Publications

Gyimesi, Martina, Oikari, Lotta E., Yu, Chieh, Sutherland, Heidi G., Nyholt, Dale R., Griffiths, Lyn R., Van Wijnen, Andre J., Okolicsanyi, Rachel K., Haupt, Larisa M. (2024) CpG methylation changes in human mesenchymal and neural stem cells in response to in vitro niche modifications. Biochimie, 223, pp.147-157. [eprints.qut.edu.au/248640/]

Kentistou, Katherine A., Kaisinger, Lena R, Stankovic, Stasa, Vaudel, Marc, Mendes de Oliveira, Edson, Messina, Andrea, Walters, Robin G, Liu, Xiaoxi, Busch, Alexander S, Helgason, Hannes, et al. (2024) Understanding the genetic complexity of puberty timing across the allele frequency spectrum. Nature Genetics, 56 (7), pp.1397-1411. [eprints.qut.edu.au/253310/]

Duwalage, Kalpani Ishara, Wynn, Moe Thandar, Mengersen, Kerrie, Nyholt, Dale, Perrin, Dimitri, Robert, Paul Frederic (2023) Predicting Carcass Weight of Grass-Fed Beef Cattle before Slaughter Using Statistical Modelling. Animals, 13 (12), pp.Article number: 1968. [eprints.qut.edu.au/242584/]

Ghaffar, Ammarah, Nyholt, Dale R (2023) Genome-wide imputed differential expression enrichment analysis identifies trait-relevant tissues. Frontiers in Genetics, 13, pp.Article number: 1008511. [eprints.qut.edu.au/244232/]

Ghaffar, Ammarah, Nyholt, Dale R, other, and (2023) Integrating eQTL and GWAS data characterises established and identifies novel migraine risk loci. Human Genetics, 142 (8), pp.1113-1137. [eprints.qut.edu.au/244222/]

Harder, Aster V E, Terwindt, Gisela M, Nyholt, Dale R, van den Maagdenberg, Arn M J M (2023) Migraine genetics: Status and road forward. Cephalalgia, 43 (2). [eprints.qut.edu.au/244230/]

Islam, Md Rafiqul, Nyholt, Dale R, other, and (2023) Cross-trait analyses identify shared genetics between migraine, headache, and glycemic traits, and a causal relationship with fasting proinsulin. Human Genetics, 142 (8), pp.1149-1172. [eprints.qut.edu.au/244214/]

Mehta, Divya, de Boer, Irene, Sutherland, Heidi G., Pijpers, Judith A., Bron, Charlene, Bainomugisa, Charlotte, Haupt, Larisa M., van den Maagdenberg, Arn M.J.M., Griffiths, Lyn R., Nyholt, Dale R., et al. (2023) Alterations in DNA methylation associate with reduced migraine and headache days after medication withdrawal treatment in chronic migraine patients: a longitudinal study. Clinical Epigenetics, 15, pp.Article number: 190. [eprints.qut.edu.au/245785/]

Rahmioglu, Nilufer, Mortlock, Sally, Ghiasi, Marzieh, Moller, Peter L., Stefansdottir, Lilja, Galarneau, Geneviève, Turman, Constance, Danning, Rebecca, Law, Matthew H, Sapkota, Yadav, et al. (2023) The genetic basis of endometriosis and comorbidity with other pain and inflammatory conditions. Nature Genetics, 55 (3), pp.423-436. [eprints.qut.edu.au/244221/]

Tasnim, Sana, Nyholt, Dale R (2023) Migraine and thyroid dysfunction: Co-occurrence, shared genes and biological mechanisms. European Journal of Neurology, 30 (6), pp.1815-1827. [eprints.qut.edu.au/244225/]

Tasnim, Sana, Wilson, Scott G, Walsh, John P., Nyholt, Dale R, other, and (2023) Shared genetics and causal relationships between migraine and thyroid function traits. Cephalalgia, 43 (2). [eprints.qut.edu.au/244215/]

Tasnim, Sana, Wilson, Scott G., Walsh, John P., Nyholt, Dale R (2023) Cross-Trait Genetic Analyses Indicate Pleiotropy and Complex Causal Relationships between Headache and Thyroid Function Traits. Genes, 14 (1), pp.Article number: 16. [eprints.qut.edu.au/244226/]

Yang, Yuanhao, Zhou, Yuan, Nyholt, Dale R, Yap, Chloe X., Tannenberg, Rudolph K., Wang, Ying, Wu, Yang, Zhu, Zhihong, Taylor, Bruce V., Gratten, Jacob (2023) The shared genetic landscape of blood cell traits and risk of neurological and psychiatric disorders. Cell Genomics, 3 (2), pp.Article number: 100249. [eprints.qut.edu.au/244233/]

Adewuyi, Emmanuel O., O'Brien, Eleanor K., Nyholt, Dale R., Porter, Tenielle, Laws, Simon M. (2022) A large-scale genome-wide cross-trait analysis reveals shared genetic architecture between Alzheimer's disease and gastrointestinal tract disorders. Communications Biology, 5 (1), pp.Article number: 691. [eprints.qut.edu.au/240513/]

Adewuyi, Emmanuel Olorunleke, Mehta, Divya, Nyholt, Dale, other, and (2022) Genetic overlap analysis of endometriosis and asthma identifies shared loci implicating sex hormones and thyroid signalling pathways. Human Reproduction, 37 (2), pp.366-383. [eprints.qut.edu.au/227189/]

Blokland, Gabriëlla A.M., Grove, Jakob, Chen, Chia Yen, Cotsapas, Chris, Tobet, Stuart, Handa, Robert, Ripke, Stephan, Neale, Benjamin M., Corvin, Aiden, Walters, James T.R., et al. (2022) Sex-Dependent Shared and Nonshared Genetic Architecture Across Mood and Psychotic Disorders. Biological Psychiatry, 91 (1), pp.102-117. [eprints.qut.edu.au/229995/]

Hautakangas, Heidi, Winsvold, Bendik S., Ruotsalainen, Sanni E., Bjornsdottir, Gyda, Harder, Aster V.E., Kogelman, Lisette J.A., Thomas, Laurent F., Noordam, Raymond, Benner, Christian, Gormley, Padhraig, et al. (2022) Genome-wide analysis of 102,084 migraine cases identifies 123 risk loci and subtype-specific risk alleles. Nature Genetics, 54 (2), pp.152-160. [eprints.qut.edu.au/233623/]

Islam, Md Rafiqul, Nyholt, Dale R (2022) Glucose-Related Traits and Risk of Migraine—A Potential Mechanism and Treatment Consideration. Genes, 13 (5), pp.Article number: 730. [eprints.qut.edu.au/231165/]

Islam, Md Rafiqul, Nyholt, Dale, other, and (2022) Genetic Overlap Analysis Identifies a Shared Etiology between Migraine and Headache with Type 2 Diabetes. Genes, 13 (10), pp.Article number: 1845. [eprints.qut.edu.au/236331/]

Mitchell, Brittany L, Diaz-Torres, Santiago, Bivol, Svetlana, Cuellar-Partida, Gabriel, Gerring, Zachary F, Martin, Nicholas G, Medland, Sarah E, Grasby, Katrina L, Nyholt, Dale R, Rentería, Miguel E, et al. (2022) Elucidating the relationship between migraine risk and brain structure using genetic data. Brain, 145 (9), pp.3214–3224. [eprints.qut.edu.au/233593/]

Mullins, Niamh, Kang, Joo Eun, Campos, Adrian I., Coleman, Jonathan R.I., Edwards, Alexis C., Galfalvy, Hanga, Levey, Daniel F., Lori, Adriana, Shabalin, Andrey, Starnawska, Anna, et al. (2022) Dissecting the Shared Genetic Architecture of Suicide Attempt, Psychiatric Disorders, and Known Risk Factors. Biological Psychiatry, 91 (3), pp.313-327. [eprints.qut.edu.au/238890/]

Pain, Oliver, Hodgson, Karen, Trubetskoy, Vassily, Ripke, Stephan, Marshe, Victoria S., Adams, Mark J., Byrne, Enda M., Campos, Adrian I., Carrillo-Roa, Tania, Cattaneo, Annamaria, et al. (2022) Identifying the Common Genetic Basis of Antidepressant Response. Biological Psychiatry Global Open Science, 2 (2), pp.115-126. [eprints.qut.edu.au/238891/]

Sathyanarayanan, Anita, Tanha, Hamzeh M., Mehta, Divya, Nyholt, Dale R. (2022) Integrative multi-omic analysis identifies genetically influenced DNA methylation biomarkers for breast and prostate cancers. Communications Biology, 5 (1), pp.Article number: 594. [eprints.qut.edu.au/233529/]

Tanha, Hamzeh M., Nyholt, Dale R., other, and (2022) Genetic analyses identify pleiotropy and causality for blood proteins and highlight Wnt/β-catenin signalling in migraine. Nature Communications, 13 (1), pp.Article number: 2593. [eprints.qut.edu.au/233527/]

Tanha, Hamzeh M., Sathyanarayanan, Anita, Mehta, Divya, Nyholt, Dale R. (2022) Shared genetic influences between blood analyte levels and risk of severe COVID-19. Cell Reports, 41 (8), pp.Article number: 111708. [eprints.qut.edu.au/237171/]

Adewuyi, Emmanuel O., Mehta, Divya, Sapkota, Yadav, Auta, Asa, Yoshihara, Kosuke, Nyegaard, Mette, Griffiths, Lyn R., Montgomery, Grant W., Chasman, Daniel I., Nyholt, Dale R. (2021) Genetic analysis of endometriosis and depression identifies shared loci and implicates causal links with gastric mucosa abnormality. Human Genetics, 140 (3), pp.529–552. [eprints.qut.edu.au/204783/]

Adewuyi, Emmanuel, O’Brien, Eleanor, Nyholt, Dale, Porter, Tenielle, Laws, Simon (2021) Cross–trait analysis of Alzheimer’s disease and gastrointestinal tract disorders identifies shared loci highlighting immune-related and statin pathways [eprints.qut.edu.au/233686/]

Andlauer, Till F.M., Guzman-Parra, Jose, Streit, Fabian, Strohmaier, Jana, González, Maria José, Gil Flores, Susana, Cabaleiro Fabeiro, Francisco J., del Río Noriega, Francisco, Perez, Fermin Perez, Haro González, Jesus, et al. (2021) Bipolar multiplex families have an increased burden of common risk variants for psychiatric disorders. Molecular Psychiatry, 26 (4), pp.1286-1298. [eprints.qut.edu.au/229876/]

Bainomugisa, Charlotte K., Sutherland, Heidi G., Parker, Richard, Mcrae, Allan F., Haupt, Larisa M., Griffiths, Lyn R., Heath, Andrew, Nelson, Elliot C., Wright, Margaret J., Hickie, Ian B., et al. (2021) Using Monozygotic Twins to Dissect Common Genes in Posttraumatic Stress Disorder and Migraine. Frontiers in Neuroscience, 15, pp.Article number: 678350. [eprints.qut.edu.au/212502/]

Cuellar-Partida, Gabriel, Tung, Joyce Y., Eriksson, Nicholas, Albrecht, Eva, Aliev, Fazil, Andreassen, Ole A., Barroso, Inês, Beckmann, Jacques S., Boks, Marco P., Boomsma, Dorret I., et al. (2021) Genome-wide association study identifies 48 common genetic variants associated with handedness. Nature Human Behaviour, 5 (1), pp.59-70. [eprints.qut.edu.au/211069/]

Kho, Pik Fang, Mortlock, Sally, Rogers, Peter A.W., Nyholt, Dale R., Montgomery, Grant W., Spurdle, Amanda B., Glubb, Dylan M., O'Mara, Tracy A., other, and (2021) Genetic analyses of gynecological disease identify genetic relationships between uterine fibroids and endometrial cancer, and a novel endometrial cancer genetic risk region at the WNT4 1p36.12 locus. Human Genetics, 140 (9), pp.1353-1365. [eprints.qut.edu.au/213790/]

Mitchell, Brittany L., Thorp, Jackson G., Wu, Yeda, Campos, Adrian I., Nyholt, Dale R., Gordon, Scott D., Whiteman, David C., Olsen, Catherine M., Hickie, Ian B., Martin, Nicholas G., et al. (2021) Polygenic Risk Scores Derived from Varying Definitions of Depression and Risk of Depression. JAMA Psychiatry, 78 (10), pp.1152-1160. [eprints.qut.edu.au/213793/]

Ni, Guiyan, Zeng, Jian, Revez, Joana A., Wang, Ying, Zheng, Zhili, Ge, Tian, Restuadi, Restuadi, Kiewa, Jacqueline, Nyholt, Dale R., Coleman, Jonathan R.I., et al. (2021) A comparison of ten polygenic score methods for psychiatric disorders applied across multiple cohorts. Biological Psychiatry, 90 (9), pp.611-620. [eprints.qut.edu.au/210583/]

Rodrigo, Linduni M., Nyholt, Dale R. (2021) Imputation and Reanalysis of ExomeChip Data Identifies Novel, Conditional and Joint Genetic Effects on Parkinson’s Disease Risk. Genes, 12 (5), pp.Article number: 689. [eprints.qut.edu.au/210582/]

Ruth, Katherine S, Day, Felix R, Hussain, Jazib, Martínez-Marchal, Ana, Aiken, Catherine E, Azad, Ajuna, Thompson, Deborah J, Knoblochova, Lucie, Abe, Hironori, Tarry-Adkins, Jane L, et al. (2021) Genetic insights into biological mechanisms governing human ovarian ageing. Nature, 596 (7872), pp.393-397. [eprints.qut.edu.au/214298/]

Seviiri, Mathias, Law, Matthew H, Ong, Jue Sheng, Gharahkhani, Puya, Nyholt, Dale R, Hopkins, Peter, Chambers, Daniel, Campbell, Scott, Isbel, Nicole M, Soyer, H Peter, et al. (2021) Polygenic Risk Scores Stratify Keratinocyte Cancer Risk among Solid Organ Transplant Recipients with Chronic Immunosuppression in a High Ultraviolet Radiation Environment. The Journal of Investigative Dermatology, 141 (12), pp.2866-2875.e2. [eprints.qut.edu.au/211076/]

Seviiri, Mathias, Law, Matthew H, Ong, Jue Sheng, Gharahkhani, Puya, Nyholt, Dale R, Olsen, Catherine M, Whiteman, David C, MacGregor, Stuart (2021) Polygenic risk scores allow risk stratification for keratinocyte cancer in organ transplant recipients. The Journal of Investigative Dermatology, 141 (2), pp.325-333.e6. [eprints.qut.edu.au/203093/]

Seviiri, Mathias, Law, Matthew H, Ong, Jue-Sheng, Gharahkhani, Puya, Nyholt, Dale R, Olsen, Catherine M, Whiteman, David C, MacGregor, Stuart (2021) Polyunsaturated fatty acid levels and the risk of keratinocyte cancer : A Mendelian randomization analysis. Cancer Epidemiology, Biomarkers and Prevention, 30 (8), pp.1591-1598. [eprints.qut.edu.au/211078/]

Tanha, Hamzeh M, Martin, Nicholas G, Whitfield, John B, Nyholt, Dale R, other, and (2021) Association and genetic overlap between clinical chemistry tests and migraine. Cephalalgia, 41 (11-12), pp.1208-1221. [eprints.qut.edu.au/214327/]

Tanha, Hamzeh M, Sathyanarayanan, Anita, Nyholt, Dale R, other, and, Griffiths, Lyn (2021) Genetic overlap and causality between blood metabolites and migraine. American Journal of Human Genetics, 108 (11), pp.2086-2098. [eprints.qut.edu.au/214223/]

Tanha, Hamzeh M., Medland, Sarah, Martin, Nicholas G, Nyholt, Dale R (2021) Genetic correlation analysis does not associate male pattern baldness with COVID-19. Journal of the American Academy of Dermatology, 85 (4), pp.971-973. [eprints.qut.edu.au/211077/]

Adewuyi, Emmanuel Olorunleke, Sapkota, Yadav, Auta, Asa, Yoshihara, Kosuke, Nyegaard, Mette, Griffiths, Lyn, Montgomery, Grant W., Chasman, Daniel I., Nyholt, Dale, other, and (2020) Shared molecular genetic mechanisms underlie endometriosis and migraine comorbidity. Genes, 11 (3), pp.Article number: 268. [eprints.qut.edu.au/199655/]

Børte, Sigrid, Zwart, John-Anker, Skogholt, Anne Heidi, Gabrielsen, Maiken Elvestad, Thomas, Laurent F, Fritsche, Lars G, Surakka, Ida, Nielsen, Jonas B, Zhou, Wei, Wolford, Brooke N, et al. (2020) Mitochondrial genome-wide association study of migraine - the HUNT Study. Cephalalgia, 40 (6), pp.625-634. [eprints.qut.edu.au/203092/]

Bryois, Julien, Skene, Nathan G., Hansen, Thomas Folkmann, Kogelman, Lisette J.A., Watson, Hunna J., Liu, Zijing, Adan, Roger, Alfredsson, Lars, Ando, Tetsuya, Andreassen, Ole, et al. (2020) Genetic identification of cell types underlying brain complex traits yields insights into the etiology of Parkinson’s disease. Nature Genetics, 52 (5), pp.482-493. [eprints.qut.edu.au/229815/]

Coleman, Jonathan R.I., Gaspar, Héléna A., Bryois, Julien, Byrne, Enda M., Forstner, Andreas J., Holmans, Peter A., de Leeuw, Christiaan A., Mattheisen, Manuel, McQuillin, Andrew, Whitehead Pavlides, Jennifer M., et al. (2020) The Genetics of the Mood Disorder Spectrum: Genome-wide Association Analyses of More Than 185,000 Cases and 439,000 Controls. Biological Psychiatry, 88 (2), pp.169-184. [eprints.qut.edu.au/238040/]

Dube, Umber, Ibanez, Laura, Budde, John P., Benitez, Bruno A., Davis, Albert A., Harari, Oscar, Iles, M. M., Law, Matthew H., Brown, Kevin M., Agee, Michelle, et al. (2020) Overlapping genetic architecture between Parkinson disease and melanoma. Acta Neuropathologica, 139 (2), pp.347-364. [eprints.qut.edu.au/230057/]

Guo, Yanjun, Rist, Pamela M., Daghlas, Iyas, Giulianini, Franco, Gormley, Padhraig, Anttila, Verneri, Winsvold, Bendik S., Palta, Priit, Esko, Tonu, Pers, Tune H., et al. (2020) A genome-wide cross-phenotype meta-analysis of the association of blood pressure with migraine. Nature Communications, 11, pp.Article number: 3368. [eprints.qut.edu.au/233424/]

Hasdemir, Can, Gokcay, Figen, Orman, Mehmet N., Kocabas, Umut, Payzin, Serdar, Sahin, Hatice, Nyholt, Dale R., Antzelevitch, Charles (2020) Recognition and clinical implications of high prevalence of migraine in patients with Brugada syndrome and drug-induced type 1 Brugada pattern. Journal of Cardiovascular Electrophysiology, 31 (12), pp.3311-3317. [eprints.qut.edu.au/211075/]

Laisk, Triin, Soares, Ana Luiza G., Ferreira, Teresa, Painter, Jodie N., Censin, Jenny C., Laber, Samantha, Bacelis, Jonas, Chen, Chia Yen, Lepamets, Maarja, Lin, Kuang, et al. (2020) The genetic architecture of sporadic and multiple consecutive miscarriage. Nature Communications, 11 (1), pp.Article number: 5980. [eprints.qut.edu.au/211072/]

Landi, Maria Teresa, Bishop, D. Timothy, MacGregor, Stuart, Machiela, Mitchell J., Stratigos, Alexander J., Ghiorzo, Paola, Brossard, Myriam, Calista, Donato, Choi, Jiyeon, Fargnoli, Maria Concetta, et al. (2020) Genome-wide association meta-analyses combining multiple risk phenotypes provide insights into the genetic architecture of cutaneous melanoma susceptibility. Nature Genetics, 52 (5), pp.494-504. [eprints.qut.edu.au/211071/]

Li, Chen, Stoma, Svetlana, Lotta, Luca A., Warner, Sophie, Albrecht, Eva, Allione, Alessandra, Arp, Pascal P., Broer, Linda, Buxton, Jessica L., Da Silva Couto Alves, Alexessander, et al. (2020) Genome-wide Association Analysis in Humans Links Nucleotide Metabolism to Leukocyte Telomere Length. American Journal of Human Genetics, 106 (3), pp.389-404. [eprints.qut.edu.au/211073/]

Mitchell, Brittany, Thorp, Jackson, Evans, David, Nyholt, Dale, Martin, Nicholas, Lupton, Michelle (2020) Exploring the genetic relationship between hearing impairment and Alzheimer’s disease. Alzheimer’s & Dementia: Diagnosis, Assessment and Disease Monitoring, 12 (1), pp.Article number: e12108. [eprints.qut.edu.au/206652/]

Nyholt, Dale R. (2020) Migraine, Human Genetics and a Passion for Science. Twin Research and Human Genetics, 23 (2), pp.105-106. [eprints.qut.edu.au/211074/]

Sargurupremraj, Muralidharan, Suzuki, Hideaki, Jian, Xueqiu, Sarnowski, Chloé, Evans, Tavia E., Bis, Joshua C., Eiriksdottir, Gudny, Sakaue, Saori, Terzikhan, Natalie, Habes, Mohamad, et al. (2020) Cerebral small vessel disease genomics and its implications across the lifespan. Nature Communications, 11, pp.Article number: 6285. [eprints.qut.edu.au/233425/]

Sathyanarayanan, Anita, Gupta, Rohit, Thompson, Rik, Nyholt, Dale, Bauer, Denis, Hiriyur Nagaraj, Shivashankar (2020) A comparative study of multi-omics integration tools for cancer driver gene identification and tumour subtyping. Briefings in Bioinformatics, 21 (6), pp.1920-1936. [eprints.qut.edu.au/197177/]

Clark, David W, Okada, Yukinori, Moore, Kristjan H S, Mason, Dan, Pirastu, Nicola, Gandin, Ilaria, Mattsson, Hannele, Barnes, Catriona L K, Lin, Kuang, Zhao, Jing Hua, et al. (2019) Associations of autozygosity with a broad range of human phenotypes. Nature Communications, 10, pp.Article number: 4957. [eprints.qut.edu.au/214224/]

Gallagher, C.S., Mäkinen, N., Harris, H R, Rahmioglu, N, Uimari, O, Cook, J P, Shigesi, N, Ferreira, T, Velez-Edwards, D R, Edwards, T L, et al. (2019) Genome-wide association and epidemiological analyses reveal common genetic origins between uterine leiomyomata and endometriosis. Nature Communications, 10 (1), pp.Article number: 4857. [eprints.qut.edu.au/202932/]

Grove, Jakob, Ripke, Stephan, Als, Thomas D., Mattheisen, Manuel, Walters, Raymond K., Won, Hyejung, Pallesen, Jonatan, Agerbo, Esben, Andreassen, Ole A., Anney, Richard, et al. (2019) Identification of common genetic risk variants for autism spectrum disorder. Nature Genetics, 51 (3), pp.431-444. [eprints.qut.edu.au/199331/]

Karlsson Linnér, Richard, Biroli, Pietro, Kong, Edward, Meddens, S. Fleur W., Wedow, Robbee, Fontana, Mark Alan, Lebreton, Maël, Tino, Stephen P., Abdellaoui, Abdel, Hammerschlag, Anke R., 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. Nature Genetics, 51 (2), pp.245-257. [eprints.qut.edu.au/230657/]

Pelzer, Nadine, Louter, Mark, van Zwet, Erik, Nyholt, Dale, Ferrari, Michel, van den Maagdenberg, Arn, Haan, Joost, Terwindt, Gisela (2019) Linking migraine frequency with family history of migraine. Cephalalgia, 39 (2), pp.229-236. [eprints.qut.edu.au/123193/]

Periyasamy, Sathish, John, Sujit, Padmavati, Raman, Rajendren, Preeti, Thirunavukkarasu, Priyadarshini, Gratten, Jake, Vinkhuyzen, Anna, McRae, Allan, Holliday, Elizabeth, Nyholt, Dale, et al. (2019) Association of schizophrenia risk with disordered niacin metabolism in an Indian genome-wide association study. JAMA Psychiatry, 76 (10), pp.1026-1034. [eprints.qut.edu.au/132356/]

van den Maagdenberg, Arn, Nyholt, Dale, Anttila, Verneri (2019) Novel hypotheses emerging from GWAS in migraine?. Journal of Headache and Pain, 20 (1), pp.Article number: 5 1-7. [eprints.qut.edu.au/132355/]

van der Spek, Ashley, Broer, Linda, Draisma, Harmen, Pool, Rene, Albrecht, Eva, Beekman, Marian, Mangino, Massimo, Raag, Mait, Nyholt, Dale, Dharuri, Harish, et al. (2019) Metabolomics reveals a link between homocysteine and lipid metabolism and leukocyte telomere length: the ENGAGE consortium. Scientific Reports, 9 (1), pp.Article number: 11623 1-12. [eprints.qut.edu.au/132357/]

Anttila, Verneri, Bulik-Sullivan, Brendan, Finucane, Hilary, Walters, Raymond, Bras, Jose, Duncan, Laramie, Escott-Price, Valentina, Falcone, Guido, Gormley, Padhraig, Malik, Rainer, et al. (2018) Analysis of shared heritability in common disorders of the brain. Science, 360 (6395), pp.Article number: eaap8757 1-12. [eprints.qut.edu.au/123228/]

Gerring, Zac, McRae, Allan, Montgomery, Grant, Nyholt, Dale (2018) Genome-wide DNA methylation profiling in whole blood reveals epigenetic signatures associated with migraine. BMC Genomics, 19, pp.Article number: 69 1-10. [eprints.qut.edu.au/123192/]

Gerring, Zac, Powell, Joseph, Montgomery, Grant, Nyholt, Dale (2018) Genome-wide analysis of blood gene expression in migraine implicates immune-inflammatory pathways. Cephalalgia, 38 (2), pp.292-303. [eprints.qut.edu.au/223158/]

Gormley, Padhraig, Kurki, Mitja I., Hiekkala, Marjo Eveliina, Veerapen, Kumar, Häppölä, Paavo, Mitchell, Adele A., Lal, Dennis, Palta, Priit, Surakka, Ida, Kaunisto, Mari Anneli, et al. (2018) Common variant burden contributes to the familial aggregation of migraine in 1,589 families. Neuron, 98 (4), pp.743-753.e4. [eprints.qut.edu.au/202429/]

Gormley, Padhraig, Kurki, Mitja, Hiekkala, Marjo Eveliina, Veerapen, Kumar, Häppölä, Paavo, Mitchell, Adele A., Lal, Dennis, Palta, Priit, Surakka, Ida, Hamalainen, Eija, et al. (2018) Correction : Common variant burden contributes to the familial aggregation of migraine in 1,589 families. Neuron, 99 (5). [eprints.qut.edu.au/203238/]

Lupton, Michelle, Medland, Sarah, Gordon, Scott, Goncalves, Tabatha, Macgregor, Stuart, Mackey, David, Young, Terri, Duffy, David, Visscher, Peter, Wray, Naomi, et al. (2018) Accuracy of inferred APOE genotypes for a range of genotyping arrays and imputation reference panels. Journal of Alzheimer's Disease, 64 (1), pp.49-54. [eprints.qut.edu.au/123187/]

Painter, Jodie N., O'Mara, Tracy A., Cheng, Timothy H.T., Gorman, Maggie, Martin, Lynn, Hodson, Shirley, Martin, Nicholas G., Henders, Anjali K., Attia, John, McEvoy, Mark, et al. (2018) Genetic overlap between endometriosis and endometrial cancer: Evidence from cross-disease genetic correlation and GWAS meta-analyses. Cancer Medicine, 7 (5), pp.1978-1987. [eprints.qut.edu.au/200896/]

Turcot, Valerie, Lu, Yingchang (Kevin), Highland, Heather, Schurmann, Claudia, Justice, Anne, Fine, Rebecca, Bradfield, Jonathan, Esko, Tonu, Giri, Ayush, Graff, Mariaelisa, et al. (2018) Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity. Nature Genetics, 50 (1), pp.26-41. [eprints.qut.edu.au/123225/]

Wray, Naomi, Ripke, Stephan, Mattheisen, Manuel, Trzaskowski, Maciej, Byrne, Enda, Abdellaoui, Abdel, Adams, Mark, Agerbo, Esben, Air, Tracy, Andlauer, Till, et al. (2018) Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depression. Nature Genetics, 50 (5), pp.668-681. [eprints.qut.edu.au/123226/]

Yang, Yuanhao, Zhao, Huiying, Boomsma, Dorret, Ligthart, Lannie, Belin, Andrea, Smith, George Davey, Esko, Tonu, Freilinger, Tobias, Folkmann Hansen, Thomas, Ikram, M. Arfan, et al. (2018) Molecular genetic overlap between migraine and major depressive disorder. European Journal of Human Genetics, 26 (8), pp.1202-1216. [eprints.qut.edu.au/123194/]