Safdar Abbas

1.2k total citations
66 papers, 803 citations indexed

About

Safdar Abbas is a scholar working on Molecular Biology, Genetics and Mechanical Engineering. According to data from OpenAlex, Safdar Abbas has authored 66 papers receiving a total of 803 indexed citations (citations by other indexed papers that have themselves been cited), including 26 papers in Molecular Biology, 14 papers in Genetics and 9 papers in Mechanical Engineering. Recurrent topics in Safdar Abbas's work include Hydraulic Fracturing and Reservoir Analysis (9 papers), Genetics and Neurodevelopmental Disorders (6 papers) and Drilling and Well Engineering (6 papers). Safdar Abbas is often cited by papers focused on Hydraulic Fracturing and Reservoir Analysis (9 papers), Genetics and Neurodevelopmental Disorders (6 papers) and Drilling and Well Engineering (6 papers). Safdar Abbas collaborates with scholars based in Pakistan, China and United States. Safdar Abbas's co-authors include R. U. Lemieux, Romain Prioul, Muhammad Umair, Brice Lecampion, Kunwar Shailubhai, Elizaveta Gordeliy, Anthony Peirce, Leonard R. Forte, Madiha Zaynab and Nam Soo Joo and has published in prestigious journals such as Proceedings of the National Academy of Sciences, SHILAP Revista de lepidopterología and PLoS ONE.

In The Last Decade

Safdar Abbas

60 papers receiving 786 citations

Peers

Safdar Abbas
Jiwon Choi South Korea
Yan Pan China
Joana Moreira Portugal
Ran Zhou China
Wu Zhou China
Jiwon Choi South Korea
Safdar Abbas
Citations per year, relative to Safdar Abbas Safdar Abbas (= 1×) peers Jiwon Choi

Countries citing papers authored by Safdar Abbas

Since Specialization
Citations

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

Fields of papers citing papers by Safdar Abbas

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Safdar Abbas

This figure shows the co-authorship network connecting the top 25 collaborators of Safdar Abbas. A scholar is included among the top collaborators of Safdar Abbas 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 Safdar Abbas. Safdar Abbas 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.
Aslam, Muhammad, et al.. (2025). A Novel Homozygous Loss-of-Function Variant in GPR156 Delineates Non-syndromic Hearing Loss. Biochemical Genetics. 64(1). 89–95. 1 indexed citations
2.
Swain, Swadhin, Safdar Abbas, Ning Li, et al.. (2025). Modulation of plant growth and development through altered ethylene binding affinity of the ethylene receptor ETR1. BMC Plant Biology. 25(1). 436–436. 1 indexed citations
3.
Dahmoune, Farid, et al.. (2025). Optimizing dehydrated soups with advanced algorithms: A novel application of D-Optimal mixture design and NSGA-II for healthier formulations. Chemometrics and Intelligent Laboratory Systems. 263. 105443–105443.
4.
Peirce, Anthony, Safdar Abbas, & Emmanuel Detournay. (2025). The Sunset Solution: Closure on Leaking Proppant. Rock Mechanics and Rock Engineering. 2 indexed citations
5.
Peirce, Anthony, Safdar Abbas, & Emmanuel Detournay. (2024). The Sunset Solution: Closure on Leaking Proppant. 1 indexed citations
6.
Afsar, Tayyaba, Hongxia Fu, Zain Ali, et al.. (2024). Loss-of-function variant in the LRR domain of SLITRK2 implicated in a neurodevelopmental disorder. Frontiers in Genetics. 14. 1308116–1308116. 1 indexed citations
7.
Afsar, Tayyaba, Ahmed Waqas, Safdar Abbas, et al.. (2023). A Novel Variant in the PAX4 Gene Causes Maturity-Onset Diabetes of the Young (MODY), Type IX with Neurodevelopmental Disorder. SHILAP Revista de lepidopterología. 2(2).
8.
Abbas, Safdar, et al.. (2023). Haemato-biochemical Changes and Various Risk Factors Associated with Bovine Coronavirus Infection in Cattle Calves. Pakistan Journal of Zoology. 56(4). 1 indexed citations
9.
Abbasi, Sumra Wajid, Safdar Abbas, Ikhlak Ahmed, et al.. (2023). A GHRHR founder mutation causes isolated growth hormone deficiency type IV in a consanguineous Pakistani family. Frontiers in Endocrinology. 14. 1066182–1066182. 2 indexed citations
10.
Zaynab, Madiha, Yasir Sharif, Safdar Abbas, et al.. (2021). Saponin toxicity as key player in plant defense against pathogens. Toxicon. 193. 21–27. 72 indexed citations
11.
Ali, Maroof, Hidayat Hussain, Amjad Hussain, et al.. (2021). Hepatoprotective Screening of Seriphidium kurramense (Qazilb.) Y.R. Ling. BioMed Research International. 2021(1). 9026731–9026731. 1 indexed citations
12.
Umair, Muhammad, Safdar Abbas, Abdur Rauf, et al.. (2020). Identification of a novel biallelic missense variant in the KIAA0825 underlies postaxial polydactyly type A. Genomics. 112(4). 2729–2733. 7 indexed citations
13.
Umair, Muhammad, Amjad Khan, Safdar Abbas, et al.. (2019). Biallelic Missense Mutation in the ECEL1 Underlies Distal Arthrogryposis Type 5 (DA5D). Frontiers in Pediatrics. 7. 343–343. 13 indexed citations
14.
Ahmed, Rizwan Raheem, Christian Windpassinger, Muhammad Salim, et al.. (2019). Genetic Study of Khyber-Pukhtunkhwa Resident Pakistani Families Presenting Primary Microcephaly With Intellectual Disability. Journal of the Pakistan Medical Association. 69(0). 1–1. 5 indexed citations
15.
Khan, Amjad, Rongrong Wang, Muhammad Umair, et al.. (2019). Homozygous missense variant in the TTN gene causing autosomal recessive limb-girdle muscular dystrophy type 10. BMC Medical Genetics. 20(1). 166–166. 13 indexed citations
16.
Younus, Muhammad, Farooq Ahmad, Muhammad Bilal, et al.. (2019). SGCD Homozygous Nonsense Mutation (p.Arg97∗) Causing Limb-Girdle Muscular Dystrophy Type 2F (LGMD2F) in a Consanguineous Family, a Case Report. Frontiers in Genetics. 9. 727–727. 16 indexed citations
17.
Gordeliy, Elizaveta, Safdar Abbas, & Anthony Peirce. (2018). Modeling nonplanar hydraulic fracture propagation using the XFEM: An implicit level-set algorithm and fracture tip asymptotics. International Journal of Solids and Structures. 159. 135–155. 25 indexed citations
18.
Abbas, Safdar, Javid Hussain, Fazal Mabood, et al.. (2017). Knowledge of Medicinal Plants for Children Diseases in the Environs of District Bannu, Khyber Pakhtoonkhwa (KPK). Frontiers in Pharmacology. 8. 430–430. 16 indexed citations
19.
Gordeliy, Elizaveta, Safdar Abbas, & Romain Prioul. (2016). Modeling of Near-Wellbore Fracture Reorientation Using a Fluid-Coupled 2D XFEM Algorithm. 50th U.S. Rock Mechanics/Geomechanics Symposium. 4 indexed citations
20.
Abbas, Safdar, Elizaveta Gordeliy, & Anthony Peirce. (2016). Modeling Multiple Curved Fractures Connected through a Wellbore Using a Fluid-Coupled XFEM Algorithm. 50th U.S. Rock Mechanics/Geomechanics Symposium. 2 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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