Amr Al‐Saif

1.3k total citations
14 papers, 1.0k citations indexed

About

Amr Al‐Saif is a scholar working on Molecular Biology, Radiology, Nuclear Medicine and Imaging and Genetics. According to data from OpenAlex, Amr Al‐Saif has authored 14 papers receiving a total of 1.0k indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Molecular Biology, 4 papers in Radiology, Nuclear Medicine and Imaging and 4 papers in Genetics. Recurrent topics in Amr Al‐Saif's work include Corneal surgery and disorders (4 papers), Corneal Surgery and Treatments (3 papers) and RNA Interference and Gene Delivery (2 papers). Amr Al‐Saif is often cited by papers focused on Corneal surgery and disorders (4 papers), Corneal Surgery and Treatments (3 papers) and RNA Interference and Gene Delivery (2 papers). Amr Al‐Saif collaborates with scholars based in United States, Saudi Arabia and Oman. Amr Al‐Saif's co-authors include Saeed Bohlega, Futwan Al‐Mohanna, John D. Gottsch, Danielle N. Meadows, Nicholas Katsanis, Allen O. Eghrari, Lisa Davey, David McGaughey, Jimmy Huynh and Andrew S. McCallion and has published in prestigious journals such as Annals of Neurology, Genome Research and The American Journal of Human Genetics.

In The Last Decade

Amr Al‐Saif

14 papers receiving 1.0k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Amr Al‐Saif United States	12	520	286	198	193	164	14	1.0k
James R. Lupski United States	10	672 1.3×	108 0.4×	90 0.5×	195 1.0×	210 1.3×	10	1.3k
Julián Esteve-Rudd United States	13	510 1.0×	80 0.3×	94 0.5×	299 1.5×	101 0.6×	18	748
Ginat Narkis Israel	14	528 1.0×	56 0.2×	72 0.4×	43 0.2×	95 0.6×	23	836
Hani Levkovitch-Verbin Israel	18	509 1.0×	457 1.6×	44 0.2×	909 4.7×	134 0.8×	39	1.3k
Silvia Pasini United States	15	381 0.7×	53 0.2×	44 0.2×	204 1.1×	184 1.1×	22	760
Frédéric Lebrun-Julien Switzerland	11	606 1.2×	57 0.2×	52 0.3×	226 1.2×	433 2.6×	12	1.0k
Bernard Arnaud France	14	1.5k 2.9×	211 0.7×	88 0.4×	390 2.0×	293 1.8×	23	1.8k
Francesca Pasutto Germany	20	665 1.3×	303 1.1×	39 0.2×	794 4.1×	34 0.2×	41	1.3k
Sébastien Augustin France	21	778 1.5×	116 0.4×	29 0.1×	307 1.6×	110 0.7×	33	1.1k
Catherine Braine United States	10	409 0.8×	67 0.2×	87 0.4×	339 1.8×	82 0.5×	11	756

Countries citing papers authored by Amr Al‐Saif

Since Specialization

Citations

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

Fields of papers citing papers by Amr Al‐Saif

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Amr Al‐Saif. 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 Amr Al‐Saif. The network helps show where Amr Al‐Saif may publish in the future.

Co-authorship network of co-authors of Amr Al‐Saif

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

All Works

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14 of 14 papers shown

Bohlega, Saeed, Hussam Abou‐Al‐Shaar, Brian F. Meyer, et al.. (2019). Autosomal recessive ADCY5-Related dystonia and myoclonus: Expanding the genetic spectrum of ADCY5-Related movement disorders. Parkinsonism & Related Disorders. 64. 145–149. 20 indexed citations

Al‐Saif, Amr. (2019). Gene therapy of hematological disorders: current challenges. Gene Therapy. 26(7-8). 296–307. 13 indexed citations

Langston, Rebekah G., Iakov N. Rudenko, Ravindran Kumaran, et al.. (2018). Differences in Stability, Activity and Mutation Effects Between Human and Mouse Leucine-Rich Repeat Kinase 2. Neurochemical Research. 44(6). 1446–1459. 9 indexed citations

Bohlega, Saeed, et al.. (2013). Mutation of fibulin-1 causes a novel syndrome involving the central nervous system and connective tissues. European Journal of Human Genetics. 22(5). 640–643. 11 indexed citations

Al‐Saif, Amr, Saeed Bohlega, & Futwan Al‐Mohanna. (2012). Loss of ERLIN2 function leads to juvenile primary lateral sclerosis. Annals of Neurology. 72(4). 510–516. 51 indexed citations

Al‐Saif, Amr, Futwan Al‐Mohanna, & Saeed Bohlega. (2011). A mutation in sigma‐1 receptor causes juvenile amyotrophic lateral sclerosis. Annals of Neurology. 70(6). 913–919. 349 indexed citations

Shuaib, Taghreed, Nadia Alhashmi, Mohammad Ghaziuddin, et al.. (2011). Propionic Acidemia Associated With Visual Hallucinations. Journal of Child Neurology. 27(6). 799–803. 20 indexed citations

Riazuddin, S. Amer, Eranga N. Vithana, Yangjian Liu, et al.. (2010). Missense mutations in the sodium borate cotransporter SLC4A11 cause late-onset Fuchs corneal dystrophya. Human Mutation. 31(11). 1261–1268. 109 indexed citations

Riazuddin, Sheikh, Norann A. Zaghloul, Amr Al‐Saif, et al.. (2010). Missense Mutations in TCF8 Cause Late-Onset Fuchs Corneal Dystrophy and Interact with FCD4 on Chromosome 9p. The American Journal of Human Genetics. 86(1). 45–53. 147 indexed citations

10.

McGlumphy, Elyse J., S. Amer Riazuddin, Amr Al‐Saif, et al.. (2010). Age-Severity Relationships in Families Linked toFCD2with Retroillumination Photography. Investigative Ophthalmology & Visual Science. 51(12). 6298–6298. 11 indexed citations

11.

Riazuddin, Sheikh, Allen O. Eghrari, Amr Al‐Saif, et al.. (2009). Linkage of a Mild Late-Onset Phenotype of Fuchs Corneal Dystrophy to a Novel Locus at 5q33.1-q35.2. Investigative Ophthalmology & Visual Science. 50(12). 5667–5667. 72 indexed citations

12.

Alazami, Anas M., Amr Al‐Saif, Abdulaziz Alsemari, et al.. (2008). Mutations in C2orf37, Encoding a Nucleolar Protein, Cause Hypogonadism, Alopecia, Diabetes Mellitus, Mental Retardation, and Extrapyramidal Syndrome. The American Journal of Human Genetics. 83(6). 684–691. 94 indexed citations

13.

McGaughey, David, et al.. (2007). Metrics of sequence constraint overlook regulatory sequences in an exhaustive analysis at phox2b. Genome Research. 18(2). 252–260. 100 indexed citations

14.

Khan, Arif O., Farrukh A. Shamsi, Amr Al‐Saif, & Marios Kambouris. (2004). A Novel Missense Norrie Disease Mutation Associated With a Severe Ocular Phenotype. Journal of Pediatric Ophthalmology & Strabismus. 41(6). 361–363. 4 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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