Occipital lobe gray matter volume in male patients with chronic schizophrenia: A quantitative MRI study von Onitsuka, Toshiaki, McCarley, Robert W, Kuroki, Noriomi, Dickey, Chandlee C, Kubicki, Marek, Demeo, Susan S, Frumin, Melissa, Kikinis, Ron, Jolesz, Ferenc A, Shenton, Martha E

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Occipital Lobe Gray Matter Volume in Male Patients with Chronic Schizophrenia: A Quantitative MRI Study: Revision for Schizophrenia Research, Full-length Paper von Onitsuka, Toshiaki, McCarley, Robert W., Kuroki, Noriomi, Dickey, Chandlee C., Kubicki, Marek, Demeo, Susan S., Frumin, Melissa, Kikinis, Ron, Jolesz, Ferenc A., Shenton, Martha E.

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Occipital lobe gray matter volume in male patients with chronic schizophrenia: A quantitative MRI study von Onitsuka, Toshiaki, McCarley, Robert William, Kuroki, Noriomi, Dickey, Chandlee C, Kubicki, Marek R, Demeo, Susan S, Frumin, Melissa, Kikinis, Ron, Jolesz, Ferenc A, Shenton, Martha Elizabeth

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TBCRC 048: Phase II Study of Olaparib for Metastatic Breast Cancer and Mutations in Homologous Recombination-Related Genes von Tung, Nadine M, Robson, Mark E, Ventz, Steffen, Santa-Maria, Cesar A, Nanda, Rita, Marcom, Paul K, Shah, Payal D, Ballinger, Tarah J, Yang, Eddy S, Vinayak, Shaveta, Melisko, Michelle, Brufsky, Adam, DeMeo, Michelle, Jenkins, Colby, Domchek, Susan, D'Andrea, Alan, Lin, Nancy U, Hughes, Melissa E, Carey, Lisa A, Wagle, Nick, Wulf, Gerburg M, Krop, Ian E, Wolff, Antonio C, Winer, Eric P, Garber, Judy E

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Inherited causes of clonal haematopoiesis in 97,691 whole genomes von Weinstock, Joshua S., Nandakumar, Satish K., Bao, Erik L., Szeto, Mindy D., Liao, Xiaotian, Nasser, Joseph, Laurie, Cecelia, Burugula, Bala Bharathi, Gibson, Christopher J., Lin, Amy E., Aguet, Francois, Ardlie, Kristin, Mitchell, Braxton D., Barnes, Kathleen C., Moscati, Arden, Redline, Susan, Psaty, Bruce M., Silverman, Edwin K., Weiss, Scott T., Palmer, Nicholette D., Vasan, Ramachandran S., Burchard, Esteban G., He, Jiang, Kaplan, Robert C., Smith, Nicholas L., Arnett, Donna K., Schwartz, David A., Guo, Xiuqing, Konkle, Barbara A., Custer, Brian, Peralta, Juan M., Gui, Hongsheng, Meyers, Deborah A., McGarvey, Stephen T., Chen, Ida Yii-Der, Shoemaker, M. Benjamin, Peyser, Patricia A., Broome, Jai G., Wang, Fei Fei, North, Kari E., Launer, Lenore J., Cade, Brian E., Bis, Joshua C., Cho, Michael H., Lasky-Su, Jessica, Bowden, Donald W., Cupples, L. Adrienne, Mak, Angel C. Y., Smith, Jennifer A., Kelly, Tanika N., Aslibekyan, Stella, Heckbert, Susan R., Tiwari, Hemant K., Yang, Ivana V., Heit, John A., Johnsen, Jill M., Curran, Joanne E., Wenzel, Sally E., Rao, Dabeeru C., Darbar, Dawood, Moon, Jee-Young, Tracy, Russell P., Buth, Erin J., Rafaels, Nicholas, Loos, Ruth J. F., Liu, Yongmei, Hou, Lifang, Lee, Jiwon, Kachroo, Priyadarshini, Freedman, Barry I., Levy, Daniel, Bielak, Lawrence F., Hixson, James E., Floyd, James S., Whitsel, Eric A., Ellinor, Patrick T., Irvin, Marguerite R., Fingerlin, Tasha E., Armasu, Sebastian M., Wheeler, Marsha M., Blangero, John, Williams, L. Keoki, Levy, Bruce D., Sheu, Wayne Huey-Herng, Roden, Dan M., Taylor, Kent D., Johnson, Andrew D., Auer, Paul L., Kooperberg, Charles, Laurie, Cathy C., Blackwell, Thomas W., Smith, Albert V., Lange, Ethan, Rotter, Jerome I., Kitzman, Jacob O., Lander, Eric S., Ebert, Benjamin L., Reiner, Alexander P., Jaiswal, Siddhartha, Kathiresan, Sekar

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Meta-analysis of epigenome-wide association studies in newborns and children show widespread sex differences in blood DNA methylation von Solomon, Olivia, Huen, Karen, Yousefi, Paul, Küpers, Leanne K., González, Juan R., Suderman, Matthew, Reese, Sarah E., Page, Christian M., Gruzieva, Olena, Rzehak, Peter, Gao, Lu, Bakulski, Kelly M., Novoloaca, Alexei, Allard, Catherine, Pappa, Irene, Llambrich, Maria, Vives, Marta, Jima, Dereje D., Kvist, Tuomas, Baccarelli, Andrea, White, Cory, Rezwan, Faisal I., Sharp, Gemma C., Tindula, Gwen, Bergström, Anna, Grote, Veit, Dou, John F., Isaevska, Elena, Magnus, Maria C., Corpeleijn, Eva, Perron, Patrice, Jaddoe, Vincent W.V., Nohr, Ellen A., Maitre, Lea, Foraster, Maria, Hoyo, Cathrine, Håberg, Siri E., Lahti, Jari, DeMeo, Dawn L., Zhang, Hongmei, Karmaus, Wilfried, Kull, Inger, Koletzko, Berthold, Feinberg, Jason I., Gagliardi, Luigi, Bouchard, Luigi, Ramlau-Hansen, Cecilia Høst, Tiemeier, Henning, Santorelli, Gillian, Maguire, Rachel L., Czamara, Darina, Litonjua, Augusto A., Langhendries, Jean-Paul, Plusquin, Michelle, Lepeule, Johanna, Binder, Elisabeth B., Verduci, Elvira, Dwyer, Terence, Carracedo, Ángel, Ferre, Natalia, Eskenazi, Brenda, Kogevinas, Manolis, Nawrot, Tim S., Munthe-Kaas, Monica C., Herceg, Zdenko, Relton, Caroline, Melén, Erik, Gruszfeld, Dariusz, Breton, Carrie, Fallin, M.D., Ghantous, Akram, Nystad, Wenche, Heude, Barbara, Snieder, Harold, Hivert, Marie-France, Felix, Janine F., Sørensen, Thorkild I.A., Bustamante, Mariona, Murphy, Susan K., Raikkönen, Katri, Oken, Emily, Holloway, John W., Arshad, Syed Hasan, London, Stephanie J., Holland, Nina

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Evidence of circadian disruption in patients with eosinophilic esophagitis von Mirkarimi, Sadafsadat, Salahi, Navid, Fox, Susan R., Singh, Shubha, Demeo, Mark T., Mahdavinia, Mahboobeh, Tobin, Mary C.

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Alpha-1 Antitrypsin MZ Heterozygosity Is an Endotype of Chronic Obstructive Pulmonary Disease von Ghosh, Auyon J, Hobbs, Brian D, Moll, Matthew, Saferali, Aabida, Boueiz, Adel, Yun, Jeong H, Sciurba, Frank, Barwick, Lucas, Limper, Andrew H, Flaherty, Kevin, Criner, Gerard, Brown, Kevin K, Wise, Robert, Martinez, Fernando J, Lomas, David, Castaldi, Peter J, Carey, Vincent J, DeMeo, Dawn L, Cho, Michael H, Silverman, Edwin K, Hersh, Craig P

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Dynamic incorporation of multiple in silico functional annotations empowers rare variant association analysis of large whole-genome sequencing studies at scale von Li, Xihao, Li, Zilin, Zhou, Hufeng, Gaynor, Sheila M., Liu, Yaowu, Chen, Han, Sun, Ryan, Dey, Rounak, Arnett, Donna K., Aslibekyan, Stella, Ballantyne, Christie M., Bielak, Lawrence F., Blangero, John, Boerwinkle, Eric, Bowden, Donald W., Broome, Jai G., Conomos, Matthew P., Correa, Adolfo, Cupples, L. Adrienne, Curran, Joanne E., Freedman, Barry I., Guo, Xiuqing, Hindy, George, Irvin, Marguerite R., Kardia, Sharon L. R., Kathiresan, Sekar, Khan, Alyna T., Kooperberg, Charles L., Laurie, Cathy C., Liu, X. Shirley, Mahaney, Michael C., Manichaikul, Ani W., Martin, Lisa W., Mathias, Rasika A., McGarvey, Stephen T., Mitchell, Braxton D., Montasser, May E., Moore, Jill E., Morrison, Alanna C., O’Connell, Jeffrey R., Palmer, Nicholette D., Pampana, Akhil, Peralta, Juan M., Peyser, Patricia A., Psaty, Bruce M., Redline, Susan, Rice, Kenneth M., Rich, Stephen S., Smith, Jennifer A., Tiwari, Hemant K., Tsai, Michael Y., Vasan, Ramachandran S., Wang, Fei Fei, Weeks, Daniel E., Weng, Zhiping, Wilson, James G., Yanek, Lisa R., Neale, Benjamin M., Sunyaev, Shamil R., Abecasis, Gonçalo R., Rotter, Jerome I., Willer, Cristen J., Peloso, Gina M., Natarajan, Pradeep, Lin, Xihong

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In vitro evaluation of intestinal epithelial TLR activation in preventing food allergic responses von de Kivit, Sander, Tobin, Mary C, DeMeo, Mark T, Fox, Susan, Garssen, Johan, Forsyth, Christopher B, Keshavarzian, Ali, Landay, Alan L

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Determinants of mosaic chromosomal alteration fitness von Pershad, Yash, Mack, Taralynn, Poisner, Hannah, Jakubek, Yasminka A., Stilp, Adrienne M., Mitchell, Braxton D., Lewis, Joshua P., Boerwinkle, Eric, Loos, Ruth J. F., Chami, Nathalie, Wang, Zhe, Barnes, Kathleen, Pankratz, Nathan, Fornage, Myriam, Redline, Susan, Psaty, Bruce M., Bis, Joshua C., Shojaie, Ali, Silverman, Edwin K., Cho, Michael H., Yun, Jeong H., DeMeo, Dawn, Levy, Daniel, Johnson, Andrew D., Mathias, Rasika A., Taub, Margaret A., Arnett, Donna, North, Kari E., Raffield, Laura M., Carson, April P., Doyle, Margaret F., Rich, Stephen S., Rotter, Jerome I., Guo, Xiuqing, Cox, Nancy J., Roden, Dan M., Franceschini, Nora, Desai, Pinkal, Reiner, Alex P., Auer, Paul L., Scheet, Paul A., Jaiswal, Siddhartha, Weinstock, Joshua S., Bick, Alexander G.

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Longitudinal Phenotypes and Mortality in Preserved Ratio Impaired Spirometry in the COPDGene Study von Wan, Emily S, Fortis, Spyridon, Regan, Elizabeth A, Hokanson, John, Han, MeiLan K, Casaburi, Richard, Make, Barry J, Crapo, James D, DeMeo, Dawn L, Silverman, Edwin K

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Genomic and phenotypic correlates of mosaic loss of chromosome Y in blood von Jakubek, Yasminka A, Ma, Xiaolong, Stilp, Adrienne M, Yu, Fulong, Bacon, Jason, Wong, Justin W, Aguet, Francois, Ardlie, Kristin, Arnett, Donna K, Barnes, Kathleen, Bis, Joshua C, Blackwell, Tom, Becker, Lewis C, Boerwinkle, Eric, Bowler, Russell P, Budoff, Matthew J, Carson, April P, Chen, Jiawen, Cho, Michael H, Coresh, Josef, Cox, Nancy J, de Vries, Paul S, DeMeo, Dawn L, Fardo, David W, Fornage, Myriam, Guo, Xiuqing, Hall, Michael E, Heard-Costa, Nancy, Hidalgo, Bertha, Irvin, Marguerite Ryan, Johnson, Andrew D, Jorgenson, Eric, Kenny, Eimear E, Kessler, Michael D, Levy, Daniel, Li, Yun, Lima, Joao A C, Liu, Yongmei, Locke, Adam E, Loos, Ruth J F, Machiela, Mitchell J, Mathias, Rasika A, Mitchell, Braxton D, Murabito, Joanne M, Mychaleckyj, Josyf C, North, Kari E, Orchard, Peter, Parker, Stephen C J, Pershad, Yash, Peyser, Patricia A, Pratte, Katherine A, Psaty, Bruce M, Raffield, Laura M, Redline, Susan, Rich, Stephen S, Rotter, Jerome I, Shah, Sanjiv J, Smith, Jennifer A, Smith, Aaron P, Smith, Albert, Taub, Margaret A, Tiwari, Hemant K, Tracy, Russell, Tuftin, Bjoernar, Bick, Alexander G, Sankaran, Vijay G, Reiner, Alexander P, Scheet, Paul, Auer, Paul L

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A high-resolution HLA reference panel capturing global population diversity enables multi-ancestry fine-mapping in HIV host response von Luo, Yang, Kanai, Masahiro, Choi, Wanson, Li, Xinyi, Sakaue, Saori, Yamamoto, Kenichi, Ogawa, Kotaro, Gutierrez-Arcelus, Maria, Gregersen, Peter K., Stuart, Philip E., Elder, James T., Forer, Lukas, Schönherr, Sebastian, Fuchsberger, Christian, Smith, Albert V., Fellay, Jacques, Carrington, Mary, Haas, David W., Guo, Xiuqing, Palmer, Nicholette D., Chen, Yii-Der Ida, Rotter, Jerome I., Taylor, Kent D., Rich, Stephen S., Correa, Adolfo, Wilson, James G., Kathiresan, Sekar, Cho, Michael H., Metspalu, Andres, Esko, Tonu, Okada, Yukinori, Han, Buhm, McLaren, Paul J., Raychaudhuri, Soumya

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Deep-coverage whole genome sequences and blood lipids among 16,324 individuals von Natarajan, Pradeep, Peloso, Gina M., Zekavat, Seyedeh Maryam, Montasser, May, Ganna, Andrea, Chaffin, Mark, Khera, Amit V., Zhou, Wei, Bloom, Jonathan M., Engreitz, Jesse M., Ernst, Jason, O’Connell, Jeffrey R., Ruotsalainen, Sanni E., Alver, Maris, Manichaikul, Ani, Johnson, W. Craig, Perry, James A., Poterba, Timothy, Seed, Cotton, Surakka, Ida L., Esko, Tonu, Ripatti, Samuli, Salomaa, Veikko, Correa, Adolfo, Vasan, Ramachandran S., Kellis, Manolis, Neale, Benjamin M., Lander, Eric S., Abecasis, Goncalo, Mitchell, Braxton, Rich, Stephen S., Wilson, James G., Cupples, L. Adrienne, Rotter, Jerome I., Willer, Cristen J., Kathiresan, Sekar

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A framework for detecting noncoding rare-variant associations of large-scale whole-genome sequencing studies von Li, Zilin, Li, Xihao, Zhou, Hufeng, Gaynor, Sheila M., Selvaraj, Margaret Sunitha, Arapoglou, Theodore, Quick, Corbin, Liu, Yaowu, Chen, Han, Sun, Ryan, Dey, Rounak, Arnett, Donna K., Auer, Paul L., Bielak, Lawrence F., Bis, Joshua C., Blackwell, Thomas W., Blangero, John, Boerwinkle, Eric, Bowden, Donald W., Brody, Jennifer A., Cade, Brian E., Conomos, Matthew P., Correa, Adolfo, Cupples, L. Adrienne, Curran, Joanne E., de Vries, Paul S., Duggirala, Ravindranath, Franceschini, Nora, Freedman, Barry I., Göring, Harald H. H., Guo, Xiuqing, Kalyani, Rita R., Kooperberg, Charles, Kral, Brian G., Lange, Leslie A., Lin, Bridget M., Manichaikul, Ani, Manning, Alisa K., Martin, Lisa W., Mathias, Rasika A., Meigs, James B., Mitchell, Braxton D., Montasser, May E., Morrison, Alanna C., Naseri, Take, O’Connell, Jeffrey R., Palmer, Nicholette D., Peyser, Patricia A., Psaty, Bruce M., Raffield, Laura M., Redline, Susan, Reiner, Alexander P., Reupena, Muagututi’a Sefuiva, Rice, Kenneth M., Rich, Stephen S., Smith, Jennifer A., Taylor, Kent D., Taub, Margaret A., Vasan, Ramachandran S., Weeks, Daniel E., Wilson, James G., Yanek, Lisa R., Zhao, Wei, Rotter, Jerome I., Willer, Cristen J., Natarajan, Pradeep, Peloso, Gina M., Lin, Xihong

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Aberrant activation of TCL1A promotes stem cell expansion in clonal haematopoiesis von Weinstock, Joshua S., Gopakumar, Jayakrishnan, Burugula, Bala Bharathi, Jahn, Nikolaus, Belk, Julia A., Bouzid, Hind, Daniel, Bence, Miao, Zhuang, Ly, Nghi, Mack, Taralynn M., Luna, Sofia E., Prothro, Katherine P., Mitchell, Shaneice R., Laurie, Cecelia A., Broome, Jai G., Taylor, Kent D., Guo, Xiuqing, Sinner, Moritz F., von Falkenhausen, Aenne S., Shuldiner, Alan R., O’Connell, Jeffrey R., Lewis, Joshua P., Boerwinkle, Eric, Chami, Nathalie, Kenny, Eimear E., Loos, Ruth J. F., Fornage, Myriam, Hou, Lifang, Lloyd-Jones, Donald M., Redline, Susan, Cade, Brian E., Psaty, Bruce M., Bis, Joshua C., Brody, Jennifer A., Yun, Jeong H., Qiao, Dandi, Palmer, Nicholette D., Freedman, Barry I., Bowden, Donald W., Cho, Michael H., Vasan, Ramachandran S., Yanek, Lisa R., Becker, Lewis C., Kardia, Sharon L. R., Peyser, Patricia A., He, Jiang, Rienstra, Michiel, Van der Harst, Pim, Kaplan, Robert, Heckbert, Susan R., Smith, Nicholas L., Wiggins, Kerri L., Arnett, Donna K., Irvin, Marguerite R., Tiwari, Hemant, Cutler, Michael J., Knight, Stacey, Muhlestein, J. Brent, Correa, Adolfo, Raffield, Laura M., Gao, Yan, de Andrade, Mariza, Rotter, Jerome I., Rich, Stephen S., Konkle, Barbara A., Johnsen, Jill M., Wheeler, Marsha M., Smith, J. Gustav, Melander, Olle, Nilsson, Peter M., Custer, Brian S., Duggirala, Ravindranath, Curran, Joanne E., Blangero, John, Xiao, Shujie, Yang, Mao, Gu, C. Charles, Chen, Yii-Der Ida, Lee, Wen-Jane, Marcus, Gregory M., Kane, John P., Pullinger, Clive R., Shoemaker, M. Benjamin, Darbar, Dawood, Roden, Dan M., Kooperberg, Charles, Zhou, Ying, Manson, JoAnn E., Desai, Pinkal, Johnson, Andrew D., Mathias, Rasika A., Abecasis, Goncalo R., Kang, Hyun M., Satpathy, Ansuman T., Natarajan, Pradeep, Kitzman, Jacob O., Whitsel, Eric A., Reiner, Alexander P., Bick, Alexander G., Jaiswal, Siddhartha

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Association of Mitochondrial DNA Copy Number With Brain MRI Markers and Cognitive Function: A Meta-analysis of Community-Based Cohorts von Zhang, Yuankai, Liu, Xue, Wiggins, Kerri L., Kurniansyah, Nuzulul, Guo, Xiuqing, Rodrigue, Amanda L, Zhao, Wei, Yanek, Lisa R, Ratliff, Scott M., Pitsillides, Achilleas, Aguirre Patiño, Juan Sebastian, Sofer, Tamar, Arking, Dan E., Austin, Thomas R., Beiser, Alexa S., Blangero, John, Boerwinkle, Eric, Bressler, Jan, Curran, Joanne E., Hou, Lifang, Hughes, Timothy M., Kardia, Sharon L, Launer, Lenore, Levy, Daniel, Mosley, Tom H., Nasrallah, Ilya M., Rich, Stephen S., Rotter, Jerome I., Seshadri, Sudha, Tarraf, Wassim, González, Kevin A., Ramachandran, Vasan, Yaffe, Kristine, Nyquist, Paul A, Psaty, Bruce M, DeCarli, Charles S., Smith, Jennifer A, Glahn, David C, González, Hector M, Bis, Joshua C, Fornage, Myriam, Heckbert, Susan R., Fitzpatrick, Annette L., Liu, Chunyu, Satizabal, Claudia L.

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Disease Progression Modeling in Chronic Obstructive Pulmonary Disease von Young, Alexandra L, Bragman, Felix J S, Rangelov, Bojidar, Han, MeiLan K, Galbán, Craig J, Lynch, David A, Hawkes, David J, Alexander, Daniel C, Hurst, John R

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Observational investigation of the 2013 near-Earth encounter by asteroid (367943) Duende von Moskovitz, Nicholas A., Benson, Conor James, Scheeres, Daniel, Endicott, Thomas, Polishook, David, Binzel, Richard, DeMeo, Francesca, Ryan, William, Ryan, Eileen, Willman, Mark, Hergenrother, Carl, Verveer, Arie, Lister, Tim, Birtwhistle, Peter, Sickafoose, Amanda, Nagayama, Takahiro, Gilmore, Alan, Kilmartin, Pam, Benecchi, Susan, Sheppard, Scott, Marchis, Franck, Augusteijn, Thomas, Smirnova, Olesja

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