Marwan K. Tayeh

1.8k total citations
26 papers, 1.2k citations indexed

About

Marwan K. Tayeh is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Marwan K. Tayeh has authored 26 papers receiving a total of 1.2k indexed citations (citations by other indexed papers that have themselves been cited), including 18 papers in Molecular Biology, 17 papers in Genetics and 4 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Marwan K. Tayeh's work include Genetic Syndromes and Imprinting (8 papers), Genomic variations and chromosomal abnormalities (5 papers) and Nuclear Structure and Function (4 papers). Marwan K. Tayeh is often cited by papers focused on Genetic Syndromes and Imprinting (8 papers), Genomic variations and chromosomal abnormalities (5 papers) and Nuclear Structure and Function (4 papers). Marwan K. Tayeh collaborates with scholars based in United States, Jordan and Türkiye. Marwan K. Tayeh's co-authors include Val C. Sheffield, Edwin M. Stone, Diane C. Slusarski, Robert F. Mullins, Hatem El‐Shanti, Darryl Nishimura, John S. Beck, Thomas L. Casavant, Terry A. Braun and Jian Huang and has published in prestigious journals such as Proceedings of the National Academy of Sciences, SHILAP Revista de lepidopterología and Blood.

In The Last Decade

Marwan K. Tayeh

25 papers receiving 1.2k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Marwan K. Tayeh United States 15 828 694 125 103 100 26 1.2k
Fuyuki Miya Japan 19 509 0.6× 299 0.4× 126 1.0× 99 1.0× 43 0.4× 84 1.0k
David Fenstermacher United States 12 784 0.9× 324 0.5× 90 0.7× 49 0.5× 24 0.2× 23 1.6k
Tristan Shaffer United States 4 748 0.9× 744 1.1× 77 0.6× 32 0.3× 40 0.4× 12 1.4k
Paul I.W. de Bakker United States 12 614 0.7× 699 1.0× 176 1.4× 19 0.2× 18 0.2× 12 1.5k
David J. Dow United Kingdom 11 399 0.5× 185 0.3× 136 1.1× 29 0.3× 65 0.7× 15 1.1k
Joshua Chiou United States 15 812 1.0× 566 0.8× 127 1.0× 38 0.4× 27 0.3× 22 1.4k
Masashi Yano Japan 22 436 0.5× 176 0.3× 272 2.2× 26 0.3× 41 0.4× 73 1.5k
Jessica K. Booker United States 13 304 0.4× 292 0.4× 114 0.9× 14 0.1× 59 0.6× 25 850
Tatsuro Kondoh Japan 19 655 0.8× 534 0.8× 157 1.3× 91 0.9× 252 2.5× 59 1.2k
Dwight Stambolian United States 19 507 0.6× 124 0.2× 84 0.7× 49 0.5× 38 0.4× 48 1.2k

Countries citing papers authored by Marwan K. Tayeh

Since Specialization
Citations

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

Fields of papers citing papers by Marwan K. Tayeh

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Marwan K. Tayeh. 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 Marwan K. Tayeh. The network helps show where Marwan K. Tayeh may publish in the future.

Co-authorship network of co-authors of Marwan K. Tayeh

This figure shows the co-authorship network connecting the top 25 collaborators of Marwan K. Tayeh. A scholar is included among the top collaborators of Marwan K. Tayeh 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 Marwan K. Tayeh. Marwan K. Tayeh 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.
Ly, Reynold C., Marwan K. Tayeh, & Yuan Ji. (2024). Education of Future Pharmacogenomics Laboratory Directors. 7(1). 33–41. 1 indexed citations
2.
Deignan, Joshua L., Mauricio De Castro, Vanessa L. Horner, et al.. (2023). Points to consider in the practice of postmortem genetic testing: A statement of the American College of Medical Genetics and Genomics (ACMG). Genetics in Medicine. 25(5). 100017–100017. 6 indexed citations
3.
4.
Tayeh, Marwan K., Andrea Gaedigk, Matthew P. Goetz, et al.. (2022). Clinical pharmacogenomic testing and reporting: A technical standard of the American College of Medical Genetics and Genomics (ACMG). Genetics in Medicine. 24(4). 759–768. 26 indexed citations
5.
Tayeh, Marwan K., Yang Chen, Jirair K. Bedoyan, et al.. (2022). Novel multilocus imprinting disturbances in a child with expressive language delay and intellectual disability. American Journal of Medical Genetics Part A. 188(7). 2209–2216. 4 indexed citations
6.
Akıncı, Barış, André Monteiro da Rocha, Rasimcan Meral, et al.. (2021). Cardiac phenotype in familial partial lipodystrophy. Clinical Endocrinology. 94(6). 1043–1053. 14 indexed citations
7.
Akıncı, Barış, Angela Subauste, Nevin Ajluni, et al.. (2021). Metreleptin therapy for nonalcoholic steatohepatitis: Open-label therapy interventions in two different clinical settings. Med. 2(7). 814–835.e6. 19 indexed citations
8.
Deignan, Joshua L., Caroline Astbury, Saurav Guha, et al.. (2020). Addendum: Technical standards and guidelines for spinal muscular atrophy testing. Genetics in Medicine. 23(12). 2462–2462. 3 indexed citations
9.
Gaudio, Daniela del, Marwan Shinawi, Caroline Astbury, et al.. (2020). Diagnostic testing for uniparental disomy: a points to consider statement from the American College of Medical Genetics and Genomics (ACMG). Genetics in Medicine. 22(7). 1133–1141. 93 indexed citations
10.
Sahinoz, Melis, Graham F. Brady, Rasimcan Meral, et al.. (2018). Potential association of LMNA-associated generalized lipodystrophy with juvenile dermatomyositis. SHILAP Revista de lepidopterología. 4(1). 6–6. 11 indexed citations
11.
Ajluni, Nevin, Rasimcan Meral, Adam Neidert, et al.. (2017). Spectrum of disease associated with partial lipodystrophy: lessons from a trial cohort. Clinical Endocrinology. 86(5). 698–707. 73 indexed citations
12.
Stratton, Robert F., et al.. (2012). Metastatic medulloblastoma in an adolescent with Simpson–Golabi–Behmel syndrome. American Journal of Medical Genetics Part A. 158A(10). 2534–2536. 18 indexed citations
13.
Ahram, Dina, T. Shawn Sato, Marwan K. Tayeh, et al.. (2009). A Homozygous Mutation in ADAMTSL4 Causes Autosomal-Recessive Isolated Ectopia Lentis. The American Journal of Human Genetics. 84(2). 274–278. 101 indexed citations
14.
Tayeh, Marwan K., Ephrem Chin, Vanessa Rangel Miller, et al.. (2009). Targeted comparative genomic hybridization array for the detection of single- and multiexon gene deletions and duplications. Genetics in Medicine. 11(4). 232–240. 32 indexed citations
15.
Tayeh, Marwan K., John S. Beck, Charles Searby, et al.. (2008). Genetic interaction between Bardet-Biedl syndrome genes and implications for limb patterning. Human Molecular Genetics. 17(13). 1956–1967. 58 indexed citations
16.
Tayeh, Marwan K., et al.. (2006). Bardet–Biedl syndrome genes are important in retrograde intracellular trafficking and Kupffer's vesicle cilia function. Human Molecular Genetics. 15(5). 667–677. 144 indexed citations
17.
Chiang, Annie, John S. Beck, Marwan K. Tayeh, et al.. (2006). Homozygosity mapping with SNP arrays identifiesTRIM32, an E3 ubiquitin ligase, as a Bardet–Biedl syndrome gene (BBS11). Proceedings of the National Academy of Sciences. 103(16). 6287–6292. 319 indexed citations
18.
Majeed, Hasan A., et al.. (2005). The Spectrum of Familial Mediterranean Fever Gene Mutations in Arabs: Report of a Large Series. Seminars in Arthritis and Rheumatism. 34(6). 813–818. 61 indexed citations
19.
Fath, Melissa A., Robert F. Mullins, Charles Searby, et al.. (2005). Mkks-null mice have a phenotype resembling Bardet–Biedl syndrome. Human Molecular Genetics. 14(9). 1109–1118. 148 indexed citations
20.
Al-Alami, Jamil, et al.. (2003). Familial Mediterranean fever mutation frequencies and carrier rates among a mixed Arabic population.. PubMed. 24(10). 1055–9. 49 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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