Viviana Karina Dalamón - Genetic Mutations

Author Information

Viviana Karina Dalamón is a researcher affiliated with the Laboratory of Physiology and Genetics of Hearing at the Instituto de Investigaciones en Ingeniería Genética y Biología Molecular "Dr. Héctor Torres" (INGEBI), which is part of the Consejo Nacional de Investigaciones Científicas y Técnicas (CONICET) in Buenos Aires, Argentina. Her research primarily focuses on genetic and physiological aspects of hearing, with significant contributions to understanding the molecular mechanisms underlying hearing impairments and related genetic disorders.

Research Contributions

Viviana Karina Dalamón has made substantial contributions to the field of genetics, particularly in the context of hearing impairments and related syndromes. Her research spans from identifying and characterizing novel genetic mutations associated with non-syndromic deafness to exploring the functional implications of these mutations on protein structures and cellular functions. She has also investigated genetic variants in specific populations, such as the Argentine cohort, and has contributed to understanding genetic conditions like Duchenne Muscular Dystrophy and Retinoblastoma. Her work has been published in reputable journals and has provided valuable insights into the genetic basis of various disorders, aiding in the development of diagnostic and therapeutic strategies.

Aliases

Viviana Karina Dalamón is also known by various aliases in academic publications, including V K Dalamon, V. Dalamon, Viviana Dalamón, and Viviana Dalamon.

Publication and Citation Metrics

Metric	Value
Total Citation Count	296
H-index	11
Total Paper Count	35

Publications:

Predicting pathogenicity for novel hearing loss mutations based on genetic and protein structure approaches

DOI: 10.1038/s41598-021-04081-2

Year: 2022

Theragnosis for Duchenne Muscular Dystrophy

DOI: 10.3389/fphar.2021.648390

Year: 2021

GJB2 and GJB6 Genetic Variant Curation in an Argentinean Non-Syndromic Hearing-Impaired Cohort

DOI: 10.3390/genes11101233

Year: 2020

Gap-junctional channel and hemichannel activity of two recently identified connexin 26 mutants associated with deafness

DOI: 10.1007/s00424-016-1788-7

Year: 2016

MLPA analysis of an Argentine cohort of patients with dystrophinopathy: Association of intron breakpoints hot spots with STR abundance in DMD gene

DOI: 10.1016/j.jns.2016.03.047

Year: 2016

Connexin 26 (GJB2) mutation in an Argentinean patient with keratitis-ichthyosis-deafness (KID) syndrome: a case report

DOI: 10.1186/s12881-016-0298-y

Year: 2016

Identification of four novel connexin 26 mutations in non-syndromic deaf patients: genotype–phenotype analysis in moderate cases

DOI: 10.1007/s11033-013-2814-x

Year: 2013

RB1 Germ-Line Deletions in Argentine Retinoblastoma Patients

DOI: 10.1007/BF03256222

Year: 2012

Effects of fasting and hypoxic preconditioning on the hypoxic-reoxygenated ventricular strips of the rat heart

DOI: 10.1007/BF03179844

Year: 2010

Electrical Properties and Functional Expression of Ionic Channels in Cochlear Inner Hair Cells of Mice Lacking the α10 Nicotinic Cholinergic Receptor Subunit

DOI: 10.1007/s10162-009-0164-0

Year: 2009

What are DNA Molecules?

How are Patients Monitored During TKI Therapy?

Are there preventive measures for PAH exposure?

What Preventive Measures Can Be Taken?

How are inherited genetic mutations diagnosed?

How is HbS Diagnosed?

What is the Link Between Tobacco Mutagens and Cancer?

Are There Any Research Advances for Delta F508 Mutation?

How Does CGH Work?

What are Some Examples of Medications Affected by Genetic Mutations?

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