Musharraf Jelani

956 total citations
53 papers, 643 citations indexed

About

Musharraf Jelani is a scholar working on Molecular Biology, Cell Biology and Genetics. According to data from OpenAlex, Musharraf Jelani has authored 53 papers receiving a total of 643 indexed citations (citations by other indexed papers that have themselves been cited), including 32 papers in Molecular Biology, 23 papers in Cell Biology and 20 papers in Genetics. Recurrent topics in Musharraf Jelani's work include Skin and Cellular Biology Research (12 papers), Wnt/β-catenin signaling in development and cancer (8 papers) and Hair Growth and Disorders (6 papers). Musharraf Jelani is often cited by papers focused on Skin and Cellular Biology Research (12 papers), Wnt/β-catenin signaling in development and cancer (8 papers) and Hair Growth and Disorders (6 papers). Musharraf Jelani collaborates with scholars based in Pakistan, Saudi Arabia and United Kingdom. Musharraf Jelani's co-authors include Wasim Ahmad, Jumana Y. Al‐Aama, Mona Mohammad Almramhi, Saleem Ahmed, Muhammad Ayub, Syed Sikander Azam, Reaz Uddin, Jamal Nasir, Abdul Wadood and Sulman Basit and has published in prestigious journals such as Blood, PLoS ONE and Brain.

In The Last Decade

Musharraf Jelani

49 papers receiving 640 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Musharraf Jelani Pakistan 17 401 228 142 102 56 53 643
Luciana I. Gallo Argentina 13 375 0.9× 180 0.8× 54 0.4× 47 0.5× 32 0.6× 22 644
Fiona J. Houghton Australia 17 694 1.7× 579 2.5× 61 0.4× 24 0.2× 69 1.2× 25 1.1k
Petra Ovaere Belgium 5 345 0.9× 222 1.0× 35 0.2× 52 0.5× 82 1.5× 6 796
Marie-Cécile Lenoir France 9 436 1.1× 115 0.5× 205 1.4× 88 0.9× 149 2.7× 17 815
Kerstin Thriene Germany 12 217 0.5× 229 1.0× 100 0.7× 10 0.1× 115 2.1× 15 565
Lenka Řežábková Czechia 17 606 1.5× 237 1.0× 61 0.4× 13 0.1× 14 0.3× 20 727
Paolo Pertile Italy 11 784 2.0× 748 3.3× 46 0.3× 133 1.3× 31 0.6× 16 1.2k
Alicia Cabezas Spain 11 426 1.1× 425 1.9× 56 0.4× 9 0.1× 69 1.2× 29 725
E.D. Kuhlmann Netherlands 16 499 1.2× 90 0.4× 37 0.3× 39 0.4× 62 1.1× 27 842
Lihui Wang China 16 513 1.3× 175 0.8× 36 0.3× 20 0.2× 100 1.8× 43 955

Countries citing papers authored by Musharraf Jelani

Since Specialization
Citations

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

Fields of papers citing papers by Musharraf Jelani

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Musharraf Jelani

This figure shows the co-authorship network connecting the top 25 collaborators of Musharraf Jelani. A scholar is included among the top collaborators of Musharraf Jelani 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 Musharraf Jelani. Musharraf Jelani 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.
2.
Ramzan, Khushnooda, et al.. (2024). A homozygous variant in ARHGAP39 is associated with lethal cerebellar vermis hypoplasia in a consanguineous Saudi family. Scientific Reports. 14(1). 25291–25291.
3.
Shams, Sulaiman, Nousheen Bibi, Asmat Ullah, et al.. (2023). A Novel Homozygous Nonsense Variant in the DYM Underlies Dyggve-Melchior-Clausen Syndrome in Large Consanguineous Family. Genes. 14(2). 510–510. 3 indexed citations
4.
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
5.
Rasool, Akhtar, Muhammad Ilyas, Allah Rakha, et al.. (2023). Phenotypic Classification of Eye Colour and Developmental Validation of the Irisplex System on Population Living in Malakand Division, Pakistan. Biomedicines. 11(4). 1228–1228. 2 indexed citations
6.
Ilyas, Muhammad, Musharraf Jelani, Muhammad Nadeem Abbas, et al.. (2021). A novel variant in the DSE gene leads to Ehlers–Danlos musculocontractural type 2 in a Pakistani family. Congenital Anomalies. 61(5). 177–182. 4 indexed citations
7.
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
8.
Pastore, Stephen F., Tahir Muhammad, Ricardo Harripaul, et al.. (2021). Biallelic inheritance in a single Pakistani family with intellectual disability implicates new candidate gene RDH14. Scientific Reports. 11(1). 23113–23113. 5 indexed citations
9.
Khan, Muhammad Ismail, Muhammad Latif, Atta Ullah Khan, et al.. (2020). Whole exome sequencing identified a novel missense alteration in CC2D2A causing Joubert syndrome 9 in a Pakhtun family. The Journal of Gene Medicine. 23(1). e3279–e3279. 3 indexed citations
10.
Khan, Muhammad Ismail, Soyeon Choi, Muhammad Zahid, et al.. (2018). Whole-exome sequencing analysis reveals co-segregation of a COL20A1 missense mutation in a Pakistani family with striate palmoplantar keratoderma. Genes & Genomics. 40(7). 789–795. 4 indexed citations
11.
Wadood, Abdul, Mehreen Ghufran, Ajmal Khan, et al.. (2018). Selective glycosidase inhibitors: A patent review (2012–present). International Journal of Biological Macromolecules. 111. 82–91. 38 indexed citations
12.
Ahmed, Saleem, Musharraf Jelani, Kay Childs, et al.. (2018). A missense mutation in TRAPPC6A leads to build-up of the protein, in patients with a neurodevelopmental syndrome and dysmorphic features. Scientific Reports. 8(1). 2053–2053. 26 indexed citations
13.
Adam, Soheir, et al.. (2018). The prevalence of APOL1 gene variants in a cohort of renal disease patients in Western Saudi Arabia. Saudi Journal of Kidney Diseases and Transplantation. 29(4). 793–793. 2 indexed citations
14.
Ahmed, Saleem, Mona Mohammad Almramhi, Taghreed Shuaib, et al.. (2016). The alkylglycerol monooxygenase (AGMO) gene previously involved in autism also causes a novel syndromic form of primary microcephaly in a consanguineous Saudi family. Journal of the Neurological Sciences. 363. 240–244. 18 indexed citations
15.
Jelani, Musharraf, Changsoo Kang, Mona Mohammad Almramhi, et al.. (2016). A novel homozygous PTH1R variant identified through whole-exome sequencing further expands the clinical spectrum of primary failure of tooth eruption in a consanguineous Saudi family. Archives of Oral Biology. 67. 28–33. 22 indexed citations
16.
Jelani, Musharraf, et al.. (2015). Case of Sjögren–Larsson syndrome with a large deletion in the ALDH3A2 gene confirmed by single nucleotide polymorphism array analysis. The Journal of Dermatology. 42(7). 706–709. 14 indexed citations
17.
Wali, Abdul, Lu Liu, Takuya Takeichi, et al.. (2015). Familial Primary Localized Cutaneous Amyloidosis Results from Either Dominant or Recessive Mutations in OSMR. Acta Dermato Venereologica. 95(8). 1005–1007. 7 indexed citations
18.
Ahmed, Saleem, Musharraf Jelani, Mona Mohammad Almramhi, et al.. (2015). Exome analysis identified a novel missense mutation in the CLPP gene in a consanguineous Saudi family expanding the clinical spectrum of Perrault Syndrome type-3. Journal of the Neurological Sciences. 353(1-2). 149–154. 37 indexed citations
19.
Rahman, Obaid Ur, Muhammad Aman Khan, Jawad Ahmed, et al.. (2013). Deletion mutation in BSCL2 gene underlies congenital generalized lipodystrophy in a Pakistani family. Diagnostic Pathology. 8(1). 78–78. 16 indexed citations
20.
Jelani, Musharraf, Muhammad Salman Chishti, & Wasim Ahmad. (2011). Mutation in PVRL4 gene encoding nectin-4 underlies ectodermal-dysplasia-syndactyly syndrome (EDSS1). Journal of Human Genetics. 56(5). 352–357. 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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