Tinka Hovnik

Publication Activity (10 Years)

Years Active: 2022-2023
Publications (10 Years): 6

Top Topics

Dendritic Cells

Intellectual Disability

Bioinformatics Analysis

Top Venues

International journal of molecular sciences

This page only lists publications with an associated author ORCID identifier.

Publications

Lara Slavec, Ksenija Gersak, Andreja Eberlinc, Tinka Hovnik, Luca Lovrečić, Irena Mlinarič-Raščan, Nataša Karas Kuželički
A Comprehensive Genetic Analysis of Slovenian Families with Multiple Cases of Orofacial Clefts Reveals Novel Variants in the Genes IRF6 , GRHL3 , and TBX22 . International journal of molecular sciences 24 (5) (2023)
Lara Slavec, Ksenija Gersak, Andreja Eberlinc, Tinka Hovnik, Luca Lovrečić, Irena Mlinarič-Raščan, Nataša Karas Kuželički
A Comprehensive Genetic Analysis of Slovenian Families with Multiple Cases of Orofacial Clefts Reveals Novel Variants in the Genes IRF6 , GRHL3 , and TBX22 . International journal of molecular sciences 24 (5) (2023)
Lara Slavec, Ksenija Gersak, Andreja Eberlinc, Tinka Hovnik, Luca Lovrečić, Irena Mlinarič-Raščan, Nataša Karas Kuželički
A Comprehensive Genetic Analysis of Slovenian Families with Multiple Cases of Orofacial Clefts Reveals Novel Variants in the Genes IRF6 , GRHL3 , and TBX22 . International journal of molecular sciences 24 (5) (2023)
Lara Slavec, Ksenija Gersak, Andreja Eberlinc, Tinka Hovnik, Luca Lovrečić, Irena Mlinarič-Raščan, Nataša Karas Kuželički
A Comprehensive Genetic Analysis of Slovenian Families with Multiple Cases of Orofacial Clefts Reveals Novel Variants in the Genes IRF6 , GRHL3 , and TBX22 . International journal of molecular sciences 24 (5) (2023)
Lana Stavber, Maria Joao Gaia, Tinka Hovnik, Barbara Jenko Bizjan, Maruša Debeljak, Jernej Kovac, Jasna Šuput Omladič, Tadej Battelino, Primož Kotnik, Klemen Dovc
Heterozygous NPR2 Variants in Idiopathic Short Stature. Genes 13 (6) (2022)
Tinka Hovnik, Eva Zitnik, Magdalena Avbelj Stefanija, Sara Bertok, Katarina Sedej, Vesna Bancic Silva, Tadej Battelino, Urh Groselj
An Adolescent Boy with Klinefelter Syndrome and 47,XXY/46,XX Mosaicism: Case Report and Review of Literature. Genes 13 (5) (2022)