Khadim Shah

434 total citations
31 papers, 267 citations indexed

About

Khadim Shah is a scholar working on Molecular Biology, Genetics and Cell Biology. According to data from OpenAlex, Khadim Shah has authored 31 papers receiving a total of 267 indexed citations (citations by other indexed papers that have themselves been cited), including 19 papers in Molecular Biology, 11 papers in Genetics and 8 papers in Cell Biology. Recurrent topics in Khadim Shah's work include Skin and Cellular Biology Research (6 papers), RNA regulation and disease (5 papers) and Wnt/β-catenin signaling in development and cancer (4 papers). Khadim Shah is often cited by papers focused on Skin and Cellular Biology Research (6 papers), RNA regulation and disease (5 papers) and Wnt/β-catenin signaling in development and cancer (4 papers). Khadim Shah collaborates with scholars based in Pakistan, United States and Saudi Arabia. Khadim Shah's co-authors include Wasim Ahmad, Muhammad Umair, Abdul Nasır, Tobias B. Haack, Tim M. Strom, Bader Alhaddad, Thomas Meitinger, Elisabeth Graf, Paul Coucke and Raja Hussain Ali and has published in prestigious journals such as SHILAP Revista de lepidopterología, Human Molecular Genetics and RSC Advances.

In The Last Decade

Khadim Shah

28 papers receiving 267 citations

Peers

Khadim Shah
Amjad Khan Pakistan
Janice C. Palumbos United States
Zahid Azeem Pakistan
Ofer Yizhar‐Barnea United States
Sophie Scheidecker France
Asma Ali Khan Pakistan
Alisha Wilkens United States
Xun Cheng China
A. Schinzel Switzerland
Madoka Kumai Japan
Amjad Khan Pakistan
Khadim Shah
Citations per year, relative to Khadim Shah Khadim Shah (= 1×) peers Amjad Khan

Countries citing papers authored by Khadim Shah

Since Specialization
Citations

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

Fields of papers citing papers by Khadim Shah

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Khadim Shah

This figure shows the co-authorship network connecting the top 25 collaborators of Khadim Shah. A scholar is included among the top collaborators of Khadim Shah 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 Khadim Shah. Khadim Shah 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.
Mushtaq, Muhammad Hassan, et al.. (2024). Satisfaction of patients in government medical teaching institutes of Peshawar Khyber Pakhtunkhwa, Pakistan: a cross-sectional analytical study. SHILAP Revista de lepidopterología. 74(4). 701–705.
3.
4.
5.
Rashid, Abdur, et al.. (2022). A novel homozygous missense variant p.D339N in the PKLR gene correlates with pyruvate kinase deficiency in a Pakistani family: a case report. Journal of Medical Case Reports. 16(1). 66–66. 3 indexed citations
6.
Schrauwen, Isabelle, Khadim Shah, Anushree Acharya, et al.. (2022). Syntaxin 4 is essential for hearing in human and zebrafish. Human Molecular Genetics. 32(7). 1184–1192. 3 indexed citations
7.
Shah, Khadim, Sulman Basit, Ghazanfar Ali, et al.. (2021). A novel homozygous frameshift variant in the C3orf52 gene underlying isolated hair loss in a consanguineous family. European Journal of Dermatology. 31(3). 409–411.
8.
Fozia, Fozia, Khadim Shah, Rubina Nazli, et al.. (2021). Novel splicing‐site mutation in DCAF17 gene causing Woodhouse‐Sakati syndrome in a large consanguineous family. Journal of Clinical Laboratory Analysis. 36(1). e24127–e24127. 3 indexed citations
9.
Shah, Khadim, Abdul Aziz, Fazal ur Rehman, et al.. (2021). Novel Frameshift Mutations in XPC Gene Underlie Xeroderma Pigmentosum in Pakistani Families. Indian Journal of Dermatology. 66(2). 220–222. 9 indexed citations
10.
Siraj, Sami, et al.. (2020). Mechanisms underlying the wound healing and tissue regeneration properties of Chenopodium album. 3 Biotech. 10(10). 452–452. 17 indexed citations
11.
Schrauwen, Isabelle, Syed Irfan Raza, Kwanghyuk Lee, et al.. (2018). Identification of CACNA1D variants associated with sinoatrial node dysfunction and deafness in additional Pakistani families reveals a clinical significance. Journal of Human Genetics. 64(2). 153–160. 28 indexed citations
12.
Schrauwen, Isabelle, Imen Chakchouk, Anushree Acharya, et al.. (2018). Novel digenic inheritance of PCDH15 and USH1G underlies profound non-syndromic hearing impairment. BMC Medical Genetics. 19(1). 122–122. 16 indexed citations
13.
Irfanullah, Irfanullah, Amir Zeb, Khadim Shah, et al.. (2018). Molecular and in silico analyses validates pathogenicity of homozygous mutations in the NPR2 gene underlying variable phenotypes of Acromesomelic dysplasia, type Maroteaux. The International Journal of Biochemistry & Cell Biology. 102. 76–86. 15 indexed citations
14.
Shah, Khadim, Raja Hussain Ali, Muhammad Salman Chishti, et al.. (2017). Sequence variants in nine different genes underlying rare skin disorders in 10 consanguineous families. International Journal of Dermatology. 56(12). 1406–1413. 6 indexed citations
15.
Muhammad, Noor, Abdul Aziz, Sher Alam Khan, et al.. (2017). A novel mutation in homeobox DNA binding domain of HOXC13 gene underlies pure hair and nail ectodermal dysplasia (ECTD9) in a Pakistani family. BMC Medical Genetics. 18(1). 42–42. 8 indexed citations
16.
Ahmad, Farooq, Khadim Shah, Muhammad Nasim Khan, et al.. (2017). Novel sequence variants in the LIPH and LPAR6 genes underlies autosomal recessive woolly hair/hypotrichosis in consanguineous families. Congenital Anomalies. 58(1). 24–28. 6 indexed citations
17.
Umair, Muhammad, Khadim Shah, Bader Alhaddad, et al.. (2017). Exome sequencing revealed a splice site variant in the IQCE gene underlying post-axial polydactyly type A restricted to lower limb. European Journal of Human Genetics. 25(8). 960–965. 36 indexed citations
18.
Ullah, Asmat, Muhammad Umair, Sher Alam Khan, et al.. (2017). Sequence variants in four genes underlying Bardet-Biedl syndrome in consanguineous families.. PubMed. 23. 482–494. 25 indexed citations
19.
Shah, Khadim, Raja Hussain Ali, Muhammad Ansar, et al.. (2016). Mitral regurgitation as a phenotypic manifestation of nonphotosensitive trichothiodystrophy due to a splice variant in MPLKIP. BMC Medical Genetics. 17(1). 13–13. 4 indexed citations
20.
Shah, Khadim, Muhammad Ansar, Falak Sher Khan, et al.. (2016). Recessive progressive symmetric erythrokeratoderma results from a homozygous loss-of-function mutation of KRT83 and is allelic with dominant monilethrix. Journal of Medical Genetics. 54(3). 186–189. 10 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

Breakdown of academic impact, for papers by Amjad Khan Breakdown of academic impact, for papers by Janice C. Palumbos Breakdown of academic impact, for papers by Zahid Azeem Breakdown of academic impact, for papers by Ofer Yizhar‐Barnea Breakdown of academic impact, for papers by Sophie Scheidecker Breakdown of academic impact, for papers by Asma Ali Khan Breakdown of academic impact, for papers by Alisha Wilkens Breakdown of academic impact, for papers by Xun Cheng Breakdown of academic impact, for papers by A. Schinzel Breakdown of academic impact, for papers by Madoka Kumai
Rankless by CCL
2026