Tiong Yang Tan

10.1k citations

69 papers · 2.3k indexed · 1 hit paper · h-index 25

Genetics top 1%
Molecular Biology top 10%
Pediatrics, Perinatology and Child Health top 5%
Cancer Research top 10%
Surgery

Co-authors: Susan M. White Zornitza Stark Peter G. Farlie David J. Amor Stephen F. Kingsmore David Dimmock Lauge Farnaes Michelle M. Clark
Topics: Genomics and Rare Diseases (21 papers)Genomic variations and chromosomal abnormalities (17 papers)Congenital heart defects research (11 papers)
Cited by: Genetics Molecular Biology Cancer Research
Journals: Proceedings of the National Academy of Sciences PLoS ONE Genetics
Partner nations: Australia United States United Kingdom

In The Last Decade

Tiong Yang Tan

67 papers receiving 2.2k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Meta-analysis of the diagnostic and clinical utility of genome and exome sequencing and chromosomal microarray in children with suspected genetic diseases

2018 340 citations Michelle M. Clark, Zornitza Stark et al. npj Genomic Medicine profile →

Peers

Countries citing papers authored by Tiong Yang Tan

Since Specialization

Citations

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

Fields of papers citing papers by Tiong Yang Tan

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Tiong Yang Tan. 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 Tiong Yang Tan. The network helps show where Tiong Yang Tan may publish in the future.

Co-authorship network of co-authors of Tiong Yang Tan

This figure shows the co-authorship network connecting the top 25 collaborators of Tiong Yang Tan. A scholar is included among the top collaborators of Tiong Yang Tan 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 Tiong Yang Tan. Tiong Yang Tan 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

#	Work	Indexed citations
1	Critically unwell infants and children with mitochondrial disorders diagnosed by ultrarapid genomic sequencing 2024 ·Genetics in Medicine ·(unknown),(unknown),Christopher F. Barnett,Mary‐Louise Freckmann,Matthew F. Hunter,Benjamin Kamien,Karin S. Kassahn,Sebastian Lunke,Chirag Patel,Jason Pinner,Tony Roscioli,Sarah A. Sandaradura,Hamish S. Scott,Tiong Yang Tan,(unknown),Alison G. Compton,David R. Thorburn,Zornitza Stark,John Christodoulou	1
2	The diverse pleiotropic effects of spliceosomal protein PUF60: A case series of Verheij syndrome 2022 ·American Journal of Medical Genetics Part A ·Andrew Fennell,(unknown),Samuel F. Berkovic,Carolyn Ellaway,(unknown),Michael S. Hildebrand,Smitha Kumble,(unknown),David Mowat,Gemma Poke,Sulekha Rajagopalan,Brigid M. Regan,Ingrid E. Scheffer,Zornitza Stark,Chloe Stutterd,Tiong Yang Tan,Ella Wilkins,Alison Yeung,Matthew F. Hunter	12
3	Intellectual Functioning of Children With Isolated PRS, PRS-Plus, and Syndromic PRS 2022 ·The Cleft Palate-Craniofacial Journal ·Stephanie Malarbi,(unknown),(unknown),Alice Burnett,Tiong Yang Tan,(unknown),Anastasia Pellicano,(unknown),Andrew A. Heggie,Rod W. Hunt	5
4	The chromatin remodeler ISWI acts during Drosophila development to regulate adult sleep 2021 ·Science Advances ·Naihua N. Gong,(unknown),(unknown),Emilia H. Moscato,Milán Szuperák,Qin Wang,Matthew Jensen,Santhosh Girirajan,Tiong Yang Tan,Matthew A. Deardorff,Dong Li,Yuanquan Song,Matthew S. Kayser	9
5	Parental experiences and genetic counsellor roles in Pierre Robin sequence 2020 ·Journal of Community Genetics ·(unknown),Nicky Kilpatrick,Tiong Yang Tan,(unknown),Laura Forrest	5
6	A head-to-head evaluation of the diagnostic efficacy and costs of trio versus singleton exome sequencing analysis 2019 ·European Journal of Human Genetics ·Tiong Yang Tan,Sebastian Lunke,Belinda Chong,Dean Phelan,Miriam Fanjul‐Fernández,Justine E. Marum,(unknown),Zornitza Stark,Alison Yeung,Natasha J. Brown,Chloe Stutterd,Martin B. Delatycki,Simon Sadedin,Melissa Martyn,Ilias Goranitis,Natalie Thorne,Clara Gaff,Susan M. White	35
7	Early diagnosis of Pearson syndrome in neonatal intensive care following rapid mitochondrial genome sequencing in tandem with exome sequencing 2019 ·European Journal of Human Genetics ·Lauren Akesson,Stefanie Eggers,(unknown),Belinda Chong,Emma Krzesinski,Natasha J. Brown,Tiong Yang Tan,Christopher M. Richmond,David R. Thorburn,John Christodoulou,Matthew F. Hunter,Sebastian Lunke,Zornitza Stark	14
8	Exome sequencing has higher diagnostic yield compared to simulated disease-specific panels in children with suspected monogenic disorders 2018 ·European Journal of Human Genetics ·(unknown),(unknown),Sebastian Lunke,Zornitza Stark,Alison Yeung,Natalie Thorne,Clara Gaff,Susan M. White,Tiong Yang Tan	83
9	Identification of Candidate Genes for Mayer-Rokitansky-Küster-Hauser Syndrome Using Genomic Approaches 2018 ·Sexual Development ·(unknown),(unknown),Gorjana Robevska,Jocelyn van den Bergen,Emanuele Pelosi,Cas Simons,Peter Koopman,Achmad Zulfa Juniarto,Sonia Grover,Sultana MH Faradz,Andrew Sinclair,Katie Ayers,Tiong Yang Tan	29
10	Meta-analysis of the diagnostic and clinical utility of genome and exome sequencing and chromosomal microarray in children with suspected genetic diseasesbreakdown → 2018 ·npj Genomic Medicine ·Michelle M. Clark,Zornitza Stark,Lauge Farnaes,Tiong Yang Tan,Susan M. White,David Dimmock,Stephen F. Kingsmore	340
11	A clinically driven variant prioritization framework outperforms purely computational approaches for the diagnostic analysis of singleton WES data 2017 ·European Journal of Human Genetics ·(unknown),Zornitza Stark,Harriet Dashnow,Sebastian Lunke,Tiong Yang Tan,Alison Yeung,Simon Sadedin,Natalie Thorne,Ivan Macciocca,Clara Gaff,Alicia Oshlack,Susan M. White,Paul A. James	13
12	Frontonasal Dysplasia: Towards an Understanding of Molecular and Developmental Aetiology 2016 ·Molecular Syndromology ·Peter G. Farlie,Naomi L. Baker,Patrick Yap,Tiong Yang Tan	34
13	SNP microarray abnormalities in a cohort of 28 infants with congenital diaphragmatic hernia 2015 ·American Journal of Medical Genetics Part A ·Zornitza Stark,(unknown),Trent Burgess,(unknown),Alison Yeung,Tiong Yang Tan,Natasha J. Brown,Ravi Savarirayan,Neil Patel	18
14	Developmental and genetic perspectives on Pierre Robin sequence 2013 ·American Journal of Medical Genetics Part C Seminars in Medical Genetics ·Tiong Yang Tan,Nicky Kilpatrick,Peter G. Farlie	81
15	Rare syndromes of the head and face—Pierre Robin sequence 2012 ·Wiley Interdisciplinary Reviews Developmental Biology ·Tiong Yang Tan,Peter G. Farlie	11
16	A newborn with a 790 kb chromosome 17p13.3 microduplication presenting with aortic stenosis, microcephaly and dysmorphic facial features – Is cardiac assessment necessary for all patients with 17p13.3 microduplication? 2012 ·European Journal of Medical Genetics ·(unknown),Anthony P. Y. Liu,(unknown),(unknown),Kelvin Y.K. Chan,(unknown),Mary H.Y. Tang,Tiong Yang Tan,Brian Hon‐Yin Chung	10
17	Mutations in the Heparan-Sulfate Proteoglycan Glypican 6 (GPC6) Impair Endochondral Ossification and Cause Recessive Omodysplasia 2009 ·The American Journal of Human Genetics ·Belinda Campos‐Xavier,Danielle Martinet,John F. Bateman,(unknown),Lynn Rowley,Tiong Yang Tan,A Baxová,Karl‐Henrik Gustavson,Zvi Borochowitz,A. Micheil Innes,Sheila Unger,J. Beckmann,Lauréane Mittaz,Diana Ballhausen,Andrea Superti‐Furga,Ravi Savarirayan,Luisa Bonafé	84
18	Biallelic PMS2 Mutations and a Distinctive Childhood Cancer Syndrome 2008 ·Journal of Pediatric Hematology/Oncology ·Tiong Yang Tan,Lisa Orme,Elly Lynch,Matthew Croxford,(unknown),(unknown),Lara Lipton	24
19	Molecular characterization of a novel X‐linked syndrome involving developmental delay and deafness 2007 ·American Journal of Medical Genetics Part A ·Michael S. Hildebrand,M. De Silva,Tiong Yang Tan,Elizabeth Rose,Carla Nishimura,Tanya Tolmachova,Joanne M. Hulett,Susan M. White,Jeremy D. Silver,Melanie Bahlo,Richard J. Smith,Hans‐Henrik M. Dahl	13
20	Tumour surveillance in Beckwith–Wiedemann syndrome and hemihyperplasia: A critical review of the evidence and suggested guidelines for local practice 2006 ·Journal of Paediatrics and Child Health ·Tiong Yang Tan,David J. Amor	86

About Tiong Yang Tan

Tiong Yang Tan is a scholar working on Genetics, Developmental Biology and Urology, having authored 69 papers that have together received 2.3k indexed citations. Recurring topics across this work include Genomics and Rare Diseases (21 papers), Genomic variations and chromosomal abnormalities (17 papers) and Congenital heart defects research (11 papers). The work is most often cited by research in Genetics (1.4k citations), Molecular Biology (1.1k citations) and Cancer Research (204 citations). Tiong Yang Tan has collaborated with scholars based in Australia, United States and United Kingdom. Frequent co-authors include Susan M. White, Zornitza Stark, Peter G. Farlie, David J. Amor, Stephen F. Kingsmore, David Dimmock, Lauge Farnaes, Michelle M. Clark, Christopher T. Gordon and Sebastian Lunke. Their work appears in journals such as Proceedings of the National Academy of Sciences, PLoS ONE and Genetics.

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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