Naveed Wasif

638 total citations
30 papers, 322 citations indexed

About

Naveed Wasif is a scholar working on Molecular Biology, Genetics and Cell Biology. According to data from OpenAlex, Naveed Wasif has authored 30 papers receiving a total of 322 indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Molecular Biology, 12 papers in Genetics and 8 papers in Cell Biology. Recurrent topics in Naveed Wasif's work include Skin and Cellular Biology Research (8 papers), Hair Growth and Disorders (7 papers) and dental development and anomalies (5 papers). Naveed Wasif is often cited by papers focused on Skin and Cellular Biology Research (8 papers), Hair Growth and Disorders (7 papers) and dental development and anomalies (5 papers). Naveed Wasif collaborates with scholars based in Pakistan, Germany and Saudi Arabia. Naveed Wasif's co-authors include Wasim Ahmad, Ghazanfar Ali, Sulman Basit, Muhammad Tariq, Syed Kamran‐ul‐Hassan Naqvi, Muhammad Ansar, Saadullah Khan, Musharraf Jelani, Muhammad Ayub and Eva Klopocki and has published in prestigious journals such as British Journal of Dermatology, Journal of Medical Genetics and Human Genetics.

In The Last Decade

Naveed Wasif

28 papers receiving 321 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Naveed Wasif Pakistan	11	202	112	101	101	40	30	322
Farooq Ahmad Pakistan	12	272 1.3×	39 0.3×	20 0.2×	227 2.2×	108 2.7×	38	421
Muhammad Salman Chishti Pakistan	11	268 1.3×	159 1.4×	68 0.7×	120 1.2×	2 0.1×	14	385
Xuanzhu Liu China	11	224 1.1×	123 1.1×	20 0.2×	56 0.6×	3 0.1×	14	333
Maria Rosaria Piemontese Italy	12	248 1.2×	111 1.0×	6 0.1×	141 1.4×	10 0.3×	23	393
Michiel J.R. van der Wielen Netherlands	6	176 0.9×	48 0.4×	22 0.2×	71 0.7×	3 0.1×	8	245
Chunyang Bai China	6	724 3.6×	35 0.3×	11 0.1×	238 2.4×	20 0.5×	12	782
Jost Schönberger Germany	7	351 1.7×	48 0.4×	11 0.1×	39 0.4×	6 0.1×	8	515
Amjad Khan Pakistan	12	170 0.8×	39 0.3×	4 0.0×	124 1.2×	19 0.5×	40	291
Yousef Shafeghati Iran	7	383 1.9×	56 0.5×	6 0.1×	67 0.7×	6 0.1×	32	478
Herbert Reichenbach Germany	6	308 1.5×	15 0.1×	27 0.3×	145 1.4×	26 0.7×	9	411

Countries citing papers authored by Naveed Wasif

Since Specialization

Citations

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

Fields of papers citing papers by Naveed Wasif

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Naveed Wasif

This figure shows the co-authorship network connecting the top 25 collaborators of Naveed Wasif. A scholar is included among the top collaborators of Naveed Wasif 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 Naveed Wasif. Naveed Wasif 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

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.

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.

Yasin, Muhammad, et al.. (2023). Molecular insight into CREBBP and TANGO2 variants causing intellectual disability. The Journal of Gene Medicine. 26(1). e3591–e3591. 2 indexed citations

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

Parveen, Asia, et al.. (2023). A novel frameshift variant in UBA2 causing split-hand/foot malformations in a Pakistani family. Human Genome Variation. 10(1). 16–16. 2 indexed citations

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

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

Parveen, Asia, et al.. (2020). A Novel Homozygous Frameshift Variant in DYM Causing Dyggve-Melchior-Clausen Syndrome in Pakistani Patients. Frontiers in Pediatrics. 8. 383–383. 9 indexed citations

Khan, Sher Alam, Muhammad Adnan Khan, Niamat Khan, et al.. (2020). A novel nonsense variant in SLC24A4 causing a rare form of amelogenesis imperfecta in a Pakistani family. BMC Medical Genetics. 21(1). 97–97. 8 indexed citations

10.

Parveen, Asia, et al.. (2019). A Novel Homozygous Frameshift Mutation in CCN6 Causing Progressive Pseudorheumatoid Dysplasia (PPRD) in a Consanguineous Yemeni Family. Frontiers in Pediatrics. 7. 245–245. 3 indexed citations

11.

Wasif, Naveed & Wasim Ahmad. (2012). A Novel Nonsense Mutation in RSPO4 Gene Underlies Autosomal Recessive Congenital Anonychia in a Pakistani Family. Pediatric Dermatology. 30(1). 139–141. 9 indexed citations

12.

Kalsoom, Umme, Eva Klopocki, Naveed Wasif, et al.. (2012). Whole exome sequencing identified a novel zinc-finger gene ZNF141 associated with autosomal recessive postaxial polydactyly type A. Journal of Medical Genetics. 50(1). 47–53. 41 indexed citations

13.

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

14.

Azeem, Zahid, Naveed Wasif, Sulman Basit, et al.. (2011). Congenital atrichia with papular lesions resulting from novel mutations in human hairless gene in four consanguineous families. The Journal of Dermatology. 38(8). 755–760. 9 indexed citations

15.

Basit, Sulman, Ghazanfar Ali, Naveed Wasif, Muhammad Ansar, & Wasim Ahmad. (2010). Genetic mapping of a novel hypotrichosis locus to chromosome 7p21.3–p22.3 in a Pakistani family and screening of the candidate genes. Human Genetics. 128(2). 213–220. 15 indexed citations

16.

Wasif, Naveed, Muhammad Tariq, Ghazanfar Ali, Muhammad Jawad Hassan, & Wasim Ahmad. (2010). A Novel Splice Site Mutation in theEDARGene Underlies Autosomal Recessive Hypohidrotic Ectodermal Dysplasia in a Pakistani Family. Pediatric Dermatology. 27(1). 106–108. 1 indexed citations

17.

Wasif, Naveed, et al.. (2009). A novel missense mutation in the EVC gene underlies Ellis‐van Creveld syndrome in a Pakistani family. Pediatrics International. 52(2). 240–246. 10 indexed citations

18.

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

19.

Basit, Sulman, Syed Kamran‐ul‐Hassan Naqvi, Naveed Wasif, et al.. (2008). A novel insertion mutation in the cartilage-derived morphogenetic protein-1 (CDMP1) gene underlies Grebe-type chondrodysplasia in a consanguineous Pakistani family. BMC Medical Genetics. 9(1). 102–102. 29 indexed citations

20.

Jelani, Musharraf, et al.. (2008). A novel deletion mutation in LIPH gene causes autosomal recessive hypotrichosis (LAH2). Clinical Genetics. 74(2). 184–188. 23 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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