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Journal of Affective Disorders|December 16, 1996
Linkage studies in bipolar affective disorder with markers on chromosome 21H Vallada, N Craddock, L Vasques, et al.
Nature|February 25, 2021
Sulfur sequestration promotes multicellularity during nutrient limitationBeth Kelly, Gustavo E Carrizo, Joy Edwards-Hicks, et al.
Journal of Interventional Cardiology|July 14, 2022
Clinical Factors and Outcomes When Real-World Heart Teams Overruled STS Risk Scores in TAVR CasesJackson M King, Morgan T Black, Ruyun Jin, et al.
Frontiers in Immunology|May 16, 2022
Early Post-Vaccination Gene Signatures Correlate With the Magnitude and Function of Vaccine-Induced HIV Envelope-Specific Plasma Antibodies in Infant Rhesus MacaquesK K Vidya Vijayan, Kaitlyn A Cross, Alan D Curtis, et al.
Cell Metabolism|November 13, 2018
Genetic Analysis Reveals AMPK Is Required to Support Tumor Growth in Murine Kras-Dependent Lung Cancer ModelsLillian J Eichner, Sonja N Brun, Sébastien Herzig, et al.
The Oncologist|January 11, 2018
Characteristics of Real-World Metastatic Non-Small Cell Lung Cancer Patients Treated with Nivolumab and Pembrolizumab During the Year Following ApprovalSean Khozin, Amy P Abernethy, Nathan C Nussbaum, et al.
Circulation. Arrhythmia and Electrophysiology|September 10, 2017
Resolving Bipolar Electrogram Voltages During Atrial Fibrillation Using Omnipolar MappingShouvik K Haldar, Karl Magtibay, Andreu Porta-Sanchez, et al.
Science (New York, N.Y.)|April 20, 2023
Induction of lysosomal and mitochondrial biogenesis by AMPK phosphorylation of FNIP1Nazma Malik, Bibiana I Ferreira, Pablo E Hollstein, et al.
The Lancet Regional Health. Western Pacific|September 1, 2023
Prevalence, time trends, and correlates of major depressive episode and other psychiatric conditions among young people amid major social unrest and COVID-19 in Hong Kong: a representative epidemiological study from 2019 to 2022Stephanie M Y Wong, Eric Y H Chen, Y N Suen, et al.
BMC Medical Genomics|October 26, 2018
Identifying the genetic causes for prenatally diagnosed structural congenital anomalies (SCAs) by whole-exome sequencing (WES)Gordon K C Leung, Christopher C Y Mak, Jasmine L F Fung, et al.
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