(Q47771802)

5 February 2018

title

Dense linkage disequilibrium mapping in the 15q11-q13 maternal expression domain yields evidence for association in autism (English)

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5 February 2018

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linkage disequilibrium

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10

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5 February 2018

Jonathan L Haines

9

object named as

Haines JL

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5 February 2018

author name string

Nurmi EL

1

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5 February 2018

Amin T

2

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5 February 2018

Olson LM

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5 February 2018

Jacobs MM

4

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5 February 2018

McCauley JL

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5 February 2018

Lam AY

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5 February 2018

Organ EL

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5 February 2018

Folstein SE

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5 February 2018

language of work or name

English

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publication date

1 June 2003

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5 February 2018

published in

Molecular Psychiatry

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5 February 2018

volume

8

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5 February 2018

issue

6

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5 February 2018

page(s)

624-34, 570

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5 February 2018

The epidemiology of autism: a review.

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Autism as a strongly genetic disorder: evidence from a British twin study

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The phenotypic manifestations of interstitial duplications of proximal 15q with special reference to the autistic spectrum disorders

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Three probands with autistic disorder and isodicentric chromosome 15.

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Relationship between clinical and genetic features in "inverted duplicated chromosome 15" patients

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Evaluation of potential models for imprinted and nonimprinted components of human chromosome 15q11-q13 syndromes by fine-structure homology mapping in the mouse

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Imprinting in Prader-Willi and Angelman syndromes

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Disruption of the bipartite imprinting center in a family with Angelman syndrome

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The Prader-Willi syndrome imprinting center activates the paternally expressed murine Ube3a antisense transcript but represses paternal Ube3a.

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The IC-SNURF-SNRPN transcript serves as a host for multiple small nucleolar RNA species and as an antisense RNA for UBE3A

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Imprinted expression of the murine Angelman syndrome gene, Ube3a, in hippocampal and Purkinje neurons

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The Angelman syndrome candidate gene, UBE3A/E6-AP, is imprinted in brain

21 January 2018

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The human aminophospholipid-transporting ATPase gene ATP10C maps adjacent to UBE3A and exhibits similar imprinted expression

21 January 2018

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The spectrum of mutations in UBE3A causing Angelman syndrome

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Melanosomal pH controls rate of melanogenesis, eumelanin/phaeomelanin ratio and melanosome maturation in melanocytes and melanoma cells.

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Genetic studies in autistic disorder and chromosome 15.

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Genomic screen and follow-up analysis for autistic disorder.

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Linkage-disequilibrium mapping of autistic disorder, with 15q11-13 markers

21 January 2018

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Analysis of linkage disequilibrium in gamma-aminobutyric acid receptor subunit genes in autistic disorder.

21 January 2018

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Association between a GABRB3 polymorphism and autism.

21 January 2018

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Serotonin transporter (5-HTT) and gamma-aminobutyric acid receptor subunit beta3 (GABRB3) gene polymorphisms are not associated with autism in the IMGSA families. The International Molecular Genetic Study of Autism Consortium.

21 January 2018

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Linkage disequilibrium at the Angelman syndrome gene UBE3A in autism families

21 January 2018

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Tests for linkage and association in nuclear families

21 January 2018

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A test for linkage and association in general pedigrees: the pedigree disequilibrium test

21 January 2018

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A generalization of the transmission/disequilibrium test for uncertain-haplotype transmission

21 January 2018

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21 January 2018

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21 January 2018

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Linkage disequilibrium in humans: models and data

21 January 2018

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Identification of a psoriasis susceptibility candidate gene by linkage disequilibrium mapping with a localized single nucleotide polymorphism map.

21 January 2018

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Mutation screening and transmission disequilibrium study of ATP10C in autism

21 January 2018

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https://api.crossref.org/works/10.1038%2FSJ.MP.4001283

Patterns of linkage disequilibrium in the human genome

21 January 2018

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Candidate-gene approaches for studying complex genetic traits: practical considerations

21 January 2018

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Rapid Detection of CYP1A1, CYP2D6, and NAT Variants by Multiplex Polymerase Chain Reaction and Allele-Specific Oligonucleotide Assay

21 January 2018

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Genetic variation in the 5q31 cytokine gene cluster confers susceptibility to Crohn disease

21 January 2018

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Twin and adoption studies in child and adolescent psychiatric disorders.

21 January 2018

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7 January 2021

Clinical and molecular analysis of five inv dup(15) patients.

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7 January 2021

Differential expression of putative transbilayer amphipath transporters

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7 January 2021

A full genome screen for autism with evidence for linkage to a region on chromosome 7q. International Molecular Genetic Study of Autism Consortium

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7 January 2021

Large-scale genotyping of single nucleotide polymorphisms by Pyrosequencing? and validation against the 5?nuclease (Taqman�) assay

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https://api.crossref.org/works/10.1038%2FSJ.MP.4001283

7 January 2021

Universal SNP genotyping assay with fluorescence polarization detection

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7 January 2021

GOLD--graphical overview of linkage disequilibrium

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7 January 2021

Variations on a theme: cataloging human DNA sequence variation

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7 January 2021

Prospects for whole-genome linkage disequilibrium mapping of common disease genes

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7 January 2021

A look at linkage disequilibrium

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https://api.crossref.org/works/10.1038%2FSJ.MP.4001283

7 January 2021

Identifiers

DOI

10.1038/SJ.MP.4001283

1 reference

5 February 2018

1 reference

5 February 2018