Amal Abu Rayyan

1.1k total citations
18 papers, 632 citations indexed

About

Amal Abu Rayyan is a scholar working on Molecular Biology, Sensory Systems and Genetics. According to data from OpenAlex, Amal Abu Rayyan has authored 18 papers receiving a total of 632 indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Molecular Biology, 6 papers in Sensory Systems and 6 papers in Genetics. Recurrent topics in Amal Abu Rayyan's work include Hearing, Cochlea, Tinnitus, Genetics (6 papers), RNA and protein synthesis mechanisms (5 papers) and DNA Repair Mechanisms (2 papers). Amal Abu Rayyan is often cited by papers focused on Hearing, Cochlea, Tinnitus, Genetics (6 papers), RNA and protein synthesis mechanisms (5 papers) and DNA Repair Mechanisms (2 papers). Amal Abu Rayyan collaborates with scholars based in Palestinian Territory, United States and Israel. Amal Abu Rayyan's co-authors include Moien Kanaan, Mary‐Claire King, Tom Walsh, Ming K. Lee, Karen B. Avraham, Hashem Shahin, T. Elkan Miller, Wendy Roeb, Anne Thornton and Süleyman Gülsüner and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Clinical Investigation and JNCI Journal of the National Cancer Institute.

In The Last Decade

Amal Abu Rayyan

15 papers receiving 622 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Amal Abu Rayyan Palestinian Territory 12 356 228 223 82 81 18 632
Laurence Jonard France 15 379 1.1× 102 0.4× 301 1.3× 13 0.2× 135 1.7× 36 742
Matías Morin Spain 12 529 1.5× 83 0.4× 262 1.2× 20 0.2× 85 1.0× 27 856
Eeva-Marja Sankila Finland 7 474 1.3× 318 1.4× 129 0.6× 385 4.7× 44 0.5× 16 978
Va Lip United States 12 474 1.3× 367 1.6× 82 0.4× 171 2.1× 28 0.3× 17 883
Kwanghyuk Lee United States 13 297 0.8× 145 0.6× 103 0.5× 9 0.1× 42 0.5× 23 546
Wanda S. Layman United States 10 262 0.7× 128 0.6× 194 0.9× 7 0.1× 24 0.3× 12 640
Seher Başaran Türkiye 17 278 0.8× 305 1.3× 31 0.1× 59 0.7× 104 1.3× 73 814
Mounira Hmani‐Aifa Tunisia 14 274 0.8× 124 0.5× 256 1.1× 12 0.1× 131 1.6× 19 706
Nataliya Di Donato Germany 18 463 1.3× 371 1.6× 54 0.2× 61 0.7× 20 0.2× 61 914
M Lathrop France 8 105 0.3× 65 0.3× 96 0.4× 8 0.1× 47 0.6× 18 364

Countries citing papers authored by Amal Abu Rayyan

Since Specialization
Citations

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

Fields of papers citing papers by Amal Abu Rayyan

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Amal Abu Rayyan. 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 Amal Abu Rayyan. The network helps show where Amal Abu Rayyan may publish in the future.

Co-authorship network of co-authors of Amal Abu Rayyan

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

All Works

18 of 18 papers shown
1.
Jacobson, Angela, Amal Abu Rayyan, Süleyman Gülsüner, et al.. (2025). Long-read DNA and RNA sequencing for inherited polyposis and colorectal cancer: cryptic intronic variants and multiple mutational mechanisms. Journal of Medical Genetics. 62(10). 617–623.
2.
Gülsüner, Süleyman, Amal Abu Rayyan, Jessica B. Mandell, et al.. (2024). Long-read DNA and cDNA sequencing identify cancer-predisposing deep intronic variation in tumor-suppressor genes. Genome Research. 34(11). 1825–1831. 7 indexed citations
3.
Lieberman, Sari, Ming K. Lee, Süleyman Gülsüner, et al.. (2024). TP53 missense allele predisposing to high risk of breast cancer but not pediatric cancers. JNCI Journal of the National Cancer Institute. 117(5). 1069–1073.
4.
Rayyan, Amal Abu, Ryan J. Carlson, Ming K. Lee, et al.. (2023). A paradoxical genotype-phenotype relationship: Low level of GOSR2 translation from a non-AUG start codon in a family with profound hearing loss. Human Molecular Genetics. 32(14). 2265–2268.
5.
Carlson, Ryan J., Tom Walsh, Jessica B. Mandell, et al.. (2023). Association of Genetic Diagnoses for Childhood-Onset Hearing Loss With Cochlear Implant Outcomes. JAMA Otolaryngology–Head & Neck Surgery. 149(3). 212–212. 20 indexed citations
6.
Rayyan, Amal Abu, Silvia Casadei, Zippora Brownstein, et al.. (2020). Genomic analysis of inherited hearing loss in the Palestinian population. Proceedings of the National Academy of Sciences. 117(33). 20070–20076. 38 indexed citations
7.
Pierce, Sarah B., Christina Canavati, Amal Abu Rayyan, et al.. (2020). Helicase-inactivating BRIP1 mutation yields Fanconi anemia with microcephaly and other congenital abnormalities. Molecular Case Studies. 6(5). a005652–a005652. 5 indexed citations
8.
Canavati, Christina, Karl Martin Klein, Zaid Afawi, et al.. (2019). Inclusion of hemimegalencephaly into the phenotypic spectrum of NPRL3 pathogenic variants in familial focal epilepsy with variable foci. Epilepsia. 60(6). e67–e73. 13 indexed citations
9.
Renbaum, Paul, Amal Abu Rayyan, Silvia Casadei, et al.. (2017). Genomic analysis of inherited breast cancer among Palestinian women: Genetic heterogeneity and a founder mutation in TP53. International Journal of Cancer. 141(4). 750–756. 31 indexed citations
10.
Rayyan, Amal Abu, Sarah B. Pierce, Ming K. Lee, et al.. (2016). Mutation of KREMEN1, a modulator of Wnt signaling, is responsible for ectodermal dysplasia including oligodontia in Palestinian families. European Journal of Human Genetics. 24(10). 1430–1435. 19 indexed citations
11.
Tenenbaum‐Rakover, Yardena, Ariella Weinberg‐Shukron, Paul Renbaum, et al.. (2015). Minichromosome maintenance complex component 8 (MCM8) gene mutations result in primary gonadal failure. Journal of Medical Genetics. 52(6). 391–399. 91 indexed citations
12.
Rayyan, Amal Abu, Kathy Ushakov, Liat Amir-Zilberstein, et al.. (2015). The GPSM2/LGN GoLoco motifs are essential for hearing. Mammalian Genome. 27(1-2). 29–46. 30 indexed citations
13.
Weinberg‐Shukron, Ariella, Paul Renbaum, Rachel Kalifa, et al.. (2015). A mutation in the nucleoporin-107 gene causes XX gonadal dysgenesis. Journal of Clinical Investigation. 125(11). 4295–4304. 64 indexed citations
14.
Brownstein, Zippora, Amal Abu Rayyan, Serena Sirigu, et al.. (2013). Novel myosin mutations for hereditary hearing loss revealed by targeted genomic capture and massively parallel sequencing. European Journal of Human Genetics. 22(6). 768–775. 35 indexed citations
15.
Rayyan, Amal Abu, et al.. (2011). Serotype Distribution and Drug Resistance in Streptococcus pneumoniae. 1 indexed citations
16.
Walsh, Tom, Hashem Shahin, T. Elkan Miller, et al.. (2010). Whole Exome Sequencing and Homozygosity Mapping Identify Mutation in the Cell Polarity Protein GPSM2 as the Cause of Nonsyndromic Hearing Loss DFNB82. The American Journal of Human Genetics. 87(1). 90–94. 198 indexed citations
17.
Rayyan, Amal Abu, et al.. (2010). Serotype Distribution and Drug Resistance inStreptococcus pneumoniae, Palestinian Territories. Emerging infectious diseases. 17(1). 94–96. 11 indexed citations
18.
Shahin, Hashem, Tom Walsh, Amal Abu Rayyan, et al.. (2009). Five novel loci for inherited hearing loss mapped by SNP-based homozygosity profiles in Palestinian families. European Journal of Human Genetics. 18(4). 407–413. 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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