(Q40219823)

18 September 2017

title

Molecular and genomic studies of IMMP2L and mutation screening in autism and Tourette syndrome (English)

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18 September 2017

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14

Stephen W Scherer

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18 September 2017

Thomas Schwarzbraun

2

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Peter Kroisel

12

object named as

Peter M Kroisel

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18 September 2017

Erwin Petek

1

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18 September 2017

Abdul Noor

3

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18 September 2017

Megha Patel

4

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18 September 2017

Kazuhiko Nakabayashi

5

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18 September 2017

Sanaa Choufani

6

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18 September 2017

Christian Windpassinger

7

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18 September 2017

Mara Stamenkovic

8

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18 September 2017

Mary M Robertson

9

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18 September 2017

Harald N Aschauer

10

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18 September 2017

Hugh M D Gurling

11

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18 September 2017

Klaus Wagner

13

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18 September 2017

John B Vincent

15

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18 September 2017

publication date

17 October 2006

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Molecular Genetics and Genomics

18 September 2017

published in

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18 September 2017

volume

277

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18 September 2017

issue

1

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18 September 2017

page(s)

71-81

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Defining the autism minimum candidate gene region on chromosome 7.

18 September 2017

cites work

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS00438-006-0173-1

Association and transmission analysis of the FMR1 IVS10 + 14C-T variant in autism

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS00438-006-0173-1

A new method for estimating synonymous and nonsynonymous rates of nucleotide substitution considering the relative likelihood of nucleotide and codon changes

21 January 2018

1 reference

12 December 2020

Reelin gene alleles and haplotypes as a factor predisposing to autistic disorder

1 reference

12 December 2020

An integrated view of copy number and allelic alterations in the cancer genome using single nucleotide polymorphism arrays

1 reference

12 December 2020

A mitochondrial protease with two catalytic subunits of nonoverlapping specificities.

1 reference

12 December 2020

Model-based analysis of oligonucleotide arrays: model validation, design issues and standard error application

1 reference

12 December 2020

Homozygous deletions and chromosome amplifications in human lung carcinomas revealed by single nucleotide polymorphism array analysis

1 reference

12 December 2020

Evolutionary diversification of mitochondrial proteomes: implications for human disease.

1 reference

12 December 2020

A genomewide screen of 345 families for autism-susceptibility loci

1 reference

12 December 2020

Mutation screening and association analysis of six candidate genes for autism on chromosome 7q

1 reference

12 December 2020

Model-based analysis of oligonucleotide arrays: expression index computation and outlier detection

1 reference

12 December 2020

Mitochondrial disorders: clinical and genetic features

1 reference

12 December 2020

Tourette syndrome in a pedigree with a 7;18 translocation: identification of a YAC spanning the translocation breakpoint at 18q22.3.

1 reference

12 December 2020

Mature DIABLO/Smac is produced by the IMP protease complex on the mitochondrial inner membrane

1 reference

12 December 2020

Examination of NRCAM, LRRN3, KIAA0716, and LAMB1 as autism candidate genes

1 reference

12 December 2020

Disruption of a novel gene (IMMP2L) by a breakpoint in 7q31 associated with Tourette syndrome

1 reference

12 December 2020

Signal peptides having standard and nonstandard cleavage sites can be processed by Imp1p of the mitochondrial inner membrane protease

1 reference

12 December 2020

PRODH mutations and hyperprolinemia in a subset of schizophrenic patients

1 reference

12 December 2020

Association between 7q31 markers and Tourette syndrome.

1 reference

12 December 2020

The prevalence of Gilles de la Tourette syndrome in children and adolescents with autism: a large scale study

1 reference

12 December 2020

Detection of single-nucleotide polymorphisms with the WAVE DNA fragment analysis system

1 reference

12 December 2020

Genetics of austim: complex aetiology for a heterogeneous disorder

1 reference

12 December 2020

Candidate region for Gilles de la Tourette syndrome at 7q31

1 reference

12 December 2020

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

1 reference

12 December 2020

10.1007/S00438-006-0173-1

Identifiers

DOI

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18 September 2017

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