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Page 1
A Catalogue of Structural Variation across Ancestrally Diverse Asian Genomes.
Tan JHJ, Li Z, Porta MG, Rajaby R, Lim WK, Tan YA, Jimenez RT, Teo R, Hebrard M, Ow JL, Ang S, Jeyakani J, Chong YS, Lim TH, Goh LL, Tham YC, Leong KP, Chin CWL; SG10K_Health Consortium; Davila S, Karnani N, Cheng CY, Chambers J, Tai ES, Liu J, Sim X, Sung WK, Prabhakar S, Tan P, Bertin N. Tan JHJ, et al. Among authors: sim x. Nat Commun. 2024 Nov 4;15(1):9507. doi: 10.1038/s41467-024-53620-8. Nat Commun. 2024. PMID: 39496583 Free PMC article.
Biological, clinical and population relevance of 95 loci for blood lipids.
Teslovich TM, Musunuru K, Smith AV, Edmondson AC, Stylianou IM, Koseki M, Pirruccello JP, Ripatti S, Chasman DI, Willer CJ, Johansen CT, Fouchier SW, Isaacs A, Peloso GM, Barbalic M, Ricketts SL, Bis JC, Aulchenko YS, Thorleifsson G, Feitosa MF, Chambers J, Orho-Melander M, Melander O, Johnson T, Li X, Guo X, Li M, Shin Cho Y, Jin Go M, Jin Kim Y, Lee JY, Park T, Kim K, Sim X, Twee-Hee Ong R, Croteau-Chonka DC, Lange LA, Smith JD, Song K, Hua Zhao J, Yuan X, Luan J, Lamina C, Ziegler A, Zhang W, Zee RY, Wright AF, Witteman JC, Wilson JF, Willemsen G, Wichmann HE, Whitfield JB, Waterworth DM, Wareham NJ, Waeber G, Vollenweider P, Voight BF, Vitart V, Uitterlinden AG, Uda M, Tuomilehto J, Thompson JR, Tanaka T, Surakka I, Stringham HM, Spector TD, Soranzo N, Smit JH, Sinisalo J, Silander K, Sijbrands EJ, Scuteri A, Scott J, Schlessinger D, Sanna S, Salomaa V, Saharinen J, Sabatti C, Ruokonen A, Rudan I, Rose LM, Roberts R, Rieder M, Psaty BM, Pramstaller PP, Pichler I, Perola M, Penninx BW, Pedersen NL, Pattaro C, Parker AN, Pare G, Oostra BA, O'Donnell CJ, Nieminen MS, Nickerson DA, Montgomery GW, Meitinger T, McPherson R, McCarthy MI, McArdle W, Masson D, Martin NG, Marroni… See abstract for full author list ➔ Teslovich TM, et al. Among authors: sim x. Nature. 2010 Aug 5;466(7307):707-13. doi: 10.1038/nature09270. Nature. 2010. PMID: 20686565 Free PMC article.
Identification of new genetic risk variants for type 2 diabetes.
Shu XO, Long J, Cai Q, Qi L, Xiang YB, Cho YS, Tai ES, Li X, Lin X, Chow WH, Go MJ, Seielstad M, Bao W, Li H, Cornelis MC, Yu K, Wen W, Shi J, Han BG, Sim XL, Liu L, Qi Q, Kim HL, Ng DP, Lee JY, Kim YJ, Li C, Gao YT, Zheng W, Hu FB. Shu XO, et al. Among authors: sim xl. PLoS Genet. 2010 Sep 16;6(9):e1001127. doi: 10.1371/journal.pgen.1001127. PLoS Genet. 2010. PMID: 20862305 Free PMC article.
Genome-wide association studies reveal genetic variants in CTNND2 for high myopia in Singapore Chinese.
Li YJ, Goh L, Khor CC, Fan Q, Yu M, Han S, Sim X, Ong RT, Wong TY, Vithana EN, Yap E, Nakanishi H, Matsuda F, Ohno-Matsui K, Yoshimura N, Seielstad M, Tai ES, Young TL, Saw SM. Li YJ, et al. Among authors: sim x. Ophthalmology. 2011 Feb;118(2):368-75. doi: 10.1016/j.ophtha.2010.06.016. Epub 2010 Nov 20. Ophthalmology. 2011. PMID: 21095009 Free PMC article.
Learning in glaucoma genetic risk assessment.
Zhang Z, Liu J, Kwoh CK, Sim X, Tay WT, Tan Y, Yin F, Wong TY. Zhang Z, et al. Among authors: sim x. Annu Int Conf IEEE Eng Med Biol Soc. 2010;2010:6182-5. doi: 10.1109/IEMBS.2010.5627757. Annu Int Conf IEEE Eng Med Biol Soc. 2010. PMID: 21097154
264 results