| 36525634 | Solubility and Thermodynamic Investigation of Meta-Autunite Group Uranyl Arsenate Solids with Monovalent Cations Na and K. | | 2023 |
| 37601980 | Kinetics of Na- and K- uranyl arsenate dissolution. | | 2023 |
| 37981952 | Interfacial Interactions of Uranium and Arsenic with Microplastics: From Field Detection to Controlled Laboratory Tests. | | 2023 |
| 37327584 | Accurate tumor purity determination is critical for the analysis of homologous recombination deficiency (HRD). | Transl Oncol | 2023 |
| 36867212 | EGFR and MMP-9 are associated with neointimal hyperplasia in systemic-to-pulmonary shunts in children with complex cyanotic heart disease. | | 2023 |
| 36788297 | Investigation of Shared Genetic Risk Factors Between Parkinson's Disease and Cancers. | Mov Disord | 2023 |
| 34997937 | Dairy Intake and Parkinson's Disease: A Mendelian Randomization Study. | Mov Disord | 2022 |
| 35970579 | Genome-wide Association and Meta-analysis of Age at Onset in Parkinson Disease: Evidence From the COURAGE-PD Consortium. | Neurology | 2022 |
| 35810454 | The Interaction between HLA-DRB1 and Smoking in Parkinson's Disease Revisited. | Mov Disord | 2022 |
| 34633332 | Mendelian Randomisation Study of Smoking, Alcohol, and Coffee Drinking in Relation to Parkinson's Disease. | J Parkinsons Dis | 2022 |
| 35089814 | Human skin-resident host T cells can persist long term after allogeneic stem cell transplantation and maintain recirculation potential. | Science immunology | 2022 |
| 33201861 | Congenital heart disease risk loci identified by genome-wide association study in European patients. | J Clin Invest | 2021 |
| 33998058 | A Recurrent VPS16 p.Arg187* Nonsense Variant in Early-Onset Generalized Dystonia. | Mov Disord | 2021 |
| 33559291 | Investigation of gamma secretase gene complex mutations in German population with Hidradenitis suppurativa designate a complex polygenic heritage. | Journal of the European Academy of Dermatology and Venereology | 2021 |
| 33597771 | Simple and reliable detection of CRISPR-induced on-target effects by qgPCR and SNP genotyping. | Nat Protoc | 2021 |
| 34022586 | The rare and the common: An Austrian DRPLA family harboring the European haplotype. | Parkinsonism and Related Disorders | 2021 |
| 33495596 | Shared genetic pathways contribute to risk of hypertrophic and dilated cardiomyopathies with opposite directions of effect. | Nat Genet | 2021 |
| 33164571 | <i>SCN5A</i> Mutation Type and a Genetic Risk Score Associate Variably With Brugada Syndrome Phenotype in <i>SCN5A</i> Families. | Circ Genom Precis Med | 2020 |
| 32429735 | Transethnic Genome-Wide Association Study Provides Insights in the Genetic Architecture and Heritability of Long QT Syndrome. | Circulation | 2020 |
| 31788832 | Identification of Restless Legs Syndrome Genes by Mutational Load Analysis. | Ann Neurol | 2020 |
| 32176846 | Effect of Bicarbonate, Calcium, and pH on the Reactivity of As(V) and U(VI) Mixtures. | Environmental Science & Technology | 2020 |
| 32004447 | Bi-allelic Variants in RALGAPA1 Cause Profound Neurodevelopmental Disability, Muscular Hypotonia, Infantile Spasms, and Feeding Abnormalities. | Am J Hum Genet | 2020 |
| 32105419 | Biallelic loss-of-function variants in RBL2 in siblings with a neurodevelopmental disorder. | Ann Clin Transl Neurol | 2020 |
| 31820424 | Single Nucleotide Polymorphisms in Thyroid Hormone Transporter Genes MCT8, MCT10 and Deiodinase DIO2 Contribute to Inter-Individual Variance of Executive Functions and Personality Traits. | | 2020 |
| 31978935 | Correction: Single Nucleotide Polymorphisms in Thyroid Hormone Transporter Genes MCT8, MCT10 and Deiodinase DIO2 Contribute to Inter-Individual Variance of Executive Functions and Personality Traits. | Exp Clin Endocrinol Diabetes | 2020 |
| 32675288 | Genetic determinants of the humoral immune response in MS. | Neurol Neuroimmunol Neuroinflamm | 2020 |
| 32619740 | Common and rare susceptibility genetic variants predisposing to Brugada syndrome in Thailand. | Heart Rhythm | 2020 |
| 30485545 | Understanding the role of genetic variability in LRRK2 in Indian population. | Mov Disord | 2019 |
| 29315381 | CHCHD10 mutations p.R15L and p.G66V cause motoneuron disease by haploinsufficiency. | Human Molecular Genetics | 2018 |
| 28754779 | Genome-wide association study identifies inversion in the <i>CTRB1-CTRB2</i> locus to modify risk for alcoholic and non-alcoholic chronic pancreatitis. | Gut | 2018 |
| 29961571 | MPZL2, Encoding the Epithelial Junctional Protein Myelin Protein Zero-like 2, Is Essential for Hearing in Man and Mouse. | Am J Hum Genet | 2018 |
| 29754270 | Heterozygous missense variants of LMX1A lead to nonsyndromic hearing impairment and vestibular dysfunction. | Hum Genet | 2018 |
| 29120944 | Targeted Genotyping Identifies Susceptibility Locus in Brain-derived Neurotrophic Factor Gene for Chronic Postsurgical Pain. | Anesthesiology | 2018 |
| 27814993 | Evaluation of the interaction between LRRK2 and PARK16 loci in determining risk of Parkinson's disease: analysis of a large multicenter study. | Neurobiol Aging | 2017 |
| 28604674 | Genetic diagnosis of Mendelian disorders via RNA sequencing. | Nat Commun | 2017 |
| 29017012 | Reactive Transport of U and V from Abandoned Uranium Mine Wastes. | Environmental Science & Technology | 2017 |
| 28416818 | Large-scale analyses of common and rare variants identify 12 new loci associated with atrial fibrillation. | Nat Genet | 2017 |
| 28747752 | Erratum: Large-scale analyses of common and rare variants identify 12 new loci associated with atrial fibrillation. | Nat Genet | 2017 |
| 28265093 | Common coding variant in <i>SERPINA1</i> increases the risk for large artery stroke. | Proc Natl Acad Sci U S A | 2017 |
| 27876822 | A principal component meta-analysis on multiple anthropometric traits identifies novel loci for body shape. | Nat Commun | 2016 |
| 26935894 | Low-frequency and common genetic variation in ischemic stroke: The METASTROKE collaboration. | Neurology | 2016 |
| 27197191 | Cross-Cancer Genome-Wide Analysis of Lung, Ovary, Breast, Prostate, and Colorectal Cancer Reveals Novel Pleiotropic Associations. | Cancer Res | 2016 |
| 27386562 | Novel multiple sclerosis susceptibility loci implicated in epigenetic regulation. | Sci Adv | 2016 |
| 26800703 | Sudden Cardiac Arrest and Rare Genetic Variants in the Community. | Circulation: Cardiovascular Genetics | 2016 |
| 26833246 | New loci for body fat percentage reveal link between adiposity and cardiometabolic disease risk. | Nat Commun | 2016 |
| 27225129 | Genome-wide association study identifies 74 loci associated with educational attainment. | Nature | 2016 |
| 27257045 | Length Polymorphisms in Heme Oxygenase-1 and AKI after Cardiac Surgery. | J Am Soc Nephrol | 2016 |
| 27455348 | Genome-wide association analyses identify new risk variants and the genetic architecture of amyotrophic lateral sclerosis. | Nat Genet | 2016 |
| 27450276 | Impact of manure-related DOM on sulfonamide transport in arable soils. | Journal of Contaminant Hydrology | 2016 |
| 27531917 | Genetic Modifiers for the Long-QT Syndrome: How Important Is the Role of Variants in the 3' Untranslated Region of KCNQ1? | Circ Cardiovasc Genet | 2016 |