The Gittel Silverberg MS '74 Memorial Lecture
About the Gittel Silverberg Fund for Genetic Counselor Professional Development
2020—The Role of Genetic Testing in Psychiatry: Past, Present, and Future
Speakers
JORDAN W. SMOLLER, MD, SCD
Dr. Jordan Smoller is a psychiatrist, epidemiologist, and geneticist whose research focus has been 1) understanding the genetic and environmental determinants of psychiatric disorders across the lifespan; 2) integrating genomics and neuroscience to unravel how genes affect brain structure and function; and 3) using “big data”, including electronic health records and genomics, to advance precision medicine.
Dr. Smoller earned his undergraduate degree summa cum laude at Harvard University and his medical degree at Harvard Medical School. After completing residency training in psychiatry at McLean Hospital, he received masters and doctoral degrees in epidemiology at the Harvard School of Public Health.
Dr. Smoller is the Massachusetts General Hospital (MGH) Trustees Endowed Chair in Psychiatric Neuroscience, Professor of Psychiatry at Harvard Medical School and Professor in the Department of Epidemiology at the Harvard School of Public Health in Boston. He is Associate Chief for Research in the MGH Department of Psychiatry and Director of both the Psychiatric and Neurodevelopmental Genetics Unit and the Precision Medicine Research Unit in the MGH Center for Genomic Medicine. Dr. Smoller is a Tepper Family MGH Research Scholar and also serves as Director of the Omics Unit of the MGH Division of Clinical Research and co-Director of the Partners HealthCare Biobank at MGH. He is an Associate Member of the Broad Institute and Vice President of the International Society of Psychiatric Genetics. He is Director of the Partners Healthcare Training Program in Precision and Genomic Medicine. He is lead PI of the New England Precision Medicine Consortium as part of the NIH All of Us Research Program. Dr. Smoller is also co- Chair of the All of Us Science Committee and a member of the Program’s Steering Committee and Executive Committee. He is an author of more than 400 scientific publications and is also the author of The Other Side of Normal (HarperCollins/William Morrow, 2012).
LAURA HERCHER MS ’01
Director of Student Research at Joan H. Marks Graduate Program in Human Genetics at Sarah Lawrence College
BA, Colgate. MA, Columbia University. MS, Sarah Lawrence College. In addition to coordinating all of the student research projects, she is also the director of the Ethics course and is facilitator of our Current Events/Monday Afternoon Discussion series. Laura is the co-founder of and regular contributor to The DNA Exchange, as well as the author of Anybody’s Miracle . SLC, 2004–
2017—Beyond the Trisomies
Assessing clinical utility and long term consequences as we expand the targets of prenatal genetic testing
An array of forces, including commercial pressure as well as improving technology, are expanding the options for prospective parents available through prenatal genetic testing. New offerings from cell-free fetal DNA providers, including microdeletion panels and genomic indel analysis, present an alternative to the more accurate results available through diagnostic testing. Genetic counselors must help prospective parents negotiate a long and constantly changing menu of prenatal tests. What is right now? How do we assess new tests as they enter the market? Where are we headed?
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Genome, Wired, Aeon, and Scientific American. She is co-founder of the DNA Exchange, a blog for the genetic counseling community, and a regular contributor for Mendelspod.com, where she co-hosts a monthly review of the biggest stories in genomics. Hercher was chair of the National Society of Genetic Counselor’s Ethics Advisory Group for four years, and is currently a member of the Public Policy Committee, where she has most recently led efforts to examine the ethical and social implications of our rapidly improving ability to edit the genome.
Her first novel, Anybody’s Miracle, was published in 2013.
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Blair has a passion for helping patients with pregnancies affected with congenital anomalies and genetic conditions and has served as a Fetal Center genetic counselor since graduating, first with Baylor College of Medicine and the Texas Children’s Hospital Fetal Center and now with the Fetal Center at Children’s Memorial Hermann Hospital. Blair also sees patients in UT’s high risk maternal fetal medicine clinic for routine indications such as abnormal screening results, significant family history, advanced maternal age, as well as pre-test counseling for average risk women.
In addition to clinical counseling and supervisions, Blair has been involved with the National Society of Genetic Counselors and Texas Society of Genetic Counselors. Blair served as the Prenatal Special Interest Group chair from 2011-2015 and is now the Chair of the Public Policy Committee. She also served as the Texas Society of Genetic Counselors president from 2014-2015.