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Genomics and Epigenomics in the Molecular Biology of Melanoma-A Prerequisite for Biomarkers Studies

International journal of molecular sciences, 2022-12, Vol.24 (1), p.716

2022

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ORPHAcodes use for the coding of rare diseases: comparison of the accuracy and cross country comparability

Orphanet journal of rare diseases, 2023-09, Vol.18 (1), p.1-267, Article 267

2023

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Cancer Predisposition Syndromes and Thyroid Cancer: Keys for a Short Two-Way Street

Biomedicines, 2023-07, Vol.11 (8), p.2143

2023

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Exome sequencing in a Romanian Bardet‐Biedl syndrome cohort revealed an overabundance of causal BBS12 variants

American journal of medical genetics. Part A, 2023-09, Vol.191 (9), p.2376-2391

2023

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Genetic heterogeneity in corpus callosum agenesis

Frontiers in genetics, 2022-09, Vol.13, p.958570-958570

2022

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Genetics of Hearing Impairment in North-Eastern Romania-A Cost-Effective Improved Diagnosis and Literature Review

Genes, 2020-12, Vol.11 (12), p.1506

2020

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Narrative Review: Update on the Molecular Diagnosis of Fragile X Syndrome

International journal of molecular sciences, 2023-05, Vol.24 (11), p.9206

2023

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Pallister–Killian Syndrome versus Trisomy 12p—A Clinical Study of 5 New Cases and a Literature Review

Genes, 2021-05, Vol.12 (6), p.811

2021

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Wolf-Hirschhorn Syndrome: Clinical and Genetic Study of 7 New Cases, and Mini Review

Children (Basel), 2021-09, Vol.8 (9), p.751

2021

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The Importance of Molecular Genetic Testing for Precision Diagnostics, Management, and Genetic Counseling in MODY Patients

International journal of molecular sciences, 2024-06, Vol.25 (12), p.6318

2024

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Epidermolysis Bullosa—A Different Genetic Approach in Correlation with Genetic Heterogeneity

Diagnostics (Basel), 2022-05, Vol.12 (6), p.1325

2022

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Genotype-Phenotype Correlations in 2q37-Deletion Syndrome: An Update of the Clinical Spectrum and Literature Review

Genes, 2023-02, Vol.14 (2), p.465

2023

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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, 2021-12, Vol.12 (12), p.1957

2021

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Current Data and New Insights into the Genetic Factors of Atherogenic Dyslipidemia Associated with Metabolic Syndrome

Diagnostics (Basel), 2023-07, Vol.13 (14), p.2348

2023

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Different Types of Deletions Created by Low-Copy Repeats Sequences Location in 22q11.2 Deletion Syndrome: Genotype–Phenotype Correlation

Genes, 2022-11, Vol.13 (11), p.2083

2022

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Classification of osteogenesis imperfecta: Importance for prophylaxis and genetic counseling

World journal of clinical cases, 2023-04, Vol.11 (12), p.2604-2620

2023

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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), 2021-09, Vol.11 (9), p.1560

2021

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Type of treatment of cardiac disorders - quality of life and heart-focused anxiety: The mediating role of illness perceptions

Psychology, health & medicine, 2015-07, Vol.20 (5), p.551-559

2015

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Ethnicity-related DMD Genotype Landscapes in European and Non-European Countries

Neurology. Genetics, 2021-02, Vol.7 (1), p.e536-e536

2021

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Campomelic dysplasia with dextrocardia and without sex-reversal

Archive of clinical cases, 2017-03, Vol.4 (1), p.16-22

2017

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Genotype- phenotype correlation in trisomy X: a retrospective study of a selected group of 36 patients and review of literature

Revista medico-chirurgicala a Societatii de Medici si Naturalisti din Iasi, 2013-07, Vol.117 (3), p.714-721

2013

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Phenotypic variability in Patau syndrome

Revista medico-chirurgicala a Societatii de Medici si Naturalisti din Iasi, 2013-04, Vol.117 (2), p.321-327

2013

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Improvement of genetic diagnostic strategy in velo-cardio-facial syndrome

Revista medico-chirurgicala a Societatii de Medici si Naturalisti din Iasi, 2011-07, Vol.115 (3), p.756-761

2011

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Social Representations of Cancer among Nursing Students

Psihologia sociala, 2014-07 (34), p.47-60

Panzaru, Gabriela Monica

2014

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Prenatal diagnosis of gonosomal anomalies: limitations of the FISH method and genetic counseling difficulties in 15 cases

Revista medico-chirurgicala a Societatii de Medici si Naturalisti din Iasi, 2013-04, Vol.117 (2), p.450-456

2013

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Genomics and Epigenomics in the Molecular Biology of Melanoma-A Prerequisite for Biomarkers Studies

ORPHAcodes use for the coding of rare diseases: comparison of the accuracy and cross country comparability

Cancer Predisposition Syndromes and Thyroid Cancer: Keys for a Short Two-Way Street

Exome sequencing in a Romanian Bardet‐Biedl syndrome cohort revealed an overabundance of causal BBS12 variants

Genetic heterogeneity in corpus callosum agenesis

Genetics of Hearing Impairment in North-Eastern Romania-A Cost-Effective Improved Diagnosis and Literature Review

Narrative Review: Update on the Molecular Diagnosis of Fragile X Syndrome

Pallister–Killian Syndrome versus Trisomy 12p—A Clinical Study of 5 New Cases and a Literature Review

Wolf-Hirschhorn Syndrome: Clinical and Genetic Study of 7 New Cases, and Mini Review

The Importance of Molecular Genetic Testing for Precision Diagnostics, Management, and Genetic Counseling in MODY Patients

Epidermolysis Bullosa—A Different Genetic Approach in Correlation with Genetic Heterogeneity

Genotype-Phenotype Correlations in 2q37-Deletion Syndrome: An Update of the Clinical Spectrum and Literature Review

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

Current Data and New Insights into the Genetic Factors of Atherogenic Dyslipidemia Associated with Metabolic Syndrome

Different Types of Deletions Created by Low-Copy Repeats Sequences Location in 22q11.2 Deletion Syndrome: Genotype–Phenotype Correlation

Classification of osteogenesis imperfecta: Importance for prophylaxis and genetic counseling

Novel Mutation in APC Gene Associated with Multiple Osteomas in a Family and Review of Genotype-Phenotype Correlations of Extracolonic Manifestations in Gardner Syndrome

Type of treatment of cardiac disorders - quality of life and heart-focused anxiety: The mediating role of illness perceptions

Ethnicity-related DMD Genotype Landscapes in European and Non-European Countries

Campomelic dysplasia with dextrocardia and without sex-reversal

Genotype- phenotype correlation in trisomy X: a retrospective study of a selected group of 36 patients and review of literature

Phenotypic variability in Patau syndrome

Improvement of genetic diagnostic strategy in velo-cardio-facial syndrome

Social Representations of Cancer among Nursing Students

Prenatal diagnosis of gonosomal anomalies: limitations of the FISH method and genetic counseling difficulties in 15 cases

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