Josephine Hoh

Department of Environmental Health Sciences, Yale University School of Medicine

Affiliated withYale University School of Medicine

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JoVE Journal Publications

ArticleTotal : 1	Year
Publication title Cited by 5	2016

Other Publications

Article	Year
Asthma, allergy, and airway hyperresponsiveness are not linked to the beta(2)-adrenoceptor gene. Chest\| PubMed ID: 11888952	2002
A protein kinase A-dependent molecular switch in synapsins regulates neurite outgrowth. Nature neuroscience\| PubMed ID: 11976703	2002
Pharmacogenetic analysis of adverse drug effect reveals genetic variant for susceptibility to liver toxicity. The pharmacogenomics journal\| PubMed ID: 12439739	2002
SNP haplotype tagging from DNA pools of two individuals. BMC bioinformatics\| PubMed ID: 12709267	2003
Efficiency of single-nucleotide polymorphism haplotype estimation from pooled DNA. Proceedings of the National Academy of Sciences of the United States of America\| PubMed ID: 12777616	2003
Statistical methods for analyzing microarray feature data with replications. Journal of computational biology : a journal of computational molecular cell biology\| PubMed ID: 12804089	2003
Set association analysis of SNP case-control and microarray data. Journal of computational biology : a journal of computational molecular cell biology\| PubMed ID: 12935345	2003
Mathematical multi-locus approaches to localizing complex human trait genes. Nature reviews. Genetics\| PubMed ID: 12951571	2003
Sum statistics for the joint detection of multiple disease loci in case-control association studies with SNP markers. Genetic epidemiology\| PubMed ID: 14639704	2003
Genetic dissection of diseases: design and methods. Current opinion in genetics & development\| PubMed ID: 15172663	2004
Complement factor H polymorphism in age-related macular degeneration. Science (New York, N.Y.)\| PubMed ID: 15761122	2005
Strong association of the Y402H variant in complement factor H at 1q32 with susceptibility to age-related macular degeneration. American journal of human genetics\| PubMed ID: 15895326	2005
Association of angiotensinogen gene polymorphisms with essential hypertension in African-Americans and Caucasians. Human heredity\| PubMed ID: 16210856	2005
Systematic review and meta-analysis of the association between complement factor H Y402H polymorphisms and age-related macular degeneration. Human molecular genetics\| PubMed ID: 16905558	2006
HTRA1 promoter polymorphism in wet age-related macular degeneration. Science (New York, N.Y.)\| PubMed ID: 17053108	2006
A variant of the HTRA1 gene increases susceptibility to age-related macular degeneration. Science (New York, N.Y.)\| PubMed ID: 17053109	2006
Fine-scale linkage disequilibrium mapping of age-related macular degeneration in the complement factor H gene region. The British journal of ophthalmology\| PubMed ID: 17314151	2007
HTRA1 promoter polymorphism predisposes Japanese to age-related macular degeneration. Molecular vision\| PubMed ID: 17438519	2007
Origin of dendritic cells in peripheral lymphoid organs of mice. Nature immunology\| PubMed ID: 17450143	2007
Two genetic pathways for age-related macular degeneration. Current opinion in genetics & development\| PubMed ID: 17467263	2007
Replicating genotype-phenotype associations. Nature\| PubMed ID: 17554299	2007
Linkage disequilibrium mapping for complex disease genes. Methods in molecular biology (Clifton, N.J.)\| PubMed ID: 17984540	2007
Further mapping of 10q26 supports strong association of HTRA1 polymorphisms with age-related macular degeneration. Vision research\| PubMed ID: 18207215	2008
Functional and structural implications of the complement factor H Y402H polymorphism associated with age-related macular degeneration. Investigative ophthalmology & visual science\| PubMed ID: 18263814	2008
HTRA1 variants in exudative age-related macular degeneration and interactions with smoking and CFH. Investigative ophthalmology & visual science\| PubMed ID: 18316707	2008
The signatures of autozygosity among patients with colorectal cancer. Cancer research\| PubMed ID: 18375840	2008
The NEI/NCBI dbGAP database: genotypes and haplotypes that may specifically predispose to risk of neovascular age-related macular degeneration. BMC medical genetics\| PubMed ID: 18541031	2008
Joint effects of polymorphisms in the HTRA1, LOC387715/ARMS2, and CFH genes on AMD in a Caucasian population. Molecular vision\| PubMed ID: 18682806	2008
Sequence variants in HTRA1 and LOC387715/ARMS2 and phenotype and response to photodynamic therapy in neovascular age-related macular degeneration in populations from Israel. Molecular vision\| PubMed ID: 19065273	2008
Mitochondrial DNA variants of respiratory complex I that uniquely characterize haplogroup T2 are associated with increased risk of age-related macular degeneration. PloS one\| PubMed ID: 19434233	2009
Interaction between the serotonin transporter gene (5-HTTLPR), stressful life events, and risk of depression: a meta-analysis. JAMA\| PubMed ID: 19531786	2009
CCR3: Shedding new light on a dark problem? Journal of molecular cell biology\| PubMed ID: 19684049	2009
Common variants on chromosome 2 and risk of primary open-angle glaucoma in the Afro-Caribbean population of Barbados. Proceedings of the National Academy of Sciences of the United States of America\| PubMed ID: 19805132	2009
A genome-wide association study on African-ancestry populations for asthma. The Journal of allergy and clinical immunology\| PubMed ID: 19910028	2010
Association between reduced copy-number at T-cell receptor gamma (TCRgamma) and childhood allergic asthma: A possible role for somatic mosaicism. Mutation research\| PubMed ID: 20553737	2010
Common variants near CAV1 and CAV2 are associated with primary open-angle glaucoma. Nature genetics\| PubMed ID: 20835238	2010
PDE11A associations with asthma: results of a genome-wide association scan. The Journal of allergy and clinical immunology\| PubMed ID: 20920776	2010
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. Endocrine-related cancer\| PubMed ID: 21139019	2011
Detecting essential and removable interactions in genome-wide association studies. Statistics and its interface\| PubMed ID: 21165165	2009
A comparison of association methods correcting for population stratification in case-control studies. Annals of human genetics\| PubMed ID: 21281271	2011
Genetic signatures of exceptional longevity in humans. PloS one\| PubMed ID: 22279548	2012
Disease risk prediction with rare and common variants. BMC proceedings\| PubMed ID: 22373337	2011
Genome-wide association study identifies a maternal copy-number deletion in PSG11 enriched among preeclampsia patients. BMC pregnancy and childbirth\| PubMed ID: 22748001	2012
Stage and gene specific signatures defined by histones H3K4me2 and H3K27me3 accompany mammalian retina maturation in vivo. PloS one\| PubMed ID: 23056497	2012
Scan statistics in human gene mapping. American journal of human genetics\| PubMed ID: 23122592	2012
Protoporphyrins enhance oligomerization and enzymatic activity of HtrA1 serine protease. PloS one\| PubMed ID: 25506911	2014
Genetic Predisposition to Dyslipidemia and Risk of Preeclampsia. American journal of hypertension\| PubMed ID: 25523295	2015
Neural-specific deletion of Htra2 causes cerebellar neurodegeneration and defective processing of mitochondrial OPA1. PloS one\| PubMed ID: 25531304	2014
Postnatal overexpression of the human ARMS2 gene does not induce abnormalities in retina and choroid in transgenic mouse models. Investigative ophthalmology & visual science\| PubMed ID: 25717153	2015
Loss of HtrA1-induced attenuation of TGF-β signaling in fibroblasts might not be the main mechanism of CARASIL pathogenesis. Proceedings of the National Academy of Sciences of the United States of America\| PubMed ID: 25770224	2015
Genetic Risk Score for Essential Hypertension and Risk of Preeclampsia. American journal of hypertension\| PubMed ID: 26002928	2016
Generation and characterization of mice with a conditional null allele of the HtrA4 gene. Molecular medicine reports\| PubMed ID: 26353049	2015
2016: A 'Mitochondria' Odyssey. Trends in molecular medicine\| PubMed ID: 27151392	2016