Gladys Ho

2.4k citations

43 papers · 1.4k indexed · h-index 19

Co-authors: John Christodoulou Helen Leonard Nicholas de Klerk Rahul Krishnaraj Simon Williams Stephanie Fehr Jenny Downs Bruce Bennetts
Topics: Genetics and Neurodevelopmental Disorders (13 papers)Genomics and Rare Diseases (10 papers)Metabolism and Genetic Disorders (9 papers)
Cited by: Genetics Clinical Biochemistry Cognitive Neuroscience
Journals: The Journal of Experimental Medicine Neurology International Journal of Molecular Sciences
Partner nations: Australia United States France

In The Last Decade

Gladys Ho

42 papers receiving 1.3k citations

Peers

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

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

20 of 20 papers shown

#	Work	Indexed citations
1	Genomic testing for children with interstitial and diffuse lung disease (chILD): parent satisfaction, understanding and health-related quality of life 2022 ·BMJ Open Respiratory Research ·Lauren Kelada,Claire E. Wakefield,(unknown),David Armstrong,Bruce Bennetts,Kirsten Boggs,John Christodoulou,Joanne Harrison,Gladys Ho,Nitin Kapur,(unknown),Tim McDonald,David Mowat,André Schultz,Hiran Selvadurai,Andrew Tai,Adam Jaffé	2
2	Whole Genome Sequencing, Focused Assays and Functional Studies Increasing Understanding in Cryptic Inherited Retinal Dystrophies 2022 ·International Journal of Molecular Sciences ·Benjamin M. Nash,Alan Ma,Gladys Ho,Elizabeth Farnsworth,André E. Minoche,Mark J. Cowley,Christopher Barnett,Janine Smith,(unknown),Karen Wong,Luke St Heaps,Dale Wright,Marcel E. Dinger,Bruce Bennetts,John Grigg,Robyn V. Jamieson	7
3	A narrative review of metabolomics in the era of “-omics”: integration into clinical practice for inborn errors of metabolism 2022 ·Translational Pediatrics ·(unknown),Arthavan Selvanathan,(unknown),Gladys Ho,Kaustuv Bhattacharya,Adviye Ayper Tolun	13
4	Paternal retraction of a fragile X allele to normal size, showing normal function over two generations 2021 ·American Journal of Medical Genetics Part A ·(unknown),Alison D. Archibald,David Francis,Ling Ling,Robert E. Thomas,(unknown),(unknown),(unknown),(unknown),Martin B. Delatycki,Bruce Bennetts,Gladys Ho,(unknown),Emma K. Baker,David J. Amor,David E. Godler	1
5	Australia and New Zealand renal gene panel testing in routine clinical practice of 542 families 2021 ·npj Genomic Medicine ·(unknown),Katherine Holman,Gladys Ho,Elizabeth Farnsworth,(unknown),(unknown),(unknown),(unknown),Rahul Krishnaraj,Tiffany Lai,Karen Wong,Chirag Patel,Amali Mallawaarachchi,Andrew J. Mallett,Bruce Bennetts,Stephen I. Alexander,Hugh J. McCarthy	15
6	Challenges in Diagnosing Intermediate Maple Syrup Urine Disease by Newborn Screening and Functional Validation of Genomic Results Imperative for Reproductive Family Planning 2021 ·International Journal of Neonatal Screening ·(unknown),(unknown),Gladys Ho,Bruce Bennetts,(unknown),(unknown),(unknown),Adviye Ayper Tolun,Veronica Wiley,Janice M. Fletcher,Maria Fuller,Shanti Balasubramaniam	8
7	A case of QARS1 associated epileptic encephalopathy and review of epilepsy in aminoacyl-tRNA synthetase disorders 2021 ·Brain and Development ·Denise Chan,Joëlle Rudinger‐Thirion,Magali Frugier,Lisa G. Riley,Gladys Ho,Kavitha Kothur,Shekeeb S. Mohammad	5
8	Autosomal dominant ADAR c.3019G>A (p.(G1007R)) variant is an important mimic of hereditary spastic paraplegia and cerebral palsy 2021 ·Brain and Development ·Hannah Jones,(unknown),Gladys Ho,(unknown),Velda X. Han,Simon Paget,Kirsty Stewart,(unknown),Kavitha Kothur,Christopher Troedson,Yanick J. Crow,Russell C. Dale,Shekeeb S. Mohammad	7
9	Mutations in the exocyst component EXOC2 cause severe defects in human brain development 2020 ·The Journal of Experimental Medicine ·Nicole J. Van Bergen,Syed Mukhtar Ahmed,Felicity Collins,Mark J. Cowley,Annalisa Vetro,Russell C. Dale,Daniella H. Hock,(unknown),Minal Menezes,(unknown),Gladys Ho,Tiziana Pisano,(unknown),(unknown),David A. Stroud,Marcel E. Dinger,Renzo Guerrini,Ian G. Macara,John Christodoulou	19
10	Precision Medicine Diagnostics for Rare Kidney Disease: Twitter as a Tool in Clinical Genomic Translation 2019 ·Kidney Medicine ·Andrew J. Mallett,Catherine Quinlan,Chirag Patel,Lindsay Fowles,Joanna Crawford,Michael Gattas,Richard Baer,Bruce Bennetts,Gladys Ho,Katherine Holman,Cas Simons	5
11	Adult-Diagnosed Nonsyndromic Nephronophthisis in Australian Families Caused by Biallelic NPHP4 Variants 2019 ·American Journal of Kidney Diseases ·Rebecca Hudson,Chirag Patel,Carmel M. Hawley,(unknown),Paul Snelling,Gladys Ho,Katherine Holman,Bruce Bennetts,Joanna Crawford,(unknown),Cas Simons,Andrew J. Mallett	5
12	Patient-iPSC-Derived Kidney Organoids Show Functional Validation of a Ciliopathic Renal Phenotype and Reveal Underlying Pathogenetic Mechanisms 2018 ·The American Journal of Human Genetics ·Thomas Forbes,Sara E. Howden,Kynan T. Lawlor,Belinda Phipson,Jovana Maksimovic,Lorna J. Hale,Sean B. Wilson,Catherine Quinlan,Gladys Ho,Katherine Holman,Bruce Bennetts,Joanna Crawford,Peter Trnka,Alicia Oshlack,Chirag Patel,Andrew J. Mallett,Cas Simons,Melissa H. Little	155
13	Massively parallel sequencing and targeted exomes in familial kidney disease can diagnose underlying genetic disorders 2017 ·Kidney International ·Andrew J. Mallett,Hugh J. McCarthy,Gladys Ho,Katherine Holman,Elizabeth Farnsworth,Chirag Patel,Jeffery Fletcher,Amali Mallawaarachchi,Catherine Quinlan,Bruce Bennetts,Stephen I. Alexander	57
14	Rmnd1 Mutations Are Associated with Autosomal Recessive Syndromic Nephropathy 2015 ·Nephrology ·Andrew J. Mallett,Dylan Mordaunt,(unknown),A M Walker,(unknown),Heiko Peters,Sierra R. White,Zornitza Stark,Peter Trnka,Chirag Patel,Jackie Crawford,(unknown),Elizabeth Farnsworth,Gladys Ho,S. Alexander,Bruce Bennetts,Helen Healy,Melissa H. Little,Cas Simons,Joy Yaplito‐Lee	1
15	The Molecular Bases of Phenylketonuria (PKU) in New South Wales, Australia: Mutation Profile and Correlation with Tetrahydrobiopterin (BH4) Responsiveness 2013 ·JIMD Reports ·Gladys Ho,Ian E. Alexander,Kaustuv Bhattacharya,(unknown),Carolyn Ellaway,Sue Ann Thompson,Bridget Wilcken,John Christodoulou	11
16	The spectrum of mutations identified in Cypriot patients with phenylalanine hydroxylase deficiency detected through neonatal screening 2012 ·Clinical Biochemistry ·Theodoros Georgiou,Gladys Ho,(unknown),(unknown),(unknown),(unknown),Paola Nicolaides,(unknown),John Christodoulou,Anthi Drousiotou	6
17	14q12 microdeletions excluding FOXG1 give rise to a congenital variant Rett syndrome-like phenotype 2012 ·European Journal of Human Genetics ·Carolyn Ellaway,Gladys Ho,Elisa Bettella,(unknown),Felicity Collins,Anna Hackett,F. Ellis McKenzie,Artur Darmanian,Gregory B. Peters,Kerry Fagan,John Christodoulou	44
18	Cyclin-Dependent Kinase-Like 5 (CDKL5) Mutation Screening in Rett Syndrome and Related Disorders 2010 ·Twin Research and Human Genetics ·Rose White,Gladys Ho,(unknown),Ingrid E. Scheffer,(unknown),Simone C. Yendle,Thierry Bienvenu,Juliette Nectoux,Carolyn Ellaway,Artur Darmanian,(unknown),(unknown),Bruce Bennetts,Veena Kalra,Tod Fullston,Jozef Gécz,Timothy C. Cox,John Christodoulou	27
19	Updating the profile of C-terminal MECP2 deletions in Rett syndrome 2009 ·Journal of Medical Genetics ·Ami Bebbington,Alan K. Percy,John Christodoulou,David Ravine,Gladys Ho,Peter Jacoby,Alison Anderson,M. Pineda,Bruria Ben Zeev,Nadia Bahi‐Buisson,Eric Smeets,Helen Leonard	54
20	Transient multiple acyl-CoA dehydrogenation deficiency in a newborn female caused by maternal riboflavin deficiency 2007 ·Molecular Genetics and Metabolism ·Mary Anne D. Chiong,Keow Giak Sim,Kevin Carpenter,William J. Rhead,Gladys Ho,Rikke Katrine Jentoft Olsen,John Christodoulou	33

About Gladys Ho

Gladys Ho is a scholar working on Clinical Biochemistry, Genetics and Nephrology, having authored 43 papers that have together received 1.4k indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (13 papers), Genomics and Rare Diseases (10 papers) and Metabolism and Genetic Disorders (9 papers). The work is most often cited by research in Genetics (855 citations), Clinical Biochemistry (172 citations) and Cognitive Neuroscience (219 citations). Gladys Ho has collaborated with scholars based in Australia, United States and France. Frequent 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. Their work appears in journals such as The Journal of Experimental Medicine, Neurology and International Journal of Molecular Sciences.

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