Glahn, David C.

Functional hierarchy underlies preferential connectivity disturbances in schizophrenia

Yang, G. J., Murray, J. D., Wang, X.-J., Glahn, D. C., Pearlson, G. D., Repovs, G., Krystal, J. H., & Anticevic, A. (2016) · Proceedings of the National Academy of Sciences

Functional Brain Connectivity StudiesSchizophrenia research and treatment

Cited by 153

Amygdala hyperactivation in untreated depressed individuals

Peluso, M. A. M., Glahn, D. C., Matsuo, K., Monkul, E. S., Najt, P., Zamarripa, F., Li, J., Lancaster, J. L., Fox, P. T., Gao, J.-H., et al. (2009) · Psychiatry Research: Neuroimaging

Neural and Behavioral Psychology StudiesAnxiety, Depression, Psychometrics, Treatment, Cognitive Processes

Cited by 141

Multi-site study of additive genetic effects on fractional anisotropy of cerebral white matter: Comparing meta and megaanalytical approaches for data pooling

Kochunov, P., Jahanshad, N., Sprooten, E., Nichols, T. E., Mandl, R. C., Almasy, L., Booth, T., Brouwer, R. M., Curran, J. E., de Zubicaray, G. I., et al. (2014) · NeuroImage

Advanced Neuroimaging Techniques and ApplicationsGenetic Associations and Epidemiology

Cited by 133

Testing the hypothesis of accelerated cerebral white matter aging in schizophrenia and major depression

Kochunov, P., Glahn, D. C., Rowland, L. M., Olvera, R. L., Winkler, A., Yang, Y.-H., Sampath, H., Carpenter, W. T., Duggirala, R., Curran, J., et al. (2013) · Biological Psychiatry

Schizophrenia research and treatmentAdvanced Neuroimaging Techniques and Applications

Cited by 118

Mapping Cortical Thickness in Children with 22q11.2 Deletions

Bearden, C. E., van Erp, T. G. M., Dutton, R. A., Tran, H., Zimmermann, L., Sun, D., Geaga, J. A., Simon, T. J., Glahn, D. C., Cannon, T. D., et al. (2007) · Cerebral Cortex

Genomic variations and chromosomal abnormalitiesSchizophrenia research and treatment

Cited by 92

Association of Copy Number Variation of the 15q11.2 BP1-BP2 Region With Cortical and Subcortical Morphology and Cognition

Writing Committee for the ENIGMA-CNV Working Group, van der Meer, D., Sønderby, I. E., Kaufmann, T., Walters, G. B., Abdellaoui, A., Ames, D., Amunts, K., Andersson, M., Armstrong, N. J., et al. (2020) · JAMA Psychiatry

Genomic variations and chromosomal abnormalitiesGenetics and Neurodevelopmental Disorders

Cited by 87

The Puzzle of Processing Speed, Memory, and Executive Function Impairments in Schizophrenia: Fitting the Pieces Together

Knowles, E. E. M., Weiser, M., David, A. S., Glahn, D. C., Davidson, M., & Reichenberg, A. (2015) · Biological Psychiatry

Schizophrenia research and treatmentNeural and Behavioral Psychology Studies

Cited by 77

Fronto-limbic circuitry in euthymic bipolar disorder: Evidence for prefrontal hyperactivation

Robinson, J. L., Monkul, E. S., Tordesillas-Gutiérrez, D., Franklin, C., Bearden, C. E., Fox, P. T., & Glahn, D. C. (2008) · Psychiatry Research: Neuroimaging

Bipolar Disorder and TreatmentNeural and Behavioral Psychology Studies

Cited by 75

Neural correlates of affective and non-affective cognition in obsessive compulsive disorder: A meta-analysis of functional imaging studies

Rasgon, A., Lee, W. H., Leibu, E., Laird, A., Glahn, D., Goodman, W., & Frangou, S. (2017) · European Psychiatry

Obsessive-Compulsive Spectrum DisordersNeural and Behavioral Psychology Studies

Cited by 73

Effects of copy number variations on brain structure and risk for psychiatric illness: Large‐scale studies from the ENIGMA working groups on CNVs

Sønderby, I. E., Ching, C. R. K., Thomopoulos, S. I., van der Meer, D., Sun, D., Villalon‐Reina, J. E., Agartz, I., Amunts, K., Arango, C., Armstrong, N. J., et al. (2022) · Human Brain Mapping

Genomic variations and chromosomal abnormalitiesGenetic Associations and Epidemiology

Cited by 67

Dose response of the 16p11.2 distal copy number variant on intracranial volume and basal ganglia

Sønderby, I. E., Gústafsson, Ó., Doan, N. T., Hibar, D. P., Martin-Brevet, S., Abdellaoui, A., Ames, D., Amunts, K., Andersson, M., Armstrong, N. J., et al. (2020) · Molecular Psychiatry

Genomic variations and chromosomal abnormalitiesGenetics and Neurodevelopmental Disorders

Cited by 66

Genetic influence on cognitive development between childhood and adulthood

Mollon, J., Knowles, E. E. M., Mathias, S. R., Gur, R., Peralta, J. M., Weiner, D. J., Robinson, E. B., Gur, R. E., Blangero, J., Almasy, L., et al. (2021) · Molecular Psychiatry

Cognitive Abilities and TestingGenetic Associations and Epidemiology

Cited by 57

Analysis of genetic variability and whole genome linkage of whole-brain, subcortical, and ependymal hyperintense white matter volume

Kochunov, P., Glahn, D., Winkler, A., Duggirala, R., Olvera, R. L., Cole, S., Dyer, T. D., Almasy, L., Fox, P. T., & Blangero, J. (2009) · Stroke

Cerebrovascular and genetic disordersGenetic Associations and Epidemiology

Cited by 54

A resting state fMRI analysis pipeline for pooling inference across diverse cohorts: an ENIGMA rs-fMRI protocol

Adhikari, B. M., Jahanshad, N., Shukla, D., Turner, J., Grotegerd, D., Dannlowski, U., Kugel, H., Engelen, J., Dietsche, B., Krug, A., et al. (2019) · Brain Imaging and Behavior

Functional Brain Connectivity StudiesAdvanced MRI Techniques and Applications

Cited by 53

Social isolation is linked to classical risk factors of Alzheimer’s disease-related dementias

Shafighi, K., Villeneuve, S., Rosa Neto, P., Badhwar, A., Poirier, J., Sharma, V., Medina, Y. I., Silveira, P. P., Dube, L., Glahn, D., et al. (2023) · PLOS ONE

Dementia and Cognitive Impairment ResearchHealth disparities and outcomes

Cited by 51

Whole Brain and Regional Hyperintense White Matter Volume and Blood Pressure: Overlap of Genetic Loci Produced by Bivariate, Whole-Genome Linkage Analyses

Kochunov, P., Glahn, D., Lancaster, J., Winkler, A., Kent, J. W., Olvera, R. L., Cole, S. A., Dyer, T. D., Almasy, L., Duggirala, R., et al. (2010) · Stroke

Cerebrovascular and genetic disordersGenetic Associations and Epidemiology

Cited by 46

Blood pressure and cerebral white matter share common genetic factors in Mexican Americans

Kochunov, P., Glahn, D. C., Lancaster, J., Winkler, A., Karlsgodt, K., Olvera, R. L., Curran, J. E., Carless, M. A., Dyer, T. D., Almasy, L., et al. (2011) · Hypertension

Cerebrovascular and genetic disordersAdvanced Neuroimaging Techniques and Applications

Cited by 38

Whole-genome association analyses of sleep-disordered breathing phenotypes in the NHLBI TOPMed program

Cade, B. E., Lee, J., Sofer, T., Wang, H., Zhang, M., Chen, H., Gharib, S. A., Gottlieb, D. J., Guo, X., Lane, J. M., et al. (2021) · Genome Medicine

Obstructive Sleep Apnea ResearchGenetic Associations and Epidemiology

Cited by 33

Recurrent major depression and right hippocampal volume: A bivariate linkage and association study: Recurrent Depression and Right Hippocampal Volume

Mathias, S. R., Knowles, E. E. M., Kent, J. W., McKay, D. R., Curran, J. E., de Almeida, M. A. A., Dyer, T. D., Göring, H. H. H., Olvera, R. L., Duggirala, R., et al. (2016) · Human Brain Mapping

Genetic Associations and EpidemiologyTreatment of Major Depression

Cited by 28

Independent evidence for an association between general cognitive ability and a genetic locus for educational attainment

Trampush, J. W., Lencz, T., Knowles, E., Davies, G., Guha, S., Pe'er, I., Liewald, D. C., Starr, J. M., Djurovic, S., Melle, I., et al. (2015) · American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

Genetic Associations and EpidemiologyCognitive Abilities and Testing

Cited by 24