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Publications

Impact of a cis-associated gene expression SNP on chromosome 20q11.22 on bipolar disorder susceptibility, hippocampal structure and cognitive performance.

Li M, Luo XJ, Landén M, et al. Impact of a cis-associated gene expression SNP on chromosome 20q11.22 on bipolar disorder susceptibility, hippocampal structure and cognitive performance. Br J Psychiatry. 2016;208(2):128-37. doi:10.1192/bjp.bp.114.156976

Association analysis of copy numbers of FC-gamma receptor genes for rheumatoid arthritis and other immune-mediated phenotypes.

Franke L, Bannoudi H el, Jansen DTSL, et al. Association analysis of copy numbers of FC-gamma receptor genes for rheumatoid arthritis and other immune-mediated phenotypes. Eur J Hum Genet. 2016;24(2):263-70. doi:10.1038/ejhg.2015.95

The limitations of simple gene set enrichment analysis assuming gene independence.

Tamayo P, Steinhardt G, Liberzon A, Mesirov JP. The limitations of simple gene set enrichment analysis assuming gene independence. Stat Methods Med Res. 2016;25(1):472-87. doi:10.1177/0962280212460441

New insights on the role of microglia in synaptic pruning in health and disease.

Hong S, Dissing-Olesen L, Stevens B. New insights on the role of microglia in synaptic pruning in health and disease. Curr Opin Neurobiol. 2016;36:128-34. doi:10.1016/j.conb.2015.12.004

Diversity Matters: A Revised Guide to Myelination.

Tomassy GS, Dershowitz LB, Arlotta P. Diversity Matters: A Revised Guide to Myelination. Trends Cell Biol. 2016;26(2):135-147. doi:10.1016/j.tcb.2015.09.002

Seq-ing the cortex one neuron at a time.

Chen HH, Arlotta P. Seq-ing the cortex one neuron at a time. Nat Neurosci. 2016;19(2):179-81. doi:10.1038/nn.4230

A Bright and Fast Red Fluorescent Protein Voltage Indicator That Reports Neuronal Activity in Organotypic Brain Slices.

Abdelfattah AS, Farhi SL, Zhao Y, et al. A Bright and Fast Red Fluorescent Protein Voltage Indicator That Reports Neuronal Activity in Organotypic Brain Slices. The Journal of neuroscience : the official journal of the Society for Neuroscience. 2016;36(8):2458-72. doi:10.1523/JNEUROSCI.3484-15.2016

Summaries of plenary, symposia, and oral sessions at the XXII World Congress of Psychiatric Genetics, Copenhagen, Denmark, 12-16 October 2014.

Aas M, Blokland GAM, Chawner SJRA, et al. Summaries of plenary, symposia, and oral sessions at the XXII World Congress of Psychiatric Genetics, Copenhagen, Denmark, 12-16 October 2014. Psychiatr Genet. 2016;26(1):1-47. doi:10.1097/YPG.0000000000000112

Whole exome sequencing combined with integrated variant annotation prediction identifies a causative myosin essential light chain variant in hypertrophic cardiomyopathy.

Nomura A, Tada H, Teramoto R, et al. Whole exome sequencing combined with integrated variant annotation prediction identifies a causative myosin essential light chain variant in hypertrophic cardiomyopathy. J Cardiol. 2016;67(2):133-9. doi:10.1016/j.jjcc.2015.09.003

A null mutation in ANGPTL8 does not associate with either plasma glucose or type 2 diabetes in humans.

Clapham KR, Chu AY, Wessel J, et al. A null mutation in ANGPTL8 does not associate with either plasma glucose or type 2 diabetes in humans. BMC Endocr Disord. 2016;16:7. doi:10.1186/s12902-016-0088-8