Yusra Alyafee

502 total citations
17 papers, 318 citations indexed

About

Yusra Alyafee is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Yusra Alyafee has authored 17 papers receiving a total of 318 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Molecular Biology, 8 papers in Genetics and 3 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Yusra Alyafee's work include Genetics and Neurodevelopmental Disorders (4 papers), Genomics and Rare Diseases (3 papers) and Prenatal Screening and Diagnostics (3 papers). Yusra Alyafee is often cited by papers focused on Genetics and Neurodevelopmental Disorders (4 papers), Genomics and Rare Diseases (3 papers) and Prenatal Screening and Diagnostics (3 papers). Yusra Alyafee collaborates with scholars based in Saudi Arabia, Iraq and United Kingdom. Yusra Alyafee's co-authors include Majid Alfadhel, Muhammad Umair, Abeer Al Tuwaijri, Qamre Alam, Abdulaziz Asiri, Salam Massadeh, Marwan Nashabat, Mazhor Aldosary, Manal Alaamery and Dilek Çolak and has published in prestigious journals such as The American Journal of Human Genetics, International Journal of Nanomedicine and Frontiers in Genetics.

In The Last Decade

Yusra Alyafee

17 papers receiving 317 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Yusra Alyafee Saudi Arabia	12	202	123	36	27	26	17	318
Ryoko Fukai Japan	11	190 0.9×	148 1.2×	38 1.1×	17 0.6×	20 0.8×	23	368
Lucy Crompton United Kingdom	9	488 2.4×	120 1.0×	32 0.9×	44 1.6×	16 0.6×	17	660
Jungyoon Choi South Korea	8	134 0.7×	60 0.5×	11 0.3×	22 0.8×	30 1.2×	23	395
G. Praveen Raju United States	9	273 1.4×	58 0.5×	12 0.3×	21 0.8×	59 2.3×	13	414
Roberto Micheli Italy	9	217 1.1×	69 0.6×	21 0.6×	10 0.4×	18 0.7×	16	387
Alice Abdel Aleem Egypt	13	216 1.1×	119 1.0×	48 1.3×	26 1.0×	4 0.2×	24	376
Marisol Vazquez United Kingdom	5	254 1.3×	81 0.7×	8 0.2×	27 1.0×	17 0.7×	9	491
Suzanne F. C. Miller-Delaney Ireland	7	195 1.0×	127 1.0×	32 0.9×	18 0.7×	11 0.4×	8	355
Dario Melguizo‐Sanchis Spain	9	450 2.2×	55 0.4×	58 1.6×	14 0.5×	15 0.6×	11	564
Rebecca Barnard United States	7	322 1.6×	155 1.3×	13 0.4×	45 1.7×	6 0.2×	9	560

Countries citing papers authored by Yusra Alyafee

Since Specialization

Citations

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

Fields of papers citing papers by Yusra Alyafee

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Yusra Alyafee

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

All Works

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17 of 17 papers shown

Christmas, S E, et al.. (2024). Relationships Between Polymorphisms in HLA-G 3’UTR Region and COVID-19 Disease Severity. Biochemical Genetics. 63(5). 4701–4722. 1 indexed citations

Alyafee, Yusra, et al.. (2022). Non-invasive prenatal testing for autosomal recessive disorders: A new promising approach. Frontiers in Genetics. 13. 1047474–1047474. 29 indexed citations

Tuwaijri, Abeer Al, et al.. (2022). Novel homozygous pathogenic mitochondrial DNAJC19 variant in a patient with dilated cardiomyopathy and global developmental delay. Molecular Genetics & Genomic Medicine. 10(8). e1969–e1969. 10 indexed citations

Tuwaijri, Abeer Al, Yusra Alyafee, Muhammad Umair, et al.. (2022). Congenital disorder of glycosylation with defective fucosylation 2 (FCSK gene defect): The third report in the literature with a mild phenotype. Molecular Genetics & Genomic Medicine. 11(4). e2117–e2117. 4 indexed citations

Alyafee, Yusra, et al.. (2021). Next-Generation Sequencing-Based Pre-Implantation Genetic Testing for Aneuploidy (PGT-A): First Report from Saudi Arabia. Genes. 12(4). 461–461. 28 indexed citations

Umair, Muhammad, Muhammad Farooq Khan, Marwan Nashabat, et al.. (2021). Mutated VWA8 Is Associated With Developmental Delay, Microcephaly, and Scoliosis and Plays a Novel Role in Early Development and Skeletal Morphogenesis in Zebrafish. Frontiers in Cell and Developmental Biology. 9. 736960–736960. 12 indexed citations

Alyafee, Yusra, et al.. (2021). Next Generation Sequencing Based Non-invasive Prenatal Testing (NIPT): First Report From Saudi Arabia. Frontiers in Genetics. 12. 630787–630787. 30 indexed citations

Alfadhel, Majid, Muhammad Umair, Bader Almuzzaini, et al.. (2021). Identification of the TTC26 Splice Variant in a Novel Complex Ciliopathy Syndrome with Biliary, Renal, Neurological, and Skeletal Manifestations. Molecular Syndromology. 12(3). 133–140. 8 indexed citations

Bhat, Javaid Akhter, Marwan Nashabat, Yusra Alyafee, et al.. (2020). A Missense Mutation in the UGDH Gene Is Associated With Developmental Delay and Axial Hypotonia. Frontiers in Pediatrics. 8. 71–71. 18 indexed citations

10.

Mutairi, Fuad Al, Fayhan Alroqi, Yusra Alyafee, et al.. (2020). Homozygous truncating NEK10 mutation, associated with primary ciliary dyskinesia: a case report. BMC Pulmonary Medicine. 20(1). 141–141. 13 indexed citations

11.

Umair, Muhammad, Abdulaziz Asiri, Yusra Alyafee, et al.. (2020). EMC10 homozygous variant identified in a family with global developmental delay, mild intellectual disability, and speech delay. Clinical Genetics. 98(6). 555–561. 25 indexed citations

12.

Asiri, Abdulaziz, Muhammad Umair, Yusra Alyafee, et al.. (2020). Mutated RAP1GDS1 causes a new syndrome of dysmorphic feature, intellectual disability & speech delay. Annals of Clinical and Translational Neurology. 7(6). 956–964. 16 indexed citations

13.

Alsagob, Maysoon, Mustafa A. Salih, Muddathir H. Hamad, et al.. (2019). First report of two successive deletions on chromosome 15q13 cytogenetic bands in a boy and girl: additional data to 15q13.3 syndrome with a report of high IQ patient. Molecular Cytogenetics. 12(1). 21–21. 2 indexed citations

14.

Alyafee, Yusra, et al.. (2017). Preparation of anastrozole loaded PEG-PLA nanoparticles: evaluation of apoptotic response of breast cancer cell lines. International Journal of Nanomedicine. Volume 13. 199–208. 26 indexed citations

15.

Massadeh, Salam, et al.. (2016). Synthesis of protein-coated biocompatible methotrexate-loaded PLA-PEG-PLA nanoparticles for breast cancer treatment. Europe PMC (PubMed Central). 7(1). 31996–31996. 15 indexed citations

16.

Faqeih, Eissa, Mohammed Al‐Owain, Dilek Çolak, et al.. (2014). Novel homozygous DEAF1 variant suspected in causing white matter disease, intellectual disability, and microcephaly. American Journal of Medical Genetics Part A. 164(6). 1565–1570. 12 indexed citations

17.

AlSayed, Moeenaldeen, Hamad Alzaidan, Albandary AlBakheet, et al.. (2013). Mutations in NALCN Cause an Autosomal-Recessive Syndrome with Severe Hypotonia, Speech Impairment, and Cognitive Delay. The American Journal of Human Genetics. 93(4). 721–726. 69 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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