Increased burden of ultra-rare structural variants localizing to boundaries of topologically associated domains in schizophrenia von Halvorsen, Matthew, Huh, Ruth, Oskolkov, Nikolay, Wen, Jia, Netotea, Sergiu, Giusti-Rodriguez, Paola, Karlsson, Robert, Bryois, Julien, Nystedt, Björn, Ameur, Adam, Kähler, Anna K., Ancalade, NaEshia, Farrell, Martilias, Crowley, James J., Li, Yun, Magnusson, Patrik K. E., Gyllensten, Ulf, Hultman, Christina M., Sullivan, Patrick F., Szatkiewicz, Jin P.

Volltext

Characterization of Single Gene Copy Number Variants in Schizophrenia von Szatkiewicz, Jin P., Fromer, Menachem, Nonneman, Randal J., Ancalade, NaEshia, Johnson, Jessica S., Stahl, Eli A., Rees, Elliott, Bergen, Sarah E., Hultman, Christina M., Kirov, George, O’Donovan, Michael, Owen, Michael, Holmans, Peter, Sklar, Pamela, Sullivan, Patrick F., Purcell, Shaun M., Crowley, James J., Ruderfer, Douglas M.

Volltext

Association test using Copy Number Profile Curves (CONCUR) enhances power in rare copy number variant analysis von Brucker, Amanda, Lu, Wenbin, Marceau West, Rachel, Yu, Qi-You, Hsiao, Chuhsing Kate, Hsiao, Tzu-Hung, Lin, Ching-Heng, Magnusson, Patrik K E, Sullivan, Patrick F, Szatkiewicz, Jin P, Lu, Tzu-Pin, Tzeng, Jung-Ying

Volltext

Author Correction: Increased burden of ultra-rare structural variants localizing to boundaries of topologically associated domains in schizophrenia von Halvorsen, Matthew, Huh, Ruth, Oskolkov, Nikolay, Wen, Jia, Netotea, Sergiu, Giusti-Rodriguez, Paola, Karlsson, Robert, Bryois, Julien, Nystedt, Björn, Ameur, Adam, Kähler, Anna K., Ancalade, NaEshia, Farrell, Martilias, Crowley, James J., Li, Yun, Magnusson, Patrik K. E., Gyllensten, Ulf, Hultman, Christina M., Sullivan, Patrick F., Szatkiewicz, Jin P.

Volltext

The recombinational anatomy of a mouse chromosome von Paigen, Kenneth, Szatkiewicz, Jin P, Sawyer, Kathryn, Leahy, Nicole, Parvanov, Emil D, Ng, Siemon H S, Graber, Joel H, Broman, Karl W, Petkov, Petko M

Volltext

A New Method for Detecting Associations with Rare Copy-Number Variants von Tzeng, Jung-Ying, Magnusson, Patrik K E, Sullivan, Patrick F, Szatkiewicz, Jin P

Volltext

Genome-wide association study identifies eight risk loci and implicates metabo-psychiatric origins for anorexia nervosa von Hübel, Christopher, Bryois, Julien, Hinney, Anke, Leppä, Virpi M., Mattheisen, Manuel, Medland, Sarah E., Giusti-Rodríguez, Paola, Alfredsson, Lars, Berrettini, Wade H., Boni, Claudette, Burghardt, Roland, Cichon, Sven, Cone, Roger D., Courtet, Philippe, Crowley, James J., Davis, Oliver S. P., de Zwaan, Martina, Dikeos, Dimitris, Dina, Christian, Duncan, Laramie E., Egberts, Karin, Estivill, Xavier, Favaro, Angela, Fernández-Aranda, Fernando, Fichter, Manfred M., Forstner, Andreas J., Forzan, Monica, Franklin, Christopher S., Giegling, Ina, Guillaume, Sébastien, Hakonarson, Hakon, Hatzikotoulas, Konstantinos, Hauser, Joanna, Helder, Sietske G., Herpertz-Dahlmann, Beate, Herzog, Wolfgang, Huckins, Laura M., Hudson, James I., Inoko, Hidetoshi, Janout, Vladimir, Julià, Antonio, Kalsi, Gursharan, Kaminská, Deborah, Karhunen, Leila, Keski-Rahkonen, Anna, Kim, Youl-Ri, Knudsen, Gun Peggy S., La Via, Maria C., Levitan, Robert D., Lin, Bochao Danae, Luykx, Jurjen, Marsal, Sara, Marshall, Christian R., McDevitt, Sara, McGuffin, Peter, Metspalu, Andres, Monteleone, Alessio Maria, Monteleone, Palmiero, Munn-Chernoff, Melissa A., Navratilova, Marie, O’Toole, Julie K., Palotie, Aarno, Raevuori, Anu, Ramoz, Nicolas, Reichborn-Kjennerud, Ted, Ritschel, Franziska, Roberts, Marion, Rotondo, Alessandro, Rujescu, Dan, Rybakowski, Filip, Santonastaso, Paolo, Scherer, Stephen W., Schmidt, Ulrike, Schosser, Alexandra, Slagboom, P. Eline, Sorbi, Sandro, Szatkiewicz, Jin P., Tenconi, Elena, Tortorella, Alfonso, Treasure, Janet, Tziouvas, Konstantinos, van Elburg, Annemarie A., van Furth, Eric F., Zipfel, Stephan, Bergen, Andrew W., Boden, Joseph M., Johnson, Craig, Kaye, Walter H., Mitchell, James E., Olsen, Catherine M., Woodside, D. Blake, Stuber, Garret D., Gordon, Scott, Henders, Anjali K., Juréus, Anders, Petersen, Liselotte, Wade, Tracey D., Landén, Mikael, Sullivan, Patrick F., Breen, Gerome

Volltext

The impact of educational attainment, intelligence and intellectual disability on schizophrenia: a Swedish population-based register and genetic study von Song, Jie, Yao, Shuyang, Kowalec, Kaarina, Lu, Yi, Sariaslan, Amir, Szatkiewicz, Jin P., Larsson, Henrik, Lichtenstein, Paul, Hultman, Christina M., Sullivan, Patrick F.

Volltext

Patterns of recombination activity on mouse chromosome 11 revealed by high resolution mapping von Billings, Timothy, Sargent, Evelyn E, Szatkiewicz, Jin P, Leahy, Nicole, Kwak, Il-Youp, Bektassova, Nazira, Walker, Michael, Hassold, Terry, Graber, Joel H, Broman, Karl W, Petkov, Petko M

Volltext

Otitis media: a genome-wide linkage scan with evidence of susceptibility loci within the 17q12 and 10q22.3 regions von Casselbrant, Margaretha L, Mandel, Ellen M, Jung, Jeesun, Ferrell, Robert E, Tekely, Kathleen, Szatkiewicz, Jin P, Ray, Amrita, Weeks, Daniel E

Volltext

Clozapine-induced agranulocytosis is associated with rare HLA-DQB1 and HLA-B alleles von Goldstein, Jacqueline I., Fredrik Jarskog, L., Hilliard, Chris, Alfirevic, Ana, Duncan, Laramie, Fourches, Denis, Huang, Hailiang, Lek, Monkol, Neale, Benjamin M., Ripke, Stephan, Shianna, Kevin, Szatkiewicz, Jin P., Tropsha, Alexander, van den Oord, Edwin JCG, Cascorbi, Ingolf, Dettling, Michael, Gazit, Ephraim, Goff, Donald C., Holden, Arthur L., Kelly, Deanna L., Malhotra, Anil K., Nielsen, Jimmi, Pirmohamed, Munir, Rujescu, Dan, Werge, Thomas, Levy, Deborah L., Josiassen, Richard C., Kennedy, James L., Lieberman, Jeffrey A., Daly, Mark J., Sullivan, Patrick F.

Volltext

survey of airway responsiveness in 36 inbred mouse strains facilitates gene mapping studies and identification of quantitative trait loci von Leme, Adriana S, Berndt, Annerose, Williams, Laura K, Tsaih, Shirng-Wern, Szatkiewicz, Jin P, Verdugo, Ricardo, Paigen, Beverly, Shapiro, Steven D

Volltext

Improving detection of copy-number variation by simultaneous bias correction and read-depth segmentation von Szatkiewicz, Jin P, Wang, WeiBo, Sullivan, Patrick F, Wang, Wei, Sun, Wei

Volltext

Rare tandem repeat expansions associate with genes involved in synaptic and neuronal signaling functions in schizophrenia von Wen, Jia, Trost, Brett, Engchuan, Worrawat, Halvorsen, Matthew, Pallotto, Linda M., Mitina, Aleksandra, Ancalade, NaEshia, Farrell, Martilias, Backstrom, Ian, Guo, Keyi, Pellecchia, Giovanna, Thiruvahindrapuram, Bhooma, Giusti-Rodriguez, Paola, Rosen, Jonathan David, Li, Yun, Won, Hyejung, Magnusson, Patrik K. E., Gyllensten, Ulf, Bassett, Anne S., Hultman, Christina M., Sullivan, Patrick F., Yuen, Ryan K. C., Szatkiewicz, Jin P.

Volltext

Genome-wide copy number variation association study in anorexia nervosa von Walker, Alicia, Karlsson, Robert, Szatkiewicz, Jin P, Thornton, Laura M, Yilmaz, Zeynep, Leppä, Virpi M, Savva, Androula, Lin, Tian, Sidorenko, Julia, McRae, Allan, Kirov, George, Davies, Helena L, Fundín, Bengt T, Chawner, Samuel J R A, Song, Jie, Borg, Stina, Wen, Jia, Watson, Hunna J, Munn-Chernoff, Melissa A, Baker, Jessica H, Gordon, Scott, Berrettini, Wade H, Brandt, Harry, Crawford, Steven, Halmi, Katherine A, Kaplan, Allan S, Kaye, Walter H, Mitchell, James, Strober, Michael, Woodside, D Blake, Pedersen, Nancy L, Parker, Richard, Jordan, Jennifer, Kennedy, Martin A, Birgegård, Andreas, Landén, Mikael, Martin, Nicholas G, Sullivan, Patrick F, Bulik, Cynthia M, Wray, Naomi R

Volltext

Allele-specific copy-number discovery from whole-genome and whole-exome sequencing von Wang, WeiBo, Wang, Wei, Sun, Wei, Crowley, James J, Szatkiewicz, Jin P

Volltext

Crossover interference underlies sex differences in recombination rates von Petkov, Petko M, Broman, Karl W, Szatkiewicz, Jin P, Paigen, Kenneth

Volltext

Defective carbohydrate metabolism in mice homozygous for the tubby mutation von Wang, Yun, Seburn, Kevin, Bechtel, Lawrence, Lee, Bruce Y, Szatkiewicz, Jin P, Nishina, Patsy M, Naggert, Jurgen K

Volltext

Endogenous Retinoids in the Pathogenesis of Alopecia Areata von Duncan, F. Jason, Silva, Kathleen A., Johnson, Charles J., King, Benjamin L., Szatkiewicz, Jin P., Kamdar, Sonya P., Ong, David E., Napoli, Joseph L., Wang, Jinshan, King, Lloyd E., Whiting, David A., McElwee, Kevin J., Sundberg, John P., Everts, Helen B.

Volltext

Exploration of large, rare copy number variants associated with psychiatric and neurodevelopmental disorders in individuals with anorexia nervosa von Yilmaz, Zeynep, Szatkiewicz, Jin P, Crowley, James J, Ancalade, NaEshia, Brandys, Marek K, van Elburg, Annemarie, de Kovel, Carolien G.F, Adan, Roger A.H, Hinney, Anke, Hebebrand, Johannes, Gratacos, Monica, Fernandez-Aranda, Fernando, Escaramis, Georgia, Gonzalez, Juan R, Estivill, Xavier, Zeggini, Eleftheria, Sullivan, Patrick F, Bulik, Cynthia M

Volltext