Saadullah Khan

1.2k total citations
62 papers, 645 citations indexed

About

Saadullah Khan is a scholar working on Molecular Biology, Genetics and Cell Biology. According to data from OpenAlex, Saadullah Khan has authored 62 papers receiving a total of 645 indexed citations (citations by other indexed papers that have themselves been cited), including 34 papers in Molecular Biology, 24 papers in Genetics and 18 papers in Cell Biology. Recurrent topics in Saadullah Khan's work include Skin and Cellular Biology Research (10 papers), Genomic variations and chromosomal abnormalities (7 papers) and Genetics and Neurodevelopmental Disorders (7 papers). Saadullah Khan is often cited by papers focused on Skin and Cellular Biology Research (10 papers), Genomic variations and chromosomal abnormalities (7 papers) and Genetics and Neurodevelopmental Disorders (7 papers). Saadullah Khan collaborates with scholars based in Pakistan, Germany and Saudi Arabia. Saadullah Khan's co-authors include Wasim Ahmad, Noor Muhammad, Sulman Basit, Irfanullah Irfanullah, Muzammil Ahmad Khan, Naveed Wasif, Suzanne M. Leal, Sher Alam Khan, Muhammad Umair and Muhammad Nasim Khan and has published in prestigious journals such as SHILAP Revista de lepidopterología, The American Journal of Human Genetics and Gene.

In The Last Decade

Saadullah Khan

59 papers receiving 630 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Saadullah Khan Pakistan 15 400 214 110 62 51 62 645
Rhonda E. Schnur United States 20 505 1.3× 333 1.6× 261 2.4× 18 0.3× 20 0.4× 52 919
Rita Fischetto Italy 15 486 1.2× 538 2.5× 21 0.2× 7 0.1× 22 0.4× 33 837
Brenda Watt United States 8 593 1.5× 82 0.4× 290 2.6× 18 0.3× 2 0.0× 9 860
Muzammil Ahmad Khan Pakistan 11 411 1.0× 182 0.9× 97 0.9× 4 0.1× 8 0.2× 47 558
Jean‐Baptiste Vincourt France 13 238 0.6× 75 0.4× 37 0.3× 15 0.2× 4 0.1× 21 437
Catherine R. Begy United States 9 715 1.8× 278 1.3× 43 0.4× 14 0.2× 5 0.1× 9 1.3k
Jotaro Nakanishi Japan 12 192 0.5× 25 0.1× 140 1.3× 29 0.5× 3 0.1× 19 515
Sandra M. Pasternack Germany 14 538 1.3× 98 0.5× 378 3.4× 4 0.1× 5 0.1× 21 823
Ariadna Perez‐Balaguer Spain 12 498 1.2× 56 0.3× 121 1.1× 7 0.1× 6 0.1× 14 607
Arturo Incao United States 12 176 0.4× 73 0.3× 126 1.1× 7 0.1× 2 0.0× 15 355

Countries citing papers authored by Saadullah Khan

Since Specialization
Citations

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

Fields of papers citing papers by Saadullah Khan

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Saadullah Khan

This figure shows the co-authorship network connecting the top 25 collaborators of Saadullah Khan. A scholar is included among the top collaborators of Saadullah 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 Saadullah Khan. Saadullah Khan 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.
Khan, Sher Alam, Samin Jan, Salah Ud Din, et al.. (2025). Truncated Variants in FAM20A and WDR72 Genes Underlie Autosomal Recessive Amelogenesis Imperfecta in Four Pakistani Families. Biochemical Genetics. 64(1). 1311–1323.
2.
Kalsoom, Umme, et al.. (2025). A pathogenic COL7A1 variant highlights semi-dominant inheritance in dystrophic epidermolysis bullosa. BMC Medical Genomics. 18(1). 26–26.
3.
Rawlins, Lettie E., Niamat Khan, Saadullah Khan, et al.. (2024). Expanding the genetic spectrum of hereditary motor sensory neuropathies in Pakistan. BMC Neurology. 24(1). 394–394. 1 indexed citations
4.
Khan, Sher Alam, et al.. (2024). Variants in HCFC1 and MN1 genes causing intellectual disability in two Pakistani families. BMC Medical Genomics. 17(1). 176–176. 2 indexed citations
5.
Acharya, Anushree, Saadullah Khan, Irfan Ullah, et al.. (2024). THBS1 is a new autosomal recessive non-syndromic hearing impairment gene. BMC Medical Genomics. 17(1). 291–291. 1 indexed citations
6.
Parveen, Asia, Sher Alam Khan, Noor Muhammad, et al.. (2023). Brachyolmia, dental anomalies and short stature (DASS): Phenotype and genotype analyses of Egyptian and Pakistani patients. Heliyon. 10(1). e23688–e23688.
7.
Rehman, Zia Ur, Sher Alam Khan, Samin Jan, et al.. (2023). Autosomal recessive variants c.953A>C and c.97-1G>C in NSUN2 causing intellectual disability: a molecular dynamics simulation study of loss-of-function mechanisms. Frontiers in Neurology. 14. 1168307–1168307. 5 indexed citations
8.
Khan, Saadullah, et al.. (2023). Revolutionizing Potato Farming: Dynamic Innovations Reshaping Late Blight Control in Pakistan. 2–7. 1 indexed citations
9.
Khan, Sher Alam, Saadullah Khan, Noor Muhammad, et al.. (2022). The First Report of a Missense Variant in RFX2 Causing Non-Syndromic Tooth Agenesis in a Consanguineous Pakistani Family. Frontiers in Genetics. 12. 782653–782653. 2 indexed citations
10.
Fozia, Fozia, Rubina Nazli, Nousheen Bibi, et al.. (2021). Whole Exome Sequencing Confirms Molecular Diagnostics of Three Pakhtun Families With Autosomal Recessive Epidermolysis Bullosa. Frontiers in Pediatrics. 9. 727288–727288. 1 indexed citations
11.
Khan, Sher Alam, Asmat Ullah, Nousheen Bibi, et al.. (2020). Homozygous variants of EDAR underlying hypohidrotic ectodermal dysplasia in three consanguineous families. European Journal of Dermatology. 30(4). 408–416. 5 indexed citations
12.
Ahmed, Rizwan Raheem, Christian Windpassinger, Muhammad Salim, et al.. (2019). Genetic Study of Khyber-Pukhtunkhwa Resident Pakistani Families Presenting Primary Microcephaly With Intellectual Disability. Journal of the Pakistan Medical Association. 69(0). 1–1. 5 indexed citations
13.
Muhammad, Noor, Sher Alam Khan, Waheed Ullah, et al.. (2017). A novel mutation in the HPGD gene causing primary hypertrophic osteoarthropathy with digital clubbing in a Pakistani family. Annals of Human Genetics. 82(3). 171–176. 9 indexed citations
14.
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
15.
Ullah, Waheed, Muhammad Qasim, Hazır Rahman, et al.. (2017). CTX-M-15 and OXA-10 beta lactamases in multi drug resistant Pseudomonas aeruginosa : First report from Pakistan. Microbial Pathogenesis. 105. 240–244. 18 indexed citations
16.
17.
Khan, Saadullah, Imran Ullah, Irfanullah Irfanullah, et al.. (2012). Novel homozygous mutations in the genes ARL6 and BBS10 underlying Bardet–Biedl syndrome. Gene. 515(1). 84–88. 19 indexed citations
18.
Lee, Kwanghyuk, Saadullah Khan, Muhammad Ansar, et al.. (2011). A Novel ESRRB Deletion Is a Rare Cause of Autosomal Recessive Nonsyndromic Hearing Impairment among Pakistani Families. PubMed. 2011. 1–4. 9 indexed citations
19.
Khan, Saadullah, Rabia Habib, Hina Mir, et al.. (2011). Mutations in the LPAR6 and LIPH genes underlie autosomal recessive hypotrichosis/woolly hair in 17 consanguineous families from Pakistan. Clinical and Experimental Dermatology. 36(6). 652–654. 13 indexed citations
20.
Tariq, Muhammad, Muhammad Ayub, Musharraf Jelani, et al.. (2009). Mutations in theP2RY5gene underlie autosomal recessive hypotrichosis in 13 Pakistani families. British Journal of Dermatology. 160(5). 1006–1010. 15 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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