
Konstantin Senkevich
@senkkon1
MD, PhD. @cusm_muhc @TheNeuro_MNI @McGillu @NAP_med
Genetics of movement disorders.
ID: 1186476320018092032
22-10-2019 02:56:28
169 Tweet
297 Followers
450 Following


From UCL Brain Sciences, with the support of a global team, I am thrilled to share our new disease-gene linked to Primary Familial Brain Calcification in Nature Communications. Read here how #NAA60 variants make the brain turn into calcified lumps disq.us/t/4nd64gp UCL The Neurogenetics Lab ION



I was fortunate to serve as a faculty for the Kyrgyzstan GP2 local training alongside incredible colleagues Alastair Noyce, Ed Jabbari, Cholpon Shambetova, and more who are not on Twitter. The course was a great success with the full engagement of our trainees!




In this case report, we identified the SNCA p.E46K mutation in a family with Russian ancestry. This is the third family in the world known to carry this variant. This further emphasizes the importance of genetic screening across diverse populations! …mentdisorders.onlinelibrary.wiley.com/doi/10.1002/md…



Our new paper, published today, shows lack of human genetic evidence of a role for NLRP3 inflammasome in Parkinson's disease. Why is this important? See below. Study led by Konstantin Senkevich in collaboration with Mike A. Nalls, @HamptonLLeonard and others. nature.com/articles/s4153…

New initiative by MDS Young Members Group Steering Committee to highlight the research performed by young members ece bayram Yasser Mecheri MARY WETANI AGORIWO Mehri Cholpon Shambetova Delaram @wntbrains4bkfst Konstantin Senkevich Michele Matarazzo @DeTijssen Michael Okun Bas Bloem






New research from Konstantin Senkevich Ziv Gan-Or & colleagues finds that rare heterozygous SYNJ1 variants were potentially associated with early onset #Parkinsons & variants in the Sac1 domain are associated with sporadic PD; Further study in large cohorts required nature.com/articles/s4153…

