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Bhaskar S Kolachana
Author PubWeight™ 67.05
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Top papers
Rank
Title
Journal
Year
PubWeight™
‹?›
1
The BDNF val66met polymorphism affects activity-dependent secretion of BDNF and human memory and hippocampal function.
Cell
2003
12.50
2
5-HTTLPR polymorphism impacts human cingulate-amygdala interactions: a genetic susceptibility mechanism for depression.
Nat Neurosci
2005
10.13
3
Functional analysis of genetic variation in catechol-O-methyltransferase (COMT): effects on mRNA, protein, and enzyme activity in postmortem human brain.
Am J Hum Genet
2004
5.70
4
Brain-derived neurotrophic factor val66met polymorphism affects human memory-related hippocampal activity and predicts memory performance.
J Neurosci
2003
5.11
5
The brain-derived neurotrophic factor val66met polymorphism and variation in human cortical morphology.
J Neurosci
2004
4.84
6
A susceptibility gene for affective disorders and the response of the human amygdala.
Arch Gen Psychiatry
2005
4.33
7
The distinct cognitive syndromes of Parkinson's disease: 5 year follow-up of the CamPaIGN cohort.
Brain
2009
3.03
8
Executive subprocesses in working memory: relationship to catechol-O-methyltransferase Val158Met genotype and schizophrenia.
Arch Gen Psychiatry
2003
2.82
9
Effect of catechol-O-methyltransferase val158met genotype on attentional control.
J Neurosci
2005
2.37
10
Catechol O-methyltransferase val158met genotype and neural mechanisms related to affective arousal and regulation.
Arch Gen Psychiatry
2006
1.94
11
Catechol-O-methyltransferase genotype and dopamine regulation in the human brain.
J Neurosci
2003
1.82
12
Tolcapone improves cognition and cortical information processing in normal human subjects.
Neuropsychopharmacology
2006
1.71
13
Genetic variation in AKT1 is linked to dopamine-associated prefrontal cortical structure and function in humans.
J Clin Invest
2008
1.43
14
Genetic variation in catechol-O-methyltransferase: effects on working memory in schizophrenic patients, their siblings, and healthy controls.
Biol Psychiatry
2007
1.41
15
Evidence that altered amygdala activity in schizophrenia is related to clinical state and not genetic risk.
Am J Psychiatry
2008
1.33
16
Evidence for statistical epistasis between catechol-O-methyltransferase (COMT) and polymorphisms in RGS4, G72 (DAOA), GRM3, and DISC1: influence on risk of schizophrenia.
Hum Genet
2006
1.29
17
Planning ability in Parkinson's disease is influenced by the COMT val158met polymorphism.
Mov Disord
2004
1.14
18
Catechol-O-methyltransferase val108/158met genotype predicts working memory response to antipsychotic medications.
Biol Psychiatry
2004
1.14
19
Impact of interacting functional variants in COMT on regional gray matter volume in human brain.
Neuroimage
2008
1.10
20
The BDNF Val66Met polymorphism has a gender specific influence on planning ability in Parkinson's disease.
J Neurol
2005
1.09
21
Epistatic and functional interactions of catechol-o-methyltransferase (COMT) and AKT1 on neuregulin1-ErbB signaling in cell models.
PLoS One
2010
0.88
22
Prefrontal electrophysiologic "noise" and catechol-O-methyltransferase genotype in schizophrenia.
Biol Psychiatry
2006
0.87
23
Brain-derived neurotrophic factor Val⁶⁶Met polymorphism affects resting regional cerebral blood flow and functional connectivity differentially in women versus men.
J Neurosci
2012
0.84