L Lello, M Hsu, E Widen, TG Raben - Scientific Reports, 2023 - nature.com
We use UK Biobank and a unique IVF family dataset (including genotyped embryos) to investigate sibling variation in both phenotype and genotype. We compare phenotype …
V Rodriguez, L Alameda, D Quattrone… - Psychological …, 2023 - cambridge.org
Background Schizophrenia (SZ), bipolar disorder (BD) and depression (D) run in families. This susceptibility is partly due to hundreds or thousands of common genetic variants, each …
D Serpico - Studies in History and Philosophy of Science, 2023 - Elsevier
Research in pharmacogenomics and precision medicine has recently introduced the concept of Polygenic Scores (PGSs), namely, indexes that aggregate the effects that many …
Respiratory diseases such as asthma, chronic obstructive pulmonary disease and lung cancer represent a critical area for medical research as millions of people are affected …
Background Substance use, substance use disorders (SUDs), and psychiatric disorders commonly co-occur. Genetic risk common to these complex traits is an important …
Variants of unknown/uncertain significance (VUS) pose a huge dilemma in current genetic variation screening methods and genetic counselling. Driven by methods of next generation …
Previous studies suggest an individual's risk of depression following adversity may be moderated by their genetic liability. No study, however, has examined peer victimisation, an …
L Byrne, AE Toland - Urologic Clinics, 2021 - urologic.theclinics.com
Prostate cancer (PCa) is the most common cancer among men with a lifetime risk of 12% and median age of diagnosis of 66. 1 In 2020, 191,930 new cases are expected to be …
H Lu, T Wang, J Zhang, S Zhang, S Huang, P Zeng - Human Genetics, 2021 - Springer
Genome-wide association studies (GWASs) have successfully identified a large amount of single-nucleotide polymorphisms associated with many complex phenotypes in diverse …