Mutation screening and LD mapping in the VCFS deleted region of chromosome 22q11 in schizophrenia using a novel DNA pooling approach. (Q53661663)

17 May 2018

title

Mutation screening and LD mapping in the VCFS deleted region of chromosome 22q11 in schizophrenia using a novel DNA pooling approach. (English)

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17 May 2018

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7

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17 May 2018

Michael C O'Donovan

12

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17 May 2018

author name string

N M Williams

1

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17 May 2018

G Spurlock

2

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17 May 2018

N Norton

3

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17 May 2018

H J Williams

4

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17 May 2018

M L Hamshere

5

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17 May 2018

M Krawczak

6

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17 May 2018

I Nikolov

8

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17 May 2018

L Georgieva

9

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17 May 2018

S Jones

10

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17 May 2018

A G Cardno

11

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17 May 2018

M J Owen

13

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17 May 2018

language of work or name

English

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publication date

1 January 2002

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17 May 2018

published in

Molecular Psychiatry

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17 May 2018

volume

7

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17 May 2018

page(s)

1092-1100

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17 May 2018

issue

10

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17 May 2018

https://scigraph.springernature.com/pub.10.1038/sj.mp.4001188

exact match

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cites work

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Bipolar spectrum disorders in patients diagnosed with velo-cardio-facial syndrome: does a hemizygous deletion of chromosome 22q11 result in bipolar affective disorder?

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High rates of schizophrenia in adults with velo-cardio-facial syndrome.

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Schizophrenia susceptibility associated with interstitial deletions of chromosome 22q11.

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Three new mutations in patients with myophosphorylase deficiency (McArdle disease)

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A genome-wide search for schizophrenia susceptibility genes

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Is schizophrenia a neurodevelopmental disorder?

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Chromosome 22-specific low copy repeats and the 22q11.2 deletion syndrome: genomic organization and deletion endpoint analysis

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Deletion of 150 kb in the minimal DiGeorge/velocardiofacial syndrome critical region in mouse.

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Sensorimotor gating and schizophrenia. Human and animal model studies

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Startle gating deficits occur across prepulse intensities in schizophrenic patients

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Cloning a balanced translocation associated with DiGeorge syndrome and identification of a disrupted candidate gene

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Comparative mapping of the human 22q11 chromosomal region and the orthologous region in mice reveals complex changes in gene organization

21 January 2018

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Comparative sequence analysis of 634 kb of the mouse chromosome 16 region of conserved synteny with the human velocardiofacial syndrome region on chromosome 22q11.2.

21 January 2018

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The DNA sequence of human chromosome 22

21 January 2018

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A region of mouse chromosome 16 is syntenic to the DiGeorge, velocardiofacial syndrome minimal critical region.

21 January 2018

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Molecular characterization of a serine/threonine kinase in the DiGeorge minimal critical region

21 January 2018

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BLAST 2 Sequences, a new tool for comparing protein and nucleotide sequences

21 January 2018

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Gapped BLAST and PSI-BLAST: a new generation of protein database search programs

21 January 2018

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Organization and sequence of the human gene for the mitochondrial citrate transport protein

21 January 2018

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Structural and mutational analysis of a conserved gene (DGSI) from the minimal DiGeorge syndrome critical region

21 January 2018

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Characterization and mutation analysis of goosecoid-like (GSCL), a homeodomain-containing gene that maps to the critical region for VCFS/DGS on 22q11

21 January 2018

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Isolation and characterization of a gene from the DiGeorge chromosomal region homologous to the mouse Tbx1 gene

21 January 2018

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SCAN. Schedules for Clinical Assessment in Neuropsychiatry

21 January 2018

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Universal, robust, highly quantitative SNP allele frequency measurement in DNA pools.

21 January 2018

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Performing the exact test of Hardy-Weinberg proportion for multiple alleles

21 January 2018

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Model-free analysis and permutation tests for allelic associations.

21 January 2018

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An extended transmission/disequilibrium test (TDT) for multi-allele marker loci.

21 January 2018

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Association of NOD2 leucine-rich repeat variants with susceptibility to Crohn's disease

21 January 2018

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A frameshift mutation in NOD2 associated with susceptibility to Crohn's disease

21 January 2018

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The high affinity neurotensin receptor gene (NTSR1): comparative sequencing and association studies in schizophrenia

21 January 2018

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Cheap, accurate and rapid allele frequency estimation of single nucleotide polymorphisms by primer extension and DHPLC in DNA pools

21 January 2018

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Family-based linkage disequilibrium mapping using SNP marker haplotypes: application to a potential locus for schizophrenia at chromosome 22q11

21 January 2018

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Blind Analysis of Denaturing High-Performance Liquid Chromatography as a Tool for Mutation Detection

21 January 2018

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Genotyping single nucleotide polymorphisms by primer extension and high performance liquid chromatography

21 January 2018

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Late‐Onset psychosis in the velo‐cardio‐facial syndrome

21 January 2018

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7 January 2021

Velocardiofacial manifestations and microdeletions in schizophrenic inpatients

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7 January 2021

Follow-up report of potential linkage for schizophrenia on chromosome 22q: Part 3

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7 January 2021

Sequence-ready physical map of the mouse chromosome 16 region with conserved synteny to the human velocardiofacial syndrome region on 22q11.2.

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https://api.crossref.org/works/10.1038%2FSJ.MP.4001188

7 January 2021

Monte Carlo tests for associations between disease and alleles at highly polymorphic loci

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001188

7 January 2021

Variation is the spice of life

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https://api.crossref.org/works/10.1038%2FSJ.MP.4001188

7 January 2021

Family-based association mapping provides evidence for a gene for reading disability on chromosome 15q

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7 January 2021

Identifiers

DOI

10.1038/SJ.MP.4001188

1 reference

17 May 2018

release_khvp3mnoznaqvdeozm7tlodrma

Fatcat ID

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/khvp3mnoznaqvdeozm7tlodrma

24 November 2022

mapped directly with Wikidata item

PubMed ID

12476324

1 reference

17 May 2018