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common variant
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Common variants in P2RY11 are associated with narcolepsy
2011 |
First Faculty of Medicine
publication
A common variant on chromosome 11q13 is associated with atopic dermatitis
2009 |
Second Faculty of Medicine
publication
A common variant near BDNF is associated with dietary calcium intake in adolescents
2015 |
Faculty of Science, Third Faculty of Medicine
publication
Common Variants Near ZIC1 and ZIC4 in Autopsy-Confirmed Multiple System Atrophy
2022 |
Third Faculty of Medicine
publication
Common variants in Alzheimer's disease and risk stratification by polygenic risk scores
2021 |
Second Faculty of Medicine
publication
Diagnostic method validation: High resolution melting (HRM) of small amplicons genotyping for the most common variants in the MTHFR gene
2009 |
Second Faculty of Medicine
publication
Martin-Gruber anastomosis with anomalous superficial radial innervation to ulnar dorsum of hand: a pitfall when common variants coexist
2010 |
Third Faculty of Medicine
publication
Polygenic burden in focal and generalized epilepsies
2019 |
Second Faculty of Medicine
publication
Variation in a repeat sequence determines whether a common variant of the cystic fibrosis transmembrane conductance regulator gene is pathogenic or benign
2004 |
Second Faculty of Medicine
publication
Common variants associated with breast cancer in genome-wide association studies are modifiers of breast cancer risk in BRCA1 and BRCA2 mutation carriers
2010 |
First Faculty of Medicine
publication
Genotype and haplotype analysis of TP53 gene and the risk of pancreatic cancer: an association study in the Czech Republic
2010 |
Central Library of Charles University, First Faculty of Medicine, Second Faculty of Medicine
publication
Genetics of neurodevelopmental disorders
2021 |
Second Faculty of Medicine
publication
Gene expression variations: potentialities of master regulator polymorphisms in colorectal cancer risk
2012 |
First Faculty of Medicine
publication
A catalog of genetic loci associated with kidney function from analyses of a million individuals
2019 |
First Faculty of Medicine
publication
Variations in mismatch repair genes and colorectal cancer risk and clinical outcome
2014 |
First Faculty of Medicine
publication
Biological insights from 108 schizophrenia-associated genetic loci
2014 |
Second Faculty of Medicine
publication
Schizophrenia risk from complex variation of complement component 4
2016 |
Second Faculty of Medicine
publication
Association of Obesity Susceptibility Gene Variants with Metabolic Syndrome and Related Traits in 1,443 Czech Adolescents
2013 |
Faculty of Science, Third Faculty of Medicine
publication
Discovery of new risk loci for IgA nephropathy implicates genes involved in immunity against intestinal pathogens
2014 |
First Faculty of Medicine
publication
Testicular Cancer in Monozygotic Twin Brothers with Urticaria Pigmentosa
2018 |
Second Faculty of Medicine
publication
Genetic influences on schizophrenia and subcortical brain volumes: large-scale proof of concept
2016 |
Second Faculty of Medicine
publication
Resequencing Study Confirms That Host Defense and Cell Senescence Gene Variants Contribute to the Risk of Idiopathic Pulmonary Fibrosis
2019 |
First Faculty of Medicine
publication
Pityriasis Lichenoides et Varioliformis Acuta With Numerous CD30+ Cells: A Variant Mimicking Lymphomatoid Papulosis and Other Cutaneous Lymphomas. A Clinicopathologic, Immunohistochemical, and Molecular Biological Study of 13 Cases
2012 |
Faculty of Medicine in Pilsen
publication
SLC46A1 haplotype with predicted functional impact has prognostic value in breast carcinoma
2021 |
Faculty of Medicine in Pilsen
publication
Foamy Cell Angiosarcoma is a Diagnostic Pitfall: A Case Report of an Angiosarcoma Mimicking Xanthoma
2014 |
Faculty of Medicine in Pilsen
publication
Probing the Structure and Function of the Cytosolic Domain of the Human Zinc Transporter ZnT8 with Nickel(II) Ions
2021 |
Faculty of Pharmacy in Hradec Králové
publication
International Lung Cancer Consortium: Coordinated association study of 10 potential lung cancer susceptibility variants
2010 |
First Faculty of Medicine
publication
Analysis of shared heritability in common disorders of the brain
2018 |
First Faculty of Medicine
publication
Identification of novel risk loci for restless legs syndrome in genome-wide association studies in individuals of European ancestry: a meta-analysis
2017 |
Faculty of Medicine in Pilsen, First Faculty of Medicine
publication
Replication of restless legs syndrome loci in three European populations
2009 |
Central Library of Charles University, First Faculty of Medicine