Gladys Ho

2.4k total citations
43 papers, 1.4k citations indexed

About

Gladys Ho is a scholar working on Genetics, Molecular Biology and Clinical Biochemistry. According to data from OpenAlex, Gladys Ho has authored 43 papers receiving a total of 1.4k indexed citations (citations by other indexed papers that have themselves been cited), including 27 papers in Genetics, 26 papers in Molecular Biology and 9 papers in Clinical Biochemistry. Recurrent topics in Gladys Ho's work include Genetics and Neurodevelopmental Disorders (13 papers), Genomics and Rare Diseases (10 papers) and Metabolism and Genetic Disorders (9 papers). Gladys Ho is often cited by papers focused on Genetics and Neurodevelopmental Disorders (13 papers), Genomics and Rare Diseases (10 papers) and Metabolism and Genetic Disorders (9 papers). Gladys Ho collaborates with scholars based in Australia, United States and France. Gladys Ho's co-authors include John Christodoulou, Helen Leonard, Nicholas de Klerk, Rahul Krishnaraj, Simon Williams, Stephanie Fehr, Jenny Downs, Bruce Bennetts, Katherine Holman and David Forbes and has published in prestigious journals such as The Journal of Experimental Medicine, Neurology and International Journal of Molecular Sciences.

In The Last Decade

Gladys Ho

42 papers receiving 1.3k citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
Gladys Ho Australia	19	855	778	219	172	102	43	1.4k
Katrin Õunap Estonia	25	857 1.0×	1.0k 1.3×	72 0.3×	249 1.4×	76 0.7×	106	1.8k
F. Lucy Raymond United Kingdom	25	727 0.9×	1.0k 1.3×	106 0.5×	183 1.1×	46 0.5×	51	1.8k
Lucia Galli Italy	22	544 0.6×	947 1.2×	203 0.9×	22 0.1×	77 0.8×	57	1.4k
Gregory Costain Canada	23	941 1.1×	1.2k 1.5×	192 0.9×	29 0.2×	93 0.9×	71	1.9k
Victoria Mok Siu Canada	25	868 1.0×	1.3k 1.6×	97 0.4×	44 0.3×	28 0.3×	73	1.9k
Emmanuelle Lemyre Canada	22	879 1.0×	550 0.7×	55 0.3×	45 0.3×	88 0.9×	52	1.3k
Alice Goldenberg France	20	565 0.7×	678 0.9×	50 0.2×	45 0.3×	47 0.5×	49	1.1k
Katherine Lachlan United Kingdom	19	659 0.8×	869 1.1×	122 0.6×	25 0.1×	20 0.2×	45	1.4k
Ahmet Okay Çağlayan Türkiye	18	390 0.5×	482 0.6×	88 0.4×	36 0.2×	38 0.4×	79	1.1k
Julie S. Cohen United States	22	578 0.7×	617 0.8×	76 0.3×	66 0.4×	176 1.7×	44	1.4k

Countries citing papers authored by Gladys Ho

Since Specialization

Citations

This map shows the geographic impact of Gladys Ho'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 Gladys Ho with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Gladys Ho more than expected).

Fields of papers citing papers by Gladys Ho

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Gladys Ho. 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 Gladys Ho. The network helps show where Gladys Ho may publish in the future.

Co-authorship network of co-authors of Gladys Ho

This figure shows the co-authorship network connecting the top 25 collaborators of Gladys Ho. A scholar is included among the top collaborators of Gladys Ho based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Gladys Ho. Gladys Ho is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

Kelada, Lauren, Claire E. Wakefield, David Armstrong, et al.. (2022). Genomic testing for children with interstitial and diffuse lung disease (chILD): parent satisfaction, understanding and health-related quality of life. BMJ Open Respiratory Research. 9(1). e001139–e001139. 2 indexed citations

Nash, Benjamin M., Alan Ma, Gladys Ho, et al.. (2022). Whole Genome Sequencing, Focused Assays and Functional Studies Increasing Understanding in Cryptic Inherited Retinal Dystrophies. International Journal of Molecular Sciences. 23(7). 3905–3905. 7 indexed citations

Selvanathan, Arthavan, et al.. (2022). A narrative review of metabolomics in the era of “-omics”: integration into clinical practice for inborn errors of metabolism. Translational Pediatrics. 11(10). 1704–1716. 13 indexed citations

Archibald, Alison D., David Francis, Ling Ling, et al.. (2021). Paternal retraction of a fragile X allele to normal size, showing normal function over two generations. American Journal of Medical Genetics Part A. 188(1). 304–309. 1 indexed citations

Holman, Katherine, Gladys Ho, Elizabeth Farnsworth, et al.. (2021). Australia and New Zealand renal gene panel testing in routine clinical practice of 542 families. npj Genomic Medicine. 6(1). 20–20. 15 indexed citations

Ho, Gladys, Bruce Bennetts, Adviye Ayper Tolun, et al.. (2021). Challenges in Diagnosing Intermediate Maple Syrup Urine Disease by Newborn Screening and Functional Validation of Genomic Results Imperative for Reproductive Family Planning. International Journal of Neonatal Screening. 7(2). 25–25. 8 indexed citations

Chan, Denise, Joëlle Rudinger‐Thirion, Magali Frugier, et al.. (2021). A case of QARS1 associated epileptic encephalopathy and review of epilepsy in aminoacyl-tRNA synthetase disorders. Brain and Development. 44(2). 142–147. 5 indexed citations

Jones, Hannah, Gladys Ho, Velda X. Han, et al.. (2021). Autosomal dominant ADAR c.3019G>A (p.(G1007R)) variant is an important mimic of hereditary spastic paraplegia and cerebral palsy. Brain and Development. 44(2). 153–160. 7 indexed citations

Bergen, Nicole J. Van, Syed Mukhtar Ahmed, Felicity Collins, et al.. (2020). Mutations in the exocyst component EXOC2 cause severe defects in human brain development. The Journal of Experimental Medicine. 217(10). 19 indexed citations

10.

Mallett, Andrew J., Catherine Quinlan, Chirag Patel, et al.. (2019). Precision Medicine Diagnostics for Rare Kidney Disease: Twitter as a Tool in Clinical Genomic Translation. Kidney Medicine. 1(5). 315–318. 5 indexed citations

11.

Hudson, Rebecca, Chirag Patel, Carmel M. Hawley, et al.. (2019). Adult-Diagnosed Nonsyndromic Nephronophthisis in Australian Families Caused by Biallelic NPHP4 Variants. American Journal of Kidney Diseases. 76(2). 282–287. 5 indexed citations

12.

Forbes, Thomas, Sara E. Howden, Kynan T. Lawlor, et al.. (2018). Patient-iPSC-Derived Kidney Organoids Show Functional Validation of a Ciliopathic Renal Phenotype and Reveal Underlying Pathogenetic Mechanisms. The American Journal of Human Genetics. 102(5). 816–831. 155 indexed citations

13.

Mallett, Andrew J., Hugh J. McCarthy, Gladys Ho, et al.. (2017). Massively parallel sequencing and targeted exomes in familial kidney disease can diagnose underlying genetic disorders. Kidney International. 92(6). 1493–1506. 57 indexed citations

14.

Mallett, Andrew J., Dylan Mordaunt, A M Walker, et al.. (2015). Rmnd1 Mutations Are Associated with Autosomal Recessive Syndromic Nephropathy. Nephrology. 20. 42–42. 1 indexed citations

15.

Ho, Gladys, Ian E. Alexander, Kaustuv Bhattacharya, et al.. (2013). The Molecular Bases of Phenylketonuria (PKU) in New South Wales, Australia: Mutation Profile and Correlation with Tetrahydrobiopterin (BH4) Responsiveness. JIMD Reports. 14. 55–65. 11 indexed citations

16.

Georgiou, Theodoros, et al.. (2012). The spectrum of mutations identified in Cypriot patients with phenylalanine hydroxylase deficiency detected through neonatal screening. Clinical Biochemistry. 45(7-8). 588–592. 6 indexed citations

17.

Ellaway, Carolyn, Gladys Ho, Elisa Bettella, et al.. (2012). 14q12 microdeletions excluding FOXG1 give rise to a congenital variant Rett syndrome-like phenotype. European Journal of Human Genetics. 21(5). 522–527. 44 indexed citations

18.

White, Rose, Gladys Ho, Ingrid E. Scheffer, et al.. (2010). Cyclin-Dependent Kinase-Like 5 (CDKL5) Mutation Screening in Rett Syndrome and Related Disorders. Twin Research and Human Genetics. 13(2). 168–178. 27 indexed citations

19.

Bebbington, Ami, Alan K. Percy, John Christodoulou, et al.. (2009). Updating the profile of C-terminal MECP2 deletions in Rett syndrome. Journal of Medical Genetics. 47(4). 242–248. 54 indexed citations

20.

Chiong, Mary Anne D., Keow Giak Sim, Kevin Carpenter, et al.. (2007). Transient multiple acyl-CoA dehydrogenation deficiency in a newborn female caused by maternal riboflavin deficiency. Molecular Genetics and Metabolism. 92(1-2). 109–114. 33 indexed citations

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.

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