Khushnooda Ramzan

2.1k total citations
79 papers, 1.2k citations indexed

About

Khushnooda Ramzan is a scholar working on Molecular Biology, Genetics and Sensory Systems. According to data from OpenAlex, Khushnooda Ramzan has authored 79 papers receiving a total of 1.2k indexed citations (citations by other indexed papers that have themselves been cited), including 42 papers in Molecular Biology, 25 papers in Genetics and 12 papers in Sensory Systems. Recurrent topics in Khushnooda Ramzan's work include Hearing, Cochlea, Tinnitus, Genetics (12 papers), Genomic variations and chromosomal abnormalities (8 papers) and Metabolism and Genetic Disorders (7 papers). Khushnooda Ramzan is often cited by papers focused on Hearing, Cochlea, Tinnitus, Genetics (12 papers), Genomic variations and chromosomal abnormalities (8 papers) and Metabolism and Genetic Disorders (7 papers). Khushnooda Ramzan collaborates with scholars based in Saudi Arabia, Pakistan and United States. Khushnooda Ramzan's co-authors include Faiqa Imtiaz, Sulman Basit, Sibtain Afzal, Zubair M. Ahmed, Thomas B. Friedman, Moeenaldeen AlSayed, Sheikh Riazuddin, Saima Riazuddin, Mohammed Al‐Owain and Shaheen N. Khan and has published in prestigious journals such as Journal of Clinical Investigation, SHILAP Revista de lepidopterología and Blood.

In The Last Decade

Khushnooda Ramzan

73 papers receiving 1.2k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Khushnooda Ramzan Saudi Arabia 18 644 320 236 230 112 79 1.2k
Nejat Mahdieh Iran 17 860 1.3× 394 1.2× 228 1.0× 438 1.9× 63 0.6× 95 1.6k
Bahareh Rabbani Iran 14 548 0.9× 337 1.1× 102 0.4× 185 0.8× 31 0.3× 48 1.1k
Chaim Jalas United States 23 724 1.1× 375 1.2× 127 0.5× 92 0.4× 231 2.1× 60 1.7k
Mohammed Al‐Owain Saudi Arabia 25 1.1k 1.7× 595 1.9× 110 0.5× 103 0.4× 128 1.1× 87 2.0k
Shamir Zenvirt Israel 16 618 1.0× 367 1.1× 114 0.5× 36 0.2× 173 1.5× 22 1.2k
Claudio Graziano Italy 20 695 1.1× 325 1.0× 73 0.3× 84 0.4× 96 0.9× 77 1.2k
Wadih M. Zein United States 21 762 1.2× 369 1.2× 65 0.3× 69 0.3× 246 2.2× 86 1.4k
Daniel T. Meehan United States 21 605 0.9× 181 0.6× 92 0.4× 181 0.8× 104 0.9× 34 1.5k
Jerzy Bal Poland 19 486 0.8× 244 0.8× 82 0.3× 85 0.4× 112 1.0× 113 1.1k
Sumita Danda India 16 489 0.8× 269 0.8× 128 0.5× 33 0.1× 111 1.0× 122 1.0k

Countries citing papers authored by Khushnooda Ramzan

Since Specialization
Citations

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

Fields of papers citing papers by Khushnooda Ramzan

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Khushnooda Ramzan

This figure shows the co-authorship network connecting the top 25 collaborators of Khushnooda Ramzan. A scholar is included among the top collaborators of Khushnooda Ramzan 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 Khushnooda Ramzan. Khushnooda Ramzan 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.
Ramzan, Khushnooda, et al.. (2024). A homozygous variant in ARHGAP39 is associated with lethal cerebellar vermis hypoplasia in a consanguineous Saudi family. Scientific Reports. 14(1). 25291–25291.
2.
Echahidi, Najmeddine, et al.. (2024). Genetic Analysis of Heterotaxy in a Consanguineous Cohort. Clinical Genetics. 107(2). 224–230. 1 indexed citations
3.
Al‐Ashwal, Abdullah, et al.. (2024). Clinical and molecular characterization of familial chylomicronemia in Saudi patients: a retrospective study. Frontiers in Endocrinology. 15. 1439862–1439862. 1 indexed citations
4.
Al‐Ashwal, Abdullah, et al.. (2024). Long-term treatment for Laron syndrome with IGF-1 injection over 22 years in Saudi: A cohort study. Hormone Research in Paediatrics. 1–23. 1 indexed citations
5.
Aldalaan, Abdullah M., et al.. (2021). Genetic basis of pulmonary arterial hypertension: a prospective study from a highly inbred population. Pulmonary Circulation. 11(3). 1–8.
6.
Hashmi, Jamil Amjad, et al.. (2021). A Novel Frameshift Mutation in the ITGB3 Gene Leading to Glanzmann’s Thrombasthenia in a Saudi Arabian Family. Hematology/Oncology and Stem Cell Therapy. 15(1). 21–26. 6 indexed citations
7.
Ramzan, Khushnooda, Nouf S. Al‐Numair, Nadia Sakati, et al.. (2020). Identification of Novel CDH23 Variants Causing Moderate to Profound Progressive Nonsyndromic Hearing Loss. Genes. 11(12). 1474–1474. 12 indexed citations
8.
Afzal, Sibtain, Khushnooda Ramzan, Salma M. Wakil, et al.. (2020). A novel nonsense mutation in the STS gene in a Pakistani family with X-linked recessive ichthyosis: including a very rare case of two homozygous female patients. BMC Medical Genetics. 21(1). 20–20. 4 indexed citations
9.
Khalifa, Ola, et al.. (2020). Genotype–phenotype correlation of 33 patients with maple syrup urine disease. American Journal of Medical Genetics Part A. 182(11). 2486–2500. 13 indexed citations
10.
11.
Umair, Muhammad, Naveed Wasif, Khushnooda Ramzan, et al.. (2019). Exome sequencing revealed a novel loss‐of‐function variant in the GLI3 transcriptional activator 2 domain underlies nonsyndromic postaxial polydactyly. Molecular Genetics & Genomic Medicine. 7(7). e00627–e00627. 16 indexed citations
12.
Muhammad, Noor, Sher Alam Khan, Sher Alam Khan, et al.. (2017). A novel mutation in the HPGD gene causing primary hypertrophic osteoarthropathy with digital clubbing in a Pakistani family. Annals of Human Genetics. 82(3). 171–176. 9 indexed citations
13.
Al‐Ashwal, Abdullah, Afaf Alsagheir, Khushnooda Ramzan, et al.. (2017). Clinical, Endocrine, and Molecular Genetic Analysis of a Large Cohort of Saudi Arabian Patients with Laron Syndrome. Hormone Research in Paediatrics. 88(2). 119–126. 3 indexed citations
14.
Abouelhoda, Mohamed, Mohamed El-Kalioby, Nisha Patel, et al.. (2016). Clinical genomics can facilitate countrywide estimation of autosomal recessive disease burden. Genetics in Medicine. 18(12). 1244–1249. 67 indexed citations
15.
Basit, Sulman, et al.. (2015). Xq21.31–q21.32 duplication underlies intellectual disability in a large family with five affected males. American Journal of Medical Genetics Part A. 170(1). 87–93. 15 indexed citations
16.
Wasim, Muhammad, et al.. (2015). Alterations in the RB1 gene in Pakistani patients with retinoblastoma using direct sequencing analysis.. PubMed. 21. 1085–92. 13 indexed citations
17.
Wakil, Salma M., Khushnooda Ramzan, Rana Alomar, et al.. (2013). Infantile-onset ascending hereditary spastic paraplegia with bulbar involvement due to the novel ALS2 mutation c.2761C > T. Gene. 536(1). 217–220. 21 indexed citations
18.
Alsmadi, Osama, Brian F. Meyer, Fowzan S. Alkuraya, et al.. (2008). Syndromic congenital sensorineural deafness, microtia and microdontia resulting from a novel homoallelic mutation in fibroblast growth factor 3 (FGF3). European Journal of Human Genetics. 17(1). 14–21. 32 indexed citations
19.
Riazuddin, Saima, Zubair M. Ahmed, Alan S. Fanning, et al.. (2006). Tricellulin Is a Tight-Junction Protein Necessary for Hearing. The American Journal of Human Genetics. 79(6). 1040–1051. 205 indexed citations
20.
Ahmad, Jamil, Shaheen N. Khan, Shahid Y. Khan, et al.. (2005). DFNB48, a new nonsyndromic recessive deafness locus, maps to chromosome 15q23-q25.1. Human Genetics. 116(5). 407–412. 12 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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