- Contrasting genetic architectures of schizophrenia and other complex diseases using fast variance-components analysis2015 | 2. lékařská fakulta
- Age at first birth in women is genetically associated with increased risk of schizophrenia2018 | 2. lékařská fakulta
- A common haplotype of protamine 1 and 2 genes is associated with higher sperm counts2010 | 2. lékařská fakulta
- Genetic variation in FOXP2 alters grey matter concentrations in schizophrenia patients2011 | Publikace bez příslušnosti k fakultě
- The chromosome 2p21 region harbors a complex genetic architecture for association with risk for renal cell carcinoma2012 | 2. lékařská fakulta
- BCL11A deletions result in fetal hemoglobin persistence and neurodevelopmental alterations2015 | 2. lékařská fakulta
- Do pancreatic cancer and chronic pancreatitis share the same genetic risk factors? A PANcreatic Disease ReseArch (PANDoRA) consortium investigation2018 | Lékařská fakulta v Plzni, Ústřední knihovna
- A Genetic Locus within the FMN1/GREM1 Gene Region Interacts with Body Mass Index in Colorectal Cancer Risk2023 | 1. lékařská fakulta, Lékařská fakulta v Plzni
- MARVELD2 (DFNB49) Mutations in the Hearing Impaired Central European Roma Population - Prevalence, Clinical Impact and the Common Origin2015 | 2. lékařská fakulta
- CDH13 promoter SNPs with pleiotropic effect on cardiometabolic parameters represent methylation QTLs2015 | 1. lékařská fakulta