B. Kolachana

发表

Allelic variation in GAD1 (GAD67) is associated with schizophrenia and influences cortical function and gene expression

Michael B. Mayhew, R. Straub, B. Lipska, 2007, Molecular Psychiatry.

Variation in DISC1 affects hippocampal structure and function and increases risk for schizophrenia.

A. Meyer-Lindenberg, R. Straub, M. Egan, 2005, Proceedings of the National Academy of Sciences of the United States of America.

5-HTTLPR polymorphism impacts human cingulate-amygdala interactions: a genetic susceptibility mechanism for depression

A. Meyer-Lindenberg, M. Egan, B. Kolachana, 2005, Nature Neuroscience.

COMT genotype predicts cortical-limbic D1 receptor availability measured with [11C]NNC112 and PET

B. Kolachana, D. Weinberger, M. Laruelle, 2008, Molecular Psychiatry.

Effect of COMT Val108/158 Met genotype on frontal lobe function and risk for schizophrenia

R. Straub, M. Egan, T. Goldberg, 2001, Proceedings of the National Academy of Sciences of the United States of America.

Catechol O-methyltransferase val158-met genotype and individual variation in the brain response to amphetamine

M. Egan, T. Goldberg, J. Callicott, 2003, Proceedings of the National Academy of Sciences of the United States of America.

Interactive effect of apolipoprotein e genotype and age on hippocampal activation during memory processing in healthy adults.

B. Kolachana, D. Weinberger, K. Berman, 2012, Archives of general psychiatry.

Effective connectivity of AKT1-mediated dopaminergic working memory networks and pharmacogenetics of anti-dopaminergic treatment.

J. Callicott, B. Kolachana, D. Weinberger, 2012, Brain : a journal of neurology.

Genetic variation in CACNA1C affects brain circuitries related to mental illness.

Joseph H Callicott, Daniel R Weinberger, Venkata S Mattay, 2010, Archives of general psychiatry.

Evidence that altered amygdala activity in schizophrenia is related to clinical state and not genetic risk.

Andreas Meyer-Lindenberg, Joseph H Callicott, Daniel R Weinberger, 2009, The American journal of psychiatry.

Functional Polymorphisms in PRODH Are Associated with Risk and Protection for Schizophrenia and Fronto-Striatal Structure and Function

Joseph H. Callicott, Daniel R. Weinberger, Andreas Meyer-Lindenberg, 2008, PLoS genetics.

Genetic variation in AKT1 is linked to dopamine-associated prefrontal cortical structure and function in humans.

A. Meyer-Lindenberg, R. Straub, J. Callicott, 2008, The Journal of clinical investigation.

Allelic Variation in RGS4 Impacts Functional and Structural Connectivity in the Human Brain

Andreas Meyer-Lindenberg, Michael F Egan, Joseph H Callicott, 2007, The Journal of Neuroscience.

Serotonin Transporter Genetic Variation and the Response of the Human Amygdala

M. Egan, B. Kolachana, D. Weinberger, 2002, Science.

Prefrontal-Hippocampal Coupling During Memory Processing Is Modulated by COMT Val158Met Genotype

A. Meyer-Lindenberg, B. Kolachana, D. Weinberger, 2006, Biological Psychiatry.

Prefrontal Electrophysiologic “Noise” and Catechol-O-Methyltransferase Genotype in Schizophrenia

R. Coppola, M. Egan, T. Goldberg, 2006, Biological Psychiatry.

The BDNF val66met Polymorphism Affects Activity-Dependent Secretion of BDNF and Human Memory and Hippocampal Function

M. Egan, T. Goldberg, J. Callicott, 2003, Cell.

Catechol-O-Methyltransferase Genotype and Dopamine Regulation in the Human Brain

B. Kolachana, J. Kleinman, D. Weinberger, 2003, The Journal of Neuroscience.

Executive subprocesses in working memory: relationship to catechol-O-methyltransferase Val158Met genotype and schizophrenia.

R. Coppola, M. Egan, T. Goldberg, 2003, Archives of general psychiatry.

Functional analysis of genetic variation in catechol-O-methyltransferase (COMT): effects on mRNA, protein, and enzyme activity in postmortem human brain.

M. Egan, B. Kolachana, J. Kleinman, 2004, American journal of human genetics.

Planning ability in Parkinson's disease is influenced by the COMT val158met polymorphism

T. Robbins, T. Goldberg, B. Kolachana, 2004, Movement disorders : official journal of the Movement Disorder Society.

Epistatic interactions of AKT1 on human medial temporal lobe biology and pharmacogenetic implications

J. Callicott, B. Kolachana, D. Weinberger, 2011, Molecular Psychiatry.

Effects of the BDNF Val66Met Polymorphism on White Matter Microstructure in Healthy Adults

B. Kolachana, D. Weinberger, B. Verchinski, 2013, Neuropsychopharmacology.

Brain-Derived Neurotrophic Factor val66met Polymorphism Affects Human Memory-Related Hippocampal Activity and Predicts Memory Performance

M. Egan, T. Goldberg, J. Callicott, 2003, The Journal of Neuroscience.

The Brain-derived Neurotrophic Factor Val66met Polymorphism and Variation in Human Cortical Morphology

A. Meyer-Lindenberg, R. Straub, M. Egan, 2022 .

Schizophrenia is associated with elevated amphetamine-induced synaptic dopamine concentrations: evidence from a novel positron emission tomography method.

A. Malhotra, R. Saunders, T. Su, 1997, Proceedings of the National Academy of Sciences of the United States of America.

Midbrain dopamine and prefrontal function in humans: interaction and modulation by COMT genotype

R. Nussbaum, A. Meyer-Lindenberg, B. Kolachana, 2005, Nature Neuroscience.

Effect of Catechol-O-Methyltransferase val158met Genotype on Attentional Control

M. Egan, T. Goldberg, J. Callicott, 2005, The Journal of Neuroscience.

Variation in dopamine genes influences responsivity of the human reward system

B. Kolachana, D. Weinberger, K. Berman, 2009, Proceedings of the National Academy of Sciences.

Catechol O-methyltransferase val158met genotype and neural mechanisms related to affective arousal and regulation.

Andreas Meyer-Lindenberg, Michael F Egan, Daniel R Weinberger, 2006, Archives of general psychiatry.

Kinetic Modeling of [11C]Raclopride: Combined PET-Microdialysis Studies

W C Eckelman, R E Carson, R. Saunders, 1997, Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism.

Brain-Derived Neurotrophic Factor ValMet Polymorphism Affects Resting Regional Cerebral Blood Flow and Functional Connectivity Differentially in Women Versus Men

Daniel R Weinberger, Karen F Berman, Shau-Ming Wei, 2012 .

The distinct cognitive syndromes of Parkinson's disease: 5 year follow-up of the CamPaIGN cohort.

Thomas Foltynie, Daniel R Weinberger, Stephen J Sawcer, 2009, Brain : a journal of neurology.

Impact of complex genetic variation in COMT on human brain function

Thomas E. Nichols, A. Meyer-Lindenberg, M. Egan, 2006, Molecular Psychiatry.

Neural mechanisms of genetic risk for impulsivity and violence in humans.

Giuseppe Blasi, Andreas Meyer-Lindenberg, Joseph H Callicott, 2006, Proceedings of the National Academy of Sciences of the United States of America.

Neural mechanisms of genetic risk for impulsivity and violence in humans

Ahmad R. Hariri, Joseph H. Callicott, Daniel R. Weinberger, 2006 .

An improved methodology for routine in vivo microdialysis in non-human primates

R. Saunders, B. Kolachana, D. Weinberger, 1994, Journal of Neuroscience Methods.

Evidence for a frontocortical-septal glutamatergic pathway and compensatory changes in septal glutamate uptake after cortical and fornix lesions in the rat

B. Kolachana, R. Wyatt, B. Lipska, 1991, Brain Research.

Variation in the Williams syndrome GTF2I gene and anxiety proneness interactively affect prefrontal cortical response to aversive stimuli

B. Kolachana, D. Weinberger, K. Berman, 2015, Translational Psychiatry.

A common allele in the oxytocin receptor gene (OXTR) impacts prosocial temperament and human hypothalamic-limbic structure and function

Daniel R. Weinberger, Venkata S. Mattay, Beth A. Verchinski, 2010, Proceedings of the National Academy of Sciences.

Genetic Variation in COMT: Effects on Working Memory in Schizophrenic Patients, Their Siblings, & Healthy Controls

R. Straub, M. Egan, T. Goldberg, 2013 .

Catechol-O-methyltransferase Val158Met Genotype and Resting Regional Cerebral Blood Flow in Medication-Free Patients with Schizophrenia

A. Meyer-Lindenberg, B. Kolachana, D. Weinberger, 2010 .

A susceptibility gene for affective disorders and the response of the human amygdala.

Michael F Egan, Daniel R Weinberger, Venkata S Mattay, 2005, Archives of general psychiatry.

Neurogenetic Effects of OXTR rs2254298 in the Extended Limbic System of Healthy Caucasian Adults

Daniel R. Weinberger, Venkata S. Mattay, Andreas Meyer-Lindenberg, 2011, Biological Psychiatry.

Neonatal lesions of the medial temporal lobe disrupt prefrontal cortical regulation of striatal dopamine

Daniel R. Weinberger, Bhaskar S. Kolachana, Richard C. Saunders, 1998, Nature.

In vivo characterization of extracellular GABA release in the caudate nucleus and prefrontal cortex of the rhesus monkey

R. Saunders, B. Kolachana, D. Weinberger, 1997, Synapse.

Characteristics of the Cation Cotransporter NKCC1 in Human Brain: Alternate Transcripts, Expression in Development, and Potential Relationships to Brain Function and Schizophrenia

R. Straub, J. Callicott, B. Kolachana, 2014, The Journal of Neuroscience.

Association of the Ser704Cys DISC1 polymorphism with human hippocampal formation gray matter and function during memory encoding

Fabio Sambataro, Giuseppe Blasi, Apostolos Papazacharias, 2008, The European journal of neuroscience.

Tolcapone Improves Cognition and Cortical Information Processing in Normal Human Subjects

Michael F Egan, Joseph H Callicott, Venkata Mattay, 2007, Neuropsychopharmacology.

Catechol O-Methyltransferase (COMT) mRNA Expression in the Dorsolateral Prefrontal Cortex of Patients with Schizophrenia

Daniel R Weinberger, B. Kolachana, J. Kleinman, 2003, Neuropsychopharmacology.

Incomplete penetrance of NRXN1 deletions in families with schizophrenia

R. Straub, R. Vakkalanka, B. Kolachana, 2014, Schizophrenia Research.

Genetic evidence implicating DARPP-32 in human frontostriatal structure, function, and cognition.

Andreas Meyer-Lindenberg, Michael F Egan, Joseph H Callicott, 2007, The Journal of clinical investigation.

Expression of oligodendrocyte-associated genes in dorsolateral prefrontal cortex of patients with schizophrenia

R. Vakkalanka, B. Kolachana, J. Kleinman, 2008, Schizophrenia Research.

Biological validation of increased schizophrenia risk with NRG1, ERBB4, and AKT1 epistasis via functional neuroimaging in healthy controls.

Joseph H Callicott, Daniel R Weinberger, Pierandrea Muglia, 2010, Archives of general psychiatry.

Transcriptional profiling in the human prefrontal cortex: evidence for two activational states associated with cocaine abuse

B. Kolachana, J. Kleinman, K. Becker, 2003, The Pharmacogenomics Journal.

The BDNF Val66Met polymorphism has a gender specific influence on planning ability in Parkinson’s disease

T. Robbins, T. Goldberg, B. Kolachana, 2005, Journal of Neurology.

A method for determining haploid and triploid genotypes and their association with vascular phenotypes in Williams syndrome and 7q11.23 duplication syndrome

Michael D. Gregory, C. Mervis, B. Kolachana, 2018, BMC Medical Genetics.

Evidence for statistical epistasis between catechol-O-methyltransferase (COMT) and polymorphisms in RGS4, G72 (DAOA), GRM3, and DISC1: influence on risk of schizophrenia

Daniel R. Weinberger, Kristin K. Nicodemus, Bhaskar S. Kolachana, 2007, Human Genetics.

Genetic variants in AVPR1A linked to autism predict amygdala activation and personality traits in healthy humans

A. Meyer-Lindenberg, B. Kolachana, D. Weinberger, 2009, Molecular Psychiatry.

Revisiting DARPP-32 in postmortem human brain: changes in schizophrenia and bipolar disorder and genetic associations with t-DARPP-32 expression

T M Hyde, B. Kolachana, J. Kleinman, 2014, Molecular Psychiatry.

Impact of interacting functional variants in COMT on regional gray matter volume in human brain

Joseph H. Callicott, Daniel R. Weinberger, Andreas Meyer-Lindenberg, 2009, NeuroImage.

Striatal dopamine receptors and transporters in monkeys with neonatal temporal limbic damage

R. Saunders, B. Kolachana, J. Bachevalier, 1999, Synapse.

Neuregulin1-induced cell migration is impaired in schizophrenia: association with neuregulin1 and catechol-o-methyltransferase gene polymorphisms

M. Egan, B. Kolachana, D. Weinberger, 2007, Molecular Psychiatry.

Genetic Association of ErbB4 and Human Cortical GABA Levels In Vivo

Daniel R. Weinberger, Matthew Geramita, Jun Shen, 2011, The Journal of Neuroscience.

Attenuated extracellular dopamine levels after stress and amphetamine in the nucleus accumbens of rats with neonatal ventral hippocampal damage

B. Lipska, B. Kolachana, D. Weinberger, 1999, Journal of Neural Transmission.

Differential effects of common variants in SCN2A on general cognitive ability, brain physiology, and messenger RNA expression in schizophrenia cases and control individuals.

Graham L. Baum, D. Rujescu, R. Straub, 2014, JAMA psychiatry.

Biological Effects of COMT Haplotypes and Psychosis Risk in 22q11.2 Deletion Syndrome

B. Kolachana, D. Weinberger, Abraham Weizman, 2014, Biological Psychiatry.

Evidence of biologic epistasis between BDNF and SLC6A4 and implications for depression

A. Meyer-Lindenberg, M. Egan, B. Kolachana, 2008, Molecular Psychiatry.

Genetic Variation in Catechol-O-Methyltransferase: Effects on Working Memory in Schizophrenic Patients, Their Siblings, and Healthy Controls

Terry E. Goldberg, Daniel R. Weinberger, Bhaskar S. Kolachana, 2008, Biological Psychiatry.

Epistasis between Dopamine Regulating Genes Identifies a Nonlinear Response of the Human Hippocampus During Memory Tasks

B. Kolachana, D. Weinberger, F. Sambataro, 2008, Biological Psychiatry.

The relationship between dorsolateral prefrontal N-acetylaspartate measures and striatal dopamine activity in schizophrenia∗ ∗ See accompanying Editorial, in this issue.

R. Saunders, M. Egan, J. Callicott, 1999, Biological Psychiatry.

Variation of Human Amygdala Response During Threatening Stimuli as a Function of 5′HTTLPR Genotype and Personality Style

Daniel R. Weinberger, Tommaso Scarabino, Giuseppe Blasi, 2005, Biological Psychiatry.

Neanderthal‐derived genetic variation in living humans relates to schizophrenia diagnosis, to psychotic symptom severity, and to dopamine synthesis

Michael D. Gregory, B. Kolachana, K. Berman, 2021, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Neanderthal-Derived Genetic Variation is Associated with Functional Connectivity in the Brains of Living Humans

Joseph H. Callicott, Bhaskar S. Kolachana, Karen Faith Berman, 2020, Brain Connect..

Catechol-O-methyltransferase val108/158met genotype predicts working memory response to antipsychotic medications

M. Egan, T. Goldberg, B. Kolachana, 2004, Biological Psychiatry.

WWC1 Genotype Modulates Age-Related Decline in Episodic Memory Function Across the Adult Life Span

Fabio Sambataro, Venkata S. Mattay, Herve Lemaitre, 2014, Biological Psychiatry.

Augmentation of prefrontal cortical monoaminergic activity inhibits dopamine release in the caudate nucleus: Anin vivo neurochemical assessment in the rhesus monkey

D. R. Weinberger, R. Saunders, B. Kolachana, 1995, Neuroscience.

Common Variation in the DOPA Decarboxylase (DDC) Gene and Human Striatal DDC Activity In Vivo

Michael D. Gregory, Karen F Berman, Joseph C Masdeu, 2016, Neuropsychopharmacology.

Polymorphism in the ZNF804A Gene and Variation in D1 and D2/D3 Dopamine Receptor Availability in the Healthy Human Brain: A Dual Positron Emission Tomography Study.

Michael D. Gregory, B. Kolachana, K. Berman, 2021, Biological psychiatry. Cognitive neuroscience and neuroimaging.

Catechol-o-methyltransferase enzyme activity and protein expression in human prefrontal cortex across the postnatal lifespan.

Paul J. Harrison, B. Kolachana, J. Kleinman, 2007, Cerebral cortex.

Late-Onset Alzheimer's Disease Polygenic Risk Profile Score Predicts Hippocampal Function.

Joseph H Callicott, Daniel R Weinberger, Hao Yang Tan, 2017, Biological psychiatry. Cognitive neuroscience and neuroimaging.

Brain‐Derived Neurotrophic Factor Val66Met Polymorphism Affects the Relationship Between an Anxiety‐Related Personality Trait and Resting Regional Cerebral Blood Flow

B. Kolachana, K. Berman, P. Kohn, 2016, Cerebral cortex.

Catechol-O-Methyltransferase Valine158Methionine Genotype and Resting Regional Cerebral Blood Flow in Medication-Free Patients with Schizophrenia

A. Meyer-Lindenberg, B. Kolachana, D. Weinberger, 2010, Biological Psychiatry.

Brain-Derived Neurotrophic Factor (BDNF) Val66Met Polymorphism Differentially Predicts Hippocampal Function in Medication-Free Patients with Schizophrenia

B. Kolachana, D. Weinberger, K. Berman, 2012, Molecular Psychiatry.

BDNF Val 66 Met polymorphism tunes frontolimbic circuitry during affective contextual learning

Mbemba Jabbi, Bhaskar S. Kolachana, Karen Faith Berman, 2017, NeuroImage.

Genetic Modulation of GABA Levels in the Anterior Cingulate Cortex by GAD1 and COMT

Joseph H Callicott, Daniel R Weinberger, Matthew Geramita, 2010, Neuropsychopharmacology.

EffectofCatechol-O-Methyltransferaseval 158 metGenotype onAttentionalControl

Michael E. Egan, J. Callicott, B. Kolachana, 2005 .

Effects of ibotenic acid lesion of the medial prefrontal cortex on dopamine agonist-related behaviors in the rat

B. Kolachana, D. Weinberger, K. Vladar, 1993, Pharmacology Biochemistry and Behavior.

D1 and D2 receptor modulation in rat striatum and nucleus accumbens after subchronic and chronic haloperidol treatment

B. Lipska, B. Kolachana, J. Kleinman, 1992, Brain Research.

Local pharmacological manipulation of extracellular dopamine levels in the dorsolateral prefrontal cortex and caudate nucleus in the rhesus monkey: An in vivo microdialysis study

R. Saunders, B. Kolachana, D. Weinberger, 2004, Experimental Brain Research.

Polygenic scores for psychiatric disorders in a diverse postmortem brain tissue cohort

B. Kolachana, S. Marenco, P. Auluck, 2022, European Neuropsychopharmacology.

Microdialysis in Nonhuman Primates

R. Saunders, B. Kolachana, Daniel R. Weinberger, 1997, Current protocols in neuroscience.

Epistatic and Functional Interactions of Catechol-O-Methyltransferase (COMT) and AKT1 on Neuregulin1-ErbB Signaling in Cell Models

B. Kolachana, D. Weinberger, E. Tunbridge, 2010, PloS one.

In vivo characterization of extracellular GABA release in the caudate nucleus and prefrontal cortex of the rhesus monkey

R. Saunders, B. Kolachana, D. Weinberger, 1997, Synapse.

Biological validation of increased schizophrenia risk with NRG1, ERBB4, and AKT1 epistasis via functional neuroimaging in healthy controls.

D. Rujescu, P. Muglia, I. Giegling, 2010, Archives of general psychiatry.

A variable number of tandem repeats in the 3′‐untranslated region of the dopamine transporter modulates striatal function during working memory updating across the adult age span

T. Goldberg, B. Kolachana, D. Weinberger, 2015, The European journal of neuroscience.

Brain-derived neurotrophic factor Val66Met genotype and ovarian steroids interactively modulate working memory-related hippocampal function in women: a multimodal neuroimaging study

B. Kolachana, K. Berman, P. Kohn, 2018, Molecular Psychiatry.

Genetic variation in CACNA1C affects brain circuitries related to mental illness.

R. Straub, J. Callicott, R. Vakkalanka, 2010, Archives of general psychiatry.

The distinct cognitive syndromes of Parkinson's disease: 5 year follow-up of the CamPaIGN cohort.

T. Robbins, M. Ban, A. Goris, 2009, Brain : a journal of neurology.

WWC1 Genotype Modulates Age-Related Decline in Episodic Memory Function Across the Adult Life Span

J. Callicott, B. Kolachana, D. Weinberger, 2014, Biological Psychiatry.

The Brain-Derived Neurotrophic Factor val66met Polymorphism and Variation in Human Cortical Morphology

A. Meyer-Lindenberg, R. Straub, M. Egan, 2004, The Journal of Neuroscience.

Brain-Derived Neurotrophic Factor Val66Met Polymorphism Affects Resting Regional Cerebral Blood Flow and Functional Connectivity Differentially in Women Versus Men

B. Kolachana, D. Weinberger, K. Berman, 2012, The Journal of Neuroscience.

Dorsal visual stream and LIMK1: hemideletion, haplotype, and enduring effects in children with Williams syndrome

Michael D. Gregory, Tiffany A. Nash, C. Mervis, 2023, Journal of Neurodevelopmental Disorders.