Allison A. Dilliott

998 total citations
20 papers, 271 citations indexed

About

Allison A. Dilliott is a scholar working on Molecular Biology, Neurology and Genetics. According to data from OpenAlex, Allison A. Dilliott has authored 20 papers receiving a total of 271 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Molecular Biology, 8 papers in Neurology and 6 papers in Genetics. Recurrent topics in Allison A. Dilliott's work include Amyotrophic Lateral Sclerosis Research (8 papers), Genomics and Rare Diseases (5 papers) and Neurogenetic and Muscular Disorders Research (5 papers). Allison A. Dilliott is often cited by papers focused on Amyotrophic Lateral Sclerosis Research (8 papers), Genomics and Rare Diseases (5 papers) and Neurogenetic and Muscular Disorders Research (5 papers). Allison A. Dilliott collaborates with scholars based in Canada, United States and Chile. Allison A. Dilliott's co-authors include Robert A. Hegele, Adam D. McIntyre, Henian Cao, Jacqueline S. Dron, John F. Robinson, Jian Wang, Sali M.K. Farhan, Jean‐Claude Tardif, Murray W. Huff and Guillaume Lettre and has published in prestigious journals such as Brain, Scientific Reports and International Journal of Molecular Sciences.

In The Last Decade

Allison A. Dilliott

15 papers receiving 270 citations

Peers

Allison A. Dilliott

SURGE

EDM

CCM

Elena Passeri Italy

Raitis Pečulis Latvia

Amy E. Knight Johnson United States

Cinthia E. Jannes Brazil

L. P. Kuyt Netherlands

Sophie Vallette Canada

Nicoleta Cristina Olarescu Norway

Lívia M. Mermejo Brazil

Michiyo Yamamoto Japan

Elena Passeri Italy

Allison A. Dilliott

79 ×0.5

SURGE

25 ×0.4

129 ×1.9

137 ×2.3

EDM

26 ×0.5

CCM

Citations per year, relative to Allison A. Dilliott Allison A. Dilliott (= 1×) peers Elena Passeri

Countries citing papers authored by Allison A. Dilliott

Since Specialization

Citations

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

Fields of papers citing papers by Allison A. Dilliott

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Allison A. Dilliott. 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 Allison A. Dilliott. The network helps show where Allison A. Dilliott may publish in the future.

Co-authorship network of co-authors of Allison A. Dilliott

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

All Works

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20 of 20 papers shown

Grant, Riley, Mary B. Makarious, Lara M. Lange, et al.. (2025). The Global Parkinson’s Disease Genetics (GP2) Genome Browser. medRxiv.

Maussion, Gilles, Narges Abdian, Ghazal Haghi, et al.. (2025). Transcriptome-based screening in TARDBP/TDP-43 knock-in motor neurons identifies the NEDD8-activating enzyme inhibitor MLN4924. Scientific Reports. 15(1). 28555–28555.

Dilliott, Allison A., Tiziana Petrozziello, James D. Berry, et al.. (2024). Identification of gene fusions associated with amyotrophic lateral sclerosis. Muscle & Nerve. 69(4). 477–489. 2 indexed citations

Simó, J. A., Emily Dwosh, Roberta La Piana, et al.. (2024). Enhancing variant of uncertain significance (VUS) interpretation in neurogenetics: collaborative experiences from a tertiary care centre. Journal of Medical Genetics. 62(1). 37–45.

Dilliott, Allison A., et al.. (2024). Transcriptomics of Human Brain Tissue in Parkinson’s Disease: a Comparison of Bulk and Single-cell RNA Sequencing. Molecular Neurobiology. 61(11). 8996–9015. 10 indexed citations

Dilliott, Allison A., et al.. (2023). Characterizing proteomic and transcriptomic features of missense variants in amyotrophic lateral sclerosis genes. Brain. 146(11). 4608–4621. 1 indexed citations

Dilliott, Allison A., et al.. (2023). Evaluating the Utility of REVEL and CADD for Interpreting Variants in Amyotrophic Lateral Sclerosis Genes. Human Mutation. 2023. 1–16.

Dilliott, Allison A., Guy A. Rouleau, & Sali M.K. Farhan. (2022). Lack of association of TP73 with amyotrophic lateral sclerosis in a large cohort of cases. Neurobiology of Aging. 115. 109–111. 1 indexed citations

Salem, Ahmed, et al.. (2022). Matrin3: Disorder and ALS Pathogenesis. Frontiers in Molecular Biosciences. 8. 794646–794646. 11 indexed citations

10.

Dilliott, Allison A., et al.. (2022). Sex-stratified RNA-seq analysis reveals traumatic brain injury-induced transcriptional changes in the female hippocampus conducive to dementia. Frontiers in Neurology. 13. 1026448–1026448.

11.

Iragorri, Nicolas, Sujata Mishra, Allison A. Dilliott, et al.. (2022). Cost-effectiveness of a gene sequencing test for Alzheimer’s disease in Ontario. Journal of Community Genetics. 14(2). 135–147. 1 indexed citations

12.

Dilliott, Allison A., et al.. (2022). DnaJC7 in Amyotrophic Lateral Sclerosis. International Journal of Molecular Sciences. 23(8). 4076–4076. 14 indexed citations

13.

Dron, Jacqueline S., Allison A. Dilliott, Adam D. McIntyre, et al.. (2020). Ancestry-specific profiles of genetic determinants of severe hypertriglyceridemia. Journal of clinical lipidology. 15(1). 88–96. 10 indexed citations

14.

Dron, Jacqueline S., Allison A. Dilliott, Adam D. McIntyre, et al.. (2020). Loss-of-Function CREB3L3 Variants in Patients With Severe Hypertriglyceridemia. Arteriosclerosis Thrombosis and Vascular Biology. 40(8). 1935–1941. 22 indexed citations

15.

Dilliott, Allison A., Jian Wang, Gagandeep Singh, et al.. (2020). A novel homozygous variant in REN in a family presenting with classic features of disorders involving the renin–angiotensin pathway, without renal tubular dysgenesis. American Journal of Medical Genetics Part A. 182(10). 2284–2290. 4 indexed citations

16.

Dilliott, Allison A., John F. Robinson, Robert A. Hegele, et al.. (2019). Genetic and epigenetic study of an Alzheimer’s disease family with monozygotic triplets. Brain. 142(11). 3375–3381. 11 indexed citations

17.

Dilliott, Allison A., et al.. (2018). A De Novo POLD1 Mutation Associated With Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome in a Family With Werner Syndrome. Journal of Investigative Medicine High Impact Case Reports. 6. 2735251922–2735251922. 10 indexed citations

18.

Farhan, Sali M.K., et al.. (2016). KMT2D p.Gln3575His segregating in a family with autosomal dominant choanal atresia strengthens the Kabuki/CHARGE connection. American Journal of Medical Genetics Part A. 173(1). 183–189. 14 indexed citations

19.

Farhan, Sali M.K., Allison A. Dilliott, Mahdi Ghani, et al.. (2016). The ONDRISeq panel: custom-designed next-generation sequencing of genes related to neurodegeneration. npj Genomic Medicine. 1(1). 16032–16032. 15 indexed citations

20.

Wang, Jian, Jacqueline S. Dron, Matthew R. Ban, et al.. (2016). Polygenic Versus Monogenic Causes of Hypercholesterolemia Ascertained Clinically. Arteriosclerosis Thrombosis and Vascular Biology. 36(12). 2439–2445. 145 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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