Liu JS, Juo SH, Chen WH, Chang YY, Chen SS. A case of Graves' diseases associated with intracranial moyamoya vessels and tubular stenosis of extracranial internal carotid arteries. J Formos Med Assoc. 93(9):806-9. 1994 (impact factor = 0.47)
　

Doehring CB, Sanda MG, Partin AW, Sauvageot J, Juo SH, Beaty TH, Epstein JI, Hill G, Walsh PC.             Histopathologic Characterization of Hereditary Benign Prostatic Hyperplasia. Urology. 48(4):650‑3, 1996 (impact factor = 2.1)
　

Juo SH, Beaty TH, Kwiterovich PO Jr.  Etiologic heterogeneity of hyperapobetalipoproteinemia (hyperapoB). Results from segregation analysis in families with premature coronary artery disease. Arterioscler Thromb Vasc Biol. 17: 2729-2736, 1997. (impact factor = 7.1)
　

Juo SH, Beaty TH, Duffy LD, Maestri NE, Prenger VL , Zeiger J, Lei HH, Coresh J.  A Comprehensive Analysis of a Common Disease and Its Underlying Traits. Genet Epidemiol. 14:815-820, 1997 (impact factor = 5.1)
　

Juo SH, Beaty TH, Xu J, Prenger VL, Coresh J, Kwiterovich PO Jr. Segregation Analysis of Two-Locus Models Regulating Apolipoprotein-AI Levels.  Genet Epidemiol. 15:73-86, 1998 (impact factor = 5.1)
　

Juo SH, Bredie SJH, Kiemeney LA, Demacker PNM, Stalenhoef AFH. A Common Genetic Mechanism Determine Plasma Apolipoprotein B Levels and Dense LDL Subfraction Distribution in Familial Combined Hyperlipidemia. Am J Hum Genet. 63:586-594, 1998 (impact factor = 12.6)
　

Juo SH, Beaty TH, Duffy D, Coresh J, Kwiterovich PO Jr.  No Common Major Gene for Apolipoprotein A-I and HDL₃-C Levels: Results From Bivariate Segregation Analysis. Genet Epidemiol. 16:54-68, 1999 (impact factor = 5.1)
　

Juo SH, Wyszynski DF, Beaty TH, Huang HY, Bailey-Wilson JE. Mild Association Between the A/G Polymorphism in the Promoter of the Apolipoprotein A-I Gene and Apolipoprotein A-I levels: A Meta-analysis. Am J Med Genet. 82:235-241, 1999 (impact factor = 3.5)
　

Stephan DA, Gillanders E, Vanderveen D, Fraes-Lutz D, Wistow G, Van Auken A, Quesenberry MI, Robbins CM, Bailey-Wilson J, Juo SH, Trent JM, Smith L, Brownstein MJ. Progressive juvenile-onset punctate cataracts caused by mutation of the gammaD-crystallin gene. Proc Natl. Acad. Sci. USA 96:1008‑12, 1999. (impact factor = 10.2)
　

De Oliveira e Silva ER, Kong M, Han Z, Starr C, Kass EM, Juo SH, Foster D, Dansky HM, Merkel M, Cundey K, Brinton EA, Breslow JL, Smith JD. Metabolic and Genetic Determinants of HDL Metabolism and Hepatic Lipase Activity in Normolipidemic Females.  J Lipid Res. 40:1211-1221, 1999. (impact factor = 3.9)
　

Juo SH, Pugh EW, Baffoe-Bonnie A, Kingman A, Sorant AJM, Klein A, O’Neill J, Mathias R, Wilson AF, Bailey-Wilson JE. Possible Linkage of Alcoholism, Monoamine Oxidase (MAO) Activity and P300 Amplitude to Chromosome 12q24. Genet Epidemiol. 17 Suppl 1:S193-8, 1999 (impact factor = 5.1)
　

Barnes KC, Freidhoff LR, Nickel R, Chiu YF, Juo SH, Hizawa N, Naidu RP, Ehrlich E, Duffy DL, Schou C,       Levett PN, Marsh DG, Beaty TH. Dense Mapping of Chromosome 12q13.2-q23.3 and Linkage to Asthma and     Atopy.  J Allergy Clin Immunol 104(2 Pt 1):485-491, 1999 (impact factor = 7.7)
　

Appukuttan B, Gillanders E, Juo SH, Freas-Lutz D, Ott S, Sood R, Van Auken A, Bailey-Wilson J, Wang X, Patel R, Robbins CM, Chung M, Annett G, Weinberg K, Borchert M, Trent JM, Brownstein MJ, Stout JT. Localization of a Gene for Duane's Retraction Syndrome to Chromosome 2q31. Am J Hum Genet 65(6):1639-1646, 1999 (impact factor = 12.6)
　

Juo SH, Han Z, Smith JD, Colangelo L, Liu K. Common polymorphism in promoter of microsomal triglyceride transfer protein gene influences cholesterol, ApoB, and triglyceride levels in young African American men: results from the coronary artery risk development in young adults (CARDIA) study. Arterioscler Thromb Vasc Biol. 20(5):1316-22, 2000 (impact factor = 7.1)
　

Kainu T, Juo SH, Desper R., Schäffer AA, Bailey-Wilson JE, Kallioniemi OP, et al. Somatic deletions in hereditary breast cancers implicate 13q21 as a putative novel breast cancer susceptibility locus. Proc Natl. Acad. Sci. USA 97:9603-9608, 2000 (impact factor = 10.2)
　

Juo SH, Han Z, Smith JD, Colangelo L, Liu K. Promoter Polymorphism of Hepatic Lipase Gene Influences HDL₂ But Not HDL₃ in African American Men: The CARDIA Study. J Lipid Res. 42: 258-264, 2001 (impact factor = 3.9)
　

Liu JJ, Juo SH, Terwilliger JD, Grunn A, Tong XM, Brito M, Loth JE, Kanyas K, Lerer B, Endicott J, Penchaszadeh G, Gilliam TC, Baron M.  A Follow-Up Linkage Study Supports Evidence for a Bipolar Affective Disorder Locus on Chromosome 21q22. Am J Med Genet. 105:189-194, 2001 (impact factor = 3.5)
　

Slager SL, Juo SH, Durner M, Hodge SE. Markov Chain Monte Carlo Linkage Analysis: Effect of Bin Width on the Probability of Linkage. Genet Epidemiol. 21 Suppl. 700-705, 2001 (impact factor = 5.1)
　

Liu JJ, Juo SH, Holopainen P, Terwilliger J, Tong X, Grunn A, Brito M, Green P, Mustalahti K, Mäki M, Gilliam C, Partanen J. Genomewide linkage analysis of celiac disease in Finnish families. Am J Hum Genet. 70:51-59, 2002 (impact factor = 12.3)
　

Rozenblum E, Vahteristo P, Sandberg T, Bergthorsson T, Syrjakoski K, Weaver D, Haraldsson K, Johannsdottir K, Vehmanen P, Nigam S, Golberger N, Robbins C, Pak E, Dutra A, Gillander E, Stephan DA, Bailey-Wilson J, Juo SH, Kainu T, Arason A, Barkardottir B, Nevanlinna H, Borg A, Kallioniemi OP.  A genomic map of a 6-Mb region at 13q21-q22 implicated in cancer development: identification and characterization of candidate genes. Hum Genet. 110:111-121, 2002 (impact factor = 4.3)
　

Rundek T, Elkind MS, Pittman J, Boden-Albala B, Martin S, Humphries SE, Juo SH, Sacco RL. Carotid Intima-Media Thickness is Associated with Allelic Variants of Stromelysin-1, Interleukin-6 and Hepatic Lipase Genes: The Northern Manhattan Prospective Cohort Study. Stroke 33:1420-1423, 2002 (impact factor = 5.7)
　

Liu J, Juo SH, Dewan A, Grunn A, Tong X, Brito M, Park N, Loth JE, Kanyas K, Lerer B, Endicott J, Penchaszadeh G, Knowles JA, Ott J, Gilliam TC, Baron M. Evidence for a putative bipolar disorder locus on 2p13-16 and other potential loci on 4q31, 7q34, 8q13, 9q31, 10q21-24, 13q32, 14q21 and 17q11-12. Mol Psychiatry, 8(3):333-342, 2003 (impact factor = 9.3)
　

Juo SH, Colangelo L, Han Z, Smith JD, Liu K. Confirmation of the microsomal triglyceride transfer protein genetic effect on lipids in young African American men from the CARDIA study. Arterioscler Thromb Vasc Biol. 23:912-913, 2003 (impact factor = 7.1)
　

Jawaheer D, Juo SH, Petit C, Damle A, Dowbak S, Gregersen P, McElreavey K, Ostrer H. Mapping a gene for 46,XY gonadal dysgenesis by linkage analysis. Clin Genet. 63(6):530-535, 2003 (impact factor = 3.3)
　

Yonan AL, Alarcón M, Cheng R, Magnusson PEK, Spence SJ, Palmer AA, Grunn A, Juo SH, Terwilliger JD, Liu J, Cantor RM, Geschwind DH, Gilliam TC. A Genome-wide Screen of 345 Families for Autism Susceptibility Loci. Am J Hum Genet 73(4): 886-897, 2003 (impact factor = 12.6)
　

Segurado R, Detera-Wadleigh SD, Levinson DF, Lewis CM, Gill M, Nurnberget JI Jr, Craddock N, DePaulo JR, Baron M, Gerson ES, Ekholm J, Cichon S, Turecki G, Claes S, Kelsoe JR, Schofield PR, Badenhop RF, Morissette J, Coon H, Blackwood D, Curtis D,Gilliam C, Juo SH, Berrettini WH, etc. Genome Scan meta-analysis of schizophrenia and bipolar disorder. Part III: Bipolar disorder. Am J Hum Genet. 73(1):49-62. 2003 (impact factor = 12.6)
　

Gillanders E*, Juo SH*, Holland EA, Jones M, Nancarrow D, Freas-Lutz D, Sood R, Park N, Faruque M, Markey C, Kefford RF, Palmer J, Bergman W, Bishop DT, Tucker MA, Bressac-de Paillerets B, Hansson J, The Lund Melanoma Study Group, Stark M, Gruis N, Bishop JN, Goldstein AM, Bailey-Wilson JE, Mann GJ, Trent J and Melanoma Linkage Consortium. Localization of a Novel Melanoma Susceptibility Locus to 1p22. Am J Hum Genet 73:301-313, 2003 *contributed equally (impact factor = 12.6)
　

Cheng R, Park N, Hodge SE, Juo SH. Comparison of the linkage results of two phenotypic constructs the longitudinal data from the Framingham Family Study: analyses on data measured at three time points and on the average of three measurements. BMC Genet, 4(Suppl 1):S20. 2003 (impact factor = 1.8)
　

Liang CL, Hung KS, Park N, Chan P, Juo SH. Comparison of Measurements of Refractive Errors Between the Hand-held Retinomax and on-Table Autorefractors in Cyclopleged and Non-Cyclopleged Children. Am J Ophthalmol. 136;1120-1128. 2003 (impact factor = 2.4)
　

Huusko P*, Juo SH*, Gillanders E*, Sarantaus L*, Kainu T, Vahteristo P, Allinen M, Jones M, Rapakko K, Eerola H, Markey C, Vehmanen P, Gildea D, Freas-Lutz D, Blomqvist C, Leisti J, Blanco G, Puistola U, Trent J, Bailey-Wilson J, Winqvist R, Nevanlinna H, Kallioniemi OP. Genome-wide scanning for linkage in Finnish breast cancer families.  Eur J Hum Genet, 12(2):98-104; 2004 *contributed equally (impact factor = 3.3)   
　

Wang PW, Liu RT, Juo SH, Wang ST, Hu YH, Hsieh CJ, Chen MH, Chen YY, Wu CL. Cytotoxic T lymphocyte-associated molecule-4 polymorphism and relapse of Graves' hyperthyroidism after antithyroid withdrawal. J Clin Endocrinol Metab. 2004; 89(1): 169-73. 2004 (impact factor = 6.0)
　

Liang CL, Hung KS, Park N, Chan P, Juo SH. Comparison of the Hand-held Retinomax K-plus2 and On–Table Autokeratometers in Children With and Without Cycloplegia.  J Cataract Refract Surg. 30(3):669-74. 2004 (impact factor = 1.9)
　

Juo SH, Lin H-F, Rundek T, Sabala E, Boden-Albala B, Park N, Lan MY, Sacco RL. Genetic and environmental contributions to carotid intima-media thickness and obesity phenotypes in the Northern Manhattan Family Study  Stroke. 35(10):2243-7, 2004 (impact factor = 5.9)
　

Liang CL, Yen E, Su JY, Liu C, Chang TY, Park N, Wu MJ, Lee S, Flynn JT, Juo SH. The impact of family history of high myopia on the level and the onset of myopia.  Invest Ophthalmol Vis Sci. 45:3446-3452, 2004 (impact factor = 3.6)
　

Hung KS, Liang CL, Wang CH, Chang HW, Park N, Juo SH. Outcome after traumatic frontal intracerebral haemorrhage: a comparison of unilateral and bilateral haematomas. J Clin Neurosci. 11(8):849-853, 2004 (impact factor = 0.7)
　

Park N, Juo SH, Cheng R, Liu J, Loth JE, Lilliston B, Nee J, Grunn A, Kanyas K, Lerer B, Endicott J, Gilliam TC, Baron M. Linkage analysis of psychosis in bipolar pedigrees suggests novel putative loci for bipolar disorder and shared susceptibility with schizophrenia. Mol Psychiatry. 9(12):1091-9, 2004 (impact factor = 9.3)
　

Park N, Cheng R, Juo SH, Liu J, Loth JE, Endicott J, Gilliam TC, Baron M. Absence of psychosis may influence linkage results for bipolar disorder. Mol Psychiatry. 10(3):235-7, 2005  (impact factor = 6.9)
　

Shih HH, Lin TM, Chuang JH, Eng HL, Juo SH, Huang FC, Chen CL, Chen HL. Promoter polymorphism of the CD14 endotoxin receptor gene is associated with biliary atresia and idiopathic neonatal cholestasis. Pediatrics 116:437-441, 2005 (impact factor = 4.3)
　

Juo SH, Di Tullio MR, Lin HF, Boden-Albala B, Homma S, Sacco RL. Heritability of Left Ventricular Mass and Other Morphologic Variables in Caribbean Hispanics: The Northern Manhattan Family Study. J Am Coll Cardiol 46(4):735-737, 2005 (impact factor = 9.2)
　

Lin H-F, Boden-Albala B, Juo SH*, Park N, Rundek T, Sacco RL. Heritabilities of metabolic syndrome and its components in the Northern Manhattan Family Study. Diabetologia. 48(10): 2006-12, 2005  (impact factor = 5.3) *correspondent author
　

McQueen MB, Devlin B, Faraone SV, Nimgaonkar VL, Sklar P, Smoller JW, Abou Jamra R, Albus M, Bacanu SA, Baron M, Barrett TB, Berrettini W, Blacker D, Byerley W, Cichon S, Coryell W, Craddock N, Daly MJ, Depaulo JR, Edenberg HJ, Foroud T, Gill M, Gilliam TC, Hamshere M, Jones I, Jones L, Juo SH, Kelsoe JR, Lambert D, Lange C, Lerer B, Liu J, Maier W, Mackinnon JD, McInnis MG, McMahon FJ, Murphy DL, Nothen MM, Nurnberger JI, Pato CN, Pato MT, Potash JB, Propping P, Pulver AE, Rice JP, Rietschel M, Scheftner W, Schumacher J, Segurado R, Van Steen K, Xie W, Zandi PP, Laird NM. Combined Analysis from Eleven Linkage Studies of Bipolar Disorder Provides Strong Evidence of Susceptibility Loci on Chromosomes 6q and 8q. Am J Hum Genet. 77(4): 582-595, 2005  (impact factor = 12.6)
　

Juo SH, Rundek T, Lin H-F, Chen R, Lan MY, Huang JS, Boden-Albala B, Sacco RL. Heritability of Carotid Artery Distensibility in Hispanics: the Northern Manhattan Family Study. Stroke. 36:2357-2361, 2005 (impact factor = 5.9)
　

Liang CL, Juo SH, Chang CJ. Comparison of higher-order wavefront aberrations among three different aberrometers.  J Cataract Refract Surg. 31(11):2153-2156, 2005 (impact factor = 1.9)
　

Lin H-F, Juo SH, Chen R. Comparison of the power between microsatellite and SNP markers for linkage and linkage disequilibrium mapping of an electrophysiological phenotype. BMC Genet 6(suppl 1):S7, 2005 (impact factor = 1.8)
　

Cheng R, Park N, Juo SH, Liu JJ, Loth JE, Endicott J, Gilliam TC, Baron M. Psychosis and the genetic spectrum of bipolar disorder: evidence from linkage analysis. Mol Psychiatry. 11 (1):3-5, 2006 (impact factor = 9.3)
　

Cheng R, Juo SH, Loth JE, Nee J, Ossifov I, Blumenthal R, Sharpe L, Kanyas K, Lerer B, Lilliston B, Smith M,  Trautman K, Gilliam TC, Baron M.  Genome-wide Linkage Scan in a Large Bipolar Disorder Sample from the National Institute of Mental Health Genetics Initiative Suggests Putative Loci for Bipolar Disorder, Psychosis, Suicide, and Panic Disorder. Mol Psychiatry, 2006 Jan 10; [Epub ahead of print] (impact factor = 9.3)
　

Juo SH, Wang TN, Lee JN, Wu MT, Long CU, Tsai EM. CYP17, CYP1A1 and COMT polymorphisms and the risk of adenomyosis and endometriosis in Taiwanese women. Hum Reprod. 21(6):1498-1502, 2006(impact factor = 3.7)
　

Liang CL, Wang HS, Hung KS, Hsi E, Sun A, Kuo YH, Juo SH*. Evaluation of MMP3 and TIMP1 as candidate genes for high myopia in young Taiwanese men. Am J Ophthalmol. 142(3):518-20. 2006  *correspondent author
　

Lin HF, Liao YC, Liou CW, Liu CK, Juo SH. The phosphodiesterase 4D gene for early-onset ischemic stroke among normotensive patients. J Thromb Haemost 2006 Dec 7; [Epub ahead of print] (IF=5.26) *correspondent author
　

Lin TH, Chiu HC, Su HM, Juo SH, Lee YT, Voon WC, Lai WT, Sheu SH. D-Allele of ACE Polymorphism is Associated With Increased Magnitude of QT Dispersion Prolongation in Elderly Chinese. Circ J. 2007;71(1):39-45. (IF=1.998)
　

Liang CL, Hsieh HY, Hung KS, Chang W, Tsai YY, Wang HS, Juo SH*. Systematic Assessment of the Tagging Polymorphisms of the COL1A1 Gene for High Myopia. J of Hum Genet. (IF=2.205 rank=73/131) 52(4):374-7, 2007 *correspondent author
　

Yang P, Lung FW, Jong YJ, Hsieh HY, Liang CL, SH Juo*. Association of the homeobox transcription factor gene ENGRAILED 2 (EN2) with autistic disorder in Chinese children. Neuropsychobiology (in press) 2008. (IF=2.367, rank= 43/94) *correspondent author
　

Book Chapter
　

Invited Commentary