Alexa Kidd

2.9k total citations
24 papers, 1.1k citations indexed

About

Alexa Kidd is a scholar working on Molecular Biology, Genetics and Genetics. According to data from OpenAlex, Alexa Kidd has authored 24 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Molecular Biology, 9 papers in Genetics and 6 papers in Genetics. Recurrent topics in Alexa Kidd's work include Neurogenetic and Muscular Disorders Research (5 papers), Genomic variations and chromosomal abnormalities (4 papers) and Muscle Physiology and Disorders (3 papers). Alexa Kidd is often cited by papers focused on Neurogenetic and Muscular Disorders Research (5 papers), Genomic variations and chromosomal abnormalities (4 papers) and Muscle Physiology and Disorders (3 papers). Alexa Kidd collaborates with scholars based in New Zealand, United States and United Kingdom. Alexa Kidd's co-authors include Nora Shannon, John Tolmie, Alberto Plaja, Nazneen Rahman, John Swansbury, Helen V. Firth, Alexandre Irrthum, Sarah Reid, David Fitzpatrick and Jenny Douglas and has published in prestigious journals such as Journal of Biological Chemistry, Nature Genetics and PEDIATRICS.

In The Last Decade

Alexa Kidd

24 papers receiving 1.0k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Alexa Kidd New Zealand 14 663 327 305 177 150 24 1.1k
Monika Goś Poland 19 769 1.2× 331 1.0× 94 0.3× 134 0.8× 91 0.6× 49 1.2k
Matthias Zenkel Germany 27 727 1.1× 227 0.7× 197 0.6× 116 0.7× 95 0.6× 54 2.0k
Kristiina Avela Finland 17 633 1.0× 402 1.2× 66 0.2× 118 0.7× 132 0.9× 34 1.1k
Hayley Spearman United Kingdom 13 376 0.6× 145 0.4× 116 0.4× 95 0.5× 142 0.9× 17 726
Victoria A. Robb United States 12 518 0.8× 121 0.4× 129 0.4× 132 0.7× 85 0.6× 14 872
Elisabeth Castellanos Spain 13 319 0.5× 139 0.4× 188 0.6× 78 0.4× 95 0.6× 26 620
Anas M. Alazami Saudi Arabia 22 857 1.3× 584 1.8× 100 0.3× 79 0.4× 95 0.6× 55 1.5k
Jan Osinga Netherlands 23 754 1.1× 365 1.1× 80 0.3× 342 1.9× 288 1.9× 34 1.5k
Irene Bottillo Italy 18 531 0.8× 253 0.8× 66 0.2× 122 0.7× 74 0.5× 65 1.1k
Jonna Tallila Finland 11 632 1.0× 388 1.2× 57 0.2× 141 0.8× 101 0.7× 18 924

Countries citing papers authored by Alexa Kidd

Since Specialization
Citations

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

Fields of papers citing papers by Alexa Kidd

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Alexa Kidd

This figure shows the co-authorship network connecting the top 25 collaborators of Alexa Kidd. A scholar is included among the top collaborators of Alexa Kidd 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 Alexa Kidd. Alexa Kidd 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.
Stutterd, Chloe, Alexa Kidd, Chris Florkowski, et al.. (2021). Expanding the clinical and radiological phenotypes of leukoencephalopathy due to biallelic HMBS mutations. American Journal of Medical Genetics Part A. 185(10). 2941–2950. 2 indexed citations
2.
Guimier, Anne, Fanny Bajolle, Christian Turner, et al.. (2018). PPA2 gene is involved in neonatal fatal acute dilated cardiomyopathy. Archives of Cardiovascular Diseases Supplements. 11(1). 134–134. 1 indexed citations
3.
Guimier, Anne, Fanny Bajolle, Christian Turner, et al.. (2018). PPA2 gene is involved in neonatal fatal acute dilated cardiomyopathy. Archives of Cardiovascular Diseases Supplements. 10(3-4). 282–282. 2 indexed citations
4.
Rodrigues, Miriam, et al.. (2017). The New Zealand Neuromuscular Disease Patient Registry; Five Years and a Thousand Patients. Journal of Neuromuscular Diseases. 4(3). 183–188. 6 indexed citations
5.
Rodrigues, Miriam, Alexa Kidd, Donald R. Love, & Richard Roxburgh. (2014). The New Zealand Neuromuscular Disease Registry: Rate of diagnoses confirmed by molecular testing. Journal of Clinical Neuroscience. 22(2). 434–436. 3 indexed citations
6.
Tacik, Paweł, Fabienne C. Fiesel, Shinsuke Fujioka, et al.. (2014). Three families with Perry syndrome from distinct parts of the world. Parkinsonism & Related Disorders. 20(8). 884–888. 22 indexed citations
7.
Rodrigues, Miriam, Graeme Hammond-Tooke, Alexa Kidd, et al.. (2012). The New Zealand Neuromuscular Disease Registry. Journal of Clinical Neuroscience. 19(12). 1749–1750. 20 indexed citations
8.
Scurr, Ingrid, Louise C. Wilson, Melissa Lees, et al.. (2011). Cantú syndrome: Report of nine new cases and expansion of the clinical phenotype. American Journal of Medical Genetics Part A. 155(3). 508–518. 54 indexed citations
9.
Christiaans, Imke, Theo A.M. van Os, Frank Baas, et al.. (2010). Germline SMARCB1 mutation and somatic NF2 mutations in familial multiple meningiomas. Journal of Medical Genetics. 48(2). 93–97. 105 indexed citations
10.
Smith, Melissa, et al.. (2010). Diagnosis of distal 22q11.2 deletion syndrome in a patient with a teratoid/rhabdoid tumour. European Journal of Medical Genetics. 54(3). 295–298. 19 indexed citations
11.
Racacho, Lemuel, Louanne Hudgins, Andrea Kwan, et al.. (2009). Brachydactyly A-1 mutations restricted to the central region of the N-terminal active fragment of Indian Hedgehog. European Journal of Human Genetics. 17(9). 1112–1120. 43 indexed citations
12.
Fox, Lisa M., et al.. (2007). Neonatal Hyperparathyroidism and Pamidronate Therapy in an Extremely Premature Infant. PEDIATRICS. 120(5). e1350–e1354. 34 indexed citations
13.
Twigg, Stephen R.F., Kazuya Matsumoto, Alexa Kidd, et al.. (2006). The Origin of EFNB1 Mutations in Craniofrontonasal Syndrome: Frequent Somatic Mosaicism and Explanation of the Paucity of Carrier Males. The American Journal of Human Genetics. 78(6). 999–1010. 73 indexed citations
14.
Morgan, Sonya, et al.. (2004). Genetic testing in New Zealand: the role of the general practitioner.. PubMed. 117(1206). U1178–U1178. 12 indexed citations
15.
White, Susan M., Elizabeth M. Thompson, Alexa Kidd, et al.. (2004). Growth, behavior, and clinical findings in 27 patients with Kabuki (Niikawa–Kuroki) syndrome. American Journal of Medical Genetics Part A. 127A(2). 118–127. 66 indexed citations
16.
Hanks, Sandra, Kim Coleman, Sarah Reid, et al.. (2004). Constitutional aneuploidy and cancer predisposition caused by biallelic mutations in BUB1B. Nature Genetics. 36(11). 1159–1161. 444 indexed citations
17.
McEwen, Alison, et al.. (2004). Occult cancer of the fallopian tube in a BRCA2 germline mutation carrier at prophylactic salpingo-oophorectomy. Gynecologic Oncology. 92(3). 992–994. 12 indexed citations
18.
Viprakasit, Vip, Alexa Kidd, Helena Ayyub, et al.. (2003). De novo deletion within the telomeric region flanking the human α globin locus as a cause of α thalassaemia. British Journal of Haematology. 120(5). 867–875. 26 indexed citations
19.
Stewart, Grant S., James I. Last, Tatjana Stanković, et al.. (2001). Residual Ataxia Telangiectasia Mutated Protein Function in Cells from Ataxia Telangiectasia Patients, with 5762ins137 and 7271T→G Mutations, Showing a Less Severe Phenotype. Journal of Biological Chemistry. 276(32). 30133–30141. 78 indexed citations
20.
Kidd, Alexa, et al.. (1990). Suspected adverse reactions to medicines during 1989.. PubMed. 126(16). 376–8. 5 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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