Recent advances in prenatal genetic screening and testing von Van den Veyver, Ignatia B

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The current and future impact of genome-wide sequencing on fetal precision medicine von Sabbagh, Riwa, Van den Veyver, Ignatia B.

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Prenatally diagnosed developmental abnormalities of the central nervous system and genetic syndromes: A practical review von Van den Veyver, Ignatia B.

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Non-invasive prenatal sequencing for multiple Mendelian monogenic disorders using circulating cell-free fetal DNA von Zhang, Jinglan, Li, Jianli, Saucier, Jennifer B., Feng, Yanming, Jiang, Yanjun, Sinson, Jefferson, McCombs, Anne K., Schmitt, Eric S., Peacock, Sandra, Chen, Stella, Dai, Hongzheng, Ge, Xiaoyan, Wang, Guoli, Shaw, Chad A., Mei, Hui, Breman, Amy, Xia, Fan, Yang, Yaping, Purgason, Anne, Pourpak, Alan, Chen, Zhao, Wang, Xia, Wang, Yue, Kulkarni, Shashikant, Choy, Kwong Wai, Wapner, Ronald J., Van den Veyver, Ignatia B., Beaudet, Arthur, Parmar, Sheetal, Wong, Lee-Jun, Eng, Christine M.

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Prenatal exomes and genomes – so much new and so much more to learn von Veyver, Ignatia B.

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International Society for Prenatal Diagnosis Updated Position Statement on the use of genome‐wide sequencing for prenatal diagnosis von Van den Veyver, Ignatia B., Chandler, Natalie, Wilkins‐Haug, Louise E., Wapner, Ronald J., Chitty, Lyn S.

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Parental mosaicism for apparent de novo genetic variants: Scope, detection, and counseling challenges von Zemet, Roni, Veyver, Ignatia B., Stankiewicz, Paweł

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Overview and recent developments in cell‐based noninvasive prenatal testing von Vossaert, Liesbeth, Chakchouk, Imen, Zemet, Roni, Van den Veyver, Ignatia B.

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International Society for Prenatal Diagnosis 2022 debate 3—Fetal genome sequencing should be offered to all pregnant patients von Veyver, Ignatia B., Yaron, Yuval, Deans, Zandra C.

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Take your mother's ferry: preimplantation embryo development requires maternal karyopherins for nuclear transport von Sharif, Momal, Detti, Laura, Van den Veyver, Ignatia B

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Maternally expressed NLRP2 links the subcortical maternal complex (SCMC) to fertility, embryogenesis and epigenetic reprogramming von Mahadevan, Sangeetha, Sathappan, Varsha, Utama, Budi, Lorenzo, Isabel, Kaskar, Khalied, Van den Veyver, Ignatia B.

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Deletion of Porcn in Mice Leads to Multiple Developmental Defects and Models Human Focal Dermal Hypoplasia (Goltz Syndrome) von Liu, Wei, Shaver, Timothy M, Balasa, Alfred, Ljungberg, M. Cecilia, Wang, Xiaoling, Wen, Shu, Nguyen, Hoang, Van den Veyver, Ignatia B, Singh, Shree Ram

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Improving the prenatal diagnosis of Beckwith–Wiedemann syndrome von Veyver, Ignatia B.

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Facilitating variant curation sharing for fetal precision genomics: A new venture for prenatal diagnosis von Chitty, Lyn S., Veyver, Ignatia B.

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Causative Mutations and Mechanism of Androgenetic Hydatidiform Moles von Nguyen, Ngoc Minh Phuong, Ge, Zhao-Jia, Reddy, Ramesh, Fahiminiya, Somayyeh, Sauthier, Philippe, Bagga, Rashmi, Sahin, Feride Iffet, Mahadevan, Sangeetha, Osmond, Matthew, Breguet, Magali, Rahimi, Kurosh, Lapensee, Louise, Hovanes, Karine, Srinivasan, Radhika, Van den Veyver, Ignatia B., Sahoo, Trilochan, Ao, Asangla, Majewski, Jacek, Taketo, Teruko, Slim, Rima

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The uptake of pan‐ethnic expanded carrier screening is higher when offered during preconception or early prenatal genetic counseling von Larsen, Dana, Ma, Jingmei, Strassberg, Melissa, Ramakrishnan, Rajesh, Van den Veyver, Ignatia B.

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Lower fetal fraction in clinical cell‐free DNA screening results is associated with increased risk of hypertensive disorders of pregnancy von Madala, Deeksha, Maktabi, Mohamad Ali, Sabbagh, Riwa, Erfani, Hadi, Moon, Andrea, Veyver, Ignatia B.

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DNA Methylation Dynamics in the Female Germline and Maternal-Effect Mutations That Disrupt Genomic Imprinting von Anvar, Zahra, Chakchouk, Imen, Demond, Hannah, Sharif, Momal, Kelsey, Gavin, Van den Veyver, Ignatia B

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Current controversies in prenatal diagnosis 2: The 59 genes ACMG recommends reporting as secondary findings when sequencing postnatally should be reported when detected on fetal (a... von Amor, David J., Chitty, Lyn S., Van den Veyver, Ignatia B.

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Clinical exome sequencing for fetuses with ultrasound abnormalities and a suspected Mendelian disorder von Normand, Elizabeth A, Braxton, Alicia, Nassef, Salma, Ward, Patricia A, Vetrini, Francesco, He, Weimin, Patel, Vipulkumar, Qu, Chunjing, Westerfield, Lauren E, Stover, Samantha, Dharmadhikari, Avinash V, Muzny, Donna M, Gibbs, Richard A, Dai, Hongzheng, Meng, Linyan, Wang, Xia, Xiao, Rui, Liu, Pengfei, Bi, Weimin, Xia, Fan, Walkiewicz, Magdalena, Van den Veyver, Ignatia B, Eng, Christine M, Yang, Yaping

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