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European Journal of Human Genetics : EJHG|October 28, 2021
Meiotic genes in premature ovarian insufficiency: variants in HROB and REC8 as likely genetic causesElena J Tucker, Katrina M Bell, Gorjana Robevska, et al.
Human Mutation|October 14, 2017
Functional characterization of novel NR5A1 variants reveals multiple complex roles in disorders of sex developmentGorjana Robevska, Jocelyn A van den Bergen, Thomas Ohnesorg, et al.
An International Journal on Information Fusion|April 15, 2020
Autosomal Dominantly Inherited Alzheimer Disease: Analysis of genetic subgroups by Machine LearningDiego Castillo-Barnes, Li Su, Javier Ramírez, et al.
Acta Neuropathologica Communications|March 5, 2022
Circular RNA detection identifies circPSEN1 alterations in brain specific to autosomal dominant Alzheimer's diseaseHsiang-Han Chen, Abdallah Eteleeb, Ciyang Wang, et al.
Brain : a Journal of Neurology|February 18, 2015
Early behavioural changes in familial Alzheimer's disease in the Dominantly Inherited Alzheimer NetworkJohn M Ringman, Li-Jung Liang, Yan Zhou, et al.
Age (Dordrecht, Netherlands)|February 1, 2015
Genetics of hand grip strength in mid to late lifeJessica P L Chan, Anbupalam Thalamuthu, Christopher Oldmeadow, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association|April 10, 2025
Early increase of the synaptic blood marker β-synuclein in asymptomatic autosomal dominant Alzheimer's diseasePatrick Oeckl, Benjamin Mayer, Randall J Bateman, et al.
Schizophrenia Research|October 30, 2012
Meta-analysis and brain imaging data support the involvement of VRK2 (rs2312147) in schizophrenia susceptibilityMing Li, Yi Wang, Xue-bin Zheng, et al.
Annals of Neurology|October 30, 2010
Sigma nonopioid intracellular receptor 1 mutations cause frontotemporal lobar degeneration-motor neuron diseaseAgnes A Luty, John B J Kwok, Carol Dobson-Stone, et al.
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