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Nature Communications|May 20, 2025
Whole genome sequencing improves tissue-of-origin diagnosis and treatment options for cancer of unknown primaryRichard J Rebello, Atara Posner, Ruining Dong, et al.
Brain : a Journal of Neurology|April 22, 2025
Disease-modifying effects of TMEM106B in genetic frontotemporal dementia: a longitudinal GENFI studySaira S Mirza, Maurice Pasternak, Andrew D Paterson, et al.
The British Journal of Psychiatry : the Journal of Mental Science|September 5, 2015
Impact of a cis-associated gene expression SNP on chromosome 20q11.22 on bipolar disorder susceptibility, hippocampal structure and cognitive performanceMing Li, Xiong-jian Luo, Mikael Landén, et al.
Cell Reports|February 13, 2020
Dynamic Imaging of LDH Inhibition in Tumors Reveals Rapid In Vivo Metabolic Rewiring and Vulnerability to Combination TherapyNobu Oshima, Ryo Ishida, Shun Kishimoto, et al.
The British Journal of Psychiatry : the Journal of Mental Science|March 25, 2026
The American Society of Clinical Psychopharmacology (ASCP) task force on the deprescribing of psychotropic medications for mood disorders: Delphi expert consensusJoseph F Goldberg, Holly A Swartz, Roger S McIntyre, et al.
Scientific Reports|January 14, 2021
Prediction of lithium response using genomic dataWilliam Stone, Abraham Nunes, Kazufumi Akiyama, et al.
JAMA Network Open|February 25, 2026
Recommendations for the Deprescribing of Psychotropic Medications: A Consensus Statement From the American Society of Clinical Psychopharmacology Task ForceJoseph F Goldberg, Roger S McIntyre, Holly A Swartz, et al.
Bipolar Disorders|March 24, 2022
Predictors of functional impairment in bipolar disorder: Results from 13 cohorts from seven countries by the global bipolar cohort collaborativeKatherine E Burdick, Caitlin E Millett, Anastasia K Yocum, et al.
Patterns (New York, N.Y.)|July 31, 2024
Cortical similarities in psychiatric and mood disorders identified in federated VBM analysis via COINSTACKelly Rootes-Murdy, Sandeep Panta, Ross Kelly, et al.
Neurogenetics|January 22, 2013
Mutations in SLC20A2 are a major cause of familial idiopathic basal ganglia calcificationSandy Chan Hsu, Renee L Sears, Roberta R Lemos, et al.
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