A. Reis

发表

Astrogenesis in the murine dentate gyrus is a life‐long and dynamic process

C. Alzheimer, A. Ekici, O. Basak, 2022, The EMBO journal.

Epigenetic targeting in the mouse zygote marks DNA for later methylation: a mechanism for maternal effects in development

B. Pickard, W. Reik, J. Walter, 2001, Mechanisms of Development.

Dentate gyrus astrocytes exhibit layer-specific molecular, morphological and physiological features

C. Henneberger, S. Liebner, Julia Schneider, 2022, Nature Neuroscience.

scRNA sequencing uncovers a TCF4-dependent transcription factor network regulating commissure development in mouse

A. Ekici, M. Wegner, D. Lie, 2021, Development.

Divergent genetic and epigenetic post‐zygotic isolation mechanisms in Mus and Peromyscus

H. Himmelbauer, H. Ropers, M. Hemberger, 2004, Journal of evolutionary biology.

Exome Pool-Seq in neurodevelopmental disorders

A. Ekici, C. Thiel, A. Reis, 2017, European Journal of Human Genetics.

De novo mutations in MSL3 cause an X-linked syndrome marked by impaired histone H4 lysine 16 acetylation

R. Pfundt, J. Ganesh, B. Menten, 2018, Nature Genetics.

Author Correction: CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language

Joshua C Randall, Tomas W. Fitzgerald, G. J. Swaminathan, 2018, Nature Communications.

Mechanism of KMT5B haploinsufficiency in neurodevelopment in humans and mice

Ellen F. Macnamara, Theodore G. Drivas, J. Constantino, 2023, Science advances.

Different MAPT haplotypes influence expression of total MAPT in postmortem brain tissue

T. Arzberger, O. Windl, S. Gentleman, 2023, Acta Neuropathologica Communications.

Volume contents

Singapore., France, E. Wilder, 2001, Mechanisms of Development.

Elucidating the clinical and molecular spectrum of SMARCC2-associated NDD in a cohort of 65 affected individuals

H. Mefford, C. Skinner, R. Stevenson, 2023, medRxiv.

Disturbed Wnt Signalling due to a Mutation in CCDC88C Causes an Autosomal Recessive Non-Syndromic Hydrocephalus with Medial Diverticulum

A. Ekici, E. Boltshauser, C. Thiel, 2010, Molecular Syndromology.

In-Frame Deletion and Missense Mutations of the C-Terminal Helicase Domain of SMARCA2 in Three Patients with Nicolaides-Baraitser Syndrome

A. Reis, A. Rauch, C. Zweier, 2012, Molecular Syndromology.

Mutations in STRA6 cause a broad spectrum of malformations including anophthalmia, congenital heart defects, diaphragmatic hernia, alveolar capillary dysplasia, lung hypoplasia, and mental retardation.

G. Mortier, R. Hennekam, G. Nürnberg, 2007, American journal of human genetics.

Cystathionine β-synthase as novel endogenous regulator of lymphangiogenesis via modulating VEGF receptor 2 and 3

T. Clahsen, G. Musial, F. Bock, 2022, Communications Biology.

Determinants Affecting the Clinical Implementation of a Molecularly Informed Molecular Tumor Board Recommendation: Experience from a Tertiary Cancer Center

R. Stöhr, N. Meidenbauer, E. Moskalev, 2023, Cancers.