Forkhead family transcription factor FoxO and neural differentiation Qiang WenHaitao WangWenhua Zheng Review Article 28 March 2012 Pages: 105 - 113
Mutations in the satellite cell gene MEGF10 cause a recessive congenital myopathy with minicores Steven E. BoydenLane J. MahoneyPeter B. Kang Original Article Open access 28 February 2012 Pages: 115 - 124
A novel locus for restless legs syndrome maps to chromosome 19p in an Irish pedigree Evelyn B. SkehanManal M. A. AbdulrahimCollette K. Hand Original Article 14 March 2012 Pages: 125 - 132
JPH3 repeat expansions cause a progressive akinetic-rigid syndrome with severe dementia and putaminal rim in a five-generation African-American family Susanne A. SchneiderKate E. MarshallMark S. LeDoux Original Article 25 March 2012 Pages: 133 - 140
Frequency of SMARCB1 mutations in familial and sporadic schwannomatosis Miriam J. SmithAndrew J. WallaceD. Gareth R. Evans Original Article 22 March 2012 Pages: 141 - 145
Systems genetic analysis of the effects of iron deficiency in mouse brain Leslie C. JellenErica L. UngerByron C. Jones Original Article 29 March 2012 Pages: 147 - 157
Regulation of estrogen receptor alpha gene expression in the mouse prefrontal cortex during early postnatal development Jenne M. WestberryMelinda E. Wilson Original Article 29 March 2012 Pages: 159 - 167
Axonal transport deficit in a KIF5A –/– mouse model Kathrin N. KarleDiana MöckelLudger Schöls Original Article Open access 01 April 2012 Pages: 169 - 179
Replication study of multiple sclerosis (MS) susceptibility alleles and correlation of DNA-variants with disease features in a cohort of Austrian MS patients Mascha C. SchmiedSonja ZehetmayerAlexander Zimprich Short Communication 14 March 2012 Pages: 181 - 187