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Author Details

Peter Lichtner
1996
202
67
PMIDPaper TitleJournal TitlePublished Year
36525634Solubility and Thermodynamic Investigation of Meta-Autunite Group Uranyl Arsenate Solids with Monovalent Cations Na and K.2023
37601980Kinetics of Na- and K- uranyl arsenate dissolution.2023
37981952Interfacial Interactions of Uranium and Arsenic with Microplastics: From Field Detection to Controlled Laboratory Tests.2023
37327584Accurate tumor purity determination is critical for the analysis of homologous recombination deficiency (HRD).Transl Oncol2023
36867212EGFR and MMP-9 are associated with neointimal hyperplasia in systemic-to-pulmonary shunts in children with complex cyanotic heart disease.2023
36788297Investigation of Shared Genetic Risk Factors Between Parkinson's Disease and Cancers.Mov Disord2023
34997937Dairy Intake and Parkinson's Disease: A Mendelian Randomization Study.Mov Disord2022
35970579Genome-wide Association and Meta-analysis of Age at Onset in Parkinson Disease: Evidence From the COURAGE-PD Consortium.Neurology2022
35810454The Interaction between HLA-DRB1 and Smoking in Parkinson's Disease Revisited.Mov Disord2022
34633332Mendelian Randomisation Study of Smoking, Alcohol, and Coffee Drinking in Relation to Parkinson's Disease.J Parkinsons Dis2022
35089814Human skin-resident host T cells can persist long term after allogeneic stem cell transplantation and maintain recirculation potential.Science immunology2022
33201861Congenital heart disease risk loci identified by genome-wide association study in European patients.J Clin Invest2021
33998058A Recurrent VPS16 p.Arg187* Nonsense Variant in Early-Onset Generalized Dystonia.Mov Disord2021
33559291Investigation 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 Venereology2021
33597771Simple and reliable detection of CRISPR-induced on-target effects by qgPCR and SNP genotyping.Nat Protoc2021
34022586The rare and the common: An Austrian DRPLA family harboring the European haplotype.Parkinsonism and Related Disorders2021
33495596Shared genetic pathways contribute to risk of hypertrophic and dilated cardiomyopathies with opposite directions of effect.Nat Genet2021
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 Med2020
32429735Transethnic Genome-Wide Association Study Provides Insights in the Genetic Architecture and Heritability of Long QT Syndrome.Circulation2020
31788832Identification of Restless Legs Syndrome Genes by Mutational Load Analysis.Ann Neurol2020
32176846Effect of Bicarbonate, Calcium, and pH on the Reactivity of As(V) and U(VI) Mixtures.Environmental Science &amp; Technology2020
32004447Bi-allelic Variants in RALGAPA1 Cause Profound Neurodevelopmental Disability, Muscular Hypotonia, Infantile Spasms, and Feeding Abnormalities.Am J Hum Genet2020
32105419Biallelic loss-of-function variants in RBL2 in siblings with a neurodevelopmental disorder.Ann Clin Transl Neurol2020
31820424Single Nucleotide Polymorphisms in Thyroid Hormone Transporter Genes MCT8, MCT10 and Deiodinase DIO2 Contribute to Inter-Individual Variance of Executive Functions and Personality Traits.2020
31978935Correction: 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 Diabetes2020
32675288Genetic determinants of the humoral immune response in MS.Neurol Neuroimmunol Neuroinflamm2020
32619740Common and rare susceptibility genetic variants predisposing to Brugada syndrome in Thailand.Heart Rhythm2020
30485545Understanding the role of genetic variability in LRRK2 in Indian population.Mov Disord2019
29315381CHCHD10 mutations p.R15L and p.G66V cause motoneuron disease by haploinsufficiency.Human Molecular Genetics2018
28754779Genome-wide association study identifies inversion in the <i>CTRB1-CTRB2</i> locus to modify risk for alcoholic and non-alcoholic chronic pancreatitis.Gut2018
29961571MPZL2, Encoding the Epithelial Junctional Protein Myelin Protein Zero-like 2, Is Essential for Hearing in Man and Mouse.Am J Hum Genet2018
29754270Heterozygous missense variants of LMX1A lead to nonsyndromic hearing impairment and vestibular dysfunction.Hum Genet2018
29120944Targeted Genotyping Identifies Susceptibility Locus in Brain-derived Neurotrophic Factor Gene for Chronic Postsurgical Pain.Anesthesiology2018
27814993Evaluation of the interaction between LRRK2 and PARK16 loci in determining risk of Parkinson's disease: analysis of a large multicenter study.Neurobiol Aging2017
28604674Genetic diagnosis of Mendelian disorders via RNA sequencing.Nat Commun2017
29017012Reactive Transport of U and V from Abandoned Uranium Mine Wastes.Environmental Science &amp; Technology2017
28416818Large-scale analyses of common and rare variants identify 12 new loci associated with atrial fibrillation.Nat Genet2017
28747752Erratum: Large-scale analyses of common and rare variants identify 12 new loci associated with atrial fibrillation.Nat Genet2017
28265093Common coding variant in <i>SERPINA1</i> increases the risk for large artery stroke.Proc Natl Acad Sci U S A2017
27876822A principal component meta-analysis on multiple anthropometric traits identifies novel loci for body shape.Nat Commun2016
26935894Low-frequency and common genetic variation in ischemic stroke: The METASTROKE collaboration.Neurology2016
27197191Cross-Cancer Genome-Wide Analysis of Lung, Ovary, Breast, Prostate, and Colorectal Cancer Reveals Novel Pleiotropic Associations.Cancer Res2016
27386562Novel multiple sclerosis susceptibility loci implicated in epigenetic regulation.Sci Adv2016
26800703Sudden Cardiac Arrest and Rare Genetic Variants in the Community.Circulation: Cardiovascular Genetics2016
26833246New loci for body fat percentage reveal link between adiposity and cardiometabolic disease risk.Nat Commun2016
27225129Genome-wide association study identifies 74 loci associated with educational attainment.Nature2016
27257045Length Polymorphisms in Heme Oxygenase-1 and AKI after Cardiac Surgery.J Am Soc Nephrol2016
27455348Genome-wide association analyses identify new risk variants and the genetic architecture of amyotrophic lateral sclerosis.Nat Genet2016
27450276Impact of manure-related DOM on sulfonamide transport in arable soils.Journal of Contaminant Hydrology2016
27531917Genetic Modifiers for the Long-QT Syndrome: How Important Is the Role of Variants in the 3' Untranslated Region of KCNQ1?Circ Cardiovasc Genet2016
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Technical University of Munich, Institute of Human Genetics
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German Research Center for Cardiovascular Disease (DZHK)
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Max Planck Institute of Psychiatry
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Ludwig-Maximilians-Universitat Munchen
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Erasmus University Medical Center
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Harvard T.H. Chan School of Public Health
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The Kolling Institute, University of Sydney, and Royal North Shore Hospital
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Sorbonne University, Paris Brain Institute - ICM, Inserm, CNRS
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Institute for Medical Information Processing
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National Cancer Institute, National Institutes of Health
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University of Southern California
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German Research Center for Environmental Health, Institute of Genetic Epidemiology
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Institute of Psychiatric Phenomics and Genomics (IPPG), LMU University Hospital
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University of Oxford
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William Harvey Research Institute, Queen Mary University of London
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Finnish Cardiovascular Research Center-Tampere - FCRCT, Tampere University
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University Medical Center Rotterdam
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