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2018

Journal Article

Extended twin study of alcohol use in Virginia and Australia

Verhulst, Brad, Neale, Michael C., Eaves, Lindon J., Medland, Sarah E., Heath, Andrew C., Martin, Nicholas G. and Maes, Hermine H. (2018). Extended twin study of alcohol use in Virginia and Australia. Twin Research and Human Genetics, 21 (3), 163-178. doi: 10.1017/thg.2018.21

Extended twin study of alcohol use in Virginia and Australia

2018

Journal Article

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

Bartels, Meike, Hendriks, Anne, Mauri, Matteo, Krapohl, Eva, Whipp, Alyce, Bolhuis, Koen, Conde, Lucia Colodro, Luningham, Justin, Fung Ip, Hill, Hagenbeek, Fiona, Roetman, Peter, Gatej, Raluca, Lamers, Audri, Nivard, Michel, van Dongen, Jenny, Lu, Yi, Middeldorp, Christel, van Beijsterveldt, Toos, Vermeiren, Robert, Hankemeijer, Thomas, Kluft, Cees, Medland, Sarah, Lundström, Sebastian, Rose, Richard, Pulkkinen, Lea, Vuoksimaa, Eero, Korhonen, Tellervo, Martin, Nicholas G., Lubke, Gitta ... Boomsma, Dorret I. (2018). 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. European Child & Adolescent Psychiatry, 27 (9), 1-17. doi: 10.1007/s00787-018-1169-1

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

2018

Journal Article

Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depression

Wray, Naomi R., Ripke, Stephan, Mattheisen, Manuel, Trzaskowski, Maciej, Byrne, Enda M., Abdellaoui, Abdel, Adams, Mark J., Agerbo, Esben, Air, Tracy M., Andlauer, Till M. F., Bacanu, Silviu-Alin, Baekvad-Hansen, Marie, Beekman, Aartjan F. T., Bigdeli, Tim B., Binder, Elisabeth B., Blackwood, Douglas R. H., Bryois, Julien, Buttenschon, Henriette N., Bybjerg-Grauholm, Jonas, Cai, Na, Castelao, Enrique, Christensen, Jane Hvarregaard, Clarke, Toni-Kim, Coleman, Jonathan I. R., Colodro-Conde, Lucia, Couvy-Duchesne, Baptiste, Craddock, Nick, Crawford, Gregory E., Crowley, Cheynna A. ... Sullivan, Patrick F. (2018). Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depression. Nature Genetics, 50 (5), 668-+. doi: 10.1038/s41588-018-0090-3

Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depression

2018

Journal Article

Genome-wide association meta-analysis of individuals of European ancestry identifies new loci explaining a substantial fraction of hair color variation and heritability

Hysi, Pirro G., Valdes, Ana M., Liu, Fan, Furlotte, Nicholas A., Evans, David M., Bataille, Veronique, Visconti, Alessia, Hemani, Gibran, McMahon, George, Ring, Susan M., Smith, George Davey, Duffy, David L., Zhu, Gu, Gordon, Scott D., Medland, Sarah E., Lin, Bochao D., Willemsen, Gonneke, Jan Hottenga, Jouke, Vuckovic, Dragana, Girotto, Giorgia, Gandin, Ilaria, Sala, Cinzia, Concas, Maria Pina, Brumat, Marco, Gasparini, Paolo, Toniolo, Daniela, Cocca, Massimiliano, Robino, Antonietta, Yazar, Seyhan ... Spector, Timothy D. (2018). Genome-wide association meta-analysis of individuals of European ancestry identifies new loci explaining a substantial fraction of hair color variation and heritability. Nature Genetics, 50 (5), 652-656. doi: 10.1038/s41588-018-0100-5

Genome-wide association meta-analysis of individuals of European ancestry identifies new loci explaining a substantial fraction of hair color variation and heritability

2018

Journal Article

Genome-wide association study identifies nine novel loci for 2D:4D finger ratio, a putative retrospective biomarker of testosterone exposure in utero

Warrington, Nicole M., Shevroja, Enisa, Hemani, Gibran, Hysi, Pirro G., Jiang, Yunxuan, Auton, Adam, Boer, Cindy G., Mangino, Massimo, Wang, Carol A., Kemp, John P., McMahon, George, Medina-Gomez, Carolina, Hickey, Martha, Trajanoska, Katerina, Wolke, Dieter, Ikram, Arfan M., 23 and Me Research Team, Montgomery, Grant W., Felix, Janine F., Wright, Margaret J., Mackey, David A., Jaddoe, Vincent W., Martin, Nicholas G., Tung, Joyce Y., Davey Smith, George, Pennell, Craig E., Spector, Tim D., van Meurs, Joyce, Rivadeneira, Fernando ... Evans, David M. (2018). Genome-wide association study identifies nine novel loci for 2D:4D finger ratio, a putative retrospective biomarker of testosterone exposure in utero. Human Molecular Genetics, 27 (11), 2025-2038. doi: 10.1093/hmg/ddy121

Genome-wide association study identifies nine novel loci for 2D:4D finger ratio, a putative retrospective biomarker of testosterone exposure in utero

2018

Journal Article

Nineteen and Up study (19Up): Understanding pathways to mental health disorders in young Australian twins

Couvy-Duchesne, Baptiste, O'Callaghan, Victoria, Parker, Richard, Mills, Natalie, Kirk, Katherine M., Scott, Jan, Vinkhuyzen, Anna., Hermens, Daniel F., Lind, Penelope A., Davenport, Tracey A., Burns, Jane M., Connell, Melissa, Zietsch, Brendan P., Scott, James, Wright, Margaret J., Medland, Sarah E., McGrath, John, Martin, Nicholas G., Hickie, Ian B. and Gillespie, Nathan A. (2018). Nineteen and Up study (19Up): Understanding pathways to mental health disorders in young Australian twins. BMJ Open, 8 (3) e018959, 1-13. doi: 10.1136/bmjopen-2017-018959

Nineteen and Up study (19Up): Understanding pathways to mental health disorders in young Australian twins

2018

Journal Article

Publisher Correction: protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity

Turcot, Valérie, Lu, Yingchang, Highland, Heather M., Schurmann, Claudia, Justice, Anne E., Fine, Rebecca S., Bradfield, Jonathan P., Esko, Tõnu, Giri, Ayush, Graff, Mariaelisa, Guo, Xiuqing, Hendricks, Audrey E., Karaderi, Tugce, Lempradl, Adelheid, Locke, Adam E., Mahajan, Anubha, Marouli, Eirini, Sivapalaratnam, Suthesh, Young, Kristin L., Alfred, Tamuno, Feitosa, Mary F., Masca, Nicholas G. D., Manning, Alisa K., Medina-Gomez, Carolina, Mudgal, Poorva, Ng, Maggie C. Y., Reiner, Alex P., Vedantam, Sailaja, Willems, Sara M. ... Loos, Ruth J. F. (2018). Publisher Correction: protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity. Nature Genetics, 50 (5), 1-2. doi: 10.1038/s41588-018-0082-3

Publisher Correction: protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity

2018

Journal Article

The Nature of Nurture: Using a Virtual-Parent Design to Test Parenting Effects on Children's Educational Attainment in Genotyped Families

Bates, Timothy C., Maher, Brion S., Medland, Sarah E., McAloney, Kerrie, Wright, Margaret J., Hansell, Narelle K., Kendler, Kenneth S., Martin, Nicholas G. and Gillespie, Nathan A. (2018). The Nature of Nurture: Using a Virtual-Parent Design to Test Parenting Effects on Children's Educational Attainment in Genotyped Families. Twin Research and Human Genetics, 21 (2), 73-83. doi: 10.1017/thg.2018.11

The Nature of Nurture: Using a Virtual-Parent Design to Test Parenting Effects on Children's Educational Attainment in Genotyped Families

2018

Journal Article

Gene set enrichment analysis and expression pattern exploration implicate an involvement of neurodevelopmental processes in bipolar disorder

Mühleisen, Thomas W., Reinbold, Céline S., Forstner, Andreas J., Abramova, Lilia I., Alda, Martin, Babadjanova, Gulja, Bauer, Michael, Brennan, Paul, Chuchalin, Alexander, Cruceanu, Cristiana, Czerski, Piotr M., Degenhardt, Franziska, Fischer, Sascha B., Fullerton, Janice M., Gordon, Scott D., Grigoroiu-Serbanescu, Maria, Grof, Paul, Hauser, Joanna, Hautzinger, Martin, Herms, Stefan, Hoffmann, Per, Kammerer-Ciernioch, Jutta, Khusnutdinova, Elza, Kogevinas, Manolis, Krasnov, Valery, Lacour, André, Laprise, Catherine, Leber, Markus, Lissowska, Jolanta ... Cichon, Sven (2018). Gene set enrichment analysis and expression pattern exploration implicate an involvement of neurodevelopmental processes in bipolar disorder. Journal of Affective Disorders, 228, 20-25. doi: 10.1016/j.jad.2017.11.068

Gene set enrichment analysis and expression pattern exploration implicate an involvement of neurodevelopmental processes in bipolar disorder

2018

Journal Article

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

Beaumont, Robin N., Warrington, Nicole M., Cavadino, Alana, Tyrrell, Jessica, Nodzenski, Michael, Horikoshi, Momoko, Geller, Frank, Myhre, Ronny, Richmond, Rebecca C., Paternoster, Lavinia, Bradfield, Jonathan P., Kreiner-Møller, Eskil, Huikari, Ville, Metrustry, Sarah, Lunetta, Kathryn L., Painter, Jodie N., Hottenga, Jouke-Jan, Allard, Catherine, Barton, Sheila J., Espinosa, Ana, Marsh, Julie A., Potter, Catherine, Zhang, Ge, Ang, Wei, Berry, Diane J., Bouchard, Luigi, Das, Shikta, Early Growth Genetics (EGG) Consortium, Hakonarson, Hakon ... Freathy, Rachel M. (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. Human Molecular Genetics, 27 (4) ddx429, 742-756. doi: 10.1093/hmg/ddx429

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

2018

Journal Article

No evidence of association of oxytocin polymorphisms with breastfeeding in 2 independent samples

Colodro-Conde, L., Sánchez-Romera, J. F., Lind, P. A., Zhu, G., Martin, N. G., Medland, S. E. and Ordoñana, J. R. (2018). No evidence of association of oxytocin polymorphisms with breastfeeding in 2 independent samples. Genes, Brain and Behavior, 17 (7) e12464, e12464. doi: 10.1111/gbb.12464

No evidence of association of oxytocin polymorphisms with breastfeeding in 2 independent samples

2018

Journal Article

The protocadherin 17 gene affects cognition, personality, amygdala structure and function, synapse development and risk of major mood disorders

Chang, H., Hoshina, N., Zhang, C., Ma, Y., Cao, H., Wang, Y., Wu, D. D., Bergen, S. E., Landén, M., Hultman, C. M., Preisig, M., Kutalik, Z., Castelao, E., Grigoroiu-Serbanescu, M., Forstner, A. J., Strohmaier, J., Hecker, J., Schulze, T. G., Müller-Myhsok, B., Reif, A., Mitchell, P. B., Martin, N. G., Schofield, P. R., Cichon, S., Nöthen, M. M., Walter, H., Erk, S., Heinz, A., Amin, N. ... MooDS Bipolar Consortium (2018). The protocadherin 17 gene affects cognition, personality, amygdala structure and function, synapse development and risk of major mood disorders. Molecular Psychiatry, 23 (2), 400-412. doi: 10.1038/mp.2016.231

The protocadherin 17 gene affects cognition, personality, amygdala structure and function, synapse development and risk of major mood disorders

2018

Journal Article

Meta-analysis of genome-wide association studies identifies 8 novel loci involved in shape variation of human head hair

Liu, Fan, Chen, Yan, Zhu, Gu, Hysi, Pirro G., Wu, Sijie, Adhikari, Kaustubh, Breslin, Krystal, Pośpiech, Ewelina, Hamer, Merel A., Peng, Fuduan, Muralidharan, Charanya, Acuna-Alonzo, Victor, Canizales-Quinteros, Samuel, Bedoya, Gabriel, Gallo, Carla, Poletti, Giovanni, Rothhammer, Francisco, Bortolini, Maria Catira, Gonzalez-Jose, Rolando, Zeng, Changqing, Xu, Shuhua, Jin, Li, Uitterlinden, André G., Arfan Ikram, M., van Duijn, Cornelia M., Nijsten, Tamar, Walsh, Susan, Branicki, Wojciech, Wang, Sijia ... Kayser, Manfred (2018). Meta-analysis of genome-wide association studies identifies 8 novel loci involved in shape variation of human head hair. Human Molecular Genetics, 27 (3), 559-575. doi: 10.1093/hmg/ddx416

Meta-analysis of genome-wide association studies identifies 8 novel loci involved in shape variation of human head hair

2018

Journal Article

Polygenic risk score, genome-wide association, and gene set analyses of cognitive domain deficits in schizophrenia

Nakahara, Soichiro, Medland, Sarah, Turner, Jessica A., Calhoun, Vince D., Lim, Kelvin O., Mueller, Bryon A., Bustillo, Juan R., O'Leary, Daniel S., Vaidya, Jatin G., McEwen, Sarah, Voyvodic, James, Belger, Aysenil, Mathalon, Daniel H., Ford, Judith M., Guffanti, Guia, Macciardi, Fabio, Potkin, Steven G. and van Erp, Theo G.M. (2018). Polygenic risk score, genome-wide association, and gene set analyses of cognitive domain deficits in schizophrenia. Schizophrenia Research, 201, 393-399. doi: 10.1016/j.schres.2018.05.041

Polygenic risk score, genome-wide association, and gene set analyses of cognitive domain deficits in schizophrenia

2018

Journal Article

Genomic kinship construction to enhance genetic analyses in the human connectome project data

Kochunov, Peter, Donohue, Brian, Mitchell, Braxton D., Ganjgahi, Habib, Adhikari, Bhim, Ryan, Meghann, Medland, Sarah E., Jahanshad, Neda, Thompson, Paul M., Blangero, John, Fieremans, Els, Novikov, Dmitry S., Marcus, Daniel, Van Essen, David C., Glahn, David C, Elliot Hong, L. and Nichols, Thomas E. (2018). Genomic kinship construction to enhance genetic analyses in the human connectome project data. Human Brain Mapping, 40 (5), 1677-1688. doi: 10.1002/hbm.24479

Genomic kinship construction to enhance genetic analyses in the human connectome project data

2018

Journal Article

Accuracy of inferred APOE genotypes for a range of genotyping arrays and imputation reference panels

Lupton, Michelle K., Medland, Sarah E., Gordon, Scott D., Goncalves, Tabatha, MacGregor, Stuart, Mackey, David A., Young, Terri L., Duffy, David L., Visscher, Peter M., Wray, Naomi R., Nyholt, Dale R., Bain, Lisa, Ferreira, Manuel A., Henders, Anjali K., Wallace, Leanne, Montgomery, Grant W., Wright, Margaret J. and Martin, Nicholas G. (2018). Accuracy of inferred APOE genotypes for a range of genotyping arrays and imputation reference panels. Journal of Alzheimer's Disease, 64 (1), 49-54. doi: 10.3233/JAD-171104

Accuracy of inferred APOE genotypes for a range of genotyping arrays and imputation reference panels

2018

Journal Article

Type I Error Rates and Parameter Bias in Multivariate Behavioral Genetic Models

Verhulst, Brad, Prom-Wormley, Elizabeth, Keller, Matthew, Medland, Sarah and Neale, Michael C. (2018). Type I Error Rates and Parameter Bias in Multivariate Behavioral Genetic Models. Behavior Genetics, 49 (1), 99-111. doi: 10.1007/s10519-018-9942-y

Type I Error Rates and Parameter Bias in Multivariate Behavioral Genetic Models

2018

Journal Article

Association of whole-genome and NETRIN1 signaling pathway–derived polygenic risk scores for major depressive disorder and white matter microstructure in the UK Biobank

Barbu, Miruna C., Zeng, Yanni, Shen, Xueyi, Cox, Simon R., Clarke, Toni-Kim, Gibson, Jude, Adams, Mark J., Johnstone, Mandy, Haley, Chris S., Lawrie, Stephen M., Deary, Ian J., Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium, Wray, Naomi R., Ripke, Stephan, Mattheisen, Manuel, Trzaskowski, Maciej, Byrne, Enda M., Abdellaoui, Abdel, Adams, Mark J., Agerbo, Esben, Air, Tracy M., Andlauer, Till F.M., Bacanu, Silviu-Alin, Bækvad-Hansen, Marie, Beekman, Aartjan T.F., Bigdeli, Tim B., Binder, Elisabeth B., Blackwood, Douglas H.R., Bryois, Julien ... Whalley, Heather C. (2018). Association of whole-genome and NETRIN1 signaling pathway–derived polygenic risk scores for major depressive disorder and white matter microstructure in the UK Biobank. Biological Psychiatry: Cognitive Neuroscience and Neuroimaging, 4 (1), 91-100. doi: 10.1016/j.bpsc.2018.07.006

Association of whole-genome and NETRIN1 signaling pathway–derived polygenic risk scores for major depressive disorder and white matter microstructure in the UK Biobank

2017

Journal Article

Pathways to depression by age 16 years: Examining trajectories for self-reported psychological and somatic phenotypes across adolescence

Scott, Jan, Davenport, Tracey A., Parker, Richard, Hermens, Daniel F., Lind, Penelope A., Medland, Sarah E., Wright, Margaret J., Martin, Nicholas G., Gillespie, Nathan A. and Hickie, Ian B. (2017). Pathways to depression by age 16 years: Examining trajectories for self-reported psychological and somatic phenotypes across adolescence. Journal of Affective Disorders, 230, 1-6. doi: 10.1016/j.jad.2017.12.007

Pathways to depression by age 16 years: Examining trajectories for self-reported psychological and somatic phenotypes across adolescence

2017

Journal Article

Genome-wide meta-analysis associates HLA-DQA1/DRB1 and LPA and lifestyle factors with human longevity

Joshi, Peter K., Pirastu, Nicola, Kentistou, Katherine A., Fischer, Krista, Hofer, Edith, Schraut, Katharina E., Clark, David W., Nutile, Teresa, Barnes, Catriona L. K., Timmers, Paul R. H. J., Shen, Xia, Gandin, Ilaria, McDaid, Aaron F., Hansen, Thomas Folkmann, Gordon, Scott D., Giulianini, Franco, Boutin, Thibaud S., Abdellaoui, Abdel, Zhao, Wei, Medina-Gomez, Carolina, Bartz, Traci M., Trompet, Stella, Lange, Leslie A., Raffield, Laura, Van Der Spek, Ashley, Galesloot, Tessel E., Proitsi, Petroula, Yanek, Lisa R., Bielak, Lawrence F. ... Wilson, James F. (2017). Genome-wide meta-analysis associates HLA-DQA1/DRB1 and LPA and lifestyle factors with human longevity. Nature Communications, 8 (1) 910, 910. doi: 10.1038/s41467-017-00934-5

Genome-wide meta-analysis associates HLA-DQA1/DRB1 and LPA and lifestyle factors with human longevity