia Academy, Glenside PA
Medical Genetics
Jehannine Austin, PhD, CGC, CCGC, University of British Columbia, Vancouver, BC, Canada; Brenda Finucane, MS, LGC, Geisinger Health System, Lewisburg PA; TO: Emily M. James, MS, CGC, Invitae, Pittsburgh PA; Staci Kallish, DO, Perelman Schoolhouse of Medicine at University of Pennsylvania School of Medicine, Philadelphia PA; Ian Krantz, Dr., Children'south Infirmary of Philadelphia, Philadelphia PA; Donna McDonald-McGinn, MS, LCGC, Children's Hospital of Philadelphia, Philadelphia PA; Reed Pyeritz, Dr., Perelman Schoolhouse of Medicine at University of Pennsylvania, Philadelphia PA; Ronald Rubenstein, MD, Children'due south Hospital of Philadelphia, Philadelphia PA Molecular Genetics
Laura J. Conway, PhD, CGC, Arcadia University, Glenside PA Neurogenetics
Livija Medne, MS, CGC, Children's Hospital of Philadelphia, Philadelphia PA; Elisabeth Wood, MS, CGC, Academy of Pennsylvania, Philadelphia PA
New Genomics
Cecelia A. Bellcross, PhD, CGC, Emory Genetic Counseling Plan, Atlanta GA; Jodie M. Vento, MGC, CGC, Children's Hospital of Pittsburgh, Pittsburgh PA
Prenatal
Dee Quinn, MS, CGC, Arizona Pregnancy Riskline and College of Medicine and Pharmacy, University of Arizona, Tucson AZ; Katie Stoll, MS, CGC, Genetic Back up Foundation, Olympia WA; Ronald J. Wapner, Physician, Columbia University Medical Center, New York, NY; Vivian Weinblatt, MS, LGC, Integrated Genetics of LabCorp Specialty Laboratory, Philadelphia PA
Quantitative Genetics
Lisa Schwartz, MS, EdD, CGC, The George Washington Academy, Washington, DC; Robert Wilson, Medico, PhD, University of Pennsylvania, Philadelphia PA
Dawn C. Allain, MS, LGC, Director of The Ohio State University (OSU) Genetic Counseling Graduate Plan, is a licensed genetic counselor and Assistant Professor of Clinical Internal Medicine at the OSU Wexner Medical Center in Columbus, OH. She was awarded a Master'south caste in Genetic Counseling from Northwestern Academy in 1993 and was certified by the American Lath of Genetic Counselors in 1996. Ms. Allain served as a member of the OSU Biomedical Institution Review Board from 2006 through 2014 and is a fellow member of the OSU Higher of Medicine's Center for Bioethics and Medical Humanities. She is currently a member of the National Guild of Genetic Counselors' (NSGC) Jane Engelberg Memorial Fellowship Informational Group, is a past member of the NSGC Ideals Advisory Group and is a past president the NSGC. Most recently, she authored ii chapters in a book published in October 2014, Ethical Dilemmas in Genetics and Genetic Counseling, "Testing Children for Developed Onset Weather condition," and "Ethical Issues in Genetic and Genomic Research." Carrie Atzinger, MS, CGC, is a graduate of the University of Cincinnati Genetic Counseling Plan, where she now serves equally Assistant Director. Her clinical practice specializes in pediatrics at the Cincinnati Children'southward Hospital Medical Center. In improver, whe coordinates CCHMC's Marfan/Ehlers-Danlos Syndrome Clinic and Skeletal Dysplasia Center. She has developed online courses in Cardiovascular Genetics and Laboratory Genetic Counseling in improver to updating previously available courses in Embryology and Teratology. Carrie serves as a faculty member for the CCHMC Leadership Pedagogy in Neurodevelopmental Disabilities (LEND) program, and is involved in various other authoritative aspects of the plan. Jehannine Austin, PhD, CGC, CCGC, is an Associate Professor in the Departments of Psychiatry & Department of Medical Genetics at the Academy of British Columbia in Vancouver, Canada, where she holds the Canada Enquiry Chair in Translational Psychiatric Genomics. She completed her PhD in neuropsychiatric genetics at the Academy of Wales Higher of Medicine prior to pursuing her preparation and certification in genetic counseling at the University of British Columbia. Her research interests focus on the interface between psychiatric genetics and clinical practice. She completed the kickoff randomized controlled trial to investigate the impact of genetic counselling for individuals with schizophrenia, bipolar and schizoaffective disorder. In add-on, she has co-authored a volume, How to Talk with Families about Genetics and Psychiatric Illness, and in 2012, founded the first international specialist psychiatric genetic counselling service that now trains clinicians from all over the world. Her international scholarly works, professional activities, awards and publications are numerous. Cecelia Bellcross, PhD, MS, CGC, obtained her Master of Scientific discipline degree in Medical Genetics at the University of Wisconsin-Madison Genetic Counseling plan in 1990, and her PhD from the University of Wisconsin-Madison Department of Population Wellness Sciences in 2007. Following her piece of work equally a clinical genetics advisor from 1990-2008, she completed a fellowship through the American Society of Human Genetics with the CDC'due south Office of Public Health Genomics in Atlanta in 2010. Dr. Bellcross earned her certification from the American Board of Genetic Counseling (ABGC) in 1993, and recently served on the Accreditation Council for Genetic Counseling (ACGC). She is an Assistant Professor with the Department of Human Genetics, Emory University Schoolhouse of Medicine, where she developed and is Manager of the Emory Genetic Counseling Training Program. She is frequently invited to speak at national meetings and symposia, and has more a dozen articles in a variety of peer-reviewed journals. Her areas of interest and expertise include hereditary cancer and translational genomics. Laura J. Conway, PhD, CGC, received her BS in Biology from the Massachusetts Found of Technology, her PhD in Biochemistry from the University of Wisconsin-Madison, and her MS in Genetic Counseling from Arcadia University. Since 2004, she has served as Assistant Director of the Arcadia University Genetic Counseling Plan. Her varied credentials and experience take enriched her pedagogy of avant-garde science and laboratory courses and pupil mentorship. Dr. Conway's own enquiry interests focus on how the genetic counseling profession is adapting to new technology, both in the dispensary and more globally, as a profession. She currently serves every bit Secretary/Treasurer of the National Guild of Genetic Counselors and has taken an active part in looking at various issues related to the time to come of the genetic counseling profession, including licensure and advanced degrees. Dr. Conway has been published in more a dozen peer-reviewed journals. Brenda Finucane, MS, LGC, is a licensed genetic counselor and the Associate Director of the Autism and Developmental Medicine Institute of Geisinger Health Arrangement in Lewisburg, PA. Her clinical and research activities have focused on genetic causes of neurodevelopmental disorders. Ms. Finucane has a detail interest in the behavioral and cognitive manifestations of frail X, Smith-Magenis, 15q duplication, and other syndromes that effect in circuitous intellectual and neuropsychological symptoms. Her feel with this population includes young children through adults, and she has a specific interest in research related to the natural history of behavioral and developmental disorders over the lifespan. Ms. Finucane is widely published and has been in leadership roles in professional and advancement organizations throughout her career, including a term as president of the National Lodge of Genetic Counselors in 2012. Emily M. James, MS, CGC, received her masters in genetic counseling from the University of Pittsburgh Genetic Counseling Grooming Programme, where she received the Outstanding Graduate Student Award. She is Board Certified by the American Board of Genetic Counseling. Currently, she is on the genetic counseling squad at Invitae. Previously, she served in the West Penn Allegheny Health System in the Cancer and Cardiovascular Genetics Programs. She has made poster presentations at the American Society of Human Genetics. In addition, she co-instructed a grade in clinical genetics for nurses and lectured in a form on hereditary cancer for doctor of nursing practice students at the Robert Morris Academy. She has lectured first year genetic counseling students at the University of Pittsburgh Genetic Counseling Program. Staci Chiliad. Kallish, Practice, is a dr. in the Sectionalisation of Translational Medicine and Medical Genetics at the Academy of Pennsylvania. She is Banana Professor of Clinical Medicine and is Lath Certified in both Pediatrics and Medical Genetics - Clinical Biochemical Genetics. Amidst her clinical areas of interest are cardiomyopathies, skeletal dysplasias, connective tissue disease, metabolic myopathies, muscular dystrophies, neurofibromatosis and developmental disabilities. Lisa Kessler, MS, LCGC, is a graduate of the Arcadia University Genetic Counseling Program, where she currently serves equally Clinical Coordinator and Assistant Professor. Prior to her amalgamation in the graduate plan, she served in a diverseness of positions at University of Pennsylvania, including the Departments of Psychiatry and Ophthalmology and the Division of Medical Genetics. She has numerous publications in peer-reviewed journals. Kathryn Spitzer Kim, MS, CGC, has been a genetic counselor for 28 years and has taught in a genetic counseling training programs for twenty of those years, giving her a broad perspective on the field and many years of feel teaching and critiquing best practices in the field. She currently is on faculty in the Stanford University Genetic Counseling Program. Prior to this position, she served as Director of Counseling Educational activity at the Arcadia University Genetic Counseling Programme. Additionally, she has published in several peer review journals including the Journal of Genetic Counseling, for which she served as an editor for several years. She is the author of the chapter on interviewing in A Guide to Genetic Counseling (2009) edited by Uhlmann, Schutte, and Yashar. Her personal areas of expertise and interest are the psychological foundations of genetic counseling and multicultural perspectives. Ian D. Krantz, MD, is Professor of Pediatrics and Co-manager of Individualized Medical Genetic at Children'southward Hospital of Philadelphia (CHOP) in Philadelphia, PA, and serves as Medical Director of the Arcadia University Genetic Counseling Program. He earned his MD at Tel Aviv University in 1991. He is Board Certified by the American Board of Pediatrics in both Clinical Cytogenetics and Clinical Genetics. His areas of research interest are of the molecular etiology of syndromic and not-syndromic human evolution disorders and birth defects, especially those syndromes related to nascency defects and hearing loss. In practice, as a pediatrician and clinical geneticist, his focus is on dysmorphology and pediatric genetics disorders, including Cornelia de Lange, Alagille and Pallister Killian syndromes and related disorders. In addition, he directs a genetics clinic dedicated to children with sensorineural hearing loss. Dr. Krantz is well published in peer-reviewed journals. Donna McDonald McGinn, MS, CGC, received her BA in biological science and sociology from Rosemont Higher and her MS in man genetics from Sarah Lawrence College. Later on graduation, she joined the Division of Human Genetics and Molecular Biology every bit a genetic advisor and clinical coordinator at Children's Hospital of Philadelphia (CHOP). She was recently appointed Clinical Professor of Pediatrics at the Perelman School of Medicine of the Academy of Pennsylvania and is Director of the 22q and You Center at CHOP. Her areas of expertise are clinical enquiry and genetic counseling related to the diagnosis of fissure palate and craniofacial disorders, and she has been recognized internationally for her piece of work with 22q. In 2012, she received the DiGeorge Medal of Honor for her expertise and contributions to the agreement and/or treatment of chromosome 22q deletion syndrome. She was simply the 2nd person to receive this highly esteemed honor. Livija Medne, MS, CGC is a genetic advisor who has been working in pediatric genetics at The Children'due south Infirmary of Philadelphia since 1997. For the terminal 12 years, she has focused on neurogenetic and neuromuscular disorders and has seen and counseled patients and families with both centrally mediated neurologic disorders and peripheral neuromuscular diseases. She has participated in clinical treatment trials for DMD likewise every bit several natural history trials and patient registries for other neuromuscular diseases. She serves on the Genetic Counseling Taskforce for the Muscular Dystrophy Clan. Since 2014, Livija has been working as a co-director of the Individualized Medical Genetics Center at CHOP. This newly established plan sees patients who undergo large-scale genomic testing, with the focus on exome/genome sequencing. Throughout her carreer in genetic counseling, Livija has been lecturing to medical and genetic counseling students as well as genetics and neurology fellows. Colleen Clarke Muraresku, MS, LCGC, is Senior Genetic Counselors and Program Administrator at Children's Hospital of Philadelphia. She earned her Master'south Degree in Genetic Counseling from Arcadia University, Glenside PA. Her involvement and area of expertise is in biochemical genetics, and she has nearly a dozen peer-reviewed manufactures, including being lead writer for an commodity published by Molecular Genetics and Metabolism in 2013. Reed E. Pyeritz, Physician, PhD Board certified in internal medicine and clinical genetics, earned both a PhD in biological chemistry in 1972 and his MD in 1975 at Harvard. His medical grooming was at both Brigham Hospital in Boston and Johns Hopkins Hospital in Baltimore, where he became a full professor. He served as chief of the Division of Medical Genetics at the Infirmary of the University of Pennsylvania and Professor of Medicine and Genetics at the Academy of Pennsylvania. In 2013, he became the William Smilow Professor of Medicine. He founded the National Marfan Foundation and continues to serve on its Professional Informational Lath. He has served on the editorial boards of the American Journal of Medical Genetics, the New England Journal of Medicine, Periodical of the American Medical Association, Journal of the American College of Cardiology and Circulation. He is co-editor of the standard text in his field, Principles and Exercise of Medical Genetics, the 6th edition of which was published in 2014. Dr. Pyeritz has long been recognized as an international potency on the genetics of cardiovascular disorders, about notably, Marfan syndrome and hereditary hemorrhagic telangiectasia (HHT). He was recently appointed to the Secretary's Advisory Committee on Human Inquiry Protection, U.South. Department of Health and Man Services. He has published over 500 scientific articles, reviews, editorials and chapters in textbooks. Dee Quinn, MS, CGC, has been Director of the Arizona Pregnancy Riskline since its inception in 1999, and is Clinical Lecturer in the Colleges of Medicine and Chemist's shop at the University of Arizona, where she teaches genetics and teratology to medical students, residents, and other allied wellness professionals. In addition, she provides prenatal and teratology genetic counseling at the University. She received a BSN degree from the University of Bridgeport in 1975 and her Main'southward degree in Genetic Counseling from Sarah Lawrence College in 1981. At the Academy of Connecticut from 1981-1989, Ms. Quinn provided prenatal, pediatric and cancer genetic counseling and developed the Connecticut Pregnancy Riskline. Well-recognized for her piece of work in teratology, Quinn has been first author on numerous peer-reviewed publications and has presented at national and international teratology conferences. She served equally President of the Organization of Teratology Information Specialists (OTIS) from 1999-2001 and Executive Director from 2005-2012. Ronald Rubenstein, Physician, PhD, is a pediatric pulmonologist specializing in novel pharmacotherapies and advanced techniques for diagnosis and evaluation of cystic fibrosis and noisy animate in infancy. Currently, he is an Associate Professor of Pediatrics at the Perelman School of Medicine at the University of Pennsylvania and is the Manager of the Cystic Fibrosis Center at Children'due south Hospital of Philadelphia (CHOP), Philadelphia, PA. He received his medical education from University of Texas Southwestern Medical School in Dallas, followed by a residency at Children'southward Hospital of Pittsburgh. He is Board Certified in Pediatrics and Pediatric Pulmonology by the American Board of Pediatrics. He has published dozens of articles in peer-reviewed journals. Katherine A. Schneider, MPH, CGC, is Senior Genetic Counselor at Dana-Farber Cancer Institute in Boston, MA. Ms. Schneider was awarded a Masters Degree in Public Wellness (MPH) from Yale University Schoolhouse of Medicine, New Haven, CT. Since 1991, she has been considered a leader among her peers in the field of cancer genetic counseling. Ms. Schneider is author of Counseling near Cancer: Strategies for Genetic Counseling, published by Wiley & Sons. The book is now in its third edition. She has numerous presentations at professional person meetings and nearly 50 publications in peer-reviewed journals. In improver, she was awarded the prestigious Jane Engelberg Memorial Fellowship in 1992. She currently serves on an AACR workshop to develop surveillance recommendations for children with hereditary cancer syndromes. She has been certified past the American Board of Medical Genetics (1987) and licensed in the Republic of Massachusetts (2009). Her awards and memberships are numerous and a Presidential Term for National Society of Genetic Counselors (2000 - 2004). Lisa Schwartz, MS, EdD, CGC, received her masters in genetic counseling from the Academy of Pittsburgh Genetic Counseling Training Program and her doctorate in higher education administration from The George Washington Academy. She is Board Certified past the American Lath of Genetic Counseling. She is onetime director of the University of Maryland Master's in Genetic Counseling Preparation Plan, and she currently is Banana Professor at the Department of Integrated Health Sciences, School of Medicine and Health Sciences at The George Washington Academy in Washington DC. She has extensive teaching feel and has more than two dozen publications in peer-reviewed journals. Stuart Schwartz, PhD, received his PhD from the Indiana University School of Medicine and is currently the Strategic Managing director of Cytogenetics at Laboratory Corporation of America. For the past half dozen years, he has been involved in the evolution and improvement of microarray technology and implementation of this technology in pediatric, prenatal and oncology patients. This involvement has included not merely the utilization of array engineering science for diagnosis, but also advocating for its acceptance as a routine technology in the laboratory. Dr Schwartz serves every bit the current President of the Cancer Genomics Consortium, and is a former President of the American Board of Medical Genetics every bit well every bit Cytogenetics section editor for both the American Journal of Medical Genetics and Genetics in Medicine. Dr. Schwartz has been involved with the cytogenetic diagnosis of patients since 1982 and has over 178 peer reviewed publications and 22 published invited capacity. Prior to his position at LabCorp, he was Professor of Genetics at Case Western Reserve University and Academy of Chicago. Katie Stoll, MS, CGC, was awarded a degree in genetic counseling at Brandeis University, Waltham, Massachusetts. She is Board Certified by the American Board of Genetic Counseling and licensed in the State of Washington. Since 2014, she has served every bit Director of Clinical Services at the Genetic Support Foundation in Olympia, Washington. Her previous positions were all related to providing genetic counseling services, including developing clinical genetic services in the southwest region of the state. She has made numerous presentations and is kickoff author on several peer-reviewed manufactures in genetics and prenatal journals. Jill Stopfer, MS, CGC, was awarded her degree in genetic counseling at the University of Michigan in 1988. She is Lath Certified past the American Lath of Medical Genetics and the American Board of Genetic Counseling. From 2008 - 2015, she was the Familial Cancer Coordinator at Abramson Cancer Center and Basser Centre for BRCA at University of Pennsylvania in Philadelphia, PA and was amid the first genetic counselors in the country to develop a high risk chest programme, offering family unit history cess, risk calculation and research participation. While at the University of Pennsylvania, she helped to constitute research and clinical protocols for a multidisciplinary clinical and research cancer genetics program, which has served thousands of families with a specialty in risk assessment and genetic testing and counseling families at increased risk for breast, ovarian, colon, pancreatic and other hereditary forms of cancer. In 2015, she relocated to Boston MA, and was named Associate Managing director of the Dana-Farber Cancer Establish's Heart for Cancer Genetics and Prevention. Kathleen Valverde, MS, CGC, serves as Chair, Department of Genetic Counseling at Arcadia Academy and Managing director of the Arcadia University Genetic Counseling Master'due south Plan. She is co-managing director of the Review Grade in Medical Genetics and Genetic Counseling. Active in her profession, she has served on the Clan of Genetic Counseling Program Directors (AGCPD), is a founding member of the Accreditation Council of Genetic Counseling (ACGC), was a Board member of American Board of Genetic Counseling (ABGC) and has held numerous leadership positions of the National Society of Genetic Counselors (NSGC). She was instrumental in the process that resulted in licensure for genetic counselors in the Commonwealth of Pennsylvania. Her publications are well recognized and she is a frequent invited speaker at national professional conferences. Jodie G. Vento, MGC, CGC, currently works at Children's Infirmary of Pittsburgh of UPMC as the manager of the Brain Care Plant, which have followed positions every bit Manager, Center for Rare Disease Therapy and Genetic Counseling Supervisor for Laboratory Services. She previously worked at Children's National Medical Center in Washington, DC as the coordinator for the Neurogenetics Program. Jodie received a grant through the National Coalition for Health Professional person Didactics in Genetics (NCHPEG) to develop a targeted didactics program, entitled "Genetics for the Child Neurologist". She provides supervision of genetic counseling interns from the Academy of Pittsburgh and lectures to students, nurses, and physicians. She works closely with a patient advocacy group, the United Mitochondrial Disease Foundation, on program development and annual conferences. Jodie obtained a Masters in Genetic Counseling from the University of Maryland, School of Medicine. She is a certified past the American Board of Genetic Counseling and is a member of the National Guild of Genetic Counselors. Lewis J. Waber, Dr., PhD, has a distinguished career in medical genetics and is certified in Pediatrics, Clinical Genetics and Biochemical Genetics. He was awarded a dual caste in Medicine (Physician) and Biochemistry (PhD) from Case Western Reserve followed by post-doctoral internship, residency and genetic fellowships at Johns Hopkins Hospital in Baltimore, MD. He served from 1989 - 2015 at UT Southwestern Medical Center, where he was a Distinguished Teaching Professor from 2007 - 2015 at the fourth dimension of his retirement. He was Principal or Co-Investigator for numerous enquiry grants in biochemical genetics awarded by NIH, New York Country Department of Health and Texas Department of Health. Ronald J. Wapner, MD, is Professor in Obstetrics and Gynecology, Vice Chair of Clinical Inquiry in Obstetrics and Gynecology and Director of Reproductive Genetics at Columbia University Medical Center. He earned his medical degree at Thomas Jefferson Medical Higher in Philadelphia, where he later served as Chairman of the Departments of Obstetrics and Gynecology and Director of the Divisions of Maternal-Fetal Medicine and Reproductive Genetics. He holds Board Certifications in Maternal-Fetal Medicine and Medical Genetics. Dr. Wapner is an internationally known physician and researcher specializing in reproductive genetics. He pioneered the evolution of chorionic villus sampling (CVS) and multi-fetal reduction. He has authored or co-authored over 300 publications and he has been an active investigator in the area of Maternal-Fetal Medicine. He is either a master or co-investigator for a number of NICHD sponsored multi-middle studies. He serves every bit the center Principal Investigator for the National Standards for Fetal Growth study and the NuMoM2B study at Columbia Academy in the Maternal Fetal Medicine Units Network and on numerous other high-profile grants in his field. Most recently, Dr. Wapner led a multicenter study evaluating the accuracy, efficacy and clinical advantages of prenatal diagnosis using microarray analysis. He has had a significant role in the development of multidisciplinary research studies and clinical research centers throughout his career. Vivian J Weinblatt, MS, CGC, is Managing director of Clinical and Sales Education for Integrated Genetics, a commercial laboratory specializing in genetic testing. She earned her Bachelor's degree from Cornell University and her Genetic Counseling caste from the University of California, Berkeley. Weinblatt provided prenatal genetic counseling for well-nigh twenty years, and has maintained her research interest in multiple pregnancies and cystic fibrosis screening. She is a charter fellow member of the American Board of Genetic Counseling, is a diplomate of the American Board of Medical Genetics and is licensed in the Commonwealth of Pennsylvania. She served as President of the National Social club of Genetic Counselors. Weinblatt currently provides genetics and genetic testing education for educating sales teams' at Integrated Genetics and has been recognized for her pedagogy abilities, having taught as Adjunct Professor for the Arcadia Academy Genetic Counseling program since 1996. Robert B. Wilson, Medico, PhD, received his BA in Music and his BS in Biochemistry from Chocolate-brown University, and his Doc and PhD in Genetics from the University of Pennsylvania. He completed his residency training in Clinical Pathology and his fellowship preparation in Transfusion Medicine at the Hospital of the Academy of Pennsylvania, and he was then a postal service-doctoral researcher in the Howard Hughes Medical Plant. He joined the Department of Pathology and Laboratory Medicine at the University of Pennsylvania as an Banana Professor in 1992 and is at present a Full Professor. His primary research interests are in the neurodegenerative disorder Friedreich's ataxia, in the development of small RNA therapeutics and in the statistics of genetic risk cess. During a sabbatical in 2012 - 2013, Dr. Wilson studied computer scientific discipline and advanced statistics at the Academy of Pennsylvania, culminating in graduate-level courses in Machine Learning and Avant-garde Bayesian Data Analysis. In addition to research, he is a practicing molecular genetic pathologist in the Molecular Pathology Laboratory of the Hospital of the University of Pennsylvania. He also teaches full general pathology to medical and graduate students, molecular pathology to residents and fellows, and topics related to neurodegenerative disease to neuroscience graduate students. Elisabeth McCarty Wood, MS, CGC, is a genetic counselor in the Eye for Neurodegenerative Illness Research at the Academy of Pennsylvania. She was awarded a Master'southward degree in Genetic Counseling from the Academy of Pittsburgh in 2003 and was certified past the American Board of Genetic Counseling in 2005. Ms. Wood has specialized in the genetics of neurodegenerative disease since 2003, including involvement in molecular and clinical research for frontotemporal degeneration, amyotrophic lateral sclerosis, Alzheimer disease, and Parkinson disease. She has participated as a member of the REVEAL Iv research team, and is currently a fellow member of the genetic testing and education commission for the Alzheimer'south Prevention Initiative APOE4 Treatment Trial. She recently authored ii capacity, one on the genetics of frontotemporal degeneration in the book What If It's Not Alzheimer'south, and the 2d on amyotrophic lateral sclerosis in Genetic Counseling for Adult Neurogenetic Disease. CEUs for Genetic Counselors CEUs are available for active registrants, simply. One time Lath certified, inactivated registrants may re-enroll for CEUs at a significantly discounted rate. Contact Audrey: Audrey@BLCommunications.us The National Gild of Genetic Counselors (NSGC) has authorized Category 1 CEUs for this Class every bit follows: - For individuals who have non previously completed the course for CEUs, including lectures and tutorials: seven.82 CEUs or 78.21 Contact Hours.
- New and updated lectures and tutorials only, for individuals who have previously completed the grade for CEUs betwixt October 5, 2015 – Oct v, 2017: 2.9 CEUs or 29.fifteen Contact Hours and obtained CEUs prior to January i, 2017.
- New and updated lectures and tutorials just, for individuals who have previously completed the grade for CEUs prior to January 1, 2014: 7.25 CEUs or 72.51 Contact Hours.
Genetic Counselors are not eligible for ABGC-approved CEUs toward recertification until the letter awarding diplomate condition is received. Exceptions are outlined in guidelines set past American Board of Genetic Counseling (ABGC). Once officially certified, the American Board of Genetic Counseling (ABGC) will accept CEUs earned in this program for the purposes of certification and recertification. Practise you demand help determining which CEU group you qualify for or the fee schedule. Ship an e-mail to Audrey@blcommunications.usa. She will help yous determine your eligibility group as well every bit the discounted fee if you are a previous registrant. Disclaimer Statement Statements, opinions and results of studies contained in this grade are those of the presenters and do not reflect the policy or position of Arcadia University or the Management Team. Arcadia University and the Management Team exercise not provide any warranty as to their accuracy or reliability. Every reasonable endeavor has been made to faithfully reproduce the presentations and material as submitted. However, no responsibility is assumed past Arcadia University or the Management Squad for any claims, injury and/or damage to persons or property from any cause, including negligence or otherwise, or from whatever utilise or functioning of any methods, products, instruments, or ideas contained in the fabric herein. Conflict of Interest Disclosure Statement Conflict / Disclaimer The faculty members of this course have had no role in constructing any of the board examinations. Nosotros make no pretense that this course's curriculum reflects the content of either the ABGC or ABMG Board examinations. Also, the practice questions are offered as a means of gaining experience in exam taking. We make no claim that either the style of the questions or their content is representative of the either examination. For information nigh relationships of presenters with regard to commercial interests, if any, Click here. Privacy and Confidentiality All information is held with strictest conviction. BLCommunications, LLC, does not sell, rent or charter whatsoever data provided past our registrants for any reason other than for the purposes of CEU procurement. | TOPIC | Speaker | Title | CEU eligible Lecture Hours:Minutes | Tutorial Questions | | Introduction | Kathleen Valverde, MS | Report for Success | 0:00 | 0 | | Biochemical Genetics | Lewis J. Waber, Doctor, PhD | Biochemical Genetics & Metabolic Syndromes | 6:49 | 42 | | Colleen Murarasku, MS, | Mitochondrial Disorders | 1:34 | 21 | | Cancer Genetics | Jill Stopfer, MS | Breast, Ovarian and GI Cancers; New Panel Testing | four:21 | 35 | | Katherine Schneider, MS | Tumor Predisposition and Babyhood Cancers | 1:59 | thirty | | Cardiogenetics | Emily M. James, MS | Cardiovascular Genetics | 1:33 | 40 | | Cytogenetics | Stuart Schwartz, PhD | Cytogenetics and Molecular Cytogenetics | 2:00 | 22 | | Ethics | Dawn Allain, MS, LGC | Ethics of Genetic Counseling | 1:12 | 14 | | Genetic Counseling Principles and Do | Kathryn S. Kim, MS | Addressing Difficult Issues with Clients and Crisis Intervention | 1:00 | 11 | | Kathleen Valverde, MS | Guiding Models and Hallmarks of Patient Interactions | 0:51 | 13 | | Lisa Kessler, MS | Case Management: Theories and Concepts | 0:51 | 12 | | Carrie Atzinger, MS | Clinical Supervision and Self Care | i:00 | 10 | | Genetics and the Law | Emily M. James, MS | Genetics Nondiscrimination: The Law | 0:eighteen | fifteen | | Medical Genetics | Ian Krantz, MD | Intro to Dysmorphology | 1:17 | 12 | | Staci Kallish, DO | Common Genetic Disorders | 0:50 | 10 | | Ron Rubinstein, Md, PhD | Cystic Fibrosis | 0:45 | 10 | | Reed Pyeritz, MD, PhD | Marfan'south and other Arteriopathies | 0:47 | 10 | | Brenda Finucune, MS | Mental Retardation and FraX | one:03 | 10 | | Donna McDonald-McGinn, MS | What's New with 22q? | 0:59 | 11 | | Jehannine Austin, PhD | Genetics of Circuitous Disorders | 1:02 | 14 | | Emily Yard. James, MS | Patterns of Inheritance | 0:41 | 20 | | Molecular Genetics | Laura Conway, PhD | Molecular Genetics, Parts ane - 6 | 4:34 | 57 | | Neurogenetics | Livija Medne, MS | Childhood Neuromuscular and Neurodegenerative Disorders | two:16 | 23 | | Beth Woods, MS | Adult Neurodegenerative Disorders: Developed Onset Dementia and Parkinson'south, Alzheimer's, Huntington'due south, and Gaucher diseases
| one:48 | 20 | | New Genomics | Jodie Vento | WES, OLIGO, Microarray | i:44 | 31 | | Cecelia Bellcross, PhD | Genomic Medicine - Expanding Opportunities for Genetic Professionals | 1:44 | 20 | | Prenatal Genetics | Vivian Weinblatt, MS | Marker Screening & Carrier Screening | 1:55 | twenty | | Ronald J. Wapner, MD | The New Genetics: What Yous Need To Know | two:02 | 20 | | Katie Stoll, MS | Expanded Carrier Screening & NIPT | i:28 | 10 | | Dee Quinn, MS | Teratogens | 0:45 | 15 | | Quantatative Genetics | Robert Wilson, MD, PhD | Baysian Probability | 1:30 | x | | Lisa Schwartz, EdD | Hardy Weinberg Applications | 0:46 | 25 | | Course Review | Form Tutorial Review | | | 25 | The registration fee includes individual secured password-protected access to video lectures with PowerPoint slides, downloadable audios, pre- and post-tests, tutorials do questions with instant feedback, and supplemental educational materials. Discounts are bachelor for study groups of ii or more than. Password access will not be disseminated until all members of the group are registered. Your registration is valid for 9 total months following the appointment yous receive your access information, well-nigh often within three business organisation days of your registration. For case: If your registration date is Feb 20, 2018, your access will be active until November xxx, 2018. If your registration date is October ane, 2018, your access will be active until July 31, 2019. Discounts are bachelor for those who have been registered within the by five years who would similar to re-annals for the purpose of accruing CEUs or every bit a refresher for retaking the Boards. Contact Audrey Lombard Audrey@blcommunications.united states of america All fees must exist submitted in US dollars past check or online.
| Private Registration | $995 | | Grouping Registration, two - 5, per license | $950 | | Grouping Registration, 6 or more, per license | $900 | Processing Fee NSGC - approved Continuing Education Units
CEUs are applicative for Board Certified Genetic Counselors, only. Contact ABGC for exceptions. | $25 | Credit Cards Accepted Online only. The charge will appear as BLCommunications on your monthly charge carte du jour statement. - Checks may be sent payable to BLCommunications, P.O. Box 63912, Philadelphia PA 19147-7779
- A $50 fee will be applied for all returned checks or chargebacks on credit cards.
- We accept Visa, MasterCard, Discover and American Limited.
We regret that refunds will not be granted after access codes are provided. Audrey Lombard, Grade Administrator
Ph: 610-872-8730
Email: Audrey@BLCommunications.The states Bea Leopold, Managing Director
Ph: 610-872-8730
Email: BLeopold@BLCommunications.Usa Annals NOW by mail (pdf) Register Online with Credit Cards | |
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