Annette Schenck - Selected Publications#

1. Fenckova M, Blok LER, Asztalos L, Goodman DP, Cizek P, Singgih E, Glennon J, In’t Hout J, Zweier Z, Eichler EE, von Reyn CR, Bernier R, Asztalos, Schenck A. Habituation Learning is a Widely Affected Mechanism in Drosophila Models of Intellectual Disability and Autism Spectrum Disorders.
Biol Psychiatry. 2019 Aug 15;86(4):294-305 [IF=12,0]; highlighted by a Biol Psychiatry Commentary, PMID:31370964.

2. Riahi H, Brekelmans C, Foriel S, Merkling SH, Lyons TA, Itskov PM, Kleefstra T, Ribeiro C, van Rij RP, Kramer JM*, Schenck A*.The histone methyltransferase G9a regulates tolerance to oxidative stress-induced energy consumption.
PLoS Biol. 2019 Mar 12;17(3):e2006146. [IF=9,5]; highlighted by a PLoS Biol. Primer (PMID: 31002662).

3. Eidhof I, van de Warrenburg, BP, Schenck A. Biology of Genetic Ataxias (SnapShot).
Cell 2018, 175(3):890-890. [IF=33,8]

4. Eidhof I*, Baets J*, Kamsteeg EJ, Deconinck T, van Ninhuys L, Martin JJ, Schüle R, Züchner S, De Jonghe P, Schenck A$, van de Warrenburg, BP$. GDAP2 mutations implicate susceptibility to cellular stress in a new form of autosomal recessive cerebellar ataxia,
Brain 2018, 141(9):2592-2604. [IF=11,2]

5. Koemans TS, Kleefstra T, Stone MH, Chubak MC, Reijnders MRF, de Munnik S, Willemsen M, Fenckova M, Stumpel C, Bok LA, Sifuentes Saenz M, Byerly K, Baughn LB, Stegmann S, Pfundt R,van Bokhoven H, Schenck A$, Kramer JM$. Functional convergence of histone methyltransferases EHMT1 and KMT2C involved in Intellectual Disability and Autism.
PLoS Genet, 2017 Oct 25;13(10):e1006864. [IF=6,7]

6. Stessman HAF*, Xiong B*, Coe BP, Wang T, Hoekzema K, Fenckova M, Kvarnung M,…., Harich B, Castells-Nobau A, Xia K, Peeters H, Nordenskjöld M, Schenck A, Bernier R, Eichler EE. Targeted sequencing identifies 91 neurodevelopmental disorder risk genes with autism and developmental-disability biases.
Nat Genet, 2017 Apr;49(4):515-526. [IF=31,2]; (highlighted by a Nat. Genet. news & views PMID:28358133)

7. Esmaeeli-Nieh S*, Fenckova M*, Porter IM*, Motazacker MM, Nijhof B, Castells-Nobau A, Asztalos Z, Felbor U, Behjati F, Tzschach A, Weißmann R, Scherthan H, Sayfati M, Ropers HH, Kahrizi K, Najmabadi H, Swedlow JR, Schenck A$ and Kuss AW$
BOD1 is required for cognitive function in human and Drosophila
Plos Genet, 2016 May 11;12(5):e1006022. [IF=6,7]

8. Kochinke K*, Zweier C*, Nijhof B, Fenckova M, Cizek P, Honti F, Keerthikumar S, Oortveld MAW, Kleefstra T, Kramer JM, Webber C, Huynen MA, and Schenck A. Systematic Phenomics Analysis Deconvolutes Genes Mutated in Intellectual Disability into Biologically Coherent Modules.
Am J Hum Genet, 2016 Jan 7;98(1):149-64. [IF=10,1]

9. van der Voet M, Harich B, Franke B, Schenck A. ADHD-associated dopamine transporter, latrophilin and neurofibromin share a dopamine-related locomotor signature in Drosophila.
Mol Psychiatry, 2016 Apr;21(4):565-73. [IF=12,4]

10. Schenck A, Goto-Silva L, Collinet C, Rhinn M, Giner A, Habermann B, Brand M, Zerial M. The endosomal protein Appl1 mediates Akt substrate specificity and cell survival in vertebrate development.
Cell. 2008 May 2;133(3):486-97. [IF=36,2]