Yusra Alyafee

513 citations

17 papers · 326 · h-index 12

Impact in

Aging
Genetics
- Genetics and Neurodevelopmental Disorders
- Genomics and Rare Diseases
- Genetic and Kidney Cyst Diseases

Papers in

Molecular Biology 10
- Glycosylation and Glycoproteins Research 2
- Renal and related cancers 2
- Congenital heart defects research 2
Genetics 7
- Genetics and Neurodevelopmental Disorders 3
- Genomics and Rare Diseases 3
- Genomic variations and chromosomal abnormalities 3
- Genetic Syndromes and Imprinting 2

Co-authors: Muhammad Umair (11 shared papers)Majid Alfadhel (11 shared papers)Abeer Al Tuwaijri (9 shared papers)Qamre Alam (5 shared papers)Abdulaziz Asiri (5 shared papers)Dilek Çolak (3 shared papers)Namik Kaya (3 shared papers)Salam Massadeh (2 shared papers)
Journals: Frontiers in Genetics (2 papers)BMC Pulmonary Medicine (1 paper)Frontiers in Pediatrics (1 paper)Frontiers in Cell and Developmental Biology (1 paper)International Journal of Nanomedicine (1 paper)
Partner nations: Saudi Arabia United Kingdom Pakistan

In The Last Decade

Yusra Alyafee

17 papers receiving 325 citations

Peers

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-authors

The 25 scholars most cited alongside Yusra Alyafee, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Yusra Alyafee Line = papers co-authored together Yusra Alyafee links everyone, so they are left out of the graph.

All Works

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17 of 17 papers shown

#	Work
1	Mutations in NALCN Cause an Autosomal-Recessive Syndrome with Severe Hypotonia, Speech Impairment, and Cognitive Delay The American Journal of Human Genetics ·Moeenaldeen AlSayed, Hamad Alzaidan, Albandary AlBakheet, Hana Hakami, Rosan Kenana, Yusra Alyafee, Mazhor Aldosary, Alya Qari, Tarfa Al‐Sheddi, Muhammed Al-Muheiza, Wafa Al-Qubbaj, Yamina Lakmache, Hindi Al‐Hindi, Muhammad Ghaziuddin, Dilek Çolak, Namik Kaya	2013	70
2	Next Generation Sequencing Based Non-invasive Prenatal Testing (NIPT): First Report From Saudi Arabia Frontiers in Genetics ·Yusra Alyafee, Abeer Al Tuwaijri, Qamre Alam, Muhammad Umair, Shahad Haddad, Mashael Alharbi, Maryam Ballow, Mohammed Al Drees, Abdulkareem AlAbdulrahman, Aziza Al Khaldi, Majid Alfadhel	2021	32
3	Non-invasive prenatal testing for autosomal recessive disorders: A new promising approach Frontiers in Genetics ·Yusra Alyafee, Abeer Al Tuwaijri, Muhammad Umair, Mashael Alharbi, Shahad Haddad, Maryam Ballow, Latifah Alayyar, Qamre Alam, Saleh Althenayyan, Nadia Al Ghilan, Aziza Al Khaldi, Majid S. Faden, Hamad Al Sufyan, Majid Alfadhel	2022	31
4	Next-Generation Sequencing-Based Pre-Implantation Genetic Testing for Aneuploidy (PGT-A): First Report from Saudi Arabia Genes ·Yusra Alyafee, Qamre Alam, Abeer Al Tuwaijri, Muhammad Umair, Shahad Haddad, Meshael Alharbi, Hayat Ahmed Alrabiah, Maha Al-Ghuraibi, Sahar Al-Showaier, Majid Alfadhel	2021	28
5	Preparation of anastrozole loaded PEG-PLA nanoparticles: evaluation of apoptotic response of breast cancer cell lines International Journal of Nanomedicine ·Yusra Alyafee, Manal Alaamery, Shahad Bawazeer, Mansour Al Mutairi, Badr G. Alghamdi, Nawaf Alomran, Atia Sheereen, Maha H. Daghestani, Salam Massadeh	2017	26
6	EMC10 homozygous variant identified in a family with global developmental delay, mild intellectual disability, and speech delay Clinical Genetics ·Muhammad Umair, Mariam Ballow, Abdulaziz Asiri, Yusra Alyafee, Abeer Al Tuwaijri, Kheloud M. Alhamoudi, Taghrid Aloraini, Marwa Abdelhakim, Azza Althagafi, Şenay Kafkas, Lamia Alsubaie, Muhammad Talal Alrifai, Robert Hoehndorf, Ahmed Alfares, Majid Alfadhel	2020	25
7	A Missense Mutation in the UGDH Gene Is Associated With Developmental Delay and Axial Hypotonia Frontiers in Pediatrics ·Kheloud M. Alhamoudi, Javaid Akhter Bhat, Marwan Nashabat, Masheal Alharbi, Yusra Alyafee, Abdulaziz Asiri, Muhammad Umair, Majid Alfadhel	2020	19
8	Mutated RAP1GDS1 causes a new syndrome of dysmorphic feature, intellectual disability & speech delay Annals of Clinical and Translational Neurology ·Abdulaziz Asiri, Essra Aloyouni, Muhammad Umair, Yusra Alyafee, Abeer Al Tuwaijri, Kheloud M. Alhamoudi, Bader Almuzzaini, Abeer Al Baz, Deemah Alwadaani, Marwan Nashabat, Majid Alfadhel	2020	16
9	Synthesis of protein-coated biocompatible methotrexate-loaded PLA-PEG-PLA nanoparticles for breast cancer treatment Europe PMC (PubMed Central) ·Salam Massadeh, Manal Alaamery, Shatha Al-Qatanani, Saqer Alarifi, Shahad Bawazeer, Yusra Alyafee	2016	15
10	Homozygous truncating NEK10 mutation, associated with primary ciliary dyskinesia: a case report BMC Pulmonary Medicine ·Fuad Al Mutairi, Randa Alkhalaf, Abdullah Alkhorayyef, Fayhan Alroqi, Yusra Alyafee, Muhammad Umair, Nouf Fetaini, Amjad Khan, Meshael Alharbi, (unknown), Monira Alaujan, Abdulaziz Asiri, Kheloud M. Alhamoudi, Majid Alfadhel	2020	14
11	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 ·Muhammad Umair, Muhammad Farooq Khan, Mohammed Aldrees, Marwan Nashabat, Kheloud M. Alhamoudi, Muhammad Bilal, Yusra Alyafee, Abeer Al Tuwaijri, Manar Aldarwish, Ahmed Al‐Rumayyan, Hamad Alkhalaf, Mohammad Ahmad Wadaan, Majid Alfadhel	2021	13
12	Novel homozygous DEAF1 variant suspected in causing white matter disease, intellectual disability, and microcephaly American Journal of Medical Genetics Part A ·Eissa Faqeih, Mohammed Al‐Owain, Dilek Çolak, Rosan Kenana, Yusra Alyafee, Mazhor Aldosary, Abdulaziz Alsaman, Fadwa Albalawi, Dalia Al‐Sarar, Dalia Domiaty, Maha H. Daghestani, Namik Kaya	2014	12
13	Novel homozygous pathogenic mitochondrial DNAJC19 variant in a patient with dilated cardiomyopathy and global developmental delay Molecular Genetics & Genomic Medicine ·Abeer Al Tuwaijri, Yusra Alyafee, Mashael Alharbi, Maryam Ballow, Mohammed Aldrees, Qamre Alam, Rola Sleiman, Muhammad Umair, Majid Alfadhel	2022	10
14	Identification of the TTC26 Splice Variant in a Novel Complex Ciliopathy Syndrome with Biliary, Renal, Neurological, and Skeletal Manifestations Molecular Syndromology ·Majid Alfadhel, Muhammad Umair, Bader Almuzzaini, Abdulaziz Asiri, Abeer Al Tuwaijri, Khaloud Alhamoudi, Yusra Alyafee, Mohammed Al‐Owain	2021	8
15	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 ·Abeer Al Tuwaijri, Yusra Alyafee, Muhammad Umair, Arwa Alsubait, Mashael Alharbi, Hamad Al‐Eidi, Mariam Ballow, Mohammed Aldrees, Qamre Alam, Abdulkareem Al Abdulrahman, Muhammad Talal Alrifai, Majid Alfadhel	2022	4
16	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 ·Maysoon Alsagob, Mustafa A. Salih, Muddathir H. Hamad, Yusra Alyafee, Jawaher Al‐Zahrani, Albandary AlBakheet, Michael Nester, Nadia Sakati, Salma M. Wakil, Ali Al‐Odaib, Dilek Çolak, Namik Kaya	2019	2
17	Relationships Between Polymorphisms in HLA-G 3’UTR Region and COVID-19 Disease Severity Biochemical Genetics ·Ahmed Alyami, Fawziya Barnawi, S E Christmas, Yusra Alyafee, Maaweya Awadalla, Zaid Al‐Bayati, Ahmad A. Alshehri, Ahmed Saif, Lamjed Mansour	2024	1

About Yusra Alyafee

Yusra Alyafee is a scholar working on Molecular Biology, Genetics, Pediatrics, Perinatology and Child Health, Infectious Diseases and Surgery, having authored 17 papers that have together received 326 indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (3 papers), Genomics and Rare Diseases (3 papers), Prenatal Screening and Diagnostics (3 papers), Genomic variations and chromosomal abnormalities (3 papers), Glycosylation and Glycoproteins Research (2 papers), Genetic Syndromes and Imprinting (2 papers), Renal and related cancers (2 papers) and Congenital heart defects research (2 papers). The work is most often cited by research in Aging (7 citations), Genetics (98 citations), Sensory Systems (13 citations), Molecular Biology (170 citations) and Clinical Biochemistry (13 citations). Yusra Alyafee has collaborated with scholars based in Saudi Arabia, United Kingdom and Pakistan. Frequent co-authors include Muhammad Umair, Majid Alfadhel, Abeer Al Tuwaijri, Qamre Alam, Abdulaziz Asiri, Dilek Çolak, Namik Kaya, Salam Massadeh, Marwan Nashabat and Mazhor Aldosary. Their work appears in journals such as Frontiers in Genetics, BMC Pulmonary Medicine, Frontiers in Pediatrics, Frontiers in Cell and Developmental Biology and International Journal of Nanomedicine.

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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