Alison Gardner

7.0k total citations
30 papers, 1.6k citations indexed

About

Alison Gardner is a scholar working on Genetics, Molecular Biology and Genetics. According to data from OpenAlex, Alison Gardner has authored 30 papers receiving a total of 1.6k indexed citations (citations by other indexed papers that have themselves been cited), including 20 papers in Genetics, 10 papers in Molecular Biology and 5 papers in Genetics. Recurrent topics in Alison Gardner's work include Genetics and Neurodevelopmental Disorders (14 papers), Genomics and Rare Diseases (7 papers) and Neurogenetic and Muscular Disorders Research (4 papers). Alison Gardner is often cited by papers focused on Genetics and Neurodevelopmental Disorders (14 papers), Genomics and Rare Diseases (7 papers) and Neurogenetic and Muscular Disorders Research (4 papers). Alison Gardner collaborates with scholars based in Australia, United States and Netherlands. Alison Gardner's co-authors include Gabriel Kremmidiotis, Jozef Gécz, John C. Mulley, Mark Corbett, David F. Callen, Samuel F. Berkovic, Leanne M. Dibbens, Joanna Crawford, Ingrid E. Scheffer and Alastair H. MacLennan and has published in prestigious journals such as Nature Genetics, Journal of Clinical Oncology and The American Journal of Medicine.

In The Last Decade

Alison Gardner

30 papers receiving 1.5k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Alison Gardner Australia 17 799 569 339 225 194 30 1.6k
John H. Livingston United Kingdom 23 735 0.9× 181 0.3× 249 0.7× 278 1.2× 322 1.7× 56 1.8k
Andrei Verner Canada 17 670 0.8× 507 0.9× 287 0.8× 265 1.2× 78 0.4× 19 1.4k
A. C. B. Peters Netherlands 21 301 0.4× 240 0.4× 364 1.1× 196 0.9× 378 1.9× 46 1.2k
Shin‐ichiro Hamano Japan 19 340 0.4× 246 0.4× 612 1.8× 329 1.5× 363 1.9× 111 1.3k
Tsunekazu Yamano Japan 22 525 0.7× 176 0.3× 159 0.5× 274 1.2× 448 2.3× 120 1.8k
Takashi Shiihara Japan 20 346 0.4× 220 0.4× 191 0.6× 166 0.7× 132 0.7× 50 1.1k
Michael Freilinger Austria 19 447 0.6× 206 0.4× 223 0.7× 95 0.4× 220 1.1× 42 1.2k
Mark Nespeca United States 16 279 0.3× 363 0.6× 386 1.1× 162 0.7× 366 1.9× 28 1.2k
Melody Li Australia 15 517 0.6× 309 0.5× 424 1.3× 264 1.2× 79 0.4× 30 1.1k
Elida P.B. Ojopi Brazil 18 267 0.3× 273 0.5× 112 0.3× 144 0.6× 81 0.4× 30 1.4k

Countries citing papers authored by Alison Gardner

Since Specialization
Citations

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

Fields of papers citing papers by Alison Gardner

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Alison Gardner

This figure shows the co-authorship network connecting the top 25 collaborators of Alison Gardner. A scholar is included among the top collaborators of Alison Gardner 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 Alison Gardner. Alison Gardner 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.
Gardner, Alison, Clare L. van Eyk, Paul Q. Thomas, et al.. (2024). Proteomic analysis of the developing mammalian brain links PCDH19 to the Wnt/β-catenin signalling pathway. Molecular Psychiatry. 29(7). 2199–2210. 4 indexed citations
2.
Mittal, Nimisha, Chadwick T. Davis, Peter McLean, et al.. (2023). Human nuclear hormone receptor activity contributes to malaria parasite liver stage development. Cell chemical biology. 30(5). 486–498.e7. 3 indexed citations
3.
Carroll, Renée, Marie Shaw, Maria Arvio, et al.. (2020). Two novel intragenic variants in the FMR1 gene in patients with suspect clinical diagnosis of Fragile X syndrome and no CGG repeat expansion. European Journal of Medical Genetics. 63(10). 104010–104010. 4 indexed citations
4.
Shaw, Marie, Magdalena Badura‐Stronka, Alison Gardner, et al.. (2019). EXOME REPORT: Novel mutation in ATP6V1B2 segregating with autosomal dominant epilepsy, intellectual disability and mild gingival and nail abnormalities. European Journal of Medical Genetics. 63(4). 103799–103799. 12 indexed citations
5.
Corbett, Mark, Clare L. van Eyk, Dani L. Webber, et al.. (2018). Pathogenic copy number variants that affect gene expression contribute to genomic burden in cerebral palsy. npj Genomic Medicine. 3(1). 33–33. 27 indexed citations
6.
Eyk, Clare L. van, Mark Corbett, Alison Gardner, et al.. (2018). Analysis of 182 cerebral palsy transcriptomes points to dysregulation of trophic signalling pathways and overlap with autism. Translational Psychiatry. 8(1). 88–88. 22 indexed citations
7.
Corbett, Mark, Samantha J. Turner, Alison Gardner, et al.. (2017). Familial epilepsy with anterior polymicrogyria as a presentation of COL18A1 mutations. European Journal of Medical Genetics. 60(8). 437–443. 8 indexed citations
8.
Shaw, Marie, Lyndal Henden, Melanie Bahlo, et al.. (2015). Identical by descent L1CAM mutation in two apparently unrelated families with intellectual disability without L1 syndrome. European Journal of Medical Genetics. 58(6-7). 364–368. 13 indexed citations
9.
McMichael, G., Eric Haan, Alison Gardner, et al.. (2013). NKX2-1 mutation in a family diagnosed with ataxic dyskinetic cerebral palsy. European Journal of Medical Genetics. 56(9). 506–509. 16 indexed citations
10.
Huang, Lingli, Lachlan A. Jolly, Saffron A.G. Willis‐Owen, et al.. (2012). A Noncoding, Regulatory Mutation Implicates HCFC1 in Nonsyndromic Intellectual Disability. The American Journal of Human Genetics. 91(4). 694–702. 73 indexed citations
11.
Shoubridge, Cheryl, Alison Gardner, Charles E. Schwartz, et al.. (2012). Is there a Mendelian transmission ratio distortion of the c.429_452dup(24bp) polyalanine tract ARX mutation?. European Journal of Human Genetics. 20(12). 1311–1314. 5 indexed citations
12.
Corbett, Mark, Michael Schwake, Melanie Bahlo, et al.. (2011). A Mutation in the Golgi Qb-SNARE Gene GOSR2 Causes Progressive Myoclonus Epilepsy with Early Ataxia. The American Journal of Human Genetics. 88(5). 657–663. 84 indexed citations
13.
Gardner, Alison, Gloria Mattiuzzi, Stefan Faderl, et al.. (2008). Randomized Comparison of Cooked and Noncooked Diets in Patients Undergoing Remission Induction Therapy for Acute Myeloid Leukemia. Journal of Clinical Oncology. 26(35). 5684–5688. 84 indexed citations
14.
Gardner, Alison. (2007). Diagnosing Fungal Infections in Neutropenic Patients. Clinical journal of oncology nursing. 11(1). 29–32. 6 indexed citations
15.
Bais, Anthony J., et al.. (2004). Aberrant CBFA2T3B gene promoter methylation in breast tumors.. Molecular Cancer. 3(1). 22–22. 12 indexed citations
16.
Bhalla, Kavita, Hilary A. Phillips, Joanna Crawford, et al.. (2004). The de novo chromosome 16 translocations of two patients with abnormal phenotypes (mental retardation and epilepsy) disrupt the A2BP1 gene. Journal of Human Genetics. 49(6). 308–311. 121 indexed citations
17.
18.
Wallace, Robyn H., Ingrid E. Scheffer, Shaun Barnett, et al.. (2001). Neuronal Sodium-Channel α1-Subunit Mutations in Generalized Epilepsy with Febrile Seizures Plus. The American Journal of Human Genetics. 68(4). 859–865. 272 indexed citations
19.
20.
Morgan, David O., Lee Turnpenny, Judith Goodship, et al.. (1998). Inversin, a novel gene in the vertebrate left-right axis pathway, is partially deleted in the inv mouse. Nature Genetics. 20(2). 149–156. 190 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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