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| 36976765 | Large-scale analysis of structural brain asymmetries in schizophrenia via the ENIGMA consortium. | Proc Natl Acad Sci U S A | 2023 |
| 36315097 | Somatic inactivation of breast cancer predisposition genes in tumors associated with pathogenic germline variants. | Journal of the National Cancer Institute | 2023 |
| 35396271 | Contribution of large genomic rearrangements in to familial breast cancer: implications for genetic testing. | Journal of Medical Genetics | 2023 |
| 35972662 | High polygenic risk score for exceptional longevity is associated with a healthy metabolic profile. | Geroscience | 2023 |
| 37628757 | DNA Methylation Signatures of Multiple Sclerosis Occur Independently of Known Genetic Risk and Are Primarily Attributed to B Cells and Monocytes. | Int J Mol Sci | 2023 |
| 36765422 | Parity is associated with long-term differences in DNA methylation at genes related to neural plasticity in multiple sclerosis. | | 2023 |
| 36494461 | Brain ageing in schizophrenia: evidence from 26 international cohorts via the ENIGMA Schizophrenia consortium. | Mol Psychiatry | 2023 |
| 37325639 | Interferon beta treatment is a potent and targeted epigenetic modifier in multiple sclerosis. | | 2023 |
| 37296477 | Detection of germline variants with pathogenic potential in 48 patients with familial colorectal cancer by using whole exome sequencing. | BMC Med Genomics | 2023 |
| 37170696 | The utilisation of digital droplet PCR to enhance the diagnosis of bladder and pancreaticobiliary tumours in cytology specimens. | | 2023 |
| 37168552 | Multi-trait genome-wide association study identifies a novel endometrial cancer risk locus that associates with testosterone levels. | iScience | 2023 |
| 37541839 | Evaluation of Cell-Specific Epigenetic Age Acceleration in People With Multiple Sclerosis. | | 2023 |
| 37480976 | Alteration of DNA Methylation and Epigenetic Scores Associated With Features of Schizophrenia and Common Variant Genetic Risk. | | 2023 |
| 34697207 | Catastrophic chemotherapy toxicity leading to diagnosis of Fanconi anaemia due to <i>FANCD1/BRCA2</i> during adulthood: description of an emerging phenotype. | J Med Genet | 2022 |
| 35396580 | Mapping genomic loci implicates genes and synaptic biology in schizophrenia. | Nature | 2022 |
| 35974141 | Genome-wide meta-analyses reveal novel loci for verbal short-term memory and learning. | Mol Psychiatry | 2022 |
| 35387118 | Verification and Validation of a Four-Gene Panel as a Prognostic Indicator in Triple Negative Breast Cancer. | Frontiers in Oncology | 2022 |
| 36088367 | Modifier genes and Lynch syndrome: some considerations. | Hereditary Cancer in Clinical Practice | 2022 |
| 35637507 | Correction: When is a mutation not a mutation: the case of the c.594-2A>C splice variant in a woman harbouring another BRCA1 mutation in trans. | Hereditary Cancer in Clinical Practice | 2022 |
| 35489875 | Virtual Ontogeny of Cortical Growth Preceding Mental Illness. | Biol Psychiatry | 2022 |
| 35478773 | Bladder cancer survival in patients with <i>NOD2</i> or <i>CDKN2A</i> variants. | Oncotarget | 2022 |
| 36585691 | Whole-blood methylation signatures are associated with and accurately classify multiple sclerosis disease severity. | | 2022 |
| 35039523 | Integration of tumour sequencing and case-control data to assess pathogenicity of RAD51C missense variants in familial breast cancer. | npj Breast Cancer | 2022 |
| 35052430 | Capturing SNP Association across the NK Receptor and HLA Gene Regions in Multiple Sclerosis by Targeted Penalised Regression Models. | Genes | 2021 |
| 32359158 | Combined Associations of a Polygenic Risk Score and Classical Risk Factors With Breast Cancer Risk. | J Natl Cancer Inst | 2021 |
| 34117267 | Investigation of monogenic causes of familial breast cancer: data from the BEACCON case-control study. | npj Breast Cancer | 2021 |
| 34059744 | A genetic variant in telomerase reverse transcriptase (TERT) modifies cancer risk in Lynch syndrome patients harbouring pathogenic MSH2 variants. | Sci Rep | 2021 |
| 34225099 | Copy number variation in triple negative breast cancer samples associated with lymph node metastasis. | Neoplasia | 2021 |
| 34224176 | Time-resolved proteomic profiling of cigarette smoke-induced experimental chronic obstructive pulmonary disease. | Respirology | 2021 |
| 34002096 | Genome-wide association study of more than 40,000 bipolar disorder cases provides new insights into the underlying biology. | Nat Genet | 2021 |
| 34259353 | Exome sequencing of familial adenomatous polyposis-like individuals identifies both known and novel causative genes. | Clinical Genetics | 2021 |
| 34200699 | Survival of Laryngeal Cancer Patients Depending on Zinc Serum Level and Oxidative Stress Genotypes. | Biomolecules | 2021 |
| 33721710 | The MinION as a cost-effective technology for diagnostic screening of the SCN1A gene in epilepsy patients. | Epilepsy Research | 2021 |
| 33720009 | Genetic association and causal inference converge on hyperglycaemia as a modifiable factor to improve lung function. | eLife | 2021 |
| 33980861 | Evaluation of the association of heterozygous germline variants in NTHL1 with breast cancer predisposition: an international multi-center study of 47,180 subjects. | NPJ Breast Cancer | 2021 |
| 33926505 | CD36 polymorphisms and the age of disease onset in patients with pathogenic variants within the mutation cluster region of APC. | Hereditary Cancer in Clinical Practice | 2021 |
| 32648197 | Lung Cancer Occurrence-Correlation with Serum Chromium Levels and Genotypes. | Biol Trace Elem Res | 2021 |
| 33249371 | Blood cadmium levels as a marker for early lung cancer detection. | J Trace Elem Med Biol | 2021 |
| 32683684 | The "unnatural" history of colorectal cancer in Lynch syndrome: Lessons from colonoscopy surveillance. | Int J Cancer | 2021 |
| 32851660 | Mendelian randomization analyses suggest a role for cholesterol in the development of endometrial cancer. | Int J Cancer | 2021 |
| 32888145 | Prevalence of germline TP53 variants among early-onset breast cancer patients from Polish population. | Breast Cancer | 2021 |
| 34863305 | Epigenome-wide association studies: current knowledge, strategies and recommendations. | Clinical Epigenetics | 2021 |
| 34572288 | Low Blood-As Levels and Selected Genotypes Appears to Be Promising Biomarkers for Occurrence of Colorectal Cancer in Women. | Biomedicines | 2021 |
| 34675350 | Multi-tissue transcriptome-wide association study identifies eight candidate genes and tissue-specific gene expression underlying endometrial cancer susceptibility. | Commun Biol | 2021 |
| 34499690 | Survival of bladder or renal cancer in patients with CHEK2 mutations. | PLoS One | 2021 |
| 34439826 | Influence of the Levels of Arsenic, Cadmium, Mercury and Lead on Overall Survival in Lung Cancer. | Biomolecules | 2021 |
| 34381565 | Genetic testing for homologous recombination repair (HRR) in metastatic castration-resistant prostate cancer (mCRPC): challenges and solutions. | Oncotarget | 2021 |
| 35003109 | Endocannabinoid System as a Promising Therapeutic Target in Inflammatory Bowel Disease - A Systematic Review. | Frontiers in Immunology | 2021 |
| 34475139 | Sertraline hydrochloride for reducing impulsive behaviour in male, repeat-violent offenders (ReINVEST): protocol for a phase IV, double-blind, placebo-controlled, randomised clinical trial. | BMJ Open | 2021 |
| 31391148 | Transcriptomic abnormalities in peripheral blood in bipolar disorder, and discrimination of the major psychoses. | Schizophr Res | 2020 |