Abdul Wali

696 citations

34 papers · 268 indexed · h-index 12

Co-authors: Wasim Ahmad Ghazanfar Ali Muhammad Ayub Musharraf Jelani Sulman Basit Zahid Azeem Muhammad Ansar Peter John
Topics: Skin and Cellular Biology Research (8 papers)Hair Growth and Disorders (7 papers)RNA regulation and disease (6 papers)
Cited by: Urology Cell Biology Developmental Biology
Journals: British Journal of Dermatology BioMed Research International Human Genetics
Partner nations: Pakistan Saudi Arabia United States

In The Last Decade

Abdul Wali

31 papers receiving 264 citations

Peers

Countries citing papers authored by Abdul Wali

Since Specialization

Citations

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

Fields of papers citing papers by Abdul Wali

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Abdul Wali

This figure shows the co-authorship network connecting the top 25 collaborators of Abdul Wali. A scholar is included among the top collaborators of Abdul Wali 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 Abdul Wali. Abdul Wali 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	Nilotinib: Disrupting the MYC-MAX Heterocomplex 2024 ·Bioinformatics and Biology Insights ·(unknown),(unknown),(unknown),Abdul Wali,(unknown)	0
2	A Recurrent Nonsense Mutation in NECTIN4 Underlying Ectodermal Dysplasia-Syndactyly Syndrome with a Novel Phenotype in a Consanguineous Kashmiri Family 2023 ·Genetics Research ·Ghazanfar Ali,(unknown),(unknown),Zahid Azeem,(unknown),Syed Akif Raza Kazmi,Zia Ur Rehman,(unknown),(unknown),Abdul Wali,(unknown),Nasib Zaman,Muhammad Ayub,(unknown),Noor Hassan	0
3	Identification and In Silico Analysis of a Homozygous Nonsense Variant in TGM1 Gene Segregating with Congenital Ichthyosis in a Consanguineous Family 2023 ·Medicina ·(unknown),(unknown),Abdul Aziz,(unknown),Rafiullah Rafiullah,Fazal ur Rehman,(unknown),Rozeena Shaikh,Muhammad Ayub,Abdul Wali	1
4	NPHP3 splice acceptor site variant is associated with infantile nephronophthisis and asphyxiating thoracic dystrophy; A rare combination 2022 ·European Journal of Medical Genetics ·(unknown),(unknown),(unknown),(unknown),(unknown),Jamil Amjad Hashmi,Abdul Wali,Sulman Basit	1
5	Molecular, Cytogenetic, and Hematological Analysis of Chronic Myeloid Leukemia Patients and Discovery of Two Novel Translocations 2021 ·Analytical Cellular Pathology ·Muhammad Asif,Abrar Hussain,Abdul Wali,(unknown),Irfan Ali,Zafar Iqbal,Muhammad Amir,Muhammad Shafiq,Mahmood Rasool	5
6	Ethnobotanical and Biochemical Study of Berberis lycium Royle Collected from Different Areas of Azad Jammu and Kashmir 2021 ·Evidence-based Complementary and Alternative Medicine ·(unknown),Ghazanfar Ali,Syed Rizwan Abbas,(unknown),(unknown),(unknown),Abdul Wali,Muhammad Ayub,(unknown),Ahmed Khames,(unknown)	3
7	Identification of a Novel Homozygous Missense (c.443A>T:p.N148I) Mutation in BBS2 in a Kashmiri Family with Bardet‐Biedl Syndrome 2021 ·BioMed Research International ·Ghazanfar Ali,(unknown),Jia Nee Foo,Abdul Nasır,(unknown),(unknown),(unknown),Zahid Azeem,(unknown),Syed Akif Raza Kazmi,(unknown),Abdul Hameed Khan,(unknown),(unknown),Abdul Wali,(unknown),Wasim Akhtar,(unknown),(unknown)	1
8	Novel Frameshift Mutations in XPC Gene Underlie Xeroderma Pigmentosum in Pakistani Families 2021 ·Indian Journal of Dermatology ·(unknown),Khadim Shah,Abdul Aziz,Fazal ur Rehman,Yasir Ali,Abdul Malik Tareen,(unknown),Muhammad Ayub,Abdul Wali	9
9	Sequencing and Characterization of Mitochondrial Protein‐Coding Genes for Schizothorax niger (Cypriniformes: Cyprinidae) with Phylogenetic Consideration 2020 ·BioMed Research International ·(unknown),Ghazanfar Ali,Nusrat Shafi,Wasim Akhtar,Abdul Hameed Khan,(unknown),Abdul Wali,(unknown),Abdul Rehman Khan,(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown)	4
10	A rare case of three-way complex variant translocation in chronic myeloid leukemia t(6;9;22)(p21;q34;q11): A case report 2017 ·Biomedical Reports ·Muhammad Asif,Abrar Hussain,Abdul Wali,N. Ahmad,(unknown),Muhammad Amir,Irfan Ali,Peter Natesan Pushparaj,Mahmood Rasool	7
11	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
12	Mutations in the LPAR6 and LIPH genes underlie autosomal recessive hypotrichosis/woolly hair in 17 consanguineous families from Pakistan 2011 ·Clinical and Experimental Dermatology ·Saadullah Khan,Rabia Habib,Hina Mir,(unknown),(unknown),Muhammad Ayub,(unknown),(unknown),Nida Ali,Sulman Basit,Naveed Wasif,Syed Kamran‐ul‐Hassan Naqvi,Ghazanfar Ali,Abdul Wali,Muhammad Ansar,Wasim Ahmad	13
13	Digenic inheritance of an autosomal recessive hypotrichosis in two consanguineous pedigrees 2010 ·Clinical Genetics ·Sulman Basit,Abdul Wali,Abdul Aziz,Noor Muhammad,Musharraf Jelani,Wasim Ahmad	12
14	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
15	Novel missense mutations in lipase H (LIPH) gene causing autosomal recessive hypotrichosis (LAH2) 2009 ·Journal of Dermatological Science ·(unknown),(unknown),Ghazanfar Ali,Zahid Azeem,Abdul Wali,Muhammad Ansar,Wasim Ahmad	12
16	Novel mutations in G protein-coupled receptor gene (P2RY5) in families with autosomal recessive hypotrichosis (LAH3) 2008 ·Human Genetics ·Zahid Azeem,Musharraf Jelani,(unknown),Muhammad Tariq,Naveed Wasif,Syed Kamran‐ul‐Hassan Naqvi,Muhammad Ayub,Masoom Yasinzai,Muhammad Aminuddin,Abdul Wali,Ghazanfar Ali,Muhammad Salman Chishti,Wasim Ahmad	34
17	Mapping of a Gene for Alopecia with Mental Retardation Syndrome (APMR3) on Chromosome 18q11.2‐q12.2 2007 ·Annals of Human Genetics ·Abdul Wali,Ghazanfar Ali,Peter John,Kwanghyuk Lee,(unknown),Suzanne M. Leal,Wasim Ahmad	10
18	Ectodermal dysplasia of hair and nail type: mapping of a novel locus to chromosome 17p12-q21.2 2006 ·British Journal of Dermatology ·Muhammad Naeem,Musharraf Jelani,Kwanghyuk Lee,Ghazanfar Ali,(unknown),Abdul Wali,Asma Gul,Peter John,Muhammad Jawad Hassan,Suzanne M. Leal,Wasim Ahmad	17
19	Atrichia with papular lesions resulting from a novel insertion mutation in the human hairless gene 2006 ·Clinical and Experimental Dermatology ·Abdul Wali,Muhammad Ansar,Muhammad Nasim Khan,Wasim Ahmad	9
20	A novel locus for alopecia with mental retardation syndrome (APMR2) maps to chromosome 3q26.2‐q26.31 2006 ·Clinical Genetics ·Abdul Wali,Peter John,Asma Gul,Kwanghyuk Lee,(unknown),Ghazanfar Ali,(unknown),(unknown),Wasim Ahmad	11

About Abdul Wali

Abdul Wali is a scholar working on Urology, Developmental Biology and Cell Biology, having authored 34 papers that have together received 268 indexed citations. Recurring topics across this work include Skin and Cellular Biology Research (8 papers), Hair Growth and Disorders (7 papers) and RNA regulation and disease (6 papers). The work is most often cited by research in Urology (106 citations), Cell Biology (131 citations) and Developmental Biology (14 citations). Abdul Wali has collaborated with scholars based in Pakistan, Saudi Arabia and United States. Frequent co-authors include Wasim Ahmad, Ghazanfar Ali, Muhammad Ayub, Musharraf Jelani, Sulman Basit, Zahid Azeem, Muhammad Ansar, Peter John, Abdul Aziz and Muhammad Tariq. Their work appears in journals such as British Journal of Dermatology, BioMed Research International and Human Genetics.

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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