Zehra Agha

550 total citations
16 papers, 68 citations indexed

About

Zehra Agha is a scholar working on Genetics, Cell Biology and Molecular Biology. According to data from OpenAlex, Zehra Agha has authored 16 papers receiving a total of 68 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Genetics, 4 papers in Cell Biology and 3 papers in Molecular Biology. Recurrent topics in Zehra Agha's work include Genetics and Neurodevelopmental Disorders (6 papers), Genomics and Rare Diseases (4 papers) and Genomic variations and chromosomal abnormalities (3 papers). Zehra Agha is often cited by papers focused on Genetics and Neurodevelopmental Disorders (6 papers), Genomics and Rare Diseases (4 papers) and Genomic variations and chromosomal abnormalities (3 papers). Zehra Agha collaborates with scholars based in Pakistan, United States and Netherlands. Zehra Agha's co-authors include Maleeha Azam, Raheel Qamar, Zafar Iqbal, Hans van Bokhoven, Syeda Hafiza Benish Ali, Humaira Ayub, Lisenka E.L.M. Vissers, Lies H. Hoefsloot, Moeen Riaz and Christian Gilissen and has published in prestigious journals such as PLoS ONE, Gene and Heliyon.

In The Last Decade

Zehra Agha

14 papers receiving 68 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Zehra Agha Pakistan 5 38 38 11 8 5 16 68
Irman Forghani United States 6 32 0.8× 44 1.2× 6 0.5× 14 1.8× 7 1.4× 11 75
Mona Grimmel Germany 5 38 1.0× 26 0.7× 12 1.1× 15 1.9× 6 1.2× 11 93
Jullianne Diaz United States 6 62 1.6× 28 0.7× 13 1.2× 5 0.6× 9 1.8× 10 89
Francesca Mattioli Switzerland 7 90 2.4× 74 1.9× 10 0.9× 7 0.9× 5 1.0× 11 138
Eleina England United States 6 54 1.4× 43 1.1× 7 0.6× 3 0.4× 5 1.0× 10 87
Edward J. Romasko United States 4 52 1.4× 58 1.5× 11 1.0× 2 0.3× 7 1.4× 6 118
Saeed Al Tala Saudi Arabia 4 59 1.6× 45 1.2× 20 1.8× 7 0.9× 2 0.4× 4 91
Muhsin Elmas Türkiye 6 47 1.2× 32 0.8× 11 1.0× 4 0.5× 3 0.6× 25 89
Heba Y. El Khashab Saudi Arabia 7 39 1.0× 40 1.1× 10 0.9× 6 0.8× 6 1.2× 11 86
Nathalie Pouvreau France 6 55 1.4× 44 1.2× 12 1.1× 3 0.4× 13 2.6× 6 99

Countries citing papers authored by Zehra Agha

Since Specialization
Citations

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

Fields of papers citing papers by Zehra Agha

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Zehra Agha

This figure shows the co-authorship network connecting the top 25 collaborators of Zehra Agha. A scholar is included among the top collaborators of Zehra Agha 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 Zehra Agha. Zehra Agha is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

16 of 16 papers shown
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Kizilbash, Nadeem, et al.. (2023). Genome-wide CNV analysis uncovers novel pathogenic regions in cohort of five multiplex families with neurodevelopmental disorders. Heliyon. 9(9). e19718–e19718. 1 indexed citations
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Taj, Rizwan, et al.. (2023). Association of 11 variants of the dopaminergic and cognitive pathways genes with major depression, schizophrenia and bipolar disorder in the Pakistani population. International Journal of Neuroscience. 134(11). 1172–1184. 1 indexed citations
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Agha, Zehra, et al.. (2023). Novel biallelic frameshift in TRPM7 gene causes Hallermann–Streiff syndrome in a consanguineous family: a case report. Acta Neurologica Belgica. 124(1). 321–324. 1 indexed citations
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Qamar, Raheel, et al.. (2022). Contributing risk factors of common psychiatric disorders in the Pakistani population. European Archives of Psychiatry and Clinical Neuroscience. 273(4). 963–981. 2 indexed citations
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Paterson, Andrew D., Delnaz Roshandel, Liaqat Ali, et al.. (2022). Role of 19 SNPs in 10 genes with type 2 diabetes in the Pakistani population. Gene. 848. 146899–146899. 2 indexed citations
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Rafiq, Muhammad, Syed Tahir Abbas Shah, Muhammad Ansar, et al.. (2022). KIF1A novel frameshift variant p.(Ser887Profs*64) exhibits clinical heterogeneity in a Pakistani family with hereditary sensory and autonomic neuropathy type IIC. International Journal of Neuroscience. 134(6). 665–675. 2 indexed citations
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Azam, Aisha, Zehra Agha, Waqas Ahmed, et al.. (2018). ATF6 polymorphisms and protective effect in diabetic retinopathy. Meta Gene. 17. 56–60. 3 indexed citations
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Agha, Zehra, Shakeel Ahmed, Liaquat Ali, et al.. (2017). A study of ACE, eNOS and MTHFR association with psoriasis in Pakistani population. Meta Gene. 15. 65–69. 4 indexed citations
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Agha, Zehra, Zafar Iqbal, Maleeha Azam, et al.. (2014). A complex microcephaly syndrome in a Pakistani family associated with a novel missense mutation in RBBP8 and a heterozygous deletion in NRXN1. Gene. 538(1). 30–35. 12 indexed citations
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Agha, Zehra, Zafar Iqbal, Maleeha Azam, et al.. (2014). Exome Sequencing Identifies Three Novel Candidate Genes Implicated in Intellectual Disability. PLoS ONE. 9(11). e112687–e112687. 21 indexed citations
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Agha, Zehra, Zafar Iqbal, Maleeha Azam, et al.. (2013). A novel homozygous 10 nucleotide deletion in BBS10 causes Bardet–Biedl syndrome in a Pakistani family. Gene. 519(1). 177–181. 10 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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