Aamira Huq

763 total citations
20 papers, 345 citations indexed

About

Aamira Huq is a scholar working on Molecular Biology, Genetics and Physiology. According to data from OpenAlex, Aamira Huq has authored 20 papers receiving a total of 345 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Molecular Biology, 10 papers in Genetics and 5 papers in Physiology. Recurrent topics in Aamira Huq's work include Alzheimer's disease research and treatments (4 papers), Genomics and Rare Diseases (3 papers) and BRCA gene mutations in cancer (3 papers). Aamira Huq is often cited by papers focused on Alzheimer's disease research and treatments (4 papers), Genomics and Rare Diseases (3 papers) and BRCA gene mutations in cancer (3 papers). Aamira Huq collaborates with scholars based in Australia, United States and Vietnam. Aamira Huq's co-authors include Ingrid Winship, Paul Lacaze, Paul A. James, Alexis Ceecee Britten‐Jones, Thomas L. Edwards, Martin B. Delatycki, Lauren N. Ayton, Marguerite V. Evans‐Galea, Françoise Pousset and David R. Lynch and has published in prestigious journals such as Annals of Neurology, Scientific Reports and American Journal of Ophthalmology.

In The Last Decade

Aamira Huq

20 papers receiving 344 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Aamira Huq Australia 9 210 116 98 45 45 20 345
Banan Al‐Younes Saudi Arabia 12 222 1.1× 55 0.5× 92 0.9× 27 0.6× 29 0.6× 18 387
Ewa Jamroz Poland 13 241 1.1× 50 0.4× 139 1.4× 34 0.8× 91 2.0× 52 529
Deborah L. Renaud United States 11 233 1.1× 51 0.4× 79 0.8× 180 4.0× 53 1.2× 41 470
Mefford Hc 6 163 0.8× 35 0.3× 90 0.9× 24 0.5× 40 0.9× 239 337
Qingmei Shao United States 12 177 0.8× 119 1.0× 51 0.5× 39 0.9× 14 0.3× 22 383
Sonia Emperador Spain 15 450 2.1× 33 0.3× 38 0.4× 30 0.7× 43 1.0× 37 542
M. Kinoshita Japan 14 217 1.0× 198 1.7× 24 0.2× 79 1.8× 35 0.8× 39 393
Saunder Bernes United States 14 316 1.5× 109 0.9× 107 1.1× 57 1.3× 21 0.5× 16 500
F Ballesta Spain 14 246 1.2× 66 0.6× 249 2.5× 37 0.8× 46 1.0× 28 547
Bhim Singhal India 14 236 1.1× 92 0.8× 17 0.2× 147 3.3× 65 1.4× 21 506

Countries citing papers authored by Aamira Huq

Since Specialization
Citations

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

Fields of papers citing papers by Aamira Huq

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Aamira Huq

This figure shows the co-authorship network connecting the top 25 collaborators of Aamira Huq. A scholar is included among the top collaborators of Aamira Huq 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 Aamira Huq. Aamira Huq 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.
Bhalala, Oneil G., Dhamidhu Eratne, Simon M. Laws, et al.. (2025). Blood biomarker profiles in young-onset neurocognitive disorders: A cohort study. Australian & New Zealand Journal of Psychiatry. 59(4). 378–388. 1 indexed citations
2.
Mack, Heather G., Andrew Metha, Doron G. Hickey, et al.. (2024). Forty-year odyssey to Refsum disease diagnosis: impact of diagnostic delay on effective treatment. Clinical and Experimental Optometry. 108(5). 636–639. 2 indexed citations
3.
Britten‐Jones, Alexis Ceecee, Joshua R. Schultz, Heather G. Mack, et al.. (2024). Patient experiences and perceived value of genetic testing in inherited retinal diseases: a cross-sectional survey. Scientific Reports. 14(1). 5403–5403. 4 indexed citations
4.
Huq, Aamira, Bryony A. Thompson, & Ingrid Winship. (2024). Clinical application of whole genome sequencing in young onset dementia: challenges and opportunities. Expert Review of Molecular Diagnostics. 24(8). 659–675. 1 indexed citations
5.
Britten‐Jones, Alexis Ceecee, et al.. (2022). The Diagnostic Yield of Next Generation Sequencing in Inherited Retinal Diseases: A Systematic Review and Meta-analysis. American Journal of Ophthalmology. 249. 57–73. 39 indexed citations
6.
Riaz, Moeen, Aamira Huq, Joanne Ryan, et al.. (2021). Effect of APOE and a polygenic risk score on incident dementia and cognitive decline in a healthy older population. Aging Cell. 20(6). e13384–e13384. 22 indexed citations
7.
Huq, Aamira, et al.. (2021). Mainstreaming genomics: training experience of hospital medical officers at the Royal Melbourne Hospital. Internal Medicine Journal. 51(2). 268–271. 4 indexed citations
8.
Huq, Aamira, Brian Fulton‐Howard, Moeen Riaz, et al.. (2021). Polygenic score modifies risk for Alzheimer's disease in APOE ε4 homozygotes at phenotypic extremes. Alzheimer s & Dementia Diagnosis Assessment & Disease Monitoring. 13(1). e12226–e12226. 8 indexed citations
9.
Huq, Aamira, Adrienne Sexton, Paul Lacaze, et al.. (2021). Genetic testing in dementia‐A medical genetics perspective. International Journal of Geriatric Psychiatry. 36(8). 1158–1170. 8 indexed citations
10.
Zhang, Lei, Yining Bao, Moeen Riaz, et al.. (2020). Population Genomic Screening of All Young Adults in a Health-Care System: A Cost-Effectiveness Analysis. Obstetrical & Gynecological Survey. 75(2). 91–93. 3 indexed citations
11.
Schultz, Joshua R., Lisa S. Kearns, Michael Fahey, et al.. (2020). A novel AFG3L2 mutation close to AAA domain leads to aberrant OMA1 and OPA1 processing in a family with optic atrophy. Acta Neuropathologica Communications. 8(1). 93–93. 13 indexed citations
12.
Zhang, Lei, Yining Bao, Moeen Riaz, et al.. (2019). Population genomic screening of all young adults in a health-care system: a cost-effectiveness analysis. Genetics in Medicine. 21(9). 1958–1968. 54 indexed citations
13.
Huq, Aamira, Peter Fransquet, Simon M. Laws, et al.. (2019). Genetic resilience to Alzheimer's disease in APOE ε4 homozygotes: A systematic review. Alzheimer s & Dementia. 15(12). 1612–1623. 27 indexed citations
14.
Huq, Aamira, Maie Walsh, M. Finlay, et al.. (2018). Mutations in SUFU and PTCH1 genes may cause different cutaneous cancer predisposition syndromes: similar, but not the same. Familial Cancer. 17(4). 601–606. 20 indexed citations
15.
Huq, Aamira, et al.. (2018). APRT deficiency: the need for early diagnosis. BMJ Case Reports. 2018. bcr–2018. 3 indexed citations
16.
Monif, Mastura, et al.. (2018). MonoMac syndrome with associated neurological deficits and longitudinally extensive cord lesion. BMJ Case Reports. 2018. bcr–2017. 11 indexed citations
17.
Huq, Aamira, Michael Bogwitz, Alexandra Gorelik, et al.. (2017). Cohort study of Gorlin syndrome with emphasis on standardised phenotyping and quality of life assessment. Internal Medicine Journal. 47(6). 664–673. 12 indexed citations
18.
Huq, Aamira, Mark D. Pertile, Andrew M. Davis, et al.. (2016). A Novel Mechanism for Human Cardiac Ankyrin-B Syndrome due to Reciprocal Chromosomal Translocation. Heart Lung and Circulation. 26(6). 612–618. 6 indexed citations
19.
Galea, Charles A., Aamira Huq, Paul J. Lockhart, et al.. (2015). Compound heterozygous FXN mutations and clinical outcome in friedreich ataxia. Annals of Neurology. 79(3). 485–495. 106 indexed citations
20.
Huq, Aamira, et al.. (2014). Vestibular schwannoma in a patient with neurofibromatosis type 1: clinical report and literature review. Familial Cancer. 14(1). 157–160. 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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