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Psychiatry Research|October 24, 2013
Altered brain response to reward and punishment in adolescents with Anorexia nervosaAmanda Bischoff-Grethe, Danyale McCurdy, Emily Grenesko-Stevens, et al.
Journal of Thrombosis and Haemostasis : JTH|May 27, 2026
Novel SERPINC1 variants in hereditary Antithrombin Deficiency: first pathogenic deep-intronic variant, revealed by multiple genomic and transcriptomic approachesP Christian Remmelzwaal, René Mulder, Jelkje J de Boer-Bergsma, et al.
Genetics in Medicine Open|December 13, 2024
Exploring the phenotypic spectrum and osteopenia mechanisms in Yunis-Varón syndromeÉliane Beauregard-Lacroix, Alexandra Scott, Thi Tuyet Mai Nguyen, et al.
Neuropsychology Review|May 26, 2007
Functional MRI of language in aphasia: a review of the literature and the methodological challengesBruce Crosson, Keith McGregor, Kaundinya S Gopinath, et al.
Journal of Autoimmunity|July 7, 2024
Impact of coding risk variant IFNGR2 on the B cell-intrinsic IFN-γ signaling pathway in multiple sclerosisLaurens Bogers, Jasper Rip, Liza Rijvers, et al.
Heart & Lung : the Journal of Critical Care|February 22, 2023
Evaluating depressive symptoms, BDNF Val66Met, and APOE-ε4 as moderators of response to computerized cognitive training in heart failureSusan J Pressler, Miyeon Jung, Bruno Giordani, et al.
Journal of Wildlife Diseases|March 26, 2025
A Metagenomic Investigation into Apteryx rowi Dermatosis Identifies Multiple Novel Viruses and a Highly Abundant NematodeJordan T Taylor, Vivian Lee, Tracey Dearlove, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|March 28, 2019
Semaphorin4D Induces Inhibitory Synapse Formation by Rapid Stabilization of Presynaptic Boutons via MET CoactivationCátia P Frias, Jian Liang, Tom Bresser, et al.
Cancers|August 7, 2019
Loss of BAP1 Is Associated with Upregulation of the NFkB Pathway and Increased HLA Class I Expression in Uveal MelanomaZahra Souri, Annemijn P A Wierenga, Christiaan van Weeghel, et al.
American Journal of Human Genetics|June 5, 2018
βIV Spectrinopathies Cause Profound Intellectual Disability, Congenital Hypotonia, and Motor Axonal NeuropathyChih-Chuan Wang, Xilma R Ortiz-González, Sabrina W Yum, et al.
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