Vishwanathan Hucthagowder

1.8k total citations
12 papers, 521 citations indexed

About

Vishwanathan Hucthagowder is a scholar working on Molecular Biology, Genetics and Hematology. According to data from OpenAlex, Vishwanathan Hucthagowder has authored 12 papers receiving a total of 521 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Molecular Biology, 6 papers in Genetics and 4 papers in Hematology. Recurrent topics in Vishwanathan Hucthagowder's work include Connective tissue disorders research (5 papers), Multiple Myeloma Research and Treatments (4 papers) and Dermatological and Skeletal Disorders (2 papers). Vishwanathan Hucthagowder is often cited by papers focused on Connective tissue disorders research (5 papers), Multiple Myeloma Research and Treatments (4 papers) and Dermatological and Skeletal Disorders (2 papers). Vishwanathan Hucthagowder collaborates with scholars based in United States, Denmark and United Kingdom. Vishwanathan Hucthagowder's co-authors include Zsolt Urbán, Lihua Y. Marmorstein, Brad Angle, Katherine H. Kim, Nina Sausgruber, Ji-Won Choi, Michael Marble, Chester Brown, Kristen E. Holland and Robin D. Clark and has published in prestigious journals such as Blood, PLoS ONE and The American Journal of Human Genetics.

In The Last Decade

Vishwanathan Hucthagowder

12 papers receiving 510 citations

Peers

Vishwanathan Hucthagowder
B Lee United States
Julie Lozier United States
Tomoyo Sasaki United States
Somyoth Sridurongrit United States
Beatrice Sellinger United States
Dru F. Leistritz United States
Sui Lee‐Arteaga United States
Sapna Vijayakumar United States
Vishwanathan Hucthagowder
Citations per year, relative to Vishwanathan Hucthagowder Vishwanathan Hucthagowder (= 1×) peers Josephina Meester

Countries citing papers authored by Vishwanathan Hucthagowder

Since Specialization
Citations

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

Fields of papers citing papers by Vishwanathan Hucthagowder

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Vishwanathan Hucthagowder

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

All Works

12 of 12 papers shown
1.
Jelsig, Anne Marie, Zsolt Urbán, Vishwanathan Hucthagowder, Henrik Nissen, & Lilian Bomme Ousager. (2016). Novel ELN mutation in a family with supravalvular aortic stenosis and intracranial aneurysm. European Journal of Medical Genetics. 60(2). 110–113. 18 indexed citations
2.
Hucthagowder, Vishwanathan, et al.. (2016). Utility of clinical high‐depth next generation sequencing for somatic variant detection in the PIK3CA‐related overgrowth spectrum. Clinical Genetics. 91(1). 79–85. 29 indexed citations
3.
Perrino, Carmen M., et al.. (2014). Genetic alterations in renal cell carcinoma with rhabdoid differentiation. Human Pathology. 46(1). 9–16. 9 indexed citations
4.
Mullins, C. Daniel, Mack Y. Su, Vishwanathan Hucthagowder, et al.. (2013). Germinal Center B-Cells Resist Transformation by Kras Independently of Tumor Suppressor Arf. PLoS ONE. 8(6). e67941–e67941. 6 indexed citations
5.
Hucthagowder, Vishwanathan, Ta‐Chiang Liu, Alex R. Paciorkowski, et al.. (2012). Chromosome 2p15p16.1 microdeletion syndrome: 2.5 Mb deletion in a patient with renal anomalies, intractable seizures and a choledochal cyst. European Journal of Medical Genetics. 55(8-9). 485–489. 14 indexed citations
6.
Hucthagowder, Vishwanathan, Chelsea Mullins, Rakesh Nagarajan, et al.. (2012). Resequencing analysis of the candidate tyrosine kinase and RAS pathway gene families in multiple myeloma. Cancer Genetics. 205(9). 474–478. 15 indexed citations
7.
Mullins, Chelsea, Mack Y. Su, Vishwanathan Hucthagowder, et al.. (2012). Activation of K-Ras in Arf-Null Mice Is Not Sufficient for Malignant Transformation of Post-Germinal Center B-Cells. Blood. 120(21). 5016–5016. 1 indexed citations
8.
Callewaert, Bert, Marjolijn Renard, Vishwanathan Hucthagowder, et al.. (2011). New insights into the pathogenesis of autosomal‐dominant cutis laxa with report of fiveELNmutations. Human Mutation. 32(4). 445–455. 82 indexed citations
9.
Hucthagowder, Vishwanathan, Chelsea Mullins, Rakesh Nagarajan, et al.. (2010). Resequencing Analysis of the Human Candidate Ras and Receptor Tyrosine Kinase Gene Family In Multiple Myeloma. Blood. 116(21). 301–301. 2 indexed citations
10.
Urbán, Zsolt, Vishwanathan Hucthagowder, Nura Schürmann, et al.. (2009). Mutations in LTBP4 Cause a Syndrome of Impaired Pulmonary, Gastrointestinal, Genitourinary, Musculoskeletal, and Dermal Development. The American Journal of Human Genetics. 85(5). 593–605. 108 indexed citations
11.
Urbán, Zsolt, Olga A. Agapova, Vishwanathan Hucthagowder, et al.. (2007). Population Differences in Elastin Maturation in Optic Nerve Head Tissue and Astrocytes. Investigative Ophthalmology & Visual Science. 48(7). 3209–3209. 35 indexed citations
12.
Hucthagowder, Vishwanathan, Nina Sausgruber, Katherine H. Kim, et al.. (2006). Fibulin-4: A Novel Gene for an Autosomal Recessive Cutis Laxa Syndrome. The American Journal of Human Genetics. 78(6). 1075–1080. 202 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.

Explore authors with similar magnitude of impact

Rankless by CCL
2026