← back to search

Scott D. Gordon

QIMR Berghofer Medical Research Institute · AU
Area of research
Genetics · Pediatrics, Perinatology and Child Health
Research interest
Research interests include Genetic Associations and Epidemiology, Genetic Mapping and Diversity in Plants and Animals, Genetics and Neurodevelopmental Disorders, and Birth, Development, and Health.
h-index
95
citations
54,856
works
333
NIH funding
primary concept
Biology
email

Recent publications

Genomics yields biological and phenotypic insights into bipolar disorder
Nature 2025cited by 144position: middledoi
Mapping the genetic landscape across 14 psychiatric disorders
Nature 2025cited by 43position: middledoi
Associations between common genetic variants and income provide insights about the socio-economic health gradient
Nature Human Behaviour 2025cited by 24position: middledoi
Polygenic prediction of body mass index and obesity through the life course and across ancestries
Nature Medicine 2025cited by 22position: middledoi
Genome-wide association meta-analysis of childhood ADHD symptoms and diagnosis identifies new loci and potential effector genes
Nature Genetics 2025cited by 6position: middledoi
Genome-wide association analyses identify 95 risk loci and provide insights into the neurobiology of post-traumatic stress disorder
Nature Genetics 2024cited by 168position: middledoi
X-chromosome and kidney function: evidence from a multi-trait genetic analysis of 908,697 individuals reveals sex-specific and sex-differential findings in genes regulated by androgen response elements
Nature Communications 2024cited by 12position: middledoi
Multivariate genome-wide association meta-analysis of over 1 million subjects identifies loci underlying multiple substance use disorders
Nature Mental Health 2023cited by 223position: middledoi
Multi-ancestry study of the genetics of problematic alcohol use in over 1 million individuals
Nature Medicine 2023cited by 173position: middledoi
Genome-wide association study meta-analysis of dizygotic twinning illuminates genetic regulation of female fecundity
Human Reproduction 2023cited by 27position: middledoi
A saturated map of common genetic variants associated with human height
Nature 2022cited by 880position: middledoi
Genetic diversity fuels gene discovery for tobacco and alcohol use
Nature 2022cited by 502position: middledoi
Within-sibship genome-wide association analyses decrease bias in estimates of direct genetic effects
Nature Genetics 2022cited by 389position: middledoi
Genome-wide association analyses of physical activity and sedentary behavior provide insights into underlying mechanisms and roles in disease prevention
Nature Genetics 2022cited by 230position: middledoi
A Saturated Map of Common Genetic Variants Associated with Human Height from 5.4 Million Individuals of Diverse Ancestries
bioRxiv (Cold Spring Harbor Laboratory) 2022cited by 18position: middledoi
Genome-wide association study of more than 40,000 bipolar disorder cases provides new insights into the underlying biology
Nature Genetics 2021cited by 1,563position: middledoi
The Genetic Architecture of Depression in Individuals of East Asian Ancestry
JAMA Psychiatry 2021cited by 194position: middledoi
Identifying the Common Genetic Basis of Antidepressant Response
Biological Psychiatry Global Open Science 2021cited by 130position: middledoi
Genome-wide association study in almost 195,000 individuals identifies 50 previously unidentified genetic loci for eye color
Science Advances 2021cited by 86position: middledoi
Genetic association study of childhood aggression across raters, instruments, and age
Translational Psychiatry 2021cited by 76position: middledoi
Enhancing Discovery of Genetic Variants for Posttraumatic Stress Disorder Through Integration of Quantitative Phenotypes and Trauma Exposure Information
Biological Psychiatry 2021cited by 67position: middledoi
Identical twins carry a persistent epigenetic signature of early genome programming
Nature Communications 2021cited by 65position: middledoi
Polygenic Risk Scores Derived From Varying Definitions of Depression and Risk of Depression
JAMA Psychiatry 2021cited by 62position: middledoi
The Australian Genetics of Depression Study: New Risk Loci and Dissecting Heterogeneity Between Subtypes
Biological Psychiatry 2021cited by 50position: middledoi
Model-based assessment of replicability for genome-wide association meta-analysis
Nature Communications 2021cited by 40position: middledoi
Genetic identification of cell types underlying brain complex traits yields insights into the etiology of Parkinson’s disease
Nature Genetics 2020cited by 381position: middledoi
A large-scale genome-wide association study meta-analysis of cannabis use disorder
The Lancet Psychiatry 2020cited by 376position: middledoi
Genome-wide association meta-analyses combining multiple risk phenotypes provide insights into the genetic architecture of cutaneous melanoma susceptibility
Nature Genetics 2020cited by 236position: middledoi
Genome-wide gene-environment analyses of major depressive disorder and reported lifetime traumatic experiences in UK Biobank
Molecular Psychiatry 2020cited by 219position: middledoi
Genome-wide Association Analysis in Humans Links Nucleotide Metabolism to Leukocyte Telomere Length
The American Journal of Human Genetics 2020cited by 174position: middledoi

Grants

No grants ingested yet.

Frequent collaborators

Sarah E. Medland · Cardiff University5 papers (2012–2021)Anjali K. Henders · Queensland Eye Institute3 papers (2012–2017)Stuart MacGregor · The University of Queensland3 papers (2012–2019)Grant W. Montgomery · Marshall University3 papers (2012–2017)Adrián I. Campos · Virginia Commonwealth University2 papers (2021–2021)Timothy D. Spector · King's College London2 papers (2012–2012) · 2 papers (2017–2019)David C. Whiteman · University of Edinburgh2 papers (2021–2021)David L. Duffy · University of Queensland2 papers (2012–2017)Dale R. Nyholt · The University of Western Australia2 papers (2012–2021)Catherine M. Olsen · University of Manchester2 papers (2021–2021)Brittany L. Mitchell · University of Lausanne2 papers (2021–2021)Enda M. Byrne · Institut de Psychiatrie et Neurosciences de Paris2 papers (2021–2021)Naomi R. Wray · University of Oulu2 papers (2021–2021) · 1 papers (2012–2012)Danielle R. Reed · Iowa State University1 papers (2019–2019)Richard A. Sturm · National Human Genome Research Institute1 papers (2017–2017)Hitoshi Zembutsu · RIKEN Center for Integrative Medical Sciences1 papers (2012–2012) · 1 papers (2012–2012)Jinglei Lv · The University of Sydney1 papers (2020–2020)