Musharraf Jelani

956 citations

53 papers · 643 indexed · h-index 17

Co-authors: Wasim Ahmad Jumana Y. Al‐Aama Mona Mohammad Almramhi Muhammad Ayub Saleem Ahmed Reaz Uddin Sulman Basit Syed Sikander Azam
Topics: Skin and Cellular Biology Research (12 papers)Wnt/β-catenin signaling in development and cancer (8 papers)Hair Growth and Disorders (6 papers)
Cited by: Urology Cell Biology Molecular Biology
Journals: Blood PLoS ONE Brain
Partner nations: Pakistan Saudi Arabia United Kingdom

In The Last Decade

Musharraf Jelani

49 papers receiving 640 citations

Peers

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

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20 of 20 papers shown

#	Work	Indexed citations
1	Whole exome sequencing: Unlocking the molecular diagnostic odyssey in Pakhtun ethnic group of Pakistani population 2025 ·Gene ·(unknown),(unknown),(unknown),(unknown),Muhammad Nadeem Abbas,Muhammad Latif,Musharraf Jelani	0
2	Phenotypic Classification of Eye Colour and Developmental Validation of the Irisplex System on Population Living in Malakand Division, Pakistan 2023 ·Biomedicines ·(unknown),(unknown),Akhtar Rasool,Muhammad Ilyas,Allah Rakha,Sulaiman Shams,Musharraf Jelani,Fehmida Bibi,Bader Shirah,(unknown),Muhammad Imran Naseer,(unknown)	2
3	Two novel homozygous variants of ATP6V0A2 and ALDH18A1 lead to autosomal recessive cutis laxa type 2 and 3 in two Pakistani families 2023 ·The Journal of Gene Medicine ·(unknown),(unknown),Gauhar Rehman,(unknown),(unknown),Amin Jan,Jamshid Khan,Muhammad Anas,(unknown),Muhammad Umair,Osama Y. Muthaffar,(unknown),Fehmida Bibi,Muhammad Imran Naseer,Musharraf Jelani	1
4	A novel variant in the DSE gene leads to Ehlers–Danlos musculocontractural type 2 in a Pakistani family 2021 ·Congenital Anomalies ·(unknown),(unknown),Muhammad Ilyas,(unknown),Musharraf Jelani,(unknown),Muhammad Nadeem Abbas,Muhammad Ishfaq,Fawad Ali,(unknown),Stéphanie Efthymiou,(unknown),Henry Houlden	4
5	Whole Exome Sequencing Confirms Molecular Diagnostics of Three Pakhtun Families With Autosomal Recessive Epidermolysis Bullosa 2021 ·Frontiers in Pediatrics ·Fozia Fozia,Rubina Nazli,Nousheen Bibi,Sher Alam Khan,Noor Muhammad,(unknown),Saadullah Khan,Musharraf Jelani,Naveed Wasif	1
6	Two missense mutations in GPNMB cause autosomal recessive amyloidosis cutis dyschromica in the consanguineous pakistani families 2021 ·Genes & Genomics ·Obaid Ur Rahman,(unknown),Caroline Mahon,Musharraf Jelani,Changsoo Kang	3
7	Biallelic inheritance in a single Pakistani family with intellectual disability implicates new candidate gene RDH14 2021 ·Scientific Reports ·Stephen F. Pastore,Tahir Muhammad,Ricardo Harripaul,Rebecca Lau,Muhammad Tariq Masood Khan,Muhammad Ismail Khan,Omar Islam,Changsoo Kang,Muhammad Ayub,Musharraf Jelani,John B. Vincent	5
8	The prevalence of APOL1 gene variants in a cohort of renal disease patients in Western Saudi Arabia 2018 ·Saudi Journal of Kidney Diseases and Transplantation ·Soheir Adam,Maha A. Badawi,(unknown),(unknown),(unknown),Musharraf Jelani,(unknown)	2
9	Whole-exome sequencing analysis reveals co-segregation of a COL20A1 missense mutation in a Pakistani family with striate palmoplantar keratoderma 2018 ·Genes & Genomics ·Muhammad Ismail Khan,Soyeon Choi,Muhammad Zahid,Habib Ahmad,Roshan Ali,Musharraf Jelani,Changsoo Kang	4
10	Selective glycosidase inhibitors: A patent review (2012–present) 2018 ·International Journal of Biological Macromolecules ·Abdul Wadood,Mehreen Ghufran,Ajmal Khan,Syed Sikander Azam,Musharraf Jelani,Reaz Uddin	38
11	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 2016 ·Archives of Oral Biology ·Musharraf Jelani,Changsoo Kang,(unknown),(unknown),Mona Mohammad Almramhi,(unknown),Huanming Yang,Jumana Y. Al‐Aama,Muhammad Naeem,Yaser M. Alkhiary	22
12	A Novel Missense Mutation in the CLPP Gene Causing Perrault Syndrome Type 3 in a Turkish Family 2016 ·Journal of Clinical Research in Pediatric Endocrinology ·Fatma Dursun,(unknown),(unknown),Muhammad Naeem,Musharraf Jelani,Heves Kırmızıbekmez	21
13	Case of Sjögren–Larsson syndrome with a large deletion in the ALDH3A2 gene confirmed by single nucleotide polymorphism array analysis 2015 ·The Journal of Dermatology ·(unknown),Musharraf Jelani,Mona Mohammad Almramhi,(unknown),Jumana Y. Al‐Aama	14
14	Familial Primary Localized Cutaneous Amyloidosis Results from Either Dominant or Recessive Mutations in OSMR 2015 ·Acta Dermato Venereologica ·Abdul Wali,Lu Liu,Takuya Takeichi,Musharraf Jelani,Obaid Ur Rahman,(unknown),Steven Tien Guan Thng,Juneyoung Lee,Masashi Akiyama,John A. McGrath,Regina C. Betz	7
15	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 2015 ·Journal of the Neurological Sciences ·Saleem Ahmed,Musharraf Jelani,(unknown),(unknown),Mona Mohammad Almramhi,(unknown),(unknown),Jun Wang,Jamal Nasir,Jumana Y. Al‐Aama	37
16	Deletion mutation in BSCL2 gene underlies congenital generalized lipodystrophy in a Pakistani family 2013 ·Diagnostic Pathology ·Obaid Ur Rahman,(unknown),Muhammad Aman Khan,Jawad Ahmed,(unknown),Jumana Y. Al‐Aama,Muhammad Naeem,Musharraf Jelani	16
17	Mutation in PVRL4 gene encoding nectin-4 underlies ectodermal-dysplasia-syndactyly syndrome (EDSS1) 2011 ·Journal of Human Genetics ·Musharraf Jelani,Muhammad Salman Chishti,Wasim Ahmad	23
18	Mutations in theP2RY5gene underlie autosomal recessive hypotrichosis in 13 Pakistani families 2009 ·British Journal of Dermatology ·Muhammad Tariq,Muhammad Ayub,Musharraf Jelani,Sulman Basit,(unknown),Naveed Wasif,Syed Irfan Raza,(unknown),Saadullah Khan,Zahid Azeem,Masoom Yasinzai,Abdul Wali,Ghazanfar Ali,(unknown),Wasim Ahmad	15
19	A Homozygous Nonsense Mutation in the Human Desmocollin-3 (DSC3) Gene Underlies Hereditary Hypotrichosis and Recurrent Skin Vesicles 2009 ·The American Journal of Human Genetics ·Muhammad Ayub,Sulman Basit,Musharraf Jelani,Fazal Ur Rehman,Muhammad Iqbal,Masoom Yasinzai,Wasim Ahmad	53
20	A novel deletion mutation in LIPH gene causes autosomal recessive hypotrichosis (LAH2) 2008 ·Clinical Genetics ·Musharraf Jelani,Naveed Wasif,Ghazanfar Ali,(unknown),Wasim Ahmad	23

About Musharraf Jelani

Musharraf Jelani is a scholar working on Cell Biology, Urology and Genetics, having authored 53 papers that have together received 643 indexed citations. Recurring topics across this 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). The work is most often cited by research in Urology (102 citations), Cell Biology (228 citations) and Molecular Biology (401 citations). Musharraf Jelani has collaborated with scholars based in Pakistan, Saudi Arabia and United Kingdom. Frequent co-authors include Wasim Ahmad, Jumana Y. Al‐Aama, Mona Mohammad Almramhi, Muhammad Ayub, Saleem Ahmed, Reaz Uddin, Sulman Basit, Syed Sikander Azam, Abdul Wadood and Jamal Nasir. Their work appears in journals such as Blood, PLoS ONE and Brain.

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