Amjad Khan

713 total citations
40 papers, 291 citations indexed

About

Amjad Khan is a scholar working on Molecular Biology, Genetics and Developmental Biology. According to data from OpenAlex, Amjad Khan has authored 40 papers receiving a total of 291 indexed citations (citations by other indexed papers that have themselves been cited), including 23 papers in Molecular Biology, 18 papers in Genetics and 5 papers in Developmental Biology. Recurrent topics in Amjad Khan's work include Genomics and Rare Diseases (9 papers), Congenital limb and hand anomalies (5 papers) and Genomic variations and chromosomal abnormalities (5 papers). Amjad Khan is often cited by papers focused on Genomics and Rare Diseases (9 papers), Congenital limb and hand anomalies (5 papers) and Genomic variations and chromosomal abnormalities (5 papers). Amjad Khan collaborates with scholars based in Pakistan, China and Saudi Arabia. Amjad Khan's co-authors include Muhammad Umair, Rongrong Wang, Xue Zhang, Muhammad Bilal, Majid Alfadhel, Muhammad Younus, Farooq Ahmad, Safdar Abbas, Abdulaziz Asiri and Arif Mahmood and has published in prestigious journals such as New England Journal of Medicine, Movement Disorders and Genomics.

In The Last Decade

Amjad Khan

37 papers receiving 284 citations

Peers

Amjad Khan

GENET

CMN

Mathilde Nizon France

Yukiko Kuroda Japan

Marisol Mirabelli-Badenier Italy

Janice C. Palumbos United States

Xun Cheng China

Naveed Wasif Pakistan

Kelly E. Jackson United States

Simone Gana Italy

Chunyang Bai China

Yousef Shafeghati Iran

Mathilde Nizon France

Amjad Khan

239 ×1.4

153 ×1.2

GENET

26 ×0.7

45 ×1.8

CMN

14 ×0.7

Citations per year, relative to Amjad Khan Amjad Khan (= 1×) peers Mathilde Nizon

Countries citing papers authored by Amjad Khan

Since Specialization

Citations

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

Fields of papers citing papers by Amjad Khan

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Amjad Khan

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

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

Khan, Amjad, et al.. (2025). Identification of biomarkers and enrichment analysis in pancreatic adenocarcinoma through transcriptome analysis. 15(1). 1–16.

Sheraz, Muhammad, Sumaiya Khan, Saima Majeed, et al.. (2024). Burden of neurodevelopmental disorder in Lakki Marwat population of Khyber Pakhtunkhwa, Pakistan. Journal of Health Population and Nutrition. 43(1). 216–216.

Khan, Amjad, et al.. (2024). Further delineation of Wiedemann‐Rautenstrauch syndrome linked with POLR3A. Molecular Genetics & Genomic Medicine. 12(3). e2274–e2274. 1 indexed citations

Saima, Saima, Amjad Khan, Sajid Ali, et al.. (2024). Clinical genomics expands the link between erroneous cell division, primary microcephaly and intellectual disability. Neurogenetics. 25(3). 179–191. 2 indexed citations

Muzammal, Muhammad, Amjad Khan, Muhammad Ikram, et al.. (2023). Identification of GLI1 and KIAA0825 Variants in Two Families with Postaxial Polydactyly. Genes. 14(4). 869–869. 1 indexed citations

Sun, Liwei, Xueting Yang, Amjad Khan, et al.. (2023). Panoramic variation analysis of a family with neurodevelopmental disorders caused by biallelic loss-of-function variants in TMEM141, DDHD2, and LHFPL5. Frontiers of Medicine. 18(1). 81–97. 2 indexed citations

Khan, Amjad, Zhichao Miao, Shahid Niaz Khan, et al.. (2023). Exome sequencing identifies homozygous variants in MBOAT7 associated with neurodevelopmental disorder. Clinical Genetics. 105(4). 423–429. 3 indexed citations

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

Mahmood, Arif, et al.. (2021). Recalling the pathology of Parkinson's disease; lacking exact figure of prevalence and genetic evidence in Asia with an alarming outcome: A time to step‐up. Clinical Genetics. 100(6). 659–677. 12 indexed citations

10.

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

11.

Ahmad, Farooq, Qamre Alam, Tanveer Ahmad, et al.. (2021). Variants in the <b><i>PNPLA1</i></b> Gene in Families with Autosomal Recessive Congenital Ichthyosis Reveal Clinical Significance. Molecular Syndromology. 12(6). 351–361. 3 indexed citations

12.

Khan, Amjad, et al.. (2020). PDCD6IP , encoding a regulator of the ESCRT complex, is mutated in microcephaly. Clinical Genetics. 98(1). 80–85. 9 indexed citations

13.

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

14.

Sun, Liwei, et al.. (2020). Phenotypic Characterization of Intellectual Disability Caused by MBOAT7 Mutation in Two Consanguineous Pakistani Families. Frontiers in Pediatrics. 8. 585053–585053. 6 indexed citations

15.

Liu, Hongyan, et al.. (2019). Novel Compound Heterozygous Mutations in TTI2 Cause Syndromic Intellectual Disability in a Chinese Family. Frontiers in Genetics. 10. 1060–1060. 3 indexed citations

16.

Umair, Muhammad, Amjad Khan, Safdar Abbas, et al.. (2019). Biallelic Missense Mutation in the ECEL1 Underlies Distal Arthrogryposis Type 5 (DA5D). Frontiers in Pediatrics. 7. 343–343. 13 indexed citations

17.

Khan, Amjad, et al.. (2018). Identification of a Novel Nonsense ASPM Mutation in a Large Consanguineous Pakistani Family Using Targeted Next-Generation Sequencing. Genetic Testing and Molecular Biomarkers. 22(3). 159–164. 2 indexed citations

18.

Wang, Rongrong, et al.. (2017). Molecular Analysis of Twelve Pakistani Families with Nonsyndromic or Syndromic Hearing Loss. Genetic Testing and Molecular Biomarkers. 21(5). 316–321. 14 indexed citations

19.

Khan, Amjad, et al.. (2017). A novel homozygous missense mutation in BHLHA9 causes mesoaxial synostotic syndactyly with phalangeal reduction in a Pakistani family. Human Genome Variation. 4(1). 17054–17054. 10 indexed citations

20.

Kang, Huimin, Haifei Wang, Ziyao Fan, et al.. (2015). Resequencing diverse Chinese indigenous breeds to enrich the map of genomic variations in swine. Genomics. 106(5). 286–294. 6 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.

Explore authors with similar magnitude of impact