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Investigating the dark-side of the genome: a barrier to human disease variant discovery?

Biological research, 2023-07, Vol.56 (1), p.42-42, Article 42

2023

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Investigating copy number variants in schizophrenia pedigrees using a new consensus pipeline called PECAN

Scientific reports, 2024-07, Vol.14 (1), p.17518-9, Article 17518

2024

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Converting single nucleotide variants between genome builds: from cautionary tale to solution

Briefings in bioinformatics, 2021-09, Vol.22 (5)

2021

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The impact of perinatal maternal stress on the maternal and infant gut and human milk microbiomes: A scoping review protocol

PloS one, 2024-06, Vol.19 (6), p.e0304787

2024

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Evidence for parent-of-origin effects in autism spectrum disorder: a narrative review

Journal of applied genetics, 2023-05, Vol.64 (2), p.303-317

2023

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Methyl-CpG-binding protein 2 mediates overlapping mechanisms across brain disorders

Scientific reports, 2020-12, Vol.10 (1), p.22255-22255, Article 22255

2020

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Whole genome sequencing study of identical twins discordant for psychosis

Translational psychiatry, 2024-07, Vol.14 (1), p.313-6, Article 313

2024

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BRD7, a Subunit of SWI/SNF Complexes, Binds Directly to BRCA1 and Regulates BRCA1-Dependent Transcription

Cancer research (Chicago, Ill.), 2010-03, Vol.70 (6), p.2538-2547

2010

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Ultrarare Missense Variants Implicated in Utah Pedigrees Multiply Affected With Schizophrenia

Biological psychiatry global open science, 2023-10, Vol.3 (4), p.797-802

2023

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Parental opinion of consent in neonatal research

Archives of disease in childhood. Fetal and neonatal edition, 2019-07, Vol.104 (4), p.F409-F414

2019

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A critical review of life cycle assessment studies of woody biomass conversion to sugars

Philosophical transactions of the Royal Society of London. Series A: Mathematical, physical, and engineering sciences, 2021-09, Vol.379 (2206), p.20200335

2021

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DNA sequence-level analyses reveal potential phenotypic modifiers in a large family with psychiatric disorders

Molecular psychiatry, 2018-12, Vol.23 (12), p.2254-2265

2018

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Identification of a novel locus on chromosome 2q13, which predisposes to clinical vertebral fractures independently of bone density

Annals of the rheumatic diseases, 2018-03, Vol.77 (3), p.378-385

2018

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SuRFing the genomics wave: an R package for prioritising SNPs by functionality

Genome medicine, 2014-10, Vol.6 (10), p.79-79, Article 79

2014

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Genome-wide haplotype-based association analysis of major depressive disorder in Generation Scotland and UK Biobank

Translational psychiatry, 2017-11, Vol.7 (11), p.1263-9, Article 1263

2017

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GP94 Paediatric Radiation: Do we know what we are doing?

Archives of disease in childhood, 2019-06, Vol.104 (Suppl 3), p.A68

2019

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FAMILY-BASED STUDIES IN PSYCHIATRIC GENOMICS: PROGRESS AND RELEVANCE IN 2024

European neuropsychopharmacology, 2024-10, Vol.87, p.31-32

2024

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Preliminary assessment of pre-morbid DNA methylation in individuals at high genetic risk of mood disorders

Bipolar disorders, 2016-08, Vol.18 (5), p.410-422

2016

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PROGRESS UPDATE FROM THE PGC PEDIGREE SEQUENCING WORKING GROUP: RESULTS AND NOVEL METHODOLOGIES

European neuropsychopharmacology, 2024-10, Vol.87, p.33-33

2024

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W87. RARE, PATHOGENIC COPY NUMBER VARIANTS CO-SEGREGATE WITH SCHIZOPHRENIA IN PEDIGREE COHORT

European neuropsychopharmacology, 2023-10, Vol.75, p.S151-S151

2023

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T16. A BAYESIAN FRAMEWORK TO MODEL PEDIGREE-BASED CAUSALITY USING NEXT-GENERATION SEQUENCING DATA

European neuropsychopharmacology, 2022-10, Vol.63, p.e176-e177

2022

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SA22INVESTIGATING PARENT-OF-ORIGIN EFFECTS IN AUTISM SPECTRUM DISORDER USING NEXT GENERATION SEQUENCING DATA

European neuropsychopharmacology, 2019, Vol.29, p.S1199-S1200

2019

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Neutrophil-lymphocyte ratio and prediction of pathological complete response to neoadjuvant treatment in breast cancer

Journal of clinical oncology, 2022-06, Vol.40 (16_suppl), p.e12627-e12627

2022

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T84. RARE VARIANT ANALYSIS IN A PAIR OF PAKISTANI PEDIGREES WITH A HIGH LOAD OF PSYCHIATRIC ILLNESS

European neuropsychopharmacology, 2023-10, Vol.75, p.S207-S207

2023

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Independent Computerized Cognitive Remediation for Psychosis: An Investigation of Patient Experiences

The journal of nervous and mental disease, 2018-08, Vol.206 (8), p.606-613

2018

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Investigating the dark-side of the genome: a barrier to human disease variant discovery?

Investigating copy number variants in schizophrenia pedigrees using a new consensus pipeline called PECAN

Converting single nucleotide variants between genome builds: from cautionary tale to solution

The impact of perinatal maternal stress on the maternal and infant gut and human milk microbiomes: A scoping review protocol

Evidence for parent-of-origin effects in autism spectrum disorder: a narrative review

Methyl-CpG-binding protein 2 mediates overlapping mechanisms across brain disorders

Whole genome sequencing study of identical twins discordant for psychosis

BRD7, a Subunit of SWI/SNF Complexes, Binds Directly to BRCA1 and Regulates BRCA1-Dependent Transcription

Ultrarare Missense Variants Implicated in Utah Pedigrees Multiply Affected With Schizophrenia

Parental opinion of consent in neonatal research

A critical review of life cycle assessment studies of woody biomass conversion to sugars

DNA sequence-level analyses reveal potential phenotypic modifiers in a large family with psychiatric disorders

Identification of a novel locus on chromosome 2q13, which predisposes to clinical vertebral fractures independently of bone density

SuRFing the genomics wave: an R package for prioritising SNPs by functionality

Genome-wide haplotype-based association analysis of major depressive disorder in Generation Scotland and UK Biobank

GP94 Paediatric Radiation: Do we know what we are doing?

FAMILY-BASED STUDIES IN PSYCHIATRIC GENOMICS: PROGRESS AND RELEVANCE IN 2024

Preliminary assessment of pre-morbid DNA methylation in individuals at high genetic risk of mood disorders

PROGRESS UPDATE FROM THE PGC PEDIGREE SEQUENCING WORKING GROUP: RESULTS AND NOVEL METHODOLOGIES

W87. RARE, PATHOGENIC COPY NUMBER VARIANTS CO-SEGREGATE WITH SCHIZOPHRENIA IN PEDIGREE COHORT

T16. A BAYESIAN FRAMEWORK TO MODEL PEDIGREE-BASED CAUSALITY USING NEXT-GENERATION SEQUENCING DATA

SA22INVESTIGATING PARENT-OF-ORIGIN EFFECTS IN AUTISM SPECTRUM DISORDER USING NEXT GENERATION SEQUENCING DATA

Neutrophil-lymphocyte ratio and prediction of pathological complete response to neoadjuvant treatment in breast cancer

T84. RARE VARIANT ANALYSIS IN A PAIR OF PAKISTANI PEDIGREES WITH A HIGH LOAD OF PSYCHIATRIC ILLNESS

Independent Computerized Cognitive Remediation for Psychosis: An Investigation of Patient Experiences

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