A heritable form of SMARCE1-related meningiomas with important implications for follow-up and family screening E. H. GerkesJ. M. FockM. J. W. Olderode-Berends Review Article Open access 23 January 2016 Pages: 83 - 89
A novel heat shock protein alpha 8 (Hspa8) molecular network mediating responses to stress- and ethanol-related behaviors Kyle R. UrquhartYinghong ZhaoLu Lu Original Article 18 January 2016 Pages: 91 - 105
Spinocerebellar ataxia type 3/Machado-Joseph disease starting before adolescence Karina Carvalho DonisJonas Alex Morales SauteLaura Bannach Jardim Original Article 16 January 2016 Pages: 107 - 113
Recessive mutations of TMC1 associated with moderate to severe hearing loss Ayesha ImtiazAzra MaqsoodSadaf Naz Original Article 16 February 2016 Pages: 115 - 123
Slc20a2 is critical for maintaining a physiologic inorganic phosphate level in cerebrospinal fluid Nina JensenJacob Kwasi AutzenLene Pedersen Short Communication Open access 12 December 2015 Pages: 125 - 130
Multiple sclerosis in families: risk factors beyond known genetic polymorphisms Denis A. AkkadDe-Hyung LeeRalf A. Linker Short Communication 11 February 2016 Pages: 131 - 135
Mutations in GALC cause late-onset Krabbe disease with predominant cerebellar ataxia Yi-Hong ShaoKarine ChoquetBernard Brais Short Communication 26 February 2016 Pages: 137 - 141
Erratum to: Clinical and molecular study in a long-surviving patient with MLASA syndrome due to novel PUS1 mutations Michelangelo CaoMarta DonĂ Elena Pegoraro Erratum 29 February 2016 Pages: 143 - 143