Nuo Si

873 total citations
37 papers, 505 citations indexed

About

Nuo Si is a scholar working on Molecular Biology, Genetics and Surgery. According to data from OpenAlex, Nuo Si has authored 37 papers receiving a total of 505 indexed citations (citations by other indexed papers that have themselves been cited), including 18 papers in Molecular Biology, 14 papers in Genetics and 12 papers in Surgery. Recurrent topics in Nuo Si's work include Congenital Ear and Nasal Anomalies (7 papers), Reconstructive Facial Surgery Techniques (5 papers) and Congenital heart defects research (4 papers). Nuo Si is often cited by papers focused on Congenital Ear and Nasal Anomalies (7 papers), Reconstructive Facial Surgery Techniques (5 papers) and Congenital heart defects research (4 papers). Nuo Si collaborates with scholars based in China, Israel and United States. Nuo Si's co-authors include Raphaela Goldbach‐Mansky, Sofia Babay, Ángel Vera, Antonio Torrelo, Abraham Zlotogorski, Yuval Ramot, Xue Zhang, Chyi‐Chia Richard Lee, Peter W. Kim and Afzal Sheikh and has published in prestigious journals such as Gene, Clinica Chimica Acta and Journal of Translational Medicine.

In The Last Decade

Nuo Si

34 papers receiving 500 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Nuo Si China	12	288	160	85	64	60	37	505
Sofia Babay Israel	8	255 0.9×	183 1.1×	73 0.9×	61 1.0×	80 1.3×	8	449
Ritsuko Seki Japan	15	266 0.9×	104 0.7×	116 1.4×	33 0.5×	58 1.0×	48	647
Nathan A. Lemp United States	12	245 0.9×	83 0.5×	71 0.8×	39 0.6×	101 1.7×	18	568
Erika Zilahi Hungary	13	184 0.6×	130 0.8×	54 0.6×	29 0.5×	113 1.9×	19	539
Melissa Kahn United States	7	407 1.4×	284 1.8×	26 0.3×	65 1.0×	47 0.8×	9	837
Guillaume Sarrabay France	13	353 1.2×	253 1.6×	109 1.3×	69 1.1×	125 2.1×	32	558
Yanna Ding United States	6	166 0.6×	209 1.3×	63 0.7×	55 0.9×	58 1.0×	13	433
Xingwen Dong United States	9	266 0.9×	224 1.4×	69 0.8×	30 0.5×	72 1.2×	15	528
Sreeja Parameswaran United States	11	149 0.5×	142 0.9×	41 0.5×	97 1.5×	109 1.8×	29	397
Priscilla Wong China	16	492 1.7×	201 1.3×	77 0.9×	68 1.1×	300 5.0×	32	893

Countries citing papers authored by Nuo Si

Since Specialization

Citations

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

Fields of papers citing papers by Nuo Si

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Nuo Si

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

All Works

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20 of 20 papers shown

Zhou, Jian, et al.. (2025). A Novel TP63 Missense Mutation in the Sumoylation Motif Causes Isolated Split‐Hand/Foot Malformation 4: A Pedigree Report and Literature Review. Molecular Genetics & Genomic Medicine. 13(9). e70140–e70140.

Xu, Lubin, Xueqing Tang, Nuo Si, et al.. (2023). Genetic and clinical characterization of familial renal glucosuria. Clinical Kidney Journal. 17(2). sfad265–sfad265. 3 indexed citations

Zhu, Caiyun, Yang Yang, Bo Pan, et al.. (2023). Genetic Screening of Targeted Region on the Chromosome 22q11.2 in Patients with Microtia and Congenital Heart Defect. Genes. 14(4). 879–879. 2 indexed citations

Li, Na, Xiaolin Dong, Ke Shi, et al.. (2023). Model development and validation of noninvasive parameters based on coronary computed tomography angiography to predict culprit lesions in acute coronary syndromes within 3 years: value of plaque characteristics, hemodynamics and pericoronary adipose tissue. Quantitative Imaging in Medicine and Surgery. 13(7). 4325–4338. 5 indexed citations

Dong, Xiaolin, Na Li, Ke Shi, et al.. (2023). Identification of patients with acute coronary syndrome and representation of their degree of inflammation: application of pericoronary adipose tissue within different radial distances of the proximal coronary arteries. Quantitative Imaging in Medicine and Surgery. 13(6). 3644–3659. 5 indexed citations

Pan, Bo, et al.. (2022). Functional Pathway and Process Enrichment Analysis of Genes Associated With Morphological Abnormalities of the Outer Ear. Journal of Craniofacial Surgery. 34(2). 489–493. 2 indexed citations

Li, Xinru, et al.. (2021). Clinical and genetic findings in patients with congenital cataract and heart diseases. Orphanet Journal of Rare Diseases. 16(1). 242–242. 6 indexed citations

Si, Nuo, et al.. (2021). Generation of an induced pluripotent stem cell line from a congenital microtia patient with 4p16.1 microduplication involving the long-range enhancer of HMX1. Stem Cell Research. 53. 102357–102357. 6 indexed citations

Si, Nuo, et al.. (2021). Slc20a2-Deficient Mice Exhibit Multisystem Abnormalities and Impaired Spatial Learning Memory and Sensorimotor Gating but Normal Motor Coordination Abilities. Frontiers in Genetics. 12. 639935–639935. 11 indexed citations

10.

Wen, Yubing, et al.. (2021). FSGS in Chinese twins with a de novo PAX2 mutation: a case report and review of the literature. Journal of Nephrology. 34(6). 2155–2158. 6 indexed citations

11.

Si, Nuo, et al.. (2020). Identification of loss-of-function HOXA2 mutations in Chinese families with dominant bilateral microtia. Gene. 757. 144945–144945. 15 indexed citations

12.

Si, Nuo, Xiaosheng Lu, Zhe Liu, et al.. (2020). Duplications involving the long range HMX1 enhancer are associated with human isolated bilateral concha-type microtia. Journal of Translational Medicine. 18(1). 244–244. 14 indexed citations

13.

Si, Nuo, et al.. (2019). A 105 kb interstitial insertion in the Xq27.1 palindrome from pseudoautosomal region PAR1 causes a novel X-linked recessive compound phenotype. Journal of Translational Medicine. 17(1). 138–138. 2 indexed citations

14.

Si, Nuo, et al.. (2019). A novel MAF missense mutation leads to congenital nuclear cataract by impacting the transactivation of crystallin and noncrystallin genes. Gene. 692. 113–118. 12 indexed citations

15.

Si, Nuo, et al.. (2018). A novel mutation in the CRYAA gene associated with congenital cataract and microphthalmia in a Chinese family. BMC Medical Genetics. 19(1). 190–190. 16 indexed citations

16.

Si, Nuo, et al.. (2018). 17p13.3 genomic rearrangement in a Chinese family with split-hand/foot malformation with long bone deficiency: report of a complicated duplication with marked variation in phenotype. Orphanet Journal of Rare Diseases. 13(1). 106–106. 8 indexed citations

17.

Si, Nuo, et al.. (2017). Genetic Testing of the mucin 1 gene-Variable Number Tandem Repeat Single Cytosine Insertion Mutation in a Chinese Family with Medullary Cystic Kidney Disease. Chinese Medical Journal. 130(20). 2459–2464. 1 indexed citations

18.

Zhang, Qian, Nuo Si, Yaping Liu, et al.. (2017). Steroid sulfatase and filaggrin mutations in a boy with severe ichthyosis, elevated serum IgE level and moyamoya syndrome. Gene. 628. 103–108. 2 indexed citations

19.

Zhao, Zhen, Yaping Liu, Wei Yang, et al.. (2013). Novel <b><i>TRPM6</i></b> Mutations in Familial Hypomagnesemia with Secondary Hypocalcemia. American Journal of Nephrology. 37(6). 541–548. 23 indexed citations

20.

Liu, Yin, Yuval Ramot, Antonio Torrelo, et al.. (2011). Mutations in proteasome subunit β type 8 cause chronic atypical neutrophilic dermatosis with lipodystrophy and elevated temperature with evidence of genetic and phenotypic heterogeneity. Arthritis & Rheumatism. 64(3). 895–907. 266 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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