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Author Details

Yun Freudenberg-Hua
Feinstein Institutes for Medical Research
2003
22
11
PMIDPaper TitleJournal TitlePublished Year
37953324The Human Phenotype Ontology in 2024: phenotypes around the world.Nucleic Acids Res2024
35372430Psychotropic Medication Use Is Associated With Greater 1-Year Incidence of Dementia After COVID-19 Hospitalization.Front Med (Lausanne)2022
33164815Greater effect of polygenic risk score for Alzheimer's disease among younger cases who are apolipoprotein E-ε4 carriers.Neurobiol Aging2021
33774420Beyond standard pipeline and p⿯<⿯0.05 in pathway enrichment analyses.Comput Biol Chem2021
34673821Mortality in association with antipsychotic medication use and clinical outcomes among geriatric psychiatry outpatients with COVID-19.PLoS One2021
31985774Associations of Apolipoprotein E ε4 Genotype and Ball Heading With Verbal Memory in Amateur Soccer Players.JAMA Neurol2020
31920921BDNF Val<sup>66</sup>Met Positive Players Demonstrate Diffusion Tensor Imaging Consistent With Impaired Myelination Associated With High Levels of Soccer Heading: Indication of a Potential Gene-Environment Interaction Mechanism.Front Neurol2019
31695094Empirical design of a variant quality control pipeline for whole genome sequencing data using replicate discordance.Sci Rep2019
29740579The Role of Genetics in Advancing Precision Medicine for Alzheimer's Disease-A Narrative Review.Front Med (Lausanne)2018
27260402Differential burden of rare protein truncating variants in Alzheimer's disease patients compared to centenarians.Hum Mol Genet2016
25333069Disease variants in genomes of 44 centenarians.Mol Genet Genomic Med2014
22914616Testing the genomic enrichment of a large copy number variation within schizophrenia linkage regions.Psychiatr Genet2012
22701602A simple method for analyzing exome sequencing data shows distinct levels of nonsynonymous variation for human immune and nervous system genes.PLoS One2012
18192679Huntingtin-associated protein-1 is a modifier of the age-at-onset of Huntington's disease.Hum Mol Genet2008
17905754Brain-specific tryptophan hydroxylase 2 (TPH2): a functional Pro206Ser substitution and variation in the 5'-region are associated with bipolar affective disorder.Hum Mol Genet2008
16736033A summary statistic approach to sequence variation in noncoding regions of six schizophrenia-associated gene loci.Eur J Hum Genet2006
17117947Investigation of the functional variant c.-169T &gt; C of the Fc receptor-like 3 (FCRL3) gene in alopecia areata.Int J Immunogenet2006
16774540Investigation of the p.Ser278Arg polymorphism of the autoimmune regulator (AIRE) gene in alopecia areata.Tissue Antigens2006
15809674Systematic investigation of genetic variability in 111 human genes-implications for studying variable drug response.Pharmacogenomics J2005
15902657Genetic variation in the human androgen receptor gene is the major determinant of common early-onset androgenetic alopecia.Am J Hum Genet2005
15852064A family-based and case-control association study of trace amine receptor genes on chromosome 6q23 in bipolar affective disorder.Mol Psychiatry2005
14525928Single nucleotide variation analysis in 65 candidate genes for CNS disorders in a representative sample of the European population.Genome Res2003
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Collaborators

Institute of Human Genetics, University Hospital Bonn
Co-authored papers 8
Instituto de Genetica Humana, Universidad de Bonn
Co-authored papers 7
University Hospital Basel and University of Basel
Co-authored papers 6
Co-authored papers 4
SUNY Upstate Medical University
Co-authored papers 4
Co-authored papers 4
Central Institute of Mental Health, University of Mannheim
Co-authored papers 3
Philipps University of Marburg
Co-authored papers 3
Co-authored papers 2
Stanley Institute for Cognitive Genomics
Co-authored papers 2
University Hospital Bonn
Co-authored papers 2
Icahn School of Medicine at Mount Sinai
Co-authored papers 2
Medcurio Inc.
Co-authored papers 2
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Co-authored papers 1
Armand Trousseau Hospital, Sorbonne University
Co-authored papers 1
Co-authored papers 1
INSERM
Co-authored papers 1
Donders Institute for Brain, Radboud University Medical Center
Co-authored papers 1
McGill University, Canada Shriners Hospital for Children-Canada
Co-authored papers 1
Co-authored papers 1
Co-authored papers 1
American Medical Informatics Association, Oregon Health and Science University, Oregon State University, University of Colorado Anschutz Medical Campus, University of North Carolina at Chapel Hill, University of Wisconsin-Madison
Co-authored papers 1
Harvard Medical School
Co-authored papers 1
Dalhousie University
Co-authored papers 1
University of Colorado Anschutz Medical Campus
Co-authored papers 1
St. Anna Children's Cancer Research Institute (CCRI)
Co-authored papers 1
University Medical Center Groningen
Co-authored papers 1
Institute of Reproductive Genetics, University of Munster
Co-authored papers 1
Co-authored papers 1