Simultaneous Screening of the FRAXA and FRAXE Loci for Rapid Detection of FMR1 CGG and/or AFF2 CCG Repeat Expansions by Triplet-Primed PCR
Liu, Timing, Wang, Furene S., Cheah, Felicia S.H., Gu, Yanghong, Shaw, Marie, Law, Hai-Yang, Tay, Stacey K.H., Lee, Caroline G., Nelson, David L., Gecz, Jozef, Chong, Samuel S.
Published in The Journal of molecular diagnostics : JMD (01.08.2021)
Published in The Journal of molecular diagnostics : JMD (01.08.2021)
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Identification of novel microsatellite markers <1 Mb from the HBB gene and development of a single‐tube pentadecaplex PCR panel of highly polymorphic markers for preimplantation genetic diagnosis of beta‐thalassemia
Chen, Min, Tan, Arnold S. C, Cheah, Felicia S. H, Saw, Eugene E. L, Chong, Samuel S
Published in Electrophoresis (01.12.2015)
Published in Electrophoresis (01.12.2015)
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BMP4 was associated with NSCL/P in an Asian population
Chen, Qianqian, Wang, Hong, Hetmanski, Jacqueline B, Zhang, Tianxiao, Ruczinski, Ingo, Schwender, Holger, Liang, Kung Yee, Fallin, M Daniele, Redett, Richard J, Raymond, Gerald V, Wu Chou, Yah-Huei, Chen, Philip Kuo-Ting, Yeow, Vincent, Chong, Samuel S, Cheah, Felicia S H, Jabs, Ethylin Wang, Scott, Alan F, Beaty, Terri H
Published in PloS one (13.04.2012)
Published in PloS one (13.04.2012)
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Identification of Novel Microsatellite Markers Flanking the SMN1 and SMN2 Duplicated Region and Inclusion Into a Single-Tube Tridecaplex Panel for Haplotype-Based Preimplantation Genetic Testing of Spinal Muscular Atrophy
Zhao, Mingjue, Lian, Mulias, Cheah, Felicia S.H., Tan, Arnold S.C., Agarwal, Anupriya, Chong, Samuel S.
Published in Frontiers in genetics (06.11.2019)
Published in Frontiers in genetics (06.11.2019)
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Journal Article
FMR1 CGG repeat expansion mutation detection and linked haplotype analysis for reliable and accurate preimplantation genetic diagnosis of fragile X syndrome
Rajan-Babu, Indhu-Shree, Lian, Mulias, Cheah, Felicia S.H., Chen, Min, Tan, Arnold S.C., Prasath, Ethiraj B., Loh, Seong Feei, Chong, Samuel S.
Published in Expert reviews in molecular medicine (19.07.2017)
Published in Expert reviews in molecular medicine (19.07.2017)
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Germline transgenesis of zebrafish using the medaka Tol1 transposon system
Koga, Akihiko, Cheah, Felicia S.H., Hamaguchi, Satoshi, Yeo, Gare Hoon, Chong, Samuel S.
Published in Developmental dynamics (01.09.2008)
Published in Developmental dynamics (01.09.2008)
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Rapid and reliable preimplantation genetic diagnosis of common hemoglobin Bart's hydrops fetalis syndrome and hemoglobin H disease determinants using an enhanced single‐tube decaplex polymerase chain reaction assay
Chen, Min, Loh, Seong Feei, Yu, Su Ling, Nair, Suresh, Tan, Heng Hao, Nadarajah, Sadhana, Wong, Peng‐Cheang, Ng, Soon Chye, Prasath, Ethiraj B., Tan, Arnold S.C., Cheah, Felicia S.H., Saw, Eugene E.L., Chong, Samuel S.
Published in American journal of hematology (01.09.2015)
Published in American journal of hematology (01.09.2015)
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Journal Article
Phylogenetic and evolutionary relationships and developmental expression patterns of the zebrafish twist gene family
Yeo, Gare Hoon, Cheah, Felicia S. H, Winkler, Christoph, Jabs, Ethylin Wang, Venkatesh, Byrappa, Chong, Samuel S
Published in Development genes and evolution (01.06.2009)
Published in Development genes and evolution (01.06.2009)
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Journal Article
Single-tube nonaplex microsatellite PCR panel for preimplantation genetic diagnosis of Hb Bart's hydrops fetalis syndrome
Chen, Min, Chan, Jerry K. Y., Nadarajah, Sadhana, Tan, Arnold S. C., Chan, Melinda L. H., Mathew, Joyce, Saw, Eugene E. L., Lim, Cheryl, Wong, Wendy, Cheah, Felicia S. H., Law, Hai-Yang, Wong, Peng-Cheang, Chong, Samuel S.
Published in Prenatal diagnosis (01.06.2015)
Published in Prenatal diagnosis (01.06.2015)
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Fetal polymorphisms at the ABCB1-transporter gene locus are associated with susceptibility to non-syndromic oral cleft malformations
Omoumi, Ardeshir, Wang, Zihua, Yeow, Vincent, Wu-Chou, Yah-Huei, Chen, Philip K, Ruczinski, Ingo, Cheng, Joanne, Cheah, Felicia S H, Lee, Caroline G, Beaty, Terri H, Chong, Samuel S
Published in European journal of human genetics : EJHG (01.12.2013)
Published in European journal of human genetics : EJHG (01.12.2013)
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Journal Article
The FGF and FGFR Gene Family and Risk of Cleft Lip with or Without Cleft Palate
Wang, Hong, Zhang, Tianxiao, Wu, Tao, Hetmanski, Jacqueline B., Ruczinski, Ingo, Schwender, Holger, Yee Liang, Kung, Murray, Tanda, Daniele Fallin, M., Redett, Richard J., Raymond, Gerald V., Jin, Sheng-Chih, Wu Chou, Yah-Huei, Kuo-Ting Chen, Philip, Yeow, Vincent, Chong, Samuel S., Cheah, Felicia S.H., Ha Jee, Sun, Jabs, Ethylin W., Scott, Alan F., Beaty, Terri H.
Published in The Cleft palate-craniofacial journal (01.01.2013)
Published in The Cleft palate-craniofacial journal (01.01.2013)
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Zebrafish twist1 is expressed in craniofacial, vertebral, and renal precursors
Yeo, Gare-Hoon, Cheah, Felicia S. H, Jabs, Ethylin Wang, Chong, Samuel S
Published in Development genes and evolution (01.12.2007)
Published in Development genes and evolution (01.12.2007)
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Genomic, cDNA, and embryonic expression analysis of zebrafish transforming growth factor beta 3 (tgfβ3)
Cheah, Felicia S.H., Jabs, Ethylin Wang, Chong, Samuel S.
Published in Developmental dynamics (01.04.2005)
Published in Developmental dynamics (01.04.2005)
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Journal Article
Robust Preimplantation Genetic Testing of Huntington Disease by Combined Triplet-Primed PCR Analysis of the HTT CAG Repeat and Multi-Microsatellite Haplotyping
Zhao, Mingjue, Cheah, Felicia Siew Hong, Tan, Arnold Sia Chye, Lian, Mulias, Phang, Gui Ping, Agarwal, Anupriya, Chong, Samuel S.
Published in Scientific reports (11.11.2019)
Published in Scientific reports (11.11.2019)
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Journal Article
ROR2 gene is associated with risk of non-syndromic cleft palate in an Asian population
Wang, Hong, Hetmanski, Jacqueline B, Ruczinski, Ingo, Liang, Kung Yee, Fallin, M Daniele, Redett, Richard J, Raymond, Gerald V, Chou, Yah-Huei Wu, Chen, Philip Kuo-Ting, Yeow, Vincent, Chong, Samuel S, Cheah, Felicia Sh, Jabs, Ethylin Wang, Scott, Alan F, Beaty, Terri H
Published in Chinese medical journal (01.02.2012)
Published in Chinese medical journal (01.02.2012)
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Differential parental transmission of markers in RUNX2 among cleft case-parent trios from four populations
Sull, Jae Woong, Liang, Kung-Yee, Hetmanski, Jacqueline B., Fallin, Margaret Daniele, Ingersoll, Roxann G., Park, Jiwan, Wu-Chou, Yah-Huei, Chen, Philip K., Chong, Samuel S., Cheah, Felicia, Yeow, Vincent, Park, Beyoung Yun, Jee, Sun Ha, Jabs, Ethylin Wang, Redett, Richard, Jung, Euiju, Ruczinski, Ingo, Scott, Alan F., Beaty, Terri H.
Published in Genetic epidemiology (01.09.2008)
Published in Genetic epidemiology (01.09.2008)
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Journal Article
tgfβ3 regulation of chondrogenesis and osteogenesis in zebrafish is mediated through formation and survival of a subpopulation of the cranial neural crest
Cheah, Felicia S.H., Winkler, Christoph, Jabs, Ethylin Wang, Chong, Samuel S.
Published in Mechanisms of development (01.07.2010)
Published in Mechanisms of development (01.07.2010)
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Journal Article
Robust PGT-M of Huntington disease combining triplet-primed PCR of the HTT CAG repeat with multi-microsatellite haplotyping
Zhao, Mingjue, Cheah, Felicia S.H., Tan, Arnold S.C., Agarwal, Anupriya, Chong, Samuel S.
Published in Reproductive biomedicine online (01.04.2019)
Published in Reproductive biomedicine online (01.04.2019)
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Journal Article
Evidence for gene‐environment interaction in a genome wide study of nonsyndromic cleft palate
Beaty, Terri H., Ruczinski, Ingo, Murray, Jeffrey C., Marazita, Mary L., Munger, Ronald G., Hetmanski, Jacqueline B., Murray, Tanda, Redett, Richard J., Fallin, M. Daniele, Liang, Kung Yee, Wu, Tao, Patel, Poorav J., Jin, Sheng‐Chih, Zhang, Tian Xiao, Schwender, Holger, Wu‐Chou, Yah Huei, Chen, Philip K., Chong, Samuel S., Cheah, Felicia, Yeow, Vincent, Ye, Xiaoqian, Wang, Hong, Huang, Shangzhi, Jabs, Ethylin W., Shi, Bing, Wilcox, Allen J., Lie, Rolv T., Jee, Sun Ha, Christensen, Kaare, Doheny, Kimberley F., Pugh, Elizabeth W., Ling, Hua, Scott, Alan F.
Published in Genetic epidemiology (01.09.2011)
Published in Genetic epidemiology (01.09.2011)
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