Ella Wilkins

1.9k total citations
7 papers, 128 citations indexed

About

Ella Wilkins is a scholar working on Genetics, Nephrology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Ella Wilkins has authored 7 papers receiving a total of 128 indexed citations (citations by other indexed papers that have themselves been cited), including 3 papers in Genetics, 2 papers in Nephrology and 2 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Ella Wilkins's work include Genomics and Rare Diseases (2 papers), Genomic variations and chromosomal abnormalities (2 papers) and Renal Diseases and Glomerulopathies (2 papers). Ella Wilkins is often cited by papers focused on Genomics and Rare Diseases (2 papers), Genomic variations and chromosomal abnormalities (2 papers) and Renal Diseases and Glomerulopathies (2 papers). Ella Wilkins collaborates with scholars based in Australia, United Kingdom and New Zealand. Ella Wilkins's co-authors include Susan M. White, Margaret Sahhar, Alison D. Archibald, Anneke van der Walt, Justin P. Rubio, Helmut Butzkueven, Ingrid van der Mei, Melanie Bahlo, Matthew A. Brown and Bruce Taylor and has published in prestigious journals such as PLoS ONE, Parkinsonism & Related Disorders and Pediatric Nephrology.

In The Last Decade

Ella Wilkins

7 papers receiving 116 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Ella Wilkins Australia	6	69	36	24	23	17	7	128
Anne-Marie Van Der Kevie-Kersemaekers Netherlands	7	124 1.8×	10 0.3×	92 3.8×	61 2.7×	5 0.3×	13	212
Sini Kerminen Finland	4	141 2.0×	12 0.3×	39 1.6×	7 0.3×	7 0.4×	7	185
James J. O’Byrne Ireland	8	81 1.2×	13 0.4×	95 4.0×	9 0.4×	7 0.4×	24	174
Hatice Mutlu Albayrak Türkiye	7	41 0.6×	5 0.1×	67 2.8×	31 1.3×	13 0.8×	26	147
Yonit A. Addissie United States	6	66 1.0×	5 0.1×	77 3.2×	17 0.7×	13 0.8×	11	144
Meral Yirmibeş Karaoğuz Türkiye	10	94 1.4×	5 0.1×	35 1.5×	60 2.6×	5 0.3×	36	218
Angelica Rampazzo Italy	10	12 0.2×	18 0.5×	43 1.8×	9 0.4×	78 4.6×	14	241
Aziz Mhanni Canada	6	54 0.8×	5 0.1×	50 2.1×	30 1.3×	7 0.4×	10	102
Amelie T. van der Ven Germany	6	41 0.6×	13 0.4×	103 4.3×	53 2.3×	4 0.2×	9	154
Rena A. Godfrey United States	4	54 0.8×	12 0.3×	30 1.3×	5 0.2×	8 0.5×	8	96

Countries citing papers authored by Ella Wilkins

Since Specialization

Citations

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

Fields of papers citing papers by Ella Wilkins

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ella Wilkins

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

All Works

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7 of 7 papers shown

1.

Kausman, Joshua, et al.. (2025). Cracking the code: an integrated electronic medical record approach to early diagnosis of genetic kidney disease in children with microscopic haematuria. Pediatric Nephrology. 40(7). 2329–2339. 1 indexed citations

2.

Fennell, Andrew, Samuel F. Berkovic, Carolyn Ellaway, et al.. (2022). The diverse pleiotropic effects of spliceosomal protein PUF60: A case series of Verheij syndrome. American Journal of Medical Genetics Part A. 188(12). 3432–3447. 12 indexed citations

3.

Jayasinghe, Kushani, Susan M. White, Peter G. Kerr, et al.. (2019). Isolated proteinuria due to CUBN homozygous mutation – challenging the investigative paradigm. BMC Nephrology. 20(1). 330–330. 12 indexed citations

4.

Brett, Gemma R., Ella Wilkins, Anna Jarmolowicz, et al.. (2018). Genetic Counseling in the Era of Genomics: What's all the Fuss about?. Journal of Genetic Counseling. 27(5). 1010–1021. 11 indexed citations

5.

Wilkins, Ella, Alison D. Archibald, Margaret Sahhar, & Susan M. White. (2016). “It wasn't a disaster or anything”: Parents’ experiences of their child's uncertain chromosomal microarray result. American Journal of Medical Genetics Part A. 170(11). 2895–2904. 42 indexed citations

6.

Wilkins, Ella, Justin P. Rubio, Katya Kotschet, et al.. (2012). A DNA resequencing array for genes involved in Parkinson’s disease. Parkinsonism & Related Disorders. 18(4). 386–390. 9 indexed citations

7.

Jensen, Cathy, Jim Stankovich, Anneke van der Walt, et al.. (2010). Multiple Sclerosis Susceptibility-Associated SNPs Do Not Influence Disease Severity Measures in a Cohort of Australian MS Patients. PLoS ONE. 5(4). e10003–e10003. 41 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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