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Journal of Alzheimer'S Disease : JAD|October 10, 2022
Cancer and Vascular Comorbidity Effects on Dementia Risk and Neuropathology in the Oldest-OldChristian Lachner, Gregory S Day, Gamze Balci Camsari, et al.
The Journal of Clinical Endocrinology and Metabolism|July 13, 2016
The Long-Term Outcome of Boys With Partial Androgen Insensitivity Syndrome and a Mutation in the Androgen Receptor GeneA Lucas-Herald, S Bertelloni, A Juul, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association|December 25, 2025
BiomarkersLindsey A Kuchenbecker, Kevin J Thompson, Cheyenne D Hurst, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association|July 28, 2025
Novel set of plasma proteins classifies Alzheimer's dementia in African American individuals with high accuracyLindsey A Kuchenbecker, Kevin J Thompson, Cheyenne D Hurst, et al.
Science Advances|February 1, 2021
Induction of muscle-regenerative multipotent stem cells from human adipocytes by PDGF-AB and 5-azacytidineAvani Yeola, Shruthi Subramanian, Rema A Oliver, et al.
ERJ Open Research|January 10, 2024
A BEAT-PCD consensus statement: a core outcome set for pulmonary disease interventions in primary ciliary dyskinesiaRenate Kos, Myrofora Goutaki, Helene E Kobbernagel, et al.
Acta Neuropathologica Communications|October 23, 2020
Association of ABI3 and PLCG2 missense variants with disease risk and neuropathology in Lewy body disease and progressive supranuclear palsySamantha L Strickland, Hélène Morel, Christian Prusinski, et al.
Molecular Neurodegeneration|October 18, 2018
ABI3 and PLCG2 missense variants as risk factors for neurodegenerative diseases in Caucasians and African AmericansOlivia J Conway, Minerva M Carrasquillo, Xue Wang, et al.
Acta Neuropathologica|September 10, 2015
Cerebellar c9RAN proteins associate with clinical and neuropathological characteristics of C9ORF72 repeat expansion carriersTania F Gendron, Marka van Blitterswijk, Kevin F Bieniek, et al.
The Journal of Clinical Investigation|January 31, 2017
Mutations in tropomyosin 4 underlie a rare form of human macrothrombocytopeniaIrina Pleines, Joanne Woods, Stephane Chappaz, et al.
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