Malgorzata I. Srebniak

Author

Also Known As

L Govaerts, L Hoefsloot, M I Srebniak, M. I. Srebniak, M.I. Srebniak, Malgorzata I Srebniak, Malgorzata I. Srebniak, Malgorzata Ilona Srebniak, Malgorzata Srebniak, Małgorzata Srebniak

103

Publications

2.5K

Citations

H-Index

Concepts

All Affiliations

Erasmus MC Erasmus University Rotterdam Leiden University Medical Center Radboud University Medical Center Amsterdam University Medical Centers

About

Malgorzata I. Srebniak is an author at Erasmus MC specializing in medicine, prenatal diagnosis, and public health.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	11	11	547
2	Public Health	8	8	413
3	Social Sciences	1	1	42
4	Biostatistics	1	1	30
5	Cell Biology	1	1	22

Malgorzata I. Srebniak

Publications

1.6K

Citations

H-Index

Page 1

	Year	Citations
TRIDENT-2: National Implementation of Genome-wide Non-invasive Prenatal Testing as a First-Tier Screening Test in the Netherlands Karuna R. M. van der Meij, Erik A. Sistermans, Merryn Macville, The American Journal of Human Genetics	2019	364
Application of SNP array for rapid prenatal diagnosis: implementation, genetic counselling and diagnostic flow Malgorzata I. Srebniak, Marjan Boter, Grétel Oudesluijs, European Journal of Human Genetics Genetic TestingPrenatal Genetic TestingRapid Prenatal DiagnosisGeneticsMedicine	2011	107
Clinical impact of additional findings detected by genome-wide non-invasive prenatal testing: Follow-up results of the TRIDENT-2 study Lisanne van Prooyen Schuurman, Erik A. Sistermans, Diane Van Opstal, The American Journal of Human Genetics	2022	94
Prenatal SNP array testing in 1000 fetuses with ultrasound anomalies: causative, unexpected and susceptibility CNVs Malgorzata I. Srebniak, Karin E. M. Diderich, Marieke Joosten, European Journal of Human Genetics Developmental AnomalyUltrasound AnomaliesPrenatal Genetic TestingPrenatal Snp ArrayPrenatal Genetic Screening	2015	79
Genomic SNP array as a gold standard for prenatal diagnosis of foetal ultrasound abnormalities Malgorzata I. Srebniak, Marjan Boter, Grétel Oudesluijs, Molecular Cytogenetics	2012	75
Abnormal non-invasive prenatal test results concordant with karyotype of cytotrophoblast but not reflecting abnormal fetal karyotype Malgorzata I. Srebniak, Karin E. M. Diderich, Petra Noomen, Ultrasound in Obstetrics and Gynecology Mosaic Male KaryotypeGenetic TestingFertilityFetal KaryotypeGenetics	2014	69
Phenotypic variability of atypical 22q11.2 deletions not including<i>TBX1</i> Judith M.A. Verhagen, Karin E. M. Diderich, Grétel Oudesluijs, American Journal of Medical Genetics Part A Interstitial DeletionsGeneticsPathologyMolecular GeneticsDisease Gene Identification	2012	67
Noninvasive Prenatal Test Results Indicative of Maternal Malignancies: A Nationwide Genetic and Clinical Follow-Up Study Catharina J. Heesterbeek, Sietse Aukema, Robert‐Jan H. Galjaard, Journal of Clinical Oncology	2022	52
Benefits and Burdens of Using a SNP Array in Pregnancies at Increased Risk for the Common Aneuploidies Diane Van Opstal, Femke de Vries, Lutgarde Govaerts, Human Mutation FertilityGeneticsGenetic EpidemiologyReproductive HealthGynecology	2014	51
Pregnant couples at increased risk for common aneuploidies choose maximal information from invasive genetic testing Sanne Steen, Karin E. M. Diderich, Sam Riedijk, Clinical Genetics	2014	50

Page 1