Akhtar Ali

405 total citations
35 papers, 267 citations indexed

About

Akhtar Ali is a scholar working on Molecular Biology, Genetics and Rheumatology. According to data from OpenAlex, Akhtar Ali has authored 35 papers receiving a total of 267 indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Molecular Biology, 15 papers in Genetics and 4 papers in Rheumatology. Recurrent topics in Akhtar Ali's work include Hedgehog Signaling Pathway Studies (6 papers), Cleft Lip and Palate Research (5 papers) and Craniofacial Disorders and Treatments (5 papers). Akhtar Ali is often cited by papers focused on Hedgehog Signaling Pathway Studies (6 papers), Cleft Lip and Palate Research (5 papers) and Craniofacial Disorders and Treatments (5 papers). Akhtar Ali collaborates with scholars based in India, Pakistan and United States. Akhtar Ali's co-authors include Rajiva Raman, Jinyan Li, Priyanka Kumari, Masroor Ellahi Babar, Vaibhav Shukla, Ritu Karoli, Vivek Pandey, Abhishek Chandra, Anima Tripathi and C. B. Singh and has published in prestigious journals such as PLoS ONE, Gene and Environmental Research.

In The Last Decade

Akhtar Ali

29 papers receiving 260 citations

Peers

Countries citing papers authored by Akhtar Ali

Since Specialization

Citations

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

Fields of papers citing papers by Akhtar Ali

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Akhtar Ali

This figure shows the co-authorship network connecting the top 25 collaborators of Akhtar Ali. A scholar is included among the top collaborators of Akhtar Ali 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 Akhtar Ali. Akhtar Ali 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	Clinical and Molecular Profile of Duchenne Muscular Dystrophy (DMD): Case-Record Analysis From Uttar Pradesh, India 2024 ·Indian Pediatrics ·Ankur Singh, (unknown), Akhtar Ali, (unknown), (unknown), Om Mishra	0
2	Philadelphia chromosome- positive myelodysplastic syndrome with single lineage dysplasia 2023 ·Cancer Genetics ·(unknown), Vijai Tilak, (unknown), (unknown), R. Rahul, Deepak Gautam, Akhtar Ali	0
3	Cytogenetic Analysis of Chronic Myeloid Leukemia in an Eastern Indian Population 2023 ·(unknown), (unknown), Akhtar Ali, (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown)	1
4	Unilateral Syndactyly, Hemihypertrophy, and Hyperpigmentation with Mosaic 2q35 Deletion 2023 ·Indian Journal of Dermatology ·Akhtar Ali, Ajeet Kumar, (unknown), (unknown), (unknown)	0
5	Impact of Asthma on the Quality of Sleep in Young People 2021 ·Cureus ·Akhtar Ali, Deepa Kumari, (unknown), (unknown), (unknown), (unknown), (unknown), Sidra Naz, Amna Jamil, Faizan Shaukat	3
6	Water resources allocation model based on ecological priority in the arid region 2021 ·Environmental Research ·Jinyan Li, (unknown), (unknown), Akhtar Ali	37
7	Novel HOXD13 variants in syndactyly type 1b and type 1c, and a new spectrum of TP63-related disorders 2021 ·Journal of Human Genetics ·(unknown), (unknown), (unknown), Akhtar Ali	6
8	ANALYZING PATIENT SATISFACTION WITH REGARDS TO PROVISION OF FREE MEDICINES IN KHYBER PAKHTUNKHWA PAKISTAN 2021 ·(unknown), (unknown), Akhtar Ali, (unknown)	0
9	Comparison of Incidence of Myocardial Infarction in Patients With Rheumatoid Arthritis and Diabetes Mellitus 2021 ·Cureus ·(unknown), Akhtar Ali, (unknown), Ravi A. Kumar, (unknown), (unknown), (unknown), (unknown), (unknown), Amber Rizwan	6
10	SLC1A3 C3590T but not BDNF G196A is a predisposition factor for stress as well as depression, in an adolescent eastern Indian population 2020 ·BMC Medical Genetics ·(unknown), Akhtar Ali, (unknown), (unknown), (unknown)	3
11	Bioinformatics enrichment analysis of genes and pathways related to maternal type 1 diabetes associated with adverse fetal outcomes 2020 ·Journal of Diabetes and its Complications ·(unknown), Anjali Rani, Akhtar Ali, Vinay Kumar Singh, Pawan K. Dubey	5
12	Association of Kaphaja and Kapha-Pittaja Prakriti and methylenetetrahydrofolate reductase C677T allele with type 2 diabetes 2018 ·AYU (An International Quarterly Journal of Research in Ayurveda) ·(unknown), (unknown), Akhtar Ali, (unknown), (unknown), (unknown)	2
13	Novel Mutations in the Crystallin Gene in Age-Related Cataract Patients from a North Indian Population 2017 ·Molecular Syndromology ·(unknown), (unknown), Abhishek Chandra, Akhtar Ali	6
14	Co-occurrence of mosaic supernumerary isochromosome 18p and intermittent 2q13 deletions in a child with multiple congenital anomalies 2015 ·Gene ·Sushil Kumar Jaiswal, Ashok Kumar, Akhtar Ali, Amit Kumar	7
15	GLI3 mutations in syndromic and non‐syndromic polydactyly in two Indian families 2015 ·Congenital Anomalies ·(unknown), C. B. Singh, (unknown), (unknown), Akhtar Ali	12
16	A novel GLI3c.750delC truncation mutation in a multiplex Greig cephalopolysyndactyly syndrome family with an unusual phenotypic combination in a patient 2014 ·Meta Gene ·(unknown), (unknown), (unknown), Anjali Rani, (unknown), Akhtar Ali	4
17	MTHFR C677T Predisposes to POAG but Not to PACG in a North Indian Population: A Case Control Study 2014 ·PLoS ONE ·(unknown), (unknown), (unknown), Abhishek Chandra, (unknown), (unknown), Akhtar Ali, Ashim Mukherjee, Mousumi Mutsuddi	15
18	Predictors of Diabetic retinopathy in Patients with type 2 Diabetes who have normoalbuminuria 2013 ·Annals of Medical and Health Sciences Research ·Ritu Karoli, (unknown), Vaibhav Shukla, (unknown), Akhtar Ali	18
19	MTHFR 677TT Alone and IRF6 820GG Together with MTHFR 677CT, but Not MTHFR A1298C, Are Risks for Nonsyndromic Cleft Lip with or without Cleft Palate in an Indian Population 2009 ·Genetic Testing and Molecular Biomarkers ·Akhtar Ali, (unknown), Rajiva Raman	37
20	Coding Region of IRF6 Gene May Not Be Causal for Van Der Woude Syndrome in Cases from India 2009 ·The Cleft Palate-Craniofacial Journal ·Akhtar Ali, (unknown), Rajiva Raman	4

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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