Al‐Walid Mohsen

2.6k total citations
67 papers, 1.9k citations indexed

About

Al‐Walid Mohsen is a scholar working on Molecular Biology, Clinical Biochemistry and Physiology. According to data from OpenAlex, Al‐Walid Mohsen has authored 67 papers receiving a total of 1.9k indexed citations (citations by other indexed papers that have themselves been cited), including 51 papers in Molecular Biology, 48 papers in Clinical Biochemistry and 12 papers in Physiology. Recurrent topics in Al‐Walid Mohsen's work include Metabolism and Genetic Disorders (48 papers), Mitochondrial Function and Pathology (16 papers) and Biochemical and Molecular Research (16 papers). Al‐Walid Mohsen is often cited by papers focused on Metabolism and Genetic Disorders (48 papers), Mitochondrial Function and Pathology (16 papers) and Biochemical and Molecular Research (16 papers). Al‐Walid Mohsen collaborates with scholars based in United States, Brazil and Denmark. Al‐Walid Mohsen's co-authors include Jerry Vockley, Eric S. Goetzman, Richard T. Lovell, Yu Wang, Miao He, Jung‐Ja P. Kim, Zuzana Swigoňová, Stephanie J. Mihalik, Anuradha Karunanidhi and Regina Ensenauer and has published in prestigious journals such as Journal of Biological Chemistry, Blood and Biochemistry.

In The Last Decade

Al‐Walid Mohsen

65 papers receiving 1.9k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Al‐Walid Mohsen United States 24 1.3k 831 361 152 146 67 1.9k
Mary C. Hunt Sweden 26 1.6k 1.2× 397 0.5× 398 1.1× 187 1.2× 219 1.5× 37 2.2k
Flavia Fontanesi United States 30 2.3k 1.7× 473 0.6× 184 0.5× 198 1.3× 125 0.9× 56 2.8k
Susana Alemany Spain 29 1.6k 1.2× 183 0.2× 261 0.7× 263 1.7× 241 1.7× 66 2.7k
Thomas E. Roche United States 30 1.9k 1.4× 1.2k 1.5× 400 1.1× 360 2.4× 222 1.5× 56 3.3k
Zigmund Luka United States 25 1.6k 1.2× 263 0.3× 151 0.4× 305 2.0× 410 2.8× 50 2.3k
Lei O. Li United States 20 1.4k 1.1× 182 0.2× 605 1.7× 377 2.5× 370 2.5× 23 2.3k
Eri Kubo Japan 30 1.7k 1.3× 353 0.4× 287 0.8× 147 1.0× 152 1.0× 111 2.6k
Katrin Merker Germany 13 1.2k 0.9× 194 0.2× 534 1.5× 68 0.4× 342 2.3× 14 1.9k
Françoise Bontemps Belgium 24 1.1k 0.9× 145 0.2× 266 0.7× 83 0.5× 215 1.5× 71 2.0k
Taku Amo Japan 17 749 0.6× 125 0.2× 216 0.6× 56 0.4× 165 1.1× 31 1.2k

Countries citing papers authored by Al‐Walid Mohsen

Since Specialization
Citations

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

Fields of papers citing papers by Al‐Walid Mohsen

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Al‐Walid Mohsen

This figure shows the co-authorship network connecting the top 25 collaborators of Al‐Walid Mohsen. A scholar is included among the top collaborators of Al‐Walid Mohsen 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 Al‐Walid Mohsen. Al‐Walid Mohsen 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.
Wang, Meicheng, Yu Wang, Al‐Walid Mohsen, et al.. (2024). Mitochondrial bioenergetics and cardiolipin remodeling abnormalities in mitochondrial trifunctional protein deficiency. JCI Insight. 9(17). 5 indexed citations
2.
Karunanidhi, Anuradha, et al.. (2024). A multiomics approach reveals evidence for phenylbutyrate as a potential treatment for combined D,L-2- hydroxyglutaric aciduria. Molecular Genetics and Metabolism. 142(3). 108495–108495. 3 indexed citations
3.
Zhao, Xuejun, Al‐Walid Mohsen, Stephanie J. Mihalik, et al.. (2023). Messenger RNA rescues medium-chain acyl-CoA dehydrogenase deficiency in fibroblasts from patients and a murine model. Human Molecular Genetics. 32(14). 2347–2356. 6 indexed citations
4.
Mohsen, Al‐Walid, Anuradha Karunanidhi, Claudette M. St. Croix, et al.. (2022). Mitochondrial dysfunction associated with TANGO2 deficiency. Scientific Reports. 12(1). 3045–3045. 26 indexed citations
5.
Roma, Alessia, Nawaz Ahmed, Richard Smith, et al.. (2021). Very long chain fatty acid metabolism is required in acute myeloid leukemia. Blood. 137(25). 3518–3532. 66 indexed citations
6.
Xia, Chuanwu, Zhuji Fu, Al‐Walid Mohsen, et al.. (2021). Molecular mechanism of interactions between ACAD9 and binding partners in mitochondrial respiratory complex I assembly. iScience. 24(10). 103153–103153. 18 indexed citations
7.
Alodaib, Ahmad, et al.. (2021). Characterization of variants of uncertain significance in isovaleryl-CoA dehydrogenase identified through newborn screening: An approach for faster analysis. Molecular Genetics and Metabolism. 134(1-2). 29–36. 6 indexed citations
8.
Mohsen, Al‐Walid, et al.. (2021). C-Reactive Protein for Prediction or Early Detection of Pre-Eclampsia: A Systematic Review. Gynecologic and Obstetric Investigation. 86(1-2). 13–26. 19 indexed citations
9.
Spruce, Lynn A., et al.. (2021). Mitochondrial morphology, bioenergetics and proteomic responses in fatty acid oxidation disorders. Redox Biology. 41. 101923–101923. 8 indexed citations
10.
Wang, Wei, Al‐Walid Mohsen, Guy Uechi, et al.. (2014). Complex changes in the liver mitochondrial proteome of short chain acyl-CoA dehydrogenase deficient mice. Molecular Genetics and Metabolism. 112(1). 30–39. 12 indexed citations
11.
Luis, Paula B., Jos P.N. Ruiter, Lodewijk IJlst, et al.. (2011). Role of Isovaleryl-CoA Dehydrogenase and Short Branched-Chain Acyl-CoA Dehydrogenase in the Metabolism of Valproic Acid: Implications for the Branched-Chain Amino Acid Oxidation Pathway. Drug Metabolism and Disposition. 39(7). 1155–1160. 20 indexed citations
12.
Mohsen, Al‐Walid, Sara Copeland, Jay W. Ellison, et al.. (2010). Characterization of new ACADSB gene sequence mutations and clinical implications in patients with 2-methylbutyrylglycinuria identified by newborn screening. Molecular Genetics and Metabolism. 100(4). 333–338. 28 indexed citations
13.
Wang, Yu, Al‐Walid Mohsen, Stephanie J. Mihalik, Eric S. Goetzman, & Jerry Vockley. (2010). Evidence for Physical Association of Mitochondrial Fatty Acid Oxidation and Oxidative Phosphorylation Complexes. Journal of Biological Chemistry. 285(39). 29834–29841. 133 indexed citations
14.
Goetzman, Eric S., et al.. (2007). Expression and characterization of mutations in human very long-chain acyl-CoA dehydrogenase using a prokaryotic system. Molecular Genetics and Metabolism. 91(2). 138–147. 34 indexed citations
15.
Ensenauer, Regina, Miao He, Eric S. Goetzman, et al.. (2005). Human Acyl-CoA Dehydrogenase-9 Plays a Novel Role in the Mitochondrial β-Oxidation of Unsaturated Fatty Acids. Journal of Biological Chemistry. 280(37). 32309–32316. 78 indexed citations
16.
Mohsen, Al‐Walid, et al.. (2004). Thermal unfolding of medium-chain acyl-CoA dehydrogenase and iso(3)valeryl-CoA dehydrogenase: study of the effect of genetic defects on enzyme stability. Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 1690(1). 22–32. 15 indexed citations
17.
Tiến, Nguyễn Văn, Brage Storstein Andresen, Thomas J. Corydon, et al.. (2002). Identification of isobutyryl-CoA dehydrogenase and its deficiency in humans. Molecular Genetics and Metabolism. 77(1-2). 68–79. 51 indexed citations
18.
Reinard, Thomas, et al.. (2001). Cloning of genomic and cDNA for mouse isovaleryl-CoA dehydrogenase (IVD) and evolutionary comparison to other known IVDs. Gene. 270(1-2). 253–257. 3 indexed citations
19.
Vockley, Jerry, et al.. (2000). Mammalian Branched-Chain Acyl-CoA Dehydrogenases: Molecular Cloning and Characterization of Recombinant Enzymes. Methods in enzymology on CD-ROM/Methods in enzymology. 324. 241–258. 34 indexed citations
20.
Mohsen, Al‐Walid & Jerry Vockley. (1995). Identification of the Active Site Catalytic Residue in Human Isovaleryl-CoA Dehydrogenase. Biochemistry. 34(32). 10146–10152. 37 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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