Nitin Udar

2.8k total citations
58 papers, 1.8k citations indexed

About

Nitin Udar is a scholar working on Molecular Biology, Ophthalmology and Radiology, Nuclear Medicine and Imaging. According to data from OpenAlex, Nitin Udar has authored 58 papers receiving a total of 1.8k indexed citations (citations by other indexed papers that have themselves been cited), including 39 papers in Molecular Biology, 22 papers in Ophthalmology and 14 papers in Radiology, Nuclear Medicine and Imaging. Recurrent topics in Nitin Udar's work include Retinal Diseases and Treatments (17 papers), Retinal Development and Disorders (15 papers) and DNA Repair Mechanisms (8 papers). Nitin Udar is often cited by papers focused on Retinal Diseases and Treatments (17 papers), Retinal Development and Disorders (15 papers) and DNA Repair Mechanisms (8 papers). Nitin Udar collaborates with scholars based in United States, France and Belgium. Nitin Udar's co-authors include M. Cristina Kenney, Shari R. Atilano, Kent W. Small, Anthony B. Nesburn, Marilyn Chwa, David S. Boyer, Douglas C. Wallace, Richard A. Gatti, Michael V. Miceli and S. Michal Jazwinski and has published in prestigious journals such as Journal of Clinical Oncology, Bioinformatics and PLoS ONE.

In The Last Decade

Nitin Udar

56 papers receiving 1.7k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Nitin Udar United States 25 1.1k 526 458 261 235 58 1.8k
Marta Cortón Spain 28 1.6k 1.4× 615 1.2× 205 0.4× 73 0.3× 494 2.1× 92 2.3k
Mais Hashem Saudi Arabia 23 1.1k 0.9× 192 0.4× 156 0.3× 107 0.4× 544 2.3× 51 1.8k
Samuel Shao-Min Zhang United States 15 690 0.6× 661 1.3× 393 0.9× 93 0.4× 133 0.6× 22 1.3k
Mary Kay Francis United States 16 636 0.6× 172 0.3× 115 0.3× 75 0.3× 179 0.8× 18 1.1k
Judit Baffi United States 17 731 0.6× 958 1.8× 435 0.9× 80 0.3× 64 0.3× 24 1.5k
Tarja Lamminen Finland 19 821 0.7× 183 0.3× 38 0.1× 105 0.4× 184 0.8× 35 1.3k
Nobuhiro Ibaraki Japan 15 512 0.5× 481 0.9× 269 0.6× 36 0.1× 68 0.3× 32 1.1k
Shivakumar Vasanth United States 17 611 0.5× 196 0.4× 354 0.8× 40 0.2× 486 2.1× 28 1.1k
William Samuel United States 15 573 0.5× 312 0.6× 126 0.3× 276 1.1× 37 0.2× 27 912
Kylee L. Spencer United States 14 1.0k 0.9× 2.3k 4.4× 1.4k 3.1× 49 0.2× 256 1.1× 17 2.9k

Countries citing papers authored by Nitin Udar

Since Specialization
Citations

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

Fields of papers citing papers by Nitin Udar

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Nitin Udar

This figure shows the co-authorship network connecting the top 25 collaborators of Nitin Udar. A scholar is included among the top collaborators of Nitin Udar 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 Nitin Udar. Nitin Udar 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.
Atilano, Shari R., et al.. (2021). Low frequency mitochondrial DNA heteroplasmy SNPs in blood, retina, and [RPE+choroid] of age-related macular degeneration subjects. PLoS ONE. 16(1). e0246114–e0246114. 8 indexed citations
2.
Atilano, Shari R., Steven Chang, Marilyn Chwa, et al.. (2020). Differential effects of cisplatin on cybrid cells with varying mitochondrial DNA haplogroups. PeerJ. 8. e9908–e9908. 7 indexed citations
3.
4.
Chwa, Marilyn, et al.. (2019). Corneal oxidative damage in keratoconus cells due to decreased oxidant elimination from modified expression levels of SOD enzymes, PRDX6, SCARA3, CPSF3, and FOXM1. Journal of Ophthalmic and Vision Research. 14(1). 62–62. 35 indexed citations
5.
Emig-Agius, Dorothea, Yu Jiang, Anita K. Iyer, et al.. (2018). Pisces: an accurate and versatile variant caller for somatic and germline next-generation sequencing data. Bioinformatics. 35(9). 1579–1581. 47 indexed citations
6.
Atilano, Shari R., Deepika Malik, Marilyn Chwa, et al.. (2015). Mitochondrial DNA variants can mediate methylation status of inflammation, angiogenesis and signaling genes. Human Molecular Genetics. 24(16). 4491–4503. 49 indexed citations
7.
Malik, Deepika, Payam Falatoonzadeh, Javier Cáceres‐del‐Carpio, et al.. (2014). Human Retinal Transmitochondrial Cybrids with J or H mtDNA Haplogroups Respond Differently to Ultraviolet Radiation: Implications for Retinal Diseases. PLoS ONE. 9(6). e99003–e99003. 28 indexed citations
8.
Kenney, M. Cristina, Marilyn Chwa, Shari R. Atilano, et al.. (2013). Mitochondrial DNA Variants Mediate Energy Production and Expression Levels for CFH, C3 and EFEMP1 Genes: Implications for Age-Related Macular Degeneration. PLoS ONE. 8(1). e54339–e54339. 84 indexed citations
9.
Atilano, Shari R., Marilyn Chwa, Daewon Kim, et al.. (2009). Hydrogen Peroxide Causes Mitochondrial DNA Damage in Corneal Epithelial Cells. Cornea. 28(4). 426–433. 18 indexed citations
10.
Aldave, Anthony J., et al.. (2005). Candidate Gene Screening for Posterior Polymorphous Dystrophy. Cornea. 24(2). 151–155. 30 indexed citations
11.
Aldave, Anthony J., Vivek S. Yellore, Mario A. Meallet, et al.. (2004). Lattice corneal dystrophy associated with the Ala546Asp and Pro551Gln missense changes in the TGFBI gene. American Journal of Ophthalmology. 138(5). 772–781. 33 indexed citations
12.
Udar, Nitin, et al.. (2003). Hereditary motor and sensory neuropathy type VI with optic atrophy. American Journal of Ophthalmology. 136(4). 670–677.
13.
Gatti, Richard A., Sara Becker-Catania, Helen H. Chun, et al.. (2001). The Pathogenesis of Ataxia-Telangiectasia. Clinical Reviews in Allergy & Immunology. 20(1). 87–108. 84 indexed citations
14.
Baere, Elfride De, Yoshimitsu Fukushima, Kent W. Small, et al.. (2000). Identification of BPESC1, a Novel Gene Disrupted by a Balanced Chromosomal Translocation, t(3;4)(q23;p15.2), in a Patient with BPES. Genomics. 68(3). 296–304. 19 indexed citations
15.
Udar, Nitin, Shunbin Xu, J.-O. Bay, et al.. (1999). Physical Map of the Region Surrounding the Ataxia-Telangiectasia Gene on Human Chromosome 11q22-23. Neuropediatrics. 30(4). 176–180. 4 indexed citations
16.
Telatar, Milhan, Sharon N. Teraoka, Zhijun Wang, et al.. (1998). Ataxia-Telangiectasia: Identification and Detection of Founder-Effect Mutations in the ATM Gene in Ethnic Populations. The American Journal of Human Genetics. 62(1). 86–97. 121 indexed citations
17.
Rabb, Maurice F., et al.. (1998). A North Carolina macular dystrophy phenotype in a Belizean family maps to the MCDR1 locus. American Journal of Ophthalmology. 125(4). 502–508. 24 indexed citations
18.
McCurdy, Deborah, Jenny Nguyen, Huanming Yang, et al.. (1998). MAGE Xp-2: A Member of the MAGE Gene Family Isolated from an Expression Library Using Systemic Lupus Erythematosus Sera. Molecular Genetics and Metabolism. 63(1). 3–13. 16 indexed citations
19.
Larson, Garrett P., Guoqiang Zhang, Shibin Ding, et al.. (1997). An Allelic Variant at the ATM Locus Is Implicated in Breast Cancer Susceptibility. Genetic Testing. 1(3). 165–170. 37 indexed citations
20.
Yang, Lan, Nitin Udar, Teresa Liang, et al.. (1997). CAND3: A ubiquitously expressed gene immediately adjacent and in opposite transcriptional orientation to the ATM gene at 1lq23.1. Mammalian Genome. 8(2). 129–133. 15 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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