Shaochun Ma

Mutations in GABRA1, GABRA5, GABRG2 and GABRD receptor genes are not a major factor in the pathogenesis of familial focal epilepsy preceded by febrile seizures

J. Sutcliffe, J. Haines, P. Hedera, 2006, Neuroscience Letters.

Mutations in the GABRA1 and EFHC1 genes are rare in familial juvenile myoclonic epilepsy

P. Hedera, B. Abou-Khalil, M. Blair, 2006, Epilepsy Research.

Chinese cases of early infantile epileptic encephalopathy: a novel mutation in the PCDH19 gene was proved in a mosaic male- case report

Li-ping Chen, Zongbo Chen, Pei-pei Liu, 2018, BMC Medical Genetics.

Mutation in KIF5A can also cause adult-onset hereditary spastic paraplegia

P. Hedera, M. Blair, Shaochun Ma, 2006, Neurogenetics.

Tetrathiomolybdate Protects Against Liver Injury from Acetaminophen in Mice

G. Hou, Shaochun Ma, R. Dick, 2004 .

Identification of a Novel Locus for Febrile Seizures and Epilepsy on Chromosome 21q22

J. Haines, P. Hedera, Y. Bradford, 2006, Epilepsia.

Novel variants in TBC1D24 associated with epilepsy and deafness: Report of two cases

N. Zhang, Wei Wei, Zongbo Chen, 2020, International journal of developmental neuroscience : the official journal of the International Society for Developmental Neuroscience.

The GABBR1 locus and the G1465A variant is not associated with temporal lobe epilepsy preceded by febrile seizures

J. Sutcliffe, J. Haines, P. Hedera, 2005, BMC Medical Genetics.

Reappraisal of the role of the DRD3 gene in essential tremor.

P. Hedera, F. Phibbs, T. Davis, 2008, Parkinsonism & related disorders.

Familial essential tremor with apparent autosomal dominant inheritance: Should we also consider other inheritance modes?

J. Haines, P. Hedera, Y. Bradford, 2006, Movement disorders : official journal of the Movement Disorder Society.

A case of TSC2‐PKD1 contiguous deletion syndrome: Clinical features and effective treatment for epilepsy

Wei Wei, L. Yi, Cheng-qing Yang, 2021, International journal of developmental neuroscience : the official journal of the International Society for Developmental Neuroscience.

The Genetics of Neuronal Channelopathies

J. Gargus, Shaochun Ma, 2007 .