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Science Advances|March 12, 2025
Synaptic-dependent developmental dysconnectivity in 22q11.2 deletion syndromeFilomena Grazia Alvino, Silvia Gini, Antea Minetti, et al.
Annals of Oncology : Official Journal of the European Society for Medical Oncology|April 16, 2023
Nab-paclitaxel weekly versus dose-dense solvent-based paclitaxel followed by dose-dense epirubicin plus cyclophosphamide in high-risk HR+/HER2- early breast cancer: results from the neoadjuvant part of the WSG-ADAPT-HR+/HER2- trialO Gluz, S Kuemmel, U Nitz, et al.
European Urology|August 21, 2020
Clinical Restaging and Tumor Sequencing are Inaccurate Indicators of Response to Neoadjuvant Chemotherapy for Muscle-invasive Bladder CancerRussell E N Becker, Alexa R Meyer, Aaron Brant, et al.
Annals of Oncology : Official Journal of the European Society for Medical Oncology|April 18, 2026
Clinical and molecular biomarkers for prediction of endocrine response after short preoperative endocrine therapy in the WSG ADAPT-HR+/HER2- and ADAPTcycle trials (N=7914)O Gluz, U Nitz, M Christgen, et al.
Human Molecular Genetics|January 24, 2018
Deletion size analysis of 1680 22q11.2DS subjects identifies a new recombination hotspot on chromosome 22q11.2Tingwei Guo, Alexander Diacou, Hiroko Nomaru, 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.
Human Genetics|January 9, 2016
Rare copy number variants and congenital heart defects in the 22q11.2 deletion syndromeElisabeth E Mlynarski, Michael Xie, Deanne Taylor, et al.
Schizophrenia Bulletin|February 17, 2017
Subthreshold Psychosis in 22q11.2 Deletion Syndrome: Multisite Naturalistic StudyOmri Weisman, Yael Guri, Raquel E Gur, et al.
Nature Reviews. Urology|August 5, 2026
Integrating clinically actionable biomarkers into bladder cancer care - recommendations from the International Bladder Cancer GroupPatrick J Hensley, Jeremy Y C Teoh, Roger Li, et al.
American Journal of Human Genetics|April 21, 2015
Copy-Number Variation of the Glucose Transporter Gene SLC2A3 and Congenital Heart Defects in the 22q11.2 Deletion SyndromeElisabeth E Mlynarski, Molly B Sheridan, Michael Xie, et al.
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