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1. NOVEL INSIGHTS INTO THE GENETIC ETIOLOGY OF BIPOLAR DISORDER FROM A MULTI-ANCESTRY GENOME-WIDE ASSOCIATION STUDY FROM THE PSYCHIATRIC GENOMICS CONSORTIUM
1. NOVEL INSIGHTS INTO THE GENETIC ETIOLOGY OF BIPOLAR DISORDER FROM A MULTI-ANCESTRY GENOME-WIDE ASSOCIATION STUDY FROM THE PSYCHIATRIC GENOMICS CONSORTIUM
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1. NOVEL INSIGHTS INTO THE GENETIC ETIOLOGY OF BIPOLAR DISORDER FROM A MULTI-ANCESTRY GENOME-WIDE ASSOCIATION STUDY FROM THE PSYCHIATRIC GENOMICS CONSORTIUM

Koromina, Maria

European neuropsychopharmacology, 2023-10, Vol.75, p.S56-S56 [Periódico revisado por pares]

Elsevier B.V

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Discovery of new drug indications for COVID-19: A drug repurposing approach
Discovery of new drug indications for COVID-19: A drug repurposing approach
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Discovery of new drug indications for COVID-19: A drug repurposing approach

Kumari, Priyanka ; Pradhan, Bikram ; Koromina, Maria ; Patrinos, George P ; Steen, Kristel Van Yang, Jinn-Moon

PloS one, 2022-05, Vol.17 (5), p.e0267095 [Periódico revisado por pares]

United States: Public Library of Science

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Delineating significant genome-wide associations of variants with antipsychotic and antidepressant treatment response: implications for clinical pharmacogenomics
Delineating significant genome-wide associations of variants with antipsychotic and antidepressant treatment response: implications for clinical pharmacogenomics
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Delineating significant genome-wide associations of variants with antipsychotic and antidepressant treatment response: implications for clinical pharmacogenomics

Koromina, Maria ; Koutsilieri, Stefania ; Patrinos, George P

Human genomics, 2020-01, Vol.14 (1), p.4-4, Article 4 [Periódico revisado por pares]

England: BioMed Central

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4
Genome-based therapeutic interventions for β-type hemoglobinopathies
Genome-based therapeutic interventions for β-type hemoglobinopathies
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Genome-based therapeutic interventions for β-type hemoglobinopathies

Karamperis, Kariofyllis ; Tsoumpeli, Maria T ; Kounelis, Fotios ; Koromina, Maria ; Mitropoulou, Christina ; Moutinho, Catia ; Patrinos, George P

Human genomics, 2021-06, Vol.15 (1), p.32-32, Article 32 [Periódico revisado por pares]

England: BioMed Central

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5
A novel machine learning-based approach for the computational functional assessment of pharmacogenomic variants
A novel machine learning-based approach for the computational functional assessment of pharmacogenomic variants
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A novel machine learning-based approach for the computational functional assessment of pharmacogenomic variants

Pandi, Maria-Theodora ; Koromina, Maria ; Tsafaridis, Iordanis ; Patsilinakos, Sotirios ; Christoforou, Evangelos ; van der Spek, Peter J ; Patrinos, George P

Human genomics, 2021-08, Vol.15 (1), p.51-51, Article 51 [Periódico revisado por pares]

England: BioMed Central

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6
A Novel Text-Mining Approach for Retrieving Pharmacogenomics Associations From the Literature
A Novel Text-Mining Approach for Retrieving Pharmacogenomics Associations From the Literature
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A Novel Text-Mining Approach for Retrieving Pharmacogenomics Associations From the Literature

Pandi, Maria-Theodora ; van der Spek, Peter J ; Koromina, Maria ; Patrinos, George P

Frontiers in pharmacology, 2020-11, Vol.11, p.602030-602030 [Periódico revisado por pares]

Switzerland: Frontiers Research Foundation

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7
Genome-wide analysis toward the epigenetic aetiology of myelodysplastic syndrome disease progression and pharmacoepigenomic basis of hypomethylating agents drug treatment response
Genome-wide analysis toward the epigenetic aetiology of myelodysplastic syndrome disease progression and pharmacoepigenomic basis of hypomethylating agents drug treatment response
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Genome-wide analysis toward the epigenetic aetiology of myelodysplastic syndrome disease progression and pharmacoepigenomic basis of hypomethylating agents drug treatment response

Siamoglou, Stavroula ; Boers, Ruben ; Koromina, Maria ; Boers, Joachim ; Tsironi, Anna ; Chatzilygeroudi, Theodora ; Lazaris, Vasileios ; Verigou, Evgenia ; Kourakli, Alexandra ; van IJcken, Wilfred F J ; Gribnau, Joost ; Symeonidis, Argiris ; Patrinos, George P

Human genomics, 2023-04, Vol.17 (1), p.37-37, Article 37 [Periódico revisado por pares]

England: BioMed Central

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8
Exome-Wide Analysis of the DiscovEHR Cohort Reveals Novel Candidate Pharmacogenomic Variants for Clinical Pharmacogenomics
Exome-Wide Analysis of the DiscovEHR Cohort Reveals Novel Candidate Pharmacogenomic Variants for Clinical Pharmacogenomics
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Exome-Wide Analysis of the DiscovEHR Cohort Reveals Novel Candidate Pharmacogenomic Variants for Clinical Pharmacogenomics

Pandi, Maria-Theodora ; Williams, Marc S ; van der Spek, Peter ; Koromina, Maria ; Patrinos, George P

Genes, 2020-05, Vol.11 (5), p.561 [Periódico revisado por pares]

Switzerland: MDPI AG

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9
VARIANT TO FUNCTION: INNOVATION AND INSIGHTS FROM FINE-MAPPING AND HIGH-THROUGHPUT ASSAYS
VARIANT TO FUNCTION: INNOVATION AND INSIGHTS FROM FINE-MAPPING AND HIGH-THROUGHPUT ASSAYS
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VARIANT TO FUNCTION: INNOVATION AND INSIGHTS FROM FINE-MAPPING AND HIGH-THROUGHPUT ASSAYS

Koromina, Maria ; Ripke, Stephan ; Edenberg, Howard

European neuropsychopharmacology, 2023-10, Vol.75, p.S5-S5 [Periódico revisado por pares]

Elsevier B.V

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10
Rethinking Drug Repositioning and Development with Artificial Intelligence, Machine Learning, and Omics
Rethinking Drug Repositioning and Development with Artificial Intelligence, Machine Learning, and Omics
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Rethinking Drug Repositioning and Development with Artificial Intelligence, Machine Learning, and Omics

Koromina, Maria ; Pandi, Maria-Theodora ; Patrinos, George P.

Omics (Larchmont, N.Y.), 2019-11, Vol.23 (11), p.539-548 [Periódico revisado por pares]

United States: Mary Ann Liebert, Inc., publishers

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