Usha Kini

8.4k total citations
99 papers, 1.5k citations indexed

About

Usha Kini is a scholar working on Genetics, Surgery and Molecular Biology. According to data from OpenAlex, Usha Kini has authored 99 papers receiving a total of 1.5k indexed citations (citations by other indexed papers that have themselves been cited), including 28 papers in Genetics, 26 papers in Surgery and 21 papers in Molecular Biology. Recurrent topics in Usha Kini's work include Genomic variations and chromosomal abnormalities (10 papers), Pharmacological Effects and Toxicity Studies (8 papers) and Genetics and Neurodevelopmental Disorders (8 papers). Usha Kini is often cited by papers focused on Genomic variations and chromosomal abnormalities (10 papers), Pharmacological Effects and Toxicity Studies (8 papers) and Genetics and Neurodevelopmental Disorders (8 papers). Usha Kini collaborates with scholars based in India, United Kingdom and United States. Usha Kini's co-authors include Gus A. Baker, Naghme Adab, Jill Clayton‐Smith, Helen Coyle, Jon A. Gregg, Jenny C. Taylor, Alistair T. Pagnamenta, George Mawer, Rebecca Bromley and Samantha J.L. Knight and has published in prestigious journals such as SHILAP Revista de lepidopterología, Neurology and Human Molecular Genetics.

In The Last Decade

Usha Kini

93 papers receiving 1.5k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Usha Kini India 21 485 472 382 373 295 99 1.5k
G. Léna France 25 325 0.7× 356 0.8× 211 0.6× 284 0.8× 182 0.6× 73 1.9k
Ingeborg Barišić Croatia 25 488 1.0× 851 1.8× 525 1.4× 328 0.9× 163 0.6× 90 2.2k
Daniela Zuccarello Italy 22 718 1.5× 290 0.6× 647 1.7× 503 1.3× 115 0.4× 61 1.9k
I Pascual-Castroviejo Spain 25 448 0.9× 377 0.8× 495 1.3× 124 0.3× 270 0.9× 170 2.1k
Stephen R. Braddock United States 25 525 1.1× 296 0.6× 538 1.4× 302 0.8× 41 0.1× 71 1.7k
Matthias Kieslich Germany 20 334 0.7× 288 0.6× 97 0.3× 109 0.3× 235 0.8× 95 1.4k
Salvatore Savasta Italy 23 542 1.1× 182 0.4× 366 1.0× 62 0.2× 265 0.9× 120 1.6k
Ryutaro Kira Japan 21 274 0.6× 284 0.6× 226 0.6× 65 0.2× 391 1.3× 97 1.5k
Maria Paola Bonasoni Italy 18 319 0.7× 607 1.3× 340 0.9× 622 1.7× 78 0.3× 109 1.7k
Maria Piccione Italy 21 408 0.8× 192 0.4× 384 1.0× 80 0.2× 82 0.3× 78 1.0k

Countries citing papers authored by Usha Kini

Since Specialization
Citations

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

Fields of papers citing papers by Usha Kini

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Usha Kini

This figure shows the co-authorship network connecting the top 25 collaborators of Usha Kini. A scholar is included among the top collaborators of Usha Kini 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 Usha Kini. Usha Kini 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.
Hanington, Lucy, Andrew Parrish, John Taylor, et al.. (2025). Impact of rapid genomic testing on clinical outcomes of acutely unwell children presenting with severe epilepsy. European Journal of Human Genetics. 33(10). 1324–1332.
2.
Bértoli, Marta, Tania Attié‐Bitach, Antonio Rausell, et al.. (2024). The phenotype of MEGF8-related Carpenter syndrome (CRPT2) is refined through the identification of eight new patients. European Journal of Human Genetics. 32(7). 864–870.
3.
Kini, Usha. (2023). Genetics and orofacial clefts: a clinical perspective. BDJ. 234(12). 947–952. 8 indexed citations
4.
Park, Yohan, Saskia B. Wortmann, Adam C. Gunning, et al.. (2021). Functional interpretation of ATAD3A variants in neuro-mitochondrial phenotypes. Genome Medicine. 13(1). 55–55. 20 indexed citations
5.
Douzgou, Sofia, Hui Liang, Kay Metcalfe, et al.. (2019). The clinical presentation caused by truncating CHD8 variants. Clinical Genetics. 96(1). 72–84. 26 indexed citations
6.
Kumar, E. V. K. Suresh, et al.. (2016). PLASMID PROFILE AND CURING, BIOFILM DETECTION AMONG ESBL PRODUCING ISOLATES OF ACINETOBACTER SPECIES. International Journal of Pharmacy and Pharmaceutical Sciences. 8(4). 39–42. 2 indexed citations
7.
Haas, Matilda, Linh Ngo, Shanshan Li, et al.. (2016). De Novo Mutations in DENR Disrupt Neuronal Development and Link Congenital Neurological Disorders to Faulty mRNA Translation Re-initiation. Cell Reports. 15(10). 2251–2265. 26 indexed citations
8.
Kini, Usha, et al.. (2014). SEROPREVALENCE OF SCRUB TYPHUS AMONG FEBRILE PATIENTS – A PRELIMINARY STUDY. Asian Journal of Pharmaceutical and Clinical Research. 7(6). 19–21. 13 indexed citations
9.
Rajasimha, Harsha, Preveen Ramamoorthy, Madhuri Hegde, et al.. (2014). Organization for rare diseases India (ORDI) – addressing the challenges and opportunities for the Indian rare diseases' community. Genetics Research. 96. e009–e009. 29 indexed citations
10.
Aggarwal, Rajiv, et al.. (2011). Primary pulmonary hemosiderosis-a rare cuase of Microcytic hypochromic anemia. Current Pediatric Research. 15(1). 0. 1 indexed citations
11.
Pagnamenta, Alistair T., Stefano Lise, Victoria Harrison, et al.. (2011). Exome sequencing can detect pathogenic mosaic mutations present at low allele frequencies. Journal of Human Genetics. 57(1). 70–72. 46 indexed citations
12.
Joss, Shelagh, Usha Kini, Richard Fisher, et al.. (2011). The face of Ulnar Mammary syndrome?. European Journal of Medical Genetics. 54(3). 301–305. 12 indexed citations
13.
Kini, Usha, et al.. (2010). Sporadic synchronous ganglioneuromas in a child—case report and review. Journal of Pediatric Surgery. 45(4). 822–825. 5 indexed citations
14.
Blair, Edward, et al.. (2009). Ulnar mammary syndrome and TBX3: Expanding the phenotype. American Journal of Medical Genetics Part A. 149A(12). 2809–2812. 48 indexed citations
15.
Mawer, G. E., Michelle Briggs, Gus A. Baker, et al.. (2009). Pregnancy with epilepsy: Obstetric and neonatal outcome of a controlled study. Seizure. 19(2). 112–119. 87 indexed citations
16.
Bromley, Rebecca, et al.. (2008). The behavioral consequences of exposure to antiepileptic drugs in utero. Epilepsy & Behavior. 14(1). 197–201. 58 indexed citations
17.
Kini, Usha, et al.. (2006). Role of FNA in the medical management of minimally enlarged thyroid. Diagnostic Cytopathology. 34(3). 196–200. 14 indexed citations
18.
Kini, Usha, et al.. (2002). Comparative cytological study of lymph node tuberculosis in HIV-infected individuals and in patients with diabetes in a developing country. Diagnostic Cytopathology. 26(2). 75–75. 2 indexed citations
19.
Anandh, Urmila, et al.. (2002). Association between membranous glomerulonephritis and erythema induratum (Nodular vasculitis) - A case report. Indian Journal of Nephrology. 12(1). 27–27. 1 indexed citations
20.
Mawer, George, Jill Clayton‐Smith, Helen Coyle, & Usha Kini. (2002). Outcome of pregnancy in women attending an outpatient epilepsy clinic: adverse features associated with higher doses of sodium valproate. Seizure. 11(8). 512–518. 77 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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