Liu, Jingyu

Correspondence of DNA Methylation Between Blood and Brain Tissue and Its Application to Schizophrenia Research

Walton, E., Hass, J., Liu, J., Roffman, J. L., Bernardoni, F., Roessner, V., Kirsch, M., Schackert, G., Calhoun, V., & Ehrlich, S. (2016) · Schizophrenia Bulletin

Epigenetics and DNA MethylationSchizophrenia research and treatment

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Investigation of relationships between fMRI brain networks in the spectral domain using ICA and granger causality reveals distinct differences between schizophrenia patients and healthy controls

Demirci, O., Stevens, M. C., Andreasen, N. C., Michael, A., Liu, J., White, T., Pearlson, G. D., Clark, V. P., & Calhoun, V. D. (2009) · NeuroImage

Functional Brain Connectivity StudiesMental Health Research Topics

Cited by 126

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

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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

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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

Patterns of Co-Occurring Gray Matter Concentration Loss across the Huntington Disease Prodrome

Ciarochi, J. A., Calhoun, V. D., Lourens, S., Long, J. D., Johnson, H. J., Bockholt, H. J., Liu, J., Plis, S. M., Paulsen, J. S., & Turner, J. A. (2016) · Frontiers in Neurology

Genetic Neurodegenerative DiseasesObsessive-Compulsive Spectrum Disorders

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