Lamia Alsubaie

716 total citations
16 papers, 220 citations indexed

About

Lamia Alsubaie is a scholar working on Genetics, Molecular Biology and Genetics. According to data from OpenAlex, Lamia Alsubaie has authored 16 papers receiving a total of 220 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Genetics, 8 papers in Molecular Biology and 3 papers in Genetics. Recurrent topics in Lamia Alsubaie's work include Genomics and Rare Diseases (9 papers), Genomic variations and chromosomal abnormalities (4 papers) and Genetics and Neurodevelopmental Disorders (3 papers). Lamia Alsubaie is often cited by papers focused on Genomics and Rare Diseases (9 papers), Genomic variations and chromosomal abnormalities (4 papers) and Genetics and Neurodevelopmental Disorders (3 papers). Lamia Alsubaie collaborates with scholars based in Saudi Arabia, United States and United Kingdom. Lamia Alsubaie's co-authors include Majid Alfadhel, Ahmed Alfares, Fuad Al Mutairi, Malak Abedalthagafi, Nada Al Tassan, Musa Alharbi, Rasha Aljelaify, Robert Hoehndorf, Shakti Ramkissoon and Abeer Al Tuwaijri and has published in prestigious journals such as SHILAP Revista de lepidopterología, Bioinformatics and The Oncologist.

In The Last Decade

Lamia Alsubaie

16 papers receiving 219 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Lamia Alsubaie Saudi Arabia	8	99	97	48	47	36	16	220
R. Tanner Hagelstrom United States	9	229 2.3×	75 0.8×	38 0.8×	47 1.0×	19 0.5×	16	325
Ronny Derks Netherlands	10	221 2.2×	130 1.3×	40 0.8×	19 0.4×	31 0.9×	15	326
Leticia Fröhlich Archangelo Brazil	10	251 2.5×	54 0.6×	32 0.7×	38 0.8×	26 0.7×	18	318
Dorothée Michaux France	8	226 2.3×	110 1.1×	46 1.0×	107 2.3×	17 0.5×	8	358
Luke St Heaps Australia	10	214 2.2×	188 1.9×	38 0.8×	32 0.7×	38 1.1×	22	379
Silvia Azzarello‐Burri Switzerland	8	206 2.1×	139 1.4×	35 0.7×	63 1.3×	8 0.2×	17	303
Fergus J. Couch United States	8	209 2.1×	74 0.8×	45 0.9×	74 1.6×	15 0.4×	11	305
Alexander M. Holtz United States	8	214 2.2×	60 0.6×	17 0.4×	79 1.7×	24 0.7×	12	268
Laura A. New Canada	10	242 2.4×	75 0.8×	26 0.5×	32 0.7×	50 1.4×	16	431
Jagadeesan Madhavan India	11	186 1.9×	61 0.6×	29 0.6×	84 1.8×	22 0.6×	20	294

Countries citing papers authored by Lamia Alsubaie

Since Specialization

Citations

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

Fields of papers citing papers by Lamia Alsubaie

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Lamia Alsubaie

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

All Works

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16 of 16 papers shown

Alharbi, Wardah, Lamia Alsubaie, Abdulrahman Alswaid, et al.. (2022). The variant artificial intelligence easy scoring (VARIES) system. Computers in Biology and Medicine. 145. 105492–105492. 2 indexed citations

Alsubaie, Lamia, Abdulrahman Swaid, Wafa Eyaid, et al.. (2022). Common disease-associated gene variants in a Saudi Arabian population. Annals of Saudi Medicine. 42(1). 29–35. 16 indexed citations

Alsubaie, Lamia, Nagarajan Kathiresan, Katsuhiko Mineta, et al.. (2021). DeepSVP: integration of genotype and phenotype for structural variant prioritization using deep learning. Bioinformatics. 38(6). 1677–1684. 9 indexed citations

Eissa, Mariam Al, Lamia Alsubaie, Abdulrahman Alswaid, et al.. (2021). Genetic carrier screening for disorders included in newborn screening in the Saudi population. SHILAP Revista de lepidopterología. 4(2). 70–75. 7 indexed citations

Alsubaie, Lamia, et al.. (2021). The rate of secondary genomic findings in the Saudi population. American Journal of Medical Genetics Part A. 188(1). 83–88. 7 indexed citations

Macken, William L., Gabrielle Wheway, Karen Stals, et al.. (2021). Biallelic variants in COPB1 cause a novel, severe intellectual disability syndrome with cataracts and variable microcephaly. Genome Medicine. 13(1). 34–34. 23 indexed citations

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

Alsubaie, Lamia, Abdulrahman Swaid, Fuad Al Mutairi, et al.. (2020). Genomic testing and counseling: The contribution of next‐generation sequencing to epilepsy genetics. Annals of Human Genetics. 84(6). 431–436. 7 indexed citations

Alsubaie, Lamia, et al.. (2020). Novel mutation of the FHL1 gene associated with congenital myopathy and early respiratory muscles involvement: a case report. SHILAP Revista de lepidopterología. 3(1). 45–51. 1 indexed citations

10.

Alsubaie, Lamia, Abdulrahman Swaid, Fuad Al Mutairi, et al.. (2020). MEFV c.2230G>T p.(Ala744Ser) rs61732874 previously misclassified as pathogenic variant due to lack of a population specific database. Annals of Human Genetics. 84(5). 370–379. 1 indexed citations

11.

Alharbi, Musa, Rasha Aljelaify, Lamia Alsubaie, et al.. (2018). Durable Response to Nivolumab in a Pediatric Patient with Refractory Glioblastoma and Constitutional Biallelic Mismatch Repair Deficiency. The Oncologist. 23(12). 1401–1406. 51 indexed citations

12.

Alharbi, Musa, Rasha Aljelaify, Fatimah Alqubaishi, et al.. (2018). Rare TP53 variant associated with Li-Fraumeni syndrome exhibits variable penetrance in a Saudi family. npj Genomic Medicine. 3(1). 35–35. 7 indexed citations

13.

Alsubaie, Lamia, Saeed Al-Turki, Ali Alothaim, & Ahmed Alfares. (2018). Clinical reassessment of post-laboratory variant call format (VCF) files. SHILAP Revista de lepidopterología. 1(1). 31–36. 1 indexed citations

14.

Abulkhair, Omalkhair, Mohammed Al Balwi, Lamia Alsubaie, et al.. (2018). Prevalence of BRCA1 and BRCA2 Mutations Among High-Risk Saudi Patients With Breast Cancer. Journal of Global Oncology. 4(4). 1–9. 21 indexed citations

15.

Alfares, Ahmed, Lamia Alsubaie, Mohammed Al‐Owain, et al.. (2017). A new association between CDK5RAP2 microcephaly and congenital cataracts. Annals of Human Genetics. 82(3). 165–170. 10 indexed citations

16.

Leslie, Elizabeth J., James O’Sullivan, Michael L. Cunningham, et al.. (2015). Expanding the genetic and phenotypic spectrum of popliteal pterygium disorders. American Journal of Medical Genetics Part A. 167(3). 545–552. 32 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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