Moises Serrano

588 total citations
17 papers, 410 citations indexed

About

Moises Serrano is a scholar working on Genetics, Molecular Biology and Cancer Research. According to data from OpenAlex, Moises Serrano has authored 17 papers receiving a total of 410 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Genetics, 9 papers in Molecular Biology and 5 papers in Cancer Research. Recurrent topics in Moises Serrano's work include Genomics and Rare Diseases (8 papers), Genomic variations and chromosomal abnormalities (8 papers) and DNA Repair Mechanisms (5 papers). Moises Serrano is often cited by papers focused on Genomics and Rare Diseases (8 papers), Genomic variations and chromosomal abnormalities (8 papers) and DNA Repair Mechanisms (5 papers). Moises Serrano collaborates with scholars based in United States, Canada and Italy. Moises Serrano's co-authors include Phillip R. Musich, Zhengke Li, Yue Zou, Yunfeng Zou, Marina Roginskaya, Sheila Patrick, B. Cartwright, Valerie Fako, Zizheng Dong and Xi Wu and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Biological Chemistry and SHILAP Revista de lepidopterología.

In The Last Decade

Moises Serrano

17 papers receiving 403 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Moises Serrano United States	9	289	119	108	79	28	17	410
Clayton B. Marshall United States	9	260 0.9×	156 1.3×	63 0.6×	64 0.8×	39 1.4×	10	376
Simona Dalin United States	9	311 1.1×	102 0.9×	130 1.2×	56 0.7×	33 1.2×	13	419
Ariel Cariaga-Martínez Spain	11	230 0.8×	64 0.5×	51 0.5×	57 0.7×	25 0.9×	17	355
Alicia Subtil‐Rodríguez Spain	8	374 1.3×	139 1.2×	63 0.6×	200 2.5×	39 1.4×	10	540
Jelle Verbeeck Belgium	12	346 1.2×	50 0.4×	49 0.5×	170 2.2×	34 1.2×	16	469
Kateryna Kubaichuk Finland	8	236 0.8×	76 0.6×	133 1.2×	24 0.3×	36 1.3×	14	346
William A. Scaringe United States	14	468 1.6×	66 0.6×	126 1.2×	169 2.1×	13 0.5×	22	609
Beatrix A. Olofsson United States	5	331 1.1×	62 0.5×	55 0.5×	34 0.4×	25 0.9×	7	390
Moritz Menzel Germany	7	236 0.8×	61 0.5×	28 0.3×	69 0.9×	39 1.4×	9	339
Jessica Shu Nan Li United States	4	487 1.7×	56 0.5×	36 0.3×	207 2.6×	15 0.5×	6	592

Countries citing papers authored by Moises Serrano

Since Specialization

Citations

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

Fields of papers citing papers by Moises Serrano

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Moises Serrano

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

All Works

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17 of 17 papers shown

Barseghyan, Hayk, Andy Wing Chun Pang, Ben Clifford, et al.. (2023). Comparative Benchmarking of Optical Genome Mapping and Chromosomal Microarray Reveals High Technological Concordance in CNV Identification and Additional Structural Variant Refinement. Genes. 14(10). 1868–1868. 6 indexed citations

Martin, Megan, et al.. (2023). P510: Validation of parent of origin detection for de novo events identified on SNP microarray in a postnatal population. SHILAP Revista de lepidopterología. 1(1). 100557–100557. 1 indexed citations

Davis, Kyle, Colleen G. Bilancia, Megan Martin, et al.. (2022). NeuroSCORE is a genome-wide omics-based model that identifies candidate disease genes of the central nervous system. Scientific Reports. 12(1). 5427–5427. 1 indexed citations

Vanzo, Rena, Aparna Prasad, Charles H. Hensel, et al.. (2020). The Temple Grandin Genome: Comprehensive Analysis in a Scientist with High-Functioning Autism. Journal of Personalized Medicine. 11(1). 21–21. 3 indexed citations

Costain, Gregory, Susan Walker, Bob Argiropoulos, et al.. (2019). Rare copy number variations affecting the synaptic gene DMXL2 in neurodevelopmental disorders. Journal of Neurodevelopmental Disorders. 11(1). 3–3. 6 indexed citations

Wassman, E. Robert, Karen J. Ho, Kyle Davis, et al.. (2019). Critical exon indexing improves clinical interpretation of copy number variants in neurodevelopmental disorders. Neurology Genetics. 5(6). e378–e378. 2 indexed citations

Davis, Kyle, Moises Serrano, Sara Loddo, et al.. (2019). Parent-of-Origin Effects in 15q11.2 BP1-BP2 Microdeletion (Burnside-Butler) Syndrome. International Journal of Molecular Sciences. 20(6). 1459–1459. 23 indexed citations

Prasad, Aparna, Rena Vanzo, Patricia Mowery‐Rushton, et al.. (2018). Clinical utility of exome sequencing in individuals with large homozygous regions detected by chromosomal microarray analysis. BMC Medical Genetics. 19(1). 46–46. 19 indexed citations

Hensel, Charles H., Rena Vanzo, Megan Martin, et al.. (2017). Analytical and Clinical Validity Study of FirstStepDx PLUS: A Chromosomal Microarray Optimized for Patients with Neurodevelopmental Conditions. PLoS Currents. 9. 7 indexed citations

10.

Wu, Xi, Zizheng Dong, Valerie Fako, et al.. (2016). FASN regulates cellular response to genotoxic treatments by increasing PARP-1 expression and DNA repair activity via NF-κB and SP1. Proceedings of the National Academy of Sciences. 113(45). 73 indexed citations

11.

Ho, Karen J., Rena Vanzo, Charles H. Hensel, et al.. (2016). Clinical Performance of an Ultrahigh Resolution Chromosomal Microarray Optimized for Neurodevelopmental Disorders. BioMed Research International. 2016. 1–7. 15 indexed citations

12.

Hilton, Benjamin, Zhengke Li, Phillip R. Musich, et al.. (2015). ATR Plays a Direct Antiapoptotic Role at Mitochondria, which Is Regulated by Prolyl Isomerase Pin1. Molecular Cell. 60(1). 35–46. 65 indexed citations

13.

Wang, Yan, Phillip R. Musich, Moises Serrano, et al.. (2013). Effects of DSP4 on the Noradrenergic Phenotypes and Its Potential Molecular Mechanisms in SH-SY5Y Cells. Neurotoxicity Research. 25(2). 193–207. 13 indexed citations

14.

Serrano, Moises, Zhengke Li, Phillip R. Musich, et al.. (2012). DNA-PK, ATM and ATR collaboratively regulate p53–RPA interaction to facilitate homologous recombination DNA repair. Oncogene. 32(19). 2452–2462. 90 indexed citations

15.

Wu, Xi, Moises Serrano, Yue Zou, & Jian‐Ting Zhang. (2012). Abstract 2124: Non-homologues end joining mediates fatty acid synthase(FASN)-associated resistance to DNA-damaging chemotherapeutics. Cancer Research. 72(8_Supplement). 2124–2124. 1 indexed citations

16.

Li, Zhengke, et al.. (2011). XPA-Mediated Regulation of Global Nucleotide Excision Repair by ATR Is p53-Dependent and Occurs Primarily in S-Phase. PLoS ONE. 6(12). e28326–e28326. 23 indexed citations

17.

Shell, Steven M., Zhengke Li, Nikolozi Shkriabai, et al.. (2009). Checkpoint Kinase ATR Promotes Nucleotide Excision Repair of UV-induced DNA Damage via Physical Interaction with Xeroderma Pigmentosum Group A. Journal of Biological Chemistry. 284(36). 24213–24222. 62 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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