Search Results - "Simpson NH"

Copy number variation burden does not predict severity of neurodevelopmental phenotype in children with a sex chromosome trisomy.

Authors: Mountford HS Bishop DVM Thompson PA et al.

Source: American journal of medical genetics. Part C, Seminars in medical genetics [Am J Med Genet C Semin Med Genet] 2020 Jun; Vol. 184 (2), pp. 256-266. Date of Electronic Publication: 2020 May 26.

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

Journal Info: Publisher: Wiley-Blackwell Country of Publication: United States NLM ID: 101235745 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1552-4876 (Electronic) Linking ISSN: 15524868 NLM ISO Abbreviation: Am J Med Genet C Semin Med Genet Subsets: MEDLINE

Genome-wide analyses of individual differences in quantitatively assessed reading- and language-related skills in up to 34,000 people.

Authors: Eising E Mirza-Schreiber N de Zeeuw EL et al.

Source: Proceedings of the National Academy of Sciences of the United States of America [Proc Natl Acad Sci U S A] 2022 Aug 30; Vol. 119 (35), pp. e2202764119. Date of Electronic Publication: 2022 Aug 23.

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

Journal Info: Publisher: National Academy of Sciences Country of Publication: United States NLM ID: 7505876 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1091-6490 (Electronic) Linking ISSN: 00278424 NLM ISO Abbreviation: Proc Natl Acad Sci U S A Subsets: MEDLINE

Genome-wide analysis identifies a role for common copy number variants in specific language impairment.

Authors: Simpson NH Ceroni F Reader RH et al.

Corporate Authors: Simpson NH Ceroni F Reader RH et al.

Source: European journal of human genetics : EJHG [Eur J Hum Genet] 2015 Oct; Vol. 23 (10), pp. 1370-7. Date of Electronic Publication: 2015 Jan 14.

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

Journal Info: Publisher: Nature Publishing Group Country of Publication: England NLM ID: 9302235 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1476-5438 (Electronic) Linking ISSN: 10184813 NLM ISO Abbreviation: Eur J Hum Genet Subsets: MEDLINE

Reply to Pembrey et al: 'ZNF277 microdeletions, specific language impairment and the meiotic mismatch methylation (3M) hypothesis'.

Authors: Ceroni F Simpson NH Francks C et al.

Corporate Authors: Ceroni F Simpson NH Francks C et al.

Source: European journal of human genetics : EJHG [Eur J Hum Genet] 2015 Sep; Vol. 23 (9), pp. 1113-5. Date of Electronic Publication: 2014 Dec 24.

Publication Type: Journal Article; Comment

Journal Info: Publisher: Nature Publishing Group Country of Publication: England NLM ID: 9302235 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1476-5438 (Electronic) Linking ISSN: 10184813 NLM ISO Abbreviation: Eur J Hum Genet Subsets: MEDLINE

Stage 2 Registered Report: Variation in neurodevelopmental outcomes in children with sex chromosome trisomies: testing the double hit hypothesis.

Authors: Newbury DF Simpson NH Thompson PA et al.

Source: Wellcome open research [Wellcome Open Res] 2021 Jun 01; Vol. 3, pp. 85. Date of Electronic Publication: 2021 Jun 01 (Print Publication: 2018).

Publication Type: Journal Article; Comment

Journal Info: Publisher: Wellcome Trust Country of Publication: England NLM ID: 101696457 Publication Model: eCollection Cited Medium: Print ISSN: 2398-502X (Print) Linking ISSN: 2398502X NLM ISO Abbreviation: Wellcome Open Res Subsets: PubMed not MEDLINE

Copy Number Variation Screen Identifies a Rare De Novo Deletion at Chromosome 15q13.1-13.3 in a Child with Language Impairment.

Authors: Pettigrew KA Reeves E Leavett R et al.

Source: PloS one [PLoS One] 2015 Aug 11; Vol. 10 (8), pp. e0134997. Date of Electronic Publication: 2015 Aug 11 (Print Publication: 2015).

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

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

Correction: Exome Sequencing in an Admixed Isolated Population Indicates NFXL1 Variants Confer a Risk for Specific Language Impairment.

Authors: Villanueva P Nudel R Hoischen A et al.

Corporate Authors: Villanueva P Nudel R Hoischen A et al.

Source: PLoS genetics [PLoS Genet] 2015 Jun 26; Vol. 11 (6), pp. e1005336. Date of Electronic Publication: 2015 Jun 26 (Print Publication: 2015).

Publication Type: Published Erratum

Journal Info: Publisher: Public Library of Science Country of Publication: United States NLM ID: 101239074 Publication Model: eCollection Cited Medium: Internet ISSN: 1553-7404 (Electronic) Linking ISSN: 15537390 NLM ISO Abbreviation: PLoS Genet Subsets: PubMed not MEDLINE

Lack of replication for the myosin-18B association with mathematical ability in independent cohorts.

Authors: Pettigrew KA Fajutrao Valles SF Moll K et al.

Corporate Authors: Pettigrew KA Fajutrao Valles SF Moll K et al.

Source: Genes, brain, and behavior [Genes Brain Behav] 2015 Apr; Vol. 14 (4), pp. 369-76. Date of Electronic Publication: 2015 Apr 01.

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

Journal Info: Publisher: Munksgaard Country of Publication: England NLM ID: 101129617 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1601-183X (Electronic) Linking ISSN: 1601183X NLM ISO Abbreviation: Genes Brain Behav Subsets: MEDLINE

Exome sequencing in an admixed isolated population indicates NFXL1 variants confer a risk for specific language impairment.

Authors: Villanueva P Nudel R Hoischen A et al.

Corporate Authors: Villanueva P Nudel R Hoischen A et al.

Source: PLoS genetics [PLoS Genet] 2015 Mar 17; Vol. 11 (3), pp. e1004925. Date of Electronic Publication: 2015 Mar 17 (Print Publication: 2015).

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: 101239074 Publication Model: eCollection Cited Medium: Internet ISSN: 1553-7404 (Electronic) Linking ISSN: 15537390 NLM ISO Abbreviation: PLoS Genet Subsets: MEDLINE

Homozygous microdeletion of exon 5 in ZNF277 in a girl with specific language impairment.

Authors: Ceroni F Simpson NH Francks C et al.

Corporate Authors: Ceroni F Simpson NH Francks C et al.

Source: European journal of human genetics : EJHG [Eur J Hum Genet] 2014 Oct; Vol. 22 (10), pp. 1165-71. Date of Electronic Publication: 2014 Feb 12.

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

Journal Info: Publisher: Nature Publishing Group Country of Publication: England NLM ID: 9302235 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1476-5438 (Electronic) Linking ISSN: 10184813 NLM ISO Abbreviation: Eur J Hum Genet Subsets: MEDLINE

Genome-wide screening for DNA variants associated with reading and language traits.

Authors: Gialluisi A Newbury DF Wilcutt EG et al.

Corporate Authors: Gialluisi A Newbury DF Wilcutt EG et al.

Source: Genes, brain, and behavior [Genes Brain Behav] 2014 Sep; Vol. 13 (7), pp. 686-701. Date of Electronic Publication: 2014 Aug 29.

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

Journal Info: Publisher: Munksgaard Country of Publication: England NLM ID: 101129617 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1601-183X (Electronic) Linking ISSN: 1601183X NLM ISO Abbreviation: Genes Brain Behav 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

Genome-wide association analyses of child genotype effects and parent-of-origin effects in specific language impairment.

Authors: Nudel R Simpson NH Baird G et al.

Corporate Authors: Nudel R Simpson NH Baird G et al.

Source: Genes, brain, and behavior [Genes Brain Behav] 2014 Apr; Vol. 13 (4), pp. 418-29. Date of Electronic Publication: 2014 Mar 24.

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

Journal Info: Publisher: Munksgaard Country of Publication: England NLM ID: 101129617 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1601-183X (Electronic) Linking ISSN: 1601183X NLM ISO Abbreviation: Genes Brain Behav Subsets: MEDLINE

A deletion involving CD38 and BST1 results in a fusion transcript in a patient with autism and asthma.

Authors: Ceroni F Sagar A Simpson NH et al.

Source: Autism research : official journal of the International Society for Autism Research [Autism Res] 2014 Apr; Vol. 7 (2), pp. 254-63. Date of Electronic Publication: 2014 Mar 13.

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

Journal Info: Publisher: John Wiley & Sons, Inc Country of Publication: United States NLM ID: 101461858 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1939-3806 (Electronic) Linking ISSN: 19393806 NLM ISO Abbreviation: Autism Res Subsets: MEDLINE

Stage 1 Registered Report: Variation in neurodevelopmental outcomes in children with sex chromosome trisomies: protocol for a test of the double hit hypothesis.

Authors: Newbury DF Simpson NH Thompson PA et al.

Source: Wellcome open research [Wellcome Open Res] 2018 Feb 12; Vol. 3, pp. 10. Date of Electronic Publication: 2018 Feb 12 (Print Publication: 2018).

Publication Type: Journal Article

Journal Info: Publisher: Wellcome Trust Country of Publication: England NLM ID: 101696457 Publication Model: eCollection Cited Medium: Print ISSN: 2398-502X (Print) Linking ISSN: 2398502X NLM ISO Abbreviation: Wellcome Open Res Subsets: PubMed not MEDLINE

Next-generation DNA sequencing identifies novel gene variants and pathways involved in specific language impairment.

Authors: Chen XS Reader RH Hoischen A et al.

Source: Scientific reports [Sci Rep] 2017 Apr 25; Vol. 7, pp. 46105. Date of Electronic Publication: 2017 Apr 25.

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

Associations of HLA alleles with specific language impairment.

Authors: Nudel R Simpson NH Baird G et al.

Corporate Authors: Nudel R Simpson NH Baird G et al.

Source: Journal of neurodevelopmental disorders [J Neurodev Disord] 2014 Jan 17; Vol. 6 (1), pp. 1. Date of Electronic Publication: 2014 Jan 17.

Publication Type: Journal Article

Journal Info: Publisher: BioMed Central Country of Publication: England NLM ID: 101483832 Publication Model: Electronic Cited Medium: Print ISSN: 1866-1947 (Print) Linking ISSN: 18661947 NLM ISO Abbreviation: J Neurodev Disord Subsets: PubMed not MEDLINE

Bcl-2 over-expression reduces growth rate and prolongs G1 phase in continuous chemostat cultures of hybridoma cells.

Authors: Simpson NH Singh RP Emery AN et al.

Source: Biotechnology and bioengineering [Biotechnol Bioeng] 1999 Jul 20; Vol. 64 (2), pp. 174-86.

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

Journal Info: Publisher: Wiley Country of Publication: United States NLM ID: 7502021 Publication Model: Print Cited Medium: Print ISSN: 0006-3592 (Print) Linking ISSN: 00063592 NLM ISO Abbreviation: Biotechnol Bioeng Subsets: MEDLINE

Malpractice in outpatient psychotherapy.

Authors: Pope KS Simpson NH Weiner MF

Source: American journal of psychotherapy [Am J Psychother] 1978 Oct; Vol. 32 (4), pp. 593-602.

Publication Type: Journal Article

Journal Info: Publisher: American Psychiatric Association Country of Publication: United States NLM ID: 0110672 Publication Model: Print Cited Medium: Print ISSN: 0002-9564 (Print) Linking ISSN: 00029564 NLM ISO Abbreviation: Am J Psychother Subsets: MEDLINE

In hybridoma cultures, deprivation of any single amino acid leads to apoptotic death, which is suppressed by the expression of the bcl-2 gene.

Authors: Simpson NH Singh RP Perani A et al.

Source: Biotechnology and bioengineering [Biotechnol Bioeng] 1998 Jul 05; Vol. 59 (1), pp. 90-8.

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

Journal Info: Publisher: Wiley Country of Publication: United States NLM ID: 7502021 Publication Model: Print Cited Medium: Print ISSN: 0006-3592 (Print) Linking ISSN: 00063592 NLM ISO Abbreviation: Biotechnol Bioeng Subsets: MEDLINE