Iris A L M van Rooij (Iris Alm van Rooij)

ResearcherID ORCID

Publication Activity (10 Years)

Years Active: 2019-2022
Publications (10 Years): 6

Top Topics

Patient Reported

Genome Wide Association Study

Dna Methylation

Top Venues

Children (Basel, Switzerland)

Medical science educator

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

Publications

Sander Groen In 't Woud, Carlo Maj, Kirsten Y Renkema, Nine V A M Knoers, Tessel Galesloot, Iris A L M van Rooij, Sita H Vermeulen, Wout F J Feitz, Nel Roeleveld, Michiel F Schreuder, Loes F M van der Zanden, null null
A Genome-Wide Association Study into the Aetiology of Congenital Solitary Functioning Kidney. Biomedicines 10 (12) (2022)
Eva E Amerstorfer, Eberhard Schmiedeke, Inbal Samuk, Cornelius E J Sloots, Iris A L M van Rooij, Ekkehart Jenetzky, Paola Midrio, null Arm-Net Consortium
Clinical Differentiation between a Normal Anus, Anterior Anus, Congenital Anal Stenosis, and Perineal Fistula: Definitions and Consequences-The ARM-Net Consortium Consensus. Children (Basel, Switzerland) 9 (6) (2022)
Sander Groen In 't Woud, Carlo Maj, Kirsten Y Renkema, Nine V A M Knoers, Tessel Galesloot, Iris A L M van Rooij, Sita H Vermeulen, Wout F J Feitz, Nel Roeleveld, Michiel F Schreuder, Loes F M van der Zanden, null null
A Genome-Wide Association Study into the Aetiology of Congenital Solitary Functioning Kidney. Biomedicines 10 (12) (2022)
Femmie de Vegt, Johannes D M Otten, Diederik R H de Bruijn, Helma Pluk, Iris A L M van Rooij, Thom F Oostendorp
Research in Action-Students' Perspectives on the Integration of Research Activities in Undergraduate Biomedical Curricula. Medical science educator 31 (2) (2021)
Gabriel C Dworschak, Iris A L M van Rooij, Heiko Martin Reutter
The Role of De Novo Variants in Formation of Human Anorectal Malformations. Genes 12 (9) (2021)
Iris A L M van Rooij, Kerstin U Ludwig, Julia Welzenbach, Nina Ishorst, Michelle Thonissen, Tessel E Galesloot, Edwin Ongkosuwito, Stefaan J Bergé, Khalid Aldhorae, Augusto Rojas-Martinez, Lambertus Alm Kiemeney, Joris Robert Vermeesch, Han Brunner, Nel Roeleveld, Koen Devriendt, Titiaan Dormaar, Greet Hens, Michael Knapp, Carine E L Carels, Elisabeth Mangold
Non-Syndromic Cleft Lip with or without Cleft Palate: Genome-Wide Association Study in Europeans Identifies a Suggestive Risk Locus at 16p12.1 and Supports SH3PXD2A as a Clefting Susceptibility Gene. Genes 10 (12) (2019)