FIND

researchers

DISCOVER

relevant articles

PROMOTE

your research

now for free

Ivy Ng

Research Profile

Geographic Areas

Singapore

Disorders

Chemicals & Drugs

Procedures

Genes & Molecular Sequences

Alleles

Concepts & Ideas

Physiology

Living Beings

Asian Continental Ancestry Group

Co-author Network

Publications

TOP 3
Maggie S Brett; Angeline Lai; Zhihui Li; Eileen C P Lim; Ivy S L Ng; Min Hwee Yong; Ene-Choo Tan
De novo 3q22.1 q24 deletion associated with multiple congenital anomalies, growth retardation and intellectual disability.
Saumya Shekhar Jamuar; Angeline Hwei Meeng Lai; Ah Moy Tan; Ee Shien Tan; Mei-Yoke Chan; Ivy S L Ng
Use of deferiprone for iron chelation in patients with transfusion-dependent thalassaemia.
Dollyn Liying Quek; Yen-Yek Ng; Wen Wang; Arnold S C Tan; Guek-Im Tang-Lim; Ivy S L Ng; Hai-Yang Law; Samuel S Chong
Rapid carrier screening for beta-thalassemia by single-step allele-specific PCR and detection.

Register for free to view:

Visualized networks:

See your personal network in
sophisticated graphical views

GeoTargeted Searches:

Locate experts around the world
and connect with global collaborators

Research Profiles:

See the research activity
of experts around the globe

Geonetwork of Ivy Ng (preview)

Cities where this author has publications
Cities where co-authors of this author have publications

Flash Player Required

All Publications

2013: Maggie S Brett; Angeline Lai; Zhihui Li; Eileen C P Lim; Ivy S L Ng; Min Hwee Yong; Ene-Choo Tan
De novo 3q22.1 q24 deletion associated with multiple congenital anomalies, growth retardation and intellectual disability.
Gene 2013;517(1):82-8.
2011: Saumya Shekhar Jamuar; Angeline Hwei Meeng Lai; Ah Moy Tan; Ee Shien Tan; Mei-Yoke Chan; Ivy S L Ng
Use of deferiprone for iron chelation in patients with transfusion-dependent thalassaemia.
Journal of paediatrics and child health 2011;47(11):812-7.
2007: Dollyn Liying Quek; Yen-Yek Ng; Wen Wang; Arnold S C Tan; Guek-Im Tang-Lim; Ivy S L Ng; Hai-Yang Law; Samuel S Chong
Rapid carrier screening for beta-thalassemia by single-step allele-specific PCR and detection.
Clinical biochemistry 2007;40(5-6):427-30.
2006: Youyou Zhou; Kun Tang; Hai-Yang Law; Ivy S L Ng; Caroline G L Lee; Samuel S Chong
FMR1 CGG repeat patterns and flanking haplotypes in three Asian populations and their relationship with repeat instability.
Annals of human genetics 2006;70(Pt 6):784-96.
2006: Terri H beaty; Jacqueline B Hetmanski; MARGARET D FALLIN; Ji Wan Park; J W Sull; Iain McIntosh; Kung-Yee Liang; Craig VanderKolk; Richard Redett; Simeon Boyd; Ethylin Jabs; Samuel S Chong; F S H Cheah; Yah-Huei Wu Chou; Philip K T Chen; Yen-Feng Chiu; Vincent K L Yeow; Ivy S L Ng; J Cheng; Shau-Ku Huang; X Ye; Hong Wang; Roxann G Ingersoll; Alan F Scott
Analysis of candidate genes on chromosome 2 in oral cleft case-parent trios from three populations.
Human genetics 2006;120(4):501-18.
2006: S W Lim; Yi Zhao; Eva Chua; Hai-Yang Law; Yih Yuen; Ratnagopal Pavanni; Meng-Cheong Wong; Ivy S L Ng; CS Yoon; Kim-Yoong Puong; S H Lim; Eng-King Tan
Genetic analysis of SCA2, 3 and 17 in idiopathic Parkinson's disease.
Neuroscience letters 2006;403(1-2):11-4.
2006: Hai-Yang Law; Hong-Yuan Luo; Wen Wang; Julia F V Ho; Hossein Najmabadi; Ivy S L Ng; Martin H Steinberg; David H K Chui; Samuel S Chong
Determining the cause of patchwork HBA1 and HBA2 genes: recurrent gene conversion or crossing over fixation events.
Haematologica 2006;91(3):297-302.
2005: Eng-King Tan; Yi Zhao; Kim-Yoong Puong; Hai-Yang Law; Ling-Ling Chan; Kenneth Yew; Hui Shen; Vandana R Chandran; Yih Yuen; Ratnagopal Pavanni; Meng-Cheong Wong; Ivy S L Ng
Expanded FMR1 alleles are rare in idiopathic Parkinson's disease.
Neurogenetics 2005;6(1):51-2.
2005: A H M Lai; E S Tan; Hai-Yang Law; CS Yoon; Ivy S L Ng
SMN1 deletions among singaporean patients with spinal muscular atrophy.
Annals of the Academy of Medicine, Singapore 2005;34(1):73-7.
2004: Eng-King Tan; Yi Zhao; Kim-Yoong Puong; Hai-Yang Law; Ling-Ling Chan; Kenneth Yew; Christopher Tan; Hui Shen; Vandana R Chandran; Mei-Lin Teoh; Yuan Yih; Ratnagopal Pavanni; Meng-Cheong Wong; Ivy S L Ng
Fragile X premutation alleles in SCA, ET, and parkinsonism in an Asian cohort.
Neurology 2004;63(2):362-3.
2004: Chunming Ding; Rossa W K Chiu; tze lau; Tse N Leung; Li C Chan; Amy Y Y Chan; Pimlak Charoenkwan; Ivy S L Ng; Hai-Yang Law; Edmond S K Ma; Xiangmin Xu; Chanane Wanapirak; Torpong Sanguansermsri; Can Liao; Mary Anne Tan Jin Ai; David H K Chui; Charles R Cantor; Y M Dennis Lo
MS analysis of single-nucleotide differences in circulating nucleic acids: Application to noninvasive prenatal diagnosis.
Proceedings of the National Academy of Sciences of the United States of America 2004;101(29):10762-7.
2004: Y Zhou; Hai-Yang Law; Corinne D Boehm; CS Yoon; Garry R Cutting; Ivy S L Ng; Samuel S Chong
Robust fragile X (CGG)n genotype classification using a methylation specific triple PCR assay.
Journal of medical genetics 2004;41(4):e45.
2003: Hai-Yang Law; M K L Chee; G P Tan; Ivy S L Ng
The simultaneous presence of alpha- and beta-thalassaemia alleles: a pitfall of thalassaemia screening.
Community genetics 2003;6(1):14-21.
2001: Hai-Yang Law; Ivy S L Ng; CS Yoon; Y Zhao; Meng-Cheong Wong
Trinucleotide repeat analysis of Huntington's disease gene in Singapore.
Annals of the Academy of Medicine, Singapore 2001;30(2):122-7.
2000: Gay Hui Ho; B H Phang; Ivy S L Ng; Hai-Yang Law; Khee Chee Soo; Erg-Hen Ng
Novel germline BRCA1 mutations detected in women in singapore who developed breast carcinoma before the age of 36 years.
Cancer 2000;89(4):811-6.
2000: B S Tan; Hai-Yang Law; Y Zhao; CS Yoon; Ivy S L Ng
DNA testing for fragile X syndrome in 255 males from special schools in Singapore.
Annals of the Academy of Medicine, Singapore 2000;29(2):207-12.
1997: S H Teo; DK Chan; MH Yong; Ivy S L Ng; K Y Wong; LA Knight; Lai Yun Ho
Williams syndrome--the Singapore General Hospital experience.
Annals of the Academy of Medicine, Singapore 1997;26(3):360-4.
1997: K F Cheong; LA Knight; M Tan; Ivy S L Ng
Variants of chromosome 9 in phenotypically normal individuals.
Annals of the Academy of Medicine, Singapore 1997;26(3):312-4.
1996: Ivy S L Ng; J B Ong; C L Tan; H Y Law
Early prenatal diagnosis of beta-thalassaemia in Singapore.
Annals of the Academy of Medicine, Singapore 1996;25(6):779-82.
1996: LA Knight; MH Yong; M Tan; Ivy S L Ng
Subtle translocation (18;21) confirmed by FISH in a patient with Down syndrome.
Clinical genetics 1996;50(5):430-2.
1996: Meow-Keong Thong; H Y Law; Ivy S L Ng
Molecular heterogeneity of beta-thalassaemia in Malaysia: a practical approach to diagnosis.
Annals of the Academy of Medicine, Singapore 1996;25(1):79-83.
1995: LA Knight; MH Yong; M Tan; Ivy S L Ng
Del(3) (p25.3) without phenotypic effect.
Journal of medical genetics 1995;32(12):994-5.
1994: Ivy S L Ng; J B Ong; C L Tan; H Y Law
Beta-thalassemia mutations in Singapore--a strategy for prenatal diagnosis.
Human genetics 1994;94(4):385-8.
1993: Meng-Cheong Wong; Ivy S L Ng; Swee Han Lim
Huntington's disease in five siblings.
Annals of the Academy of Medicine, Singapore 1993;22(3 Suppl):428-30.
1993: Meng-Cheong Wong; Ivy S L Ng
Huntington's disease: recent progress in gene mapping and potential local application in Singapore.
Annals of the Academy of Medicine, Singapore 1993;22(3 Suppl):534-6.