Researcher
Kris Van Den Bogaert
- Disciplines:Clinical genetics and molecular diagnostics
Affiliations
- Department of Human Genetics (Department)
Member
From1 Oct 2019 → Today
Projects
1 - 4 of 4
- Long Read Sequencing for the detection of cryptic structural variation and methylome changes in patients with developmental disorders.From11 Oct 2021 → TodayFunding: Own budget, for example: patrimony, inscription fees, gifts
- Prenatal genome sequencing to map embryonic lethal and developmental disorder genesFrom17 Sep 2020 → 25 Oct 2023Funding: Own budget, for example: patrimony, inscription fees, gifts
- IMPLEMENTATION OF GENOME-WIDE CELL-FREE DNA SEQUENCING FOR THE EARLY IDENTIFICATION AND EFFICIENT MANAGEMENT OF HIGH-RISK PREGNANCIESFrom1 Nov 2019 → 10 Oct 2023Funding: Own budget, for example: patrimony, inscription fees, gifts
- PhD position in Bioinformatics and GenomicsFrom1 Oct 2019 → 1 Oct 2023Funding: Own budget, for example: patrimony, inscription fees, gifts
Publications
1 - 10 of 42
- Expanding the phenotype of copy number variations involving NR0B1 (DAX1)(2024)
Authors: Kris Van Den Bogaert
- Population screening for 15q11-q13 duplications: corroboration of the difference in impact between maternally and paternally inherited alleles(2024)
Authors: Koenraad Devriendt, Kris Van Den Bogaert, Joris Vermeesch
Pages: 31 - 36 - IMPLEMENTATION OF GENOME-WIDE CELL-FREE DNA SEQUENCING FOR THE EARLY IDENTIFICATION AND EFFICIENT MANAGEMENT OF HIGH-RISK PREGNANCIES(2023)
Authors: Lore Lannoo, Kristel Van Calsteren, Kris Van Den Bogaert, Koenraad Devriendt
- What helps define outcomes in persistent uninterpretable non-invasive prenatal testing: Maternal factors, fetal fraction or quality scores?(2023)
Authors: Lore Lannoo, Nathalie Brison, Kris Van Den Bogaert, Joris Vermeesch, Koenraad Devriendt, Kristel Van Calsteren
Pages: 1333 - 1343 - Inactivating TDP2 missense mutation in siblings with congenital abnormalities reminiscent of fanconi anemia(2023)
Authors: Kris Van Den Bogaert, Hilde Van Esch
- Exome sequencing efficacy and phenotypic expansions involving esophageal atresia/tracheoesophageal fistula plus(2022)
Authors: Kris Van Den Bogaert
Pages: 3492 - 3504 - Rare autosomal trisomies detected by non-invasive prenatal testing: an overview of current knowledge(2022)
Authors: Lore Lannoo, Jeroen Breckpot, Nathalie Brison, Luc De Catte, Eftychia Dimitriadou, Eric Legius, Hilde Peeters, Olga Tsuiko, Joris Vermeesch, Griet Van Buggenhout, et al.
Pages: 1323 - 1330 - FOSL2 truncating variants in the last exon cause a neurodevelopmental disorder with scalp and enamel defects(2022)
Authors: Isabelle Meyts, Wim Wuyts, Leen Moens, Selket Delafontaine, Kris Van Den Bogaert, Koenraad Devriendt
Pages: 2475 - 2486 - Identifying phenotypic expansions for congenital diaphragmatic hernia plus (CDH plus ) using DECIPHER data(2022)
Authors: Kris Van Den Bogaert
Pages: 2958 - 2968 - Machine learning-based detection of immune-mediated diseases from genome-wide cell-free DNA sequencing datasets(2022)
Authors: Huiwen Che, Lore Lannoo, Nathalie Brison, Kris Van Den Bogaert, Koenraad Devriendt, Ellen De Langhe, Séverine Vermeire, Bram Verstockt, Kristel Van Calsteren, Joris Vermeesch