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

Liu J, Dong F and 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;112 (14) :E1693. Epub 2015 Mar 13. PMID: 25770224

Liu J and 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;56 (2) :1387-8. Epub 2015 Feb 25. PMID: 25717153

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

Patterson VL, Zullo AJ, Koenig C, Stoessel S, Jo H, Liu X, Han J, Choi M, DeWan AT, Thomas JL, Kuan CY and Hoh J: Neural-specific deletion of Htra2 causes cerebellar neurodegeneration and defective processing of mitochondrial OPA1. PLoS One. 2014;9 (12) :e115789. Epub 2014 Dec 22. PMID: 25531304

Jo H, Patterson V, Stoessel S, Kuan CY and Hoh J: Protoporphyrins enhance oligomerization and enzymatic activity of HtrA1 serine protease. PLoS One. 2014;9 (12) :e115362. Epub 2014 Dec 15. PMID: 25506911

Zhao L, Triche EW, Walsh KM, Bracken MB, Saftlas AF, Hoh J and Dewan AT: Genome-wide association study identifies a maternal copy-number deletion in PSG11 enriched among preeclampsia patients. BMC Pregnancy Childbirth. 2012 Jun 29;12 :61. Epub 2012 Jun 29. PMID: 22748001

Wu C, Walsh KM, Dewan AT, Hoh J and Wang Z: Disease risk prediction with rare and common variants. BMC Proc. 2011 Nov 29;5 Suppl 9 :S61. Epub 2011 Nov 29. PMID: 22373337

Wu C, DeWan A, Hoh J and Wang Z: A comparison of association methods correcting for population stratification in case-control studies. Ann Hum Genet. 2011 May;75 (3) :418-27. Epub 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 and 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;18 (1) :171-80. Epub 2011 Jan 13. PMID: 21139019

Walsh KM, Bracken MB, Murk WK, Hoh J and Dewan AT: Association between reduced copy-number at T-cell receptor gamma (TCRgamma) and childhood allergic asthma: A possible role for somatic mosaicism. Mutat Res. 2010 Aug 7;690 (1-2) :89-94. Epub 2010 May 27. PMID: 20553737

Mason AB and Hoh J: CCR3: Shedding new light on a dark problem? J Mol Cell Biol. 2009 Oct;1 (1) :17-9. Epub 2009 Aug 14. PMID: 19684049

Wu C, Zhang H, Liu X, Dewan A, Dubrow R, Ying Z, Yang Y and Hoh J: Detecting essential and removable interactions in genome-wide association studies. Stat Interface. 2009 Jan 1;2 (2) :161-170. PMID: 21165165

Zhang H, Morrison MA, Dewan A, Adams S, Andreoli M, Huynh N, Regan M, Brown A, Miller JW, Kim IK, Hoh J and 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;9 :51. Epub 2008 Jun 9. PMID: 18541031

DeWan A, Bracken MB and Hoh J: Two genetic pathways for age-related macular degeneration. Curr Opin Genet Dev. 2007 Jun;17 (3) :228-33. Epub 2007 Apr 27. PMID: 17467263

DeWan A, Klein RJ and Hoh J: Linkage disequilibrium mapping for complex disease genes. Methods Mol Biol. 2007;376 :85-107. 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 and Hoh J: HTRA1 promoter polymorphism in wet age-related macular degeneration. Science. 2006 Nov 10;314 (5801) :989-92. Epub 2006 Oct 19. PMID: 17053108

Hoh J and Ott J: Genetic dissection of diseases: design and methods. Curr Opin Genet Dev. 2004 Jun;14 (3) :229-32. PMID: 15172663