Zobrazeno 1 - 10 of 12 pro vyhledávání: '"Chui-Sheun Yoon"'
2
Data from Identification of Novel Breast Cancer Risk Loci
Autor: Ann Siew Gek Lee, Peter Ang, Yoon Sim Yap, Min-Han Tan, Chui Sheun Yoon, Hai Yang Law, Edward Sern Yuen Wong, Geok Ling Koh, Sau Yeen Loke, Prabhakaran Munusamy, Claire Hian Tzer Chan
It has been estimated that >1,000 genetic loci have yet to be identified for breast cancer risk. Here we report the first study utilizing targeted next-generation sequencing to identify single-nucleotide polymorphisms (SNP) associated with breast can
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::340547b99988bf8e5dda0b302da2abd2
https://doi.org/10.1158/0008-5472.c.6508967.v1
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3
Single-Tube Screen for Rapid Detection of Repeat Expansions in Seven Common Spinocerebellar Ataxias
Autor: Mulias Lian, Chanin Limwongse, Chui-Sheun Yoon, Caroline G Lee, Hai-Yang Law, Samuel S Chong
Publikováno v: Clinical Chemistry. 68:794-802
Background The autosomal dominantly inherited and genetically heterogeneous spinocerebellar ataxias (SCAs) exhibit highly similar clinical presentations. Many are caused by repeat expansions, of which at least 8 involve CAG repeats. Repeat expansion
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d772ec003bbbf597f2f85cf3372c7cda
https://doi.org/10.1093/clinchem/hvac011
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4
Rapid Molecular Screen of Spinocerebellar Ataxia Types 1, 2, and 3 by Triplet-Primed PCR and Melting Curve Analysis
Autor: Hai-Yang Law, Mingjue Zhao, Yun Ting Soong, Gui Ping Phang, Samuel S. Chong, Chui-Sheun Yoon, Caroline G.L. Lee, Mulias Lian
Publikováno v: The Journal of molecular diagnostics : JMD. 23(5)
The autosomal dominantly inherited spinocerebellar ataxias (SCAs) can be caused by dynamic mutations of short tandem repeats within various genes. Because of the significant clinical overlap among the various SCA types, molecular screening of multipl
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2faae3202692da7b2442333e3f5735b2
https://pubmed.ncbi.nlm.nih.gov/33618058
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6
Identification of Novel Breast Cancer Risk Loci
Autor: Ann Siew Gek Lee, Geok Ling Koh, Min-Han Tan, Edward Sern Yuen Wong, Prabhakaran Munusamy, Hai-Yang Law, Claire Hian Tzer Chan, Chui Sheun Yoon, Peter Ang, Yoon Sim Yap, Sau Yeen Loke
Publikováno v: Cancer Research. 77:5428-5437
It has been estimated that >1,000 genetic loci have yet to be identified for breast cancer risk. Here we report the first study utilizing targeted next-generation sequencing to identify single-nucleotide polymorphisms (SNP) associated with breast can
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b00bd6c7c535227f45daa5a059af76b8
https://doi.org/10.1158/0008-5472.can-17-0992
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7
Evaluation of Nanofluidics Technology for High-Throughput SNP Genotyping in a Clinical Setting
Autor: Maurice Chan, Mei Wen Chan, Ting Wei Loh, Hai Yang Law, Chui Sheun Yoon, Sint Sint Than, Jia Mei Chua, Chow Yin Wong, Wei Sean Yong, Yoon Sim Yap, Gay Hui Ho, Peter Ang, Ann Siew Gek Lee
Publikováno v: The Journal of Molecular Diagnostics. 13:305-312
The current need for high-throughput genotyping platforms for targeted validation of disease-associated single nucleotide polymorphisms (SNPs) motivated us to evaluate a novel nanofluidics platform for genotyping DNA extracted from peripheral blood a
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ed474b375a15385f46acbc01bcdd2855
https://doi.org/10.1016/j.jmoldx.2010.12.001
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8
Simplified strategy for rapid first-line screening of fragile X syndrome: closed-tube triplet-primed PCR and amplicon melt peak analysis
Autor: Hai-Yang Law, Indhu-Shree Rajan-Babu, Caroline G.L. Lee, Samuel S. Chong, Chui-Sheun Yoon
Publikováno v: Expert Reviews in Molecular Medicine
Premutation and full-mutation hyperexpansion of CGG-triplets in the X-linkedFragile X Mental Retardation 1(FMR1) gene have been implicated in fragile X-associated tremor/ataxia syndrome, fragile X-associated primary ovarian insufficiency, and fragile
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f28258436b01a50f64a331a91997e796
https://doi.org/10.1017/erm.2015.5
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10
Association of common genetic variants with breast cancer risk and clinicopathological characteristics in a Chinese population
Autor: Chow Yin Wong, Chung Lie Oey, Ann Siew Gek Lee, Puay Hoon Tan, Chui Sheun Yoon, Huihua Li, Nan Soon Wong, Yoon Sim Yap, Kong Wee Ong, C. S. Liaw, G. H. Ho, Hai-Yang Law, Preetha Madhukumar, Peter Ang, Wei Sean Yong, Raymond Ng, Maurice Chan, S. M. Ji
Publikováno v: Breast cancer research and treatment. 136(1)
Genome-wide association studies (GWAS) have identified various genetic susceptibility loci for breast cancer based mainly on European-ancestry populations. Differing linkage disequilibrium patterns exist between European and Asian populations, and th
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::941a8d28e18cb9f74370e7f9a31d694c
https://pubmed.ncbi.nlm.nih.gov/22965832
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