Molecular detection of persistent postoperative circulating tumour cells in stages II and III colon cancer patients via multiple blood sampling: prognostic significance of detectio... by Lu, C-Y, Uen, Y-H, Tsai, H-L, Chuang, S-C, Hou, M-F, Wu, D-C, Hank Juo, S-H, Lin, S-R, Wang, J-Y

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Heritabilities of the metabolic syndrome and its components in the Northern Manhattan Family Study by LIN, H.-F, BODEN-ALBALA, B, JUO, S. H, PARK, N, RUNDEK, T, SACCO, R. L

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Association between lactoferrin gene polymorphisms and aggressive periodontitis among Taiwanese patients by Wu, Y-M., Juo, S-H., Ho, Y-P., Ho, K-Y., Yang, Y-H., Tsai, C-C.

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CYP17, CYP1A1 and COMT polymorphisms and the risk of adenomyosis and endometriosis in Taiwanese women by Juo, S.H., Wang, T.N., Lee, J.N., Wu, M.T., Long, C.Y., Tsai, E.M.

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The phosphodiesterase 4D gene for early onset ischemic stroke among normotensive patients by LIN, H.‐F., LIAO, Y.‐C., LIOU, C.‐W., LIU, C.‐K., JUO, S.‐H. H.

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The Impact of Cigarette Smoking, Alcohol Drinking and Betel Quid Chewing on the Risk of Calcium Urolithiasis by Liu, Chia-Chu, Huang, Shu-Pin, Wu, Wen-Jeng, Chou, Yii-Her, Juo, S.H, Tsai, Li-Yu, Huang, Chun-Hsiung, Wu, Ming-Tsang

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Mapping a gene for 46,XY gonadal dysgenesis by linkage analysis by Jawaheer, D, Juo, S-HH, Le Caignec, C, David, A, Petit, C, Gregersen, P, Dowbak, S, Damle, A, McElreavey, K, Ostrer, H

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Localization of a Gene for Duane Retraction Syndrome to Chromosome 2q31 by Appukuttan, Binoy, Gillanders, Elizabeth, Juo, Suh-Hang, Freas-Lutz, Diana, Ott, Sandra, Sood, Raman, Van Auken, Ann, Bailey-Wilson, Joan, Wang, Xiaoguang, Patel, Reshma J., Robbins, Christiane M., Chung, Mina, Annett, Geralyn, Weinberg, Kenneth, Borchert, Mark S., Trent, Jeffrey M., Brownstein, Michael J., Stout, J. Timothy

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Dense mapping of chromosome 12q13.12-q23.3 and linkage to asthma and atopy by Barnes, Kathleen C., Freidhoff, Linda R., Nickel, Renate, Chiu, Yen-Feng, Juo, Suh-Hang, Hizawa, Nobuyuki, Naidu, Raana P., Ehrlich, Eva, Duffy, David L., Schou, Carsten, Levett, Paul N., Marsh, David G., Beaty, Terri H.

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Segregation analysis of two-locus models regulating apolipoprotein-A1 levels by Juo, S.H., Beaty, T.H., Xu, J., Prenger, V.L., Coresh, J., Kwiterovich Jr, P.O.

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Markov Chain Monte Carlo Linkage Analysis: Effect of Bin Width on the Probability of Linkage by Slager, S.L., Juo, S.H., Durner, M., Hodge, S.E.

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A Common Genetic Mechanism Determines Plasma Apolipoprotein B Levels and Dense LDL Subfraction Distribution in Familial Combined Hyperlipidemia by Juo, Suh-Hang Hank, Bredie, Sebastian J.H., Kiemeney, Lambertus A., Demacker, Pierre N.M., Stalenhoef, Anton F.H.

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A follow-up linkage study supports evidence for a bipolar affective disorder locus on chromosome 21q22 by Liu, Jianjun, Juo, Suh Hang, Terwilliger, Joseph D., Grunn, Adina, Tong, Xiaomei, Brito, Miguel, Loth, Jo Ellen, Kanyas, Kyra, Lerer, Bernard, Endicott, Jean, Penchaszadeh, Graciela, Gilliam, T. Conrad, Baron, Miron

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A comprehensive analysis of complex traits in problem 2A by Juo, S.H., Beaty, T.H., Duffy, D.L., Maestri, N.E., Prenger, V.L., Zeiger, J., Lei, H.H., Coresh, J.

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A Genomewide Screen of 345 Families for Autism-Susceptibility Loci by Yonan, Amanda L., Alarcón, Maricela, Cheng, Rong, Magnusson, Patrik K.E., Spence, Sarah J., Palmer, Abraham A., Grunn, Adina, Hank Juo, Suh-Hang, Terwilliger, Joseph D., Liu, Jianjun, Cantor, Rita M., Geschwind, Daniel H., Gilliam, T. Conrad

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The role of SIRT1/AKT/ERK pathway in ultraviolet B induced damage on human retinal pigment epithelial cells by Chou, Wen-Wen, Chen, Ku-Chung, Wang, Yung-Song, Wang, Jaw-Yuan, Liang, Chung-Ling, Juo, Suh-Hang Hank

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No common major gene for apolipoprotein A-I and HDL3-C levels: Evidence from bivariate segregation analysis by Juo, S.H.H., Beaty, T.H., Duffy, D.L., Coresh, J., Kwiterovich Jr, P.O.

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Apelin gene polymorphism influences apelin expression and obesity phenotypes in Chinese women by LIAO, Yi-Chu, CHOU, Wen-Wen, LI, Yi-Ning, CHUANG, Shih-Chang, LIN, Wen-Yi, VKS LAKKAKULA, Bhaskar, YU, Ming-Lung, HANK JUO, Suh-Hang

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The FGF2 gene in a myopia animal model and human subjects by An, Jianhong, Hsi, Edward, Zhou, Xiangtian, Tao, Yijin, Juo, Suh-Hang Hank, Liang, Chung-Ling

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Progressive Juvenile-Onset Punctate Cataracts Caused by Mutation of the γ D-crystallin Gene by Stephan, Dietrich A., Gillanders, Elizabeth, Vanderveen, Deborah, Freas-Lutz, Diana, Wistow, Graeme, Baxevanis, Andreas D., Robbins, Christiane M., VanAuken, Ann, Quesenberry, Matthew I., Bailey-Wilson, Joan, Juo, Suh-Hang Hank, Trent, Jeffrey M., Smith, Lois, Brownstein, Michael J.

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