Sumedha Sudhaman

552 total citations
10 papers, 140 citations indexed

About

Sumedha Sudhaman is a scholar working on Cancer Research, Molecular Biology and Pathology and Forensic Medicine. According to data from OpenAlex, Sumedha Sudhaman has authored 10 papers receiving a total of 140 indexed citations (citations by other indexed papers that have themselves been cited), including 4 papers in Cancer Research, 3 papers in Molecular Biology and 3 papers in Pathology and Forensic Medicine. Recurrent topics in Sumedha Sudhaman's work include Cancer Genomics and Diagnostics (3 papers), Parkinson's Disease Mechanisms and Treatments (3 papers) and Genetic factors in colorectal cancer (3 papers). Sumedha Sudhaman is often cited by papers focused on Cancer Genomics and Diagnostics (3 papers), Parkinson's Disease Mechanisms and Treatments (3 papers) and Genetic factors in colorectal cancer (3 papers). Sumedha Sudhaman collaborates with scholars based in United States, India and Canada. Sumedha Sudhaman's co-authors include B.K. Thelma, Madhuri Behari, Uday B. Muthane, Ramesh C. Juyal, Shyla T. Govindappa, Kameshwar Prasad, Uri Tabori, Melissa Edwards, Daniel A. Morgenstern and Pedro Castelo‐Branco and has published in prestigious journals such as Journal of Clinical Investigation, Neurobiology of Aging and Journal of Medical Genetics.

In The Last Decade

Sumedha Sudhaman

10 papers receiving 139 citations

Peers

Sumedha Sudhaman
Fatme Seval Ismail Germany
Mikiko Tada Japan
Diego Lopergolo Italy
Jon Landa Spain
Gorka Fernández‐Eulate France
Chiara Cappelletti Norway
Anika Bongaarts Netherlands
Martina de Majo United States
Leen Vendredy Belgium
Brianna Godlewski United States
Fatme Seval Ismail Germany
Sumedha Sudhaman
Citations per year, relative to Sumedha Sudhaman Sumedha Sudhaman (= 1×) peers Fatme Seval Ismail

Countries citing papers authored by Sumedha Sudhaman

Since Specialization
Citations

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

Fields of papers citing papers by Sumedha Sudhaman

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Sumedha Sudhaman

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

All Works

10 of 10 papers shown
1.
Das, Anirban, Daniel A. Morgenstern, Sumedha Sudhaman, et al.. (2022). Immune Checkpoint Inhibition as Single Therapy for Synchronous Cancers Exhibiting Hypermutation: An IRRDC Study. JCO Precision Oncology. 6(6). e2100286–e2100286. 9 indexed citations
2.
Achari, Rimpa Basu, Gopal Achari, Paromita Roy, et al.. (2022). Germline Biallelic Mismatch Repair Deficiency in Childhood Glioblastoma and Implications for Clinical Management. Neurology India. 70(2). 772–774. 7 indexed citations
3.
Das, Anirban, Vanessa Bianchi, Sumedha Sudhaman, et al.. (2021). Upfront Adjuvant Immunotherapy of Replication Repair–Deficient Pediatric Glioblastoma With Chemoradiation-Sparing Approach. JCO Precision Oncology. 5(5). 1426–1431. 4 indexed citations
4.
Komosa, Martin, Sumedha Sudhaman, Ricardo Leão, et al.. (2021). Dual role of allele-specific DNA hypermethylation within the TERT promoter in cancer. Journal of Clinical Investigation. 131(21). 1570–1575. 18 indexed citations
5.
Morgenstern, Daniel A., Melissa Edwards, Sumedha Sudhaman, et al.. (2020). IMMU-14. IMMUNE CHECKPOINT INHIBITOR THERAPY FOR TREATMENT OF SYNCHRONOUS CANCERS IN PAEDIATRIC PATIENTS WITH CONSTITUTIONAL MISMATCH REPAIR DEFICIENCY. Neuro-Oncology. 22(Supplement_3). iii362–iii362. 1 indexed citations
6.
Oshrine, Benjamin, Melissa Crenshaw, Melissa Edwards, et al.. (2019). B-cell acute lymphoblastic leukemia with high mutation burden presenting in a child with constitutional mismatch repair deficiency. Blood Advances. 3(12). 1795–1798. 5 indexed citations
7.
Sudhaman, Sumedha, Uday B. Muthane, Madhuri Behari, et al.. (2016). Evidence of mutations in RIC3 acetylcholine receptor chaperone as a novel cause of autosomal-dominant Parkinson's disease with non-motor phenotypes. Journal of Medical Genetics. 53(8). 559–566. 29 indexed citations
8.
Govindappa, Shyla T., Sumedha Sudhaman, B.K. Thelma, et al.. (2016). Early Onset Parkinson's disease due to DJ1 mutations: An Indian study. Parkinsonism & Related Disorders. 32. 20–24. 16 indexed citations
9.
Sudhaman, Sumedha, Kameshwar Prasad, Madhuri Behari, et al.. (2016). Discovery of a frameshift mutation in podocalyxin-like (PODXL) gene, coding for a neural adhesion molecule, as causal for autosomal-recessive juvenile Parkinsonism. Journal of Medical Genetics. 53(7). 450–456. 29 indexed citations
10.
Sudhaman, Sumedha, Madhuri Behari, Shyla T. Govindappa, et al.. (2013). VPS35 and EIF4G1 mutations are rare in Parkinson's disease among Indians. Neurobiology of Aging. 34(10). 2442.e1–2442.e3. 22 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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