Meredith Wilson

11.3k total citations
92 papers, 3.3k citations indexed

About

Meredith Wilson is a scholar working on Molecular Biology, Genetics and Geography, Planning and Development. According to data from OpenAlex, Meredith Wilson has authored 92 papers receiving a total of 3.3k indexed citations (citations by other indexed papers that have themselves been cited), including 38 papers in Molecular Biology, 27 papers in Genetics and 16 papers in Geography, Planning and Development. Recurrent topics in Meredith Wilson's work include Pacific and Southeast Asian Studies (13 papers), Genomic variations and chromosomal abnormalities (10 papers) and Congenital gastrointestinal and neural anomalies (9 papers). Meredith Wilson is often cited by papers focused on Pacific and Southeast Asian Studies (13 papers), Genomic variations and chromosomal abnormalities (10 papers) and Congenital gastrointestinal and neural anomalies (9 papers). Meredith Wilson collaborates with scholars based in Australia, United States and United Kingdom. Meredith Wilson's co-authors include David Mowat, Lesley C. Adès, Bronwyn Kerr, Ági K. Gedeon, John Christodoulou, Jennifer E. Mossop, Donald M. Caspary, David R. Moore, John C. Mulley and Florence Dastot‐Le Moal and has published in prestigious journals such as Bioinformatics, Scientific Reports and International Journal of Molecular Sciences.

In The Last Decade

Meredith Wilson

89 papers receiving 3.2k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Meredith Wilson Australia 31 1.6k 1.1k 478 342 266 92 3.3k
Bronwyn Kerr United Kingdom 32 1.6k 1.0× 1.3k 1.2× 480 1.0× 399 1.2× 170 0.6× 67 3.2k
Lina Basel‐Vanagaite Israel 32 1.9k 1.1× 1.4k 1.3× 233 0.5× 497 1.5× 182 0.7× 111 3.6k
Maria Anvret Sweden 39 2.5k 1.5× 1.3k 1.2× 287 0.6× 354 1.0× 191 0.7× 125 4.7k
Vandana Shashi United States 27 1.4k 0.9× 1.3k 1.2× 221 0.5× 230 0.7× 152 0.6× 98 2.9k
Nicholas Lench United Kingdom 36 2.7k 1.7× 1.3k 1.2× 866 1.8× 515 1.5× 204 0.8× 107 5.5k
Damien Sanlaville France 33 1.6k 1.0× 2.2k 2.0× 356 0.7× 585 1.7× 362 1.4× 189 3.7k
Gudrun Nürnberg Germany 44 2.9k 1.8× 1.6k 1.5× 272 0.6× 253 0.7× 280 1.1× 93 5.1k
John Dean United Kingdom 30 1.3k 0.8× 1.4k 1.3× 246 0.5× 575 1.7× 111 0.4× 103 3.5k
Alan Fryer United Kingdom 33 1.5k 0.9× 1.4k 1.3× 338 0.7× 581 1.7× 194 0.7× 103 4.5k
Mitsuko Nakashima Japan 39 2.5k 1.5× 1.6k 1.5× 246 0.5× 203 0.6× 170 0.6× 191 4.4k

Countries citing papers authored by Meredith Wilson

Since Specialization
Citations

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

Fields of papers citing papers by Meredith Wilson

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Meredith Wilson

This figure shows the co-authorship network connecting the top 25 collaborators of Meredith Wilson. A scholar is included among the top collaborators of Meredith Wilson 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 Meredith Wilson. Meredith Wilson is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Tummala, Hemanth, Amanda J. Walne, Roberto Buccafusca, et al.. (2022). Germline thymidylate synthase deficiency impacts nucleotide metabolism and causes dyskeratosis congenita. The American Journal of Human Genetics. 109(8). 1472–1483. 13 indexed citations
2.
Wilson, Meredith, Robert Goetti, Catherine S. Birman, et al.. (2020). A Case Series of X-Linked Deafness-2 with Sensorineural Hearing Loss, Stapes Fixation, and Perilymphatic Gusher: MR Imaging and Clinical Features of Hypothalamic Malformations. American Journal of Neuroradiology. 41(6). 1087–1093. 3 indexed citations
3.
Riley, Lisa G., Joëlle Rudinger‐Thirion, Magali Frugier, et al.. (2020). The expandingLARS2phenotypic spectrum: HLASA, Perrault syndrome with leukodystrophy, and mitochondrial myopathy. Human Mutation. 41(8). 1425–1434. 18 indexed citations
4.
Rossleigh, Monica A., et al.. (2015). DMSA Studies in Infants under One Year of Age. Contributions to nephrology. 79. 166–169.
5.
Bachmann‐Gagescu, Ruxandra, Ian G. Phelps, Jennifer C. Dempsey, et al.. (2015). KIAA0586is Mutated in Joubert Syndrome. Human Mutation. 36(9). 831–835. 52 indexed citations
6.
Hsu, Peter, Alan Ma, Meredith Wilson, et al.. (2014). CHARGE syndrome: A review. Journal of Paediatrics and Child Health. 50(7). 504–511. 120 indexed citations
7.
Elmaleh, Monique, Clarisse Baumann, Vincent Couloigner, et al.. (2012). Spectrum of Temporal Bone Abnormalities in Patients with Waardenburg Syndrome andSOX10Mutations. American Journal of Neuroradiology. 34(6). 1257–1263. 77 indexed citations
8.
Wilson, Meredith, et al.. (2011). Chief Roi Mata's domain: Challenges for a world heritage property in Vanuatu. The Historic Environment Policy & Practice. 23(2). 5–11. 9 indexed citations
9.
Compton, Alison G., Christopher Troedson, Meredith Wilson, et al.. (2010). Application of oligonucleotide array CGH in the detection of a large intragenic deletion in POLG associated with Alpers Syndrome. Mitochondrion. 11(1). 104–107. 11 indexed citations
10.
Blue, Gillian M., Andrew D. Cole, Meredith Wilson, et al.. (2007). The negative impact of Alagille syndrome on survival of infants with pulmonary atresia. Journal of Thoracic and Cardiovascular Surgery. 133(4). 1094–1096. 13 indexed citations
11.
McGaughran, Julie, et al.. (2005). Recurrence of Mowat–Wilson syndrome in siblings with the same proven mutation. American Journal of Medical Genetics Part A. 137A(3). 302–304. 32 indexed citations
12.
Bi, Weimin, Gulam Mustafa Saifi, Christine J. Shaw, et al.. (2004). Mutations of RAI1, a PHD-containing protein, in nondeletion patients with Smith-Magenis syndrome. Human Genetics. 115(6). 515–524. 81 indexed citations
13.
Wilson, Meredith, Matthew Spriggs, & Ewan Lawson. (2001). Dating the rock art of Vanuatu: AMS radiocarbon determinations from abandoned mud-wasp nests and charcoal pigment found in superimposition. ANU Open Research (Australian National University). 8 indexed citations
14.
Bedford, Stuart, Matthew Spriggs, Meredith Wilson, & Ralph Regenvanu. (1998). The Australian National University-National Museum of Vanuatu Archaeology Project: A Preliminary Report on the Establishment of Cultural Sequences and Rock Art Research. Asian perspectives. 37(2). 165–193. 21 indexed citations
15.
Mulley, John C., Kathrin Saar, Franz Rüschendorf, et al.. (1998). Gene Localization for an Autosomal Dominant Familial Periodic Fever to 12p13. The American Journal of Human Genetics. 62(4). 884–889. 63 indexed citations
16.
Sillence, David, et al.. (1995). Early prenatal diagnosis of cartilage‐hair hypoplasia (CHH) with polymorphic DNA markers. Prenatal Diagnosis. 15(2). 135–140. 4 indexed citations
17.
Ogle, Robert, Meredith Wilson, K Kozłowski, & D. Sillence. (1994). Desbuquois syndrome complicated by obstructive sleep apnoea and cervical kyphosis. American Journal of Medical Genetics. 51(3). 216–221. 9 indexed citations
18.
Adès, Lesley C., Ági K. Gedeon, Meredith Wilson, et al.. (1993). Barth syndrome: Clinical features and confirmation of gene localisation to distal Xq28. American Journal of Medical Genetics. 45(3). 327–334. 104 indexed citations
19.
Wilson, Meredith, et al.. (1989). Duplication of 5ql1.2→q13.1 from a familial (5;20) balanced insertion. American Journal of Medical Genetics. 33(2). 220–223. 8 indexed citations
20.
Ahmed, Khalil, et al.. (1976). Action of polyamines on rat ventral prostate chromatin and non histone phosphoprotein (NHP) associated protein phosphokinases (PK). 18(2). 1 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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