Ignatia B Van den Veyver (Ignatia Van den Veyver)

ORCID

Publication Activity (10 Years)

Years Active: 2019-2024
Publications (10 Years): 36

Top Venues

Prenatal diagnosis

medRxiv : the preprint server for health sciences

Reproductive sciences (Thousand Oaks, Calif.)

Clinical case reports

Baylor College of Medicine

This page only lists publications with an associated author ORCID identifier.

Affiliation History

Baylor College of Medicine

United States

Professor :: Molecular and Human Genetics

Baylor College of Medicine

United States

Professor :: Obstetrics and Gynecology

Publications

Pilar Cacheiro, Samantha Lawson, Ignatia B Van den Veyver, Gabriel Marengo, David Zocche, Stephen A Murray, Michael Henri Duyzend, Peter Nick Robinson, Damian Smedley
Lethal phenotypes in Mendelian disorders. medRxiv : the preprint server for health sciences (2024)
Pilar Cacheiro, Samantha Lawson, Ignatia B Van den Veyver, Gabriel Marengo, David Zocche, Stephen A Murray, Michael Henri Duyzend, Peter Nick Robinson, Damian Smedley
Lethal phenotypes in Mendelian disorders. medRxiv : the preprint server for health sciences (2024)
Pilar Cacheiro, Samantha Lawson, Ignatia B Van den Veyver, Gabriel Marengo, David Zocche, Stephen A Murray, Michael Henri Duyzend, Peter Nick Robinson, Damian Smedley
Lethal phenotypes in Mendelian disorders. medRxiv : the preprint server for health sciences (2024)
Pilar Cacheiro, Samantha Lawson, Ignatia B Van den Veyver, Gabriel Marengo, David Zocche, Stephen A Murray, Michael Henri Duyzend, Peter Nick Robinson, Damian Smedley
Lethal phenotypes in Mendelian disorders. medRxiv : the preprint server for health sciences (2024)
Pilar Cacheiro, Samantha Lawson, Ignatia B Van den Veyver, Gabriel Marengo, David Zocche, Stephen A Murray, Michael Henri Duyzend, Peter Nick Robinson, Damian Smedley
Lethal phenotypes in Mendelian disorders. medRxiv : the preprint server for health sciences (2024)
Pilar Cacheiro, Samantha Lawson, Ignatia B Van den Veyver, Gabriel Marengo, David Zocche, Stephen A Murray, Michael Henri Duyzend, Peter Nick Robinson, Damian Smedley
Lethal phenotypes in Mendelian disorders. medRxiv : the preprint server for health sciences (2024)
Takuya Sakyu, Samantha R Stover, Yue Wang, Patricia Ward, Manisha Gandhi, Michael C Braun, Ignatia B Van den Veyver, Weimin Bi
Compound heterozygosity of a de novo submicroscopic deletion and an inherited frameshift pathogenic variant in the PKHD1 gene in a fetus with bilaterally enlarged and echogenic kidneys, enlarged abdomen and oligohydramnios. Clinical case reports 11 (2) (2023)
Ivonne Alexandra Bedei, Tascha Gehrke, Karl-Philipp Gloning, Matthias Meyer-Wittkopf, Daria Willner, Martin Krapp, Alexander Scharf, Jan Degenhardt, Kai-Sven Heling, Peter Kozlowski, Kathrin Trautmann, Kai M Jahns, Annegret Geipel, Jan-Erik Baumüller, Lucas Wilhelm, Ingo Gottschalk, Andreas Schröer, Alexander Graf, Aline Wolter, Johanna Schenk, Axel Weber, Ignatia B Van den Veyver, Roland Axt-Fliedner
Multicenter clinical experience with non-invasive cell-free DNA screening for monosomy X and related X-chromosome variants. Prenatal diagnosis 43 (2) (2023)
Ivonne Alexandra Bedei, Tascha Gehrke, Karl-Philipp Gloning, Matthias Meyer-Wittkopf, Daria Willner, Martin Krapp, Alexander Scharf, Jan Degenhardt, Kai-Sven Heling, Peter Kozlowski, Kathrin Trautmann, Kai M Jahns, Annegret Geipel, Jan-Erik Baumüller, Lucas Wilhelm, Ingo Gottschalk, Andreas Schröer, Alexander Graf, Aline Wolter, Johanna Schenk, Axel Weber, Ignatia B Van den Veyver, Roland Axt-Fliedner
Multicenter clinical experience with non-invasive cell-free DNA screening for monosomy X and related X-chromosome variants. Prenatal diagnosis 43 (2) (2023)
Zahra Anvar, Imen Chakchouk, Momal Sharif, Sangeetha Mahadevan, Eleni Theodora Nasiotis, Li Su, Zhandong Liu, Ying-Wooi Wan, Ignatia B Van den Veyver
Loss of the Maternal Effect Gene Nlrp2 Alters the Transcriptome of Ovulated Mouse Oocytes and Impacts Expression of Histone Demethylase KDM1B. Reproductive sciences (Thousand Oaks, Calif.) (2023)
Ivonne Alexandra Bedei, Tascha Gehrke, Karl-Philipp Gloning, Matthias Meyer-Wittkopf, Daria Willner, Martin Krapp, Alexander Scharf, Jan Degenhardt, Kai-Sven Heling, Peter Kozlowski, Kathrin Trautmann, Kai M Jahns, Annegret Geipel, Jan-Erik Baumüller, Lucas Wilhelm, Ingo Gottschalk, Andreas Schröer, Alexander Graf, Aline Wolter, Johanna Schenk, Axel Weber, Ignatia B Van den Veyver, Roland Axt-Fliedner
Multicenter clinical experience with non-invasive cell-free DNA screening for monosomy X and related X-chromosome variants. Prenatal diagnosis (2023)
Ivonne Alexandra Bedei, Tascha Gehrke, Karl-Philipp Gloning, Matthias Meyer-Wittkopf, Daria Willner, Martin Krapp, Alexander Scharf, Jan Degenhardt, Kai-Sven Heling, Peter Kozlowski, Kathrin Trautmann, Kai M Jahns, Annegret Geipel, Jan-Erik Baumüller, Lucas Wilhelm, Ingo Gottschalk, Andreas Schröer, Alexander Graf, Aline Wolter, Johanna Schenk, Axel Weber, Ignatia B Van den Veyver, Roland Axt-Fliedner
Multicenter clinical experience with non-invasive cell-free DNA screening for monosomy X and related X-chromosome variants. Prenatal diagnosis (2023)
Zahra Anvar, Imen Chakchouk, Momal Sharif, Sangeetha Mahadevan, Eleni Theodora Nasiotis, Li Su, Zhandong Liu, Ying-Wooi Wan, Ignatia B Van den Veyver
Loss of the Maternal Effect Gene Nlrp2 Alters the Transcriptome of Ovulated Mouse Oocytes and Impacts Expression of Histone Demethylase KDM1B. Reproductive sciences (Thousand Oaks, Calif.) (2023)
Ivonne Alexandra Bedei, Tascha Gehrke, Karl-Philipp Gloning, Matthias Meyer-Wittkopf, Daria Willner, Martin Krapp, Alexander Scharf, Jan Degenhardt, Kai-Sven Heling, Peter Kozlowski, Kathrin Trautmann, Kai M Jahns, Annegret Geipel, Jan-Erik Baumüller, Lucas Wilhelm, Ingo Gottschalk, Andreas Schröer, Alexander Graf, Aline Wolter, Johanna Schenk, Axel Weber, Ignatia B Van den Veyver, Roland Axt-Fliedner
Multicenter clinical experience with non-invasive cell-free DNA screening for monosomy X and related X-chromosome variants. Prenatal diagnosis 43 (2) (2023)
Takuya Sakyu, Samantha R Stover, Yue Wang, Patricia Ward, Manisha Gandhi, Michael C Braun, Ignatia B Van den Veyver, Weimin Bi
Compound heterozygosity of a de novo submicroscopic deletion and an inherited frameshift pathogenic variant in the PKHD1 gene in a fetus with bilaterally enlarged and echogenic kidneys, enlarged abdomen and oligohydramnios. Clinical case reports 11 (2) (2023)
Zahra Anvar, Imen Chakchouk, Momal Sharif, Sangeetha Mahadevan, Li Su, Swathi Anikar, Fatemeh Alavi Naini, Alloysius Budi Utama, Ignatia B Van den Veyver
Comparison of Four Protocols for In Vitro Differentiation of Human Embryonic Stem Cells into Trophoblast Lineages by BMP4 and Dual Inhibition of Activin/Nodal and FGF2 Signaling. Reproductive sciences (Thousand Oaks, Calif.) (2023)
Bobby K Brar, Marisa Gilstrop Thompson, Neeta L Vora, Kelly Gilmore, Karin Blakemore, Kristen A Miller, Jessica L Giordano, Andreas Dufke, Beatrix Wong, Samantha Stover, Billie Lianoglou, Ignatia B Van den Veyver, Esther Dempsey, Mara Rosner, Karen Chong, David Chitayat, Teresa N Sparks, Mary E Norton, Ronald Wapner, Kristin Baranano, Angie C Jelin, null null
Prenatal phenotyping of fetal tubulinopathies: A multicenter retrospective case series. Prenatal diagnosis (2022)
Ignatia B Van den Veyver, Yuval Yaron, Zandra C Deans
International Society for Prenatal Diagnosis 2022 debate 3-Fetal genome sequencing should be offered to all pregnant patients. Prenatal diagnosis (2022)
Catherine G Kernie, Julia Wynn, Allison Rosenbaum, Jessica de Voest, Stephanie Galloway, Jessica L Giordano, Samantha Stover, Lauren Westerfield, Kelly Gilmore, Ronald J Wapner, Ignatia B Van den Veyver, Neeta L Vora, Rebecca G Clifton, Aaron B Caughey, Wendy K Chung
Information is power: The experiences, attitudes and needs of individuals who chose to have prenatal genomic sequencing for fetal anomalies. Prenatal diagnosis 42 (7) (2022)
Brielle Crovetti, Mohamad Ali Maktabi, Hadi Erfani, Tachjaree Panchalee, Qun Wang, Liesbeth Vossaert, Ignatia B Van den Veyver
Circulating trophoblast numbers as a potential marker for pregnancy complications. Prenatal diagnosis 42 (9) (2022)
Ignatia B Van den Veyver
Prenatal exomes and genomes - so much new and so much more to learn. Prenatal diagnosis 42 (6) (2022)
Ignatia B Van den Veyver, Natalie Jane Chandler, Louise E Wilkins-Haug, Ronald J Wapner, Lyn S Chitty, null null
International Society for Prenatal Diagnosis Updated Position Statement on the use of genome-wide sequencing for prenatal diagnosis. Prenatal diagnosis 42 (6) (2022)
Lyn S Chitty, Ignatia B Van den Veyver
Facilitating variant curation sharing for fetal precision genomics: A new venture for prenatal diagnosis. Prenatal diagnosis 42 (12) (2022)
Deeksha Madala, Mohamad Ali Maktabi, Riwa Sabbagh, Hadi Erfani, Andrea Moon, Ignatia B Van den Veyver
Lower fetal fraction in clinical cell-free DNA screening results is associated with increased risk of hypertensive disorders of pregnancy. Prenatal diagnosis 42 (10) (2022)
Roni Zemet, Ignatia B Van den Veyver, Przemyslaw Szafranski
Parental mosaicism for apparent de novo genetic variants: Scope, detection, and counseling challenges. Prenatal diagnosis 42 (7) (2022)
Ignatia B Van den Veyver
Improving the prenatal diagnosis of Beckwith-Wiedemann syndrome. Prenatal diagnosis 41 (7) (2021)
Xinming Zhuo, Qun Wang, Liesbeth Vossaert, Roseen Salman, Adriel Kim, Ignatia B Van den Veyver, Amy Breman, Arthur Beaudet
Use of amplicon-based sequencing for testing fetal identity and monogenic traits with Single Circulating Trophoblast (SCT) as one form of cell-based NIPT. PloS one 16 (4) (2021)
Liesbeth Vossaert, Imen Chakchouk, Roni Zemet, Ignatia B Van den Veyver
Overview and recent developments in cell-based noninvasive prenatal testing. Prenatal diagnosis 41 (10) (2021)
Sara E Arian, Hadi Erfani, Lauren E Westerfield, Alexandra Buffie, Salma Nassef, William E Gibbons, Ignatia B Van den Veyver
Prenatal testing in pregnancies conceived by in vitro fertilization with pre-implantation genetic testing. Prenatal diagnosis 40 (7) (2020)
Tachjaree Panchalee, Liesbeth Vossaert, Qun Wang, Brielle R Crovetti, Anne K McCombs, Ronald J Wapner, Ignatia B Van den Veyver, Arthur L Beaudet
The effect of maternal body mass index and gestational age on circulating trophoblast yield in cell-based noninvasive prenatal testing. Prenatal diagnosis 40 (11) (2020)
Sara Arian, Jessica Rubin, Imen Chakchouk, Momal Sharif, Sangeetha K Mahadevan, Hadi Erfani, Katharine Shelly, Lan Liao, Isabel Lorenzo, Rajesh Ramakrishnan, Ignatia B Van den Veyver
Reproductive Outcomes from Maternal Loss of Nlrp2 Are Not Improved by IVF or Embryo Transfer Consistent with Oocyte-Specific Defect. Reproductive sciences (Thousand Oaks, Calif.) 28 (7) (2020)
David J Amor, Lyn S Chitty, Ignatia B Van den Veyver
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 (and parental) sequencing. Prenatal diagnosis 40 (12) (2020)
Bibiana K Y Wong, Jaclyn B Murry, Rajesh Ramakrishnan, Fang He, Alfred Balasa, Gary R Stinnett, Steen E Pedersen, Robia G Pautler, Ignatia B Van den Veyver
Maternal stress in Shank3ex4-9 mice increases pup-directed care and alters brain white matter in male offspring. PloS one 14 (11) (2019)
Dana Larsen, Jingmei Ma, Melissa Strassberg, Rajesh Ramakrishnan, Ignatia B Van den Veyver
The uptake of pan-ethnic expanded carrier screening is higher when offered during preconception or early prenatal genetic counseling. Prenatal diagnosis 39 (4) (2019)
Ignatia B Van den Veyver
Prenatally diagnosed developmental abnormalities of the central nervous system and genetic syndromes: A practical review. Prenatal diagnosis 39 (9) (2019)
Riwa Sabbagh, Ignatia B Van den Veyver
The current and future impact of genome-wide sequencing on fetal precision medicine. Human genetics 139 (9) (2019)

Ignatia B Van den Veyver.css-eqlu8i{font-size:small;padding-left:4px;} (Ignatia Van den Veyver)

Publication Activity (10 Years)

Top Topics

Top Venues

Ignatia B Van den Veyver (Ignatia Van den Veyver)