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Frontiers in Endocrinology|May 19, 2025
Developing a congenital hyperinsulinism prioritized research agenda: a patient-driven international collaborative research networkTai L S Pasquini, Indraneel Banerjee, Henrik Thybo Christesen, et al.
Journal of Clinical Child and Adolescent Psychology : the Official Journal for the Society of Clinical Child and Adolescent Psychology, American Psychological Association, Division 53|November 20, 2025
Proportion and Profile of Autistic Children Not Acquiring Spoken Language Despite Receiving Evidence-Based Early InterventionsGiacomo Vivanti, Michael V Lombardo, Ashley Zitter, et al.
Ebiomedicine|May 25, 2026
Low-level mosaic variants causing the pancreatic disease congenital hyperinsulinism can be detected from blood DNAJasmin J Bennett, Thomas W Laver, Jonna M E Männistö, et al.
Pediatric Diabetes|March 16, 2022
Increased referrals for congenital hyperinsulinism genetic testing in children with trisomy 21 reflects the high burden of non-genetic risk factors in this groupThomas I Hewat, Thomas W Laver, Jayne A L Houghton, et al.
Journal of Acquired Immune Deficiency Syndromes (1999)|October 21, 2016
County-Level Vulnerability Assessment for Rapid Dissemination of HIV or HCV Infections Among Persons Who Inject Drugs, United StatesMichelle M Van Handel, Charles E Rose, Elaine J Hallisey, et al.
American Journal of Human Genetics|January 1, 2013
Next-generation sequencing reveals deep intronic cryptic ABCC8 and HADH splicing founder mutations causing hyperinsulinism by pseudoexon activationSarah E Flanagan, Weijia Xie, Richard Caswell, et al.
Bioorganic & Medicinal Chemistry|May 17, 2021
Toward the assembly and characterization of an encoded library hit confirmation platform: Bead-Assisted Ligand Isolation Mass Spectrometry (BALI-MS)Anokha S Ratnayake, Mark E Flanagan, Timothy L Foley, et al.
Journal of the American Chemical Society|May 29, 2019
Expanding Reactivity in DNA-Encoded Library Synthesis via Reversible Binding of DNA to an Inert Quaternary Ammonium SupportDillon T Flood, Shota Asai, Xuejing Zhang, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association|December 25, 2025
Basic Science and PathogenesisRebecca Bernal, Obed Okwoli Apochi, Yannick Joel Wadop Ngouongo, et al.
Cell Metabolism|January 14, 2014
Analysis of transcription factors key for mouse pancreatic development establishes NKX2-2 and MNX1 mutations as causes of neonatal diabetes in manSarah E Flanagan, Elisa De Franco, Hana Lango Allen, et al.
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