Jamil Amjad Hashmi

458 total citations
26 papers, 303 citations indexed

About

Jamil Amjad Hashmi is a scholar working on Molecular Biology, Genetics and Genetics. According to data from OpenAlex, Jamil Amjad Hashmi has authored 26 papers receiving a total of 303 indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Molecular Biology, 13 papers in Genetics and 4 papers in Genetics. Recurrent topics in Jamil Amjad Hashmi's work include Genetics and Neurodevelopmental Disorders (4 papers), Genomics and Rare Diseases (3 papers) and Cell Adhesion Molecules Research (3 papers). Jamil Amjad Hashmi is often cited by papers focused on Genetics and Neurodevelopmental Disorders (4 papers), Genomics and Rare Diseases (3 papers) and Cell Adhesion Molecules Research (3 papers). Jamil Amjad Hashmi collaborates with scholars based in Saudi Arabia, Pakistan and Denmark. Jamil Amjad Hashmi's co-authors include Yusuf Zafar, Muhammad Arshad, Shahid Mansoor, Sulman Basit, Amer Mahmood, Musaad Alfayez, Mona Elsafadi, Moustapha Kassem, Muthurangan Manikandan and Khushnooda Ramzan and has published in prestigious journals such as SHILAP Revista de lepidopterología, Scientific Reports and Neuroscience.

In The Last Decade

Jamil Amjad Hashmi

23 papers receiving 294 citations

Peers

Jamil Amjad Hashmi
Cameron Arakaki United States
Sakthikumar Ambady United States
Francesco Aulicino United Kingdom
Hadi Bayat Iran
Aurélie Dupuy France
Detu Zhu China
David Yudovich Sweden
Yumei Luo China
Emily M. Smith United States
В. В. Терских Russia
Cameron Arakaki United States
Jamil Amjad Hashmi
Citations per year, relative to Jamil Amjad Hashmi Jamil Amjad Hashmi (= 1×) peers Cameron Arakaki

Countries citing papers authored by Jamil Amjad Hashmi

Since Specialization
Citations

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

Fields of papers citing papers by Jamil Amjad Hashmi

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Jamil Amjad Hashmi. 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 Jamil Amjad Hashmi. The network helps show where Jamil Amjad Hashmi may publish in the future.

Co-authorship network of co-authors of Jamil Amjad Hashmi

This figure shows the co-authorship network connecting the top 25 collaborators of Jamil Amjad Hashmi. A scholar is included among the top collaborators of Jamil Amjad Hashmi 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 Jamil Amjad Hashmi. Jamil Amjad Hashmi 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.
Latif, Muhammad, et al.. (2024). Identification of Novel and Recurrent Variants in BTD, GBE1, AGL and ASL Genes in Families with Metabolic Disorders in Saudi Arabia. Journal of Clinical Medicine. 13(5). 1193–1193. 1 indexed citations
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Iqbal, Muhammad, et al.. (2024). Loss-of-function variant in spermidine/spermine N1-acetyl transferase like 1 (SATL1) gene as an underlying cause of autism spectrum disorder. Scientific Reports. 14(1). 5765–5765. 4 indexed citations
4.
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Hashmi, Jamil Amjad, et al.. (2022). NPHP3 splice acceptor site variant is associated with infantile nephronophthisis and asphyxiating thoracic dystrophy; A rare combination. European Journal of Medical Genetics. 65(10). 104578–104578. 1 indexed citations
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Hashmi, Jamil Amjad, et al.. (2021). A Novel Frameshift Mutation in the ITGB3 Gene Leading to Glanzmann’s Thrombasthenia in a Saudi Arabian Family. Hematology/Oncology and Stem Cell Therapy. 15(1). 21–26. 6 indexed citations
8.
Hashmi, Jamil Amjad, Sibtain Afzal, Khushnooda Ramzan, et al.. (2020). Homozygosity mapping and whole exome sequencing provide exact diagnosis of Cohen syndrome in a Saudi family. Brain and Development. 42(8). 587–593. 6 indexed citations
9.
Basit, Sulman, et al.. (2020). Centromere protein I (CENPI) is a candidate gene for X-linked steroid sensitive nephrotic syndrome. Journal of Nephrology. 33(4). 763–769. 7 indexed citations
10.
Hashmi, Jamil Amjad, et al.. (2020). Missense Mutations in theCTSCGene in Saudi Families Segregating Papillon-Lefèvre Syndrome. Annals of Dermatology. 32(1). 77–77. 3 indexed citations
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Afzal, Sibtain, et al.. (2019). A Heterozygous Mutation in the Triple Helical Region of the Alpha 1 (II) Chain of the COL2A1 Protein Causes Non-Lethal Spondyloepiphyseal Dysplasia Congenita. Genetic Testing and Molecular Biomarkers. 23(5). 310–315. 5 indexed citations
13.
Hashmi, Jamil Amjad, et al.. (2019). Novel homozygous loss-of-function mutations in RP1 and RP1L1 genes in retinitis pigmentosa patients. Ophthalmic Genetics. 40(6). 507–513. 14 indexed citations
14.
Hashmi, Jamil Amjad, et al.. (2018). An 18 bps in-frame deletion mutation in RUNX2 gene is a population polymorphism rather than a pathogenic variant. European Journal of Medical Genetics. 62(2). 124–128. 9 indexed citations
15.
Manikandan, Muthurangan, Sarah Abuelreich, Mona Elsafadi, et al.. (2018). NR2F1 mediated down-regulation of osteoblast differentiation was rescued by bone morphogenetic protein-2 (BMP-2) in human MSC. Differentiation. 104. 36–41. 16 indexed citations
16.
Elsafadi, Mona, Muthurangan Manikandan, Sami G. Almalki, et al.. (2018). TGFβ1-Induced Differentiation of Human Bone Marrow-Derived MSCs Is Mediated by Changes to the Actin Cytoskeleton. Stem Cells International. 2018. 1–14. 32 indexed citations
17.
Al‐Ayadhi, Laila, et al.. (2016). High-resolution SNP genotyping platform identified recurrent and novel CNVs in autism multiplex families. Neuroscience. 339. 561–570. 13 indexed citations
18.
Elsafadi, Mona, Muthurangan Manikandan, Muhammad Atteya, et al.. (2016). Characterization of Cellular and Molecular Heterogeneity of Bone Marrow Stromal Cells. Stem Cells International. 2016(1). 9378081–9378081. 41 indexed citations
19.
Hashmi, Jamil Amjad, Yusuf Zafar, Muhammad Arshad, Shahid Mansoor, & Shaheen Asad. (2011). Engineering cotton (Gossypium hirsutum L.) for resistance to cotton leaf curl disease using viral truncated AC1 DNA sequences. Virus Genes. 42(2). 286–296. 42 indexed citations
20.
Asad, Shaheen, Zahid Mukhtar, Jamil Amjad Hashmi, et al.. (2008). Silicon Carbide Whisker-Mediated Embryogenic Callus Transformation of Cotton (Gossypium hirsutum L.) and Regeneration of Salt Tolerant Plants. Molecular Biotechnology. 40(2). 161–169. 50 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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