Huma Arshad Cheema

622 total citations
48 papers, 267 citations indexed

About

Huma Arshad Cheema is a scholar working on Surgery, Genetics and Physiology. According to data from OpenAlex, Huma Arshad Cheema has authored 48 papers receiving a total of 267 indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Surgery, 11 papers in Genetics and 9 papers in Physiology. Recurrent topics in Huma Arshad Cheema's work include Metabolism and Genetic Disorders (8 papers), Lysosomal Storage Disorders Research (7 papers) and Pediatric Hepatobiliary Diseases and Treatments (6 papers). Huma Arshad Cheema is often cited by papers focused on Metabolism and Genetic Disorders (8 papers), Lysosomal Storage Disorders Research (7 papers) and Pediatric Hepatobiliary Diseases and Treatments (6 papers). Huma Arshad Cheema collaborates with scholars based in Pakistan, India and Saudi Arabia. Huma Arshad Cheema's co-authors include Anjum Saeed, Muhammad Yasir Zahoor, Khushnooda Ramzan, Wasim Shehzad, Nadia K. Waheed, Imran Rashid, Najim Ameziane, Muhammad Arshad Alvi, Carol J. Soroka and Emily Gao and has published in prestigious journals such as SHILAP Revista de lepidopterología, Hepatology and Gene.

In The Last Decade

Huma Arshad Cheema

41 papers receiving 261 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Huma Arshad Cheema Pakistan 9 74 70 55 53 52 48 267
Kuerbanjiang Abuduxikuer China 12 60 0.8× 114 1.6× 63 1.1× 33 0.6× 69 1.3× 33 295
Sylwia Szymańska Poland 9 88 1.2× 70 1.0× 113 2.1× 13 0.2× 49 0.9× 40 262
Kyoko Ban Japan 8 23 0.3× 57 0.8× 21 0.4× 57 1.1× 61 1.2× 19 191
Sirish Palle United States 8 24 0.3× 43 0.6× 66 1.2× 12 0.2× 63 1.2× 24 180
Hanaa El‐Karaksy Egypt 11 23 0.3× 81 1.2× 140 2.5× 49 0.9× 21 0.4× 35 342
Ronald J. Sokol United States 8 43 0.6× 297 4.2× 38 0.7× 64 1.2× 77 1.5× 8 443
Dina Ramadan Kuwait 12 71 1.0× 47 0.7× 36 0.7× 46 0.9× 99 1.9× 19 273
Norman Händel Germany 8 57 0.8× 106 1.5× 139 2.5× 6 0.1× 92 1.8× 11 343
Yasemen Eroğlu United States 10 43 0.6× 195 2.8× 72 1.3× 13 0.2× 130 2.5× 24 352
Burcu Barutçuoğlu Türkiye 11 24 0.3× 38 0.5× 86 1.6× 9 0.2× 84 1.6× 34 317

Countries citing papers authored by Huma Arshad Cheema

Since Specialization
Citations

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

Fields of papers citing papers by Huma Arshad Cheema

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Huma Arshad Cheema. 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 Huma Arshad Cheema. The network helps show where Huma Arshad Cheema may publish in the future.

Co-authorship network of co-authors of Huma Arshad Cheema

This figure shows the co-authorship network connecting the top 25 collaborators of Huma Arshad Cheema. A scholar is included among the top collaborators of Huma Arshad Cheema 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 Huma Arshad Cheema. Huma Arshad Cheema 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.
Rahman, Fatima, Abolfazl Rad, Gabriela Oprea, et al.. (2024). Bi-allelic MYMX variants cause a syndromic congenital myopathy with recognizable facial palsy, growth restriction, and dysmorphism. European Journal of Human Genetics. 33(4). 552–555.
2.
Zahid, Muhammad, et al.. (2024). Aromatase deficiency due to novel CYP19A1 mutation: a rare cause of maternal and fetal virilization. Case Reports in Perinatal Medicine. 13(1). 20230032–20230032.
3.
Cheema, Huma Arshad, et al.. (2023). Clinical and Genetic Description of Hereditary Chronic Pancreatitis in Pakistani Children. The Turkish Journal of Gastroenterology. 34(10). 1088–1098.
4.
Skrahin, Aliaksandr, Huma Arshad Cheema, Nuzhat Rana, et al.. (2023). Secondary findings in a large Pakistani cohort tested with whole genome sequencing. Life Science Alliance. 6(3). e202201673–e202201673. 2 indexed citations
5.
Saeed, Anjum, et al.. (2023). Corticosterone Methyl Oxidase Type 1 (CMO1) Deficiency Due to CYP11B2 Mutation: Two Case Reports. Cureus. 15(5). e39181–e39181. 1 indexed citations
6.
Cheema, Huma Arshad, et al.. (2023). The mutational landscape of genetic cholestatic diseases in Pakistani children. SHILAP Revista de lepidopterología. 73(8). 1610–1621.
7.
Cheema, Huma Arshad, et al.. (2022). Kleefstra Syndrome with Severe Sensory Neural Deafness and <em>De Novo</em> Novel Mutation. Journal of College of Physicians And Surgeons Pakistan. 32(2). 236–238. 3 indexed citations
8.
Imran, Imran, et al.. (2021). Spectrum of Clinical Presentation of Celiac Disease in Pediatric Population. Cureus. 13(6). e15582–e15582. 6 indexed citations
9.
Cheema, Huma Arshad, Aida M. Bertoli‐Avella, Volha Skrahina, et al.. (2020). Genomic testing in 1019 individuals from 349 Pakistani families results in high diagnostic yield and clinical utility. npj Genomic Medicine. 5(1). 44–44. 29 indexed citations
10.
Cheema, Huma Arshad, et al.. (2020). Mutational spectrum of SMPD1 gene in Pakistani Niemann-Pick disease patients. Pakistan Journal of Medical Sciences. 36(3). 479–484. 7 indexed citations
11.
Cheema, Huma Arshad, et al.. (2019). Spectrum of UGT1A1 variants in Pakistani children affected with inherited unconjugated hyperbilirubinemias. Clinical Biochemistry. 69. 30–35. 5 indexed citations
12.
Alvi, Muhammad Arshad, et al.. (2018). Ribavirin free direct-acting antivirals in adolescents with hepatitis C and thalassemia. 12(3). 1 indexed citations
13.
Cheema, Huma Arshad, et al.. (2018). Berardinelli-seip Congenital Generalised Lipodystrophy. Journal of College of Physicians And Surgeons Pakistan. 28(5). 406–408. 3 indexed citations
14.
Cheema, Huma Arshad, et al.. (2018). Is Hepatovenocaval Syndrome A Different Entity From Budd-chiari Syndrome In Children?. Journal of College of Physicians And Surgeons Pakistan. 28(5). 344–347. 1 indexed citations
15.
Cheema, Huma Arshad, et al.. (2017). Mucopolysaccharidoses - Clinical Spectrum and Frequency of Different Types.. PubMed. 27(2). 80–83. 8 indexed citations
16.
Cheema, Huma Arshad, et al.. (2017). Celiac Crisis: A Rare Or Rarely Recognized Disease.. PubMed. 28(4). 672–675. 8 indexed citations
17.
Cheema, Huma Arshad, et al.. (2017). Effectiveness and Safety of Sofosbuvir in Treatment-NäiveChildren with Hepatitis C Infection.. PubMed. 27(7). 423–426. 14 indexed citations
18.
Cheema, Huma Arshad, et al.. (2016). Congenital hepatic fibrosis: clinical presentation, laboratory features and management at a tertiary care hospital of Lahore.. PubMed. 66(8). 984–8. 10 indexed citations
19.
Cheema, Huma Arshad, et al.. (2016). Spectrum of Inherited Metabolic Disorders in Pakistani Children Presenting at a Tertiary Care Centre.. PubMed. 26(6). 498–502. 20 indexed citations
20.
Mahmood, Umair, Imran Rashid, Huma Arshad Cheema, et al.. (2012). Detection of common mutations in the GALT gene through ARMS. Gene. 509(2). 291–294. 9 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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