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  1. No Access

    Article

    Additive or Interactive Associations of Food Allergies with Glutathione S-Transferase Genes in Relation to ASD and ASD Severity in Jamaican Children

    To investigate additive and interactive associations of food allergies with three glutathione S-transferase (GST) genes in relation to ASD and ASD severity in Jamaican children. Using data from 344 1:1 age- an...

    Sepideh Saroukhani, Maureen Samms-Vaughan in Journal of Autism and Developmental Disord… (2024)

  2. Article

    Open Access

    Multi-omics and pathway analyses of genome-wide associations implicate regulation and immunity in verbal declarative memory performance

    Uncovering the functional relevance underlying verbal declarative memory (VDM) genome-wide association study (GWAS) results may facilitate the development of interventions to reduce age-related memory decline ...

    Hao Mei, Jeannette Simino, Lianna Li, Fan Jiang in Alzheimer's Research & Therapy (2024)

  3. Article

    Open Access

    Factors associated with blood mercury concentrations and their interactions with three glutathione S-transferase genes (GSTT1, GSTM1, and GSTP1): an exposure assessment study of typically develo** Jamaican children

    Jamaican soil is abundant in heavy metals including mercury (Hg). Due to availability and ease of access, fish is a traditional dietary component in Jamaica and a significant source of Hg exposure. Mercury is ...

    Sheikh Farzana Zaman, Maureen Samms-Vaughan, Sepideh Saroukhani in BMC Pediatrics (2024)

  4. Article

    Open Access

    Identification of circulating proteins associated with general cognitive function among middle-aged and older adults

    Identifying circulating proteins associated with cognitive function may point to biomarkers and molecular process of cognitive impairment. Few studies have investigated the association between circulating prot...

    Adrienne Tin, Alison E. Fohner, Qiong Yang, Jennifer A. Brody in Communications Biology (2023)

  5. No Access

    Article

    Multivariate genetic analysis of personality and cognitive traits reveals abundant pleiotropy

    Personality and cognitive function are heritable mental traits whose genetic foundations may be distributed across interconnected brain functions. Previous studies have typically treated these complex mental t...

    Guy Hindley, Alexey A. Shadrin, Dennis van der Meer in Nature Human Behaviour (2023)

  6. Article

    Open Access

    Genome-wide meta-analyses reveal novel loci for verbal short-term memory and learning

    Understanding the genomic basis of memory processes may help in combating neurodegenerative disorders. Hence, we examined the associations of common genetic variants with verbal short-term memory and verbal le...

    Jari Lahti, Samuli Tuominen, Qiong Yang, Giulio Pergola in Molecular Psychiatry (2022)

  7. Article

    Open Access

    Clonal hematopoiesis of indeterminate potential, DNA methylation, and risk for coronary artery disease

    Age-related changes to the genome-wide DNA methylation (DNAm) pattern observed in blood are well-documented. Clonal hematopoiesis of indeterminate potential (CHIP), characterized by the age-related acquisition...

    M d Mesbah Uddin, Ngoc Quynh H. Nguyen, Bing Yu, Jennifer A. Brody in Nature Communications (2022)

  8. Article

    Open Access

    Markers of kidney function, genetic variation related to cognitive function, and cognitive performance in the UK Biobank

    Chronic kidney disease has been linked to worse cognition. However, this association may be dependent on the marker of kidney function used, and studies assessing modification by genetics are lacking. This stu...

    Erin L. Richard, Linda K. McEvoy, Ian J. Deary, Gail Davies in BMC Nephrology (2022)

  9. Article

    Open Access

    New insights into the genetic etiology of Alzheimer’s disease and related dementias

    Characterization of the genetic landscape of Alzheimer’s disease (AD) and related dementias (ADD) provides a unique opportunity for a better understanding of the associated pathophysiological processes. We per...

    Céline Bellenguez, Fahri Küçükali, Iris E. Jansen, Luca Kleineidam in Nature Genetics (2022)

  10. Article

    Open Access

    Correction: Association of low-frequency and rare coding variants with information processing speed

    Jan Bressler, Gail Davies, Albert V. Smith, Yasaman Saba in Translational Psychiatry (2022)

  11. Article

    Open Access

    Epigenome-wide association study of serum urate reveals insights into urate co-regulation and the SLC2A9 locus

    Elevated serum urate levels, a complex trait and major risk factor for incident gout, are correlated with cardiometabolic traits via incompletely understood mechanisms. DNA methylation in whole blood captures ...

    Adrienne Tin, Pascal Schlosser, Pamela R. Matias-Garcia in Nature Communications (2021)

  12. Article

    Open Access

    Association of low-frequency and rare coding variants with information processing speed

    Measures of information processing speed vary between individuals and decline with age. Studies of aging twins suggest heritability may be as high as 67%. The Illumina HumanExome Bead Chip genoty** array was...

    Jan Bressler, Gail Davies, Albert V. Smith, Yasaman Saba in Translational Psychiatry (2021)

  13. No Access

    Article

    Interaction of Blood Manganese Concentrations with GSTT1 in Relation to Autism Spectrum Disorder in Jamaican Children

    Using data from 266 age- and sex-matched pairs of Jamaican children with autism spectrum disorder (ASD) and typically develo** (TD) controls (2–8 years), we investigated whether glutathione S-transferase the...

    Mohammad H. Rahbar, Maureen Samms-Vaughan in Journal of Autism and Developmental Disord… (2021)

  14. Article

    Open Access

    Mitochondrial DNA copy number can influence mortality and cardiovascular disease via methylation of nuclear DNA CpGs

    Mitochondrial DNA copy number (mtDNA-CN) has been associated with a variety of aging-related diseases, including all-cause mortality. However, the mechanism by which mtDNA-CN influences disease is not currentl...

    Christina A. Castellani, Ryan J. Longchamps, Jason A. Sumpter in Genome Medicine (2020)

  15. No Access

    Article

    Perinatal Factors Associated with Autism Spectrum Disorder in Jamaican Children

    Mode of delivery, preterm birth, and low birth weight (LBW) are hypothesized to be associated with autism spectrum disorder (ASD) in the offspring. Using data from 343 ASD cases (2–8 years) and their age- and ...

    Sepideh Saroukhani, Maureen Samms-Vaughan in Journal of Autism and Developmental Disord… (2020)

  16. Article

    Open Access

    Genome-wide association study of cognitive function in diverse Hispanics/Latinos: results from the Hispanic Community Health Study/Study of Latinos

    Cognitive function such as reasoning, attention, memory, and language is strongly correlated with brain aging. Compared to non-Hispanic whites, Hispanics/Latinos have a higher risk of cognitive impairment and ...

    Xueqiu Jian, Tamar Sofer, Wassim Tarraf, Jan Bressler in Translational Psychiatry (2020)

  17. Article

    Open Access

    Global differences in the prevalence of the CpG island methylator phenotype of colorectal cancer

    CpG Island Methylator Phenotype (CIMP) is an epigenetic phenotype in CRC characterized by hypermethylation of CpG islands in promoter regions of tumor suppressor genes, leading to their transcriptional silenci...

    Shailesh Mahesh Advani, Pragati Shailesh Advani, Derek W. Brown in BMC Cancer (2019)

  18. Article

    Open Access

    An integrative cross-omics analysis of DNA methylation sites of glucose and insulin homeostasis

    Despite existing reports on differential DNA methylation in type 2 diabetes (T2D) and obesity, our understanding of its functional relevance remains limited. Here we show the effect of differential methylation...

    Jun Liu, Elena Carnero-Montoro, Jenny van Dongen, Samantha Lent in Nature Communications (2019)

  19. Article

    Open Access

    Author Correction: Study of 300,486 individuals identifies 148 independent genetic loci influencing general cognitive function

    Christina M. Lill, who contributed to analysis of data, was inadvertently omitted from the author list in the originally published version of this article. This has now been corrected in both the PDF and HTML ...

    Gail Davies, Max Lam, Sarah E. Harris, Joey W. Trampush in Nature Communications (2019)

  20. Article

    Open Access

    Meta-analysis of epigenome-wide association studies of cognitive abilities

    Cognitive functions are important correlates of health outcomes across the life-course. Individual differences in cognitive functions are partly heritable. Epigenetic modifications, such as DNA methylation, ar...

    Riccardo E. Marioni, Allan F. McRae, Jan Bressler, Elena Colicino in Molecular Psychiatry (2018)

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