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Author Details

Paul J Gallins
2005
46
25
PMIDPaper TitleJournal TitlePublished Year
36921087Genetic Modifiers of Cystic Fibrosis Lung Disease Severity: Whole-Genome Analysis of 7,840 Patients.Am J Respir Crit Care Med2023
35128485Leveraging TOPMed imputation server and constructing a cohort-specific imputation reference panel to enhance genotype imputation among cystic fibrosis patients.HGG Adv2022
36006120A Population-Based Human In Vitro Approach to Quantify Inter-Individual Variability in Responses to Chemical Mixtures.Toxics2022
36071064A resource for integrated genomic analysis of the human liver.Scientific Reports2022
36055212Identification and single-base gene-editing functional validation of a cis-EPO variant as a genetic predictor for EPO-increasing therapies.Am J Hum Genet2022
33193632Exploring the Limits of Combined Image/'omics Analysis for Non-cancer Histological Phenotypes.Frontiers in Genetics2020
31868224A New Liver Expression Quantitative Trait Locus Map From 1,183 Individuals Provides Evidence for Novel Expression Quantitative Trait Loci of Drug Response, Metabolic, and Sex-Biased Phenotypes.Clin Pharmacol Ther2020
31293616A Review and Tutorial of Machine Learning Methods for Microbiome Host Trait Prediction.Frontiers in Genetics2019
29641994A Common Allele in FGF21 Associated with Sugar Intake Is Associated with Body Shape, Lower Total Body-Fat Percentage, and Higher Blood Pressure.Cell Reports2018
28853905Airway Mucosal Host Defense Is Key to Genomic Regulation of Cystic Fibrosis Lung Disease Severity.Am J Respir Crit Care Med2018
30197785A Zero-inflated Beta-binomial Model for Microbiome Data Analysis.Stat2018
28973375Editor's Highlight: Comparative Dose-Response Analysis of Liver and Kidney Transcriptomic Effects of Trichloroethylene and Tetrachloroethylene in B6C3F1 Mouse.Toxicological Sciences2017
28674633Corrigendum: Novel variation at chr11p13 associated with cystic fibrosis lung disease severity.Hum Genome Var2017
27902686Genomic Characterization of Metformin Hepatic Response.PLoS Genet2016
27408752Novel variation at chr11p13 associated with cystic fibrosis lung disease severity.Hum Genome Var2016
26417704Genome-wide association meta-analysis identifies five modifier loci of lung disease severity in cystic fibrosis.Nat Commun2015
25622337Population-based in vitro hazard and concentration-response assessment of chemicals: the 1000 genomes high-throughput screening study.Environ Health Perspect2015
25574903Polymorphisms associated with expression of BPIFA1/BPIFB1 and lung disease severity in cystic fibrosis.American Journal of Respiratory Cell and Molecular Biology2015
25640674Gene expression in transformed lymphocytes reveals variation in endomembrane and HLA pathways modifying cystic fibrosis pulmonary phenotypes.Am J Hum Genet2015
24728292Heritability and genomics of gene expression in peripheral blood.Nat Genet2014
22773346Linkage and association of successful aging to the 6q25 region in large Amish kindreds.Age (Dordr)2013
21750925Mitochondrial haplogroup X is associated with successful aging in the Amish.Hum Genet2012
22306846Vitamin D receptor and Alzheimer's disease: a genetic and functional study.Neurobiol Aging2012
22722634Novel late-onset Alzheimer disease loci variants associate with brain gene expression.Neurology2012
22481475The ARMS2 A69S variant and bilateral advanced age-related macular degeneration.Retina2012
21668908Successful aging shows linkage to chromosomes 6, 7, and 14 in the Amish.Ann Hum Genet2011
21488853A genome-wide linkage screen in the Amish with Parkinson disease points to chromosome 6.Ann Hum Genet2011
21169531Dissection of chromosome 16p12 linkage peak suggests a possible role for CACNG3 variants in age-related macular degeneration susceptibility.Invest Ophthalmol Vis Sci2011
21460841Common variants at MS4A4/MS4A6E, CD2AP, CD33 and EPHA1 are associated with late-onset Alzheimer's disease.Nat Genet2011
21455292Using genetic variation and environmental risk factor data to identify individuals at high risk for age-related macular degeneration.PLoS One2011
20182747Analysis of the indel at the ARMS2 3'UTR in age-related macular degeneration.Hum Genet2010
20885792Dementia revealed: novel chromosome 6 locus for late-onset Alzheimer disease provides genetic evidence for folate-pathway abnormalities.PLoS Genet2010
20697030Meta-analysis confirms CR1, CLU, and PICALM as alzheimer disease risk loci and reveals interactions with APOE genotypes.Arch Neurol2010
19933179Inverse association of female hormone replacement therapy with age-related macular degeneration and interactions with ARMS2 polymorphisms.Invest Ophthalmol Vis Sci2010
20374233Analysis of single nucleotide polymorphisms in the NOS2A gene and interaction with smoking in age-related macular degeneration.Ann Hum Genet2010
18061132Phenotype analysis of patients with the risk variant LOC387715 (A69S) in age-related macular degeneration.Am J Ophthalmol2008
18067970Peripheral reticular pigmentary change is associated with complement factor H polymorphism (Y402H) in age-related macular degeneration.Ophthalmology2008
18325906C3 R102G polymorphism increases risk of age-related macular degeneration.Hum Mol Genet2008
18084039Deletion of CFHR3 and CFHR1 genes in age-related macular degeneration.Hum Mol Genet2008
17724217Haplotypes spanning the complement factor H gene are protective against age-related macular degeneration.Invest Ophthalmol Vis Sci2007
17210853Neovascular age-related macular degeneration and its association with LOC387715 and complement factor H polymorphism.Arch Ophthalmol2007
17576744Protective effect of complement factor B and complement component 2 variants in age-related macular degeneration.Hum Mol Genet2007
17241667Independent effects of complement factor H Y402H polymorphism and cigarette smoking on risk of age-related macular degeneration.Ophthalmology2007
16642439Cigarette smoking strongly modifies the association of LOC387715 and age-related macular degeneration.Am J Hum Genet2006
16828512Complement factor H increases risk for atrophic age-related macular degeneration.Ophthalmology2006
15761120Complement factor H variant increases the risk of age-related macular degeneration.Science2005
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Cleveland Institute for Computational Biology, Case Western Reserve University
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John P. Hussman Institute for Human Genomics.
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The Center for Applied Genomics, Children's Hospital of Philadelphia
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