Search Results - "Addis, L."

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

Authors: Addis, L. Chiang, T. Clarke, T. et al.

Source: Genes, Brain & Behavior. Mar2014, Vol. 13 Issue 3, p333-340. 8p.

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

Authors: Newbury, D. F. Paracchini, S. Scerri, T. S. et al.

Source: Behavior Genetics. Jan2011, Vol. 41 Issue 1, p90-104. 15p. 4 Charts.

Subjects: Dyslexia, Specific language impairment in children, Learning disability genetics, Linkage (Genetics), Cohort analysis

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

Authors: Addis, L. Friederici, A. D. Kotz, S. A. et al.

Source: Genes, Brain & Behavior. Aug2010, Vol. 9 Issue 6, p545-561. 17p. 2 Diagrams, 6 Charts, 2 Graphs.

Pavement of the future.

Authors: Addis, L. E.

Source: Good Roads.; June 7 1919, Vol. 17, p245

Digitizing: printless part programming comes of age.

Authors: Mason, Burt Harvey, Addis L.

Source: Tooling & Production; September 1990, Vol. 56, p188-189, 2p

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

Authors: Falcaro, M. Pickles, A. Newbury, D. F. et al.

Source: Genes, Brain & Behavior. Jun2008, Vol. 7 Issue 4, p393-402. 10p. 2 Charts, 5 Graphs.

GWAS of extended prescription analgesic use identifies genetic loci in chronic pain.

Authors: Harlow CE Uzochukwu E Fernando HA et al.

Source: Nature communications [Nat Commun] 2026 May 28; Vol. 17 (1). Date of Electronic Publication: 2026 May 28.

Publication Type: Journal Article

Journal Info: Publisher: Nature Pub. Group Country of Publication: England NLM ID: 101528555 Publication Model: Electronic Cited Medium: Internet ISSN: 2041-1723 (Electronic) Linking ISSN: 20411723 NLM ISO Abbreviation: Nat Commun Subsets: MEDLINE

Exome sequencing and analysis of 44,028 British South Asians enriched for high autozygosity.

Authors: Kim HI DeBoever C Walter K et al.

Corporate Authors: Kim HI DeBoever C Walter K et al.

Source: Nature genetics [Nat Genet] 2026 Apr; Vol. 58 (4), pp. 821-830. Date of Electronic Publication: 2026 Mar 27.

Publication Type: Journal Article

Journal Info: Publisher: Nature Pub. Co Country of Publication: United States NLM ID: 9216904 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1546-1718 (Electronic) Linking ISSN: 10614036 NLM ISO Abbreviation: Nat Genet Subsets: MEDLINE

Phenotypic and genetic spectrum of epilepsy with myoclonic atonic seizures.

Authors: Tang S Addis L Smith A et al.

Corporate Authors: Tang S Addis L Smith A et al.

Source: Epilepsia [Epilepsia] 2020 May; Vol. 61 (5), pp. 995-1007. Date of Electronic Publication: 2020 May 29.

Publication Type: Journal Article; Research Support, Non-U.S. Gov't

Journal Info: Publisher: Blackwell Science Country of Publication: United States NLM ID: 2983306R Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1528-1167 (Electronic) Linking ISSN: 00139580 NLM ISO Abbreviation: Epilepsia Subsets: MEDLINE

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

Authors: Addis L Ahn JW Dobson R et al.

Source: Human mutation [Hum Mutat] 2015 Sep; Vol. 36 (9), pp. 842-50. Date of Electronic Publication: 2015 Jun 30.

Publication Type: Journal Article; Research Support, Non-U.S. Gov't

Journal Info: Publisher: Wiley-Liss Country of Publication: United States NLM ID: 9215429 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1098-1004 (Electronic) Linking ISSN: 10597794 NLM ISO Abbreviation: Hum Mutat Subsets: MEDLINE

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

Authors: Derkach A Chiang T Gong J et al.

Source: Bioinformatics (Oxford, England) [Bioinformatics] 2014 Aug 01; Vol. 30 (15), pp. 2179-88. Date of Electronic Publication: 2014 Apr 14.

Publication Type: Journal Article; Research Support, Non-U.S. Gov't

Journal Info: Publisher: Oxford University Press Country of Publication: England NLM ID: 9808944 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1367-4811 (Electronic) Linking ISSN: 13674803 NLM ISO Abbreviation: Bioinformatics Subsets: MEDLINE

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

Authors: Simpson NH Addis L Brandler WM et al.

Corporate Authors: Simpson NH Addis L Brandler WM et al.

Source: Developmental medicine and child neurology [Dev Med Child Neurol] 2014 Apr; Vol. 56 (4), pp. 346-53. Date of Electronic Publication: 2013 Oct 09.

Publication Type: Journal Article; Research Support, Non-U.S. Gov't

Journal Info: Publisher: Blackwell Country of Publication: England NLM ID: 0006761 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1469-8749 (Electronic) Linking ISSN: 00121622 NLM ISO Abbreviation: Dev Med Child Neurol Subsets: MEDLINE

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

Authors: Lesca G Rudolf G Bruneau N et al.

Source: Nature genetics [Nat Genet] 2013 Sep; Vol. 45 (9), pp. 1061-6. Date of Electronic Publication: 2013 Aug 11.

Publication Type: Journal Article; Research Support, Non-U.S. Gov't

Journal Info: Publisher: Nature Pub. Co Country of Publication: United States NLM ID: 9216904 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1546-1718 (Electronic) Linking ISSN: 10614036 NLM ISO Abbreviation: Nat Genet Subsets: MEDLINE

Mutations in GRIN2A cause idiopathic focal epilepsy with rolandic spikes.

Authors: Lemke JR Lal D Reinthaler EM et al.

Source: Nature genetics [Nat Genet] 2013 Sep; Vol. 45 (9), pp. 1067-72. Date of Electronic Publication: 2013 Aug 11.

Publication Type: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't

Journal Info: Publisher: Nature Pub. Co Country of Publication: United States NLM ID: 9216904 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1546-1718 (Electronic) Linking ISSN: 10614036 NLM ISO Abbreviation: Nat Genet Subsets: MEDLINE

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

Authors: Strug LJ Addis L Chiang T et al.

Source: PloS one [PLoS One] 2012; Vol. 7 (7), pp. e40696. Date of Electronic Publication: 2012 Jul 18.

Publication Type: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't

Journal Info: Publisher: Public Library of Science Country of Publication: United States NLM ID: 101285081 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1932-6203 (Electronic) Linking ISSN: 19326203 NLM ISO Abbreviation: PLoS One Subsets: MEDLINE

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

Authors: Addis L Sproviero W Thomas SV et al.

Source: Journal of medical genetics [J Med Genet] 2018 Sep; Vol. 55 (9), pp. 607-616. Date of Electronic Publication: 2018 May 22.

Publication Type: Journal Article; Research Support, Non-U.S. Gov't

Journal Info: Publisher: British Medical Association Country of Publication: England NLM ID: 2985087R Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1468-6244 (Electronic) Linking ISSN: 00222593 NLM ISO Abbreviation: J Med Genet Subsets: MEDLINE

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

Authors: Addis L Virdee JK Vidler LR et al.

Source: Scientific reports [Sci Rep] 2017 Feb 27; Vol. 7 (1), pp. 66. Date of Electronic Publication: 2017 Feb 27.

Publication Type: Journal Article; Research Support, Non-U.S. Gov't

Journal Info: Publisher: Nature Publishing Group Country of Publication: England NLM ID: 101563288 Publication Model: Electronic Cited Medium: Internet ISSN: 2045-2322 (Electronic) Linking ISSN: 20452322 NLM ISO Abbreviation: Sci Rep Subsets: MEDLINE

Idiopathic focal epilepsies: the "lost tribe".

Transliterated Title: Idiopathic focal epilepsies: the "lost tribe".

Authors: Pal DK Ferrie C Addis L et al.

Source: Epileptic disorders : international epilepsy journal with videotape [Epileptic Disord] 2016 Sep 01; Vol. 18 (3), pp. 252-88.

Publication Type: Journal Article; Review

Journal Info: Publisher: Wiley Country of Publication: United States NLM ID: 100891853 Publication Model: Print Cited Medium: Internet ISSN: 1950-6945 (Electronic) Linking ISSN: 12949361 NLM ISO Abbreviation: Epileptic Disord Subsets: MEDLINE

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

Authors: Panjwani N Wilson MD Addis L et al.

Source: Annals of clinical and translational neurology [Ann Clin Transl Neurol] 2016 Jun 02; Vol. 3 (7), pp. 512-22. Date of Electronic Publication: 2016 Jun 02 (Print Publication: 2016).

Publication Type: Journal Article

Journal Info: Publisher: Wiley Periodicals, Inc on behalf of American Neurological Association Country of Publication: United States NLM ID: 101623278 Publication Model: eCollection Cited Medium: Print ISSN: 2328-9503 (Print) Linking ISSN: 23289503 NLM ISO Abbreviation: Ann Clin Transl Neurol Subsets: PubMed not MEDLINE

Analysis of rare copy number variation in absence epilepsies.

Authors: Addis L Rosch RE Valentin A et al.

Source: Neurology. Genetics [Neurol Genet] 2016 Mar 22; Vol. 2 (2), pp. e56. Date of Electronic Publication: 2016 Mar 22 (Print Publication: 2016).

Publication Type: Journal Article

Journal Info: Publisher: Published for the American Academy of Neurology by Wolters Kluwer Country of Publication: United States NLM ID: 101671068 Publication Model: eCollection Cited Medium: Print ISSN: 2376-7839 (Print) Linking ISSN: 23767839 NLM ISO Abbreviation: Neurol Genet Subsets: PubMed not MEDLINE