Nadia Ali

747 total citations
73 papers, 433 citations indexed

About

Nadia Ali is a scholar working on Physiology, Genetics and Clinical Psychology. According to data from OpenAlex, Nadia Ali has authored 73 papers receiving a total of 433 indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Physiology, 13 papers in Genetics and 10 papers in Clinical Psychology. Recurrent topics in Nadia Ali's work include Lysosomal Storage Disorders Research (11 papers), Family and Disability Support Research (8 papers) and Glycogen Storage Diseases and Myoclonus (8 papers). Nadia Ali is often cited by papers focused on Lysosomal Storage Disorders Research (11 papers), Family and Disability Support Research (8 papers) and Glycogen Storage Diseases and Myoclonus (8 papers). Nadia Ali collaborates with scholars based in United States, Tunisia and Pakistan. Nadia Ali's co-authors include Emily C. Lisi, Cynthia R. Cimino, Dawn A. Laney, Scott Gillespie, Stephanie Cagle, Samir Belal, John D. Coates, Karrie A. Weber, Cecelia Bellcross and Saloua Mrabet and has published in prestigious journals such as SHILAP Revista de lepidopterología, Neurology and Applied Microbiology and Biotechnology.

In The Last Decade

Nadia Ali

57 papers receiving 422 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Nadia Ali United States 11 169 78 61 60 52 73 433
Emanuela Zagni Italy 7 73 0.4× 110 1.4× 44 0.7× 29 0.5× 24 0.5× 17 431
Michela Traglia Italy 18 88 0.5× 77 1.0× 40 0.7× 184 3.1× 96 1.8× 29 852
Andrea B. Schote Germany 13 95 0.6× 32 0.4× 37 0.6× 78 1.3× 37 0.7× 25 506
Giorgio Pistis Italy 16 53 0.3× 52 0.7× 74 1.2× 152 2.5× 31 0.6× 31 687
Anna Verri Italy 13 86 0.5× 30 0.4× 174 2.9× 58 1.0× 31 0.6× 38 493
Leontine W. ten Hoopen Netherlands 12 166 1.0× 18 0.2× 93 1.5× 186 3.1× 105 2.0× 25 514
Leanne Wallace Australia 13 40 0.2× 56 0.7× 27 0.4× 130 2.2× 34 0.7× 21 591
Xuejiao Chen China 13 56 0.3× 34 0.4× 47 0.8× 60 1.0× 27 0.5× 35 669
Analia Tomova Bulgaria 16 68 0.4× 56 0.7× 39 0.6× 69 1.1× 15 0.3× 44 822
Yakov A. Tsepilov Russia 16 106 0.6× 33 0.4× 146 2.4× 186 3.1× 32 0.6× 57 758

Countries citing papers authored by Nadia Ali

Since Specialization
Citations

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

Fields of papers citing papers by Nadia Ali

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Nadia Ali

This figure shows the co-authorship network connecting the top 25 collaborators of Nadia Ali. A scholar is included among the top collaborators of Nadia Ali 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 Nadia Ali. Nadia Ali 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.
Ali, Nadia, et al.. (2025). Comparison of Tibiofemoral and Patellofemoral Mobilization in Improving Pain, Rom and Functional Disability in Patellofemoral Pain Syndrome. British Journal of Multidisciplinary and Advanced Studies. 6(1). 30–40.
2.
Sassi, Samia Ben, et al.. (2025). Genetic association study between rs2234253 (p.T96K) variant of TREM2 and Alzheimer’s disease in a Tunisian population. Neurological Research. 47(4). 290–295. 1 indexed citations
3.
Hipp, Heather S., et al.. (2024). Women’s healthcare providers’ knowledge and practices surrounding fragile-X associated primary ovarian insufficiency (FXPOI). Journal of Assisted Reproduction and Genetics. 42(2). 499–508.
4.
Ali, Nadia, et al.. (2024). Reflections on my international genetic counseling rotations: Contrasts in practice between India and the United States. SHILAP Revista de lepidopterología. 2(Suppl 2). 101871–101871. 1 indexed citations
5.
King, Andrew P., Nadia Ali, Cecelia Bellcross, et al.. (2023). Healthcare Experiences of African American Women with the Fragile X Premutation. Journal of Racial and Ethnic Health Disparities. 11(6). 3390–3400.
6.
Ali, Nadia, et al.. (2023). Cognitive impairment in multiple sclerosis: Utility of electroencephalography. Multiple Sclerosis and Related Disorders. 70. 104502–104502. 4 indexed citations
7.
Ali, Nadia, et al.. (2023). Genetic counselors' perceptions of student supervision across service delivery models. Journal of Genetic Counseling. 32(6). 1314–1324. 1 indexed citations
8.
9.
Ali, Nadia, et al.. (2022). Primary Care Providers’ Use of Genetic Services in the Southeast United States: Barriers, Facilitators, and Strategies. Journal of Primary Care & Community Health. 13. 4267754912–4267754912. 7 indexed citations
10.
Ali, Nadia, et al.. (2022). The diagnostic experience of women with fragile X–associated primary ovarian insufficiency (FXPOI). Journal of Assisted Reproduction and Genetics. 40(1). 179–190. 8 indexed citations
11.
12.
Ali, Nadia, et al.. (2021). Knowledge and attitudes toward epilepsy among teachers in Tunisia. Epilepsy & Behavior. 123. 108260–108260. 9 indexed citations
13.
Shahid, Muhammad, et al.. (2020). Frequency of anxiety and depression in patients with melasma. Journal of Pakistan Association of Dermatology. 30(1). 81–85. 4 indexed citations
14.
Ali, Nadia, et al.. (2019). Epileptic seizures and occupational exposure to solvents: a cases series. ˜La œMedicina del lavoro. 110(1). 56–62.
15.
16.
Fradj, Mohamed Kacem Ben, Lilia Kraoua, Faouzi Mâazoul, et al.. (2018). <b><i>TOP3B</i></b>: A Novel Candidate Gene in Juvenile Myoclonic Epilepsy?. Cytogenetic and Genome Research. 154(1). 1–5. 16 indexed citations
17.
Ali, Nadia, et al.. (2015). Les critères prédictifs d’une épilepsie pharmacorésistante chez l’enfant. Revue Neurologique. 171(10). 730–735. 10 indexed citations
18.
Ali, Nadia, et al.. (2015). Novel presenilin 1 mutation (p.I83T) in Tunisian family with early-onset Alzheimer's disease. Neurobiology of Aging. 36(10). 2904.e9–2904.e11. 9 indexed citations
19.
Ali, Nadia & Stephanie Cagle. (2014). Psychological Health in Adults with Morquio Syndrome. JIMD Reports. 20. 87–93. 17 indexed citations
20.
Ahmed, Alia, Chester B. Whitley, Kyle Rudser, et al.. (2013). Neurocognitive and neuropsychiatric phenotypes associated with the mutation L238Q of the α-L-iduronidase gene in Hurler–Scheie syndrome. Molecular Genetics and Metabolism. 111(2). 123–127. 24 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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