Dana Marafi

1.1k total citations
24 papers, 171 citations indexed

About

Dana Marafi is a scholar working on Molecular Biology, Genetics and Genetics. According to data from OpenAlex, Dana Marafi has authored 24 papers receiving a total of 171 indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Molecular Biology, 14 papers in Genetics and 3 papers in Genetics. Recurrent topics in Dana Marafi's work include Genomics and Rare Diseases (7 papers), RNA modifications and cancer (5 papers) and Genetics and Neurodevelopmental Disorders (4 papers). Dana Marafi is often cited by papers focused on Genomics and Rare Diseases (7 papers), RNA modifications and cancer (5 papers) and Genetics and Neurodevelopmental Disorders (4 papers). Dana Marafi collaborates with scholars based in United States, Kuwait and Egypt. Dana Marafi's co-authors include Davut Pehli̇van, Mohammed Almannai, Richard A. Gibbs, Jennifer E. Posey, James R. Lupski, Ayman W. El‐Hattab, Valory Pavlik, Jawid M. Fatih, Shalini N. Jhangiani and Bernhard Suter and has published in prestigious journals such as Nucleic Acids Research, Neurology and British Journal of Haematology.

In The Last Decade

Dana Marafi

21 papers receiving 171 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Dana Marafi United States 8 88 70 22 20 16 24 171
Matilda R. Jackson Australia 8 54 0.6× 78 1.1× 17 0.8× 21 1.1× 19 1.2× 14 155
Ping Yee Billie Au Canada 9 119 1.4× 121 1.7× 18 0.8× 6 0.3× 14 0.9× 21 216
Bryan Sayson Canada 7 70 0.8× 48 0.7× 16 0.7× 26 1.3× 7 0.4× 8 160
Jessica Sebastian United States 6 64 0.7× 92 1.3× 12 0.5× 5 0.3× 13 0.8× 11 146
Ya-Hui Lin United Kingdom 6 159 1.8× 46 0.7× 40 1.8× 13 0.7× 8 0.5× 10 216
Claudia Soler‐Alfonso United States 12 197 2.2× 135 1.9× 13 0.6× 16 0.8× 10 0.6× 21 333
Naomi Meeks United States 8 86 1.0× 50 0.7× 9 0.4× 9 0.5× 11 0.7× 16 169
Thuong Ha Australia 6 77 0.9× 47 0.7× 13 0.6× 5 0.3× 20 1.3× 13 136
Fernanda T. Bellucco Brazil 9 107 1.2× 140 2.0× 10 0.5× 18 0.9× 10 0.6× 24 233
Naila Cristina Vilaça Lourenço Brazil 9 125 1.4× 129 1.8× 8 0.4× 8 0.4× 46 2.9× 16 214

Countries citing papers authored by Dana Marafi

Since Specialization
Citations

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

Fields of papers citing papers by Dana Marafi

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Dana Marafi

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

All Works

20 of 20 papers shown
1.
Marafi, Dana, et al.. (2024). Tribal Founder EMC1 Variant in 5 Kuwaiti Families Expands Phenotypic Spectrum of EMC1 -Related Disorder. Neurology Genetics. 10(3). e200156–e200156.
2.
3.
Marafi, Dana. (2024). Founder mutations and rare disease in the Arab world. Disease Models & Mechanisms. 17(6). 2 indexed citations
4.
Marafi, Dana, Ruizhi Duan, Jawid M. Fatih, et al.. (2024). Genomic Balancing Act: deciphering DNA rearrangements in the complex chromosomal aberration involving 5p15.2, 2q31.1, and 18q21.32. European Journal of Human Genetics. 33(2). 231–238. 4 indexed citations
5.
Al-Tawari, Asma, Dina Ramadan, Nawal Makhseed, et al.. (2023). Biotin-thiamine responsive basal ganglia disease: a retrospective review of the clinical, radiological and molecular findings of cases in Kuwait with novel variants. Orphanet Journal of Rare Diseases. 18(1). 271–271. 5 indexed citations
6.
Marafi, Dana, Mais Hashem, Firdous Abdulwahab, et al.. (2023). Human ‘knockouts’ of CSF3 display severe congenital neutropenia. British Journal of Haematology. 203(3). 477–480. 3 indexed citations
7.
Marafi, Dana, Ruizhi Duan, Shalini N. Jhangiani, et al.. (2023). Novel LSS variants in alopecia and intellectual disability syndrome: New case report and clinical spectrum of LSS ‐related rare disease traits. Clinical Genetics. 104(3). 344–349.
8.
Al‐Balool, Haya H., Alice Gardham, Emma Wakeling, et al.. (2023). Expanding the allelic spectrum of ELOVL4‐related autosomal recessive neuro‐ichthyosis. Molecular Genetics & Genomic Medicine. 11(12). e2256–e2256. 4 indexed citations
9.
Du, Haowei, Angad Jolly, Christopher M. Grochowski, et al.. (2023). HMZDupFinder: a robust computational approach for detecting intragenic homozygous duplications from exome sequencing data. Nucleic Acids Research. 52(4). e18–e18. 2 indexed citations
10.
Eldomery, Mohammad K., Lorraine Potocki, Dana Marafi, et al.. (2022). De novo heterozygous variants in SLC30A7 are a candidate cause for Joubert syndrome. American Journal of Medical Genetics Part A. 188(8). 2360–2366. 3 indexed citations
11.
Calame, Daniel G., Tadahiro Mitani, Jawid M. Fatih, et al.. (2022). Novel RETREG1 (FAM134B) founder allele is linked to HSAN2B and renal disease in a Turkish family. American Journal of Medical Genetics Part A. 188(7). 2153–2161. 3 indexed citations
12.
Calame, Daniel G., Jawid M. Fatih, Isabella Herman, et al.. (2021). Deep clinicopathological phenotyping identifies a previously unrecognized pathogenic EMD splice variant. Annals of Clinical and Translational Neurology. 8(10). 2052–2058.
13.
Herman, Isabella, Angad Jolly, Haowei Du, et al.. (2021). Quantitative dissection of multilocus pathogenic variation in an Egyptian infant with severe neurodevelopmental disorder resulting from multiple molecular diagnoses. American Journal of Medical Genetics Part A. 188(3). 735–750. 7 indexed citations
14.
Calame, Daniel G., Isabella Herman, Jawid M. Fatih, et al.. (2021). Risk of sudden cardiac death in EXOSC5‐related disease. American Journal of Medical Genetics Part A. 185(8). 2532–2540. 10 indexed citations
15.
Calame, Daniel G., Jawid M. Fatih, Isabella Herman, et al.. (2021). Biallelic Pathogenic Variants in TNNT3 Associated With Congenital Myopathy. Neurology Genetics. 7(3). e589–e589. 9 indexed citations
16.
Marafi, Dana, Tadahiro Mitani, Haowei Du, et al.. (2021). Neurodevelopmental disorder in an Egyptian family with a biallelic ALKBH8 variant. American Journal of Medical Genetics Part A. 185(4). 1288–1293. 15 indexed citations
17.
Herman, Isabella, Michael A. Lopez, Dana Marafi, et al.. (2020). Clinical exome sequencing in the diagnosis of pediatric neuromuscular disease. Muscle & Nerve. 63(3). 304–310. 17 indexed citations
18.
Bizargity, Peyman, Haley Streff, Yi-Shan Lee, et al.. (2019). GNA11 brain somatic pathogenic variant in an individual with phacomatosis pigmentovascularis. Neurology Genetics. 5(6). e366–e366. 2 indexed citations
19.
Pillai, Nishitha R., Dana Marafi, Sónia Monteiro, et al.. (2018). Novel deletion of 6p21.31p21.1 associated with laryngeal cleft, developmental delay, dysmorphic features and vascular anomaly. European Journal of Medical Genetics. 62(6). 103531–103531. 3 indexed citations
20.
Marafi, Dana, Bernhard Suter, Rebecca Schultz, et al.. (2018). Spectrum and time course of epilepsy and the associated cognitive decline in MECP2 duplication syndrome. Neurology. 92(2). e108–e114. 28 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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