Liesbeth Vossaert

Publication Activity (10 Years)

Years Active: 2018-2024
Publications (10 Years): 12

Top Topics

Computed Tomography

Low Birth Weight

Genome Wide Association Study

Top Venues

Clinical genetics

Prenatal diagnosis

American journal of medical genetics. Part A

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

Publications

Christian M Parobek, Roni Zemet, Matthew A Shanahan, Brian A Burnett, Elizabeth Mizerik, Jill Anne Rosenfeld, Liesbeth Vossaert, Steven L Clark, Jill V Hunter, Seema R Lalani
Clinical exome sequencing uncovers genetic disorders in neonates with suspected hypoxic-ischemic encephalopathy: A retrospective analysis. Clinical genetics 106 (1) (2024)
Christian M Parobek, Roni Zemet, Matthew A Shanahan, Brian A Burnett, Elizabeth Mizerik, Jill Anne Rosenfeld, Liesbeth Vossaert, Steven L Clark, Jill V Hunter, Seema R Lalani
Clinical exome sequencing uncovers genetic disorders in neonates with suspected hypoxic-ischemic encephalopathy: A retrospective analysis. Clinical genetics (2024)
Christian M Parobek, Roni Zemet, Matthew A Shanahan, Brian A Burnett, Elizabeth Mizerik, Jill Anne Rosenfeld, Liesbeth Vossaert, Steven L Clark, Jill V Hunter, Seema R Lalani
Clinical exome sequencing uncovers genetic disorders in neonates with suspected hypoxic-ischemic encephalopathy: A retrospective analysis. Clinical genetics 106 (1) (2024)
Christian M Parobek, Roni Zemet, Matthew A Shanahan, Brian A Burnett, Elizabeth Mizerik, Jill Anne Rosenfeld, Liesbeth Vossaert, Steven L Clark, Jill V Hunter, Seema R Lalani
Clinical exome sequencing uncovers genetic disorders in neonates with suspected hypoxic-ischemic encephalopathy: A retrospective analysis. Clinical genetics (2024)
Christian M Parobek, Roni Zemet, Matthew A Shanahan, Brian A Burnett, Elizabeth Mizerik, Jill Anne Rosenfeld, Liesbeth Vossaert, Steven L Clark, Jill V Hunter, Seema R Lalani
Clinical exome sequencing uncovers genetic disorders in neonates with suspected hypoxic-ischemic encephalopathy: A retrospective analysis. Clinical genetics 106 (1) (2024)
Christian M Parobek, Roni Zemet, Matthew A Shanahan, Brian A Burnett, Elizabeth Mizerik, Jill Anne Rosenfeld, Liesbeth Vossaert, Steven L Clark, Jill V Hunter, Seema R Lalani
Clinical exome sequencing uncovers genetic disorders in neonates with suspected hypoxic-ischemic encephalopathy: A retrospective analysis. Clinical genetics 106 (1) (2024)
Sujal Manohar, Yoel Gofin, Haley Streff, Liesbeth Vossaert, Pamela Camacho, Chaya N Murali
A familial deletion of 10p12.1 associated with thrombocytopenia. American journal of medical genetics. Part A (2023)
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)
Pengfei Liu, Liesbeth Vossaert
Emerging technologies for prenatal diagnosis: The application of whole genome and RNA sequencing. Prenatal diagnosis 42 (6) (2022)
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)
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)
Liesbeth Vossaert, Qun Wang, Roseen Salman, Xinming Zhuo, Chunjing Qu, David Henke, Ron Seubert, Jennifer Chow, Lance U'ren, Brennan Enright, Jackie Stilwell, Eric Kaldjian, Yaping Yang, Chad Shaw, Brynn Levy, Ronald Wapner, Amy Breman, Ignatia Van den Veyver, Arthur L Beaudet
Reliable detection of subchromosomal deletions and duplications using cell-based noninvasive prenatal testing. Prenatal diagnosis 38 (13) (2018)