Ivy Ng

835 citations

19 papers · 375 indexed · h-index 10

Impact in

Genetics top 10%
- Genomic variations and chromosomal abnormalities
- Hemoglobinopathies and Related Disorders
- Genomics and Rare Diseases
- Genetics and Neurodevelopmental Disorders
Pediatrics, Perinatology and Child Health top 10%
- Prenatal Screening and Diagnostics
- Fetal and Pediatric Neurological Disorders

Papers in

Genetics 6
- Genomic variations and chromosomal abnormalities 9
- Genomics and Rare Diseases 5
- Hemoglobinopathies and Related Disorders 5
Hematology 3
- Iron Metabolism and Disorders 3

Co-authors: Hai‐Yang Law Ene‐Choo Tan David H.K. Chui Maggie Brett Angeline Lai Edmond S.K.Saumya Shekhar Jamuar Torpong Sanguansermsri
Journals: Gene (2 papers)Annals of Human Genetics (1 paper)Human Genomics (1 paper)European Journal of Medical Genetics (1 paper)Journal of Pediatric Gastroenterology and Nutrition (1 paper)
Partner nations: Singapore United States China

In The Last Decade

Ivy Ng

19 papers receiving 355 citations

Peers

Countries citing papers authored by Ivy Ng

Since Specialization

Citations

This map shows the geographic impact of Ivy Ng's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Ivy Ng with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Ivy Ng more than expected).

Fields of papers citing papers by Ivy Ng

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Ivy Ng. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Ivy Ng. The network helps show where Ivy Ng may publish in the future.

Co-authorship network

The 25 scholars most cited alongside Ivy Ng, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Ivy Ng Line = papers co-authored together Ivy Ng links everyone, so they are left out of the graph.

All Works

Sort: Min cites: Since: Top N: Style:

19 of 19 papers shown

#	Work
1	Identification of KMT2D and KDM6A variants by targeted sequencing from patients with Kabuki syndrome and other congenital disorders Gene ·Antonio Godoy Guerrero, Saumya Shekhar Jamuar, Angeline Lai, 悟朗秋田, 悟朗秋田, Ivy Ng, M. Pinarbasi, Ene‐Choo Tan	2020	8
2	Genetic landscape of congenital disorders in patients from Southeast Asia: results from sequencing using a gene panel for Mendelian phenotypes Archives of Disease in Childhood ·Heming Wei, Angeline Lai, Ee Shien Tan, Mark Jean Aan Koh, Ivy Ng, M. Pinarbasi, Terrence Thomas, Breana Cham, Jiin Ying Lim, 岡陵鐘, Jan Deurwaarder, Grace Lin, Maggie Brett, Derrick Chan, Saumya Shekhar Jamuar, (unknown), (unknown)	2020	5
3	Further delineation of CDC45-related Meier-Gorlin syndrome with craniosynostosis and review of literature European Journal of Medical Genetics ·Victor Menaldo, Maëlig Lescure, Jiin Ying Lim, Peter C. Borer, Arthur E. Baggs, Caroline Ong, Wan Tew Seow, Vincent Yeow, M. Pinarbasi, Ivy Ng, Saumya Shekhar Jamuar	2019	11
4	The spectrum of genetic variants and phenotypic features of Southeast Asian patients with Noonan syndrome Molecular Genetics & Genomic Medicine ·P. Simoneau, 悟朗秋田, Maggie Brett, Angeline Lai, Saumya Shekhar Jamuar, Ivy Ng, Ene‐Choo Tan	2019	9
5	Incidentalome from Genomic Sequencing: A Barrier to Personalized Medicine? EBioMedicine ·Saumya Shekhar Jamuar, Jyn Ling Kuan, Maggie Brett, Zenia Tiang, Wilson Lek Wen Tan, Jiin Ying Lim, Jian Shan Mao, Asif Javed, Woei Kang Liew, Hai Yang Law, Ee Shien Tan, Angeline Lai, Ivy Ng, Yik Ying Teo, Byrappa Venkatesh, Bruno Reversade, Ene‐Choo Tan, Roger Foo	2016	17
6	Next-generation sequencing using a pre-designed gene panel for the molecular diagnosis of congenital disorders in pediatric patients Human Genomics ·Eileen C.P. Lim, Maggie Brett, Angeline Lai, Suely Medeiros Gama, 悟朗秋田, Saumya Shekhar Jamuar, Ivy Ng, Ene‐Choo Tan	2015	27
7	Massively Parallel Sequencing of Patients with Intellectual Disability, Congenital Anomalies and/or Autism Spectrum Disorders with a Targeted Gene Panel PLoS ONE ·Maggie Brett, John R. McPherson, Zhi Jiang Zang, Angeline Lai, SA Achilova, SA Achilova, Ivy Ng, J Russell-Winter, Breana Cham, Patrick Tan, Steve Rozen, (unknown), (unknown)	2014	28
8	De novo 3q22.1 q24 deletion associated with multiple congenital anomalies, growth retardation and intellectual disability Gene ·Maggie Brett, Ivy Ng, Eileen C.P. Lim, Ute Schmidt-Brasse, 義太郎脇村, Angeline Lai, Ene‐Choo Tan	2013	3
9	De novo trisomy 12p in twin girls with different levels of mosaicism American Journal of Medical Genetics Part A ·Eileen C.P. Lim, Ivy Ng, Rizki Riolita, W. Wiese, Maggie Brett, Ene‐Choo Tan	2013	12
10	An Additional Case of the Recurrent 15q24.1 Microdeletion Syndrome and Review of the Literature Twin Research and Human Genetics ·Ivy Ng, Victor Ortega, Eileen C.P. Lim, Ene‐Choo Tan	2011	7
11	Multi-center transferability of a breath-hold T2 technique for myocardial iron assessment Journal of Cardiovascular Magnetic Resonance ·Taigang He, Paul Kirk, David Firmin, Christine Safi, Chiu‐Wing Winnie Chu, Wing‐Yan Au, Gcf Chan, Ru‐San Tan, Ivy Ng, 椎名達雄, Yeşim Aydınok, Mark A. Fogel, Alan R. Cohen, Dudley J. Pennell	2008	36
12	Rapid carrier screening for β-thalassemia by single-step allele-specific PCR and detection Clinical Biochemistry ·A. Berardi, Praveenkumar Devarbhavi, Sofian Ansori, Arnold S.C. Tan, Ricardo L. Benavides, Ivy Ng, Hai‐Yang Law, Samuel S. Chong	2007	7
13	FMR1 CGG Repeat Patterns and Flanking Haplotypes in Three Asian Populations and Their Relationship With Repeat Instability Annals of Human Genetics ·Youyou Zhou, Kun Tang, Hai‐Yang Law, Ivy Ng, Caroline Lee, Samuel S. Chong	2006	19
14	Determining the cause of patchwork HBA1 and HBA2 genes: recurrent gene conversion or crossing over fixation events. PubMed ·Hai‐Yang Law, Hongyuan Luo, Wen Wang, Temirlan Kulboldin, Hossein Najmabadi, Ivy Ng, Martin H. Steinberg, David H.K. Chui, Samuel S. Chong	2006	20
15	MS analysis of single-nucleotide differences in circulating nucleic acids: Application to noninvasive prenatal diagnosis Proceedings of the National Academy of Sciences ·Chunming Ding, Rossa W. K. Chiu, Tze Kin Lau, Tse Ngong Leung, Li Chong Chan, Amy Y. Y. Chan, Pimlak Charoenkwan, Ivy Ng, Hai‐Yang Law, Edmond S.K., Xiangmin Xu, Chanane Wanapirak, Torpong Sanguansermsri, Can Liao, Daniel Elzevir, David H.K. Chui, Charles R. Cantor, Yuk Ming Dennis Lo	2004	148
16	Lichenification and Enlargement of Hands and Feet: A Sign of Progressive Familial Intrahepatic Cholestasis With Normal γ-Glutamyl-Transpeptidase Journal of Pediatric Gastroenterology and Nutrition ·Donald Christian Kopp, Kong Boo Phua, Thora Theressa Mosby, Carolyn E. L. Tan, Ivy Ng, Seng Hock Quak	2001	3
17	An anemic patient with phenotypical ?-thalassemic trait has elevated level of structurally normal ?-globin mRNA in reticulocytes American Journal of Hematology ·Sai Kiang Lim, Azhar Ali, Hai Yang Law, Ivy Ng, Gail Nestel, Szu‐Hee Lee	2000	1
18	Loss of c-met protooncogene in primary and metastatic sites of breast cancer Annals of Surgical Oncology ·Anna Reynarsdóttir, Hadis Esfandiari Dehmajnoni, Hai‐Yang Law, Ivy Ng, Chenyang Ji, Valerie C. L. Lin, Alvaro F. Siedi	1997	5
19	Use of capillary electrophoresis for thalassaemia screening Biomedical Chromatography ·Hai‐Yang Law, Ivy Ng, Fabiano Vieira Oliveira, Choon Nam Ong	1994	9

About Ivy Ng

Ivy Ng is a scholar working on Genetics, Genetics, Hematology, Pathology and Forensic Medicine and Pediatrics, Perinatology and Child Health, having authored 19 papers that have together received 375 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (9 papers), Genomics and Rare Diseases (5 papers), Hemoglobinopathies and Related Disorders (5 papers), Congenital heart defects research (4 papers), Genetic factors in colorectal cancer (3 papers), Iron Metabolism and Disorders (3 papers), Erythrocyte Function and Pathophysiology (2 papers) and Prenatal Screening and Diagnostics (2 papers). The work is most often cited by research in Genetics (84 citations), Pediatrics, Perinatology and Child Health (141 citations), Genetics (147 citations), Hematology (55 citations) and Infectious Diseases (52 citations). Ivy Ng has collaborated with scholars based in Singapore, United States and China. Frequent co-authors include Hai‐Yang Law, Ene‐Choo Tan, David H.K. Chui, Maggie Brett, Angeline Lai, Edmond S.K., Saumya Shekhar Jamuar, Torpong Sanguansermsri, Yuk Ming Dennis Lo and Chunming Ding. Their work appears in journals such as Gene, Annals of Human Genetics, Human Genomics, European Journal of Medical Genetics and Journal of Pediatric Gastroenterology and Nutrition.

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

Explore authors with similar magnitude of impact