Elina Molou - Concepedia

Author

Elina Molou

National and Kapodistrian University of Athens

Also Known As

Elina Molou

Publications

177

Citations

H-Index

Concepts

All Affiliations

National and Kapodistrian University of Athens Children's Hospital Agia Sophia Institute of Child Health IASO General Hospital Screen

About

Elina Molou is an author at National and Kapodistrian University of Athens specializing in medicine, genetics, and molecular diagnostics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	5	5	66
2	Public Health	2	2	27
3	Education	1	1	11
4	Biochemistry	1	1	12
5	Biostatistics	1	1	15

Elina Molou

Publications

150

Citations

H-Index

Page 1

	Year	Citations
Expanded newborn screening in Greece: 30 months of experience Yannis L. Loukas, Georgios‐Stefanos Soumelas, Yannis Dotsikas, Journal of Inherited Metabolic Disease	2010	43
High incidence of partial biotinidase deficiency cases in newborns of Greek origin Georgia Thodi, Kleopatra H. Schulpis, Elina Molou, Gene Greek OriginInherited Metabolic DiseaseHigh IncidencePediatrics	2013	26
Study of the effect of CYP2C19 polymorphisms on omeprazole pharmacokinetics by utilizing validated LC–MS/MS and Real Time-PCR methods Maria Koukoula, Yannis Dotsikas, Elina Molou, Journal of Chromatography B Molecular PharmacologyPharmacologyCyp2c19 PolymorphismsPharmacogenomicsPharmacotherapy	2016	17
Clinical diagnostic Next-Generation sequencing: The case of <i>CFTR</i> carrier screening Yannis L. Loukas, Georgia Thodi, Elina Molou, Scandinavian Journal of Clinical and Laboratory Investigation Genetic TestingGeneticsAcog PanelGenetic EpidemiologyPathology	2015	15
Hawkinsinuria in two unrelated Greek newborns: identification of a novel variant, biochemical findings and treatment Georgia Thodi, Kleopatra H. Schulpis, Yannis Dotsikas, Journal of Pediatric Endocrinology and Metabolism	2015	15
Glucose-6-Phosphate Dehydrogenase (G6PD) deficiency in Greek newborns: The Mediterranean C563T mutation screening Elina Molou, Kleopatra H. Schulpis, Georgia Thodi, Scandinavian Journal of Clinical and Laboratory Investigation GeneticsGenetic EpidemiologyHuman PolymorphismPathologyMolecular Genetics	2014	12
Mutational analysis for biotinidase deficiency of a Greek patients’ cohort ascertained through expanded newborn screening Georgia Thodi, Elina Molou, Vassiliki Georgiou, Journal of Human Genetics Genetic TestingMutational AnalysisGenetic DisorderMedicineGenetics	2011	11
Mutational analysis of <i>GALT</i> gene in Greek patients with galactosaemia: identification of two novel mutations and clinical evaluation Kleopatra H. Schulpis, Georgia Thodi, Konstantinos Iakovou, Scandinavian Journal of Clinical and Laboratory Investigation GeneticsMotor DevelopmentPathologyEducationMolecular Genetics	2017	11

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