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Bioinformatics (Oxford, England)|February 9, 2017
PatternMarkers & GWCoGAPS for novel data-driven biomarkers via whole transcriptome NMFGenevieve L Stein-O'Brien, Jacob L Carey, Wai Shing Lee, et al.
Nature Communications|July 9, 2025
Early developmental origins of cortical disorders modeled in human neural stem cellsXoel Mato-Blanco, Suel-Kee Kim, Alexandre Jourdon, et al.
Translational Psychiatry|September 19, 2019
Clinical and genetic validity of quantitative bipolarityHeather A Bruce, Peter Kochunov, Braxton Mitchell, et al.
Molecular Psychiatry|March 7, 2023
Genome-wide significant risk loci for mood disorders in the Old Order Amish founder populationElizabeth M Humphries, Kwangmi Ahn, Rachel L Kember, et al.
Molecular Psychiatry|May 13, 2022
Rare variants implicate NMDA receptor signaling and cerebellar gene networks in risk for bipolar disorderNaushaba Hasin, Lace M Riggs, Tatyana Shekhtman, et al.
Molecular Psychiatry|June 30, 2018
Rediscovering the value of families for psychiatric genetics researchDavid C Glahn, Vishwajit L Nimgaonkar, Henriette Raventós, et al.
Biorxiv : the Preprint Server for Biology|September 18, 2025
Inhibition of autophagy-lysosomal function exacerbates microglial and monocyte lipid metabolism reprograming and dysfunction after brain injuryAmir A Mehrabani-Tabari, Nivedita Hegdekar, Brian R Herb, et al.
Research Square|November 24, 2025
Inhibition of autophagy-lysosomal function exacerbates microglial and monocyte lipid metabolism reprograming and dysfunction after brain injuryAmir A Mehrabani-Tabari, Nivedita Hegdekar, Brian R Herb, et al.
Human Molecular Genetics|March 24, 2017
High resolution time-course mapping of early transcriptomic, molecular and cellular phenotypes in Huntington's disease CAG knock-in mice across multiple genetic backgroundsSeth A Ament, Jocelynn R Pearl, Andrea Grindeland, et al.
Scientific Reports|February 9, 2017
Motivational, proteostatic and transcriptional deficits precede synapse loss, gliosis and neurodegeneration in the B6.HttQ111/+ model of Huntington's diseaseRobert M Bragg, Sydney R Coffey, Rory M Weston, et al.
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