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2019 Journal Article Concordance of genetic variation that increases risk for tourette syndrome and that influences its underlying neurocircuitryMufford, Mary, Cheung, Josh, Jahanshad, Neda, van der Merwe, Celia, Ding, Linda, Groenewold, Nynke, Koen, Nastassja, Chimusa, Emile R., Dalvie, Shareefa, Ramesar, Raj, Knowles, James A., Lochner, Christine, Hibar, Derrek P., Paschou, Peristera, van den Heuvel, Odile A., Medland, Sarah E., Scharf, Jeremiah M., Mathews, Carol A., Thompson, Paul M., Stein, Dan J. and Psychiatric Genomics Consortium - Tourette Syndrome working group (2019). Concordance of genetic variation that increases risk for tourette syndrome and that influences its underlying neurocircuitry. Translational Psychiatry, 9 (1) 120. doi: 10.1038/s41398-019-0452-3 |
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2019 Journal Article The CODATwins Project: the current status and recent findings of COllaborative Project of Development of Anthropometrical Measures in TwinsSilventoinen, K., Jelenkovic, A., Yokoyama, Y., Sund, R., Sugawara, M., Tanaka, M., Matsumoto, S., Bogl, L. H., Freitas, D. L., Maia, J. A., Hjelmborg, J. V.B., Aaltonen, S., Piirtola, M., Latvala, A., Calais-Ferreira, L., Oliveira, V. C., Ferreira, P. H., Ji, F., Ning, F., Pang, Z., Ordoñana, J. R., Sánchez-Romera, J. F., Colodro-Conde, L., Burt, S. A., Klump, K. L., Martin, N. G., Medland, S. E., Montgomery, G. W., Kandler, C. ... Kaprio, J. (2019). The CODATwins Project: the current status and recent findings of COllaborative Project of Development of Anthropometrical Measures in Twins. Twin Research and Human Genetics, 22 (6) PII S1832427419000355, 1-9. doi: 10.1017/thg.2019.35 |
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2019 Journal Article Novel genetic loci affecting facial shape variation in humansXiong, Ziyi, Dankova, Gabriela, Howe, Laurence J., Lee, Myoung Keun, Hysi, Pirro G., de Jong, Markus A., Zhu, Gu, Adhikari, Kaustubh, Li, Dan, Li, Yi, Pan, Bo, Feingold, Eleanor, Marazita, Mary L., Shaffer, John R., McAloney, Kerrie, Xu, Shu-Hua, Jin, Li, Wang, Sijia, de Vrij, Femke Ms, Lendemeijer, Bas, Richmond, Stephen, Zhurov, Alexei, Lewis, Sarah, Sharp, Gemma C., Paternoster, Lavinia, Thompson, Holly, Gonzalez-Jose, Rolando, Bortolini, Maria Catira, Canizales-Quinteros, Samuel ... Kayser, Manfred (2019). Novel genetic loci affecting facial shape variation in humans. eLife, 8 e49898. doi: 10.7554/eLife.49898 |
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2019 Conference Publication GWAS on the Internet: systematic review of online news and blog articles about GWAS publications from 2005 to 2018Morosoli, Jose J., Colodro-Conde, Lucia, Barlow, Fiona K. and Medland, Sarah (2019). GWAS on the Internet: systematic review of online news and blog articles about GWAS publications from 2005 to 2018. 49th Annual Meeting of the Behavior-Genetics-Association (BGA), Stockholm Sweden, Jun 26-29, 2019. NEW YORK: SPRINGER. |
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2019 Journal Article Altered structural brain asymmetry in autism spectrum disorder in a study of 54 datasetsPostema, Merel C., van Rooij, Daan, Anagnostou, Evdokia, Arango, Celso, Auzias, Guillaume, Behrmann, Marlene, Filho, Geraldo Busatto, Calderoni, Sara, Calvo, Rosa, Daly, Eileen, Deruelle, Christine, Di Martino, Adriana, Dinstein, Ilan, Duran, Fabio Luis S., Durston, Sarah, Ecker, Christine, Ehrlich, Stefan, Fair, Damien, Fedor, Jennifer, Feng, Xin, Fitzgerald, Jackie, Floris, Dorothea L., Freitag, Christine M., Gallagher, Louise, Glahn, David C., Gori, Ilaria, Haar, Shlomi, Hoekstra, Liesbeth, Jahanshad, Neda ... Francks, Clyde (2019). Altered structural brain asymmetry in autism spectrum disorder in a study of 54 datasets. Nature Communications, 10 (1) 4958, 4958. doi: 10.1038/s41467-019-13005-8 |
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2019 Journal Article Associations of autozygosity with a broad range of human phenotypesClark, 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, Deelen, Patrick, Rohde, Rebecca, Schurmann, Claudia, Guo, Xiuqing, Giulianini, Franco, Zhang, Weihua, Medina-Gomez, Carolina, Karlsson, Robert, Bao, Yanchun, Bartz, Traci M., Baumbach, Clemens, Biino, Ginevra, Bixley, Matthew J., Brumat, Marco, Chai, Jin-Fang, Corre, Tanguy, Cousminer, Diana L., Dekker, Annelot M., Eccles, David A. ... Wilson, James F. (2019). Associations of autozygosity with a broad range of human phenotypes. Nature Communications, 10 (1) 4957, 4957. doi: 10.1038/s41467-019-12283-6 |
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2019 Journal Article Association of copy number variation of the 15q11.2 BP1-BP2 region with cortical and subcortical morphology and cognitionVan Der Meer, Dennis, Sønderby, Ida E., Kaufmann, Tobias, Walters, G. Bragi, Abdellaoui, Abdel, Ames, David, Amunts, Katrin, Andersson, Micael, Armstrong, Nicola J., Bernard, Manon, Blackburn, Nicholas B., Blangero, John, Boomsma, Dorret I., Brodaty, Henry, Brouwer, Rachel M., Bülow, Robin, Cahn, Wiepke, Calhoun, Vince D., Caspers, Svenja, Cavalleri, Gianpiero L., Ching, Christopher R. K., Cichon, Sven, Ciufolini, Simone, Corvin, Aiden, Crespo-Facorro, Benedicto, Curran, Joanne E., Dalvie, Shareefa, Dazzan, Paola, De Geus, Eco J. C. ... Andreassen, Ole A. (2019). Association of copy number variation of the 15q11.2 BP1-BP2 region with cortical and subcortical morphology and cognition. JAMA Psychiatry, 77 (4), 1-11. doi: 10.1001/jamapsychiatry.2019.3779 |
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2019 Journal Article Genome-wide association and epidemiological analyses reveal common genetic origins between uterine leiomyomata and endometriosisGallagher, 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., Mortlock, S., Ruhioglu, Z., Day, F., Becker, C. M., Karhunen, V., Martikainen, H., Järvelin, M.-R., Cantor, R. M., Ridker, P. M., Terry, K. L., Buring, J. E., Gordon, S. D., Medland, S. E., Montgomery, G. W., Nyholt, D. R., Hinds, D. A., Tung, J. Y., Perry, J. R. B., Lind, P. A. ... Morton, C. C. (2019). Genome-wide association and epidemiological analyses reveal common genetic origins between uterine leiomyomata and endometriosis. Nature Communications, 10 (1) 4857, 4857. doi: 10.1038/s41467-019-12536-4 |
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2019 Journal Article Genetic architecture of subcortical brain structures in 38,851 individualsSatizabal, Claudia L., Adams, Hieab H. H., Hibar, Derrek P., White, Charles C., Knol, Maria J., Stein, Jason L., Scholz, Markus, Sargurupremraj, Muralidharan, Jahanshad, Neda, Roshchupkin, Gennady V., Smith, Albert V., Bis, Joshua C., Jian, Xueqiu, Luciano, Michelle, Hofer, Edith, Teumer, Alexander, van der Lee, Sven J., Yang, Jingyun, Yanek, Lisa R., Lee, Tom V., Li, Shuo, Hu, Yanhui, Koh, Jia Yu, Eicher, John D., Desrivières, Sylvane, Arias-Vasquez, Alejandro, Chauhan, Ganesh, Athanasiu, Lavinia, Rentería, Miguel E. ... Ikram, M. Arfan (2019). Genetic architecture of subcortical brain structures in 38,851 individuals. Nature Genetics, 51 (11), 1624-1636. doi: 10.1038/s41588-019-0511-y |
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2019 Conference Publication ANTICIPATING INDIVIDUAL RESPONSES TO PRECISION PSYCHIATRY BASED ON GENETIC INFORMATION: THE ROLE OF GENETIC LITERACY, COGNITIVE STYLES, AND PERSONAL VALUESGarcia, Jose Morosoli, Grasby, Katrina, Conde, Lucia Colodro, Barlow, Fiona K. and Medland, Sarah E. (2019). ANTICIPATING INDIVIDUAL RESPONSES TO PRECISION PSYCHIATRY BASED ON GENETIC INFORMATION: THE ROLE OF GENETIC LITERACY, COGNITIVE STYLES, AND PERSONAL VALUES. 27th World Congress of Psychiatric Genetics (WCPG), Los Angeles Ca, Oct 26-31, 2019. AMSTERDAM: ELSEVIER. doi: 10.1016/j.euroneuro.2019.07.196 |
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2019 Conference Publication Insights from the largest genetic study of sporadic and recurrent miscarriageLaisk, T., Soares, A., Ferreira, T., Painter, J. N., Laber, S., Bacelis, J., Chen, C., Lepamets, M., Lin, K., Liu, S., Millwood, I. Y., Ramu, A., Southcombe, J., Andersen, M. S., Yang, L., Becker, C., Gordon, S. D., Bybjerg-Grauholm, J., Helgeland, O., Hougaard, D. M., Jin, X., Johansson, S., Juodakis, J., Kartsonaki, C., Kukuskina, V., Lind, P., Metspalu, A., Montgomery, G. W., Morris, A. P. ... Lindgren, C. M. (2019). Insights from the largest genetic study of sporadic and recurrent miscarriage. 52nd Conference of the European-Society-of-Human-Genetics (ESHG), Gothenburg Sweden, Jun 15-18, 2019. LONDON: NATURE PUBLISHING GROUP. |
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2019 Journal Article Public understanding of behavioral genetics: Integrating heuristic thinking, motivated reasoning and planned social change theories for better communication strategiesMorosoli, J. J., Colodro-Conde, L., Barlow, F. K. and Medland, S. E. (2019). Public understanding of behavioral genetics: Integrating heuristic thinking, motivated reasoning and planned social change theories for better communication strategies. Behavior Genetics, 49 (5), 469-477. doi: 10.1007/s10519-019-09964-9 |
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2019 Journal Article Metabolomics reveals a link between homocysteine and lipid metabolism and leukocyte telomere length: the ENGAGE consortiumVan der Spek, Ashley, Broer, Linda, Draisma, Harmen H. M., Pool, René, Albrecht, Eva, Beekman, Marian, Mangino, Massimo, Raag, Mait, Nyholt, Dale R., Dharuri, Harish K., Codd, Veryan, Amin, Najaf, de Geus, Eco J. C., Deelen, Joris, Demirkan, Ayse, Yet, Idil, Fischer, Krista, Haller, Toomas, Henders, Anjali K., Isaacs, Aaron, Medland, Sarah E., Montgomery, Grant W., Mooijaart, Simon P., Strauch, Konstantin, Suchiman, H. Eka D., Vaarhorst, Anika A. M., van Heemst, Diana, Wang-Sattler, Rui, Whitfield, John B. ... Gieger, Christian (2019). Metabolomics reveals a link between homocysteine and lipid metabolism and leukocyte telomere length: the ENGAGE consortium. Scientific Reports, 9 (1) 11623, 11623. doi: 10.1038/s41598-019-47282-6 |
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2019 Journal Article Genetic and environmental risk factors in the non-medical use of over-the-counter or prescribed analgesics, and their relationship to major classes of licit and illicit substance use and misuse in a population-based sample of young adult twinsGillespie, Nathan A., Bates, Timothy C., Hickie, Ian B., Medland, Sarah E., Verhulst, Brad, Kirkpatrick, Robert M., Kendler, Kenneth S., Martin, Nicholas G. and Benotsch, Eric G. (2019). Genetic and environmental risk factors in the non-medical use of over-the-counter or prescribed analgesics, and their relationship to major classes of licit and illicit substance use and misuse in a population-based sample of young adult twins. Addiction, 114 (12) add.14750, 2229-2240. doi: 10.1111/add.14750 |
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2019 Journal Article Genome-wide association study identifies eight risk loci and implicates metabo-psychiatric origins for anorexia nervosaWatson, Hunna J., Yilmaz, Zeynep, Thornton, Laura M., Hübel, Christopher, Coleman, Jonathan R. I., Gaspar, Héléna A., Bryois, Julien, Hinney, Anke, Leppä, Virpi M., Mattheisen, Manuel, Medland, Sarah E., Ripke, Stephan, Yao, Shuyang, Giusti-Rodríguez, Paola, Hanscombe, Ken B., Purves, Kirstin L., Adan, Roger A. H., Alfredsson, Lars, Ando, Tetsuya, Andreassen, Ole A., Baker, Jessica H., Berrettini, Wade H., Boehm, Ilka, Boni, Claudette, Perica, Vesna Boraska, Buehren, Katharina, Burghardt, Roland, Cassina, Matteo, Cichon, Sven ... Bulik, Cynthia M. (2019). Genome-wide association study identifies eight risk loci and implicates metabo-psychiatric origins for anorexia nervosa. Nature Genetics, 51 (8), 1207-1214. doi: 10.1038/s41588-019-0439-2 |
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2019 Journal Article Genome-Wide Association Studies Identify Multiple Genetic Loci Influencing Eyebrow Color Variation in EuropeansPeng, Fuduan, Zhu, Gu, Hysi, Pirro G., Eller, Ryan J., Chen, Yan, Li, Yi, Hamer, Merel A., Zeng, Changqing, Hopkins, Racquel L., Jacobus, Case L., Wallace, Paige L., Uitterlinden, André G., Ikram, M. Arfan, Nijsten, Tamar, Duffy, David L., Medland, Sarah E., Spector, Timothy D., Walsh, Susan, Martin, Nicholas G., Liu, Fan and Kayser, Manfred (2019). Genome-Wide Association Studies Identify Multiple Genetic Loci Influencing Eyebrow Color Variation in Europeans. Journal of Investigative Dermatology, 139 (7), 1601-1605. doi: 10.1016/j.jid.2018.12.029 |
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2019 Journal Article The psychosocial impact of nausea and vomiting during pregnancy as a predictor of postpartum depressionBray, Nicola, Grasby, Katrina L., Lind, Penelope A., Painter, Jodie N., Colodro-Conde, Lucía and Medland, Sarah E. (2019). The psychosocial impact of nausea and vomiting during pregnancy as a predictor of postpartum depression. Journal of Health Psychology, 26 (7), 135910531985904-1072. doi: 10.1177/1359105319859048 |
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2019 Journal Article Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity (Nature Genetics, (2018), 50, 1, (26-41), 10.1038/s41588-017-0011-x)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. (2019). Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity (Nature Genetics, (2018), 50, 1, (26-41), 10.1038/s41588-017-0011-x). Nature Genetics, 51 (7), 1191-1192. doi: 10.1038/s41588-019-0447-2 |
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2019 Journal Article Publisher Correction: Genome-wide association meta-analysis of individuals of European ancestry identifies new loci explaining a substantial fraction of hair color variation and heritabilityHysi, 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. (2019). Publisher Correction: 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, 51 (7), 1190-1190. doi: 10.1038/s41588-019-0446-3 |
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2019 Journal Article Maternal and fetal genetic effects on birth weight and their relevance to cardio-metabolic risk factorsWarrington, Nicole M., Beaumont, Robin N., Horikoshi, Momoko, Day, Felix R., Helgeland, Øyvind, Laurin, Charles, Bacelis, Jonas, Peng, Shouneng, Hao, Ke, Feenstra, Bjarke, Wood, Andrew R., Mahajan, Anubha, Tyrrell, Jessica, Robertson, Neil R., Rayner, N. William, Qiao, Zhen, Moen, Gunn-Helen, Vaudel, Marc, Marsit, Carmen J., Chen, Jia, Nodzenski, Michael, Schnurr, Theresia M., Zafarmand, Mohammad H., Bradfield, Jonathan P., Grarup, Niels, Kooijman, Marjolein N., Li-Gao, Ruifang, Geller, Frank, Paternoster, Lavinia ... Freathy, Rachel M. (2019). Maternal and fetal genetic effects on birth weight and their relevance to cardio-metabolic risk factors. Nature Genetics, 51 (5), 804-814. doi: 10.1038/s41588-019-0403-1 |
