Spectroscopic and in vitro Investigations of Fe(2+)/α‐Ketoglutarate‐Dependent Enzymes Involved in Nucleic Acid Repair and Modification

por Schmidl, David, Lindlar né Jonasson, Niko S. W., Menke, Annika, Schneider, Sabine, Daumann, Lena J.
Publicado 2022

Drug-Resistant Juvenile Myoclonic Epilepsy: Misdiagnosis of Progressive Myoclonus Epilepsy

por Martin, Sarah, Strzelczyk, Adam, Lindlar, Silvia, Krause, Kristina, Reif, Philipp S., Menzler, Katja, Chiocchetti, Andreas G., Rosenow, Felix, Knake, Susanne, Klein, Karl Martin
Publicado 2019

Transcriptomic signatures of neuronal differentiation and their association with risk genes for autism spectrum and related neuropsychiatric disorders

por Chiocchetti, A G, Haslinger, D, Stein, J L, de la Torre-Ubieta, L, Cocchi, E, Rothämel, T, Lindlar, S, Waltes, R, Fulda, S, Geschwind, D H, Freitag, C M
Publicado 2016

The phenotypic and genotypic spectrum of epilepsy and intellectual disability in adults: Implications for genetic testing

por von Brauchitsch, Sophie, Haslinger, Denise, Lindlar, Silvia, Thiele, Holger, Bernsen, Natalie, Zahnert, Felix, Reif, Philipp S., Balcik, Yunus, Au, Ping Yee Billie, Josephson, Colin B., Altmüller, Janine, Strzelczyk, Adam, Knake, Susanne, Rosenow, Felix, Chiocchetti, Andreas, Klein, Karl Martin
Publicado 2023

Loss of the Chr16p11.2 ASD candidate gene QPRT leads to aberrant neuronal differentiation in the SH-SY5Y neuronal cell model

por Haslinger, Denise, Waltes, Regina, Yousaf, Afsheen, Lindlar, Silvia, Schneider, Ines, Lim, Chai K., Tsai, Meng-Miao, Garvalov, Boyan K., Acker-Palmer, Amparo, Krezdorn, Nicolas, Rotter, Björn, Acker, Till, Guillemin, Gilles J., Fulda, Simone, Freitag, Christine M., Chiocchetti, Andreas G.
Publicado 2018