(Q33277435)

2 March 2018

title

Case-control and family-based association studies of candidate genes in autistic disorder and its endophenotypes: TPH2 and GLO1. (English)

1 reference

2 March 2018

0 references

1 reference

17

1 reference

2 March 2018

Tiziana Pascucci

object named as

Tiziana Pascucci

14

0 references

Maurizio Elia

object named as

Maurizio Elia

11

0 references

Rainald Moessner

5

object named as

Rainald Moessner

1 reference

2 March 2018

author name string

Roberto Sacco

1

1 reference

2 March 2018

Veruska Papaleo

2

1 reference

2 March 2018

Jorg Hager

3

1 reference

2 March 2018

Francis Rousseau

4

1 reference

2 March 2018

Roberto Militerni

6

1 reference

2 March 2018

Carmela Bravaccio

7

1 reference

2 March 2018

Simona Trillo

8

1 reference

2 March 2018

Cindy Schneider

9

1 reference

2 March 2018

Raun Melmed

10

1 reference

2 March 2018

Paolo Curatolo

12

1 reference

2 March 2018

Barbara Manzi

13

1 reference

2 March 2018

Stefano Puglisi-Allegra

15

1 reference

2 March 2018

Karl-Ludvig Reichelt

16

1 reference

2 March 2018

publication date

8 March 2007

1 reference

2 March 2018

published in

BMC Medical Genetics

1 reference

2 March 2018

volume

8

1 reference

2 March 2018

page(s)

11

1 reference

2 March 2018

https://scigraph.springernature.com/pub.10.1186/1471-2350-8-11

exact match

0 references

cites work

Searching for ways out of the autism maze: genetic, epigenetic and environmental clues

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1851007

The developmental neurobiology of autism spectrum disorder.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1851007

Selective serotonin reuptake inhibitors in autism: a review of efficacy and tolerability.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1851007

The neuropathology of autism: a review

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1851007

Amygdala responsiveness is modulated by tryptophan hydroxylase-2 gene variation.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1851007

Paraoxonase gene variants are associated with autism in North America, but not in Italy: possible regional specificity in gene-environment interactions.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1851007

Allelic heterogeneity at the serotonin transporter locus (SLC6A4) confers susceptibility to autism and rigid-compulsive behaviors

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1851007

Possible association between autism and variants in the brain-expressed tryptophan hydroxylase gene (TPH2).

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1851007

Molecular genetics of autism spectrum disorder.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1851007

Association between the HOXA1 A218G polymorphism and increased head circumference in patients with autism

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1851007

Glyoxalase I--structure, function and a critical role in the enzymatic defence against glycation

21 June 2018

2 references

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1851007

21 June 2018

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1851007

A unique central tryptophan hydroxylase isoform

31 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1851007

Synthesis of serotonin by a second tryptophan hydroxylase isoform

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1851007

Genetic perspectives on the serotonin transporter

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1851007

Genetics of austim: complex aetiology for a heterogeneous disorder

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1851007

Inference of population structure using multilocus genotype data

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1851007

Microcephaly and macrocephaly in autism

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1851007

The TDT and other family-based tests for linkage disequilibrium and association

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1851007

Platelet serotonin, a possible marker for familial autism

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1851007

Centiles for adult head circumference

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1851007

Physical growth: National Center for Health Statistics percentiles

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1851007

Proteomic studies identified a single nucleotide polymorphism in glyoxalase I as autism susceptibility factor.

21 June 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-8-11

Tryptophan hydroxylase-2 controls brain serotonin synthesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-8-11

Macrocephaly in autism and other pervasive developmental disorders.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-8-11

The family based association test method: strategies for studying general genotype--phenotype associations.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-8-11

Family-based association study of TPH1 and TPH2 polymorphisms in autism.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-8-11

Transmission disequilibrium of polymorphic variants in the tryptophan hydroxylase-2 gene in children and adolescents with obsessive-compulsive disorder

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-8-11

Altered neocortical cell density and layer thickness in serotonin transporter knockout mice: a quantitation study.

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1851007

Additive effects of serotonin transporter and tryptophan hydroxylase-2 gene variation on emotional processing.

31 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1851007

31 October 2018

Identifiers

DOI

10.1186/1471-2350-8-11

1 reference

2 March 2018

PMC publication ID

1851007

1 reference

2 March 2018

PubMed publication ID

17346350

1 reference

2 March 2018