|
| 36533321 | RE: Extending the vulnerability-stress model of mental disorders: three-dimensional ÿ environment ÿ coping interaction study in anxiety. | | 2023 |
| 37308599 | The human genome harbours widespread exclusive yin yang haplotypes. | | 2023 |
| 35067685 | Weighted burden analysis in 200,000 exome-sequenced subjects characterises rare variant effects on BMI. | International Journal of Obesity | 2022 |
| 35396580 | Mapping genomic loci implicates genes and synaptic biology in schizophrenia. | Nature | 2022 |
| 35396579 | Rare coding variants in ten genes confer substantial risk for schizophrenia. | Nature | 2022 |
| 36044383 | Study of variants in genes implicated in rare familial migraine syndromes and their association with migraine in 200,000 exome-sequenced UK Biobank participants. | Annals of Human Genetics | 2022 |
| 35382908 | Identification of specific genes involved in schizophrenia aetiology - what difference does it make? | British Journal of Psychiatry | 2022 |
| 35749744 | Clinical features of UK Biobank subjects carrying protein-truncating variants in genes implicated in schizophrenia pathogenesis. | Psychiatric Genetics | 2022 |
| 35931093 | Concerns about the use of polygenic embryo screening for psychiatric and cognitive traits. | Lancet Psychiatry | 2022 |
| 35410376 | Exome sequencing in bipolar disorder identifies AKAP11 as a risk gene shared with schizophrenia. | Nat Genet | 2022 |
| 35604335 | Identification of specific genes involved in schizophrenia aetiology - what difference does it make? - CORRIGENDUM. | British Journal of Psychiatry | 2022 |
| 33910933 | Analysis of 200 000 exome-sequenced UK Biobank subjects illustrates the contribution of rare genetic variants to hyperlipidaemia. | Journal of Medical Genetics | 2022 |
| 33893496 | Investigation of Association of Rare, Functional Genetic Variants With Heavy Drinking and Problem Drinking in Exome Sequenced UK Biobank Participants. | Alcohol and Alcoholism | 2022 |
| 34216101 | Analysis of rare coding variants in 200,000 exome-sequenced subjects reveals novel genetic risk factors for type 2 diabetes. | Diabetes/Metabolism Research and Reviews | 2022 |
| 34688815 | Exploration of weighting schemes based on allele frequency and annotation for weighted burden association analysis of complex phenotypes. | Gene | 2022 |
| 34722352 | Analysis of 200,000 Exome-Sequenced UK Biobank Subjects Implicates Genes Involved in Increased and Decreased Risk of Hypertension. | Pulse | 2021 |
| 33970751 | Analysis of whole genome sequenced cases and controls shows that the association of variants in , , and with late onset Alzheimer's disease is driven by linkage disequilibrium with ε2/ε3/ε4 alleles. | Journal of Neurogenetics | 2021 |
| 34074949 | Haploinsufficiency of the HIRA gene may not always produce severe neurodevelopmental consequences. | Psychiatric Genetics | 2021 |
| 34002096 | Genome-wide association study of more than 40,000 bipolar disorder cases provides new insights into the underlying biology. | Nat Genet | 2021 |
| 34050118 | Analysis of 200â¿¿000 exome-sequenced UK Biobank subjects fails to identify genes influencing probability of developing a mood disorder resulting in psychiatric referral. | Psychiatric Genetics | 2021 |
| 33449327 | The reality of sex. | Irish Journal of Medical Science | 2021 |
| 33558082 | Corrigendum to "Analysis of exome-sequenced UK Biobank subjects implicates genes affecting risk of hyperlipidaemia " [131/1-2 (2020) 277-283]. | Molecular Genetics and Metabolism | 2021 |
| 33258115 | Mini-review: Role of the PI3K/Akt pathway and tyrosine phosphatases in Alzheimer's disease susceptibility. | Annals of Human Genetics | 2021 |
| 33333475 | Analysis of 50,000 exome-sequenced UK Biobank subjects fails to identify genes influencing probability of developing a mood disorder resulting in psychiatric referral. | Journal of Affective Disorders | 2021 |
| 34789511 | Should all babies have their genome sequenced at birth? | BMJ | 2021 |
| 31112269 | Assessment of Potential Clinical Role for Exome Sequencing in Schizophrenia. | Schizophrenia Bulletin | 2020 |
| 32020597 | Weighted burden analysis of exome-sequenced late-onset Alzheimer's cases and controls provides further evidence for a role for PSEN1 and suggests involvement of the PI3K/Akt/GSK-3β and WNT signalling pathways. | Annals of Human Genetics | 2020 |
| 31925776 | LD scores are associated with differences in allele frequencies between populations but LD score regression can still distinguish confounding from polygenicity. | Annals of Human Genetics | 2020 |
| 33752217 | Variants in ACE2 and TMPRSS2 Genes Are Not Major Determinants of COVID-19 Severity in UK Biobank Subjects. | Human Heredity | 2020 |
| 33100243 | Author's reply. | British Journal of Psychiatry | 2020 |
| 32747172 | Analysis of exome-sequenced UK Biobank subjects implicates genes affecting risk of hyperlipidaemia. | Molecular Genetics and Metabolism | 2020 |
| 32741288 | Study of Transgender Patients: Conclusions Are Not Supported by Findings. | American Journal of Psychiatry | 2020 |
| 32796235 | Do damaging variants of SLC6A9, the gene for the glycine transporter 1 (GlyT-1), protect against schizophrenia? | Psychiatric Genetics | 2020 |
| 33412546 | Multiple Linear Regression Allows Weighted Burden Analysis of Rare Coding Variants in an Ethnically Heterogeneous Population. | Human Heredity | 2020 |
| 32554502 | Pseudouridylation defect due to <i>DKC1</i> and <i>NOP10</i> mutations causes nephrotic syndrome with cataracts, hearing impairment, and enterocolitis. | Proc Natl Acad Sci U S A | 2020 |
| 31530798 | NRXN1 is associated with enlargement of the temporal horns of the lateral ventricles in psychosis. | Transl Psychiatry | 2019 |
| 31685041 | A possible role for sarcosine in the management of schizophrenia. | British Journal of Psychiatry | 2019 |
| 30258123 | A weighted burden test using logistic regression for integrated analysis of sequence variants, copy number variants and polygenic risk score. | European Journal of Human Genetics | 2019 |
| 30859703 | Genetic association and functional characterization of MCPH1 gene variation in bipolar disorder and schizophrenia. | American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics | 2019 |
| 30906985 | Clinical relevance of genome-wide polygenic score may be less than claimed. | Annals of Human Genetics | 2019 |
| 30900968 | Pursuing parity: genetic tests for psychiatric conditions in the UK National Health Service. | British Journal of Psychiatry | 2019 |
| 30664045 | In-silico investigation of coding variants potentially affecting the functioning of the glutamatergic N-methyl-D-aspartate receptor in schizophrenia. | Psychiatric Genetics | 2019 |
| 29148569 | Exome sequence analysis and follow up genotyping implicates rare ULK1 variants to be involved in susceptibility to schizophrenia. | Annals of Human Genetics | 2018 |
| 28895126 | Construction of an Exome-Wide Risk Score for Schizophrenia Based on a Weighted Burden Test. | Annals of Human Genetics | 2018 |
| 28847325 | Letter to the Editor: Schizophrenia does not represent the extreme of a normally distributed trait. | Psychological Medicine | 2018 |
| 28805183 | Letter to the Editor: Association between smoking and psychosis may be mediated by maternal smoking during pregnancy. | Psychological Medicine | 2018 |
| 29930110 | Analysis of shared heritability in common disorders of the brain. | Science | 2018 |
| 30160659 | Polygenic risk score for schizophrenia is more strongly associated with ancestry than with schizophrenia. | Psychiatric Genetics | 2018 |
| 29923609 | Mini-review: Update on the genetics of schizophrenia. | Annals of Human Genetics | 2018 |
| 29672343 | Polygenic risk score for schizophrenia is not strongly associated with the expression of specific genes or gene sets. | Psychiatric Genetics | 2018 |