Muhammad Umair

17.2k total citations
149 papers, 1.8k citations indexed

About

Muhammad Umair is a scholar working on Molecular Biology, Genetics and Developmental Biology. According to data from OpenAlex, Muhammad Umair has authored 149 papers receiving a total of 1.8k indexed citations (citations by other indexed papers that have themselves been cited), including 85 papers in Molecular Biology, 59 papers in Genetics and 19 papers in Developmental Biology. Recurrent topics in Muhammad Umair's work include Congenital limb and hand anomalies (19 papers), Genomics and Rare Diseases (16 papers) and Hedgehog Signaling Pathway Studies (16 papers). Muhammad Umair is often cited by papers focused on Congenital limb and hand anomalies (19 papers), Genomics and Rare Diseases (16 papers) and Hedgehog Signaling Pathway Studies (16 papers). Muhammad Umair collaborates with scholars based in Pakistan, Saudi Arabia and China. Muhammad Umair's co-authors include Majid Alfadhel, Wasim Ahmad, Farooq Ahmad, Muhammad Bilal, Chen Chen, Asmat Ullah, Safdar Abbas, Yusra Alyafee, Amjad Khan and Sulman Basit and has published in prestigious journals such as SHILAP Revista de lepidopterología, PLoS ONE and Scientific Reports.

In The Last Decade

Muhammad Umair

134 papers receiving 1.8k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Muhammad Umair Pakistan 24 860 574 208 133 127 149 1.8k
Xinping Yang China 27 1.2k 1.4× 289 0.5× 71 0.3× 59 0.4× 76 0.6× 74 2.0k
Muhammad Wajid Pakistan 22 918 1.1× 243 0.4× 49 0.2× 154 1.2× 30 0.2× 87 1.8k
Li Zeng China 24 1000 1.2× 193 0.3× 19 0.1× 111 0.8× 15 0.1× 79 1.9k
Wenyong Li China 19 311 0.4× 149 0.3× 45 0.2× 365 2.7× 31 0.2× 93 1.3k
Pengfei Liu China 28 1.1k 1.3× 724 1.3× 5 0.0× 196 1.5× 147 1.2× 147 2.3k
Ming Qi China 17 909 1.1× 353 0.6× 5 0.0× 174 1.3× 58 0.5× 84 1.8k
Hideo Nishimura Japan 21 250 0.3× 158 0.3× 21 0.1× 57 0.4× 339 2.7× 112 1.5k
George Papanikolaou Greece 19 357 0.4× 49 0.1× 6 0.0× 81 0.6× 80 0.6× 80 3.3k
Kenichi Iwasaki Japan 21 337 0.4× 67 0.1× 6 0.0× 178 1.3× 35 0.3× 91 1.2k
Yuanyuan Xiao China 23 809 0.9× 243 0.4× 3 0.0× 47 0.4× 107 0.8× 88 1.6k

Countries citing papers authored by Muhammad Umair

Since Specialization
Citations

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

Fields of papers citing papers by Muhammad Umair

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Muhammad Umair

This figure shows the co-authorship network connecting the top 25 collaborators of Muhammad Umair. A scholar is included among the top collaborators of Muhammad Umair 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 Muhammad Umair. Muhammad Umair 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.
Aslam, Muhammad, et al.. (2025). A Novel Homozygous Loss-of-Function Variant in GPR156 Delineates Non-syndromic Hearing Loss. Biochemical Genetics. 64(1). 89–95. 1 indexed citations
2.
Umair, Muhammad, Zaheer Ahmed, Bilal Shaker, et al.. (2024). A novel homozygous FAM92A gene (CIBAR1) variant further confirms its association with non‐syndromic postaxial polydactyly type A9 (PAPA9). Clinical Genetics. 106(4). 488–493. 2 indexed citations
3.
Zeb, Shah, Zhen Yang, Riming Hu, et al.. (2023). Electronic structure and oxygen vacancy tuning of Co & Ni co-doped W18O49 nanourchins for efficient TEA gas sensing. Chemical Engineering Journal. 465. 142815–142815. 82 indexed citations
4.
Alangari, Abdullah, et al.. (2023). Assessment of attitudes towards the use of preimplantation genetic diagnosis in a single center in Riyadh, Saudi Arabia. Journal of Genetic Counseling. 32(5). 1032–1039.
5.
Umair, Muhammad. (2023). Rare genetic disorders: Beyond whole‐exome sequencing. The Journal of Gene Medicine. 25(10). e3503–e3503. 14 indexed citations
6.
7.
Ajmal, Amar, Arif Mahmood, Mohammed Ageeli Hakami, et al.. (2023). Computer-assisted drug repurposing for thymidylate kinase drug target in monkeypox virus. Frontiers in Cellular and Infection Microbiology. 13. 1159389–1159389. 33 indexed citations
8.
Afsar, Tayyaba, Ahmed Waqas, Safdar Abbas, et al.. (2023). A Novel Variant in the PAX4 Gene Causes Maturity-Onset Diabetes of the Young (MODY), Type IX with Neurodevelopmental Disorder. SHILAP Revista de lepidopterología. 2(2).
9.
Rehman, Gauhar, Amin Jan, Jamshid Khan, et al.. (2023). Two novel homozygous variants of ATP6V0A2 and ALDH18A1 lead to autosomal recessive cutis laxa type 2 and 3 in two Pakistani families. The Journal of Gene Medicine. 25(10). e3522–e3522. 1 indexed citations
10.
Bilal, Muhammad, et al.. (2022). Genetic overview of postaxial polydactyly: Updated classification. Clinical Genetics. 103(1). 3–15. 11 indexed citations
11.
Mahmood, Arif, Abdus Samad, Abid Ali Shah, et al.. (2022). A novel biallelic variant in the Popeye domain‐containing protein 1 ( POPDC1 ) underlies limb girdle muscle dystrophy type 25. Clinical Genetics. 103(2). 219–225. 12 indexed citations
12.
Thayananthan, Vijey, et al.. (2022). The Handover and Performance Analysis of LTE Network with Traditional and SDN Approaches. Wireless Communications and Mobile Computing. 2022(1). 5 indexed citations
13.
Khan, Amjad, Fadhel A. Alomar, Muhammad Umair, et al.. (2022). SPTBN5, Encoding the βV-Spectrin Protein, Leads to a Syndrome of Intellectual Disability, Developmental Delay, and Seizures. Frontiers in Molecular Neuroscience. 15. 877258–877258. 11 indexed citations
14.
15.
Schönewolf‐Greulich, Bitten, Alexandra Afenjar, Magalie Barth, et al.. (2021). Clinical and molecular delineation of PUS3 ‐associated neurodevelopmental disorders. Clinical Genetics. 100(5). 628–633. 26 indexed citations
16.
Khan, Amjad, Anne Molitor, Sylvain Mayeur, et al.. (2021). A Homozygous Missense Variant in PPP1R1B/DARPP‐32 Is Associated With Generalized Complex Dystonia. Movement Disorders. 37(2). 365–374. 9 indexed citations
17.
Alyafee, Yusra, et al.. (2021). Next-Generation Sequencing-Based Pre-Implantation Genetic Testing for Aneuploidy (PGT-A): First Report from Saudi Arabia. Genes. 12(4). 461–461. 28 indexed citations
18.
Khan, Amjad, Zhichao Miao, Muhammad Umair, et al.. (2020). Two Cases of Recessive Intellectual Disability Caused by NDST1 and METTL23 Variants. Genes. 11(9). 1021–1021. 11 indexed citations
19.
Umair, Muhammad, Muhammad Bilal, Raja Hussain Ali, et al.. (2019). Whole‐exome sequencing revealed a nonsense mutation in STKLD1 causing non‐syndromic pre‐axial polydactyly type A affecting only upper limb. Clinical Genetics. 96(2). 134–139. 8 indexed citations
20.
Zaynab, Madiha, et al.. (2018). TRANSCRIPTOME AND PROTEOMICS INTERACTION REVEALS LOW SEED GERMINATION OF CYCLOBALNOPSIS GILVA TO SAVE FOREST ECOLOGY. Applied Ecology and Environmental Research. 16(5). 5681–5692. 2 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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