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Simona Serban Sosoi

Observed names: S Serban Sosoi, S Serban-Sosoi, S Șerban-Șoșoi, S. Sosoi, SIMONA ȘOȘOI, Simona Serban Şoşoi, Simona Serban-Sosoi, Simona Serban‑Sosoi, Simona Sosoi, Simona Ş. Şoşoi, Simona Șerban-Sosoi, Simona Șerban-Șoșoi
OpenAlex ID: A5011069805
Impact of Intermediate Hyperglycemia and Diabetes on Immune Dysfunction in Tuberculosis
2020 · Clare Eckold, Vinod Kumar, et al. · Clinical Infectious Diseases · 77
Sildenafil and tadalafil reduce the risk of contrast-induced nephropathy by modulating the oxidant/antioxidant balance in a murine model
2019 · Andrei Mihai Iordache, Anca Oana Docea, et al. · Food and Chemical Toxicology · 42
Prenatal and postnatal findings in a 10.6 Mb interstitial deletion at 10p11.22-p12.31
2015 · Simona Sosoi, Ioana Streata, et al. · Journal of Human Genetics · 40
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A Novel Nutraceutical Formulation Can Improve Motor Activity and Decrease the Stress Level in a Murine Model of Middle-Age Animals
2021 · Dimitris Tsoukalas, Ovidiu Zlatian, et al. · Journal of Clinical Medicine · 36
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Association of cytokine gene polymorphisms with osteoarthritis susceptibility
2018 · Otilia Rogoveanu, Daniela Calina, et al. · Experimental and Therapeutic Medicine · 32
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Determination of autophagy gene ATG16L1 polymorphism in human colorectal cancer.
2014 · Elena Raluca Nicoli, Theodor Dumitrescu, et al. · PubMed · 29
The Phenotypic Spectrum of 15q13.3 Region Duplications: Report of 5 Patients
2021 · Magdalena Budisteanu, Sorina Mihaela Papuc, et al. · Genes · 22
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Terminal Deletion 2q37.3 in a Patient with Klippel-Trenaunay-Weber Syndrome
2013 · Ileana Puiu, Alin Stoica, et al. · Fetal and Pediatric Pathology · 18
Cytogenetic Analysis of Sporadic First-Trimester Miscarriage Specimens Using Karyotyping and QF-PCR: A Retrospective Romanian Cohort Study
2022 · Gabriela Popescu-Hobeanu, Anca-Lelia Riza, et al. · Genes · 12
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Phenotype Heterogeneity in 3q29 Microduplication Syndrome.
2020 · Ioana Streata, Anca-Lelia Riza, et al. · PubMed · 8
A 14q31.1-q32.11 deletion case: Genotype – Neurological Phenotype Correlations in 14q interstitial deletion syndrome
2020 · EUGENIA ROZA, IOANA STREAȚĂ, et al. · ROMANIAN BIOTECHNOLOGICAL LETTERS · 6
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Polymorphisms in autophagy genes and active pulmonary tuberculosis susceptibility in Romania
2017 · Mihai Gabriel Cucu, Ioana Streața, et al. · Revista română de medicină de laborator · 5
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A rare occurrence of three consecutive autosomal trisomic pregnancies in a couple without offspring
2016 · F. Burada, S. Sosoi, et al. · Clinical and Experimental Obstetrics & Gynecology · 5
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The Value of Parental Karyotyping in Recurrent Pregnancy Loss Lies in Individual Risk Assessments
2024 · Gabriela Popescu-Hobeanu, Simona Serban Sosoi, et al. · Medicina · 4
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Pathogenic Copy Number Variations Involved in the Genetic Etiology of Syndromic and Non-Syndromic Intellectual Disability—Data from a Romanian Cohort
2022 · Ioana Streață, Alexandru Caramizaru, et al. · Diagnostics · 4
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Expanding the Clinical Phenotype of 19q Interstitial Deletions: A New Case with 19q13.32-q13.33 Deletion and Short Review of the Literature
2022 · Elena-Silvia Shelby, Michael Morris, et al. · Genes · 3
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Greig Cephalopolysyndactyly Contiguous Gene Syndrome: Case Report and Literature Review
2021 · Kinga Kozma, Marius Bembea, et al. · Genes · 3
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Prenatal diagnosis of a pure 15q distal trisomy derived from a maternal pericentric inversion: A case report
2021 · Florin Burada, Ioana Streata, et al. · Experimental and Therapeutic Medicine · 3
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Adverse Histopathological Features in Colorectal Cancer Associated with KRAS rs61764370 SNP: A Preliminary Study
2026 · Tradian Ciprian Berisha, Mihai Gabriel Cucu, et al. · Biomedicines · 1
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Array CGH - A Powerful Tool in Molecular Diagnostic of Pathogenic Microdeletions - Williams-Beuren Syndrome - A Case Report.
2016 · I Streață, S Șerban-Șoșoi, et al. · PubMed · 1
Phenotypic Spectrum in Three Romanian Patients with 8q23–q24 Deletions
2026 · Alexandru Caramizaru, Ioana Streata, et al. · International Journal of Molecular Sciences
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P140 Clinical caracterization of a new case with chromosome 3 terminal microdeletion, involving chl1 gene
2017 · IO Focsa, M Ioana, et al.
Works count: 22
Citation count: 351
H-index: 9
I10-index: 9
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