ACC	anterior cingulate cortex
ADLTE	autosomal-dominant lateral temporal epilepsy
ApoER2	apolipoprotein E2
ARX	aristaless-related homeobox gene
ASD	autism spectrum disorders
ATXN7	ataxin 7
CCK	cholecystokinin
CNS	central nervous system
CNTN6	contactin 6
DCX	doublecortin
DTI	diffusion tractography imaging
ETL7	temporal lobe epilepsy-7
GFP	green fluorescent protein
HCN	hyperpolarization-activated cyclic nucleotide–gated
HdEEG	high-density electroencephalography
ILS	isolated lissencephaly sequence
IQ	intelligence quotient
LCH	lissencephaly with cerebellar hypoplasia
LGI1	leucine-rich, glioma inactivated 1 gene
LIS1	lissencephaly 1
LIS2	lissencephaly 2
LIS3	lissencephaly 3
LTD	long-term depression
LTE	lateral temporal epilepsy
LTP	long-term potentiation
MAP2	microtubule-associated protein 2
MDS	Miller-Dieker syndrome
MEMRI	manganese-enhanced MRI
NCAM2	neural cell adhesion molecule 2
PAFAH1B1	platelet-activating factor acetylhydrolase IB subunit α
PDD-NOS	pervasive developmental disorder-not otherwise specified
PFC	prefrontal cortex
PPI	pre-pulse inhibition
PTP	post tetanic potentiation
PV	parvalbumin
RELN	Reelin gene (human)
Reln	Reelin gene (mouse)
RELN	Reelin glycoprotein (human)
Reln	Reelin glycoprotein (mouse)
ROI	region-of-interest
SBH	subcortical band heterotopia
SCA37	spinocerebellar ataxia type 37
SCA7	spinocerebellar ataxia type 7
SNP	single nucleotide polymorphism
SYP1	synaptophysin 1
TUBA1A	α tubulin 1A
VENs	von Economo neurons
VLDLR	very low-density lipoprotein receptor