Liu J, Li Y, Hoh J: Generation and characterization of mice with a conditional null allele of the HtrA4 gene. Mol Med Rep. 2015 Nov; 2015 Sep 3. PMID: 26353049

Spracklen CN, Saftlas AF, Triche EW, Bjonnes A, Keating B, Saxena R, Breheny PJ, Dewan AT, Robinson JG, Hoh J, Ryckman KK: Genetic Predisposition to Dyslipidemia and Risk of Preeclampsia. Am J Hypertens. 2015 Jul; 2014 Dec 17. PMID: 25523295

Smith CJ, Saftlas AF, Spracklen CN, Triche EW, Bjonnes A, Keating B, Saxena R, Breheny PJ, Dewan AT, Robinson JG, Hoh J, Ryckman KK: Genetic Risk Score for Essential Hypertension and Risk of Preeclampsia. Am J Hypertens. 2015 May 23; 2015 May 23. PMID: 26002928

Liu J, Dong F, Hoh J: Loss of HtrA1-induced attenuation of TGF-β signaling in fibroblasts might not be the main mechanism of CARASIL pathogenesis. Proc Natl Acad Sci U S A. 2015 Apr 7; 2015 Mar 13. PMID: 25770224

Liu J, Hoh J: Postnatal overexpression of the human ARMS2 gene does not induce abnormalities in retina and choroid in transgenic mouse models. Invest Ophthalmol Vis Sci. 2015 Feb 25; 2015 Feb 25. PMID: 25717153

Patterson VL, Zullo AJ, Koenig C, Stoessel S, Jo H, Liu X, Han J, Choi M, DeWan AT, Thomas JL, Kuan CY, Hoh J: Neural-specific deletion of Htra2 causes cerebellar neurodegeneration and defective processing of mitochondrial OPA1. PLoS One. 2014; 2014 Dec 22. PMID: 25531304

Jo H, Patterson V, Stoessel S, Kuan CY, Hoh J: Protoporphyrins enhance oligomerization and enzymatic activity of HtrA1 serine protease. PLoS One. 2014; 2014 Dec 15. PMID: 25506911

Zhao L, Triche EW, Walsh KM, Bracken MB, Saftlas AF, Hoh J, Dewan AT: Genome-wide association study identifies a maternal copy-number deletion in PSG11 enriched among preeclampsia patients. BMC Pregnancy Childbirth. 2012 Jun 29; 2012 Jun 29. PMID: 22748001

Wu C, Walsh KM, Dewan AT, Hoh J, Wang Z: Disease risk prediction with rare and common variants. BMC Proc. 2011 Nov 29; 2011 Nov 29. PMID: 22373337

Wu C, DeWan A, Hoh J, Wang Z: A comparison of association methods correcting for population stratification in case-control studies. Ann Hum Genet. 2011 May; 2011 Jan 31. PMID: 21281271

Walsh KM, Choi M, Oberg K, Kulke MH, Yao JC, Wu C, Jurkiewicz M, Hsu LI, Hooshmand SM, Hassan M, Janson ET, Cunningham JL, Vosburgh E, Sackler RS, Lifton RP, Dewan AT, Hoh J: 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. Endocr Relat Cancer. 2011 Feb; 2011 Jan 13. PMID: 21139019

Mason AB, Hoh J: CCR3: Shedding new light on a dark problem? J Mol Cell Biol. 2009 Oct; 2009 Aug 14. PMID: 19684049

Wu C, Zhang H, Liu X, Dewan A, Dubrow R, Ying Z, Yang Y, Hoh J: Detecting essential and removable interactions in genome-wide association studies. Stat Interface. 2009 Jan 1. PMID: 21165165

Zhang H, Morrison MA, Dewan A, Adams S, Andreoli M, Huynh N, Regan M, Brown A, Miller JW, Kim IK, Hoh J, Deangelis MM: The NEI/NCBI dbGAP database: genotypes and haplotypes that may specifically predispose to risk of neovascular age-related macular degeneration. BMC Med Genet. 2008 Jun 9; 2008 Jun 9. PMID: 18541031

DeWan A, Bracken MB, Hoh J: Two genetic pathways for age-related macular degeneration. Curr Opin Genet Dev. 2007 Jun; 2007 Apr 27. PMID: 17467263

DeWan A, Klein RJ, Hoh J: Linkage disequilibrium mapping for complex disease genes. Methods Mol Biol. 2007. PMID: 17984540

Dewan A, Liu M, Hartman S, Zhang SS, Liu DT, Zhao C, Tam PO, Chan WM, Lam DS, Snyder M, Barnstable C, Pang CP, Hoh J: HTRA1 promoter polymorphism in wet age-related macular degeneration. Science. 2006 Nov 10; 2006 Oct 19. PMID: 17053108

Hoh J, Ott J: Genetic dissection of diseases: design and methods. Curr Opin Genet Dev. 2004 Jun. PMID: 15172663