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Author Details
Full Name
Yun Freudenberg-Hua
Affiliation
Feinstein Institutes for Medical Research
ORCID
Career Start Year
2003
Papers
22
H Index
11
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
37953324
The Human Phenotype Ontology in 2024: phenotypes around the world.
Nucleic Acids Res
2024
35372430
Psychotropic Medication Use Is Associated With Greater 1-Year Incidence of Dementia After COVID-19 Hospitalization.
Front Med (Lausanne)
2022
33164815
Greater effect of polygenic risk score for Alzheimer's disease among younger cases who are apolipoprotein E-ε4 carriers.
Neurobiol Aging
2021
33774420
Beyond standard pipeline and p⿯<⿯0.05 in pathway enrichment analyses.
Comput Biol Chem
2021
34673821
Mortality in association with antipsychotic medication use and clinical outcomes among geriatric psychiatry outpatients with COVID-19.
PLoS One
2021
31985774
Associations of Apolipoprotein E ε4 Genotype and Ball Heading With Verbal Memory in Amateur Soccer Players.
JAMA Neurol
2020
31920921
BDNF 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 Neurol
2019
31695094
Empirical design of a variant quality control pipeline for whole genome sequencing data using replicate discordance.
Sci Rep
2019
29740579
The Role of Genetics in Advancing Precision Medicine for Alzheimer's Disease-A Narrative Review.
Front Med (Lausanne)
2018
27260402
Differential burden of rare protein truncating variants in Alzheimer's disease patients compared to centenarians.
Hum Mol Genet
2016
25333069
Disease variants in genomes of 44 centenarians.
Mol Genet Genomic Med
2014
22914616
Testing the genomic enrichment of a large copy number variation within schizophrenia linkage regions.
Psychiatr Genet
2012
22701602
A simple method for analyzing exome sequencing data shows distinct levels of nonsynonymous variation for human immune and nervous system genes.
PLoS One
2012
18192679
Huntingtin-associated protein-1 is a modifier of the age-at-onset of Huntington's disease.
Hum Mol Genet
2008
17905754
Brain-specific tryptophan hydroxylase 2 (TPH2): a functional Pro206Ser substitution and variation in the 5'-region are associated with bipolar affective disorder.
Hum Mol Genet
2008
16736033
A summary statistic approach to sequence variation in noncoding regions of six schizophrenia-associated gene loci.
Eur J Hum Genet
2006
17117947
Investigation of the functional variant c.-169T > C of the Fc receptor-like 3 (FCRL3) gene in alopecia areata.
Int J Immunogenet
2006
16774540
Investigation of the p.Ser278Arg polymorphism of the autoimmune regulator (AIRE) gene in alopecia areata.
Tissue Antigens
2006
15809674
Systematic investigation of genetic variability in 111 human genes-implications for studying variable drug response.
Pharmacogenomics J
2005
15902657
Genetic variation in the human androgen receptor gene is the major determinant of common early-onset androgenetic alopecia.
Am J Hum Genet
2005
15852064
A family-based and case-control association study of trace amine receptor genes on chromosome 6q23 in bipolar affective disorder.
Mol Psychiatry
2005
14525928
Single nucleotide variation analysis in 65 candidate genes for CNS disorders in a representative sample of the European population.
Genome Res
2003
1 - 22 of 22
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