2015 - Fellow of the Australian Academy of Health and Medical Science
2014 - Fellow of the American Association for the Advancement of Science (AAAS)
Genetics, Genome-wide association study, Single-nucleotide polymorphism, Heritability and Genetic association are his primary areas of study. His Locus, Quantitative trait locus, Candidate gene, Allele and Gene investigations are all subjects of Genetics research. His work deals with themes such as Schizophrenia, Bipolar disorder, Internal medicine, Disease and Genetic architecture, which intersect with Genome-wide association study.
His Single-nucleotide polymorphism study combines topics in areas such as Eye color, Case-control study and Polymorphism. The study incorporates disciplines such as Demography, Genetic correlation, Genetic variation and Human height in addition to Heritability. He usually deals with Twin study and limits it to topics linked to Developmental psychology and Personality, Genetic determinism and Risk factor.
Nicholas G. Martin mostly deals with Genetics, Genome-wide association study, Heritability, Single-nucleotide polymorphism and Twin study. Locus, Allele, Gene, Quantitative trait locus and Candidate gene are subfields of Genetics in which his conducts study. Nicholas G. Martin has included themes like Schizophrenia, Bioinformatics, Disease, Genetic association and Genetic architecture in his Genome-wide association study study.
His study looks at the intersection of Heritability and topics like Demography with Cohort and Body mass index. His Single-nucleotide polymorphism study frequently draws connections to adjacent fields such as Internal medicine. His research integrates issues of Developmental psychology and Psychiatry in his study of Twin study.
Nicholas G. Martin mainly focuses on Genome-wide association study, Genetics, Clinical psychology, Genetic association and Depression. His biological study spans a wide range of topics, including Meta-analysis, Schizophrenia and Genetic architecture. His study ties his expertise on Bipolar disorder together with the subject of Genetics.
His research investigates the link between Clinical psychology and topics such as Major depressive disorder that cross with problems in Genetic heterogeneity. His study in Genetic association is interdisciplinary in nature, drawing from both Evolutionary biology, Heritability and Mendelian randomization. As part of his studies on Heritability, he frequently links adjacent subjects like Demography.
Nicholas G. Martin spends much of his time researching Genome-wide association study, Genetics, Genetic association, Schizophrenia and Genetic architecture. The subject of his Genome-wide association study research is within the realm of Single-nucleotide polymorphism. Nicholas G. Martin interconnects Methylation, Allele and Cannabis in the investigation of issues within Single-nucleotide polymorphism.
His Schizophrenia research includes elements of Major depressive disorder and Depression. His studies deal with areas such as Cerebral cortex, Cortex and Evolutionary biology as well as Genetic architecture. His Heritability study incorporates themes from Genetic variation and Genotype.
This overview was generated by a machine learning system which analysed the scientist’s body of work. If you have any feedback, you can contact us here.
Common SNPs explain a large proportion of the heritability for human height
Jian Yang;Beben Benyamin;Brian P. McEvoy;Scott Gordon.
Nature Genetics (2010)
Breast cancer and hormone replacement therapy: collaborative reanalysis of data from 51 epidemiological studies of 52 705 women with breast cancer and 108 411 women without breast cancer
E. E. Calle;C. W. Heath;R. J. Coates;J. M. Liff.
The Lancet (1997)
Biological, clinical and population relevance of 95 loci for blood lipids
Tanya M. Teslovich;Kiran Musunuru;Albert V. Smith;Andrew C. Edmondson.
Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index
Elizabeth K. Speliotes;Elizabeth K. Speliotes;Cristen J. Willer;Sonja I. Berndt;Keri L. Monda.
Nature Genetics (2010)
Hundreds of variants clustered in genomic loci and biological pathways affect human height
Hana Lango Allen;Karol Estrada;Guillaume Lettre;Sonja I. Berndt.
Discovery and refinement of loci associated with lipid levels
Cristen J. Willer;Ellen M. Schmidt;Sebanti Sengupta;Gina M. Peloso;Gina M. Peloso;Gina M. Peloso.
Nature Genetics (2013)
Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs
S. Hong Lee;Stephan Ripke;Stephan Ripke;Benjamin M. Neale;Benjamin M. Neale;Stephen V. Faraone.
Nature Genetics (2013)
Breast cancer and hormonal contraceptives : collaborative reanalysis of individual data on 53.297 women with breast cancer and 100.239 women without breast cancer from 54 epidemiological studies
E. E. Calle;C. W. Heath;H. L. Miracle-McMahill;R. J. Coates.
The Lancet (1996)
Defining the role of common variation in the genomic and biological architecture of adult human height
Andrew R. Wood;Tonu Esko;Jian Yang;Sailaja Vedantam.
Nature Genetics (2014)
Large-scale genome-wide association analysis of bipolar disorder identifies a new susceptibility locus near ODZ4
Pamela Sklar;Pamela Sklar;Stephan Ripke;Stephan Ripke;Laura J. Scott;Ole A. Andreassen.
Nature Genetics (2011)
Profile was last updated on December 6th, 2021.
Research.com Ranking is based on data retrieved from the Microsoft Academic Graph (MAG).
The ranking h-index is inferred from publications deemed to belong to the considered discipline.
If you think any of the details on this page are incorrect, let us know.
We appreciate your kind effort to assist us to improve this page, it would be helpful providing us with as much detail as possible in the text box below: