IGNATIA VAN DEN VEYVER to Congenital Abnormalities
This is a "connection" page, showing publications IGNATIA VAN DEN VEYVER has written about Congenital Abnormalities.
Connection Strength
1.351
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Prenatal Metabolomics Analysis and Fetal Congenital Anomalies and Genetic Conditions: A Review of Current Literature. Prenat Diagn. 2025 11; 45(12):1544-1558.
Score: 0.692
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Loss of the maternal effect gene NLRP2 impairs embryonic and extra-embryonic development, revealing a novel genetic cause of congenital anomalies?. Biol Reprod. 2026 04 13; 114(4):1469-1485.
Score: 0.180
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The Perspectives and Experiences of Prospective Parents Declining Diagnostic Prenatal Genome Sequencing in Continuing Pregnancies With Fetal Structural Anomalies. Prenat Diagn. 2026 05; 46(5-6):727-736.
Score: 0.175
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Diagnostic Yield of Exome Sequencing for Pregnancies With and Without Fetal Anomalies and for Stillbirth. Prenat Diagn. 2025 09; 45(10):1313-1324.
Score: 0.169
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Promises, pitfalls and practicalities of prenatal whole exome sequencing. Prenat Diagn. 2018 01; 38(1):10-19.
Score: 0.098
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Rare variant enrichment analysis supports GREB1L as a contributory driver gene in the etiology of Mayer-Rokitansky-K?ster-Hauser syndrome. HGG Adv. 2023 07 13; 4(3):100188.
Score: 0.036