Skip directly to search Skip directly to A to Z list Skip directly to navigation Skip directly to page options Skip directly to site content

Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Jan 25, 2025. (Total: 235671Documents)
   dataset        GWAS Only
Filtered By:

Previous    

Records 1 - 4 (of 4 Records)

Query Trace: Disease and CLSTN2[original query]
Whole-genome sequencing reveals new Alzheimer's disease-associated rare variants in loci related to synaptic function and neuronal development.
medRxiv : the preprint server for health sciences 2020 Nov .
Prokopenko Dmitry, Morgan Sarah L, Mullin Kristina, Hofmann Oliver, Chapman Brad, Kirchner Rory, Amberkar Sandeep, Wohlers Inken, Lange Christoph, Hide Winston, Bertram Lars, Tanzi Rudolph
Whole-genome sequencing reveals new Alzheimer's disease-associated rare variants in loci related to synaptic function and neuronal development.
Alzheimer's & dementia : the journal of the Alzheimer's Association 2021 Apr .
Prokopenko Dmitry, Morgan Sarah L, Mullin Kristina, Hofmann Oliver, Chapman Brad, Kirchner Rory, , Amberkar Sandeep, Wohlers Inken, Lange Christoph, Hide Winston, Bertram Lars, Tanzi Rudolph
APOL1 Kidney Risk Variants and Proteomics.
Clinical journal of the American Society of Nephrology : CJASN 2022 4 17 (5): 684-692.
Chen Teresa K, Surapaneni Aditya L, Arking Dan E, Ballantyne Christie M, Boerwinkle Eric, Chen Jingsha, Coresh Josef, Köttgen Anna, Susztak Katalin, Tin Adrienne, Yu Bing, Grams Morgan
KLKB1 and CLSTN2 are associated with HDL-mediated cholesterol efflux capacity in a genome-wide association study.
Atherosclerosis 2023 2 368 1-11.
Schachtl-Riess Johanna F, Schönherr Sebastian, Lamina Claudia, Forer Lukas, Coassin Stefan, Streiter Gertraud, Kheirkhah Azin, Li Yong, Meiselbach Heike, Di Maio Silvia, Eckardt Kai-Uwe, Köttgen Anna, Kronenberg Florian,
TOP