Publications

My publication record to includes 134 peer reviewed publications with >19,500 citations and an H-index of 56 (Scopus, January 29, 2026). An additional seven papers published on medRxiv and bioRxiv between 2024 and 2025 are listed.

Preprints

• Bartels M, van de Weijer MP, Azcona-Granada N, et al. (2025) Epigenome-wide association study meta-analysis of wellbeing. bioRxiv, Preprint server, doi: 10.1101/2025.09.08.674802
• Mitchell BL, Gilroy D, Wallace LA, et al. (2025) Cohort profile: Cell-omics Resource of the Australian Genetics of Depression Study (AGDS:Cell-o). medRxiv, Preprint server, doi: 10.1101/2025.09.16.2533587
• Syed R, Benca-Bachman CE, Huggett SB, et al. (2025) CONSILIENCE-GWAS: A Web Resource for Parsed Heritability & Polygenic Score Analysis of Human GWAS Using Heterogeneous Functional Genomics Data. medRxiv, Preprint server, doi: 10.1101/2025.10.24.25338727
• Mitchell BL, Skelton M, Wang R, et al. (2025) Genome-wide meta-analysis identifies genetic risk factors and implicates multiple body systems in panic attacks and disorder. medRxiv, Preprint server, doi: 10.1101/2025.06.15.25329656
• Jayasinghe GJMSR, Zhu G, Pandeya N, et al. (2025) A large-scale genome-wide association meta-analysis for nevus count provides direct insights into the genetics of melanoma. medRxiv, Preprint server, doi:10.1101/2025.02.25.25322831
• van der Veen T, Tesfaye M, Yang JMK, et al. (2025) Immune, Developmental, and Synaptic Pathways Define Bipolar Disorder Clinical Heterogeneity. medRxiv, Preprint server, doi:10.1101/2025.06.23.25330155
• Boltz TA, Chu BB, Liao C, et al. (2024) A blended genome and exome sequencing method captures genetic variation in an unbiased, high-quality, and cost-effective manner. bioRxiv, Preprint server, doi:10.1101/2024.09.06.611689

Peer-reviewed Journal Articles

• Shin M, Crouse JJ, Lin T, et al. (2026) Atypical depression is associated with a distinct clinical, neurobiological, treatment response and polygenic risk profile. Biol Psychiatry, Epub ahead of print, doi: 10.1016/j.biopsych.2026.01.003
• Walker A, Mitchell BL, Lin T, et al. (2026) Genetic and Phenotypic Associations with Sustained Antidepressant Use in Major Depressive Disorder. JAMA Psychiatry, Epub ahead of print, doi: 10.1001/jamapsychiatry.2025.4372
• Bivol S, Seviiri M, Colodro-Conde L, et al. (2025) An Exploration of the Genetic Architecture of Pregnancy-Related Linea Nigra and Its Relationship With Pigmentation Phenotypes. Twin Res Hum Genet, Epub ahead of print, doi: 10.1017/thg.2025.10026
• Grotzinger AD, Werme J, Peyrot WJ, et al. (2026) Mapping the genetic landscape across 14 psychiatric disorders. Nature, 649(8096):406-415, doi: 10.1038/s41586-025-09820-3
• Sepulveda DT, Thorp JG, Lind PA, Martin NG, Medland SE, Mitchell BL. (2025) Exploring the Relationship between Polygenic Scores, Community-Shared Socioeconomic Indicators and Major Depressive Disorder Outcome. Twin Res Hum Genet, 1-9, doi:10.1017/thg.2025.10011
• O’Connell KS, Koromina M, van der Veen T, et al. (2025) Genomics yields biological and phenotypic insights into bipolar disorder. Nature, 639:968–975, doi:10.1038/s41586-024-08468-9
• Lind PA, Parker RK, Northwood K, Siskind DJ, Medland SE. (2025) Clozapine Efficacy and Adverse Drug Reactions Among a Nationwide Study of 1021 Australians Prescribed Clozapine: The ClozaGene Study. Schizophr Bull, 51(2):458-469, doi:10.1093/schbul/sbae065
• Johnson EC, Lai D, Miller AP, et al. (2025) Multi-ancestral genome-wide association study of clinically defined nicotine dependence reveals strong genetic correlations with other substance use disorders and health-related traits. Psychol Med, 55:e234, doi:10.1017/S0033291725100883
• Hatzikotoulas K, Southam L, Stefansdottir L, et al. (2025) Translational genomics of osteoarthritis in 1,962,069 individuals. Nature, 641(8065):1217-1224, doi:10.1038/s41586-025-08771-z
• MDD Working Group et al. (2025) Trans-ancestry genome-wide study of depression identifies 697 associations implicating cell types and pharmacotherapies. Cell, 188(3):640-652.e9, doi:10.1016/10.1016/j.cell.2024.12.002
• Shin M, Crouse JJ, Byrne EM, et al. (2024) Changes in sleep patterns in people with a history of depression during the COVID-19 pandemic: a natural experiment. BMJ Ment Health, 27(1), doi:10.1136/bmjment-2024-301067
• Monistrol-Mula A, Felez-Nobrega M, Byrne EM, et al. (2024) The effect of polygenic liability to mental disorders on COVID-19 outcomes in people with depression: the mediating role of anxiety. Psychol Med, 54(15):1-10, doi:10.1017/s0033291724001983
• Kentistou KA, Kaisinger LR, Stankovic S, et al. (2024) Understanding the genetic complexity of puberty timing across the allele frequency spectrum. Nat Genet, 56(7):1397-1411, doi:10.1038/s41588-024-01798-4
• Boltz TA, Chu BB, Liao C, et al. (2024) A blended genome and exome sequencing method captures genetic variation in an unbiased, high-quality, and cost-effective manner. bioRxiv, Preprint server, doi:10.1101/2024.09.06.611689
• Zhou H, Kember RL, Deak JD, et al. (2023) Multi-ancestry study of the genetics of problematic alcohol use in over 1 million individuals. Nat Med, 29(12):3184-3192, doi:10.1038/s41591-023-02653-5
• Wang X, Walker A, Revez JA, et al. (2023) Polygenic risk prediction: why and when out-of-sample prediction R(2) can exceed SNP-based heritability. Am J Hum Genet, 110(7):1207-1215, doi:10.1016/j.ajhg.2023.06.006
• Mathieson I, Day FR, Barban N, et al. (2023) Genome-wide analysis identifies genetic effects on reproductive success and ongoing natural selection at the FADS locus. Nat Hum Behav, 7(5):790-801, doi:10.1038/s41562-023-01528-6
• Lind PA, Siskind DJ, Hickie IB, et al. (2023) Preliminary results from the Australian Genetics of Bipolar Disorder Study: A nation-wide cohort. Aust N Z J Psychiatry, 57(11):1428-1442, doi:10.1177/00048674231195571
• Lind PA, Medland SE. (2023) censusADHD Study: An Australian-wide medication-based recruitment study for Attention-Deficit/Hyperactivity Disorder. Aust N Z J Psychiatry, 57(2):252-263, doi:10.1177/00048674221089234
• Howe LJ, Rasheed H, Jones PR, et al. (2023) Educational attainment, health outcomes and mortality: a within-sibship Mendelian randomization study. Int J Epidemiol, 52(5):1579-1591, doi:10.1093/ije/dyad079
• Gomez L, Díaz-Torres S, Colodro-Conde L, et al. (2023) Phenotypic and genetic factors associated with donation of DNA and consent to record linkage for prescription history in the Australian Genetics of Depression Study. Eur Arch Psychiatry Clin Neurosci, 273(6):1359-1368, doi:10.1007/s00406-022-01527-0
• Garcia-Marin LM, Mulcahy A, Byrne EM, et al. (2023) Discontinuation of antidepressant treatment: a retrospective cohort study on more than 20,000 participants. Ann Gen Psychiatry, 22(1):49, doi:10.1186/s12991-023-00480-z
• Wang Z, Emmerich A, Pillon NJ, et al. (2022) Genome-wide association analyses of physical activity and sedentary behavior provide insights into underlying mechanisms and roles in disease prevention. Nat Genet, 54(9):1332-1344, doi:10.1038/s41588-022-01165-1
• Saunders GRB, Wang X, Chen F, et al. (2022) Genetic diversity fuels gene discovery for tobacco and alcohol use. Nature, 612(7941):720-724, doi:10.1038/s41586-022-05477-4
• Pain O, Hodgson K, Trubetskoy V, et al. (2022) Identifying the Common Genetic Basis of Antidepressant Response. Biol Psychiatry Glob Open Sci, 2(2):115-126, doi:10.1016/j.bpsgos.2021.7.8
• Okbay A, Wu Y, Wang N, et al. (2022) Polygenic prediction of educational attainment within and between families from genome-wide association analyses in 3 million individuals. Nat Genet, 54(4):437-449, doi:10.1038/s41588-022-01016-z
• Mullins N, Kang J, Campos AI, et al. (2022) Dissecting the Shared Genetic Architecture of Suicide Attempt, Psychiatric Disorders, and Known Risk Factors. Biol Psychiatry, 91(3):313-327, doi:10.1016/j.biopsych.2021.5.29
• Medland SE, Grasby KL, Jahanshad N, et al. (2022) Ten years of enhancing neuro-imaging genetics through meta-analysis: An overview from the ENIGMA Genetics Working Group. Hum Brain Mapp, 43(1):292-299, doi:10.1002/hbm.25311
• Howe LJ, Nivard MG, Morris TT, et al. (2022) Within-sibship genome-wide association analyses decrease bias in estimates of direct genetic effects. Nat Genet, 54(5):581-592, doi:10.1038/s41588-022-01062-7
• Campos AI, Byrne EM, Mitchell BL, et al. (2022) Impact of CYP2C19 metaboliser status on SSRI response: a retrospective study of 9500 participants of the Australian Genetics of Depression Study. Pharmacogenomics J, 22(2):130-135, doi:10.1038/s41397-022-00267-7
• Blokland GAM, Grove J, Chen CY, et al. (2022) Sex-Dependent Shared and Nonshared Genetic Architecture Across Mood and Psychotic Disorders. Biol Psychiatry, 91(1):102-117, doi:10.1016/j.biopsych.2021.2.972
• Bivol S, Mellick GD, Gratten J, et al. (2022) Australian Parkinson’s Genetics Study (APGS): pilot (n=1532). BMJ Open, 12(2):e052032, doi:10.1136/bmjopen-2021-052032
• Ni G, Zeng J, Revez JA, et al. (2021) A Comparison of Ten Polygenic Score Methods for Psychiatric Disorders Applied Across Multiple Cohorts. Biol Psychiatry, 90(9):611-620, doi:10.1016/j.biopsych.2021.04.018
• Munn-Chernoff MA, Johnson EC, Chou YL, et al. (2021) Shared genetic risk between eating disorder- and substance-use-related phenotypes: Evidence from genome-wide association studies. Addict Biol, 26(1):e12880, doi:10.1111/adb.12880
• Mills MC, Tropf FC, Brazel DM, et al. (2021) Identification of 371 genetic variants for age at first sex and birth linked to externalising behaviour. Nat Hum Behav, 5(12):1717-1730, doi:10.1038/s41562-021-01135-3
• McGuire D, Jiang Y, Liu M, et al. (2021) Model-based assessment of replicability for genome-wide association meta-analysis. Nat Commun, 12(1):1964, doi:10.1038/s41467-021-21226-z
• Giannakopoulou O, Lin K, Meng X, et al. (2021) The Genetic Architecture of Depression in Individuals of East Asian Ancestry: A Genome-Wide Association Study. JAMA Psychiatry, 78(11):1258-1269, doi:10.1001/jamapsychiatry.2021.2099
• Tilot AK, Khramtsova EA, Liang D, et al . (2021) The Evolutionary History of Common Genetic Variants Influencing Human Cortical Surface Area. Cereb Cortex, 31(4):1873-87, doi: 10.1093/cercor/bhaa327
• Campos AI, Mulcahy A, Thorp JG, et al. (2021) Understanding genetic risk factors for common side effects of antidepressant medications. Commun Med (Lond), 0.0729166666666667, doi:10.1038/s43856-021-00046-8
• Bray N, Grasby KL, Lind PA, Painter JN, Colodro-Conde L, Medland SE. (2021) The psychosocial impact of nausea and vomiting during pregnancy as a predictor of postpartum depression. J Health Psychol, 26(7):1061-1072, doi:10.1177/1359105319859048
• Borg D, Rae K, Fiveash C, et al. (2021) Queensland Family Cohort: a study protocol. BMJ Open, 11(6):e044463, doi:10.1136/bmjopen-2020-044463
• Andlauer TFM, Guzman-Parra J, Streit F, et al. (2021) Bipolar multiplex families have an increased burden of common risk variants for psychiatric disorders. Mol Psychiatry, 26(4):1286-1298, doi:10.1038/s41380-019-0558-2
• Amare AT, Schubert KO, Hou L, et al. (2021) Association of polygenic score for major depression with response to lithium in patients with bipolar disorder. Mol Psychiatry, 26(6):2457-2470, doi:10.1038/s41380-020-0689-5
• Slutske WS, Lind PA. (2020) Contributions of Nicholas Martin to Gambling Disorder Research. Twin Res Hum Genet, 23(2):127-128, doi:10.1017/thg.2020.34
• Shen X, Howard DM, Adams MJ, et al. (2020) A phenome-wide association and Mendelian Randomisation study of polygenic risk for depression in UK Biobank. Nat Commun, 11(1):2301, doi:10.1038/s41467-020-16022-0
• Laisk T, Soares ALG, Ferreira T, et al. (2020) The genetic architecture of sporadic and multiple consecutive miscarriage. Nat Commun, 11(1):5980, doi:10.1038/s41467-020-19742-5
• Johnson EC, Demontis D, Thorgeirsson TE, et al. (2020) A large-scale genome-wide association study meta-analysis of cannabis use disorder. Lancet Psychiatry, 7(12):1032-1045, doi:10.1016/s2215-0366(20)30339-4
• Hofer E, Roshchupkin GV, Adams HHH, et al. (2020) Genetic correlations and genome-wide associations of cortical structure in general population samples of 22,824 adults. Nat Commun, 11(1):4796, doi:10.1038/s41467-020-18367-y
• Grasby KL, Jahanshad N, Painter JN, et al. (2020) The genetic architecture of the human cerebral cortex. Science, 367(6484), doi:10.1126/science.aay6690 [‡second equal author]
• Glanville KP, Coleman JRI, Hanscombe KB, et al. (2020) Classical Human Leukocyte Antigen Alleles and C4 Haplotypes Are Not Significantly Associated With Depression. Biol Psychiatry, 87(5):419-430, doi:10.1016/j.biopsych.2019.06.31
• Coleman JRI, Peyrot WJ, Purves KL, et al. (2020) Genome-wide gene-environment analyses of major depressive disorder and reported lifetime traumatic experiences in UK Biobank. Mol Psychiatry, 25(7):1430-1446, doi:10.1038/s41380-019-0546-6
• Coleman JRI, Gaspar HA, Bryois J, Breen G. (2020) The Genetics of the Mood Disorder Spectrum: Genome-wide Association Analyses of More Than 185,000 Cases and 439,000 Controls. Biol Psychiatry, 88(2):169-184, doi:10.1016/j.biopsych.2019.10.015
• Maclean EI, Andrew B, Lind, PA, et al. (2020) Rethinking Measurement of Parenting Stress in ADHD-Affected Families: A Principal Components Analysis of the Disruptive Behaviour Stress Inventory. ** J Child Fam Stud**, 29:3253–3264, doi:10.1007/s10826-020-01799-x
• Warrington NM, Beaumont RN, Horikoshi M, et al. (2019) Maternal and fetal genetic effects on birth weight and their relevance to cardio-metabolic risk factors. Nat Genet, 51(5):804-814, doi:10.1038/s41588-019-0403-1
• Polimanti R, Peterson RE, Ong JS, et al. (2019) Evidence of causal effect of major depression on alcohol dependence: findings from the psychiatric genomics consortium. Psychol Med, 49(7):1218-1226, doi:10.1017/s0033291719000667
• Mitchell BL, Campos AI, Rentería ME, et al. (2019) Twenty-Five and Up (25Up) Study: A New Wave of the Brisbane Longitudinal Twin Study. Twin Res Hum Genet, 22(3):154-163, doi:10.1017/thg.2019.27
• Liu M, Jiang Y, Wedow R, et al. (2019) Association studies of up to 1.2 million individuals yield new insights into the genetic etiology of tobacco and alcohol use. Nat Genet, 51(2):237-244, doi:10.1038/s41588-018-0307-5
• Karlsson Linnér R, Biroli P, Kong E, et al. (2019) Genome-wide association analyses of risk tolerance and risky behaviors in over 1 million individuals identify hundreds of loci and shared genetic influences. Nat Genet, 51(2):245-257, doi:10.1038/s41588-018-0309-3
• Grove J, Ripke S, Als TD, et al. (2019) Identification of common genetic risk variants for autism spectrum disorder. Nat Genet, 51(3):431-444, doi:10.1038/s41588-019-0344-8
• Gallagher CS, Mäkinen N, Harris HR, et al. (2019) Genome-wide association and epidemiological analyses reveal common genetic origins between uterine leiomyomata and endometriosis. Nat Commun, 10(1):4857, doi:10.1038/s41467-019-12536-4
• Evangelou E, Gao H, Chu C, et al. (2019) New alcohol-related genes suggest shared genetic mechanisms with neuropsychiatric disorders. Nat Hum Behav, 3(9):950-961, doi:10.1038/s41562-019-0653-z
• Dudding T, Haworth S, Lind PA, et al. (2019) Genome wide analysis for mouth ulcers identifies associations at immune regulatory loci. Nat Commun, 10(1):1052, doi:10.1038/s41467-019-08923-6
• Czamara D, Eraslan G, Page CM, et al. (2019) Integrated analysis of environmental and genetic influences on cord blood DNA methylation in new-borns. Nat Commun, 10(1):2548, doi:10.1038/s41467-019-10461-0
• Barbu MC, Zeng Y, Shen X, et al. (2019) Association of Whole-Genome and NETRIN1 Signaling Pathway-Derived Polygenic Risk Scores for Major Depressive Disorder and White Matter Microstructure in the UK Biobank. Biol Psychiatry Cogn Neurosci Neuroimaging, 4(1):91-100, doi:10.1016/j.bpsc.2018.07.006
• Choi KW, Chen C, Stein MB, et al. (2019) Assessment of Bidirectional Relationships Between Physical Activity and Depression Among Adults: A 2-Sample Mendelian Randomization Study. JAMA Psychiatry, 6(4):399–408, doi:10.1001/jamapsychiatry.2018.4175
• Wray NR, Ripke S, Mattheisen M, et al. (2018) Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depression. Nat Genet, 50(5):668-681, doi:10.1038/s41588-018-0090-3
• Walters RK, Polimanti R, Johnson EC, et al. (2018) Transancestral GWAS of alcohol dependence reveals common genetic underpinnings with psychiatric disorders. Nat Neurosci, 21(12):1656-1669, doi:10.1038/s41593-018-0275-1
• Scott J, Davenport TA, Parker R, et al. (2018) Pathways to depression by age 16 years: Examining trajectories for self-reported psychological and somatic phenotypes across adolescence. J Affect Disord, 230:1-6, doi:10.1016/j.jad.2017.12.007
• Peyrot WJ, Van der Auwera S, Milaneschi Y, et al. (2018) Does Childhood Trauma Moderate Polygenic Risk for Depression? A Meta-analysis of 5765 Subjects From the Psychiatric Genomics Consortium. Biol Psychiatry, 84(2):138-147, doi:10.1016/j.biopsych.2017.09.009
• Minică CC, Verweij KJH, van der Most PJ, et al. (2018) Genome-wide association meta-analysis of age at first cannabis use. Addiction, 113(11):2073-2086, doi:10.1111/add.14368
• Lee JJ, Wedow R, Okbay A, et al. (2018) Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals. Nat Genet, 50(8):1112-1121, doi:10.1038/s41588-018-0147-3
• de Jong S, Diniz MJA, Saloma A, et al. (2018) Applying polygenic risk scoring for psychiatric disorders to a large family with bipolar disorder and major depressive disorder. Commun Biol, 1:163, doi:10.1038/s42003-018-0155-y
• Arnau-Soler A, Adams MJ; Generation Scotland; Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium, et al. (2018) Genome-wide interaction study of a proxy for stress-sensitivity and its prediction of major depressive disorder. PLoS One, 13(12):e0209160, doi: 10.1371/journal.pone.0209160
• Couvy-Duchesne B, O’Callaghan V, Parker R, et al. (2018) Nineteen and Up study (19Up): understanding pathways to mental health disorders in young Australian twins. BMJ Open, 8(3):e018959, doi:10.1136/bmjopen-2017-018959
• Colodro-Conde L, Sánchez-Romera JF, Lind PA, et al. (2018) No evidence of association of oxytocin polymorphisms with breastfeeding in 2 independent samples. Genes Brain Behav, 17(7):e12464, doi:10.1111/gbb.12464
• Beaumont RN, Warrington NM, Cavadino A, et al. (2018) Genome-wide association study of offspring birth weight in 86 577 women identifies five novel loci and highlights maternal genetic effects that are independent of fetal genetics. Hum Mol Genet, 27(4):742-756, doi:10.1093/hmg/ddx429
• Milaneschi Y, Lamers F, Peyrot WJ, et al. (2017) Genetic Association of Major Depression With Atypical Features and Obesity-Related Immunometabolic Dysregulations. JAMA Psychiatry, 74(12):1214-1225, doi:10.1001/jamapsychiatry.2017.3016
• Day FR, Thompson DJ, Helgason H, et al. (2017) Genomic analyses identify hundreds of variants associated with age at menarche and support a role for puberty timing in cancer risk. Nat Genet, 49(6):834-841, doi:10.1038/ng.3841
• Colodro-Conde L, Cross SM, Lind PA, et al. (2017) Cohort Profile: Nausea and vomiting during pregnancy genetics consortium (NVP Genetics Consortium). Int J Epidemiol, 46(2):e17, doi:10.1093/ije/dyv360
• Weiss A, Baselmans BM, Hofer E, et al. (2016) Personality Polygenes, Positive Affect, and Life Satisfaction. Twin Res Hum Genet, 19(5):407-17, doi:10.1017/thg.2016.65
• Tyrrell J, Richmond RC, Palmer TM, et al. (2016) Genetic Evidence for Causal Relationships Between Maternal Obesity-Related Traits and Birth Weight. JAMA, 315(11):1129-40, doi:10.1001/jama.2016.1975
• Parmar PG, Taal HR, Timpson NJ, et al. (2016) International Genome-Wide Association Study Consortium Identifies Novel Loci Associated With Blood Pressure in Children and Adolescents. Circ Cardiovasc Genet, 9(3):266-278, doi:10.1161/circgenetics.115.001190
• Okbay A, Beauchamp JP, Fontana MA, et al. (2016) Genome-wide association study identifies 74 loci associated with educational attainment. Nature, 533(7604):539-42, doi:10.1038/nature17671
• Okbay A, Baselmans BM, De Neve JE, et al. (2016) Genetic variants associated with subjective well-being, depressive symptoms, and neuroticism identified through genome-wide analyses. Nat Genet, 48(6):624-33, doi:10.1038/ng.3552
• Nivard MG, Verweij KJ, Minică CC, Treur JL, Vink JM, Boomsma DI. (2016) Connecting the dots, genome-wide association studies in substance use. Mol Psychiatry, 21(6):733-5, doi:10.1038/mp.2016.14
• Marioni RE, Ritchie SJ, Joshi PK, et al. (2016) Genetic variants linked to education predict longevity. Proc Natl Acad Sci U S A, 113(47):13366-13371, doi:10.1073/pnas.1605334113
• Long EC, Verhulst B, Neale MC, et al. (2016) The Genetic and Environmental Contributions to Internet Use and Associations With Psychopathology: A Twin Study. Twin Res Hum Genet, 19(1):1-9, doi:10.1017/thg.2015.91
• Lang M, Leménager T, Streit F, et al. (2016) Genome-wide association study of pathological gambling. Eur Psychiatry, 36:38-46, doi:10.1016/j.eurpsy.2016.04.001
• Colodro-Conde L, Jern P, Johansson A, et al. (2016) Nausea and Vomiting During Pregnancy is Highly Heritable. Behav Genet, 46(4):481-91, doi:10.1007/s10519-016-9781-7
• Barban N, Jansen R, de Vlaming R, et al. (2016) Genome-wide analysis identifies 12 loci influencing human reproductive behavior. Nat Genet, 48(12):1462-1472, doi:10.1038/ng.3698
• Peyrot WJ, Lee SH, Milaneschi Y, et al. (2015) The association between lower educational attainment and depression owing to shared genetic effects? Results in ~25,000 subjects. Mol Psychiatry, 20(6):735-43, doi:10.1038/mp.2015.50
• Joshi PK, Esko T, Mattsson H, et al. (2015) Directional dominance on stature and cognition in diverse human populations. Nature, 523(7561):459-462, doi:10.1038/nature14618
• de Zeeuw EL, van Beijsterveldt CE, Glasner TJ, et al. (2014) Polygenic scores associated with educational attainment in adults predict educational achievement and ADHD symptoms in children. Am J Med Genet B Neuropsychiatr Genet, 165B(6):510-20, doi: 10.1002/ajmg.b.32254
• Evangelou E, Kerkhof HJ, Styrkarsdottir U, et al. (2014) A meta-analysis of genome-wide association studies identifies novel variants associated with osteoarthritis of the hip. Ann Rheum Dis, 73(12):2130-6, doi:10.1136/annrheumdis-2012-203114
• Stephens SH, Hartz SM, Hoft NR, et al. (2013) Distinct loci in the CHRNA5/CHRNA3/CHRNB4 gene cluster are associated with onset of regular smoking. Genet Epidemiol, 37(8):846-59, doi:10.1002/gepi.21760
• Rietveld CA, Medland SE, Derringer J, et al. (2013) GWAS of 126,559 individuals identifies genetic variants associated with educational attainment. Science, 340(6139):1467-71, doi:10.1126/science.1235488
• McRae AF, Richter MM, Lind PA. (2013) Case-control association testing of common variants from sequencing of DNA pools. PLoS One, 8(6):e65410, doi:10.1371/journal.pone.0065410
• Lind PA, Zhu G, Montgomery GW, et al. (2013) Genome-wide association study of a quantitative disordered gambling trait. Addict Biol, 18(3):511-22, doi:10.1111/j.1369-1600.2012.00463.x
• den Hoed M, Eijgelsheim M, Esko T, et al. (2013) Identification of heart rate-associated loci and their effects on cardiac conduction and rhythm disorders. Nat Genet, 45(6):621-31, doi:10.1038/ng.2610
• Lind PA, Macgregor S, Heath AC, et al. (2012) Association between in vivo alcohol metabolism and genetic variation in pathways that metabolize the carbon skeleton of ethanol and NADH reoxidation in the alcohol challenge twin study. Alcohol Clin Exp Res, 36(12):2074-85, doi:10.1111/j.1530-0277.2012.01829.x
• Conway CC, Keenan-Miller D, Hammen C, Lind PA, Najman JM, Brennan PA. (2012) Coaction of stress and serotonin transporter genotype in predicting aggression at the transition to adulthood. J Clin Child Adolesc Psychol, 41(1):53-63, doi:10.1080/15374416.2012.632351
• Webb A, Lind PA, Kalmijn J, et al. (2011) The investigation into CYP2E1 in relation to the level of response to alcohol through a combination of linkage and association analysis. Alcohol Clin Exp Res, 35(1):10-8, doi:10.1111/j.1530-0277.2010.01317.x
• Heath AC, Whitfield JB, Martin NG, et al. (2011) A quantitative-trait genome-wide association study of alcoholism risk in the community: findings and implications. Biol Psychiatry, 70(6):513-8, doi:10.1016/j.biopsych.2011.02.028
• Brennan PA, Hammen C, Sylvers P, et al. (2011) Interactions between the COMT Val108/158Met polymorphism and maternal prenatal smoking predict aggressive behavior outcomes. Biol Psychol, 87(1):99-105, doi:10.1016/j.biopsycho.2011.02.013
• Benyamin B, Middelberg RP, Lind PA, et al. (2011) GWAS of butyrylcholinesterase activity identifies four novel loci, independent effects within BCHE and secondary associations with metabolic risk factors. Hum Mol Genet, 20(22):4504-14, doi:10.1093/hmg/ddr375
• Lind PA, Macgregor S, Vink JM, et al. (2010) A genomewide association study of nicotine and alcohol dependence in Australian and Dutch populations. Twin Res Hum Genet, 13(1):10-29, , doi:10.1017/S183242740002003X
• Lind PA, Luciano M, Wright MJ, Montgomery GW, Martin NG, Bates TC. (2010) Dyslexia and DCDC2: normal variation in reading and spelling is associated with DCDC2 polymorphisms in an Australian population sample. Eur J Hum Genet, 18(6):668-73, doi:10.1038/ejhg.2009.237
• Hansell NK, Agrawal A, Whitfield JB, et al. (2010) Linkage analysis of alcohol dependence symptoms in the community. Alcohol Clin Exp Res, 34(1):158-63, doi:10.1111/j.1530-0277.2009.01077.x
• Conway CC, Hammen C, Brennan PA, Lind PA, Najman JM. (2010) Interaction of chronic stress with serotonin transporter and catechol-O-methyltransferase polymorphisms in predicting youth depression. Depress Anxiety, 27(8):737-45, doi:10.1002/da.20715
• Bates TC, Lind PA, Luciano M, Montgomery GW, Martin NG, Wright MJ. (2010) Dyslexia and DYX1C1: deficits in reading and spelling associated with a missense mutation. Mol Psychiatry, 15(12):1190-6, doi:10.1038/mp.2009.120
• Macgregor S, Lind PA, Bucholz KK, et al. (2009) Associations of ADH and ALDH2 gene variation with self report alcohol reactions, consumption and dependence: an integrated analysis. Hum Mol Genet, 18(3):580-93, doi:10.1093/hmg/ddn372
• Luciano M, Miyajima F, Lind PA, et al. (2009) Variation in the dysbindin gene and normal cognitive function in three independent population samples. Genes Brain Behav, 8(2):218-27, doi:10.1111/j.1601-183X.2008.00462.x
• Lind PA, Luciano M, Horan MA, et al. (2009) No association between Cholinergic Muscarinic Receptor 2 (CHRM2) genetic variation and cognitive abilities in three independent samples. Behav Genet, 39(5):513-23, doi:10.1007/s10519-009-9274-z
• Lind PA, Eriksson CJ, Wilhelmsen KC. (2009) Association between harmful alcohol consumption behavior and dopamine transporter (DAT1) gene polymorphisms in a male Finnish population. Psychiatr Genet, 19(3):117-25, doi:10.1097/YPG.0b013e32832a4f7b
• Hansell NK, Agrawal A, Whitfield JB, et al. (2009) *Can we identify genes for alcohol consumption in samples ascertained for heterogeneous purposes? *. Alcohol Clin Exp Res, 33(4):729-39, doi:10.1111/j.1530-0277.2008.00890.x
• Cornes BK, Medland SE, Lind PA, Nyholt DR, Montgomery GW, Martin NG. (2009) Genetic variation in female BMI increases with number of children born but failure to replicate association between GNbeta3 variants and increased BMI in parous females. Twin Res Hum Genet, 12(3):276-85, doi:10.1375/twin.12.3.276
• Cornes BK, Lind PA, Medland SE, Montgomery GW, Nyholt DR, Martin NG. (2009) Replication of the association of common rs9939609 variant of FTO with increased BMI in an Australian adult twin population but no evidence for gene by environment (G x E) interaction. Int J Obes (Lond), 33(1):75-9, doi:10.1038/ijo.2008.223
• Wray NR, James MR, Handoko HY, et al. (2008) Association study of candidate variants from brain-derived neurotrophic factor and dystrobrevin-binding protein 1 with neuroticism, anxiety, and depression. Psychiatr Genet, 18(5):219-25, doi:10.1097/YPG.0b013e3283050aee
• Wray NR, James MR, Dumenil T, et al. (2008) Association study of candidate variants of COMT with neuroticism, anxiety and depression. Am J Med Genet B Neuropsychiatr Genet, 147b(7):1314-8, doi:10.1002/ajmg.b.30744
• Macgregor S, Hottenga JJ, Lind PA, et al. (2008) Vitamin D receptor gene polymorphisms have negligible effect on human height. Twin Res Hum Genet, 11(5):488-94, doi:10.1375/twin.11.5.488
• Luciano M, Lind PA, Deary IJ, et al. (2008) Testing replication of a 5-SNP set for general cognitive ability in six population samples. Eur J Hum Genet, 16(11):1388-95, doi:10.1038/ejhg.2008.100
• Lind PA, MacGregor S, Montgomery GW, Heath AC, Martin NG, Whitfield JB. (2008) Effects of GABRA2 variation on physiological, psychomotor and subjective responses in the alcohol challenge twin study. Twin Res Hum Genet, 11(2):174-82, doi:10.1375/twin.11.2.174
• Lind PA, Macgregor S, Agrawal A, et al. (2008) The role of GABRA2 in alcohol dependence, smoking, and illicit drug use in an Australian population sample. Alcohol Clin Exp Res, 32(10):1721-31, doi:10.1111/j.1530-0277.2008.00768.x
• Lind PA, Eriksson CJ, Wilhelmsen KC. (2008) The role of aldehyde dehydrogenase-1 (ALDH1A1) polymorphisms in harmful alcohol consumption in a Finnish population. Hum Genomics, 3(1):24-35, doi:10.1186/1479-7364-3-1-24
• Hansell NK, Agrawal A, Whitfield JB, et al. (2008) Long-term stability and heritability of telephone interview measures of alcohol consumption and dependence. Twin Res Hum Genet, 11(3):287-305, doi:10.1375/twin.11.3.287
• Ehlers CL, Lind PA, Wilhelmsen KC. (2008) Association between single nucleotide polymorphisms in the mu opioid receptor gene (OPRM1) and self-reported responses to alcohol in American Indians. BMC Med Genet, 0.399305555555556, doi:10.1186/1471-2350-9-35
• Ehlers CL, Gilder DA, Slutske WS, Lind PA, Wilhelmsen KC. (2008) Externalizing disorders in American Indians: comorbidity and a genome wide linkage analysis. Am J Med Genet B Neuropsychiatr Genet, 147b(6):690-8, doi:10.1002/ajmg.b.30666
• Bates TC, Luciano M, Lind PA, et al. (2008) Recently-derived variants of brain-size genes ASPM, MCPH1, CDK5RAP and BRCA1 not associated with general cognition, reading or language. Intelligence, 36(6):689-93, doi:10.1016/j.intell.2008.04.001
• Mekel-Bobrov N, Posthuma D, Gilbert SL, et al. (2007) The ongoing adaptive evolution of ASPM and Microcephalin is not explained by increased intelligence. Hum Mol Genet, 16(6):600-8, doi:10.1093/hmg/ddl487
• Luciano M, Lind PA, Duffy DL, et al. (2007) A haplotype spanning KIAA0319 and TTRAP is associated with normal variation in reading and spelling ability. Biol Psychiatry, 62(7):811-7, doi:10.1016/j.biopsych.2007.03.007
• Francks C, Maegawa S, Laurén J, et al. (2007) LRRTM1 on chromosome 2p12 is a maternally suppressed gene that is associated paternally with handedness and schizophrenia. Mol Psychiatry, 12(12):1129-39, 1057, doi:10.1038/sj.mp.4002053
• Ehlers CL, Slutske WS, Lind PA, Wilhelmsen KC. (2007) Association between single nucleotide polymorphisms in the cannabinoid receptor gene (CNR1) and impulsivity in southwest California Indians. Twin Res Hum Genet, 10(6):805-11, doi:10.1375/twin.10.6.805
• Schuckit MA, Wilhelmsen K, Smith TL, et al. (2005) Autosomal linkage analysis for the level of response to alcohol. Alcohol Clin Exp Res, 29(11):1976-82, doi:10.1097/01.alc.0000187598.82921.27
• Lind PA, Daniel RM, Monk C, Dunn RV. (2004) Esterase catalysis of substrate vapour: enzyme activity occurs at very low hydration. Biochim Biophys Acta, 1702(1):103-10, doi:10.1016/j.bbapap.2004.08.005

Book Chapters

• Couvy-Duchesne B, Bottani S, Camenen E, et al. (2023) Main Existing Datasets for Open Brain Research on Humans. In Machine Learning for Brain Disorders, edited by O. Colliot, 753-804, doi:10.1007/978-1-0716-3195-9_24

Conference Presentations (Only first author presentations)

• Lind PA, Medland SE (2024) Continuity of ADHD care experienced by Australian children in the censusADHD Study: An exploration using Medicare record linkage. Paper presented at the 7th Annual Conference of the Australasian ADHD Professionals Association, Brisbane, QLD, Australia (July 25-27).
• Lind PA, Mitchell B, Byrne E, Medland SE, Martin NG (2023) Polygenic risk scores for lifespan, BMI, and chronic pain predict a medication-based Rx-Risk Comorbidity Index in the Australian Genetics of Depression Study. Paper presented at the 14th International Congress of Human Genetics, Cape Town, South Africa (Feb 22-26).
• Lind PA, Siskind DJ, Hickie IB, Martin NG, Medland SE (2022) Retrospective reporting of medication discontinuation in the Australian Genetics of Bipolar Disorder Study. Paper presented at the 42nd Annual Society for Mental Health Research Conference, Hobart, Tasmania (March 24-26).
• Lind PA, Gizer I, Piasecki TM, Slutske WS, Martin NG (2020) Exploring the genetic architecture of disordered gambling and the influence of genetics of risk of gambling on substance use. Paper presented at the virtual 50th Behavior Genetics Association Meeting (June 26).
• Lind PA, McRae AF, Whiteman DC, Whitfield JB (2018) The association between genetic variation in the Alcohol Dehydrogenase gene cluster and alcohol use and abuse and esophageal squamous cell carcinoma (ESCC) risk. Paper presented at the 40th Annual Society for Mental Health Research Conference (November 28-30).
• Lind PA (2016) Genetic contributions to addiction. Invited paper presented at the 25th Annual RBWH Healthcare Symposium: Genomics in Health and Disease (September 12-16).
• Lind PA, MacGregor S, Richter MM, Heath AC, Montgomery GW, Martin NG, Whitfield JB (2008) The road to skid row: How ADH gene variation leads to alcohol dependence. Paper presented at the 16th World Congress of Psychiatric Genetics, Osaka, Japan (Oct 11-15).
• Lind PA, Luciano M, Wright MJ, Montgomery GW, Martin NG, Bates TC (2007) DCDC2 is associated with normal variation in reading and spelling ability in a large Australian population sample. Paper presented at the 6th Australasian Human Gene Mapping Conference, Brisbane, Australia (Aug 29-31).
• Lind PA (2006) A molecular approach to comorbidity: overlapping candidate genes for alcoholism and depression. Paper presented at the ISBRA 2006 World Congress on Alcohol Research, Sydney, Australia (Sept 10-13)

Conference Posters (Only when presentating author)

• Lind PA, Mitchell B, Martin NG, Medland SE (2024) A genome-wide association meta-analysis of lithium response including the recently recruited Australian Genetics of Bipolar Disorder Study cohort. Poster presented at the Annual Meeting of The World Congress in Psychiatric Genetics, Singapore (Oct 15-19).
• Lind PA, Mitchell B, Martin NG, Medland SE (2023) Higher levels of chronic illness in the Australian Genetics of Bipolar Disorder Study are associated with genetic risk for reduced lifespan, increased BMI, and increased sites of chronic pain: a polygenic risk score analysis. Poster presented at the Annual Meeting of The American Society of Human Genetics, Washington DC, USA (Nov 1-5).
• Lind PA, Hickie LB, Siskind Dj, Olsen CM, Whiteman DC, Martin NG, Medland SE (2021) Polygenic risk scores for Bipolar Disorder predict age of onset of Bipolar Disorder and the number of psychiatric comorbidities experienced by participants in the population-based Genetics of Bipolar Disorder Study. Poster presented at the virtual American Society of Human Genetics Meeting (Oct 18-22).
• Lind PA, Piasecki T, Gizer I, Slutske WS, Martin NG (2020) Exploring the shared genetic architecture between disordered gambling, substance use and other psychiatric disorders. Poster presented at the virtual World Congress of Pyschiatric Genetics Meeting (Oct 19-21).
• Lind PA, Compos A, Colodro-Conde L, Medland SE, Slutske WS, Martin NG (2019) Prediction of pathological gambling and problematic gambling behaviours by Bipolar Disorder and Parkinson’s disease: A polygenic risk score analysis. Poster presented at the American Society of Human Genetics Meeting, Houston, USA (Oct 15-19).
• Lind PA, Colodro-Conde L, Couvy-Duchesne B, Painter JN, Wright M, Montgomery G, Nyholt D, Medland SE (2018) Severity of nausea and vomiting during pregnancy predicted by psychiatric and psychological traits. Poster presented at the American Society of Human Genetics Meeting, San Francisco, USA (Oct 16-20). Petrofes C, Andrew B, Lind PA (2018) Investigating potential risk factors for problematic internet use among Australian university students. Poster presented at the 2018 Australian and New Zealand Addiction Conference, Gold Coast, QLD (May 28-30).
• Lind PA, McRae AF, Whiteman DC, Whitfield JB (2018) The role of genetic variation in the Alcohol Dehydrogenase (ADH) gene cluster on hazardous alcohol consumption, alcohol use disorders and esophageal squamous cell carcinoma risk. Poster presented at the 2018 Australiana nd New Zealand Addiction Conference, Gold Coast, QLD (May 28-30).
• Lind PA, Benjamin DA, Buchwald J, Cesarini D, Gabrielsen ME, Hällfors JK, Johannesson M, Kaprio J, Korhonen T, Krokan HE, Loukola AM, Magnusson PKE, Medland SE, Rose RJ, Skorpen F, Stovner EB (2015) Snus use is not associated with variation in the CHRNA5-CHRNA3-CHRNB4 gene cluster in Sweden, Norway and Finland. Poster presented at the 65th Annual Meeting of The American Society of Human Genetics, Baltimore, USA (Oct 6-10).
• Lind PA, Hay DA, Cicero TJ, Martin NG, Medland SE (2013) Shared genetic vulnerability for Attention Deficit Hyperactivity Disorder, Substance Use and Gambling in Australian Adolescents. Poster presented at the American Society of Human Genetics Meeting, Boston, MA, USA (Oct 22-26).
• Lind PA, Cesarini D, Benjamin DJ, Koellinger PD, Magnusson PKE, Johannesson M, Medland SE (2012) Genetic Analysis of Tobacco Use in the Swedish twin registry: Genome-wide Association Studies of Cigarette and Snus Consumption. Poster presented at the American Society of Human Genetics Meeting, San Francisco, USA (Nov 6-10).
• Lind PA, MacGregor S, Wray N, Montgomery GW, Heath AC, Martin NG, Whitfield JB (2007) The Role of GABRA2 Genetic Variation in Risk for Alcohol Dependence and Comorbid Psychiatric Disorders. Poster presented at the 30th Annual Research Society on Alcoholism Scientific Meeting, Chicago, USA (July 7-12). Alcoholism Clinical and Experimental Research (2007) 31(6): 71A-71A.
• Lind PA, MacGregor S, Montgomery GW, Whitfield JB, Martin NG (2006) Allelic Variation in GABRA2 is Associated with the Response of Body Sway and Motor Coordination to Alcohol. Poster presented at the ISBRA World Congress on Alcohol Research, Sydney, Australia (Sept 10-13). Alcoholism Clinical and Experimental Research (2006) 30(9): 153A-153A.
• Lind PA, Eriksson CJP, Wilhelmsen, KC (2004) Genome Wide Allelic Association Study of Alcohol Consumption Behavior in a Finnish Population. Poster presented at the American Society of Human Genetics Meeting, Toronto, Canada (Oct 26-30).
• Lind PA, Lee JV, Feiler HS, Eriksson CJP, Wilhelmsen, KC (2003) Genome Wide Allelic Association Study of Alcohol Consumption Behavior in a Finnish Population. Poster presented at the 26th Annual Research Society on Alcoholism Scientific Meeting, Fort Lauderdale, Florida, USA (June 21-25).