Uppala Radhakrishna

4.9k total citations
81 papers, 2.1k citations indexed

About

Uppala Radhakrishna is a scholar working on Molecular Biology, Genetics and Epidemiology. According to data from OpenAlex, Uppala Radhakrishna has authored 81 papers receiving a total of 2.1k indexed citations (citations by other indexed papers that have themselves been cited), including 40 papers in Molecular Biology, 26 papers in Genetics and 17 papers in Epidemiology. Recurrent topics in Uppala Radhakrishna's work include Epigenetics and DNA Methylation (11 papers), Congenital heart defects research (8 papers) and Hidradenitis Suppurativa and Treatments (8 papers). Uppala Radhakrishna is often cited by papers focused on Epigenetics and DNA Methylation (11 papers), Congenital heart defects research (8 papers) and Hidradenitis Suppurativa and Treatments (8 papers). Uppala Radhakrishna collaborates with scholars based in United States, India and Switzerland. Uppala Radhakrishna's co-authors include Stylianos E. Antonarakis, Sangeetha Vishweswaraiah, Ray Bahado‐Singh, Buket Aydas, Hamid Mehenni, Chittibabu Guda, J. V. Solanki, Nitish K. Mishra, Swapan K. Nath and Ken McElreavey and has published in prestigious journals such as Nature Genetics, PLoS ONE and Scientific Reports.

In The Last Decade

Uppala Radhakrishna

79 papers receiving 2.0k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Uppala Radhakrishna United States	25	1.0k	758	252	241	216	81	2.1k
Ursula G. Froster Germany	23	900 0.9×	886 1.2×	334 1.3×	156 0.6×	103 0.5×	79	2.0k
Shubha R. Phadke India	23	908 0.9×	826 1.1×	245 1.0×	145 0.6×	100 0.5×	268	2.4k
Rika Kosaki Japan	25	1.3k 1.2×	846 1.1×	297 1.2×	109 0.5×	75 0.3×	113	2.3k
Ruth Newbury‐Ecob United Kingdom	25	2.0k 1.9×	1.3k 1.7×	310 1.2×	285 1.2×	53 0.2×	64	3.2k
Francesca Faravelli Italy	22	869 0.8×	1.2k 1.5×	262 1.0×	102 0.4×	100 0.5×	61	2.9k
Jeffrey E. Ming United States	28	1.9k 1.8×	1.6k 2.1×	548 2.2×	163 0.7×	237 1.1×	68	5.4k
Vazken M. Der Kaloustian Canada	29	1.5k 1.4×	958 1.3×	336 1.3×	252 1.0×	103 0.5×	121	2.7k
Roberto Mendoza‐Londono Canada	26	1.0k 1.0×	1.2k 1.5×	174 0.7×	124 0.5×	78 0.4×	85	2.1k
Hülya Kayserili Türkiye	35	2.8k 2.7×	1.7k 2.3×	331 1.3×	170 0.7×	150 0.7×	152	4.4k
Beyhan Tüysüz Türkiye	24	1.4k 1.3×	988 1.3×	231 0.9×	134 0.6×	127 0.6×	139	2.5k

Countries citing papers authored by Uppala Radhakrishna

Since Specialization

Citations

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

Fields of papers citing papers by Uppala Radhakrishna

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Uppala Radhakrishna

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

Radhakrishna, Uppala, Iltefat Hamzavi, Jignesh Prajapati, et al.. (2025). Impaired Molecular Mechanisms Contributing to Chronic Pain in Patients with Hidradenitis Suppurativa: Exploring Potential Biomarkers and Therapeutic Targets. International Journal of Molecular Sciences. 26(3). 1039–1039. 1 indexed citations

Radhakrishna, Uppala, Rupa Radhakrishnan, Srinivas B. Muvvala, et al.. (2024). Prenatal opioid exposure significantly impacts placental protein kinase C (PKC) and drug transporters, leading to drug resistance and neonatal opioid withdrawal syndrome. Frontiers in Neuroscience. 18. 1442915–1442915. 2 indexed citations

Radhakrishna, Uppala, et al.. (2024). New Horizons in Cancer Progression and Metastasis: Hippo Signaling Pathway. Biomedicines. 12(11). 2552–2552. 2 indexed citations

Radhakrishna, Uppala, Senthilkumar Sadhasivam, Rupa Radhakrishnan, et al.. (2024). Placental cytochrome P450 methylomes in infants exposed to prenatal opioids: exploring the effects of neonatal opioid withdrawal syndrome on health horizons. Frontiers in Genetics. 14. 1292148–1292148. 3 indexed citations

Radhakrishna, Uppala, Swapan K. Nath, Avinash M. Veerappa, et al.. (2023). Placental microRNA methylome signatures may serve as biomarkers and therapeutic targets for prenatally opioid-exposed infants with neonatal opioid withdrawal syndrome. Frontiers in Genetics. 14. 1215472–1215472. 3 indexed citations

Vishweswaraiah, Sangeetha, Ali Yılmaz, Xiaobei Pan, et al.. (2023). Integrative Analysis Unveils the Correlation of Aminoacyl-tRNA Biosynthesis Metabolites with the Methylation of the SEPSECS Gene in Huntington’s Disease Brain Tissue. Genes. 14(9). 1752–1752. 2 indexed citations

Radhakrishna, Uppala, Devendrasinh Jhala, Maulikkumar Patel, et al.. (2023). Hidradenitis suppurativa associated telomere‐methylome dysregulations in blood. Journal of the European Academy of Dermatology and Venereology. 38(2). 393–403. 8 indexed citations

Radhakrishna, Uppala, Devendrasinh Jhala, Maulikkumar Patel, et al.. (2023). Hidradenitis suppurativa presents a methylome dysregulation capable to explain the pro‐inflammatory microenvironment: Are theseDNAmethylations potential therapeutic targets?. Journal of the European Academy of Dermatology and Venereology. 37(10). 2109–2123. 13 indexed citations

Bahado‐Singh, Ray, Sangeetha Vishweswaraiah, Onur Türkoğlu, Stewart F. Graham, & Uppala Radhakrishna. (2023). Alzheimer’s Precision Neurology: Epigenetics of Cytochrome P450 Genes in Circulating Cell-Free DNA for Disease Prediction and Mechanism. International Journal of Molecular Sciences. 24(3). 2876–2876. 15 indexed citations

10.

Vishweswaraiah, Sangeetha, et al.. (2023). Differential methylation of microRNA encoding genes may contribute to high myopia. Frontiers in Genetics. 13. 1089784–1089784. 11 indexed citations

11.

Shao, Xiaojian, Sangeetha Vishweswaraiah, Miroslava Čuperlović‐Culf, et al.. (2022). Dementia with Lewy bodies post-mortem brains reveal differentially methylated CpG sites with biomarker potential. Communications Biology. 5(1). 1279–1279. 2 indexed citations

12.

Bahado‐Singh, Ray, Sangeetha Vishweswaraiah, Buket Aydas, et al.. (2020). Precision cardiovascular medicine: artificial intelligence and epigenetics for the pathogenesis and prediction of coarctation in neonates. The Journal of Maternal-Fetal & Neonatal Medicine. 35(3). 457–464. 30 indexed citations

13.

Radhakrishna, Uppala, Swapan K. Nath, Ken McElreavey, et al.. (2012). Genome-wide linkage and copy number variation analysis reveals 710 kb duplication on chromosome 1p31.3 responsible for autosomal dominant omphalocele. Journal of Medical Genetics. 49(4). 270–276. 9 indexed citations

14.

Bashamboo, Anu, Bruno Ferraz‐de‐Souza, Diana Lourenço, et al.. (2010). Human Male Infertility Associated with Mutations in NR5A1Encoding Steroidogenic Factor 1. The American Journal of Human Genetics. 87(5). 736–736. 3 indexed citations

15.

Beiraghi, Soraya, Swapan K. Nath, David Hutchings, et al.. (2007). Autosomal Dominant Nonsyndromic Cleft Lip and Palate: Significant Evidence of Linkage at 18q21.1. The American Journal of Human Genetics. 81(1). 180–188. 16 indexed citations

16.

Nath, Swapan K., Mahmoud Taleb Al‐Ali, Najib Al‐Khaja, et al.. (2006). Genomewide Linkage Scan for Split–Hand/Foot Malformation with Long-Bone Deficiency in a Large Arab Family Identifies Two Novel Susceptibility Loci on Chromosomes 1q42.2-q43 and 6q14.1. The American Journal of Human Genetics. 80(1). 105–111. 24 indexed citations

17.

Radhakrishna, Uppala, Dorothea Bornholdt, Hamish S. Scott, et al.. (1999). The Phenotypic Spectrum of GLI3 Morphopathies Includes Autosomal Dominant Preaxial Polydactyly Type-IV and Postaxial Polydactyly Type-A/B; No Phenotype Prediction from the Position of GLI3 Mutations. The American Journal of Human Genetics. 65(3). 645–655. 127 indexed citations

18.

Patel, Rajesh, et al.. (1997). UNUSUAL SILENT BLOOD CHIMERISM IN HOLSTEIN-FRIESIAN BULL. The Indian Journal of Animal Sciences. 67(2). 152–153. 3 indexed citations

19.

Mehenni, Hamid, et al.. (1997). Peutz-Jeghers Syndrome: Confirmation of Linkage to Chromosome 19p13.3 and Identification of a Potential Second Locus, on 19q13.4. The American Journal of Human Genetics. 61(6). 1327–1334. 102 indexed citations

20.

Sheth, Frenny, et al.. (1996). Incomplete Gonadal Dysgenesis. Urologia Internationalis. 56(1). 57–60. 4 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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