Margot R F Reijnders
5PUBLICATIONS
32CO-AUTHORS
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Publications (5)
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|Nov 17, 2020
Germline AGO2 mutations impair RNA interference and human neurological development.Davor Lessel, Daniela M Zeitler, Margot R F Reijnders
|Apr 30, 2020
Characterization of SETD1A haploinsufficiency in humans and Drosophila defines a novel neurodevelopmental syndrome.Joost Kummeling, Diante E Stremmelaar, Nicholas Raun
|Oct 26, 2017
Functional convergence of histone methyltransferases EHMT1 and KMT2C involved in intellectual disability and autism spectrum disorder.Tom S Koemans, Tjitske Kleefstra, Melissa C Chubak
|Oct 21, 2017
Variation in a range of mTOR-related genes associates with intracranial volume and intellectual disability.M R F Reijnders, M Kousi, G M van Woerden
|Aug 02, 2016
Meta-analysis of 2,104 trios provides support for 10 new genes for intellectual disability.Stefan H Lelieveld, Margot R F Reijnders, Rolph Pfundt
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Frequent Collaborators
3 joint publications
Christian Gilissen
2 joint publications
Patrick Rump
2 joint publications
Kirsty McWalter
1 joint publications
M Klein
1 joint publications
B Franke
1 joint publications
Max H Stone
1 joint publications
Levinus A Bok
1 joint publications
Linda B Baughn
1 joint publications
Rolph Pfundt
1 joint publications
Jamie M Kramer
