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Barbara Testa

Observed name: B Testa
ORCID: 0000-0003-3516-2379
Observed ORCID: 0000-0003-3516-2379
OpenAlex ID: A5070590730
The lectin-like oxidized LDL receptor-1: a new potential molecular target in colorectal cancer
2016 · Michela Murdocca, Ruggiero Mango, et al. · Oncotarget · 55
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The Short Form of the Glasgow Composite Measure Pain Scale in Post-operative Analgesia Studies in Dogs: A Scoping Review
2021 · Barbara Testa, Jacqueline Reid, et al. · Frontiers in Veterinary Science · 43
Genetics and Genomics of Breast Cancer: update and translational perspectives
2020 · Michela Biancolella, Barbara Testa, et al. · Seminars in Cancer Biology · 35
Deletion of REXO1L1 locus in a patient with malabsorption syndrome, growth retardation, and dysmorphic features: a novel recognizable microdeletion syndrome?
2015 · Maria Rosaria D’Apice, Antonio Novelli, et al. · BMC Medical Genetics · 34
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Membrane Cholesterol Modulates LOX-1 Shedding in Endothelial Cells
2015 · Magda Gioia, Giulia Vindigni, et al. · PLoS ONE · 27
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Simulative and experimental investigation on the cleavage site that generates the soluble human LOX-1
2013 · Silvia Biocca, Tania Arcangeli, et al. · Archives of Biochemistry and Biophysics · 21
Breast cancer in West Africa: molecular analysis of BRCA genes in early-onset breast cancer patients in Burkina Faso
2021 · Michela Biancolella, Nabonswindé Lamoussa Marie Ouédraogo, et al. · Human Genomics · 19
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Molecular Analysis and Reclassification of NSD1 Gene Variants in a Cohort of Patients with Clinical Suspicion of Sotos Syndrome
2023 · Barbara Testa, Giuseppina Conteduca, et al. · Genes · 15
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Identification of alternative transcripts of NSD1 gene in Sotos Syndrome patients and healthy subjects
2022 · Giuseppina Conteduca, Barbara Testa, et al. · Gene · 13
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Cognitive, adaptive and behavioral profile in Sotos syndrome children with 5q35 microdeletion or intragenic variants
2023 · Martina Siracusano, Assia Riccioni, et al. · American Journal of Medical Genetics Part A · 10
NSD1 Mutations in Sotos Syndrome Induce Differential Expression of Long Noncoding RNAs, miR646 and Genes Controlling the G2/M Checkpoint
2022 · Giuseppina Conteduca, Davide Cangelosi, et al. · Life · 10
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Androgen- and insulin-related gene signature using a specific low density oligoarray AndroChip 2 in peripheral blood mononuclear cells in agonists, recreational athletes and sedentary subjects.
2011 · D Minella, M Biancolella, et al. · PubMed · 6
SOS1 over-expression in genital skin fibroblasts from hirsute women: a putative role of the SOS1/RAS pathway in the pathogenesis of hirsutism.
2012 · D Minella, F Wannenes, et al. · PubMed · 5
A pilot study on the transcriptional response of androgen- and insulin-related genes in peripheral blood mononuclear cells induced by testosterone administration in hypogonadal men.
2011 · M G Giganti, D Minella, et al. · PubMed · 5
Exome Analysis Reveals Novel Missense and Deletion Variants in the CC2D2A Gene as Causative of Joubert Syndrome
2023 · Rute Luísa Cabrita Pinto, Silvia Viaggi, et al. · Genes · 4
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A New Variant in the NALCN Channel Is Responsible for Cerebellar Ataxia and Cognitive Impairment
2025 · Rute Luísa Cabrita Pinto, Roberto Fancellu, et al. · Genes · 2
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Pleomorphic Parotid Adenoma in a Child Affected with Cri du Chat Syndrome: Clinical, Cytogenetic, and Molecular Analysis
2024 · Cesare Danesino, Federico Biglioli, et al. · International Journal of Molecular Sciences · 2
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Derivation of the IGGi006-A stem cell line from a patient with CAPRIN1 haploinsufficiency
2025 · Giuseppina Conteduca, Chiara Baldo, et al. · Stem Cell Research · 1
Impact of NSD1 Alternative Transcripts in Actin Filament Formation and Cellular Division Pathways in Fibroblasts
2024 · Giuseppina Conteduca, Davide Cangelosi, et al. · Genes · 1
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Generation of IGGi003-A induced pluripotent stem cell line from a patient with Sotos Syndrome carrying c.1633delA NSD1 variant in exon 5
2024 · Giuseppina Conteduca, Chiara Baldo, et al. · Stem Cell Research · 1
Generation of induced pluripotent stem cell lines from a patient with Sotos syndrome carrying 5q35 microdeletion
2022 · Giuseppina Conteduca, Chiara Baldo, et al. · Stem Cell Research · 1
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Coexistence of Two Novel Mutations in CDKN2A and PMS1 Genes in a Single Patient Identifies a New and Severe Cancer Predisposition Syndrome
2017 · Marco Cassone, Leila Baghernajad Salehi, et al. · Oncomedicine · 1
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Uncommon causal variants of the ADA2 gene in patients with reduced enzyme activity and nonconfirmatory genetic testing
2025 · Alice Grossi, Alessia Cafaro, et al. · The Journal of Allergy and Clinical Immunology In Practice
Breast cancer in Western Africa: A pilot molecular analysis of BRCA genes in early- onset breast cancer patients in Burkina Faso
2021 · Michela Biancolella, Nabonswindé Lamoussa Marie Ouedraogo, et al. · Research Square
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Profiling gene expression in peripheral blood mononuclear cells (PBMC) reflects the changes related to androgen and insulin metabolism pathway in recreational and competitive athletes.
2009 · Daniela Minella, Michela Biancolella, et al. · Cineca Institutional Research Information System (Tor Vergata University)
Works count: 26
Citation count: 311
H-index: 10
I10-index: 11
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