Geeske  van Woerden

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Dr. Geeske van Woerden (GM)

Publications

1. The non-canonical thioreductase Tmx2b is essential for neuronal survival during zebrafish embryonic brain development.

Dekker J, Lam W, van der Linde HC, Ophorst F, de Konink C, Schot R, Kremers GJ, Sanderson LE, Berdowski WM, van Woerden GM, Mancini GMS, van Ham TJ
in Development (Cambridge, England) 2025

2. Biallelic MED29 variants cause pontocerebellar hypoplasia with cataracts.

Arkush L, van Woerden GM, Ziv L, Marek-Yagel D, Fonseca R, Brevé E, Barel O, Shalva N, Veber A, Anikster Y, Ben-Ami Raichman D, Musallam B, Marcu S, Nissenkorn A, Mandel H, Kushner SA, Ben Zeev B, Heimer G
in European journal of human genetics : EJHG 2025

3. Investigating the neuronal role of the proteasomal ATPase subunit gene PSMC5 in neurodevelopmental proteasomopathies.

Küry S, Stanton JE, van Woerden GM, Bosc-Rosati A, Hsieh TC, Bray L, Oloudé M, Rosenfelt C, Scott-Boyer MP, Most V, Wang T, Papendorf JJ, de Konink C, Deb W, Vignard V, Studencka-Turski M, Besnard T, Hajdukowicz AM, Thiel FG, Wolfgramm S, Florenceau L, Cuinat S, Marsac S, Verrès Y, Dangoumau A, Poirier L, Wentzensen IM, Tuttle A, Forster C, Striesow J, Golnik R, Ortiz D, Jenkins L, Rosenfeld JA, Ziegler A, Houdayer C, Bonneau D, Torti E, Begtrup A, Monaghan KG, Mullegama SV, Volker-Touw CMLN, van Gassen KLI, Oegema R, de Pagter MS, Steindl K, Rauch A, Ivanovski I, McDonald K, Boothe E, Dauber A, Baker J, Fabie NAV, Bernier RA, Turner TN, Srivastava S, Dies KA, Swanson LC, Costin C, Abdulrazak A, Jobling RK, Pappas J, Rabin R, Niyazov D, Chun-Hui Tsai A, Kovak K, Beck DB, Malicdan MCV, Adams DR, Wolfe L, Ganetzky RD, Muraresku CC, Babikyan D, Sedláček Z, Hančárová M, Timberlake AT, Saif HA, Nestler B, King K, Hajianpour MJ, Costain G, Prendergast D, Li C, Geneviève D, Vitobello A, Sorlin A, Philippe C, Harel T, Toker O, Sabir A, Lim D, Hamilton MJ, Bryson LJ, Cleary E, Weber S, Hoffman TL, Cueto-González AM, Tizzano EF, Gómez-Andrés D, Codina-Solà M, Ververi A, Pavlidou E, Lambropoulos A, Garganis K, Rio M, Levy J, Langas SJ, McRae AM, Lessard MK, D
in Nature communications 2025

4. 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

5. autoMEA: machine learning-based burst detection for multi-electrode array datasets.

Hernandes V, Heuvelmans AM, Gualtieri V, Meijer DH, van Woerden GM, Greplova E
in Frontiers in neuroscience 2024

6. CAMK2; four genes, one syndrome? Delineation of genotype-phenotype correlations.

Cheung JS, van Woerden GM, Veenma DCM
in Current opinion in neurobiology 2024

7. Purkinje cell intrinsic activity shapes cerebellar development and function

in Cold Spring Harbor Laboratory 2024

8. Loss of CAMK2G affects intrinsic and motor behavior but has minimal impact on cognitive behavior.

9. Focused ultrasound neuromodulation on a multiwell MEA.

Saccher M, Kawasaki S, Onori MP, van Woerden GM, Giagka V, Dekker R
in Bioelectronic medicine 2022

10. 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
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