Doris Škorić‐Milosavljević

Author

Amsterdam University Medical Centers ORCID

Also Known As

D Skoric-Milosavljevic, Doris Milosavljević, Doris Skoric-Milosavljevic, Doris Škorić-Milosavljević, Doris Škorić‐Milosavljević, Škorić-Milosavljević, Doris

Publications

562

Citations

H-Index

Concepts

All Affiliations

Amsterdam University Medical Centers Leiden University Medical Center University Medical Center Groningen University of Amsterdam Amsterdam UMC Location University of Amsterdam

DŠ

About

Doris Škorić‐Milosavljević is an author at Amsterdam University Medical Centers specializing in medicine, genetics, and cardiovascular genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	5	5	139
2	Public Health	2	2	38
3	Allergy	1	1	22
4	Emergency Medicine	1	1	51
5	Molecular Genetics	1	1	28

Doris Škorić‐Milosavljević

Publications

357

Citations

H-Index

Page 1

	Year	Citations
Enhancing rare variant interpretation in inherited arrhythmias through quantitative analysis of consortium disease cohorts and population controls Roddy Walsh, Najim Lahrouchi, Florence Kyndt, Genetics in Medicine	2020	100
<i>SCN5A</i> Mutation Type and a Genetic Risk Score Associate Variably With Brugada Syndrome Phenotype in <i>SCN5A</i> Families Yanushi D. Wijeyeratne, Michael W.T. Tanck, Yuka Mizusawa, Circulation Genomic and Precision Medicine	2020	63
Yield and Pitfalls of Ajmaline Testing in the Evaluation of Unexplained Cardiac Arrest and Sudden Unexplained Death Rafik Tadros, Eline A. Nannenberg, Krystien V.V. Lieve, JACC. Clinical electrophysiology Cardiogenic ShockCardiopulmonary ResuscitationCardiovascular DiseaseMedicineForensic Medicine	2017	51
Common Genetic Variants Contribute to Risk of Transposition of the Great Arteries Doris Škorić‐Milosavljević, Rafik Tadros, Fernanda M. Bosada, Circulation Research	2021	38
<i>GATA6</i> mutations: Characterization of two novel patients and a comprehensive overview of the GATA6 genotypic and phenotypic spectrum Doris Škorić‐Milosavljević, Fleur V.Y. Tjong, Julien Barc, American Journal of Medical Genetics Part A Gata6 MutationsGeneticsPathologyMolecular GeneticsNovel Patients	2019	28
Biallelic loss-of-function variants in PLD1 cause congenital right-sided cardiac valve defects and neonatal cardiomyopathy Najim Lahrouchi, Alex V. Postma, Christian Salazar, Journal of Clinical Investigation CardiomyopathyHeart FailureDevelopmental BiologyPld1 InhibitionCardiovascular Disease	2021	27
Two cases of <i>RIT1</i> associated Noonan syndrome: Further delineation of the clinical phenotype and review of the literature Doris Škorić‐Milosavljević, Eline Overwater, Saskia Tamminga, American Journal of Medical Genetics Part A Ras-mapk PathwayAllergyAutoimmune DiseaseGenetic DisorderGenetics	2016	22
Rare variants in KDR, encoding VEGF Receptor 2, are associated with tetralogy of Fallot Doris Škorić‐Milosavljević, Najim Lahrouchi, Fernanda M. Bosada, Genetics in Medicine	2021	17
Common genetic variants improve risk stratification after the atrial switch operation for transposition of the great arteries Odilia I. Woudstra, Doris Škorić‐Milosavljević, Barbara J.M. Mulder, International Journal of Cardiology Allelic VariantAtrial Switch OperationCardiovascular DiseaseGeneticsEvolutionary Biology	2022	11

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