Josephine Hoh

Asthma, allergy, and airway hyperresponsiveness are not linked to the beta(2)-adrenoceptor gene.

A protein kinase A-dependent molecular switch in synapsins regulates neurite outgrowth.

Pharmacogenetic analysis of adverse drug effect reveals genetic variant for susceptibility to liver toxicity.

SNP haplotype tagging from DNA pools of two individuals.

Efficiency of single-nucleotide polymorphism haplotype estimation from pooled DNA.

Statistical methods for analyzing microarray feature data with replications.

Set association analysis of SNP case-control and microarray data.

Mathematical multi-locus approaches to localizing complex human trait genes.

Sum statistics for the joint detection of multiple disease loci in case-control association studies with SNP markers.

Genetic dissection of diseases: design and methods.

Complement factor H polymorphism in age-related macular degeneration.

Strong association of the Y402H variant in complement factor H at 1q32 with susceptibility to age-related macular degeneration.

Association of angiotensinogen gene polymorphisms with essential hypertension in African-Americans and Caucasians.

Systematic review and meta-analysis of the association between complement factor H Y402H polymorphisms and age-related macular degeneration.

HTRA1 promoter polymorphism in wet age-related macular degeneration.

A variant of the HTRA1 gene increases susceptibility to age-related macular degeneration.

Fine-scale linkage disequilibrium mapping of age-related macular degeneration in the complement factor H gene region.

HTRA1 promoter polymorphism predisposes Japanese to age-related macular degeneration.

Origin of dendritic cells in peripheral lymphoid organs of mice.

Two genetic pathways for age-related macular degeneration.

Replicating genotype-phenotype associations.

Linkage disequilibrium mapping for complex disease genes.

Further mapping of 10q26 supports strong association of HTRA1 polymorphisms with age-related macular degeneration.

Functional and structural implications of the complement factor H Y402H polymorphism associated with age-related macular degeneration.

HTRA1 variants in exudative age-related macular degeneration and interactions with smoking and CFH.

The signatures of autozygosity among patients with colorectal cancer.

The NEI/NCBI dbGAP database: genotypes and haplotypes that may specifically predispose to risk of neovascular age-related macular degeneration.

Joint effects of polymorphisms in the HTRA1, LOC387715/ARMS2, and CFH genes on AMD in a Caucasian population.

Sequence variants in HTRA1 and LOC387715/ARMS2 and phenotype and response to photodynamic therapy in neovascular age-related macular degeneration in populations from Israel.

Mitochondrial DNA variants of respiratory complex I that uniquely characterize haplogroup T2 are associated with increased risk of age-related macular degeneration.

Interaction between the serotonin transporter gene (5-HTTLPR), stressful life events, and risk of depression: a meta-analysis.

CCR3: Shedding new light on a dark problem?

Common variants on chromosome 2 and risk of primary open-angle glaucoma in the Afro-Caribbean population of Barbados.

A genome-wide association study on African-ancestry populations for asthma.

Association between reduced copy-number at T-cell receptor gamma (TCRgamma) and childhood allergic asthma: A possible role for somatic mosaicism.

Common variants near CAV1 and CAV2 are associated with primary open-angle glaucoma.

PDE11A associations with asthma: results of a genome-wide association scan.

A pilot genome-wide association study shows genomic variants enriched in the non-tumor cells of patients with well-differentiated neuroendocrine tumors of the ileum.

Detecting essential and removable interactions in genome-wide association studies.

A comparison of association methods correcting for population stratification in case-control studies.

Genetic signatures of exceptional longevity in humans.

Disease risk prediction with rare and common variants.

Genome-wide association study identifies a maternal copy-number deletion in PSG11 enriched among preeclampsia patients.

Stage and gene specific signatures defined by histones H3K4me2 and H3K27me3 accompany mammalian retina maturation in vivo.

Scan statistics in human gene mapping.

Protoporphyrins enhance oligomerization and enzymatic activity of HtrA1 serine protease.

Genetic Predisposition to Dyslipidemia and Risk of Preeclampsia.

Neural-specific deletion of Htra2 causes cerebellar neurodegeneration and defective processing of mitochondrial OPA1.

Postnatal overexpression of the human ARMS2 gene does not induce abnormalities in retina and choroid in transgenic mouse models.

Loss of HtrA1-induced attenuation of TGF-β signaling in fibroblasts might not be the main mechanism of CARASIL pathogenesis.

Genetic Risk Score for Essential Hypertension and Risk of Preeclampsia.

Generation and characterization of mice with a conditional null allele of the HtrA4 gene.

2016: A 'Mitochondria' Odyssey.