Vyne van der Schoot - Erasmus MC | 人才画像

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论文共 16 篇作者统计合作学者相似作者

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Exploring Uncertainties Regarding Unsolicited Findings in Genetic Testing

Vyne van der Schoot, Eline van der Meer,Marij A. Hillen,Helger G. Yntema,Han G. Brunner,Anke J. M. Oerlemans

PATIENT EDUCATION AND COUNSELING (2024)

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Knowledge on Genetic Cause and Awareness of Reproductive Options in Patients with Inherited Retinal Dystrophies

Virginie Verhoeven,Malou Heijligers,Sonja de Munnik,Pam Heutinck,Vyne Van der Schoot,Marianne van Tienhoven,Lies Hoefsloot,Anneke Kievit, A. Thiadens, Magda Meester-Smoor,Caroline Klaver

EUROPEAN JOURNAL OF HUMAN GENETICS (2024): 374-374

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Response to the Comment on Diderich Et Al. "the Role of a Multidisciplinary Team in Managing Variants of Uncertain Clinical Significance in Prenatal Genetic Diagnosis" (EJMG 66(10),104844)

Karin E. M. Diderich,Jasmijn E. Klapwijk,Vyne van der Schoot,Myrthe van den Born,Martina Wilke,Marieke Joosten,Kyra E. Stuurman,Lies H. Hoefsloot,Diane Van Opstal,Hennie T. Bruggenwirth,Malgorzata I. Srebniak

European Journal of Medical Genetics (2024): 104884

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Limited Additional Value of Karyotyping Cultured Amniotic Fluid Cell Colonies in Addition to Microarray on Uncultured Cells for Confirmation of Abnormal Non-Invasive Prenatal Testing Results

Stephany H. Donze,Malgorzata I. Srebniak,Karin E. M. Diderich,Myrthe van den Born,Robert-Jan Galjaard,Lutgarde C. P. Govaerts,Vyne van der Schoot,Maarten F. C. M. Knapen,Marieke Joosten,Diane Van Opstal

PRENATAL DIAGNOSISno. 4 (2024): 401-408

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Clinical Geneticists' Views on and Experiences with Unsolicited Findings in Next-Generation Sequencing: "A Great Technology Creating New Dilemmas"

Vyne van der Schoot,Carlijn Damste,Helger Yntema,Han Brunner,Anke Oerlemans

EUROPEAN JOURNAL OF HUMAN GENETICS（2023）

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Challenges and Pragmatic Solutions in Pre-Test and Post-Test Genetic Counseling for Prenatal Exome Sequencing

Karin E. M. Diderich,Jasmijn E. Klapwijk,Vyne van der Schoot,Hennie Bruggenwirth,Marieke Joosten,Malgorzata Srebniak

APPLICATION OF CLINICAL GENETICS (2023): 89-97

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Reporting uncertain prenatal exome sequencing results: how do medical students handle uncertainty

Jasmijn E. Klapwijk,Marike G. Polak,Karin E. M. Diderich,Malgorzata I. Srebniak,Hennie T. Bruggenwirth,Stina Lou,Ida Vogel,Vyne van der Schoot,Iris M. Bakkeren,Katinka Dijkstra,Sam Riedijk

EUROPEAN JOURNAL OF HUMAN GENETICS（2022）

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Whole Exome Sequencing of Known Eye Genes Reveals Genetic Causes for High Myopia

Annechien E. G. Haarman,Alberta A. H. J. Thiadens,Marianne van Tienhoven,Sjoukje E. Loudon,J. E. M. M. Annelies de Klein,Erwin Brosens,Jan Roelof Polling,Vyne van der Schoot,Arjan Bouman,Anneke J. A. Kievit,Lies H. Hoefsloot,Caroline C. W. Klaver,Virginie J. M. Verhoeven

Human Molecular Genetics（2022）

引用18浏览0WOS引用

Lessons Learned from Unsolicited Findings in Clinical Exome Sequencing of 16,482 Individuals

Vyne van der Schoot,Lonneke Haer-Wigman,Ilse Feenstra,Femke Tammer,Anke J. M. Oerlemans,Martine P. A. van Koolwijk,Frans van Agt,Yvonne H. J. M. Arens,Han G. Brunner,Lisenka E. L. M. Vissers,Helger G. Yntema

European Journal of Human Genetics（2021）

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