Jamal Nasir

6.9k total citations · 2 hit papers
68 papers, 3.9k citations indexed

About

Jamal Nasir is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Genetics. According to data from OpenAlex, Jamal Nasir has authored 68 papers receiving a total of 3.9k indexed citations (citations by other indexed papers that have themselves been cited), including 37 papers in Molecular Biology, 22 papers in Cellular and Molecular Neuroscience and 15 papers in Genetics. Recurrent topics in Jamal Nasir's work include Genetic Neurodegenerative Diseases (19 papers), Mitochondrial Function and Pathology (12 papers) and Neurological disorders and treatments (7 papers). Jamal Nasir is often cited by papers focused on Genetic Neurodegenerative Diseases (19 papers), Mitochondrial Function and Pathology (12 papers) and Neurological disorders and treatments (7 papers). Jamal Nasir collaborates with scholars based in United Kingdom, Canada and United States. Jamal Nasir's co-authors include Michael R. Hayden, Anthony G. Phillips, John R. OʼKusky, Jutta Zeisler, María José Lafuente, Joy M. Richman, Jamey D. Marth, Stan Floresco, Virginia M. Diewert and Roshni R. Singaraja and has published in prestigious journals such as Nature, Cell and Proceedings of the National Academy of Sciences.

In The Last Decade

Jamal Nasir

64 papers receiving 3.8k citations

Hit Papers

A YAC Mouse Model for Huntington’s Disease with Full-Leng... 1995 2026 2005 2015 1999 1995 200 400 600

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Jamal Nasir United Kingdom 27 2.8k 1.9k 1.1k 435 343 68 3.9k
Miguel Lafarga Spain 40 3.6k 1.3× 962 0.5× 697 0.7× 595 1.4× 485 1.4× 174 5.8k
Marı́a T. Berciano Spain 39 3.2k 1.2× 803 0.4× 558 0.5× 506 1.2× 462 1.3× 139 5.1k
John Kamholz United States 45 2.8k 1.0× 2.1k 1.1× 862 0.8× 671 1.5× 600 1.7× 138 5.5k
Cécile Martinat France 21 1.7k 0.6× 852 0.5× 896 0.8× 204 0.5× 215 0.6× 55 2.7k
Geert Callewaert Belgium 39 2.5k 0.9× 1.1k 0.6× 583 0.5× 153 0.4× 669 2.0× 90 4.1k
Jeffrey A. Loeb United States 38 1.6k 0.6× 1.8k 1.0× 416 0.4× 233 0.5× 358 1.0× 113 4.4k
Alfred Bach Germany 20 2.0k 0.7× 1.2k 0.6× 382 0.4× 219 0.5× 322 0.9× 24 3.6k
Carlos Gilberto Carlotti Brazil 34 1.5k 0.6× 833 0.4× 489 0.5× 181 0.4× 221 0.6× 184 3.9k
Cathleen Lutz United States 33 2.8k 1.0× 1.1k 0.6× 861 0.8× 566 1.3× 227 0.7× 82 4.3k
Nicholas D. Mazarakis United Kingdom 36 2.5k 0.9× 1.0k 0.6× 883 0.8× 1.3k 3.0× 127 0.4× 63 4.2k

Countries citing papers authored by Jamal Nasir

Since Specialization
Citations

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

Fields of papers citing papers by Jamal Nasir

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Jamal Nasir

This figure shows the co-authorship network connecting the top 25 collaborators of Jamal Nasir. A scholar is included among the top collaborators of Jamal Nasir 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 Jamal Nasir. Jamal Nasir 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, Waqas, et al.. (2024). Design and Analysis of a Quad-Band Antenna for IoT and Wearable RFID Applications. Electronics. 13(4). 700–700. 9 indexed citations
2.
Vadgama, Nirmal, Douglas Lamont, John Hardy, Jamal Nasir, & Ruth C. Lovering. (2019). Distinct proteomic profiles in monozygotic twins discordant for ischaemic stroke. Molecular and Cellular Biochemistry. 456(1-2). 157–165. 7 indexed citations
3.
Vadgama, Nirmal, Alan Pittman, Michael A. Simpson, et al.. (2019). De novo single-nucleotide and copy number variation in discordant monozygotic twins reveals disease-related genes. European Journal of Human Genetics. 27(7). 1121–1133. 19 indexed citations
4.
Ahmed, Saleem, Musharraf Jelani, Mona Mohammad Almramhi, et al.. (2015). Exome analysis identified a novel missense mutation in the CLPP gene in a consanguineous Saudi family expanding the clinical spectrum of Perrault Syndrome type-3. Journal of the Neurological Sciences. 353(1-2). 149–154. 37 indexed citations
5.
Zubair, Muhammad, et al.. (2011). Atmospheric influences on satellite communications. PRZEGLĄD ELEKTROTECHNICZNY. 261–264. 14 indexed citations
6.
Kerr, Jonathan R., Alan Maclean, Margarita V. Chibalina, et al.. (2010). Altered expression and coregulation of dopamine signalling genes in schizophrenia and bipolar disorder. Neuropathology and Applied Neurobiology. 37(2). 206–219. 55 indexed citations
7.
Liu, Bigang, et al.. (2008). ALG‐2 interacting protein AIP1: a novel link between D1 and D3 signalling. European Journal of Neuroscience. 27(7). 1626–1633. 13 indexed citations
8.
Nasir, Jamal, et al.. (2007). Abnormal vibration‐induced illusion of movement in idiopathic focal dystonia: An endophenotypic marker?. Movement Disorders. 23(3). 373–377. 41 indexed citations
9.
Sperandio, Sabina, Karen S. Poksay, Ian de Belle, et al.. (2004). Paraptosis: mediation by MAP kinases and inhibition by AIP-1/Alix. Cell Death and Differentiation. 11(10). 1066–1075. 307 indexed citations
10.
Nasir, Jamal, María José Lafuente, Kui Duan, et al.. (2000). Human huntingtin-associated protein (HAP-1) gene: genomic organisation and an intragenic polymorphism. Gene. 254(1-2). 181–187. 4 indexed citations
11.
OʼKusky, John R., Jamal Nasir, Francesca Cicchetti, André Parent, & Michael R. Hayden. (1999). Neuronal degeneration in the basal ganglia and loss of pallido-subthalamic synapses in mice with targeted disruption of the Huntington's disease gene. Brain Research. 818(2). 468–479. 69 indexed citations
12.
Hodgson, John, N. Agopyan, Claire‐Anne Gutekunst, et al.. (1999). A YAC Mouse Model for Huntington’s Disease with Full-Length Mutant Huntingtin, Cytoplasmic Toxicity, and Selective Striatal Neurodegeneration. Neuron. 23(1). 181–192. 669 indexed citations breakdown →
13.
Metzler, Martina, Nansheng Chen, Cheryl D. Helgason, et al.. (1999). Life Without Huntingtin. Journal of Neurochemistry. 72(3). 1009–1018. 33 indexed citations
14.
Nasir, Jamal & Chris Walton. (1996). Lesson of the Week: Adrenal mass with virilisation: importance of endocrine investigation. BMJ. 313(7061). 872–873. 3 indexed citations
15.
Lin, Biaoyang, Jamal Nasir, Michael A. Kalchman, et al.. (1995). Structural analysis of the 5′ region of mouse and human huntington disease genes reveals conservation of putative promoter region and di- and trinucleotide polymorphisms. Genomics. 25(3). 707–715. 33 indexed citations
16.
Clarke, L., Jamal Nasir, Hanfang Zhang, et al.. (1994). Murine α-l-Iduronidase: cDNA Isolation and Expression. Genomics. 24(2). 311–316. 25 indexed citations
17.
Lin, Biaoyang, Jamal Nasir, Helen Macdonald, et al.. (1994). Sequence of the murine Huntington dusease gene: evidence for conservation, and polymorphism in a triplet (CCG) repeat alternate splicing. Human Molecular Genetics. 3(1). 85–92. 57 indexed citations
18.
Goldberg, Y. Paul, Susan E. Andrew, Gordon B. Hutchinson, et al.. (1993). Identification of an Alu retrotransposition event in close proximity to a strong candidate gene for Huntington's disease. Nature. 362(6418). 370–373. 41 indexed citations
19.
Goldberg, Y. Paul, Biaoyang Lin, Susan E. Andrew, et al.. (1992). Cloning and mapping of the  -adducin gene close to D4S95 and assessment of its relationship to Huntington disease. Human Molecular Genetics. 1(9). 669–675. 20 indexed citations
20.
Nasir, Jamal, Mark Maconochie, & Donna M. Brown. (1991). Co-amplification of L1 line elements with localised low copy repeats in Giemsa dark bands: implications for genome organisation. Nucleic Acids Research. 19(12). 3255–3260. 15 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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