Get started
Author

Ivy Ng

MS analysis of single-nucleotide differences in circulating nucleic acids: Application to noninvasive prenatal diagnosis
2004 · Chunming Ding, Rossa W. K. Chiu, et al. · Proceedings of the National Academy of Sciences · 194
International reproducibility of single breathhold T2* MR for cardiac and liver iron assessment among five thalassemia centers
2010 · Paul Kirk, Taigang He, et al. · Journal of Magnetic Resonance Imaging · 159
PDF
Down syndrome in diverse populations
2016 · Paul Kruszka, Antonio R. Porras, et al. · American Journal of Medical Genetics Part A · 98
Multi-center transferability of a breath-hold T2 technique for myocardial iron assessment
2008 · Taigang He, Paul Kirk, et al. · Journal of Cardiovascular Magnetic Resonance · 47
PDF
Massively Parallel Sequencing of Patients with Intellectual Disability, Congenital Anomalies and/or Autism Spectrum Disorders with a Targeted Gene Panel
2014 · Maggie Brett, John McPherson, et al. · PLoS ONE · 39
PDF
Singapore Undiagnosed Disease Program: Genomic Analysis aids Diagnosis and Clinical Management
2020 · Neha S Bhatia, Jiin Ying Lim, et al. · Archives of Disease in Childhood · 35
De novo trisomy 12p in twin girls with different levels of mosaicism
2013 · Eileen C.P. Lim, Ivy S.L. Ng, et al. · American Journal of Medical Genetics Part A · 34
Next-generation sequencing using a pre-designed gene panel for the molecular diagnosis of congenital disorders in pediatric patients
2015 · Eileen C. P. Lim, Maggie Brett, et al. · Human Genomics · 31
PDF
Determining the cause of patchwork HBA1 and HBA2 genes: recurrent gene conversion or crossing over fixation events.
2006 · Hai-Yang Law, Hong-Yuan Luo, et al. · PubMed · 26
Incidentalome from Genomic Sequencing: A Barrier to Personalized Medicine?
2016 · Saumya Shekhar Jamuar, Jyn Ling Kuan, et al. · EBioMedicine · 25
PDF
Identification of KMT2D and KDM6A variants by targeted sequencing from patients with Kabuki syndrome and other congenital disorders
2020 · Chui-Sun Yap, Saumya Shekhar Jamuar, et al. · Gene · 22
FMR1 CGG Repeat Patterns and Flanking Haplotypes in Three Asian Populations and Their Relationship With Repeat Instability
2006 · Youyou Zhou, Kun Tang, et al. · Annals of Human Genetics · 21
Further delineation of CDC45-related Meier-Gorlin syndrome with craniosynostosis and review of literature
2019 · Chun Yi Ting, Neha Singh Bhatia, et al. · European Journal of Medical Genetics · 19
Genetic landscape of congenital disorders in patients from Southeast Asia: results from sequencing using a gene panel for Mendelian phenotypes
2020 · Heming Wei, Angeline Lai, et al. · Archives of Disease in Childhood · 13
Academic Medicine: Vision to Reality
2013 · Ranga R Krishnan, Ivy Ng · Annals of the Academy of Medicine Singapore · 13
PDF
The spectrum of genetic variants and phenotypic features of Southeast Asian patients with Noonan syndrome
2019 · Ai‐Ling Koh, Ee‐Shien Tan, et al. · Molecular Genetics & Genomic Medicine · 12
PDF
An Additional Case of the Recurrent 15q24.1 Microdeletion Syndrome and Review of the Literature
2011 · Ivy S. L. Ng, Wai-Hoe Chin, et al. · Twin Research and Human Genetics · 12
PDF
Use of capillary electrophoresis for thalassaemia screening
1994 · Hai‐Yang Law, Ivy Ng, et al. · Biomedical Chromatography · 10
Rapid carrier screening for β-thalassemia by single-step allele-specific PCR and detection
2007 · Dollyn Liying Quek, Yen-Yek Ng, et al. · Clinical Biochemistry · 8
De novo 3q22.1 q24 deletion associated with multiple congenital anomalies, growth retardation and intellectual disability
2013 · Maggie S. Brett, Ivy S.L. Ng, et al. · Gene · 6
Loss of c-met protooncogene in primary and metastatic sites of breast cancer
1997 · Eng-Hen Ng, Huey-Bee Pey, et al. · Annals of Surgical Oncology · 6
Lichenification and Enlargement of Hands and Feet: A Sign of Progressive Familial Intrahepatic Cholestasis With Normal γ-Glutamyl-Transpeptidase
2001 · Boo C. Ooi, Kong B. Phua, et al. · Journal of Pediatric Gastroenterology and Nutrition · 4
An anemic patient with phenotypical ?-thalassemic trait has elevated level of structurally normal ?-globin mRNA in reticulocytes
2000 · Sai-Kiang Lim, Azhar bin Ali, et al. · American Journal of Hematology · 2
PDF
Genomic garden: From societal and scientific impacts to biodiversity conservation
2025 · Abner Herbert Lim, Cedric Chuan Young Ng, et al. · Cell Genomics · 1
Postnatal growth and development in patients with sex chromosome aneuploidies excluding Turner syndrome – The Singapore experience
2026 · Jiin Ying Lim, Natalie Yi Ting Koh, et al. · Translational Science of Rare Diseases
PDF
Works count: 33
Citation count: 837
H-index: 13
I10-index: 18
Year
Topic
Type