Nicholas G Martin

发表

ViewPoint and ViewDist: Utilities for Rapid Graphing of Linkage Distributions and Identification of Outliers

Harry N Beeby, Sarah E Medland, Nicholas G Martin, 2006, Behavior genetics.

Ridgecounter: A program for obtaining semi-automated finger ridge counts

Sarah E Medland, Nicholas G Martin, Daniel A Park, 2007, Annals of human biology.

A Fast Method for Estimating Statistical Power of Multivariate GWAS in Real Case Scenarios: Examples from the Field of Imaging Genetics

Sarah E Medland, Nicholas G Martin, Paul M Thompson, 2018, Behavior genetics.

Modeling of the Hemodynamic Responses in Block Design fMRI Studies

Nicholas G Martin, Paul M Thompson, Katie L McMahon, 2014, Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism.

A Genomewide Association Study of Nicotine and Alcohol Dependence in Australian and Dutch Populations

Nicholas G Martin, Dorret I Boomsma, Gonneke Willemsen, 2010, Twin Research and Human Genetics.

META-ANALYSIS OF GENOME-WIDE ASSOCIATION STUDIES IDENTIFIES THREE NEW RISK LOCI FOR ATOPIC DERMATITIS

Christian Gieger, Nicholas J Timpson, Manuel A. R. Ferreira, 2011, Nature Genetics.

Use of latent profile analysis to identify eating disorder phenotypes in an adult Australian twin cohort.

Nicholas G Martin, Ross D Crosby, N. Martin, 2006, Archives of general psychiatry.

Monoacylglycerol lipase (MGLL) polymorphism rs604300 interacts with childhood adversity to predict cannabis dependence symptoms and amygdala habituation: Evidence from an endocannabinoid system-level analysis.

Ting Wang, Daofeng Li, Nicholas G Martin, 2015, Journal of abnormal psychology.

Genetic architecture of subcortical brain structures in 38,851 individuals

Benjamin S Aribisala, Tien Yin Wong, Wiro J Niessen, 2019, Nature Genetics.

Evaluation of HapMap data in six populations of European descent

Heikki Mannila, Markus Perola, Leena Peltonen, 2008, European Journal of Human Genetics.

Heritability and genetic correlation between the cerebral cortex and associated white matter connections

Olivier Salvado, Jurgen Fripp, Vincent Doré, 2016, Human brain mapping.

Genetic influences on schizophrenia and subcortical brain volumes: large-scale proof-of-concept and roadmap for future studies

Anbupalam Thalamuthu, Thomas E. Nichols, Manuel Mattheisen, 2016, Nature Neuroscience.

Correction: Corrigendum: Novel loci affecting iron homeostasis and their effects in individuals at risk for hemochromatosis

Christian Gieger, Thomas Meitinger, Andres Metspalu, 2015, Nature Communications.

A variant in FTO shows association with melanoma risk not due to BMI

Marko Hočevar, Florence Demenais, Kari Stefansson, 2013, Nature Genetics.

Genetic and environmental influences on cannabis use initiation and problematic use: a meta-analysis of twin studies.

Sarah E Medland, Nicholas G Martin, Michael C Neale, 2010, Addiction.

Association between endometriosis and the interleukin 1A (IL1A) locus.

Yadav Sapkota, Mark McEvoy, Rodney J Scott, 2015, Human reproduction.

Integrative analysis of omics summary data reveals putative mechanisms underlying complex traits

Ting Qi, Nicholas G Martin, Jian Yang, 2018, Nature Communications.

Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection

Jakob Grove, Esben Agerbo, Robert Plomin, 2018, Nature Genetics.

Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts

Christian Gieger, Thomas Meitinger, Mario Falchi, 2009, Nature Genetics.

Toward the development of a global induced pluripotent stem cell library.

Nicholas G Martin, Shinya Yamanaka, Marc Peschanski, 2013, Cell stem cell.

Estimation of the Rate of SNP Genotyping Errors From DNA Extracted From Different Tissues

Nicholas G Martin, Peter M Visscher, P. Visscher, 2005, Twin Research and Human Genetics.

Population Differences in Finger-Length Ratios: Ethnicity or Latitude?

Sarah E Medland, Nicholas G Martin, Dennis McFadden, 2006, Archives of sexual behavior.

A three-single-nucleotide polymorphism haplotype in intron 1 of OCA2 explains most human eye-color variation.

Wei Chen, Nicholas G Martin, David L Duffy, 2007, American journal of human genetics.

Two-locus Linkage Analysis Applied to Putative Quantitative Trait Loci for Lipoprotein(a) Levels

Nicholas G Martin, Harold Snieder, Cornelis Kluft, 2003, Twin Research.

Interactive effects of MC1R and OCA2 on melanoma risk phenotypes.

Wei Chen, Nicholas G Martin, David L Duffy, 2003, Human molecular genetics.

Dose response of the 16p11.2 distal copy number variant on intracranial volume and basal ganglia

Vincent Frouin, Norman Delanty, Katrin Amunts, 2018, Molecular Psychiatry.

Novel genetic loci associated with hippocampal volume

Benjamin S Aribisala, Wiro J Niessen, Peter Kochunov, 2017, Nature Communications.

Genetic effects on alcohol dependence risk: re-evaluating the importance of psychiatric and other heritable risk factors

Nicholas G Martin, Andrew C Heath, Pamela A F Madden, 2004, Psychological Medicine.

Dyslexia and DCDC2: normal variation in reading and spelling is associated with DCDC2 polymorphisms in an Australian population sample

Nicholas G Martin, Timothy C. Bates, Margaret J Wright, 2010, European Journal of Human Genetics.

Predicting White Matter Integrity from Multiple Common Genetic Variants

Ming-Chang Chiang, Arthur W Toga, Neda Jahanshad, 2012, Neuropsychopharmacology.

Genetic linkage to chromosome 22q12 for a heavy-smoking quantitative trait in two independent samples.

Leena Peltonen, Nicholas G Martin, Jaakko Kaprio, 2007, American journal of human genetics.

Genome-wide association analyses identify multiple loci associated with central corneal thickness and keratoconus

Tin Aung, Paul Mitchell, Ching-Yu Cheng, 2013, Nature Genetics.

A Comprehensive Neuropsychiatric Study of Elderly Twins: The Older Australian Twins Study

Henry Brodaty, Wei Wen, Peter R Schofield, 2009, Twin Research and Human Genetics.

Quantitative trait loci for CD4:CD8 lymphocyte ratio are associated with risk of type 1 diabetes and HIV-1 immune control.

Nicole Soranzo, Manuel A. R. Ferreira, Sarah E Medland, 2010, American journal of human genetics.

Genome-wide association study identifies novel genetic variants contributing to variation in blood metabolite levels

Christian Gieger, Toomas Haller, Andres Metspalu, 2015, Nature Communications.

Genomic inflation factors under polygenic inheritance

Mark I McCarthy, Reedik Mägi, Nicholas G Martin, 2011, European Journal of Human Genetics.

Development of a global network of induced pluripotent stem cell haplobanks.

Nicholas G Martin, Shinya Yamanaka, Marc Peschanski, 2015, Regenerative medicine.

Novel genetic loci underlying human intracranial volume identified through genome-wide association

Benjamin S Aribisala, Wiro J Niessen, Peter Kochunov, 2016, Nature Neuroscience.

Multivariate Genetic Analysis of Chronic Pelvic Pain and Associated Phenotypes

Nicholas G Martin, Susan A Treloar, Stephen H Kennedy, 2005, Behavior genetics.

Sex differences in heritability of BMI: a comparative study of results from twin studies in eight countries.

Jennifer R Harris, Nicholas G Martin, Dorret I Boomsma, 2003, Twin research : the official journal of the International Society for Twin Studies.

A locus on 19p13 modifies risk of breast cancer in BRCA1 mutation carriers and is associated with hormone receptor–negative breast cancer in the general population

Christiana Kartsonaki, Mads Thomassen, Julian Peto, 2010, Nature Genetics.

Robust estimation of experimentwise P values applied to a genome scan of multiple asthma traits identifies a new region of significant linkage on chromosome 20q13.

Nicholas G Martin, Peter M Visscher, Paul R Burton, 2005, American journal of human genetics.

Common variants in the trichohyalin gene are associated with straight hair in Europeans.

Manuel A. R. Ferreira, Sarah E Medland, Nicholas G Martin, 2009, American journal of human genetics.

Genome-wide association study of smoking initiation and current smoking.

Leena Peltonen, Nicholas G Martin, Cornelia van Duijn, 2009, American journal of human genetics.

Genome-wide physical activity interactions in adiposity. A meta-analysis of 200,452 adults

Claude Bouchard, Christian Gieger, Tuija Tammelin, 2017 .

Genome‐wide association analysis links multiple psychiatric liability genes to oscillatory brain activity

Jian Zhang, Neda Jahanshad, Sarah E Medland, 2017, bioRxiv.

A genomewide scan for intelligence identifies quantitative trait loci on 2q and 6p.

Danielle Posthuma, Nicholas G Martin, Dorret I Boomsma, 2005, American journal of human genetics.

Telomere length in circulating leukocytes is associated with lung function and disease

Christian Gieger, Melanie Waldenberger, Nilesh J Samani, 2013, European Respiratory Journal.

Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs

Jianxin Shi, Susmita Datta, Aribert Rothenberger, 2013, Nature Genetics.

Genetic Evidence for Causal Relationships Between Maternal Obesity-Related Traits and Birth Weight.

Tom M Palmer, Debbie A Lawlor, Marie-France Hivert, 2016, JAMA.

A genome scan for eye color in 502 twin families: most variation is due to a QTL on chromosome 15q.

Sarah E Medland, Nicholas G Martin, Jeffrey M Trent, 2004, Twin research : the official journal of the International Society for Twin Studies.

Genome-wide association study identifies 30 Loci Associated with Bipolar Disorder

Jakob Grove, Esben Agerbo, Andres Metspalu, 2017, bioRxiv.

CNV-association meta-analysis in 191,161 European adults reveals new loci associated with anthropometric traits

Yadav Sapkota, Thomas Meitinger, Andres Metspalu, 2017, Nature Communications.

Large-scale gene-centric meta-analysis across 32 studies identifies multiple lipid loci.

Tom R. Gaunt, Fotios Drenos, Meena Kumari, 2012, American journal of human genetics.

Alzheimer's Disease Risk Gene, GAB2, is Associated with Regional Brain Volume Differences in 755 Young Healthy Twins

Arthur W Toga, Neda Jahanshad, Sarah E Medland, 2012, Twin Research and Human Genetics.

A population-based study of Australian twins with melanoma suggests a strong genetic contribution to liability.

Nicholas G Martin, Philippa Youl, David C Whiteman, 2009, The Journal of investigative dermatology.

Childhood aggression and the co-occurrence of behavioural and emotional problems: results across ages 3–16 years from multiple raters in six cohorts in the EU-ACTION project

Robert Plomin, Justin M. Luningham, Sebastian Lundström, 2018, European Child & Adolescent Psychiatry.

Genome-wide association studies identify four ER negative–specific breast cancer risk loci

Patrick Neven, Michael Jones, Wei Lu, 2013, Nature Genetics.

The genetics of coronary heart disease: the contribution of twin studies.

Nicholas G Martin, Dorret I Boomsma, Nancy L Pedersen, 2003, Twin research : the official journal of the International Society for Twin Studies.

Genome-wide association study identifies loci influencing concentrations of liver enzymes in plasma

Christian Gieger, Yusuke Nakamura, Philippe Froguel, 2011, Nature Genetics.

Five endometrial cancer risk loci identified through genome-wide association analysis

Hui Zhao, Mark McEvoy, Julian Peto, 2016, Nature Genetics.

Heritability of the shape of subcortical brain structures in the general population

Wiro J Niessen, Neda Jahanshad, Nicholas G Martin, 2016, Nature Communications.

A common variant at the TERT-CLPTM1L locus is associated with estrogen receptor–negative breast cancer

Jane E. Carpenter, Peter Kraft, Gary K. Chen, 2011, Nature Genetics.

Genetic and Phenotypic Stability of Measures of Neuroticism Over 22 Years

Nicholas G Martin, Peter M Visscher, Patrick F Sullivan, 2007, Twin Research and Human Genetics.

Choice of Residential Location: Chance, Family Influences, or Genes?

Nicholas G Martin, Andrew C Heath, N. Martin, 2005, Twin Research and Human Genetics.

Twins Eye Study in Tasmania (TEST): Rationale and Methodology to Recruit and Examine Twins

Cong Sun, Nicholas G Martin, David A Mackey, 2009, Twin Research and Human Genetics.

Cortical Thickness Trajectories across the Lifespan: Data from 17,075 healthy individuals aged 3-90 years

Yang Wang, Patricia Gruner, Won Hee Lee, 2020, bioRxiv.

Polymorphisms in Nevus-Associated Genes MTAP, PLA2G6, and IRF4 and the Risk of Invasive Cutaneous Melanoma

Nicholas G Martin, David C Whiteman, David L Duffy, 2011, Twin Research and Human Genetics.

Subcortical Volume Trajectories across the Lifespan: Data from 18,605 healthy individuals aged 3-90 years

Yang Wang, Patricia Gruner, Won Hee Lee, 2020, bioRxiv.

Imaging genomics.

Nicholas G Martin, Paul M Thompson, Margaret J Wright, 2010, Current opinion in neurology.

Relative Finger Lengths, Sex Differences, and Psychological Traits

Sarah E Medland, Nicholas G Martin, J. Loehlin, 2009, Archives of sexual behavior.

Genetic variation of individual alpha frequency (IAF) and alpha power in a large adolescent twin sample.

Nicholas G Martin, Margaret J Wright, G. Geffen, 2006, International journal of psychophysiology : official journal of the International Organization of Psychophysiology.

A twin study of alcohol dependence, binge eating, and compensatory behaviors.

Nicholas G Martin, Andrew C Heath, Alexis E Duncan, 2013, Journal of studies on alcohol and drugs.

Common and specific genetic influences on EEG power bands delta, theta, alpha, and beta

Nicholas G Martin, Margaret J Wright, Brendan P. Zietsch, 2007, Biological Psychology.

Genome-wide association and longitudinal analyses reveal genetic loci linking pubertal height growth, pubertal timing and childhood adiposity.

Nicholas J Timpson, Clive Osmond, Mark I McCarthy, 2013, Human molecular genetics.

Sequence variants in three loci influence monocyte counts and erythrocyte volume.

Sarah E Medland, Nicholas G Martin, Dorret I Boomsma, 2009, American journal of human genetics.

Genome-wide linkage analysis of multiple measures of neuroticism of 2 large cohorts from Australia and the Netherlands.

Nicholas G Martin, Peter M Visscher, Patrick F Sullivan, 2008, Archives of general psychiatry.

Genetic Variance in a Component of the Language Acquisition Device: ROBO1 Polymorphisms Associated with Phonological Buffer Deficits

Sarah E Medland, Nicholas G Martin, Timothy C. Bates, 2011, Behavior genetics.

Limitations of DSM-IV Operationalizations of Alcohol Abuse and Dependence in a Sample of Australian Twins

Nicholas G Martin, Andrew C Heath, Pamela A F Madden, 2005, Twin Research and Human Genetics.

Evidence for Shared Genetic Influences on Self-Reported ADHD and Autistic Symptoms in Young Adult Australian Twins

Nicholas G Martin, N. Martin, J. Constantino, 2008, Twin Research and Human Genetics.

Variants in TF and HFE explain approximately 40% of genetic variation in serum-transferrin levels.

Leena Peltonen, Nicholas G Martin, Peter M Visscher, 2009, American journal of human genetics.

A single SNP in an evolutionary conserved region within intron 86 of the HERC2 gene determines human blue-brown eye color.

Nicholas G Martin, David L Duffy, D. Duffy, 2008, American journal of human genetics.

Contribution of genetic variation to transgenerational inheritance of DNA methylation

Nicholas G Martin, Peter M Visscher, Gibran Hemani, 2014, Genome Biology.

Genetic variants in LPL, OASL and TOMM40/APOE-C1-C2-C4 genes are associated with multiple cardiovascular-related traits

Manuel A. R. Ferreira, Nicholas G Martin, Andrew C Heath, 2011, BMC Medical Genetics.

Genetic and Nongenetic Variation Revealed for the Principal Components of Human Gene Expression

Nicholas G Martin, Peter M Visscher, Joseph E Powell, 2013, Genetics.

Do Candidate Genes Affect the Brain’s White Matter Microstructure? Large-Scale Evaluation of 6,165 Diffusion MRI Scans

Peter Kochunov, Thomas E. Nichols, Neda Jahanshad, 2017, bioRxiv.

Hypermethylation in the ZBTB20 gene is associated with major depressive disorder

Fei Gao, Alexis Battle, Jun Wang, 2014, Genome Biology.

High-density fine-mapping of a chromosome 10q26 linkage peak suggests association between endometriosis and variants close to CYP2C19.

Nicholas G Martin, Andrew Morris, Susan A Treloar, 2011, Fertility and sterility.

The ongoing adaptive evolution of ASPM and Microcephalin is not explained by increased intelligence.

Nitzan Mekel-Bobrov, Bruce T Lahn, Danielle Posthuma, 2007, Human molecular genetics.

A simple method to localise pleiotropic susceptibility loci using univariate linkage analyses of correlated traits

Nicholas G Martin, Peter M Visscher, David L Duffy, 2006, European Journal of Human Genetics.

Sexual Orientation and Psychiatric Vulnerability: A Twin Study of Neuroticism and Psychoticism

Nicholas G Martin, Margaret J Wright, Brendan P. Zietsch, 2011, Archives of sexual behavior.

Identification of heart rate-associated loci and their effects on cardiac conduction and rhythm disorders

Claude Bouchard, William Wheeler, Peter Kraft, 2014 .

Genetic architecture of circulating lipid levels

Christian Gieger, Igor Rudan, Harry Campbell, 2011, European Journal of Human Genetics.

IRF4 variants have age-specific effects on nevus count and predispose to melanoma.

Nicole Soranzo, Johan Hansson, Nicholas G Martin, 2010, American journal of human genetics.

Genetic contribution to individual variation in binocular rivalry rate

Nicholas G Martin, Margaret J Wright, Steven Mark Miller, 2010, Proceedings of the National Academy of Sciences.

Cholinergic nicotinic receptor genes implicated in a nicotine dependence association study targeting 348 candidate genes with 3713 SNPs.

Nicholas G Martin, Scott F. Saccone, Laura Jean Bierut, 2007, Human molecular genetics.

Genetic influences on individual differences in longitudinal changes in global and subcortical brain volumes: Results of the ENIGMA plasticity working group

Anbupalam Thalamuthu, Xue Hua, Neda Jahanshad, 2017, Human brain mapping.

Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies

Christian Gieger, Inês Barroso, Peter Kraft, 2010, Nature Genetics.