Monica Cristina Pânzaru (Monica-Cristina Panzaru, Monica-Cristina Pânzaru, Monica Cristina Panzaru)

Publication Activity (10 Years)

Years Active: 2021-2024
Publications (10 Years): 16

Top Topics

Duchenne Muscular Dystrophy

Genome Wide Association

Top Venues

International journal of molecular sciences

Diagnostics (Basel, Switzerland)

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

Publications

Lăcrămioara Ionela Butnariu, Delia Andreia Bizim, Carmen Oltean, Cristina Rusu, Monica Cristina Pânzaru, Gabriela Păduraru, Nicoleta Gimiga, Gabriela Ghiga, Ștefana-Maria Moisă, Elena Tarca, Iuliana Magdalena Starcea, Setalia Popa, Laura Mihaela Trandafir
The Importance of Molecular Genetic Testing for Precision Diagnostics, Management, and Genetic Counseling in MODY Patients. International journal of molecular sciences 25 (12) (2024)
Lăcrămioara Ionela Butnariu, Delia Andreia Bizim, Carmen Oltean, Cristina Rusu, Monica Cristina Pânzaru, Gabriela Păduraru, Nicoleta Gimiga, Gabriela Ghiga, Ștefana-Maria Moisă, Elena Tarca, Iuliana Magdalena Starcea, Setalia Popa, Laura Mihaela Trandafir
The Importance of Molecular Genetic Testing for Precision Diagnostics, Management, and Genetic Counseling in MODY Patients. International journal of molecular sciences 25 (12) (2024)
Eva-Cristiana Gavril, Irina Nucă, Monica Cristina Pânzaru, Anca Viorica Ivanov, Cosmin Teodor Mihai, Lucian-Mihai Antoci, Cristian-Gabriel Ciobanu, Cristina Rusu, Roxana Popescu
Genotype-Phenotype Correlations in 2q37-Deletion Syndrome: An Update of the Clinical Spectrum and Literature Review. Genes 14 (2) (2023)
Ioana Balinisteanu, Monica Cristina Pânzaru, Lavinia Caba, Maria-Christina Ungureanu, Andreea Florea, Ana Maria Grigore, Eusebiu Vlad Gorduza
Cancer Predisposition Syndromes and Thyroid Cancer: Keys for a Short Two-Way Street. Biomedicines 11 (8) (2023)
Eva-Cristiana Gavril, Irina Nucă, Monica Cristina Pânzaru, Anca Viorica Ivanov, Cosmin Teodor Mihai, Lucian-Mihai Antoci, Cristian-Gabriel Ciobanu, Cristina Rusu, Roxana Popescu
Genotype-Phenotype Correlations in 2q37-Deletion Syndrome: An Update of the Clinical Spectrum and Literature Review. Genes 14 (2) (2023)
Eva-Cristiana Gavril, Irina Nucă, Monica Cristina Pânzaru, Anca Viorica Ivanov, Cosmin Teodor Mihai, Lucian-Mihai Antoci, Cristian-Gabriel Ciobanu, Cristina Rusu, Roxana Popescu
Genotype-Phenotype Correlations in 2q37-Deletion Syndrome: An Update of the Clinical Spectrum and Literature Review. Genes 14 (2) (2023)
Lăcrămioara Ionela Butnariu, Eusebiu Vlad Gorduza, Elena Tarca, Monica Cristina Pânzaru, Setalia Popa, Simona Stoleriu, Vasile Valeriu Lupu, Ancuta Lupu, Elena Cojocaru, Laura Mihaela Trandafir, Ștefana-Maria Moisă, Andreea Florea, Laura Stătescu, Minerva Codruţa Bădescu
Current Data and New Insights into the Genetic Factors of Atherogenic Dyslipidemia Associated with Metabolic Syndrome. Diagnostics (Basel, Switzerland) 13 (14) (2023)
Cristian-Gabriel Ciobanu, Irina Nucă, Roxana Popescu, Lucian-Mihai Antoci, Lavinia Caba, Anca Viorica Ivanov, Karina-Alexandra Cojocaru, Cristina Rusu, Cosmin Teodor Mihai, Monica Cristina Pânzaru
Narrative Review: Update on the Molecular Diagnosis of Fragile X Syndrome. International journal of molecular sciences 24 (11) (2023)
Daniela Luminita Zob, Iolanda Augustin, Lavinia Caba, Monica Cristina Pânzaru, Setalia Popa, Alina Delia Popa, Laura Florea, Eusebiu Vlad Gorduza
Genomics and Epigenomics in the Molecular Biology of Melanoma-A Prerequisite for Biomarkers Studies. International journal of molecular sciences 24 (1) (2022)
Eva-Cristiana Gavril, Roxana Popescu, Irina Nucă, Cristian-Gabriel Ciobanu, Lăcrămioara Ionela Butnariu, Cristina Rusu, Monica Cristina Pânzaru
Different Types of Deletions Created by Low-Copy Repeats Sequences Location in 22q11.2 Deletion Syndrome: Genotype-Phenotype Correlation. Genes 13 (11) (2022)
Daniela Luminita Zob, Iolanda Augustin, Lavinia Caba, Monica Cristina Pânzaru, Setalia Popa, Alina Delia Popa, Laura Florea, Eusebiu Vlad Gorduza
Genomics and Epigenomics in the Molecular Biology of Melanoma-A Prerequisite for Biomarkers Studies. International journal of molecular sciences 24 (1) (2022)
Daniela Luminita Zob, Iolanda Augustin, Lavinia Caba, Monica Cristina Pânzaru, Setalia Popa, Alina Delia Popa, Laura Florea, Eusebiu Vlad Gorduza
Genomics and Epigenomics in the Molecular Biology of Melanoma-A Prerequisite for Biomarkers Studies. International journal of molecular sciences 24 (1) (2022)
Monica Cristina Pânzaru, Lavinia Caba, Laura Florea, Elena Emanuela Braha, Eusebiu Vlad Gorduza
Epidermolysis Bullosa-A Different Genetic Approach in Correlation with Genetic Heterogeneity. Diagnostics (Basel, Switzerland) 12 (6) (2022)
Cristina Antohi, Danisia Haba, Lavinia Caba, Mihai Liviu Ciofu, Vasile-Liviu Drug, Oana-Bogdana Bărboi, Bogdan Ionuț Dobrovăț, Monica Cristina Pânzaru, Nicoleta Carmen Gorduza, Vasile Valeriu Lupu, Doina Dimofte, Cristina Gug, Eusebiu Vlad Gorduza
Novel Mutation in APC Gene Associated with Multiple Osteomas in a Family and Review of Genotype-Phenotype Correlations of Extracolonic Manifestations in Gardner Syndrome. Diagnostics (Basel, Switzerland) 11 (9) (2021)
Eva-Cristiana Gavril, Alina-Costina Luca, Alexandrina-Stefania Curpan, Roxana Popescu, Irina Resmerita, Monica Cristina Pânzaru, Lacramioara Ionela Butnariu, Eusebiu Vlad Gorduza, Mihaela Gramescu, Cristina Rusu
Wolf-Hirschhorn Syndrome: Clinical and Genetic Study of 7 New Cases, and Mini Review. Children (Basel, Switzerland) 8 (9) (2021)
Roxana Popescu, Mihaela Grămescu, Lavinia Caba, Monica Cristina Pânzaru, Lăcrămioara Butnariu, Elena Braha, Setalia Popa, Cristina Rusu, Georgeta Cardos, Monica Zeleniuc, Violeta Martiniuc, Cristina Gug, Luminita Păduraru, Maria Stamatin, Carmen C Diaconu, Eusebiu Vlad Gorduza
A Case of Inherited t(4;10)(q26;q26.2) Chromosomal Translocation Elucidated by Multiple Chromosomal and Molecular Analyses. Case Report and Review of the Literature. Genes 12 (12) (2021)