Search Results - "Schellenberg G"

Genetic overlap between Alzheimer's disease and Parkinson's disease at the MAPT locus.

Authors: Desikan, R S Schork, A J Wang, Y et al.

Source: Molecular Psychiatry. Dec2015, Vol. 20 Issue 12, p1588-1595. 8p.

Subjects: Genetics of Alzheimer's disease, Parkinson's disease & genetics, Single nucleotide polymorphisms, Alleles, Neurodegeneration

De novo mutation in the dopamine transporter gene associates dopamine dysfunction with autism spectrum disorder.

Authors: Hamilton, P J Campbell, N G Sharma, S et al.

Source: Molecular Psychiatry. Dec2013, Vol. 18 Issue 12, p1315-1323. 9p.

Subjects: Dopamine, Autism spectrum disorders, Drosophila melanogaster, Central nervous system, Leucine

High-density SNP association study and copy number variation analysis of the AUTS1 and AUTS5 loci implicate the IMMP2L–DOCK4 gene region in autism susceptibility.

Authors: Maestrini, E. Pagnamenta, A. T. Lamb, J. A. et al.

Source: Molecular Psychiatry. Sep2010, Vol. 15 Issue 9, p954-968. 15p. 1 Diagram, 5 Charts, 1 Graph.

Subjects: Autism spectrum disorders, Chromosomes, Disease susceptibility, Genes

Geographic Terms: Europe

Evidence for multiple loci from a genome scan of autism kindreds.

Authors: Schellenberg, G. D. Dawson, G. Sung, Y. J. et al.

Source: Molecular Psychiatry. Nov2006, Vol. 11 Issue 11, p1049-1060. 12p. 2 Charts, 7 Graphs.

Subjects: Genetics of autism, Human genome, Immunogenetics, Linkage (Genetics), Microsatellite repeats, Intellectual disabilities, Brain diseases, Autism in children

Autism and the serotonin transporter: the long and short of it.

Authors: Devlin, B. Cook Jr., E. H. Coon, H. et al.

Source: Molecular Psychiatry. Dec2005, Vol. 10 Issue 12, p1110-1116. 7p. 4 Charts.

Subjects: Autism, Autism in children, Diagnosis of autism, Serotonin, Genetics, Developmental disabilities

Apolipoprotein E genotypes and outcome from out of hospital cardiac arrest.

Authors: Longstreth W T Schellenberg G D Fahrenbruch C E et al.

Source: Journal of Neurology, Neurosurgery & Psychiatry. Oct2003, Vol. 74 Issue 10, p1441-1443. 3p.

Evidence for genetic linkage of autism to chromosomes 7 and 4.

Authors: Schellenberg, G. D. Dawson, G. Sung, Y. J. et al.

Source: Molecular Psychiatry. Nov2006, Vol. 11 Issue 11, p979-979. 1p. 1 Graph.

Subjects: Charts, diagrams, etc., Genetics of autism

Homozygosity mapping and Werner's syndrome.

Authors: Schellenberg, G D Martin, G M Wijsman, E M et al.

Source: Lancet. 4/18/1992, Vol. 339 Issue 8799, p1002-1002. 1p.

Apolipoprotein E genotype and Alzheimer's disease.

Authors: Payami, H Kaye, J Heston, L L et al.

Source: Lancet. 9/18/1993, Vol. 342 Issue 8873, p738-738. 1p.

Subjects: Alleles, Alzheimer's disease, Apolipoproteins, Comparative studies, Genes, Research methodology, Medical cooperation, Research, Evaluation research, Relative medical risk, Odds ratio

Is APOE ε4 required for Alzheimer's disease to develop in TREM2 p.R47H variant carriers?

Authors: Guerreiro, R. Orme, T. Naj, A. C. et al.

Source: Neuropathology & Applied Neurobiology. Feb2019, Vol. 45 Issue 2, p187-189. 3p.

ABCB1 genotype and CSF beta-amyloid in Alzheimer disease.

Authors: Kohen R Shofer JB Korvatska O et al.

Source: Journal of Geriatric Psychiatry & Neurology. 06/01/2011, Vol. 24 Issue 2, p63-66. 4p.

P2.067 Resolving mode-of-inheritance and association of PRKN with PD in a comprehensive sequence and copy-number-variation (CNV) analysis of 3800 subjects

Authors: Payami, H. Kay, D. Stevens, C. et al.

Source: Parkinsonism & Related Disorders. Dec2009 Supplement 2, Vol. 15, pS106-S107. 0p.

Genome wide association study meta-analysis of neuropathologic lesions of Alzheimer's disease and related dementias in a multi-site autopsy cohort.

Authors: Cholerton B Godrich D Pasteris J et al.

Corporate Authors: Cholerton B Godrich D Pasteris J et al.

Source: PLoS genetics [PLoS Genet] 2026 Jun 29; Vol. 22 (6), pp. e1012170. Date of Electronic Publication: 2026 Jun 29 (Print Publication: 2026).

Publication Type: Journal Article; Meta-Analysis

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

Genome-wide association studies of TDP-43 proteinopathy and hippocampal sclerosis reveal shared genetic associations with APOE and TMEM106B.

Authors: Godrich D Pasteris J Martin ER et al.

Corporate Authors: Godrich D Pasteris J Martin ER et al.

Source: Alzheimer's & dementia : the journal of the Alzheimer's Association [Alzheimers Dement] 2025 Nov; Vol. 21 (11), pp. e70760.

Publication Type: Journal Article; Research Support, N.I.H., Extramural

Journal Info: Publisher: John Wiley & Sons, Ltd Country of Publication: United States NLM ID: 101231978 Publication Model: Print Cited Medium: Internet ISSN: 1552-5279 (Electronic) Linking ISSN: 15525260 NLM ISO Abbreviation: Alzheimers Dement Subsets: MEDLINE

NIAGADS: A data repository for Alzheimer's disease and related dementia genomics.

Authors: Kuzma A Valladares O Greenfest-Allen E et al.

Corporate Authors: Kuzma A Valladares O Greenfest-Allen E et al.

Source: Alzheimer's & dementia : the journal of the Alzheimer's Association [Alzheimers Dement] 2025 Jun; Vol. 21 (6), pp. e70255.

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

Journal Info: Publisher: John Wiley & Sons, Ltd Country of Publication: United States NLM ID: 101231978 Publication Model: Print Cited Medium: Internet ISSN: 1552-5279 (Electronic) Linking ISSN: 15525260 NLM ISO Abbreviation: Alzheimers Dement Subsets: MEDLINE

Rare coding variants from ADSP R5 whole-genome sequencing implicate novel genes in Alzheimer's disease.

Authors: Lee WP Wang H Leung YY et al.

Source: Research square [Res Sq] 2026 Mar 31. Date of Electronic Publication: 2026 Mar 31.

Publication Type: Journal Article; Preprint

Journal Info: Country of Publication: United States NLM ID: 101768035 Publication Model: Electronic Cited Medium: Internet ISSN: 2693-5015 (Electronic) Linking ISSN: 26935015 NLM ISO Abbreviation: Res Sq Subsets: PubMed not MEDLINE

Multi-ancestry exome-wide study identifies variants associated with Alzheimer's disease protection.

Authors: Khurshid Z Farrell JJ Tong T et al.

Corporate Authors: Khurshid Z Farrell JJ Tong T et al.

Source: Journal of Alzheimer's disease : JAD [J Alzheimers Dis] 2026 Feb; Vol. 109 (3), pp. 1274-1286. Date of Electronic Publication: 2025 Dec 22.

Publication Type: Journal Article

Journal Info: Publisher: SAGE Publications Country of Publication: United States NLM ID: 9814863 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1875-8908 (Electronic) Linking ISSN: 13872877 NLM ISO Abbreviation: J Alzheimers Dis Subsets: MEDLINE

Cerebral amyloid angiopathy impacts neurofibrillary tangle burden and cognition.

Authors: Godrich D Pasteris J Martin ER et al.

Source: Brain communications [Brain Commun] 2024 Nov 22; Vol. 6 (6), pp. fcae369. Date of Electronic Publication: 2024 Nov 22 (Print Publication: 2024).

Publication Type: Journal Article

Journal Info: Publisher: Oxford University Press Country of Publication: England NLM ID: 101755125 Publication Model: eCollection Cited Medium: Internet ISSN: 2632-1297 (Electronic) Linking ISSN: 26321297 NLM ISO Abbreviation: Brain Commun Subsets: PubMed not MEDLINE

Author Correction: Genetic, transcriptomic, histological, and biochemical analysis of progressive supranuclear palsy implicates glial activation and novel risk genes.

Authors: Farrell K Humphrey J Chang T et al.

Corporate Authors: Farrell K Humphrey J Chang T et al.

Source: Nature communications [Nat Commun] 2024 Nov 13; Vol. 15 (1), pp. 9828. Date of Electronic Publication: 2024 Nov 13.

Publication Type: Published Erratum

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; PubMed not MEDLINE

Genetic, transcriptomic, histological, and biochemical analysis of progressive supranuclear palsy implicates glial activation and novel risk genes.

Authors: Farrell K Humphrey J Chang T et al.

Corporate Authors: Farrell K Humphrey J Chang T et al.

Source: Nature communications [Nat Commun] 2024 Sep 09; Vol. 15 (1), pp. 7880. Date of Electronic Publication: 2024 Sep 09.

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

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