Joris Robert Vermeesch (Joris R Vermeesch, Joris Vermeesch)

ORCID

Publication Activity (10 Years)

Years Active: 2018-2024
Publications (10 Years): 38

Top Venues

Genes

Prenatal diagnosis

Nature communications

Clinical chemistry

KULeuven

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

Affiliation History

KULeuven

Belgium

Professor :: Department of Human Genetics

Publications

Adrian Odrzywolski, Beyhan Tüysüz, Philippe Debeer, Erika Souche, Arnout Voet, Boyan Dimitrov, Paulina Krzesińska, Joris Robert Vermeesch, Przemko Tylzanowski
Gollop-Wolfgang Complex Is Associated with a Monoallelic Variation in WNT11 . Genes 15 (1) (2024)
Adrian Odrzywolski, Beyhan Tüysüz, Philippe Debeer, Erika Souche, Arnout Voet, Boyan Dimitrov, Paulina Krzesińska, Joris Robert Vermeesch, Przemko Tylzanowski
Gollop-Wolfgang Complex Is Associated with a Monoallelic Variation in WNT11 . Genes 15 (1) (2024)
Catharina J Heesterbeek, Liesbeth Lenaerts, Vivianne C G Tjan-Heijnen, Frédéric Amant, Maartje C van Rij, Miel Theunis, Christine E M De Die-Smulders, Joris Robert Vermeesch, Merryn V E Macville, null null
Comprehensive Recommendations for the Clinical Management of Pregnant Women With Noninvasive Prenatal Test Results Suspicious of a Maternal Malignancy. JCO oncology practice (2024)
Kate E Stanley, Tatjana Jatsenko, Stefania Tuveri, Dhanya Sudhakaran, Lore Lannoo, Kristel Van Calsteren, Marie de Borre, Ilse Van Parijs, Leen Van Coillie, Kris Van Den Bogaert, Rodrigo De Almeida Toledo, Liesbeth Lenaerts, Sabine Tejpar, Kevin Punie, Laura Yissel Rengifo, Peter Vandenberghe, Bernard Thienpont, Joris Robert Vermeesch
Cell type signatures in cell-free DNA fragmentation profiles reveal disease biology. Nature communications 15 (1) (2024)
Catharina J Heesterbeek, Liesbeth Lenaerts, Vivianne C G Tjan-Heijnen, Frédéric Amant, Maartje C van Rij, Miel Theunis, Christine E M De Die-Smulders, Joris Robert Vermeesch, Merryn V E Macville, null null
Comprehensive Recommendations for the Clinical Management of Pregnant Women With Noninvasive Prenatal Test Results Suspicious of a Maternal Malignancy. JCO oncology practice 20 (8) (2024)
Kate E Stanley, Tatjana Jatsenko, Stefania Tuveri, Dhanya Sudhakaran, Lore Lannoo, Kristel Van Calsteren, Marie de Borre, Ilse Van Parijs, Leen Van Coillie, Kris Van Den Bogaert, Rodrigo De Almeida Toledo, Liesbeth Lenaerts, Sabine Tejpar, Kevin Punie, Laura Yissel Rengifo, Peter Vandenberghe, Bernard Thienpont, Joris Robert Vermeesch
Cell type signatures in cell-free DNA fragmentation profiles reveal disease biology. Nature communications 15 (1) (2024)
Adrian Odrzywolski, Beyhan Tüysüz, Philippe Debeer, Erika Souche, Arnout Voet, Boyan Dimitrov, Paulina Krzesińska, Joris Robert Vermeesch, Przemko Tylzanowski
Gollop-Wolfgang Complex Is Associated with a Monoallelic Variation in WNT11 . Genes 15 (1) (2024)
Kate E Stanley, Tatjana Jatsenko, Stefania Tuveri, Dhanya Sudhakaran, Lore Lannoo, Kristel Van Calsteren, Marie de Borre, Ilse Van Parijs, Leen Van Coillie, Kris Van Den Bogaert, Rodrigo De Almeida Toledo, Liesbeth Lenaerts, Sabine Tejpar, Kevin Punie, Laura Yissel Rengifo, Peter Vandenberghe, Bernard Thienpont, Joris Robert Vermeesch
Cell type signatures in cell-free DNA fragmentation profiles reveal disease biology. Nature communications 15 (1) (2024)
Kate E Stanley, Tatjana Jatsenko, Stefania Tuveri, Dhanya Sudhakaran, Lore Lannoo, Kristel Van Calsteren, Marie de Borre, Ilse Van Parijs, Leen Van Coillie, Kris Van Den Bogaert, Rodrigo De Almeida Toledo, Liesbeth Lenaerts, Sabine Tejpar, Kevin Punie, Laura Yissel Rengifo, Peter Vandenberghe, Bernard Thienpont, Joris Robert Vermeesch
Cell type signatures in cell-free DNA fragmentation profiles reveal disease biology. Nature communications 15 (1) (2024)
Adrian Odrzywolski, Beyhan Tüysüz, Philippe Debeer, Erika Souche, Arnout Voet, Boyan Dimitrov, Paulina Krzesińska, Joris Robert Vermeesch, Przemko Tylzanowski
Gollop-Wolfgang Complex Is Associated with a Monoallelic Variation in WNT11 . Genes 15 (1) (2024)
Adrian Odrzywolski, Beyhan Tüysüz, Philippe Debeer, Erika Souche, Arnout Voet, Boyan Dimitrov, Paulina Krzesińska, Joris Robert Vermeesch, Przemko Tylzanowski
Gollop-Wolfgang Complex Is Associated with a Monoallelic Variation in WNT11 . Genes 15 (1) (2024)
Lisanne Vervoort, Nicolas Dierckxsens, Marta Sousa Santos, Senne Meynants, Erika Souche, Ruben Cools, Tracy Heung, Koen Devriendt, Hilde Peeters, Donna M McDonald-McGinn, Ann Swillen, Jeroen Breckpot, Beverly S Emanuel, Hilde Van Esch, Anne Susan Bassett, Joris Robert Vermeesch
Multiple paralogues and recombination mechanisms drive the high incidence of 22q11.2 Deletion Syndrome. bioRxiv : the preprint server for biology (2024)
Maria Siermann, Ophelia Valcke, Joris Robert Vermeesch, Taneli Raivio, Olga Tšuiko, Pascal Borry
Limitations, concerns and potential: attitudes of healthcare professionals toward preimplantation genetic testing using polygenic risk scores. European journal of human genetics : EJHG (2023)
Lisa Hui, Katie Ellis, Dora Mayen, Mark Domenic Pertile, Rebecca Riemers, Lu-Ming Sun, Joris Robert Vermeesch, Neeta L Vora, Lyn S Chitty
Position statement from the International Society for Prenatal Diagnosis (ISPD) on the use of non-invasive prenatal testing (NIPT) for the detection of fetal chromosomal conditions in singleton pregnancies. Prenatal diagnosis (2023)
Yingjie Zhao, Yujue Wang, Lijie Shi, Donna M McDonald-McGinn, T Blaine Crowley, Daniel E McGinn, Oanh T Tran, Daniella Miller, Jhih-Rong Lin, Elaine H Zackai, H Richard Johnston, Eva W C Chow, Jacob A S Vorstman, Claudia Vingerhoets, Therese van Amelsvoort, Doron Gothelf, Ann Swillen, Jeroen Breckpot, Joris Robert Vermeesch, Stephan Eliez, Maude Schneider, Marianne B M van den Bree, Michael J Owen, Wendy R Kates, Gabriela M Repetto, Vandana Shashi, Kelly Schoch, Carrie E Bearden, M Cristina Digilio, Marta Unolt, Carolina Putotto, Bruno Marino, Maria Pontillo, Marco Armando, Stefano Vicari, Kathleen Angkustsiri, Linda Campbell, Tiffany Busa, Damian Heine-Suñer, Kieran C Murphy, Declan G M Murphy, Sixto García-Miñaúr, Luis Fernández, null null, Zhengdong D Zhang, Elizabeth Goldmuntz, Raquel E Gur, Beverly S Emanuel, Deyou Zheng, Christian R Marshall, Anne Susan Bassett, Tao Wang, Bernice E Morrow
Chromatin regulators in the TBX1 network confer risk for conotruncal heart defects in 22q11.2DS. NPJ genomic medicine 8 (1) (2023)
Marie De Borre, Huiwen Che, Qian Yu, Lore Lannoo, Kobe De Ridder, Leen Vancoillie, Pauline Dreesen, Mika Van Den Ackerveken, Mio Aerden, Eva Galle, Jeroen Breckpot, Joachim Van Keirsbilck, Wilfried Gyselaers, Koenraad Devriendt, Joris Robert Vermeesch, Kristel Van Calsteren, Bernard Thienpont
Cell-free DNA methylome analysis for early preeclampsia prediction. Nature medicine (2023)
Olga Tsuiko, Yasmine El Ayeb, Tatjana Jatsenko, Joke Allemeersch, Cindy Melotte, Jia Ding, Sophie Debrock, Karen Peeraer, Arne Vanhie, Anne De Leener, Céline Pirard, Candice Kluyskens, Ellen Denayer, Eric Legius, Joris Robert Vermeesch, Hilde Brems, Eftychia Dimitriadou
Preclinical workup using long-read amplicon sequencing provides families with de novo pathogenic variants access to universal preimplantation genetic testing. Human reproduction (Oxford, England) (2023)
Olga Tsuiko, Yasmine El Ayeb, Tatjana Jatsenko, Joke Allemeersch, Cindy Melotte, Jia Ding, Sophie Debrock, Karen Peeraer, Arne Vanhie, Anne De Leener, Céline Pirard, Candice Kluyskens, Ellen Denayer, Eric Legius, Joris Robert Vermeesch, Hilde Brems, Eftychia Dimitriadou
Preclinical workup using long-read amplicon sequencing provides families with de novo pathogenic variants access to universal preimplantation genetic testing. Human reproduction (Oxford, England) 38 (3) (2023)
Margot van Riel, Yan Zhao, Tatjana Jatsenko, Lore Lannoo, Dirk Timmerman, Joris Robert Vermeesch
Ultrasensitive Microhaplotype-Based Detection of Minor Alleles in Cervical Samples of Pregnant Women Identifies Sperm Rather Than Fetal DNA. Clinical chemistry (2023)
Lore Lannoo, Joke Van Camp, Nathalie Brison, Ilse Parijs, Leen Vancoillie, Kris Van Den Bogaert, Joris Robert Vermeesch, Koen Devriendt, Kristel Van Calsteren
What helps define outcomes in persistent uninterpretable non-invasive prenatal testing: Maternal factors, fetal fraction or quality scores? Prenatal diagnosis (2023)
Ilse Parijs, Nathalie Brison, Leen Vancoillie, Machteld Baetens, Bettina Blaumeiser, Sébastien Boulanger, Julie Désir, Boyan Dimitrov, Nathalie Fieremans, Katrien Janssens, Sandra Janssens, Axel Marichal, Björn Menten, Colombine Meunier, Kim Van Berkel, Ann Van Den Bogaert, Koenraad Devriendt, Kris Van Den Bogaert, Joris Robert Vermeesch
Population screening for 15q11-q13 duplications: corroboration of the difference in impact between maternally and paternally inherited alleles. European journal of human genetics : EJHG (2023)
Olga Tsuiko, Yasmine El Ayeb, Tatjana Jatsenko, Joke Allemeersch, Cindy Melotte, Jia Ding, Sophie Debrock, Karen Peeraer, Arne Vanhie, Anne De Leener, Céline Pirard, Candice Kluyskens, Ellen Denayer, Eric Legius, Joris Robert Vermeesch, Hilde Brems, Eftychia Dimitriadou
Preclinical workup using long-read amplicon sequencing provides families with de novo pathogenic variants access to universal preimplantation genetic testing. Human reproduction (Oxford, England) 38 (3) (2023)
Liesbeth Lenaerts, Miel Theunis, Frédéric Amant, Joris Robert Vermeesch
Non-invasive prenatal testing: when results suggests maternal cancer. Medizinische Genetik : Mitteilungsblatt des Berufsverbandes Medizinische Genetik e.V 35 (4) (2023)
Liesbeth Lenaerts, Miel Theunis, Frédéric Amant, Joris Robert Vermeesch
Non-invasive prenatal testing: when results suggests maternal cancer. Medizinische Genetik : Mitteilungsblatt des Berufsverbandes Medizinische Genetik e.V 35 (4) (2023)
null null, Martine De Rycke, Antonio Capalbo, Edith Coonen, Giovanni Coticchio, Francesco Fiorentino, Veerle Goossens, Saria Mcheik, Carmen Rubio, Karen D Sermon, Ioannis A Sfontouris, Claudia Spits, Joris Robert Vermeesch, Nathalie Vermeulen, Dagan Wells, Filippo Zambelli, Georgia Kakourou
ESHRE survey results and good practice recommendations on managing chromosomal mosaicism. Human reproduction open 2022 (4) (2022)
Lisanne Vervoort, Joris Robert Vermeesch
The 22q11.2 Low Copy Repeats. Genes 13 (11) (2022)
Joris Robert Vermeesch, Liesbeth Lenaerts
Commentary on Multiple Copy Number Variants Detected by Noninvasive Prenatal Testing. Clinical chemistry 68 (5) (2022)
Stefania Tuveri, Koen Debackere, Lukas Marcelis, Nicolas Dierckxsens, Jonas Demeulemeester, Eftychia Dimitriadou, Daan Dierickx, Pierre Lefesvre, Karen Deraedt, Carlos Graux, Lucienne Michaux, Jan Cools, Thomas Tousseyn, Joris Robert Vermeesch, Iwona Wlodarska
Primary mediastinal large B-cell lymphoma is characterized by large-scale copy-neutral loss of heterozygosity. Genes, chromosomes & cancer 61 (10) (2022)
Tine De Coster, Heleen Masset, Olga Tšuiko, Maaike Catteeuw, Yan Zhao, Nicolas Dierckxsens, Ainhoa Larreategui Aparicio, Eftychia Dimitriadou, Sophie Debrock, Karen Peeraer, Marta de Ruijter-Villani, Katrien Smits, Ann Van Soom, Joris Robert Vermeesch
Parental genomes segregate into distinct blastomeres during multipolar zygotic divisions leading to mixoploid and chimeric blastocysts. Genome biology 23 (1) (2022)
Huiwen Che, Tatjana Jatsenko, Liesbeth Lenaerts, Luc Dehaspe, Leen Vancoillie, Nathalie Brison, Ilse Parijs, Kris Van Den Bogaert, Daniela Fischerova, Ruben Heremans, Chiara Landolfo, Antonia Carla Testa, Adriaan Vanderstichele, Lore Liekens, Valentina Pomella, Agnieszka Wozniak, Christophe Dooms, Els Wauters, Sigrid Hatse, Kevin Punie, Patrick Neven, Hans P M W Wildiers, Sabine Tejpar, Diether Lambrechts, An Coosemans, Dirk Timmerman, Peter Vandenberghe, Michael Jiří Halaška, Joris Robert Vermeesch
Pan-Cancer Detection and Typing by Mining Patterns in Large Genome-Wide Cell-Free DNA Sequencing Datasets. Clinical chemistry 68 (9) (2022)
Heleen Masset, Olga Tšuiko, Joris Robert Vermeesch
Genome-wide abnormalities in embryos: Origins and clinical consequences. Prenatal diagnosis 41 (5) (2021)
Priit Paluoja, Hindrek Teder, Amin Ardeshirdavanai, Baran Bayindir, Joris Robert Vermeesch, Andres Salumets, Kaarel Krjutškov, Priit Palta
Systematic evaluation of NIPT aneuploidy detection software tools with clinically validated NIPT samples. PLoS computational biology 17 (12) (2021)
Lore Lannoo, Liesbeth Lenaerts, Kris Van Den Bogaert, Huiwen Che, Nathalie Brison, Koen Devriendt, Frédéric Amant, Joris Robert Vermeesch, Kristel Van Calsteren
Non-invasive prenatal testing suggesting a maternal malignancy: What do we tell the prospective parents in Belgium? Prenatal diagnosis 41 (10) (2021)
Huiwen Che, Darine Villela, Eftychia Dimitriadou, Cindy Melotte, Nathalie Brison, Maria Neofytou, Kris Van Den Bogaert, Olga Tsuiko, Koen Devriendt, Eric Legius, Masoud Zamani Esteki, Thierry Voet, Joris Robert Vermeesch
Noninvasive prenatal diagnosis by genome-wide haplotyping of cell-free plasma DNA. Genetics in medicine : official journal of the American College of Medical Genetics 22 (5) (2020)
Glenn E Palomaki, Rossa W K Chiu, Mark Domenic Pertile, Erik A Sistermans, Yuval Yaron, Joris Robert Vermeesch, Neeta L Vora, Robert G Best, Louise Wilkins-Haug
International Society for Prenatal Diagnosis Position Statement: cell free (cf)DNA screening for Down syndrome in multiple pregnancies. Prenatal diagnosis 41 (10) (2020)
Dagan Wells, Joris Robert Vermeesch, Joe Leigh Simpson
Current Controversies in Prenatal Diagnosis 3: Gene editing should replace embryo selection following PGD. Prenatal diagnosis 39 (5) (2020)
Masoud Zamani Esteki, Triin Viltrop, Olga Tšuiko, Airi Tiirats, Mariann Koel, Margit Nõukas, Olga Žilina, Katre Teearu, Heidi Marjonen, Hanna Kahila, Jeroen Meekels, Viveca Söderström-Anttila, Anne-Maria Suikkari, Aila Tiitinen, Reedik Mägi, Sulev Kõks, Nina Kaminen-Ahola, Ants Kurg, Thierry Voet, Joris Robert Vermeesch, Andres Salumets
In vitro fertilization does not increase the incidence of de novo copy number alterations in fetal and placental lineages. Nature medicine 25 (11) (2019)
Alena Zablotskaya, Hilde Van Esch, Kevin J Verstrepen, Guy Froyen, Joris Robert Vermeesch
Mapping the landscape of tandem repeat variability by targeted long read single molecule sequencing in familial X-linked intellectual disability. BMC medical genomics 11 (1) (2018)

Joris Robert Vermeesch.css-eqlu8i{font-size:small;padding-left:4px;} (Joris R Vermeesch, Joris Vermeesch)

Publication Activity (10 Years)

Top Topics

Top Venues

Joris Robert Vermeesch (Joris R Vermeesch, Joris Vermeesch)