Asmat Ullah

996 total citations
86 papers, 667 citations indexed

About

Asmat Ullah is a scholar working on Molecular Biology, Genetics and Developmental Biology. According to data from OpenAlex, Asmat Ullah has authored 86 papers receiving a total of 667 indexed citations (citations by other indexed papers that have themselves been cited), including 40 papers in Molecular Biology, 33 papers in Genetics and 10 papers in Developmental Biology. Recurrent topics in Asmat Ullah's work include Hedgehog Signaling Pathway Studies (10 papers), Genomic variations and chromosomal abnormalities (10 papers) and Congenital limb and hand anomalies (10 papers). Asmat Ullah is often cited by papers focused on Hedgehog Signaling Pathway Studies (10 papers), Genomic variations and chromosomal abnormalities (10 papers) and Congenital limb and hand anomalies (10 papers). Asmat Ullah collaborates with scholars based in Pakistan, Denmark and Saudi Arabia. Asmat Ullah's co-authors include Wasim Ahmad, Muhammad Umair, Farooq Ahmad, Saif Ur Rehman, Mohd Yazid Bajuri, Muhammad Imran Asjad, Ali Ahmadian, Sulman Basit, Bruno Antonio Pansera and Raja Hussain Ali and has published in prestigious journals such as Journal of Clinical Oncology, SHILAP Revista de lepidopterología and Blood.

In The Last Decade

Asmat Ullah

72 papers receiving 658 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Asmat Ullah Pakistan 16 313 259 130 78 76 86 667
I. Naruse Japan 10 191 0.6× 68 0.3× 30 0.2× 57 0.7× 32 0.4× 21 486
A. Çevik Tufan Türkiye 16 304 1.0× 118 0.5× 18 0.1× 51 0.7× 70 0.9× 39 682
Y. Kitamura Japan 11 379 1.2× 38 0.1× 2 0.0× 9 0.1× 27 0.4× 21 706
Sylvie Bourthoumieu France 15 205 0.7× 138 0.5× 90 1.2× 63 0.8× 40 619
Daniel J. Salchow Germany 16 160 0.5× 94 0.4× 4 0.0× 55 0.7× 42 0.6× 60 793
Sylvie Manouvrier‐Hanu France 18 504 1.6× 395 1.5× 80 0.6× 3 0.0× 99 1.3× 57 846
R T Howell United Kingdom 17 215 0.7× 253 1.0× 3 0.0× 23 0.3× 75 1.0× 32 635
Heidrun Holland Germany 18 304 1.0× 91 0.4× 2 0.0× 39 0.5× 61 0.8× 44 872
Antonio Miranda‐Duarte Mexico 16 277 0.9× 92 0.4× 9 0.1× 31 0.4× 14 0.2× 76 792
Maogang Jiang China 10 109 0.3× 17 0.1× 3 0.0× 56 0.7× 12 0.2× 13 342

Countries citing papers authored by Asmat Ullah

Since Specialization
Citations

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

Fields of papers citing papers by Asmat Ullah

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Asmat Ullah

This figure shows the co-authorship network connecting the top 25 collaborators of Asmat Ullah. A scholar is included among the top collaborators of Asmat Ullah 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 Asmat Ullah. Asmat Ullah 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.
Xing, Hongyan, Asmat Ullah, Naveed Ullah Khan, et al.. (2025). Engineered polyphenol-keratin nanocarriers enhance probiotic delivery and ameliorate obese ulcerative colitis. Colloids and Surfaces B Biointerfaces. 256(Pt 2). 115035–115035. 1 indexed citations
2.
Banwait, Mandeep K., Zofia Piotrowska, Karen Yun, et al.. (2025). Clinical factors and molecular co-alterations impact outcomes in patients receiving first-line osimertinib for EGFR-mutated non-small cell lung cancer. Lung Cancer. 208. 108747–108747.
3.
Wilson, Machelle, et al.. (2025). Impact of quadruplet induction therapy on stem cell mobilization yields in newly diagnosed multiple myeloma. Transfusion Clinique et Biologique. 32(2). 195–198.
4.
Khan, Fiqe, et al.. (2025). A Distinctive Case of Hemophagocytic Lymphohistiocytosis in Chronic Lymphocytic Leukemia. Journal of Investigative Medicine High Impact Case Reports. 13. 1646174209–1646174209.
5.
Hussain, Muhammad M., et al.. (2024). Investigating The Mediating Role Of Work Engagement In The Relationship Between Personality And Work Performance Among Freelancers. MIGRATION LETTERS. 21(S7). 1732–1745. 1 indexed citations
6.
Ullah, Asmat, Rashmi Verma, Allen C. Gao, et al.. (2024). A phase I/II study of enzalutamide in combination with indomethacin in men with castration-resistant prostate cancer (CRPC).. Journal of Clinical Oncology. 42(16_suppl). e17027–e17027. 1 indexed citations
7.
Ullah, Asmat, et al.. (2023). Clinical exome sequencing reveals a novel pathogenic variant in KIF12 underlying cholestasis with highly variable phenotypes. Clinical Genetics. 105(1). 106–108. 2 indexed citations
8.
9.
Parveen, Asia, Sher Alam Khan, Noor Muhammad, et al.. (2023). Brachyolmia, dental anomalies and short stature (DASS): Phenotype and genotype analyses of Egyptian and Pakistani patients. Heliyon. 10(1). e23688–e23688.
10.
Ullah, Asmat, Abid Ali Shah, Abdus Samad, et al.. (2022). Clinical and genetic characterization of patients segregating variants in KPTN, MINPP1, NGLY1, AP4B1, and SON underlying neurodevelopmental disorders: Genetic and phenotypic expansion. International Journal of Developmental Neuroscience. 82(8). 788–804. 5 indexed citations
11.
Ullah, Asmat, Ubaid Ullah, Farooq Ahmad, et al.. (2021). Loss of Function Variants in the XPC Causes Severe Xeroderma Pigmentosum in Three Large Consanguineous Families. Klinische Pädiatrie. 234(3). 123–129.
12.
13.
Raja, Ghazala Kaukab, et al.. (2020). Sequence variants in three genes underlying leukodystrophy in Pakistani families. International Journal of Developmental Neuroscience. 80(5). 380–388. 3 indexed citations
14.
Ullah, Asmat, et al.. (2019). Screening, diagnosis and genetic study of breast cancer patients in Pakistan. Pakistan Journal of Medical Sciences. 36(1). 2 indexed citations
15.
Ullah, Asmat, et al.. (2019). MEROPENEM INDUCED HEPATIC DERANGEMENT: A CASE REPORT. Journal of Postgraduate Medical Institute. 33(4).
16.
Khan, Feroz, et al.. (2019). A novel frameshift variant in BHLHA9 underlies mesoaxial synostotic syndactyly associated with postaxial polydactyly. European Journal of Medical Genetics. 62(8). 103688–103688. 4 indexed citations
17.
Abdullah, Abdullah, Zahid Azeem, Muhammad Bilal, et al.. (2019). Variants in GLI3 Cause Greig Cephalopolysyndactyly Syndrome. Genetic Testing and Molecular Biomarkers. 23(10). 744–750. 8 indexed citations
18.
Ullah, Asmat, et al.. (2013). Fracture Shaft of Humerus Treated with A Functional Brace. 25(3). 15–19.
19.
Ullah, Asmat, et al.. (2012). Micro-econometric Analysis of Impact of Remittances on Household’s Welfare: Empirical Evidence from District Peshawar. SHILAP Revista de lepidopterología.
20.
Asif, Hafiz Muhammad, et al.. (2011). Comparative study of similarity and identity of human albumin with some selected organism albumin. Journal of Medicinal Plants Research. 5(19). 1 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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