List of works - Laura Addis

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

scientific article

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

scientific article published on 02 June 2016

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

scientific article published on 05 February 2009

Analysis of rare copy number variation in absence epilepsies.

scientific article published on 22 March 2016

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

scientific article

CMIP and ATP2C2 modulate phonological short-term memory in language impairment

scientific article published on 30 July 2009

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

scientific article published on 27 February 2017

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

scientific article published on 26 December 2013

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

scientific article published on 11 August 2013

Identification and characterization of the integrin alpha2beta1 binding motif in chondroadherin mediating cell attachment

scientific article

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

scientific article published on 22 May 2018

Idiopathic focal epilepsies: the "lost tribe".

scientific article

Imaging and genetics of language and cognition in pediatric epilepsy ⬇️

scientific article published on October 30, 2012

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

scientific article

Investigation of dyslexia and SLI risk variants in reading- and language-impaired subjects.

scientific article

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

scientific article published on 23 May 2015

Mutations in GRIN2A cause idiopathic focal epilepsy with rolandic spikes

scientific article published on 11 August 2013

Phenotypic and genetic spectrum of epilepsy with myoclonic atonic seizures

scientific article published on 29 May 2020

Purification, crystallization and preliminary X-ray diffraction analysis of human chondroadherin

scientific article published on 23 May 2008

The genetics of reading disability in an often excluded sample: novel loci suggested for reading disability in Rolandic epilepsy.

scientific article

List of works by Laura Addis

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

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

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

Analysis of rare copy number variation in absence epilepsies.

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

CMIP and ATP2C2 modulate phonological short-term memory in language impairment

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

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

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

Identification and characterization of the integrin alpha2beta1 binding motif in chondroadherin mediating cell attachment

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

Idiopathic focal epilepsies: the "lost tribe".

Imaging and genetics of language and cognition in pediatric epilepsy ⬇️

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

Investigation of dyslexia and SLI risk variants in reading- and language-impaired subjects.

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

Mutations in GRIN2A cause idiopathic focal epilepsy with rolandic spikes

Phenotypic and genetic spectrum of epilepsy with myoclonic atonic seizures

Purification, crystallization and preliminary X-ray diffraction analysis of human chondroadherin

The genetics of reading disability in an often excluded sample: novel loci suggested for reading disability in Rolandic epilepsy.