The Evidence for Association of ATP2B2 Polymorphisms with Autism in Chinese Han Population

Evaluation of copy number variations reveals novel candidate genes in autism spectrum disorder-associated pathways

(2012) Anthony J. Griswold et al.   HUMAN MOLECULAR GENETICS

Purkinje cell dysfunction and delayed death in plasma membrane calcium ATPase 2-heterozygous mice

(2012) Amanda K. Fakira et al.   MOLECULAR AND CELLULAR NEUROSCIENCE

The association of rs4307059 and rs35678 markers with autism spectrum disorders is replicated in Italian families

(2012) Paola Prandini et al.   PSYCHIATRIC GENETICS

Common genetic variants, acting additively, are a major source of risk for autism

(2012) Lambertus Klei et al.   Molecular Autism

Converging Evidence for an Association of ATP2B2 Allelic Variants with Autism in Male Subjects

(2011) Jérôme Carayol et al.   BIOLOGICAL PSYCHIATRY

Do common variants play a role in risk for autism? Evidence and theoretical musings

(2010) Bernie Devlin et al.   BRAIN RESEARCH

A genome-wide scan for common alleles affecting risk for autism

(2010) R. Anney et al.   HUMAN MOLECULAR GENETICS

The Novel PMCA2 Pump MutationTommyImpairs Cytosolic Calcium Clearance in Hair Cells and Links to Deafness in Mice

(2010) Mario Bortolozzi et al.   JOURNAL OF BIOLOGICAL CHEMISTRY

Reduced expression of the Ca2+transporter protein PMCA2 slows Ca2+dynamics in mouse cerebellar Purkinje neurones and alters the precision of motor coordination

(2010) Ruth M. Empson et al.   JOURNAL OF PHYSIOLOGY-LONDON

A plasma membrane Ca2+ ATPase isoform at the postsynaptic density

(2010) A.C. Burette et al.   NEUROSCIENCE

A genome-wide linkage and association scan reveals novel loci for autism

(2009) Lauren A. Weiss et al.   NATURE

Common genetic variants on 5p14.1 associate with autism spectrum disorders

(2009) Kai Wang et al.   NATURE

Molecular interactions of the plasma membrane calcium ATPase 2 at pre- and post-synaptic sites in rat cerebellum

(2009) M.L. Garside et al.   NEUROSCIENCE

Genetic Calcium Signaling Abnormalities in the Central Nervous System: Seizures, Migraine, and Autism

(2008) J. Jay Gargus   Annals of the New York Academy of Sciences

Altered calcium homeostasis in autism-spectrum disorders: evidence from biochemical and genetic studies of the mitochondrial aspartate/glutamate carrier AGC1

(2008) L Palmieri et al.   MOLECULAR PSYCHIATRY

Genome-wide association studies for complex traits: consensus, uncertainty and challenges

(2008) Mark I. McCarthy et al.   NATURE REVIEWS GENETICS

The Novel Mouse Mutation Oblivion Inactivates the PMCA2 Pump and Causes Progressive Hearing Loss

(2008) Sarah L. Spiden et al.   PLoS Genetics