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Neuroscience and Biobehavioral Reviews|July 23, 2019
From pattern classification to stratification: towards conceptualizing the heterogeneity of Autism Spectrum DisorderThomas Wolfers, Dorothea L Floris, Richard Dinga, et al.
Prostate International|October 1, 2016
Asia prostate cancer study (A-CaP Study) launch symposiumHideyuki Akaza, Yoshihiko Hirao, Choung-Soo Kim, et al.
European Urology|September 1, 2021
The Additive Diagnostic Value of Prostate-specific Membrane Antigen Positron Emission Tomography Computed Tomography to Multiparametric Magnetic Resonance Imaging Triage in the Diagnosis of Prostate Cancer (PRIMARY): A Prospective Multicentre StudyLouise Emmett, James Buteau, Nathan Papa, et al.
Biological Psychiatry|August 24, 2024
Unique Functional Neuroimaging Signatures of Genetic Versus Clinical High Risk for PsychosisCharles H Schleifer, Sarah E Chang, Carolyn M Amir, et al.
European Urology|July 8, 2026
ProBIOPSY: A Multidisciplinary International Consensus on Standards for Prostate BiopsyDaria Chernysheva, Francesco Di Bello, Giulio Avesani, et al.
BJU International|November 1, 2014
Development of a standardised training curriculum for robotic surgery: a consensus statement from an international multidisciplinary group of expertsKamran Ahmed, Reenam Khan, Alexandre Mottrie, et al.
Urologic Oncology|January 13, 2021
Oncological outcomes of salvage radical prostatectomy for recurrent prostate cancer in the contemporary era: A multicenter retrospective studyGiancarlo Marra, Robert Jeffrey Karnes, Giorgio Calleris, et al.
Molecular Autism|June 27, 2017
The EU-AIMS Longitudinal European Autism Project (LEAP): design and methodologies to identify and validate stratification biomarkers for autism spectrum disordersEva Loth, Tony Charman, Luke Mason, et al.
Molecular Autism|June 27, 2017
The EU-AIMS Longitudinal European Autism Project (LEAP): clinical characterisationTony Charman, Eva Loth, Julian Tillmann, et al.
American Journal of Human Genetics|December 25, 2019
Complete Sequence of the 22q11.2 Allele in 1,053 Subjects with 22q11.2 Deletion Syndrome Reveals Modifiers of Conotruncal Heart DefectsYingjie Zhao, Alexander Diacou, H Richard Johnston, et al.
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