Maria Asif

434 total citations
13 papers, 147 citations indexed

About

Maria Asif is a scholar working on Cell Biology, Molecular Biology and Genetics. According to data from OpenAlex, Maria Asif has authored 13 papers receiving a total of 147 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Cell Biology, 5 papers in Molecular Biology and 4 papers in Genetics. Recurrent topics in Maria Asif's work include Microtubule and mitosis dynamics (5 papers), Genomics and Rare Diseases (4 papers) and Genetics and Neurodevelopmental Disorders (2 papers). Maria Asif is often cited by papers focused on Microtubule and mitosis dynamics (5 papers), Genomics and Rare Diseases (4 papers) and Genetics and Neurodevelopmental Disorders (2 papers). Maria Asif collaborates with scholars based in Germany, Pakistan and United Kingdom. Maria Asif's co-authors include Muhammad Sajid Hussain, Shahid Mahmood Baig, Peter Nürnberg, Angelika A. Noegel, Ambrin Fatima, Anja Fromm, Jens Schuster, İlknur Sur‐Erdem, Jörg Piontek and Muhammad Tariq and has published in prestigious journals such as PLoS Genetics, Cells and Journal of Translational Medicine.

In The Last Decade

Maria Asif

12 papers receiving 144 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Maria Asif Germany	7	67	32	31	27	26	13	147
Stephanie N. Giamberardino United States	7	97 1.4×	10 0.3×	9 0.3×	22 0.8×	25 1.0×	14	171
Laura Lorioli Italy	6	68 1.0×	19 0.6×	18 0.6×	16 0.6×	87 3.3×	10	151
Nora Aljawini Saudi Arabia	4	54 0.8×	12 0.4×	23 0.7×	11 0.4×	30 1.2×	6	120
Bryan Sayson Canada	7	70 1.0×	21 0.7×	7 0.2×	48 1.8×	35 1.3×	8	160
Huanzheng Li China	8	158 2.4×	9 0.3×	25 0.8×	63 2.3×	20 0.8×	29	248
Yae-Huei Liou Taiwan	6	83 1.2×	11 0.3×	8 0.3×	14 0.5×	63 2.4×	13	205
Weiqian Yan China	8	60 0.9×	17 0.5×	15 0.5×	10 0.4×	18 0.7×	17	169
Karen LaRocque-Abramson United States	7	143 2.1×	36 1.1×	20 0.6×	23 0.9×	5 0.2×	7	296
Zoltán Grosz Hungary	8	81 1.2×	9 0.3×	44 1.4×	18 0.7×	20 0.8×	20	170
Rachel Y. Diao United States	5	173 2.6×	28 0.9×	14 0.5×	8 0.3×	45 1.7×	6	266

Countries citing papers authored by Maria Asif

Since Specialization

Citations

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

Fields of papers citing papers by Maria Asif

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Maria Asif

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

All Works

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13 of 13 papers shown

Schuler, Matthew S., et al.. (2024). Valproic Acid-Induced Thrombocytopenia in Treatment-Resistant GABRB3 Genetic Epilepsy: A Case Report. Cureus. 16(3). e57030–e57030. 2 indexed citations

Asif, Maria, et al.. (2024). Investigating the effects of a single ASPM variant (c.8508_8509) on brain architecture among siblings in a consanguineous Pakistani family. Molecular Biology Reports. 51(1). 104–104.

Asif, Maria, Uzma Abdullah, Peter Nürnberg, Sigrid Tinschert, & Muhammad Sajid Hussain. (2023). Congenital Microcephaly: A Debate on Diagnostic Challenges and Etiological Paradigm of the Shift from Isolated/Non-Syndromic to Syndromic Microcephaly. Cells. 12(4). 642–642. 7 indexed citations

Asif, Maria, et al.. (2023). PREVENTIVE EFFECTS OF FIGS POWDER & GARLIC POWDER IN MALE ALBINO RATS WITH INDUCED DYSLIPIDEMIA. Biological and Clinical Sciences Research Journal. 2023(1). 372–372. 1 indexed citations

Asif, Maria, et al.. (2023). NUTRIENT TRANSFORMATION THROUGH NANOFERTILIZERS IN SOIL. Biological and Clinical Sciences Research Journal. 2023(1). 483–483. 1 indexed citations

Asif, Maria, Christian Becker, Kerstin Becker, et al.. (2022). Whole-Exome Sequencing of Pakistani Consanguineous Families Identified Pathogenic Variants in Genes of Intellectual Disability. Genes. 14(1). 48–48. 6 indexed citations

Young, Natalie, Maria Asif, Matthew P. Jackson, et al.. (2021). Biallelic SYNE2 Missense Mutations Leading to Nesprin-2 Giant Hypo-Expression Are Associated with Intellectual Disability and Autism. Genes. 12(9). 1294–1294. 9 indexed citations

Fatima, Ambrin, Uzma Abdullah, Muhammad Farooq, et al.. (2021). Rare Pathogenic Variants in Genes Implicated in Glutamatergic Neurotransmission Pathway Segregate with Schizophrenia in Pakistani Families. Genes. 12(12). 1899–1899. 4 indexed citations

Asif, Maria, Uzma Abdullah, Wolfgang Höhne, et al.. (2021). A novel missense variant of SCN4A co‐segregates with congenital essential tremor in a consanguineous Kurdish family. American Journal of Medical Genetics Part A. 188(4). 1251–1258. 2 indexed citations

10.

Kinfe, Thomas M., Maria Asif, Krishnan Chakravarthy, et al.. (2019). Unilateral L4-dorsal root ganglion stimulation evokes pain relief in chronic neuropathic postsurgical knee pain and changes of inflammatory markers: part II whole transcriptome profiling. Journal of Translational Medicine. 17(1). 205–205. 26 indexed citations

11.

Sur‐Erdem, İlknur, et al.. (2019). Nesprin-1 impact on tumorigenic cell phenotypes. Molecular Biology Reports. 47(2). 921–934. 19 indexed citations

12.

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

13.

Ahmad, Ilyas, Shahid Mahmood Baig, Muhammad Sajid Hussain, et al.. (2016). Genetic heterogeneity in Pakistani microcephaly families revisited. Clinical Genetics. 92(1). 62–68. 19 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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