Damir Musaev

1.9k total citations
14 papers, 499 citations indexed

About

Damir Musaev is a scholar working on Molecular Biology, Genetics and Nephrology. According to data from OpenAlex, Damir Musaev has authored 14 papers receiving a total of 499 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Molecular Biology, 5 papers in Genetics and 2 papers in Nephrology. Recurrent topics in Damir Musaev's work include Genetics and Neurodevelopmental Disorders (4 papers), RNA Research and Splicing (4 papers) and RNA modifications and cancer (3 papers). Damir Musaev is often cited by papers focused on Genetics and Neurodevelopmental Disorders (4 papers), RNA Research and Splicing (4 papers) and RNA modifications and cancer (3 papers). Damir Musaev collaborates with scholars based in United States, Egypt and Türkiye. Damir Musaev's co-authors include Rasim Özgür Rosti, Joseph G. Gleeson, Maha S. Zaki, Charles E. Vejnar, Antonio J. Giráldez, Jean-Denis Beaudoin, Joseph G. Gleeson, Rami Abou Jamra, Miguel A. Moreno-Mateos and Ariel Bazzini and has published in prestigious journals such as Genome Research, Developmental Cell and The American Journal of Human Genetics.

In The Last Decade

Damir Musaev

13 papers receiving 496 citations

Peers

Damir Musaev

GENET

PPCH

NEPHR

Avigail Dreazen Israel

Katja Höpker Germany

Ilenia Bernascone Italy

Angelo Molinaro Italy

Yael Laitman Israel

Roman Ulrich Müller Germany

Sarah E. Conduit Australia

Véronique Chauvet France

Alberto Dinarello Italy

Aurélien Trimouille France

Avigail Dreazen Israel

Damir Musaev

408 ×1.1

60 ×0.6

52 ×0.5

GENET

13 ×0.3

PPCH

28 ×0.6

NEPHR

Citations per year, relative to Damir Musaev Damir Musaev (= 1×) peers Avigail Dreazen

Countries citing papers authored by Damir Musaev

Since Specialization

Citations

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

Fields of papers citing papers by Damir Musaev

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Damir Musaev

This figure shows the co-authorship network connecting the top 25 collaborators of Damir Musaev. A scholar is included among the top collaborators of Damir Musaev 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 Damir Musaev. Damir Musaev 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

Youlten, Scott E., Caroline Hoppe, Curtis W. Boswell, et al.. (2025). In vivo differentiation of embryonic cells devoid of key reprogramming factors. Cell Reports. 44(11). 116498–116498.

Musaev, Damir, Charles E. Vejnar, Valeria Yartseva, et al.. (2024). UPF1 regulates mRNA stability by sensing poorly translated coding sequences. Cell Reports. 43(4). 114074–114074. 6 indexed citations

Vejnar, Charles E., Carter M. Takacs, Valeria Yartseva, et al.. (2019). Genome wide analysis of 3′ UTR sequence elements and proteins regulating mRNA stability during maternal-to-zygotic transition in zebrafish. Genome Research. 29(7). 1100–1114. 48 indexed citations

Shaheen, Ranad, Nan Jiang, Fatema Alzahrani, et al.. (2019). Bi-allelic Mutations in FAM149B1 Cause Abnormal Primary Cilium and a Range of Ciliopathy Phenotypes in Humans. The American Journal of Human Genetics. 104(4). 731–737. 21 indexed citations

Tang, Yin, Charles E. Vejnar, Jean-Denis Beaudoin, et al.. (2019). Brd4 and P300 Confer Transcriptional Competency during Zygotic Genome Activation. Developmental Cell. 49(6). 867–881.e8. 93 indexed citations

Breuss, Martin W., An Nguyen, Qiong Song, et al.. (2018). Mutations in LNPK, Encoding the Endoplasmic Reticulum Junction Stabilizer Lunapark, Cause a Recessive Neurodevelopmental Syndrome. The American Journal of Human Genetics. 103(2). 296–304. 22 indexed citations

Marin‐Valencia, Isaac, Gaia Novarino, Anide Johansen, et al.. (2017). A homozygous founder mutation in TRAPPC6B associates with a neurodevelopmental disorder characterised by microcephaly, epilepsy and autistic features. Journal of Medical Genetics. 55(1). 48–54. 35 indexed citations

Rosti, Rasim Özgür, Bethany N. Sotak, Stephanie Bielas, et al.. (2017). Homozygous mutation in NUP107 leads to microcephaly with steroid-resistant nephrotic condition similar to Galloway-Mowat syndrome. Journal of Medical Genetics. 54(6). 399–403. 56 indexed citations

Marin‐Valencia, Isaac, Andreas Gerondopoulos, Maha S. Zaki, et al.. (2017). Homozygous Mutations in TBC1D23 Lead to a Non-degenerative Form of Pontocerebellar Hypoplasia. The American Journal of Human Genetics. 101(3). 441–450. 43 indexed citations

10.

Rosti, Rasim Özgür, Esra Dikoglu, Maha S. Zaki, et al.. (2016). Extending the mutation spectrum for Galloway–Mowat syndrome to include homozygous missense mutations in the WDR73 gene. American Journal of Medical Genetics Part A. 170(4). 992–998. 26 indexed citations

11.

Jerber, Julie, Maha S. Zaki, Jumana Y. Al‐Aama, et al.. (2016). Biallelic Mutations in TMTC3, Encoding a Transmembrane and TPR-Containing Protein, Lead to Cobblestone Lissencephaly. The American Journal of Human Genetics. 99(5). 1181–1189. 33 indexed citations

12.

Breuss, Martin W., Thai B. Nguyen, Anjana Srivatsan, et al.. (2016). Uner Tan syndrome caused by a homozygousTUBB2Bmutation affecting microtubule stability. Human Molecular Genetics. 26(2). ddw383–ddw383. 11 indexed citations

13.

Breuss, Martin W., Tipu Sultan, Kiely N. James, et al.. (2016). Autosomal-Recessive Mutations in the tRNA Splicing Endonuclease Subunit TSEN15 Cause Pontocerebellar Hypoplasia and Progressive Microcephaly. The American Journal of Human Genetics. 99(1). 228–235. 44 indexed citations

14.

Johansen, Anide, Rasim Özgür Rosti, Damir Musaev, et al.. (2016). Mutations in MBOAT7 , Encoding Lysophosphatidylinositol Acyltransferase I, Lead to Intellectual Disability Accompanied by Epilepsy and Autistic Features. The American Journal of Human Genetics. 99(4). 912–916. 61 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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