Recent advances in prenatal genetic screening and testing

Autor Van den Veyver, Ignatia B.
Vydáno v F1000Res (2016)

The current and future impact of genome-wide sequencing on fetal precision medicine

Autor Sabbagh, Riwa, Van den Veyver, Ignatia B.
Vydáno v Hum Genet (2019)

Genome-Wide Sequencing for Prenatal Detection of Fetal Single-Gene Disorders

Autor Van den Veyver, Ignatia B., Eng, Christine M.
Vydáno v Cold Spring Harb Perspect Med (2015)

Counseling Challenges with Variants of Uncertain Significance and Incidental Findings in Prenatal Genetic Screening and Diagnosis

Autor Westerfield, Lauren, Darilek, Sandra, van den Veyver, Ignatia B.
Vydáno v J Clin Med (2014)

Do recent US Supreme Court rulings on patenting of genes and genetic diagnostics affect the practice of genetic screening and diagnosis in prenatal and reproductive care?

Autor Chandrasekharan, Subhashini, McGuire, Amy L., Van den Veyver, Ignatia B.
Vydáno v Prenat Diagn (2014)

Neuroimaging Aspects of Aicardi Syndrome

Autor Hopkins, Bobbi, Sutton, V. Reid, Lewis, Richard Alan, Van den Veyver, Ignatia, Clark, Gary
Vydáno 2008

Maternally expressed NLRP2 links the subcortical maternal complex (SCMC) to fertility, embryogenesis and epigenetic reprogramming

Autor Mahadevan, Sangeetha, Sathappan, Varsha, Utama, Budi, Lorenzo, Isabel, Kaskar, Khalied, Van den Veyver, Ignatia B.
Vydáno v Sci Rep (2017)

Erratum: Maternally expressed NLRP2 links the subcortical maternal complex (SCMC) to fertility, embryogenesis and epigenetic reprogramming

Autor Mahadevan, Sangeetha, Sathappan, Varsha, Utama, Budi, Lorenzo, Isabel, Kaskar, Khalied, Van den Veyver, Ignatia B.
Vydáno v Sci Rep (2017)

Independent variant analysis of TEAD1 and OCEL1 in 38 Aicardi syndrome patients

Autor Wong, Bibiana K. Y., Sutton, Vernon R., Lewis, Richard A., Van den Veyver, Ignatia B.
Vydáno v Mol Genet Genomic Med (2017)

Terminal Osseous Dysplasia with Pigmentary Defects Maps to Human Chromosome Xq27.3-Xqter

Autor Zhang, Wenzheng, Amir, Ruthie, Stockton, David W., Van den Veyver, Ignatia B., Bacino, Carlos A., Zoghbi, Huda Y.
Vydáno 2000

Expression profiling of clonal lymphocyte cell cultures from Rett syndrome patients

Autor Delgado, Ivan J, Kim, Dong Sun, Thatcher, Karen N, LaSalle, Janine M, Van den Veyver, Ignatia B
Vydáno 2006

Ophthalmologic findings in Aicardi syndrome

Autor Fruhman, Gary, Eble, Tanya N., Gambhir, Nikki, Sutton, V. Reid, Van den Veyver, Ignatia B., Lewis, Richard A.
Vydáno 2012

A genome-wide screen for copy number alterations in an adolescent pilot cohort with Müllerian anomalies

Autor Murry, Jaclyn B., Santos, Xiomara, Wang, Xiaoling, Wan, Ying-Wooi, Van den Veyver, Ignatia B., Dietrich, Jennifer E.
Vydáno v Fertil Steril (2014)

Chronic Maternal Low-Protein Diet in Mice Affects Anxiety, Night-Time Energy Expenditure and Sleep Patterns, but Not Circadian Rhythm in Male Offspring

Autor Crossland, Randy F., Balasa, Alfred, Ramakrishnan, Rajesh, Mahadevan, Sangeetha K., Fiorotto, Marta L., Van den Veyver, Ignatia B.
Vydáno v PLoS One (2017)

Correction: Chronic Maternal Low-Protein Diet in Mice Affects Anxiety, Night-Time Energy Expenditure and Sleep Patterns, but Not Circadian Rhythm in Male Offspring

Autor Crossland, Randy F., Balasa, Alfred, Ramakrishnan, Rajesh, Mahadevan, Sangeetha K., Fiorotto, Marta L., Van den Veyver, Ignatia B.
Vydáno v PLoS One (2018)

Use of amplicon-based sequencing for testing fetal identity and monogenic traits with Single Circulating Trophoblast (SCT) as one form of cell-based NIPT

Autor Zhuo, Xinming, Wang, Qun, Vossaert, Liesbeth, Salman, Roseen, Kim, Adriel, Van den Veyver, Ignatia, Breman, Amy, Beaudet, Arthur
Vydáno v PLoS One (2021)

A Genome-Wide Screen for Copy Number Alterations in Aicardi Syndrome

Autor Wang, Xiaoling, Sutton, V. Reid, Eble, Tanya, Lewis, Richard Alan, Gunaratne, Preethi, Patel, Ankita, Van den Veyver, Ignatia B.
Vydáno 2009

Terminal Osseous Dysplasia With Pigmentary Defects (TODPD): Follow-Up of the First Reported Family, Characterization of the Radiological Phenotype, and Refinement of the Linkage Re...

Autor Brunetti-Pierri, Nicola, Lachman, Ralph, Lee, Kwanghyuk, Leal, Suzanne M., Piccolo, Pasquale, Van den Veyver, Ignatia B., Bacino, Carlos A.
Vydáno 2010

GENOME-WIDE ARRAY-BASED COPY NUMBER PROFILING IN HUMAN PLACENTAS FROM UNEXPLAINED STILLBIRTHS

Autor Harris, R. Alan, Ferrari, Francesca, Ben-Shachar, Shay, Wang, Xiaoling, Saade, George, Van Den Veyver, Ignatia, Facchinetti, Fabio, Aagaard-Tillery, Kjersti
Vydáno 2011

Deletion of Porcn in Mice Leads to Multiple Developmental Defects and Models Human Focal Dermal Hypoplasia (Goltz Syndrome)

Autor Liu, Wei, Shaver, Timothy M., Balasa, Alfred, Ljungberg, M. Cecilia, Wang, Xiaoling, Wen, Shu, Nguyen, Hoang, Van den Veyver, Ignatia B.
Vydáno 2012