Gareth Baynam

11.8k total citations · 1 hit paper
136 papers, 2.4k citations indexed

About

Gareth Baynam is a scholar working on Genetics, Molecular Biology and Pulmonary and Respiratory Medicine. According to data from OpenAlex, Gareth Baynam has authored 136 papers receiving a total of 2.4k indexed citations (citations by other indexed papers that have themselves been cited), including 79 papers in Genetics, 39 papers in Molecular Biology and 17 papers in Pulmonary and Respiratory Medicine. Recurrent topics in Gareth Baynam's work include Genomics and Rare Diseases (51 papers), Genomic variations and chromosomal abnormalities (14 papers) and BRCA gene mutations in cancer (10 papers). Gareth Baynam is often cited by papers focused on Genomics and Rare Diseases (51 papers), Genomic variations and chromosomal abnormalities (14 papers) and BRCA gene mutations in cancer (10 papers). Gareth Baynam collaborates with scholars based in Australia, United States and United Kingdom. Gareth Baynam's co-authors include Hugh Dawkins, Jack Goldblatt, Tudor Groza, Ana Rath, Sebastian Köhler, Chris Mungall, Peter N. Le Souëf, Melissa Haendel, Peter N. Robinson and Nicole Vasilevsky and has published in prestigious journals such as Nature, Cell and Nature Communications.

In The Last Decade

Gareth Baynam

122 papers receiving 2.4k 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.

How many rare diseases are there?

2019 279 citations Gareth Baynam, Tudor Groza et al. profile →

Peers

Gareth Baynam

GENET

MB

PRM

PHEOH

SURGE

Brian H. Shirts United States

Domenica Taruscio Italy

Zornitza Stark Australia

Eimear E. Kenny United States

B.J. Rimel United States

Paul R. Billings United States

Jerry Halpern United States

Gad Abraham Australia

Lee-may Chen United States

Peter Farndon United Kingdom

Brian H. Shirts United States

Gareth Baynam

909 ×0.8

GENET

911 ×1.1

MB

205 ×0.8

PRM

136 ×0.6

PHEOH

177 ×0.8

SURGE

Citations per year, relative to Gareth Baynam Gareth Baynam (= 1×) peers Brian H. Shirts

Countries citing papers authored by Gareth Baynam

Since Specialization

Citations

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

Fields of papers citing papers by Gareth Baynam

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Gareth Baynam

This figure shows the co-authorship network connecting the top 25 collaborators of Gareth Baynam. A scholar is included among the top collaborators of Gareth Baynam 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 Gareth Baynam. Gareth Baynam 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

1.

Baynam, Gareth, et al.. (2025). Rare care – Cross-sector care coordination. European Journal of Medical Genetics. 74. 104995–104995.

2.

Wang, Xiaocong, David A. Pearce, Gareth Baynam, et al.. (2025). Digital health technology use in clinical trials of rare diseases: a systematic review. Communications Medicine. 5(1). 449–449.

3.

Abraham, Mary B., Aris Siafarikas, A. M. Blackmore, et al.. (2025). Septo-optic dysplasia and gastroschisis: trends in birth prevalence and association with maternal age. European Journal of Pediatrics. 184(5). 297–297.

4.

Baynam, Gareth, et al.. (2025). A precision public health approach to improving rare disease diagnosis and care for aboriginal people, the first 15 years. SHILAP Revista de lepidopterología. 3. 100091–100091.

5.

Baynam, Gareth, Adam L. Hartman, Prescilla Carrion, et al.. (2024). Global health for rare diseases through primary care. The Lancet Global Health. 12(7). e1192–e1199. 12 indexed citations

6.

Groza, Tudor, Chun‐Hung Chan, David A. Pearce, & Gareth Baynam. (2024). Realising the potential impact of artificial intelligence for rare diseases – A framework. SHILAP Revista de lepidopterología. 3. 100057–100057.

7.

Hartman, Adam L., Gareth Baynam, Lara Bloom, et al.. (2024). Telehealth for rare disease care, research, and education across the globe: A review of the literature by the IRDiRC telehealth task force. European Journal of Medical Genetics. 72. 104977–104977. 2 indexed citations

8.

Karnebeek, Clara D.M. van, Anne O’Donnell‐Luria, Gareth Baynam, et al.. (2024). Leaving no patient behind! Expert recommendation in the use of innovative technologies for diagnosing rare diseases. Orphanet Journal of Rare Diseases. 19(1). 357–357. 7 indexed citations

9.

Matthews, Harold, Meng Yuan, Giorgos Bouritsas, et al.. (2024). A 3D Clinical Face Phenotype Space of Genetic Syndromes Using a Triplet-Based Singular Geometric Autoencoder. IEEE Access. 13. 7258–7272.

10.

Zammit, Claire, Gareth Baynam, Emma Kowal, et al.. (2024). “Equity” in genomic health policies: a review of policies in the international arena. Frontiers in Public Health. 12. 1464701–1464701. 1 indexed citations

11.

Nevin, Suzanne M., Deepak Gill, Lauren Kelada, et al.. (2023). The psychosocial impact of childhood dementia on children and their parents: a systematic review. Orphanet Journal of Rare Diseases. 18(1). 277–277. 5 indexed citations

12.

Farlow, Ashley, Georgia Tsambos, Gareth Baynam, et al.. (2023). Indigenous Australian genomes show deep structure and rich novel variation. Nature. 624(7992). 593–601. 15 indexed citations

13.

Hansen, Michèle, et al.. (2023). Surfacing undiagnosed disease: consideration, counting and coding. Frontiers in Pediatrics. 11. 1283880–1283880. 3 indexed citations

14.

Matthews, Harold, Michael A. Patton, Peter Hammond, et al.. (2022). Refining nosology by modelling variation among facial phenotypes: the RASopathies. Journal of Medical Genetics. 60(3). 285–293. 2 indexed citations

15.

McKenzie, F. Ellis, Kym Mina, Bert Callewaert, et al.. (2021). Severe congenital cutis laxa: Identification of novel homozygous LOX gene variants in two families. Clinical Genetics. 100(2). 168–175. 1 indexed citations

16.

Koromina, Maria, et al.. (2021). Ethics and Equity in Rare Disease Research and Healthcare. Personalized Medicine. 18(4). 407–416. 1 indexed citations

17.

Junaid, Mohammed, Linda Slack‐Smith, Kingsley Wong, et al.. (2021). Epidemiology of Rare Craniofacial Anomalies: Retrospective Western Australian Population Data Linkage Study. The Journal of Pediatrics. 241. 162–172.e9. 11 indexed citations

18.

Ferdinand, Angeline, Jeromey Temple, Yin Paradies, et al.. (2021). Culturally competent communication in Indigenous disability assessment: a qualitative study. International Journal for Equity in Health. 20(1). 68–68. 7 indexed citations

19.

Baynam, Gareth, Nicholas Pachter, F. Ellis McKenzie, et al.. (2015). AB002. The rare and undiagnosed diseases diagnostic service. Annals of Translational Medicine. 4(2). 3–3.

20.

Baynam, Gareth, Mark R. Davis, Kym Mina, et al.. (2015). A germline MTOR mutation in Aboriginal Australian siblings with intellectual disability, dysmorphism, macrocephaly, and small thoraces. American Journal of Medical Genetics Part A. 167(7). 1659–1667. 31 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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