Nadira Ali

1.1k total citations
15 papers, 576 citations indexed

About

Nadira Ali is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Cardiology and Cardiovascular Medicine. According to data from OpenAlex, Nadira Ali has authored 15 papers receiving a total of 576 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Molecular Biology, 4 papers in Cellular and Molecular Neuroscience and 4 papers in Cardiology and Cardiovascular Medicine. Recurrent topics in Nadira Ali's work include Genetic Neurodegenerative Diseases (4 papers), Mitochondrial Function and Pathology (2 papers) and Heme Oxygenase-1 and Carbon Monoxide (2 papers). Nadira Ali is often cited by papers focused on Genetic Neurodegenerative Diseases (4 papers), Mitochondrial Function and Pathology (2 papers) and Heme Oxygenase-1 and Carbon Monoxide (2 papers). Nadira Ali collaborates with scholars based in United Kingdom, United States and Australia. Nadira Ali's co-authors include John Powell, Hugh S. Markus, Ynte M. Ruigrok, R. Swaminathan, Jane Molloy, Faisal Ali, Shahir Hamdulay, Dorian O. Haskard, Justin C. Mason and Gillian P. Bates and has published in prestigious journals such as Blood, Neurology and Stroke.

In The Last Decade

Nadira Ali

15 papers receiving 556 citations

Peers

Nadira Ali

CCM

PHYSI

RHEUM

CMN

Antonio Ruocco Italy

Wenli Sheng China

Mesia Steed United States

Katina M. Wilson United States

D Christmann France

B. A. J. Veldman Netherlands

Xiqiong Han China

Yasuhiro Kumai Japan

Tomonori Segawa Japan

Antonio Ruocco Italy

Nadira Ali

284 ×1.4

178 ×1.2

CCM

98 ×0.7

PHYSI

84 ×0.6

RHEUM

59 ×0.6

CMN

Citations per year, relative to Nadira Ali Nadira Ali (= 1×) peers Antonio Ruocco

Countries citing papers authored by Nadira Ali

Since Specialization

Citations

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

Fields of papers citing papers by Nadira Ali

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Nadira Ali

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

All Works

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15 of 15 papers shown

Landles, Christian, Georgina F Osborne, Nadira Ali, et al.. (2024). Mutant huntingtin protein decreases with CAG repeat expansion: implications for therapeutics and bioassays. Brain Communications. 6(6). fcae410–fcae410. 7 indexed citations

Ali, Nadira, et al.. (2021). Ovarian indirect inguinal hernia. ANZ Journal of Surgery. 92(4). 918–920. 1 indexed citations

Landles, Christian, Nadira Ali, Rachel Flomen, et al.. (2020). Subcellular Localization And Formation Of Huntingtin Aggregates Correlates With Symptom Onset And Progression In A Huntington’S Disease Model. Brain Communications. 2(2). fcaa066–fcaa066. 33 indexed citations

Ali, Nadira, et al.. (2020). A rare case of transient duodenal volvulus in an elderly patient. Journal of Medical Imaging and Radiation Oncology. 65(1). 79–81. 1 indexed citations

Franich, Nicholas R., Miriam A. Hickey, Chunni Zhu, et al.. (2019). Phenotype onset in Huntington’s disease knock‐in mice is correlated with the incomplete splicing of the mutant huntingtin gene. Journal of Neuroscience Research. 97(12). 1590–1605. 33 indexed citations

Pido-Lopez, Jeffrey, Ralph André, Agnesska C. Benjamin, et al.. (2018). In vivo neutralization of the protagonist role of macrophages during the chronic inflammatory stage of Huntington’s disease. Scientific Reports. 8(1). 11447–11447. 22 indexed citations

Dumont, Odile, Andrea S. Bauer, Damien Calay, et al.. (2012). Protein kinase Cϵ activity induces anti-inflammatory and anti-apoptotic genes via an ERK1/2- and NF-κB-dependent pathway to enhance vascular protection. Biochemical Journal. 447(2). 193–204. 12 indexed citations

Ali, Faisal, Nadira Ali, Andrea S. Bauer, et al.. (2009). PPARδ and PGC1α act cooperatively to induce haem oxygenase-1 and enhance vascular endothelial cell resistance to stress. Cardiovascular Research. 85(4). 701–710. 56 indexed citations

Kinderlerer, Anne, Isabel Pombo Grégoire, Shahir Hamdulay, et al.. (2008). Heme oxygenase-1 expression enhances vascular endothelial resistance to complement-mediated injury through induction of decay-accelerating factor: a role for increased bilirubin and ferritin. Blood. 113(7). 1598–1607. 72 indexed citations

10.

Staines, Norman A., et al.. (2004). Constraints on the Efficacy of Mucosal Tolerance in Treatment of Human and Animal Arthritic Diseases. Annals of the New York Academy of Sciences. 1029(1). 250–259. 9 indexed citations

11.

Wolfe, Charles, et al.. (2001). Increased Common Carotid Intima-Media Thickness in UK African Caribbeans and Its Relation to Chronic Inflammation and Vascular Candidate Gene Polymorphisms. Stroke. 32(11). 2465–2471. 44 indexed citations

12.

Hassan, Ahamad, et al.. (2001). Atrial natriuretic peptide gene G664A polymorphism and the risk of ischemic cerebrovascular disease. Neurology. 57(9). 1726–1728. 11 indexed citations

13.

Markus, Hugh S., Ynte M. Ruigrok, Nadira Ali, & John Powell. (1998). Endothelial Nitric Oxide Synthase Exon 7 Polymorphism, Ischemic Cerebrovascular Disease, and Carotid Atheroma. Stroke. 29(9). 1908–1911. 128 indexed citations

14.

Ali, Nadira, John Powell, R. Swaminathan, & Hugh S. Markus. (1997). The relationship between MTHFR genotype, serum homocysteine and folate levels. Biochemical Society Transactions. 25(3). 386S–386S. 3 indexed citations

15.

Markus, Hugh S., et al.. (1997). A Common Polymorphism in the Methylenetetrahydrofolate Reductase Gene, Homocysteine, and Ischemic Cerebrovascular Disease. Stroke. 28(9). 1739–1743. 144 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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