Leticia Olavarrieta

Statistics

Publications

Citations

1.1K

H-Index

Active since

2002

Affiliations

Centre for Biomedical Network Research on Rare Diseases(Current)

Centro de Investigaciones Biológicas Margarita Salas

Hospital Universitario Ramón y Cajal

Instituto Cajal

Marqués de Valdecilla University Hospital

Leticia Olavarrieta is an author at Centre for Biomedical Network Research on Rare Diseases specializing in life sciences, molecular genetics, and genetics.

ORCID

Publications per year

2002–2017

Publications

Mutations in the seed region of human miR-96 are responsible for nonsyndromic progressive hearing loss

Ángeles Mencía, Silvia Modamio‐Høybjør, Nick Redshaw et al. · Nature Genetics · 2009 · 555 citations

Life Sciences, Genetics, Molecular Genetics +14

DFNA8/12 caused by TECTA mutations is the most identified subtype of nonsyndromic autosomal dominant hearing loss

Michael S. Hildebrand, Matías Morin, Nicole C. Meyer et al. · Human Mutation · 2011 · 93 citations · Full text

Life Sciences, Genetics, Molecular Genetics +12

DNA Knotting Caused by Head-on Collision of Transcription and Replication

Leticia Olavarrieta, Pablo Hernández, Dora B. Krimer et al. · Journal of Molecular Biology · 2002 · 83 citations

Life Sciences, Molecular Biology, Molecular Genetics +12

Supercoiling, knotting and replication fork reversal in partially replicated plasmids

Leticia Olavarrieta · Nucleic Acids Research · 2002 · 74 citations · Full text

Life Sciences, Genetics, Molecular Biology +17

Three deaf mice: mouse models for TECTA-based human hereditary deafness reveal domain-specific structural phenotypes in the tectorial membrane

P. Kevin Legan, Richard J. Goodyear, Matías Morin et al. · Human Molecular Genetics · 2013 · 57 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

1–5 of 11