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Heritability and genomics of gene expression in peripheral blood
Wright, Fred A, Sullivan, Patrick F, Brooks, Andrew I, Zou, Fei, Sun, Wei, Xia, Kai, Madar, Vered, Jansen, Rick, Chung, Wonil, Zhou, Yi-Hui, Abdellaoui, Abdel, Batista, Sandra, Butler, Casey, Chen, Guanhua, Chen, Ting-Huei, D'Ambrosio, David, Gallins, Paul, Ha, Min Jin, Hottenga, Jouke Jan, Huang, Shunping, Kattenberg, Mathijs, Kochar, Jaspreet, Middeldorp, Christel M, Qu, Ani, Shabalin, Andrey, Tischfield, Jay, Todd, Laura, Tzeng, Jung-Ying, van Grootheest, Gerard, Vink, Jacqueline M, Wang, Qi, Wang, Wei, Wang, Weibo, Willemsen, Gonneke, Smit, Johannes H, de Geus, Eco J, Yin, Zhaoyu, Penninx, Brenda W J H, Boomsma, Dorret I
Published in Nature genetics (01.05.2014)
Published in Nature genetics (01.05.2014)
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Genome-Wide Analysis of Copy Number Variants in Attention Deficit Hyperactivity Disorder: The Role of Rare Variants and Duplications at 15q13.3
Williams, Nigel M., Franke, Barbara, Mick, Eric, Anney, Richard J.L., Freitag, Christine M., Gill, Michael, Thapar, Anita, O'Donovan, Michael C., Owen, Michael J., Holmans, Peter, Kent, Lindsey, Middleton, Frank, Zhang-James, Yanli, Liu, Lu, Meyer, Jobst, Nguyen, Thuy Trang, Romanos, Jasmin, Romanos, Marcel, Seitz, Christiane, Renner, Tobias J., Walitza, Susanne, Warnke, Andreas, Palmason, Haukur, Buitelaar, Jan, Rommelse, Nanda, Vasquez, Alejandro Arias, Hawi, Ziarih, Langley, Kate, Sergeant, Joseph, Steinhausen, Hans-Christoph, Roeyers, Herbert, Biederman, Joseph, Zaharieva, Irina, Hakonarson, Hakon, Elia, Josephine, Lionel, Anath C., Crosbie, Jennifer, Marshall, Christian R., Schachar, Russell, Scherer, Stephen W., Todorov, Alexandre, Smalley, Susan L., Loo, Sandra, Nelson, Stanley, Shtir, Corina, Asherson, Philip, Reif, Andreas, Lesch, Klaus-Peter, Faraone, Stephen V.
Published in The American journal of psychiatry (01.02.2012)
Published in The American journal of psychiatry (01.02.2012)
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Outcomes of hematopoietic cell transplantation using donors or recipients with inherited chromosomally integrated HHV-6
Hill, Joshua A., Magaret, Amalia S., Hall-Sedlak, Ruth, Mikhaylova, Anna, Huang, Meei-Li, Sandmaier, Brenda M., Hansen, John A., Jerome, Keith R., Zerr, Danielle M., Boeckh, Michael
Published in Blood (24.08.2017)
Published in Blood (24.08.2017)
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Investigating the Contribution of Common Genetic Variants to the Risk and Pathogenesis of ADHD
Stergiakouli, Evangelia, Hamshere, Marian, Holmans, Peter, Langley, Kate, Zaharieva, Irina, Hawi, Ziarah, Kent, Lindsey, Gill, Michael, Williams, Nigel, Owen, Michael J., O'Donovan, Michael, Thapar, Anita
Published in The American journal of psychiatry (01.02.2012)
Published in The American journal of psychiatry (01.02.2012)
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De Novo and Inherited Loss-of-Function Variants in TLK2: Clinical and Genotype-Phenotype Evaluation of a Distinct Neurodevelopmental Disorder
Reijnders, Margot R.F., Miller, Kerry A., Alvi, Mohsan, Goos, Jacqueline A.C., Lees, Melissa M., de Burca, Anna, Henderson, Alex, Kraus, Alison, Mikat, Barbara, de Vries, Bert B.A., Isidor, Bertrand, Kerr, Bronwyn, Marcelis, Carlo, Schluth-Bolard, Caroline, Deshpande, Charu, Ruivenkamp, Claudia A.L., Wieczorek, Dagmar, Baralle, Diana, Blair, Edward M., Engels, Hartmut, Lüdecke, Hermann-Josef, Eason, Jacqueline, Santen, Gijs W.E., Clayton-Smith, Jill, Chandler, Kate, Tatton-Brown, Katrina, Payne, Katelyn, Helbig, Katherine, Radtke, Kelly, Nugent, Kimberly M., Cremer, Kirsten, Strom, Tim M., Bird, Lynne M., Sinnema, Margje, Bitner-Glindzicz, Maria, van Dooren, Marieke F., Alders, Marielle, Koopmans, Marije, Brick, Lauren, Kozenko, Mariya, Harline, Megan L., Klaassens, Merel, Steinraths, Michelle, Cooper, Nicola S., Edery, Patrick, Yap, Patrick, Terhal, Paulien A., van der Spek, Peter J., Lakeman, Phillis, Taylor, Rachel L., Littlejohn, Rebecca O., Pfundt, Rolph, Mercimek-Andrews, Saadet, Stegmann, Alexander P.A., Kant, Sarina G., McLean, Scott, Joss, Shelagh, Swagemakers, Sigrid M.A., Douzgou, Sofia, Wall, Steven A., Küry, Sébastien, Calpena, Eduardo, Koelling, Nils, McGowan, Simon J., Twigg, Stephen R.F., Mathijssen, Irene M.J., Nellaker, Christoffer, Brunner, Han G., Wilkie, Andrew O.M.
Published in American journal of human genetics (07.06.2018)
Published in American journal of human genetics (07.06.2018)
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A new highly penetrant form of obesity due to deletions on chromosome 16p11.2
Walters, R. G., Jacquemont, S., Valsesia, A., de Smith, A. J., Martinet, D., Andersson, J., Falchi, M., Chen, F., Andrieux, J., Lobbens, S., Delobel, B., Stutzmann, F., El-Sayed Moustafa, J. S., Chèvre, J.-C., Lecoeur, C., Vatin, V., Bouquillon, S., Buxton, J. L., Boute, O., Holder-Espinasse, M., Cuisset, J.-M., Lemaitre, M.-P., Ambresin, A.-E., Brioschi, A., Gaillard, M., Giusti, V., Fellmann, F., Ferrarini, A., Hadjikhani, N., Campion, D., Guilmatre, A., Goldenberg, A., Calmels, N., Mandel, J.-L., Le Caignec, C., David, A., Isidor, B., Cordier, M.-P., Dupuis-Girod, S., Labalme, A., Sanlaville, D., Béri-Dexheimer, M., Jonveaux, P., Leheup, B., Õunap, K., Bochukova, E. G., Henning, E., Keogh, J., Ellis, R. J., MacDermot, K. D., van Haelst, M. M., Vincent-Delorme, C., Plessis, G., Touraine, R., Philippe, A., Malan, V., Mathieu-Dramard, M., Chiesa, J., Blaumeiser, B., Kooy, R. F., Caiazzo, R., Pigeyre, M., Balkau, B., Sladek, R., Bergmann, S., Mooser, V., Waterworth, D., Reymond, A., Vollenweider, P., Waeber, G., Kurg, A., Palta, P., Esko, T., Metspalu, A., Nelis, M., Elliott, P., Hartikainen, A.-L., McCarthy, M. I., Peltonen, L., Carlsson, L., Jacobson, P., Sjöström, L., Huang, N., Hurles, M. E., O’Rahilly, S., Farooqi, I. S., Männik, K., Jarvelin, M.-R., Pattou, F., Meyre, D., Walley, A. J., Coin, L. J. M., Blakemore, A. I. F., Froguel, P., Beckmann, J. S.
Published in Nature (London) (04.02.2010)
Published in Nature (London) (04.02.2010)
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Several common variants modulate heart rate, PR interval and QRS duration
Holm, Hilma, Gudbjartsson, Daniel F, Arnar, David O, Thorleifsson, Gudmar, Thorgeirsson, Gudmundur, Stefansdottir, Hrafnhildur, Gudjonsson, Sigurjon A, Jonasdottir, Aslaug, Mathiesen, Ellisiv B, Njølstad, Inger, Nyrnes, Audhild, Wilsgaard, Tom, Hald, Erin M, Hveem, Kristian, Stoltenberg, Camilla, Løchen, Maja-Lisa, Kong, Augustine, Thorsteinsdottir, Unnur, Stefansson, Kari
Published in Nature genetics (01.02.2010)
Published in Nature genetics (01.02.2010)
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Mitochondria, Cybrids, Aging, and Alzheimer's Disease
Swerdlow, R H, Koppel, S, Weidling, I, Hayley, C, Ji, Y, Wilkins, H M
Published in Progress in molecular biology and translational science (2017)
Published in Progress in molecular biology and translational science (2017)
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Comparison of host susceptibilities to native and exotic pathogens provides evidence for pathogen-imposed selection in forest trees
Freeman, Jules S., Hamilton, Matthew G., Lee, David J., Pegg, Geoff S., Brawner, Jeremy T., Tilyard, Paul A., Potts, Brad M.
Published in The New phytologist (01.03.2019)
Published in The New phytologist (01.03.2019)
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Transposons, environmental changes, and heritable induced phenotypic variability
Piacentini, Lucia, Fanti, Laura, Specchia, Valeria, Bozzetti, Maria Pia, Berloco, Maria, Palumbo, Gino, Pimpinelli, Sergio
Published in Chromosoma (01.08.2014)
Published in Chromosoma (01.08.2014)
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Patterns and Mechanisms of Ancestral Histone Protein Inheritance in Budding Yeast
Radman-Livaja, Marta, Verzijlbergen, Kitty F., Weiner, Assaf, van Welsem, Tibor, Friedman, Nir, Rando, Oliver J., van Leeuwen, Fred
Published in PLoS biology (01.06.2011)
Published in PLoS biology (01.06.2011)
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The Complex Genetic Architecture of the Metabolome
Chan, Eva K. F., Rowe, Heather C., Hansen, Bjarne G., Kliebenstein, Daniel J.
Published in PLoS genetics (01.11.2010)
Published in PLoS genetics (01.11.2010)
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A practical model for the identification of congenital cataracts using machine learning
Lin, Duoru, Chen, Jingjing, Lin, Zhuoling, Li, Xiaoyan, Zhang, Kai, Wu, Xiaohang, Liu, Zhenzhen, Huang, Jialing, Li, Jing, Zhu, Yi, Chen, Chuan, Zhao, Lanqin, Xiang, Yifan, Guo, Chong, Wang, Liming, Liu, Yizhi, Chen, Weirong, Lin, Haotian
Published in EBioMedicine (01.01.2020)
Published in EBioMedicine (01.01.2020)
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Genome-wide association study reveals greater polygenic loading for schizophrenia in cases with a family history of illness
Bigdeli, Tim B., Ripke, Stephan, Bacanu, Silviu-Alin, Lee, Sang Hong, Wray, Naomi R., Gejman, Pablo V., Rietschel, Marcella, Cichon, Sven, St Clair, David, Corvin, Aiden, Kirov, George, McQuillin, Andrew, Gurling, Hugh, Rujescu, Dan, Andreassen, Ole A., Werge, Thomas, Blackwood, Douglas H. R., Pato, Carlos N., Pato, Michele T., Malhotra, Anil K., O'Donovan, Michael C., Kendler, Kenneth S., Fanous, Ayman H.
Published in American journal of medical genetics. Part B, Neuropsychiatric genetics (01.03.2016)
Published in American journal of medical genetics. Part B, Neuropsychiatric genetics (01.03.2016)
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Evolution of Paget's disease of bone in adults inheriting SQSTM1 mutations
Cundy, Tim, Rutland, Michael D., Naot, Dorit, Bolland, Mark
Published in Clinical endocrinology (Oxford) (01.09.2015)
Published in Clinical endocrinology (Oxford) (01.09.2015)
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