Setareh Moghadasi - Concepedia

Author

Setareh Moghadasi

Leiden University Medical Center ORCID

Also Known As

Moghadasi, Setareh, S. Moghadasi, Setareh Moghadasi

Publications

613

Citations

H-Index

Concepts

All Affiliations

Leiden University Medical Center Rigshospitalet Copenhagen University Hospital The Ohio State University Aalborg University Hospital

About

Setareh Moghadasi is an author at Leiden University Medical Center specializing in medicine, genetics, and bioinformatics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	4	4	257
2	Public Health	1	1	148
3	Social Sciences	1	1	48
4	Biostatistics	1	1	148
5	Epidemiology	1	1	148

Setareh Moghadasi

Publications

546

Citations

H-Index

Page 1

	Year	Citations
Large scale multifactorial likelihood quantitative analysis of <i>BRCA1</i> and <i>BRCA2</i> variants: An ENIGMA resource to support clinical variant classification Michael T. Parsons, Emma Tudini, Hongyan Li, Human Mutation GeneticsGenetic EpidemiologyPathologyMultifactorial Likelihood AnalysisDisease Gene Identification	2019	148
<i>BRCA2</i> Hypomorphic Missense Variants Confer Moderate Risks of Breast Cancer Hermela Shimelis, Romy L.S. Mesman, Catharina Von Nicolai, Cancer Research	2017	90
The <i>BRCA1</i> c. 5096G>A p.Arg1699Gln (R1699Q) intermediate risk variant: breast and ovarian cancer risk estimation and recommendations for clinical management from the ENIGMA consortium Setareh Moghadasi, Huong Meeks, Maaike P.G. Vreeswijk, Journal of Medical Genetics	2017	77
DLG4-related synaptopathy: a new rare brain disorder Agustí Rodríguez‐Palmero, Melissa M. Boerrigter, David Gómez‐Andrés, Genetics in Medicine Molecular NeuroscienceCorticobasal DegenerationNeurological DisorderDegenerative DiseaseDlg4-related Synaptopathy	2021	48
Downregulation of Vertebrate Tel (ETV6) and <i>Drosophila</i> Yan Is Facilitated by an Evolutionarily Conserved Mechanism of F-Box-Mediated Ubiquitination M. Guy Roukens, Mariam Alloul‐Ramdhani, Setareh Moghadasi, Molecular and Cellular Biology GeneticsGenomic MechanismMolecular GeneticsCell DifferentiationTranscriptional Regulation	2008	41
Functional Categorization of <i>BRCA1</i> Variants of Uncertain Clinical Significance in Homologous Recombination Repair Complementation Assays Peter Bouwman, Ingrid van der Heijden, Hanneke van der Gulden, Clinical Cancer Research	2020	38
Genetic Testing and Clinical Management Practices for Variants in Non-<i>BRCA1</i>/<i>2</i> Breast (and Breast/Ovarian) Cancer Susceptibility Genes: An International Survey by the Evidence-Based Network for the Interpretation of Germline Mutant Alleles (ENIGMA) Clinical Working Group Sarah M. Nielsen, Diana Eccles, Iris L. Romero, JCO Precision Oncology	2018	27
Variants of Uncertain Significance in <i>BRCA1</i> and <i>BRCA2</i> assessment of in silico analysis and a proposal for communication in genetic counselling Setareh Moghadasi, Nandy Hofland, Joyce N Wouts, Journal of Medical Genetics	2012	22
A terminal 3p26.3 deletion is not associated with dysmorphic features and intellectual disability in a four‐generation family Setareh Moghadasi, Arie van Haeringen, Lieke Langendonck, American Journal of Medical Genetics Part A	2014	20
Putting genome-wide sequencing in neonates into perspective Pleuntje J. van der Sluijs, Emmelien Aten, Daniela Q.C.M. Barge‐Schaapveld, Genetics in Medicine SequencingNeonatologyNewborn ScreeningGenome-wide SequencingNext-generation Sequencing	2018	20

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