contact
- g.vanwoerden@erasmusmc.nl
- +31 10 7044732
- Room: Ee1483
- Dr. Molewaterplein 40, Faculty Building, Rotterdam, The Netherlands
Dr. Geeske van Woerden (GM)
- Position: PhD, Associate Professor, Erasmus MC
- Lab Head in:
Publications
1. Running in the FAMILY: understanding and predicting the intergenerational transmission of mental illness.
van Houtum LAEM, Baaré WFC, Beckmann CF, Castro-Fornieles J, Cecil CAM, Dittrich J, Ebdrup BH, Fegert JM, Havdahl A, Hillegers MHJ, Kalisch R, Kushner SA, Mansuy IM, Mežinska S, Moreno C, Muetzel RL, Neumann A, Nordentoft M, Pingault JB, Preisig M, Raballo A, Saunders J, Sprooten E, Sugranyes G, Tiemeier H, van Woerden GM, Vandeleur CL, van Haren NEM
in European child & adolescent psychiatry 2024
2. Loss of CAMK2G affects intrinsic and motor behavior but has minimal impact on cognitive behavior.
in Frontiers in neuroscience 2023
3. Focused ultrasound neuromodulation on a multiwell MEA.
Saccher M, Kawasaki S, Onori MP, van Woerden GM, Giagka V, Dekker R
in Bioelectronic medicine 2022
4. Case Report: Developmental Delay and Acute Neuropsychiatric Episodes Associated With a Mutation in the Gene (c.328G>A p.Glu110Lys).
Dwyer BK, Veenma DCM, Chang K, Schulman H, Van Woerden GM
in Frontiers in pharmacology 2022
5. The MAP3K7 gene: further delineation of clinical characteristics and genotype/phenotype correlations.
van Woerden GM, Senden R, de Konink C, Trezza RA, Baban A, Bassetti JA, van Bever Y, Bird LM, van Bon BW, Brooks AS, Guan Q, Klee EW, Marcelis C, Rosado JM, Schimmenti LA, Shikany AR, Terhal PA, Nicole Weaver K, Wessels MW, van Wieringen H, Hurst AC, Gooch CF, Steindl K, Joset P, Rauch A, Tartaglia M, Niceta M, Elgersma Y, Demirdas S
in Human mutation 2022
6. Adult gene reinstatement restores the learning and plasticity deficits of knockout mice.
Rigter PMF, Wallaard I, Aghadavoud Jolfaei M, Kingma J, Post L, Elgersma M, Elgersma Y, van Woerden GM
in iScience 2022
7. TAOK1 is associated with neurodevelopmental disorder and essential for neuronal maturation and cortical development.
van Woerden GM, Bos M, de Konink C, Distel B, Trezza RA, Shur NE, Barañano K, Mahida S, Chassevent A, Schreiber A, Erwin AL, Gripp KW, Rehman F, Brulleman S, Mc Cormack R, de Geus G, Kalsner L, Sorlin A, Bruel AL, Koolen DA, Gabriel MK, Rossi M, Fitzpatrick DR, Wilkie AOM, Calpena E, Johnson D, Brooks A, van Slegtenhorst M, Fleischer J, Groepper D, Lindstrom K, Micheil Innes A, Goodwin A, Humberson J, Noyes A, Langley KG, Telegrafi A, Blevins A, Hoffman J, Guillen Sacoto MJ, Juusola J, Monaghan KG, Punj S, Simon M, Pfundt R, Elgersma Y, Kleefstra T
in Human mutation 2021
8. Role of calcium/calmodulin-dependent kinase 2 in neurodevelopmental disorders.
9. RHEB/mTOR hyperactivity causes cortical malformations and epileptic seizures through increased axonal connectivity.
Proietti Onori M, Koene LMC, Schäfer CB, Nellist M, de Brito van Velze M, Gao Z, Elgersma Y, van Woerden GM
in PLoS biology 2021
10. The Diagnostic Journey of a Patient with Prader-Willi-Like Syndrome and a Unique Homozygous Variant; Bio-Molecular Analysis and Review of the Literature.
Pellikaan K, van Woerden GM, Kleinendorst L, Rosenberg AGW, Horsthemke B, Grosser C, van Zutven LJCM, van Rossum EFC, van der Lely AJ, Resnick JL, Brüggenwirth HT, van Haelst MM, de Graaff LCG
in Genes 2021