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The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|February 28, 2024
DNA G-Quadruplex Is a Transcriptional Control Device That Regulates MemoryPaul R Marshall, Joshua Davies, Qiongyi Zhao, et al.
NPJ Genomic Medicine|July 2, 2025
Assessing the diagnostic impact of blood transcriptome profiling in a pediatric cohort previously assessed by genome sequencingHuayun Hou, Kyoko E Yuki, Gregory Costain, et al.
The Journal of Experimental Medicine|January 31, 2020
Sequential ubiquitination of NLRP3 by RNF125 and Cbl-b limits inflammasome activation and endotoxemiaJuan Tang, Sha Tu, Guoxin Lin, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 21, 2018
Haploinsufficiency of vascular endothelial growth factor related signaling genes is associated with tetralogy of FallotMiriam S Reuter, Rebekah Jobling, Rajiv R Chaturvedi, et al.
Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association for Cancer Research, Cosponsored by the American Society of Preventive Oncology|October 28, 2010
Characterization of 9p24 risk locus and colorectal adenoma and cancer: gene-environment interaction and meta-analysisJonathan D Kocarnik, Carolyn M Hutter, Martha L Slattery, et al.
Molecular Autism|April 12, 2014
Recurrent duplications of the annexin A1 gene (ANXA1) in autism spectrum disordersCatarina T Correia, Inês C Conceição, Bárbara Oliveira, et al.
Bioorganic & Medicinal Chemistry Letters|January 3, 2006
Imidazo[1,2-b][1,2,4]triazines as alpha2/alpha3 subtype selective GABA A agonists for the treatment of anxietyAndrew S R Jennings, Richard T Lewis, Michael G N Russell, et al.
JAMA Network Open|April 29, 2026
Streamlining Inherited Cancer Identification via an EMR-Integrated Risk Assessment Platform: A Nonrandomized Clinical TrialLori A Orlando, Kathleen F Mittendorf, Nathan A Bihlmeyer, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 16, 2014
A high-resolution copy-number variation resource for clinical and population geneticsMohammed Uddin, Bhooma Thiruvahindrapuram, Susan Walker, et al.
Journal of Medical Genetics|January 22, 2013
Deletions in 16q24.2 are associated with autism spectrum disorder, intellectual disability and congenital renal malformationGregory Ryan Handrigan, David Chitayat, Anath C Lionel, et al.
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