Dear Colleagues,
Please apply and/or bring this postdoctoral opportunity to the attention
of your best students and colleagues. Details are below and in the
attachment. All best wishes,
Karen
________________________________
/Karen Faith Berman, M.D./
Chief, Clinical & Translational Neuroscience Branch
Section on Integrative Neuroimaging
Psychosis & Cognitive Studies Section
National Institutes of Health, NIMH
Intramural Research Program
9000 Rockville Pike, MSC 1365
Building 10, Room 3C103A
Bethesda, MD 20892-1365
phone: 301/496-7603
fax: 301/480-7795
_karen.berman(a)nih.gov_ <mailto:karen.berman@nih.gov>
*_POSTDOCTORAL FELLOWSHIP IN MULTIMODAL NEUROIMAGING_*
*SECTION ON INTEGRATIVE NEUROIMAGING*
*CLINICAL & TRANSLATIONAL NEUROSCIENCE BRANCH*
*NATIONAL INSTITUTE OF MENTAL HEALTH, NIH *
*INTRAMURAL RESEARCH PROGRAM, DHHS, BETHESDA, MD*
The Section on Integrative Neuroimaging in the Clinical & Translational
Neuroscience Branch of the National Institute of Mental Health
Intramural Research Program (NIMH IRP), at the National Institutes of
Health (NIH), invites outstanding individuals to apply for a two to five
year post-doctoral fellowship at one of the premier research sites in
the world. The renowned NIH Clinical Center on the 300 acre Bethesda
campus of the NIH, near Washington D.C., houses unsurpassed,
state-of-the-art neuroimaging facilities (MRI, PET and MEG) all
dedicated to research, as well as superb clinical facilities, and an
exciting, interactive research community of hundreds of talented
colleagues. The strong scientific environment and outstanding resources
at NIH make this a unique opportunity for an innovative scientist.
The Branch takes a multidisciplinary approach, with multimodal
neuroimaging (sMRI, rMRI, fMRI, DTI, PET, MEG) at its core, but also
integrates genetic, neurochemical, neuropsychological, and clinical
investigations to study normal human higher cognitive function
throughout the lifespan, as well as neuropsychiatric disorders such as
Williams syndrome and schizophrenia. The successful candidate will have
particular leadership opportunities within our longitudinal study of
Williams syndrome; will have access to large, unique, archival datasets;
and will help to design new studies. The position is open to (1) recent
Ph.D.'s in experimental psychology, cognitive neuroscience,
neuroscience, neuropharmacology, or other applicable disciplines; and
(2) M.D.'s with training in psychiatry, neurology, nuclear medicine,
radiology or other relevant fields. Applicants should have a
demonstrated record of excellent scientific writing skills as well as
excellent interpersonal and presentation skill. In addition, experience
with any of the following will be an advantage: developmental/pediatric
neuroimaging, multimodal neuroimaging techniques (MRI, PET, MEG),
conducting cognitive neuroscience experiments, and/or neuroimaging of
clinical populations. Experience with SPM, FSL, Freesurfer, UNIX/LINUX/
and/or programming skills (MATLAB, C++; Python) is desirable, but not
required.
The position is open immediately and applications will be accepted until
the position is filled. A curriculum vitae, letter of interest
outlining experience and research goals, and three letters forwarded
directly from recommenders should be sent to: Karen Berman, M.D.; C/O
Jasmin B. Czarapata, Ph.D.; NIH Building 10, Rm 3C209; 9000 Rockville
Pike; Bethesda MD 20892-1365 USA. (301) 435-7645, or electronically to
_jasmins(a)mail.nih.gov_ <mailto:jasmins@mail.nih.gov>
DHHS and NIH are Equal Opportunity Employers.
A FEW REPRESENTATIVE PUBS…
Eisenberg DP, Ianni AM, Wei SM, Kohn P, Kolachana B, Apud J, Weinberger
DR, Berman KF: Brainderived
neurotrophic factor (BDNF) Val66Met polymorphism differentially affects
hippocampal function in
medication-free patients with schizophrenia. *Molecular Psychiatry*,
18(6):713-720, 2013.
Jabbi M, Kippenhan JS, Kohn P, Marenco S, Mervis CB, Morris CA,
Meyer-Lindenberg A, Berman KF:
The Williams syndrome chromosome 7q11.23 hemideletion confers
hypersocial, anxious personality via
altered insula structure and function. *Proceedings of the National
Academy of Sciences *Apr
3;109(14):E860-6, 2012.
Dreher JC, Kohn P, Kolachana B, Weinberger DR and Berman KF: Variation
in dopamine genes
influences responsivity of the human reward system. *Proceedings of the
National Academy of Science*
106: 617-622, 2009.
Meyer-Lindenberg A, Hariri A, Munuz KE, Mervis CB, Mattay VS, Morris CA
and Berman KF: Neural
correlates of genetically abnormal social cognition in Williams
syndrome. *Nature Neuroscience *8:991-993,
2005.
Kippenhan JS, Olsen RK, Mervis CB, Morris CA, Kohn PD, Meyer-Lindenberg
A and Berman KF:
Genetic contributions to human gyrification: Sulcal morphometry in
Williams syndrome. *Journal of*
*Neuroscience *25:7840-7846, 2005.
Buchsbaum BR, Olsen RK, Koch PF and Berman KF: Human dorsal and ventral
auditory streams
subserve rehearsal-based and echoic processes during verbal working
memory. *Neuron *48:687-97, 2005.
Meyer-Lindenberg A, Mervis CB, Sarpal D, Koch P, Steele S, Kohn P,
Marenco S, Morris CA, Das S,
Kippenhan JS, Mattay VS, Weinberger DR and Berman KF: Functional,
structural and metabolic
abnormalities of the hippocampal function in Williams syndrome. Journal
of Clinical Investigation
115:1888-1895, 2005.
Meyer-Lindenberg A, Kohn PD, Kolachana B, Kippenhan JS, McInerney-Leo
A, Nussbaum R,
Weinberger DR, and Berman KF: Midbrain dopamine and prefrontal function
in humans: Interaction and
modulation by COMT genotype. *Nature Neuroscience *8:594-596, 2005.
Meyer-Lindenberg A, Kohn P, Mervis CB, Kippenhan JS, Olsen RK, Morris
CA, and Berman KF:
Neural basis of genetically determined visuospatial construction deficit
in Williams syndrome. *Neuron*
43:623-631, 2004. (accompanying commentary: “Fulfilling the Promise of
the Cognitive Neurosciences,”
*Neuron *43:595-596, 2004)
Meyer-Lindenberg A, Miletich RS, Kohn PD, Esposito G, Carson RE,
Quarantelli M, Weinberger DR
and Berman KF: Reduced prefrontal activity predicts exaggerated striatal
dopaminergic function in
schizophrenia. *Nature Neuroscience *5:267-271, 2002.