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Page 1
Association of SNTB1 with High Myopia.
Cheong KX, Yong RYY, Tan MMH, Tey FLK, Ang BCH. Cheong KX, et al. Among authors: yong ryy. Curr Eye Res. 2021 Jan;46(1):144-150. doi: 10.1080/02713683.2020.1772835. Epub 2020 Jun 21. Curr Eye Res. 2021. PMID: 32452213
Association of VIPR2 and ZMAT4 with high myopia.
Cheong KX, Yong RYY, Tan MMH, Tey FLK, Ang BCH. Cheong KX, et al. Among authors: yong ryy. Ophthalmic Genet. 2020 Feb;41(1):41-48. doi: 10.1080/13816810.2020.1737951. Epub 2020 Mar 13. Ophthalmic Genet. 2020. PMID: 32166996
Identification of an INa-dependent and Ito-mediated proarrhythmic mechanism in cardiomyocytes derived from pluripotent stem cells of a Brugada syndrome patient.
Ma D, Liu Z, Loh LJ, Zhao Y, Li G, Liew R, Islam O, Wu J, Chung YY, Teo WS, Ching CK, Tan BY, Chong D, Ho KL, Lim P, Yong RYY, Panama BK, Kaplan AD, Bett GCL, Ware J, Bezzina CR, Verkerk AO, Cook SA, Rasmusson RL, Wei H. Ma D, et al. Among authors: yong ryy. Sci Rep. 2018 Jul 26;8(1):11246. doi: 10.1038/s41598-018-29574-5. Sci Rep. 2018. PMID: 30050137 Free PMC article.
A Brugada syndrome proband with compound heterozygote SCN5A mutations identified from a Chinese family in Singapore.
Tan BY, Yong RY, Barajas-Martinez H, Dumaine R, Chew YX, Wasan PS, Ching CK, Ho KL, Gan LS, Morin N, Chong AP, Yap SH, Neo JL, Yap EP, Moochhala S, Chong DT, Chow W, Seow SC, Hu D, Uttamchandani M, Teo WS. Tan BY, et al. Among authors: yong ry. Europace. 2016 Jun;18(6):897-904. doi: 10.1093/europace/euv058. Epub 2015 Mar 31. Europace. 2016. PMID: 25829473
Toward male individualization with rapidly mutating y-chromosomal short tandem repeats.
Ballantyne KN, Ralf A, Aboukhalid R, Achakzai NM, Anjos MJ, Ayub Q, Balažic J, Ballantyne J, Ballard DJ, Berger B, Bobillo C, Bouabdellah M, Burri H, Capal T, Caratti S, Cárdenas J, Cartault F, Carvalho EF, Carvalho M, Cheng B, Coble MD, Comas D, Corach D, D'Amato ME, Davison S, de Knijff P, De Ungria MC, Decorte R, Dobosz T, Dupuy BM, Elmrghni S, Gliwiński M, Gomes SC, Grol L, Haas C, Hanson E, Henke J, Henke L, Herrera-Rodríguez F, Hill CR, Holmlund G, Honda K, Immel UD, Inokuchi S, Jobling MA, Kaddura M, Kim JS, Kim SH, Kim W, King TE, Klausriegler E, Kling D, Kovačević L, Kovatsi L, Krajewski P, Kravchenko S, Larmuseau MH, Lee EY, Lessig R, Livshits LA, Marjanović D, Minarik M, Mizuno N, Moreira H, Morling N, Mukherjee M, Munier P, Nagaraju J, Neuhuber F, Nie S, Nilasitsataporn P, Nishi T, Oh HH, Olofsson J, Onofri V, Palo JU, Pamjav H, Parson W, Petlach M, Phillips C, Ploski R, Prasad SP, Primorac D, Purnomo GA, Purps J, Rangel-Villalobos H, Rębała K, Rerkamnuaychoke B, Gonzalez DR, Robino C, Roewer L, Rosa A, Sajantila A, Sala A, Salvador JM, Sanz P, Schmitt C, Sharma AK, Silva DA, Shin KJ, Sijen T, Sirker M, Siváková D, Skaro V, Solano-Matamoros C, Souto L, Stenzl V, Sudoyo… See abstract for full author list ➔ Ballantyne KN, et al. Among authors: yong ry. Hum Mutat. 2014 Aug;35(8):1021-32. doi: 10.1002/humu.22599. Epub 2014 Jul 14. Hum Mutat. 2014. PMID: 24917567 Free PMC article.
A global analysis of Y-chromosomal haplotype diversity for 23 STR loci.
Purps J, Siegert S, Willuweit S, Nagy M, Alves C, Salazar R, Angustia SM, Santos LH, Anslinger K, Bayer B, Ayub Q, Wei W, Xue Y, Tyler-Smith C, Bafalluy MB, Martínez-Jarreta B, Egyed B, Balitzki B, Tschumi S, Ballard D, Court DS, Barrantes X, Bäßler G, Wiest T, Berger B, Niederstätter H, Parson W, Davis C, Budowle B, Burri H, Borer U, Koller C, Carvalho EF, Domingues PM, Chamoun WT, Coble MD, Hill CR, Corach D, Caputo M, D'Amato ME, Davison S, Decorte R, Larmuseau MH, Ottoni C, Rickards O, Lu D, Jiang C, Dobosz T, Jonkisz A, Frank WE, Furac I, Gehrig C, Castella V, Grskovic B, Haas C, Wobst J, Hadzic G, Drobnic K, Honda K, Hou Y, Zhou D, Li Y, Hu S, Chen S, Immel UD, Lessig R, Jakovski Z, Ilievska T, Klann AE, García CC, de Knijff P, Kraaijenbrink T, Kondili A, Miniati P, Vouropoulou M, Kovacevic L, Marjanovic D, Lindner I, Mansour I, Al-Azem M, Andari AE, Marino M, Furfuro S, Locarno L, Martín P, Luque GM, Alonso A, Miranda LS, Moreira H, Mizuno N, Iwashima Y, Neto RS, Nogueira TL, Silva R, Nastainczyk-Wulf M, Edelmann J, Kohl M, Nie S, Wang X, Cheng B, Núñez C, Pancorbo MM, Olofsson JK, Morling N, Onofri V, Tagliabracci A, Pamjav H, Volgyi A, Barany G, Pawlowski R, Maciejewska A… See abstract for full author list ➔ Purps J, et al. Among authors: yong ry. Forensic Sci Int Genet. 2014 Sep;12(100):12-23. doi: 10.1016/j.fsigen.2014.04.008. Epub 2014 Apr 28. Forensic Sci Int Genet. 2014. PMID: 24854874 Free PMC article.
Genome-wide association study identifies ZFHX1B as a susceptibility locus for severe myopia.
Khor CC, Miyake M, Chen LJ, Shi Y, Barathi VA, Qiao F, Nakata I, Yamashiro K, Zhou X, Tam PO, Cheng CY, Tai ES, Vithana EN, Aung T, Teo YY, Wong TY, Moriyama M, Ohno-Matsui K, Mochizuki M, Matsuda F; Nagahama Study Group; Yong RY, Yap EP, Yang Z, Pang CP, Saw SM, Yoshimura N. Khor CC, et al. Among authors: yong ry. Hum Mol Genet. 2013 Dec 20;22(25):5288-94. doi: 10.1093/hmg/ddt385. Epub 2013 Aug 9. Hum Mol Genet. 2013. PMID: 23933737
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