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Exploration of empirical Bayes hierarchical modeling for the analysis of genome-wide association study data.

GILL, MICHAEL; HERON, ELIZABETH ANN; GALLAGHER, LOUISE (2011)

Functionality of promoter microsatellites of arginine vasopressin receptor 1A (AVPR1A): implications for Autism.

ANNEY, RICHARD JAMES LEON; GILL, MICHAEL; GALLAGHER, LOUISE (BIOMED CENTRAL, 2011)

Mental health problems in children with prader-willi syndrome.

GALLAGHER, LOUISE (2012)

Individual common variants exert weak effects on the risk for autism spectrum disorderspi.

ANNEY, RICHARD; MERIKANGAS, ALISON; HERON, ELIZABETH; GILL, MICHAEL; GALLAGHER, LOUISE (2012)

A novel approach of homozygous haplotype sharing identifies candidate genes in autism spectrum disorder.

ANNEY, RICHARD; MERIKANGAS, ALISON; MCGRATH, JANE; GALLAGHER, LOUISE (2012)

Abnormal functional connectivity in autism spectrum disorder is associated with disrupted white matter microstructural organisation

GALLAGHER, LOUISE (2013)

A novel approach of homozygous haplotype sharing identifies candidate genes in autism spectrum disorder.

GILL, MICHAEL; GALLAGHER, LOUISE (2011)

Assessing Problem based learning in Child and Adolescent Psychiatry at the Trinity College Dublin Ireland

GILL, MICHAEL; GALLAGHER, LOUISE; FRODL, THOMAS (2012)

The phenotypic manifestations of rare genic CNVs in autism spectrum disorder.

HERON, ELIZABETH; GILL, MICHAEL; ANNEY, RICHARD; CORVIN, AIDEN; GALLAGHER, LOUISE (2014)

Recurrent Rearrangements of Chromosome 1q21.1 and Variable Pediatric Phenotypes

GALLAGHER, LOUISE; GILL, MICHAEL (Massachusetts Medical Society, 2008)

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Exploration of empirical Bayes hierarchical modeling for the analysis of genome-wide association study data.

Functionality of promoter microsatellites of arginine vasopressin receptor 1A (AVPR1A): implications for Autism.

Mental health problems in children with prader-willi syndrome.

Individual common variants exert weak effects on the risk for autism spectrum disorderspi.

A novel approach of homozygous haplotype sharing identifies candidate genes in autism spectrum disorder.

Abnormal functional connectivity in autism spectrum disorder is associated with disrupted white matter microstructural organisation

A novel approach of homozygous haplotype sharing identifies candidate genes in autism spectrum disorder.

Assessing Problem based learning in Child and Adolescent Psychiatry at the Trinity College Dublin Ireland

The phenotypic manifestations of rare genic CNVs in autism spectrum disorder.

Recurrent Rearrangements of Chromosome 1q21.1 and Variable Pediatric Phenotypes

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All of TARA

This Collection

Discover

Author

Subject

Date Issued

Sponsor

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Exploration of empirical Bayes hierarchical modeling for the analysis of genome-wide association study data.

Functionality of promoter microsatellites of arginine vasopressin receptor 1A (AVPR1A): implications for Autism.

Mental health problems in children with prader-willi syndrome.

Individual common variants exert weak effects on the risk for autism spectrum disorderspi.

A novel approach of homozygous haplotype sharing identifies candidate genes in autism spectrum disorder.

Abnormal functional connectivity in autism spectrum disorder is associated with disrupted white matter microstructural organisation

A novel approach of homozygous haplotype sharing identifies candidate genes in autism spectrum disorder.

Assessing Problem based learning in Child and Adolescent Psychiatry at the Trinity College Dublin Ireland

The phenotypic manifestations of rare genic CNVs in autism spectrum disorder.

Recurrent Rearrangements of Chromosome 1q21.1 and Variable Pediatric Phenotypes