Ambrin Fatima

705 total citations
33 papers, 254 citations indexed

About

Ambrin Fatima is a scholar working on Molecular Biology, Genetics and Cellular and Molecular Neuroscience. According to data from OpenAlex, Ambrin Fatima has authored 33 papers receiving a total of 254 indexed citations (citations by other indexed papers that have themselves been cited), including 23 papers in Molecular Biology, 12 papers in Genetics and 4 papers in Cellular and Molecular Neuroscience. Recurrent topics in Ambrin Fatima's work include Genetics and Neurodevelopmental Disorders (8 papers), Genomics and Rare Diseases (4 papers) and Mitochondrial Function and Pathology (4 papers). Ambrin Fatima is often cited by papers focused on Genetics and Neurodevelopmental Disorders (8 papers), Genomics and Rare Diseases (4 papers) and Mitochondrial Function and Pathology (4 papers). Ambrin Fatima collaborates with scholars based in Pakistan, Sweden and Germany. Ambrin Fatima's co-authors include Niklas Dahl, Shahid Mahmood Baig, Jens Schuster, Joakim Klar, Gerald Wolf, Muhammad Tariq, Zafar Ali, Maria Sobol, Mario Engelmann and Mariarosa Spina and has published in prestigious journals such as Frontiers in Microbiology, PLoS Genetics and BMC Genomics.

In The Last Decade

Ambrin Fatima

32 papers receiving 250 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Ambrin Fatima Pakistan 9 149 64 56 44 19 33 254
Sara L. Domínguez United States 10 143 1.0× 37 0.6× 70 1.3× 57 1.3× 17 0.9× 14 337
Melissa Andrew United States 9 152 1.0× 142 2.2× 31 0.6× 27 0.6× 52 2.7× 14 353
L. Smirnova Russia 11 135 0.9× 61 1.0× 27 0.5× 28 0.6× 29 1.5× 35 372
Noa Avisar Israel 9 121 0.8× 48 0.8× 34 0.6× 101 2.3× 6 0.3× 18 341
Md Shaki Mostaid Bangladesh 11 162 1.1× 71 1.1× 15 0.3× 80 1.8× 11 0.6× 23 337
Petra Mohácsik Hungary 10 86 0.6× 49 0.8× 21 0.4× 18 0.4× 32 1.7× 15 349
Mukesh Varshney Sweden 11 101 0.7× 63 1.0× 19 0.3× 35 0.8× 14 0.7× 24 275
Shoko Takemura Japan 11 109 0.7× 24 0.4× 97 1.7× 76 1.7× 16 0.8× 21 325
Handojo Kusumo United States 8 157 1.1× 20 0.3× 65 1.2× 77 1.8× 52 2.7× 11 341
Angela C. Gauthier United States 10 108 0.7× 29 0.5× 33 0.6× 52 1.2× 63 3.3× 17 330

Countries citing papers authored by Ambrin Fatima

Since Specialization
Citations

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

Fields of papers citing papers by Ambrin Fatima

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ambrin Fatima

This figure shows the co-authorship network connecting the top 25 collaborators of Ambrin Fatima. A scholar is included among the top collaborators of Ambrin Fatima 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 Ambrin Fatima. Ambrin Fatima 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.
Irshad, Saba, Ambrin Fatima, Fernanda A. Correa, et al.. (2024). Genome sequencing reveals novel causative structural and single nucleotide variants in Pakistani families with congenital hypogonadotropic hypogonadism. BMC Genomics. 25(1). 787–787. 1 indexed citations
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Fatima, Ambrin, Asmat Ali, Zafar Iqbal, et al.. (2024). Exome sequencing in four families with neurodevelopmental disorders: genotype–phenotype correlation and identification of novel disease-causing variants in VPS13B and RELN. Molecular Genetics and Genomics. 299(1). 55–55. 1 indexed citations
4.
Jameel, Muhammad, Justyna Iwaszkiewicz, Muhammad Tariq, et al.. (2023). A homozygous founder variant in PDE2A causes paroxysmal dyskinesia with intellectual disability. Clinical Genetics. 104(3). 324–333. 5 indexed citations
5.
Schuster, Jens, Joakim Klar, Ambrin Fatima, et al.. (2022). ZEB2 haploinsufficient Mowat-Wilson syndrome induced pluripotent stem cells show disrupted GABAergic transcriptional regulation and function. Frontiers in Molecular Neuroscience. 15. 988993–988993. 1 indexed citations
6.
Iqbal, Naveed, Faheem Nawaz, Ting Yang, et al.. (2022). The SARS-CoV-2 differential genomic adaptation in response to varying UVindex reveals potential genomic resources for better COVID-19 diagnosis and prevention. Frontiers in Microbiology. 13. 922393–922393. 3 indexed citations
7.
Schuster, Jens, et al.. (2020). Generation of two human iPSC lines (UUIGPi013-A and UUIPGi014-A) from cases with Down syndrome and full trisomy for chromosome 21 (T21). Stem Cell Research. 49. 102081–102081. 1 indexed citations
8.
Klar, Joakim, Maria Sobol, Mansoureh Shahsavani, et al.. (2020). DNA methylation changes in Down syndrome derived neural iPSCs uncover co-dysregulation of ZNF and HOX3 families of transcription factors. Clinical Epigenetics. 12(1). 9–9. 22 indexed citations
9.
Fatima, Ambrin, Joakim Klar, Muhammad Tariq, et al.. (2020). Aberrant splicing due to a novel RPS7 variant causes Diamond-Blackfan Anemia associated with spontaneous remission and meningocele. International Journal of Hematology. 112(6). 894–899. 6 indexed citations
10.
Fatima, Ambrin, et al.. (2020). Generation of a human Neurochondrin deficient iPSC line KICRi002-A-3 using CRISPR/Cas9. Stem Cell Research. 44. 101758–101758. 3 indexed citations
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Schuster, Jens, Maria Sobol, Ambrin Fatima, et al.. (2019). Mowat-Wilson syndrome: Generation of two human iPS cell lines (UUIGPi004A and UUIGPi005A) from siblings with a truncating ZEB2 gene variant. Stem Cell Research. 39. 101518–101518. 5 indexed citations
14.
Tariq, Muhammad, Zafar Ali, Ambrin Fatima, et al.. (2019). Whole exome sequencing identifies novel variant underlying hereditary spastic paraplegia in consanguineous Pakistani families. Journal of Clinical Neuroscience. 67. 19–23. 9 indexed citations
15.
Baig, Shahid Mahmood, Ambrin Fatima, Muhammad Tariq, et al.. (2018). Hereditary brain tumor with a homozygous germline mutation in PMS2: pedigree analysis and prenatal screening in a family with constitutional mismatch repair deficiency (CMMRD) syndrome. Familial Cancer. 18(2). 261–265. 2 indexed citations
16.
Klar, Joakim, Jörg Piontek, Susanne Milatz, et al.. (2017). Altered paracellular cation permeability due to a rare CLDN10B variant causes anhidrosis and kidney damage. PLoS Genetics. 13(7). e1006897–e1006897. 51 indexed citations
17.
Ali, Zafar, Joakim Klar, M. Inam Jameel, et al.. (2016). Novel SACS mutations associated with intellectual disability, epilepsy and widespread supratentorial abnormalities. Journal of the Neurological Sciences. 371. 105–111. 20 indexed citations
18.
Fatima, Ambrin, Shaida A. Andrabi, Gerald Wolf, Mario Engelmann, & Mariarosa Spina. (2012). Urocortin 1 administered into the hypothalamic supraoptic nucleus inhibits food intake in freely fed and food-deprived rats. Amino Acids. 44(3). 879–885. 8 indexed citations
19.
Fatima, Ambrin, et al.. (2009). Urocortin 1 administered into the hypothalamic supraoptic nucleus affects open-field behaviour in rats. Amino Acids. 38(5). 1407–1414. 4 indexed citations
20.
Fatima, Ambrin, et al.. (2007). Minocycline, a possible neuroprotective agent in Leber’s hereditary optic neuropathy (LHON): Studies of cybrid cells bearing 11778 mutation. Neurobiology of Disease. 28(3). 237–250. 26 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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