Mohsin Shahzad

1.6k total citations · 1 hit paper
30 papers, 668 citations indexed

About

Mohsin Shahzad is a scholar working on Molecular Biology, Sensory Systems and Otorhinolaryngology. According to data from OpenAlex, Mohsin Shahzad has authored 30 papers receiving a total of 668 indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Molecular Biology, 13 papers in Sensory Systems and 5 papers in Otorhinolaryngology. Recurrent topics in Mohsin Shahzad's work include Hearing, Cochlea, Tinnitus, Genetics (12 papers), Ear Surgery and Otitis Media (5 papers) and RNA and protein synthesis mechanisms (5 papers). Mohsin Shahzad is often cited by papers focused on Hearing, Cochlea, Tinnitus, Genetics (12 papers), Ear Surgery and Otitis Media (5 papers) and RNA and protein synthesis mechanisms (5 papers). Mohsin Shahzad collaborates with scholars based in Pakistan, United States and Saudi Arabia. Mohsin Shahzad's co-authors include Saima Riazuddin, Zubair M. Ahmed, Sheikh Riazuddin, Thomas B. Friedman, Shaheen N. Khan, Atteeq U. Rehman, Robert J. Morell, Shahid Y. Khan, Inna A. Belyantseva and Erich T. Boger and has published in prestigious journals such as Scientific Reports, The American Journal of Human Genetics and RSC Advances.

In The Last Decade

Mohsin Shahzad

28 papers receiving 656 citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Tuning diffusion coefficient, ionic conductivity, and transference number in rGO/BaCoO ₃ electrode material for optimized supercapacitor energy storage

2025 26 citations Mohsin Shahzad, Farooq Ahmad et al. RSC Advances profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Mohsin Shahzad Pakistan	13	355	303	132	85	76	30	668
Kiyomi Hamaguchi Japan	12	226 0.6×	153 0.5×	55 0.4×	84 1.0×	57 0.8×	36	535
Ye‐Ri Kim South Korea	13	265 0.7×	174 0.6×	66 0.5×	42 0.5×	18 0.2×	26	518
Gaoying Sun China	13	352 1.0×	346 1.1×	121 0.9×	12 0.1×	23 0.3×	25	736
Wenhao Xu United States	14	470 1.3×	94 0.3×	43 0.3×	110 1.3×	9 0.1×	33	753
Jingfang Wu China	12	409 1.2×	295 1.0×	33 0.3×	12 0.1×	64 0.8×	34	748
Sung K. Moon United States	15	140 0.4×	171 0.6×	62 0.5×	9 0.1×	115 1.5×	33	535
Julie A. Alosi United States	9	170 0.5×	197 0.7×	38 0.3×	13 0.2×	30 0.4×	12	406
Chunjie Tian South Korea	12	139 0.4×	206 0.7×	74 0.6×	11 0.1×	45 0.6×	17	367
Aida Nourbakhsh United States	10	398 1.1×	58 0.2×	39 0.3×	26 0.3×	15 0.2×	21	698

Countries citing papers authored by Mohsin Shahzad

Since Specialization

Citations

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

Fields of papers citing papers by Mohsin Shahzad

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Mohsin Shahzad

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

All Works

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20 of 20 papers shown

Shah, Abdul Bari, et al.. (2025). Isolation, characterization, antidiabetic and antityrosinase potentials of compounds isolated from Anabasis Articulata. Applied Food Research. 5(1). 100949–100949.

Shahzad, Mohsin, et al.. (2025). Tuning diffusion coefficient, ionic conductivity, and transference number in rGO/BaCoO ₃ electrode material for optimized supercapacitor energy storage. RSC Advances. 15(8). 6308–6323. 26 indexed citations breakdown →

Shahzad, Mohsin, Javed Akram, Kausar Malik, et al.. (2024). A Missense Variant in HACE1 Is Associated with Intellectual Disability, Epilepsy, Spasticity, and Psychomotor Impairment in a Pakistani Kindred. Genes. 15(5). 580–580.

Arshad, Muhammad, et al.. (2023). FRMD7 Gene Alterations in a Pakistani Family Associated with Congenital Idiopathic Nystagmus. Genes. 14(2). 346–346. 2 indexed citations

Basharat, Zarrin, Muhammad Shakeel, Mohsin Shahzad, et al.. (2022). Genomic analysis of Chryseobacterium indologenes and conformational dynamics of the selected DD-peptidase. Research in Microbiology. 174(1-2). 103990–103990. 10 indexed citations

Khan, Shahid Y., Xiaodong Jiao, Asma Ali Khan, et al.. (2022). Next-generation whole exome sequencing to delineate the genetic basis of primary congenital glaucoma. Scientific Reports. 12(1). 17218–17218. 5 indexed citations

Irfan, Ahmad, Muhammad Imran, Muhammad Khalid, et al.. (2021). Phenolic and flavonoid contents in Malva sylvestris and exploration of active drugs as antioxidant and anti-COVID19 by quantum chemical and molecular docking studies. Journal of Saudi Chemical Society. 25(8). 101277–101277. 36 indexed citations

Imran, Muhammad, Ajaz Hussain, Jalal Uddin, et al.. (2021). In silico screening, SAR and kinetic studies of naturally occurring flavonoids against SARS CoV-2 main protease. Arabian Journal of Chemistry. 15(1). 103473–103473. 10 indexed citations

Booth, Kevin T., Mureed Hussain, Kathy Frees, et al.. (2020). Novel loss-of-function mutations in COCH cause autosomal recessive nonsyndromic hearing loss. Human Genetics. 139(12). 1565–1574. 16 indexed citations

10.

Richard, Élodie M., D.L. Polla, Muhammad Zaman Khan Assir, et al.. (2019). Bi-allelic Variants in METTL5 Cause Autosomal-Recessive Intellectual Disability and Microcephaly. The American Journal of Human Genetics. 105(4). 869–878. 69 indexed citations

11.

Waryah, Ali Muhammad, et al.. (2017). Genetic Testing of Non-familial Deaf Patients for CIB2 and GJB2 Mutations: Phenotype and Genetic Counselling. Biochemical Genetics. 55(5-6). 410–420. 3 indexed citations

12.

Rehman, Atteeq U., Jonathan E. Bird, Rabia Faridi, et al.. (2016). Mutational Spectrum ofMYO15Aand the Molecular Mechanisms of DFNB3 Human Deafness. Human Mutation. 37(10). 991–1003. 55 indexed citations

13.

Nayak, Gowri, Lukáš Varga, Mohsin Shahzad, et al.. (2015). Molecular genetics of MARVELD2 and clinical phenotype in Pakistani and Slovak families segregating DFNB49 hearing loss. Human Genetics. 134(4). 423–437. 15 indexed citations

14.

Shahzad, Mohsin, Cecilia Herráiz, Rizwan Yousaf, et al.. (2015). Identification and functional characterization of natural human melanocortin 1 receptor mutant alleles in Pakistani population. Pigment Cell & Melanoma Research. 28(6). 730–735. 3 indexed citations

15.

Shaikh, Rehan Sadiq, Robert A. Sisk, Mohsin Shahzad, et al.. (2014). Homozygous missense variant in the human CNGA3 channel causes cone-rod dystrophy. European Journal of Human Genetics. 23(4). 473–480. 24 indexed citations

16.

Iqbal, Zafar, Kornelia Neveling, Mohsin Shahzad, et al.. (2012). Targeted Next Generation Sequencing Reveals a Novel Intragenic Deletion of the TPO Gene in a Family with Intellectual Disability. Archives of Medical Research. 43(4). 312–316. 10 indexed citations

17.

Rehman, Atteeq U., Robert J. Morell, Kwanghyuk Lee, et al.. (2011). Mutations of GIPC3 cause nonsyndromic hearing loss DFNB72 but not DFNB81 that also maps to chromosome 19p. Human Genetics. 130(6). 759–765. 34 indexed citations

18.

Waryah, Ali Muhammad, Zubair M. Ahmed, Daniel Choo, et al.. (2011). Molecular and clinical studies of X-linked deafness among Pakistani families. Journal of Human Genetics. 56(7). 534–540. 10 indexed citations

19.

Rehman, Atteeq U., Robert J. Morell, Inna A. Belyantseva, et al.. (2010). Targeted Capture and Next-Generation Sequencing Identifies C9orf75, Encoding Taperin, as the Mutated Gene in Nonsyndromic Deafness DFNB79. The American Journal of Human Genetics. 86(3). 378–388. 145 indexed citations

20.

Riazuddin, Saima, Mohsin Shahzad, Tayyab Husnaın, et al.. (2009). Identities and frequencies of mutations of the otoferlin gene (OTOF) causing DFNB9 deafness in Pakistan. Clinical Genetics. 75(3). 237–243. 79 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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