L. Addis

发表

Imaging and genetics of language and cognition in pediatric epilepsy

Jack J. Lin, B. Hermann, D. Pal, 2013, Epilepsy & Behavior.

Microdeletions of ELP4 Are Associated with Language Impairment, Autism Spectrum Disorder, and Mental Retardation

D. Pinto, S. Scherer, D. Collier, 2015, Human mutation.

Idiopathic focal epilepsies: the "lost tribe".

A. Ioannides, P. Striano, Katsuhiro Kobayashi, 2016, Epileptic disorders : international epilepsy journal with videotape.

Genetic and phenotypic effects of phonological short‐term memory and grammatical morphology in specific language impairment

A. Pickles, A. Pickles, A. Monaco, 2008, Genes, brain, and behavior.

Phenotypic and genetic spectrum of epilepsy with myoclonic atonic seizures

S. Topp, M. Simpson, P. Fallon, 2020, Epilepsia.

Explorer CMIP and ATP 2 C 2 Modulate Phonological Short-Term Memory in Language Impairment

Dorothy V. M. Bishop, Gillian Baird, Dianne F. Newbury, 2009 .

A microRNA‐328 binding site in PAX6 is associated with centrotemporal spikes of rolandic epilepsy

E. Wirrell, D. Mandelbaum, L. Strug, 2016, Annals of clinical and translational neurology.

Analysis of rare copy number variation in absence epilepsies

R. Rosch, L. Nashef, A. Valentín, 2016, Neurology: Genetics.

GRIN2A mutations in acquired epileptic aphasia and related childhood focal epilepsies and encephalopathies with speech and language dysfunction

Anne de Saint Martin, N. Burnashev, T. Tsintsadze, 2013, Nature Genetics.

Mutations in GRIN2A cause idiopathic focal epilepsy with rolandic spikes

U. Stephani, H. Lerche, J. Serratosa, 2013, Nature Genetics.

Increased prevalence of sex chromosome aneuploidies in specific language impairment and dyslexia

G. Baird, P. Bolton, J. Knight, 2013, Developmental Medicine & Child Neurology.

Association analysis using next-generation sequence data from publicly available control groups: the robust variance score statistic

Andriy Derkach, Ian Tomlinson, Lisa J. Strug, 2014, Bioinform..

Epilepsy-associated GRIN2A mutations reduce NMDA receptor trafficking and agonist potency – molecular profiling and functional rescue

D. Collier, D. Pal, L. Vidler, 2017, Scientific Reports.

Identification of new risk factors for rolandic epilepsy: CNV at Xp22.31 and alterations at cholinergic synapses

S. Newhouse, D. Mandelbaum, Jacqueline A Taylor, 2018, Journal of Medical Genetics.

A whole-genome scan and fine-mapping linkage study of auditory-visual synesthesia reveals evidence of linkage to chromosomes 2q24, 5q33, 6p12, and 12p12.

Jean-Baptiste Cazier, Simon Baron-Cohen, Laura Addis, 2009, American journal of human genetics.

Evidence for linkage of migraine in Rolandic epilepsy to known 1q23 FHM2 and novel 17q22 genetic loci

E. Novotny, D. Mandelbaum, L. Strug, 2014, Genes, brain, and behavior.

Investigation of Dyslexia and SLI Risk Variants in Reading- and Language-Impaired Subjects

J. B. Talcott, A. Monaco, J. Talcott, 2010, Behavior genetics.

A locus for an auditory processing deficit and language impairment in an extended pedigree maps to 12p13.31-q14.3

A. Monaco, S. Pääbo, A. Friederici, 2010, Genes, brain, and behavior.

CMIP and ATP2C2 Modulate Phonological Short-Term Memory in Language Impairment

Dorothy V.M. Bishop, Gillian Baird, Dianne F. Newbury, 2009, American journal of human genetics.

The Genetics of Reading Disability in an Often Excluded Sample: Novel Loci Suggested for Reading Disability in Rolandic Epilepsy

E. Novotny, D. Mandelbaum, L. Strug, 2012, PloS one.

Epilepsy-associated GRIN2A mutations reduce NMDA receptor trafficking and agonist potency – molecular profiling and functional rescue

L. Vidler, L. Addis, J. Virdee, 2017, Scientific Reports.

Analysis of rare copy number variation in absence epilepsies

R. Rosch, D. Pal, A. Makoff, 2016 .

Association analysis using next-generation sequence data from publicly available control groups: the robust variance score statistic

R. Houlston, I. Tomlinson, L. Strug, 2014, Bioinform..