Subscribe to this collection to receive daily e-mail notification of new additions

Preview	Issue Date	Title	Author(s)
	2018	Genome-wide gene-environment interaction in depression: a systematic evaluation of candidate genes: the childhood trauma working-group of PGC-MDD	Van der Auwera, S.; Peyrot, W.; Milaneschi, Y.; Hertel, J.; Baune, B.; Breen, G.; Byrne, E.; Dunn, E.; Fisher, H.; Homuth, G.; Levinson, D.; Lewis, C.; Mills, N.; Mullins, N.; Nauck, M.; Pistis, G.; Preisig, M.; Rietschel, M.; Ripke, S.; Sullivan, P.; et al.
	2018	Analysis of 182 cerebral palsy transcriptomes points to dysregulation of trophic signalling pathways and overlap with autism	Van Eyk, C.; Corbett, M.; Gardner, A.; Van Bon, B.; Broadbent, J.; Harper, K.; MacLennan, A.; Gecz, J.
	2018	Guidelines for whole genome bisulphite sequencing of intact and FFPET DNA on the Illumina HiSeq X Ten	Nair, S.; Luu, P.-.L.; Qu, W.; Maddugoda, M.; Huschtscha, L.; Reddel, R.; Chenevix-Trench, G.; Toso, M.; Kench, J.; Horvath, L.; Hayes, V.; Stricker, P.; Hughes, T.; White, D.; Rasko, J.; Wong, J.-.L.; Clark, S.
	2018	A genotype-first approach identifies an intellectual disability-overweight syndrome caused by PHIP haploinsufficiency	Jansen, S.; Hoischen, A.; Coe, B.; Carvill, G.; van Esch, H.; Bosch, D.; Andersen, U.; Baker, C.; Bauters, M.; Bernier, R.; van Bon, B.; Claahsen-van der Grinten, H.; Gecz, J.; Gilissen, C.; Grillo, L.; Hackett, A.; Kleefstra, T.; Koolen, D.; Kvarnung, M.; Larsen, M.; et al.
	2018	Lack of ovarian skew in an allodapine bee and the evolution of casteless social behaviour	Dew, R.; Tierney, S.; Schwarz, M.
	2018	A genome-wide scan for signatures of selection in Azeri and Khuzestani buffalo breeds	Mokhber, M.; Moradi-Shahrbabak, M.; Sadeghi, M.; Moradi-Shahrbabak, H.; Stella, A.; Nicolzzi, E.; Rahmaninia, J.; Williams, J.
	2018	Neutron scanning reveals unexpected complexity in the enamel thickness of an herbivorous Jurassic reptile	Jones, M.; Lucas, P.; Tucker, A.; Watson, A.; Sertich, J.; Foster, J.; Williams, R.; Garbe, U.; Bevitt, J.; Salvemini, F.
	2017	Human evolution: a tale from ancient genomes	Llamas, B.; Willerslev, E.; Orlando, L.
	2017	An emerging female phenotype with loss-of-function mutations in the Aristaless-related homeodomain transcription factor ARX	Mattiske, T.; Moey, C.; Vissers, L.; Thorne, N.; Georgeson, P.; Bakshi, M.; Shoubridge, C.
	2017	Neanderthal behaviour, diet, and disease inferred from ancient DNA in dental calculus	Weyrich, L.; Duchene, S.; Soubrier, J.; Arriola, L.; Llamas, B.; Breen, J.; Morris, A.; Alt, K.; Caramelli, D.; Dresely, V.; Farrell, M.; Farrer, A.; Francken, M.; Gully, N.; Haak, W.; Hardy, K.; Harvati, K.; Held, P.; Holmes, E.; Kaidonis, J.; et al.
	2017	Novel missense mutation in the bZIP transcription factor, MAF, associated with congenital cataract, developmental delay, seizures and hearing loss (Aymé-Gripp syndrome)	Javadiyan, S.; Craig, J.; Sharma, S.; Lower, K.; Casey, T.; Haan, E.; Souzeau, E.; Burdon, K.
	2017	Soil DNA metabarcoding and high-throughput sequencing as a forensic tool: considerations, potential limitations and recommendations	Young, J.; Austin, J.; Weyrich, L.
	2017	Functional equivalence of the SOX2 and SOX3 transcription factors in the developing mouse brain and testes	Adikusuma, F.; Pederick, D.; McAninch, D.; Hughes, J.; Thomas, P.
	2017	Unravelling mummies: cryptic diversity, host specificity, trophic and coevolutionary interactions in psyllid-parasitoid food webs	Hall, A.; Steinbauer, M.; Taylor, G.; Johnson, S.; Cook, J.; Riegler, M.
	2017	YY1 haploinsufficiency causes an intellectual disability syndrome featuring transcriptional and chromatin dysfunction	Gabriele, M.; Vulto-van Silfhout, A.; Germain, P.; Vitriolo, A.; Kumar, R.; Douglas, E.; Haan, E.; Kosaki, K.; Takenouchi, T.; Rauch, A.; Steindl, K.; Frengen, E.; Misceo, D.; Pedurupillay, C.; Stromme, P.; Rosenfeld, J.; Shao, Y.; Craigen, W.; Schaaf, C.; Rodriguez-Buritica, D.; et al.
	2017	Efficient chromosomal-scale DNA looping in Escherichia coli using multiple DNA-looping elements	Hao, N.; Sneppen, K.; Shearwin, K.; Dodd, I.
	2017	Gonadal mosaicism of a novel IQSEC2 variant causing female limited intellectual disability and epilepsy	Ewans, L.; Field, M.; Zhu, Y.; Turner, G.; Leffler, M.; Dinger, M.; Cowley, M.; Buckley, M.; Scheffer, I.; Jackson, M.; Roscioli, T.; Shoubridge, C.
	2017	Mitochondrion to endoplasmic reticulum apposition length in zebrafish embryo spinal progenitors is unchanged in response to perturbations associated with Alzheimer’s disease	Newman, M.; Halter, L.; Lim, A.; Lardelli, M.
	2017	A paleogenetic perspective on the early population history of the high altitude Andes	Fehren-Schmitz, L.; Harkins, K.; Llamas, B.
	2017	bíogo: a simple high-performance bioinformatics toolkit for the Go language	Kortschak, R.; Snyder, J.; Maragkakis, M.; Adelson, D.