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Plenary Speakers
Summary of Gene
Workshops for COMT,DAOA(G72), DISC1 and SLC6A3 (DAT): Findings.
Saturday, October 15. 8:45-9:45 a.m. |
Pasko Rakic earned his M.D. and Ph.D. degrees in medicine,
developmental biology and genetics. He is currently the Duberg
Professor of Neuroscience and Chairman of the Department of
Neurobiology at Yale University School of Medicine. His research
has focused on development of the cerebral cortex, including
the fundamental issues of the regulation of neuronal production
and the interaction between neuronal and glial cells during
their migration to the cortex. He and his colleagues have
characterized several genes and morphoregulatory molecules
involved regulation of the proliferation, migration, differentiation
and death of neurons. Subsequent studies of the remapping
of the proliferative ventricular zone upon the expanding cerebral
cortex in various mammalian species lead to the postulate
of the “radial unit” and “protomap” hypotheses of cortical
development and evolution. Additionally, Rakic’s lab studies
synaptogenesis and emergence of transmitters and their receptors
involved in cortical microcircuitry. These studies have provided
the contemporary framework for our current understanding of
normal and pathological development of the human brain and
the pathogenesis of congenital disorders of higher brain functions.
Rakic is an author on hundreds of scientific papers and has
received numerous awards and honors that include election
to the National Academy of Sciences USA and the American Academy
of Arts and Sciences, as well as Presidency of the Society
for Neuroscience.
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David Bartel:
Small RNAs that Repress Gene Expression
Sunday, October 16. 8:15 - 9:15 a.m. |
Not
all molecules that regulate gene expression are transcription
factors or other proteins. Some are RNAs. This talk will focus
on micro RNAs, which are an abundant class of tiny endogenous
RNAs that direct the repression of protein-coding genes. Although
the functions of microRNAs are just beginning to be understood,
it is increasingly clear that they play a wide-spread role
in the regulation and evolution of human genes, making it
inevitable that their dysfunction will ultimately be linked
to numerous human diseases.
Dr. David Bartel is a member of the Whitehead
Institute, a professor of biology at MIT, and an investigator
of the Howard Hughes Medical Institute. His doctoral work
was carried out at Harvard University in the laboratory of
Jack Szostak, where he developed combinatorial techniques
to create new catalytic RNAs. Since then his lab has created
ribozymes that can catalyze the types of reactions that would
have been needed early in evolution, including RNA-templated
RNA synthesis.
Dr. Bartel has also contributed to the discovery
and understanding of small regulatory RNAs needed to “silence”
genes during normal frowth and development of plants, animals,
and fungi. His lab was among those to report that animals
have a large number of endogeneous regulatory RNAs, called
“miroRNAs.” They also found micro RNAs in plants and discovered
another type of small regulatory RNA known as “heterochromatic
siRNAs” in fungi. Bartel and colleagues developed methods
to confidently predict the genes that are regulated by plant
micro RNAs, and their recent work in animals indicated that
microRNAs regulate the expression of more than one-third of
the human genes, including many genes important in human cancers
and other diseases.
Dr. Bartel shared the 2002 American Academy
of Arts and Sciences Newcomb Cleveland Prize and was awarded
the 2005 National Academy of Sciences Award in Molecular Biology.
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Nora Volkow:
Imaging the Addicted Brain
Monday, October 17. 8:15 - 9:15 a.m.
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Nora
D. Volkow, M.D., became Director of the National Institute
on Drug Abuse (NIDA) in May 2003. A leader in drug addiction
research, she is the first woman to serve as NICA’s director
since the founding of the institute.
Dr. Volkow came to NIDA from Brookhaven National
Laboratory (BNL) where she held concurrent positions including
associate director for life sciences, Director of Nuclear
Medicine, and Director of the NIDA=Department of Energy Regional
Neuroimaging Center. In addition, Dr. Volkow was a professor
in the Department of Psychiatry and Associate Dean of the
Medical School at the State University of New York (SUNY)-Stony
Brook.
Dr. Volkow brings to NIDA a long record of
accomplishment in drug addiction research. She is a recognized
expert on the brain’s do[amine system with her research focusing
on the brains of addicted, obese and aging individuals. Her
studies have documented changes in the dopamine system affecting
the actions of frontal brain regions involved with motivation,
drive, and pleasure, and the decline of brain dopamine function
with age.
At Brookhaven, Dr. Volkow was the first to
use imaging to investigate neurochemical changes that occur
during drug addiction. Her primary focus was on mechanisms
underlying the reinforcing, addictive, and toxic properties
of drugs of abuse in the human brain. She investigated the
neurochemical mechanisms underlying the reinforcing, addictive,
and toxic properties of drugs of abuse in the human brain.
She investigated the neurochemical mechanisms that influence
the way individuals respond to drugs of abuse and the potential
link to vulnerability to drug abuse, alcoholism, or other
impulse behaviors.
Dr. Volkow has used imaging to study the rewarding
and therapeutic effects of stimulant drugs. By conducting
a systematic comparison of the pharmacological effects of
cocaine and methylphenidate (a drug to treat children with
attention deficit disorder), her studies have highlighted
the importance of pharmacokinetics in enabling the reinforcing
effects of stimulant drugs. These studies have shown that
stimulant drugs, when used therapeutically, simplify dopamine
signals in the brain and also results in improved attention
and performance.
Her work includes more that 275 peer-reviewed
publications, three edited books, and more than 50 book chapters
and non-peer reviewed manuscripts. The recipient of multiple
awards, she was elected to membership in the institute of
Medicine in the National Academy of Sciences and was names
"innovator of the Year" in 2000 by U.S. News and
World Report.
Dr. Volkow received her B.A. from Modern American
School, Mexico City, Mexico, her M.D. from the National University
of Mexico, Mexico City, and her postdoctoral training in psychiatry
at New York University. In addition to BNL and SUNY-Stony
Brook, Dr. Volkow has woorked at the University of Texas Medical
School and Seine Anne Psychiatric Hospital in Paris, France. |
Eric Lander:
Biology as Information: Genomics and Medicine
Monday, October 17. 3:45 - 4:45 p.m. |
Eric
Lander is founding director of the Broad Institute of MIT and
Harvard. As one of the principal leaders of the Human Genome
Project, Lander and colleagues are using these findings to explore
the molecular mechanisms underlying the basis of human disease.
Lander is also professor of biology at MIT,
Professor of Systems Biology at Harvard Medical School and
member of the Whitehead Institute for Biomedical Research.
He founded the Whitehead Institute/MIT Center for Genome Research
in 1990. This Center became part of the newly founded Broad
Institute in 2003.
Over the past 15 years, Lander and colleagues
have developed many of the key tools and generated many of
the key information resources of modern mammalian genomics.
They have also applied these tools and data to pioneer new
ways to understand the basis of disease. Their work includes:
mapping and sequencing of the human, mouse and other genomes;
understanding the functional elements encoded in genomes through
comparative analysis; understanding the genetic variation
in the human population and its relationship to disease susceptibility;
understanding the distinctive cellular signatures of diseases
and of response to drugs; and understanding the mutations
underlying cancer. They have also developed new analytical
and laboratory techniques for genomics, which have been applied
to a wide range of common diseases, including cancer, diabetes,
inflammatory diseases and many other genetic illnesses.
Lander’s honors and awards include the MacArthur
Foundation Prize Fellowship in 1987, the Woodrow Wilson Prize
for Public Service from Princeton University in 1998, the
City of Medicine Award in 2001, the Gairdner Foundation International
Award of Canada in 2002, and the AAAS Award for Public Understanding
of Science and Technology in 2004. He was elected a member
of the U.S. National Academy of Sciences in 1997 and the U.S.
Institute of Medicine in 1999. He has served on governing
and advisory boards for various government agencies, academic
institutions, scientific societies and corporations.
In addition to his research, Lander is an enthusiastic
teacher. He has taught MIT’s core introductory biology course
for a decade and, in 1992, won the Baker Memorial Award for
Undergraduate Teaching at MIT. He has lectured to both scientific
and lay audiences about the medical and social implications
of genetics, and delivered a special Millennium Lecture at
the White House in 2000.
Lander earned his B.A. in mathematics from
Princeton University in 1978 and Ph.D. in mathematics from
Oxford University in 1981 as a Rhodes Scholar. He was an assistant
and associate professor of managerial economics at the Harvard
Business School from 1981–1990. |
Edward Scolnick:
Are there sequence Defined Risk Genes for Schizophrenia or
Bipolar Disorder?
Tuesday, October 18. 11:00 a.m. - 12:00 p.m. |
| Schizophrenia
and bipolar disorder are devastating illnesses that affect
as much as 3 percen6t of the world population. The pathogenesis
of these diseases is poorly understood. This talk will examine
what models and data are available with regards to pathogenesis.
The perspective for examining the data will be; (1) is the
data clear enough to encourage industry to invest practical
utility for a physician caring for the patients with either
illness?
Dr. Scolnick is currently an Associate Member
of the Broad Institute of MIT and Harvard and Director of
the Broad’s Psychiatric Diseases Initiative.
From 1982 to 2003, Dr. Scolnick served in multiple
capacities as president, Merck Research laboratories and Executive
Vice President for Science and Technology. Merck & Company,
Inc. Prior to joining Merck, Dr. Scolnick worked at the National
Cancer Institute where this work demonstrated the cellular
origin of sarcoma virus oncogenes in Mammals and defined specific
genes that cause human cancer. He also worked at the National
Heart Institute where his work defined the stop signals in
genetic code and the biochemical mechanism that produces the
stops.
Dr. Scholnick was elected to the National Academy
of Sciences in 1984 and to the American Academy of Arts and
Sciences in 1993. He became a member of the Institute of Medicine
in 1996.
Dr. Scolnick’s commitment to the mental health
field is evidenced by memberships on the Board of Directors
for McLean Hospital and the McGovern Institute for Brain Research.
From 1998 to 2002, he served as a member of the Council of
the National Institute of Mental Health. Dr. Scolnick holds
an A.B. from Harvard College and a M.D. from Harvard University
Medical School. |
Educational Sessions
Nick Craddock:
Summary of Gene Workshops for COMT, DAOA(G72), DISC1 and
SLC6A3 (DAT): Findings
Tuesday, October 18, 12:00 p.m. - 1:00 p.m.
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Dr. Craddock's main research focus is the molecular genetic
investigation of mood disorders, particularly Bipolar and
related affective disorders. He is following a program of
work that uses positional and candidate gene approaches to
(a) identify susceptibility and course-modifying genes for
these disorders, and (b) investigate gene environment interactions
and co-actions in disease pathogenesis. He has a major interest
in gender-specific effects in mood disorders - particularly
the puerperal triggering of bipolar episodes. He also has
an interest in the neuropsychiatric phenotype associated with
Darier's disease. His clinical interests lie in the area of
provision of services and information for patients with Bipolar
Disorder and for their relatives and caregivers - particularly
in relation to pregnancy and childbirth.
At the Boston meeting, Nick has organized an
invitation only "Gene Workshops"where four genes
of particular interest are identified with some of the key
common issues and facilitate working towards improved approaches.
The genes to be discussed are:
- DISC1 (Chair: John Rice)
- SLC6A3 (DAT) (Chair: Cathy Barr, Co-Chair
Gerome Breen)
- DAOA (formerly G72) (Chair: Markus Nothen,Co-Chairs:
Thomas Schulze, Johannes Schumacher)
- COMT (Chair: Michael O'Donovan, Co-Chair:
Stephen Glatt).
As a summary to the Gene Workshops, Dr. Craddock's
plenary session will summarize succinctly the information
gathered and presented by the the Gene Workshop Chairs who,
with the help of their co-Chairs, have collated the current
data for each gene (including published data and that submitted
to the Boston Meeting as abstracts for all psychiatric phenotypes).
The aim of the Plenary Session is to present an overview of
the current state of knowledge for the four genes and thereby
to identify common issues that may inform our general approach
to psychiatric genetics studies.
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