ℹ️
🇬🇧
Search
Search for publications relevant for "genetics association studies"
genetics association studies
Publication
Class
Person
Publication
Programmes
publication
Lack of association between the Val158Met catechol-O-methyltransferase gene polymorphism and methamphetamine dependence
2011 |
Central Library of Charles University, Faculty of Medicine in Hradec Králové
publication
Genetics of schizophrenia
2006 |
Publication without faculty affiliation
publication
Genetics of schizophrenia
+1
2006 |
Faculty of Medicine in Hradec Králové
publication
Genetics of schizophrenia
2006 |
First Faculty of Medicine
publication
Genomewide association study using a high-density single nucleotide polymorphism array and case-control design identifies a novel essential hypertension susceptibility locus in the promoter region of endothelial NO synthase
2012 |
Faculty of Medicine in Pilsen
publication
Restless legs syndrome in Czech patients with multiple sclerosis: an epidemiological and genetic study
2010 |
First Faculty of Medicine
publication
Ornithine decarboxylase G316A genotype and colorectal cancer risk
2011 |
First Faculty of Medicine
publication
Association between polymorphisms of TAS2R16 and susceptibility to colorectal cancer
2017 |
Faculty of Medicine in Pilsen, First Faculty of Medicine
publication
Restless legs syndrome in Czech patients with multiple sclerosis: An epidemiological and genetic study
2012 |
First Faculty of Medicine
publication
Molecular epidemiology of Type 1 diabetes mellitus
Publication without faculty affiliation
publication
Genetics of anxiety disorders
2013 |
Faculty of Medicine in Hradec Králové
publication
Volunteer's Willingness to Genetic Testing - Lack of the Understanding of the Matter
2009 |
Central Library of Charles University
publication
Multi-ancestry genome-wide association study of 21,000 cases and 95,000 controls identifies new risk loci for atopic dermatitis
2015 |
Second Faculty of Medicine
publication
Are genes encoding proteoglycans really associated with the risk of anterior cruciate ligament rupture?
2017 |
Faculty of Physical Education and Sport
publication
Common variants in Alzheimer's disease and risk stratification by polygenic risk scores
2021 |
Second Faculty of Medicine
publication
Genetic variation of cisplatin-induced ototoxicity in non-cranial-irradiated pediatric patients using a candidate gene approach: The International PanCareLIFE Study
2020 |
Second Faculty of Medicine
publication
Genetic Associations Between Modifiable Risk Factors and Alzheimer Disease
2023 |
Second Faculty of Medicine
publication
Association of candidate pharmacogenetic markers with platinum-induced ototoxicity: PanCareLIFE dataset
2020 |
Second Faculty of Medicine
publication
Association of Single Nucleotide Polymorphisms from Angiogenesis-Related Genes, ANGPT2, TLR2 and TLR9, with Spontaneous Preterm Labor
2022 |
Faculty of Medicine in Hradec Králové
publication
Vitamin D receptor (VDR) gene polymorphisms and expression profile influence upon the immunological imbalance in Turner syndrome
2020 |
Faculty of Science
publication
Usefulness of current candidate genetic markers to identify childhood cancer patients at risk for platinum-induced ototoxicity: Results of the European PanCareLIFE cohort study
2020 |
Second Faculty of Medicine
publication
Association of Rare APOE Missense Variants V236E and R251G With Risk of Alzheimer Disease
2022 |
Second Faculty of Medicine