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Author Details

Andrew A Hicks
Institute for Biomedicine, Affiliated institute of the University of Lubeck
1990
182
66
PMIDPaper TitleJournal TitlePublished Year
36599941Participant perspective on the recall-by-genotype research approach: a mixed-method embedded study with participants of the CHRIS study.Eur J Hum Genet2023
37811477Fluorescent reporter of  <i>Caenorhabditis elegans</i> Parkin: Regulators of its abundance and role in autophagy-lysosomal dynamics.Open Res Eur2023
36973269The small GTPase Rit2 modulates LRRK2 kinase activity, is required for lysosomal function and protects against alpha-synuclein neuropathology.NPJ Parkinsons Dis2023
36768321Increased Levels of the Parkinson's Disease-Associated Gene ITPKB Correlate with Higher Expression Levels of α-Synuclein, Independent of Mutation Status.Int J Mol Sci2023
36764358Role of Ceramides and Sphingolipids in Parkinson's Disease.J Mol Biol2023
37072441Molecular phenotypes of mitochondrial dysfunction in clinically non-manifesting heterozygous PRKN variant carriers.NPJ Parkinsons Dis2023
36478228Mitochondrial DNA heteroplasmy distinguishes disease manifestation in PINK1/PRKN-linked Parkinson's disease.Brain2023
36599941Participant perspective on the recall-by-genotype research approach: a mixed-method embedded study with participants of the CHRIS study.Eur J Hum Genet2023
37811477Fluorescent reporter of  <i>Caenorhabditis elegans</i> Parkin: Regulators of its abundance and role in autophagy-lysosomal dynamics.Open Res Eur2023
36973269The small GTPase Rit2 modulates LRRK2 kinase activity, is required for lysosomal function and protects against alpha-synuclein neuropathology.NPJ Parkinsons Dis2023
37072441Molecular phenotypes of mitochondrial dysfunction in clinically non-manifesting heterozygous PRKN variant carriers.NPJ Parkinsons Dis2023
36478228Mitochondrial DNA heteroplasmy distinguishes disease manifestation in PINK1/PRKN-linked Parkinson's disease.Brain2023
36768321Increased Levels of the Parkinson's Disease-Associated Gene ITPKB Correlate with Higher Expression Levels of α-Synuclein, Independent of Mutation Status.Int J Mol Sci2023
36764358Role of Ceramides and Sphingolipids in Parkinson's Disease.J Mol Biol2023
34637685Prospective epidemiological, molecular, and genetic characterization of a novel coronavirus disease in the Val Venosta/Vinschgau: the CHRIS COVID-19 study protocol.Pathog Glob Health2022
35513611A genome on shaky ground: exploring the impact of mitochondrial DNA integrity on Parkinson's disease by highlighting the use of cybrid models.Cell Mol Life Sci2022
36361881Induced Pluripotent Stem Cell (iPSC) Lines from a Family with Resistant Epileptic Encephalopathy Caused by Compound Heterozygous Mutations in <i>SZT2</i> Gene.Int J Mol Sci2022
35952933Pain sensitivity is modulated by affective temperament: Results from the population-based CHRIS Affective Disorder (CHRIS-AD) study.J Affect Disord2022
35697829Differential and shared genetic effects on kidney function between diabetic and non-diabetic individuals.Commun Biol2022
35572147Functional Screening of Parkinson's Disease Susceptibility Genes to Identify Novel Modulators of α-Synuclein Neurotoxicity in <i>Caenorhabditis elegans</i>.Front Aging Neurosci2022
35189566Generation of an induced pluripotent stem cell line (EURACi014-A) from a Parkinson's disease patient with an A53T mutation in the SNCA gene by an integration-free reprogramming method.Stem Cell Res2022
35022422A multi-omics study of circulating phospholipid markers of blood pressure.Sci Rep2022
35177612Dihydroceramide- and ceramide-profiling provides insights into human cardiometabolic disease etiology.Nat Commun2022
35121197Generation and characterization of induced pluripotent stem cell (iPSC) lines of two asymptomatic individuals carrying a heterozygous exon 7 deletion in Parkin (PRKN) and two non-carriers from the same family.Stem Cell Res2022
34637685Prospective epidemiological, molecular, and genetic characterization of a novel coronavirus disease in the Val Venosta/Vinschgau: the CHRIS COVID-19 study protocol.Pathog Glob Health2022
35697829Differential and shared genetic effects on kidney function between diabetic and non-diabetic individuals.Commun Biol2022
35572147Functional Screening of Parkinson's Disease Susceptibility Genes to Identify Novel Modulators of α-Synuclein Neurotoxicity in <i>Caenorhabditis elegans</i>.Front Aging Neurosci2022
35513611A genome on shaky ground: exploring the impact of mitochondrial DNA integrity on Parkinson's disease by highlighting the use of cybrid models.Cell Mol Life Sci2022
36361881Induced Pluripotent Stem Cell (iPSC) Lines from a Family with Resistant Epileptic Encephalopathy Caused by Compound Heterozygous Mutations in <i>SZT2</i> Gene.Int J Mol Sci2022
35952933Pain sensitivity is modulated by affective temperament: Results from the population-based CHRIS Affective Disorder (CHRIS-AD) study.J Affect Disord2022
35189566Generation of an induced pluripotent stem cell line (EURACi014-A) from a Parkinson's disease patient with an A53T mutation in the SNCA gene by an integration-free reprogramming method.Stem Cell Res2022
35121197Generation and characterization of induced pluripotent stem cell (iPSC) lines of two asymptomatic individuals carrying a heterozygous exon 7 deletion in Parkin (PRKN) and two non-carriers from the same family.Stem Cell Res2022
35177612Dihydroceramide- and ceramide-profiling provides insights into human cardiometabolic disease etiology.Nat Commun2022
35022422A multi-omics study of circulating phospholipid markers of blood pressure.Sci Rep2022
32989287Genome-wide association study identifies 48 common genetic variants associated with handedness.Nat Hum Behav2021
33895538Task matters - challenging the motor system allows distinguishing unaffected Parkin mutation carriers from mutation-free controls.Parkinsonism Relat Disord2021
33453124Association of mitochondrial DNA copy number with metabolic syndrome and type 2 diabetes in 14 176 individuals.J Intern Med2021
33561612Genetic variants in levodopa-induced dyskinesia (LID): A systematic review and meta-analysis.Parkinsonism Relat Disord2021
33558525Publisher Correction: Sex-dimorphic genetic effects and novel loci for fasting glucose and insulin variability.Nat Commun2021
33981014Balancing scientific interests and the rights of participants in designing a recall by genotype study.Eur J Hum Genet2021
32989287Genome-wide association study identifies 48 common genetic variants associated with handedness.Nat Hum Behav2021
33402679Sex-dimorphic genetic effects and novel loci for fasting glucose and insulin variability.Nat Commun2021
34409038Generation of hiPSC-Derived Functional Dopaminergic Neurons in Alginate-Based 3D Culture.Front Cell Dev Biol2021
34685691The SZT2 Interactome Unravels New Functions of the KICSTOR Complex.Cells2021
34434164Frequency of Heterozygous Parkin (<i>PRKN</i>) Variants and Penetrance of Parkinson's Disease Risk Markers in the Population-Based CHRIS Cohort.Front Neurol2021
34599261Exome-wide association study of levodopa-induced dyskinesia in Parkinson's disease.Sci Rep2021
33895538Task matters - challenging the motor system allows distinguishing unaffected Parkin mutation carriers from mutation-free controls.Parkinsonism Relat Disord2021
33561612Genetic variants in levodopa-induced dyskinesia (LID): A systematic review and meta-analysis.Parkinsonism Relat Disord2021
33558525Publisher Correction: Sex-dimorphic genetic effects and novel loci for fasting glucose and insulin variability.Nat Commun2021
34434164Frequency of Heterozygous Parkin (<i>PRKN</i>) Variants and Penetrance of Parkinson's Disease Risk Markers in the Population-Based CHRIS Cohort.Front Neurol2021
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Collaborators

Peter P Pramstaller
Co-authored papers 142
Harry Campbell
Co-authored papers 66
Caroline Hayward
Co-authored papers 65
Igor Rudan
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Cornelia M van Duijn
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Co-authored papers 62
James F Wilson
Co-authored papers 62
Alan F Wright
Co-authored papers 52
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Erasmus University Medical Center
Co-authored papers 52
Irene Pichler
Co-authored papers 50
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Co-authored papers 48
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King's College London
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Ozren Polasek
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Sarah H Wild
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Bruce M Psaty
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Eric Boerwinkle
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Markus Perola
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Nicholas J Wareham
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Kari Stefansson
University of Iceland
Co-authored papers 37
Luigi Ferrucci
National Institute on Aging, National Institutes of Health
Co-authored papers 36
Andres Metspalu
Co-authored papers 36
Peter Vollenweider
Lausanne University Hospital and University of Lausanne
Co-authored papers 36
Fernando Rivadeneira
University Medical Center Rotterdam
Co-authored papers 36
Release 1.2