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European Journal of Medical Genetics|November 21, 2016
Novel ELN mutation in a family with supravalvular aortic stenosis and intracranial aneurysmAnne Marie Jelsig, Zsolt Urban, Vishwanathan Hucthagowder, et al.
Human Pathology|December 3, 2014
Genetic alterations in renal cell carcinoma with rhabdoid differentiationCarmen M Perrino, Vishwanathan Hucthagowder, Michael Evenson, et al.
American Journal of Human Genetics|May 11, 2006
Fibulin-4: a novel gene for an autosomal recessive cutis laxa syndromeVishwanathan Hucthagowder, Nina Sausgruber, Katherine H Kim, et al.
Investigative Ophthalmology & Visual Science|June 27, 2007
Population differences in elastin maturation in optic nerve head tissue and astrocytesZsolt Urban, Olga Agapova, Vishwanathan Hucthagowder, et al.
Cancer Genetics|December 4, 2019
Utility of copy number variants in the classification of intracranial ependymomaMichael Evenson, Chunyu Cai, Vishwanathan Hucthagowder, et al.
Cancer Genetics|September 4, 2012
Resequencing analysis of the candidate tyrosine kinase and RAS pathway gene families in multiple myelomaVishwanathan Hucthagowder, Rekha Meyer, Chelsea Mullins, et al.
Plos One|July 5, 2013
Germinal center B-cells resist transformation by Kras independently of tumor suppressor ArfChelsea D Mullins, Mack Y Su, Vishwanathan Hucthagowder, et al.
European Journal of Medical Genetics|May 15, 2012
Chromosome 2p15p16.1 microdeletion syndrome: 2.5 Mb deletion in a patient with renal anomalies, intractable seizures and a choledochal cystVishwanathan Hucthagowder, Ta-Chiang Liu, Alex R Paciorkowski, et al.
Human Mutation|February 11, 2011
New insights into the pathogenesis of autosomal-dominant cutis laxa with report of five ELN mutationsBert Callewaert, Marjolijn Renard, Vishwanathan Hucthagowder, et al.
American Journal of Human Genetics|October 20, 2009
Mutations in LTBP4 cause a syndrome of impaired pulmonary, gastrointestinal, genitourinary, musculoskeletal, and dermal developmentZsolt Urban, Vishwanathan Hucthagowder, Nura Schürmann, et al.
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