Asma Ali Khan

749 total citations
20 papers, 275 citations indexed

About

Asma Ali Khan is a scholar working on Molecular Biology, Genetics and Cardiology and Cardiovascular Medicine. According to data from OpenAlex, Asma Ali Khan has authored 20 papers receiving a total of 275 indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Molecular Biology, 11 papers in Genetics and 2 papers in Cardiology and Cardiovascular Medicine. Recurrent topics in Asma Ali Khan's work include Genetics and Neurodevelopmental Disorders (6 papers), Mitochondrial Function and Pathology (3 papers) and RNA modifications and cancer (3 papers). Asma Ali Khan is often cited by papers focused on Genetics and Neurodevelopmental Disorders (6 papers), Mitochondrial Function and Pathology (3 papers) and RNA modifications and cancer (3 papers). Asma Ali Khan collaborates with scholars based in Pakistan, United States and United Kingdom. Asma Ali Khan's co-authors include Sheikh Riazuddin, Muhammad Zaman Khan Assir, Rabia Faridi, Thomas B. Friedman, Javed Akram, Saima Riazuddin, Mohsin Shahzad, Mohd Asnizam Asari, Michael Hoa and William G. Newman and has published in prestigious journals such as PLoS ONE, Scientific Reports and The American Journal of Human Genetics.

In The Last Decade

Asma Ali Khan

15 papers receiving 274 citations

Peers

Asma Ali Khan

GENET

OPHTH

Mahmoud Taleb Al‐Ali United Arab Emirates

María Isabel López-Molina Spain

Antonella Fabretto Italy

Adrian Dockery Ireland

Qing Fu China

María González‐del Pozo Spain

Khadim Shah Pakistan

Heather B. Steele-Stallard United Kingdom

Lucas Fares‐Taie France

Motoshi Hayano Japan

Mahmoud Taleb Al‐Ali United Arab Emirates

Asma Ali Khan

174 ×0.9

150 ×1.8

GENET

16 ×0.4

5 ×0.2

4 ×0.2

OPHTH

Citations per year, relative to Asma Ali Khan Asma Ali Khan (= 1×) peers Mahmoud Taleb Al‐Ali

Countries citing papers authored by Asma Ali Khan

Since Specialization

Citations

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

Fields of papers citing papers by Asma Ali Khan

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Asma Ali Khan. 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 Asma Ali Khan. The network helps show where Asma Ali Khan may publish in the future.

Co-authorship network of co-authors of Asma Ali Khan

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

All Works

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20 of 20 papers shown

Faridi, Rabia, Pamela Stratton, Noemi Salmeri, et al.. (2024). Homozygous novel truncating variant of CLPP associated with severe Perrault syndrome. Clinical Genetics. 105(5). 584–586. 4 indexed citations

Shahzad, Mohsin, Javed Akram, Kausar Malik, et al.. (2024). A Missense Variant in HACE1 Is Associated with Intellectual Disability, Epilepsy, Spasticity, and Psychomotor Impairment in a Pakistani Kindred. Genes. 15(5). 580–580.

Beusekom, Ellen van, Sílvia Albert, Johanna M. van Hagen, et al.. (2024). Generation of induced pluripotent stem cell lines from two unrelated patients affected by intellectual disability carrying homozygous variants in SGIP1. Stem Cell Research. 77. 103442–103442.

Khan, Asma Ali, Muhammad Anees, Hidayat Ullah, et al.. (2024). Exome Sequencing of Consanguineous Pashtun Families With Familial Epilepsy Reveals Causative and Candidate Variants in TSEN54 , MOCS2 , and OPHN1. Clinical Genetics. 107(1). 98–103.

Khan, Asma Ali, et al.. (2023). Comparison of Acid Base Status and Electrolytes in Individuals with Prediabetes, Diabetes and Normoglycemia. Pakistan Armed Forces Medical Journal. 73(SUPPL-1). S344–347.

Khan, Shahid Y., Xiaodong Jiao, Asma Ali Khan, et al.. (2022). Next-generation whole exome sequencing to delineate the genetic basis of primary congenital glaucoma. Scientific Reports. 12(1). 17218–17218. 5 indexed citations

Faridi, Rabia, Cristina Fenollar‐Ferrer, Raymond T. O’Keefe, et al.. (2021). New insights into Perrault syndrome, a clinically and genetically heterogeneous disorder. Human Genetics. 141(3-4). 805–819. 28 indexed citations

Khan, Asma Ali, et al.. (2020). Evaluation of a recurrent mutation in HGF gene responsible for non-syndromic hereditary deafness in Kashmiri population. Advancements in Life Sciences. 7(4). 281–286. 1 indexed citations

Khan, Shahid Y., Muhammad Ali, Wendy Lee, et al.. (2020). Whole genome sequencing data of multiple individuals of Pakistani descent. Scientific Data. 7(1). 350–350. 2 indexed citations

10.

Tona, Risa, Iván A. López, Cristina Fenollar‐Ferrer, et al.. (2020). Mouse Models of Human Pathogenic Variants of TBC1D24 Associated with Non-Syndromic Deafness DFNB86 and DFNA65 and Syndromes Involving Deafness. Genes. 11(10). 1122–1122. 11 indexed citations

11.

Richard, Élodie M., D.L. Polla, Muhammad Zaman Khan Assir, et al.. (2019). Bi-allelic Variants in METTL5 Cause Autosomal-Recessive Intellectual Disability and Microcephaly. The American Journal of Human Genetics. 105(4). 869–878. 69 indexed citations

12.

Faridi, Rabia, Risa Tona, Alessandra Brofferio, et al.. (2018). Mutational and phenotypic spectra of KCNE1 deficiency in Jervell and Lange‐Nielsen Syndrome and Romano‐Ward Syndrome. Human Mutation. 40(2). 162–176. 27 indexed citations

13.

Khan, Asma Ali, et al.. (2018). Effects of Yoga on Blood Pressure and MDA in Mild Hypertensive Patients. 1(2).

14.

Jiao, Xiaodong, Firoz Kabir, Arif O. Khan, et al.. (2016). A Common Ancestral Mutation in CRYBB3 Identified in Multiple Consanguineous Families with Congenital Cataracts. PLoS ONE. 11(6). e0157005–e0157005. 10 indexed citations

15.

Faridi, Rabia, Atteeq U. Rehman, Robert J. Morell, et al.. (2016). Mutations of SGO2 and CLDN14 collectively cause coincidental Perrault syndrome. Clinical Genetics. 91(2). 328–332. 35 indexed citations

16.

Khan, Shahid Y., Arif O. Khan, Qiwei Wang, et al.. (2015). Missense Mutations in CRYAB Are Liable for Recessive Congenital Cataracts. PLoS ONE. 10(9). e0137973–e0137973. 31 indexed citations

17.

Bonnet, Céline, Asma Ali Khan, Emmanuel Bresso, et al.. (2013). Extended spectrum of MBD5 mutations in neurodevelopmental disorders. European Journal of Human Genetics. 21(12). 1457–1461. 30 indexed citations

18.

Béri‐Dexheimer, Mylène, Céline Bonnet, Myriam Bronner, et al.. (2012). RUNX1T1, a chromatin repression protein, is a candidate gene for autosomal dominant intellectual disability. American Journal of Medical Genetics Part A. 158A(7). 1782–1784. 5 indexed citations

19.

Khan, Asma Ali, Mohd Asnizam Asari, & Abbas Hassan. (2011). Unusual presence of Wormian (sutural) bones in human skulls.. PubMed. 70(4). 291–4. 15 indexed citations

20.

Kroll, Arnold J., et al.. (2006). Bipartite proximal sesamoid bones in the foal. Pferdeheilkunde Equine Medicine. 22(4). 441–444. 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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