Genetic context drives age‐related disparities in synaptic maintenance and structure across cortical and hippocampal neuronal circuits von Heuer, Sarah E., Nickerson, Emily W., Howell, Gareth R., Bloss, Erik B.

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Targeted capture and massively parallel sequencing of 12 human exomes von Ng, Sarah B, Shendure, Jay, Turner, Emily H, Robertson, Peggy D, Flygare, Steven D, Bigham, Abigail W, Lee, Choli, Shaffer, Tristan, Wong, Michelle, Bhattacharjee, Arindam, Eichler, Evan E, Bamshad, Michael, Nickerson, Deborah A

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Whole-exome capture and sequencing identifies HEATR2 mutation as a cause of primary ciliary dyskinesia von Horani, Amjad, Druley, Todd E, Zariwala, Maimoona A, Patel, Anand C, Levinson, Benjamin T, Van Arendonk, Laura G, Thornton, Katherine C, Giacalone, Joe C, Albee, Alison J, Wilson, Kate S, Turner, Emily H, Nickerson, Deborah A, Shendure, Jay, Bayly, Philip V, Leigh, Margaret W, Knowles, Michael R, Brody, Steven L, Dutcher, Susan K, Ferkol, Thomas W

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Exome Sequencing Identifies Mutations in CCDC114 as a Cause of Primary Ciliary Dyskinesia von Knowles, Michael R., Leigh, Margaret W., Ostrowski, Lawrence E., Huang, Lu, Carson, Johnny L., Hazucha, Milan J., Yin, Weining, Berg, Jonathan S., Davis, Stephanie D., Dell, Sharon D., Ferkol, Thomas W., Rosenfeld, Margaret, Sagel, Scott D., Milla, Carlos E., Olivier, Kenneth N., Turner, Emily H., Lewis, Alexandra P., Bamshad, Michael J., Nickerson, Deborah A., Shendure, Jay, Zariwala, Maimoona A.

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Mutations in SPAG1 Cause Primary Ciliary Dyskinesia Associated with Defective Outer and Inner Dynein Arms von Knowles, Michael R., Ostrowski, Lawrence E., Loges, Niki T., Hurd, Toby, Leigh, Margaret W., Huang, Lu, Wolf, Whitney E., Carson, Johnny L., Hazucha, Milan J., Yin, Weining, Davis, Stephanie D., Dell, Sharon D., Ferkol, Thomas W., Sagel, Scott D., Olivier, Kenneth N., Jahnke, Charlotte, Olbrich, Heike, Werner, Claudius, Raidt, Johanna, Wallmeier, Julia, Pennekamp, Petra, Dougherty, Gerard W., Hjeij, Rim, Gee, Heon Yung, Otto, Edgar A., Halbritter, Jan, Chaki, Moumita, Diaz, Katrina A., Braun, Daniela A., Porath, Jonathan D., Schueler, Markus, Baktai, György, Griese, Matthias, Turner, Emily H., Lewis, Alexandra P., Bamshad, Michael J., Nickerson, Deborah A., Hildebrandt, Friedhelm, Shendure, Jay, Omran, Heymut, Zariwala, Maimoona A.

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Exome sequencing identifies MLL2 mutations as a cause of Kabuki syndrome von Bamshad, Michael J, Shendure, Jay, Ng, Sarah B, Bigham, Abigail W, Buckingham, Kati J, Hannibal, Mark C, McMillin, Margaret J, Gildersleeve, Heidi I, Beck, Anita E, Tabor, Holly K, Cooper, Gregory M, Mefford, Heather C, Lee, Choli, Turner, Emily H, Smith, Joshua D, Rieder, Mark J, Yoshiura, Koh-ichiro, Matsumoto, Naomichi, Ohta, Tohru, Niikawa, Norio, Nickerson, Deborah A

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Effect of vitamin D supplementation on Mycobacterium tuberculosis-induced innate immune responses in a Canadian Dené First Nations cohort von Larcombe, Linda, Orr, Pamela, Turner-Brannen, Emily, Slivinski, Caroline R, Nickerson, Peter W, Mookherjee, Neeloffer

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Assessing the contribution of rare variants to complex trait heritability from whole-genome sequence data von Wainschtein, Pierrick, Jain, Deepti, Zheng, Zhili, Cupples, L. Adrienne, Shadyab, Aladdin H., McKnight, Barbara, Shoemaker, Benjamin M., Mitchell, Braxton D., Psaty, Bruce M., Kooperberg, Charles, Liu, Ching-Ti, Albert, Christine M., Roden, Dan, Chasman, Daniel I., Darbar, Dawood, Lloyd-Jones, Donald M., Arnett, Donna K., Regan, Elizabeth A., Boerwinkle, Eric, Rotter, Jerome I., O’Connell, Jeffrey R., Yanek, Lisa R., de Andrade, Mariza, Allison, Matthew A., McDonald, Merry-Lynn N., Chung, Mina K., Fornage, Myriam, Chami, Nathalie, Smith, Nicholas L., Ellinor, Patrick T., Vasan, Ramachandran S., Mathias, Rasika A., Loos, Ruth J. F., Rich, Stephen S., Lubitz, Steven A., Heckbert, Susan R., Redline, Susan, Guo, Xiuqing, Chen, Y. -D Ida, Laurie, Cecelia A., Hernandez, Ryan D., McGarvey, Stephen T., Goddard, Michael E., Laurie, Cathy C., North, Kari E., Lange, Leslie A., Weir, Bruce S., Yengo, Loic, Yang, Jian, Visscher, Peter M.

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Serum Urate Lowering with Allopurinol and Kidney Function in Type 1 Diabetes von Doria, Alessandro, Galecki, Andrzej T, Spino, Cathie, Pop-Busui, Rodica, Cherney, David Z, Lingvay, Ildiko, Parsa, Afshin, Rossing, Peter, Sigal, Ronald J, Afkarian, Maryam, Aronson, Ronnie, Caramori, M. Luiza, Crandall, Jill P, de Boer, Ian H, Elliott, Thomas G, Goldfine, Allison B, Haw, J. Sonya, Hirsch, Irl B, Karger, Amy B, Maahs, David M, McGill, Janet B, Molitch, Mark E, Perkins, Bruce A, Polsky, Sarit, Pragnell, Marlon, Robiner, William N, Rosas, Sylvia E, Senior, Peter, Tuttle, Katherine R, Umpierrez, Guillermo E, Wallia, Amisha, Weinstock, Ruth S, Wu, Chunyi, Mauer, Michael

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Effect of Sickle Cell Trait and APOL1 Genotype on the Association of Soluble uPAR with Kidney Function Measures in Black Americans von Reiner, Alexander P, Raffield, Laura M, Franceschini, Nora, Auer, Paul L, Lange, Ethan M, Nickerson, Deborah A, Zakai, Neil A, Correa, Adolfo, Olson, Nels

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Three-dimensional organotypic models of human colonic epithelium to study the early stages of enteric salmonellosis von Höner zu Bentrup, Kerstin, Ramamurthy, Rajee, Ott, C. Mark, Emami, Kamal, Nelman-Gonzalez, Mayra, Wilson, James W., Richter, Emily G., Goodwin, Thomas J., Alexander, J. Stephen, Pierson, Duane L., Pellis, Neal, Buchanan, Kent L., Nickerson, Cheryl A.

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SARS-CoV-2 Epidemiology on a Public University Campus in Washington State von Weil, Ana A, Sohlberg, Sarah L, O’Hanlon, Jessica A, Casto, Amanda M, Emanuels, Anne W, Lo, Natalie K, Greismer, Emily P, Magedson, Ariana M, Wilcox, Naomi C, Kim, Ashley E, Back, Lewis, Frazar, Christian D, Pelle, Ben, Sibley, Thomas R, Ilcisin, Misja, Lee, Jover, Ryke, Erica L, Craft, J Chris, Schwabe-Fry, Kristen M, Fay, Kairsten A, Cho, Shari, Han, Peter D, Heidl, Sarah J, Pfau, Brian A, Truong, Melissa, Zhong, Weizhi, Srivatsan, Sanjay R, Harb, Katia F, Gottlieb, Geoffrey S, Hughes, James P, Nickerson, Deborah A, Lockwood, Christina M, Starita, Lea M, Bedford, Trevor, Shendure, Jay A, Chu, Helen Y

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AMPD2 Regulates GTP Synthesis and Is Mutated in a Potentially Treatable Neurodegenerative Brainstem Disorder von Akizu, Naiara, Cantagrel, Vincent, Schroth, Jana, Cai, Na, Vaux, Keith, McCloskey, Douglas, Naviaux, Robert K., Van Vleet, Jeremy, Fenstermaker, Ali G., Silhavy, Jennifer L., Scheliga, Judith S., Toyama, Keiko, Morisaki, Hiroko, Sonmez, Fatma M., Celep, Figen, Oraby, Azza, Zaki, Maha S., Al-Baradie, Raidah, Faqeih, Eissa A., Saleh, Mohammed A.M., Spencer, Emily, Rosti, Rasim Ozgur, Scott, Eric, Nickerson, Elizabeth, Gabriel, Stacey, Morisaki, Takayuki, Holmes, Edward W., Gleeson, Joseph G.

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Enrichment of colorectal cancer associations in functional regions: Insight for using epigenomics data in the analysis of whole genome sequence-imputed GWAS data von Bien, Stephanie A, Auer, Paul L, Harrison, Tabitha A, Qu, Conghui, Connolly, Charles M, Greenside, Peyton G, Chen, Sai, Berndt, Sonja I, Bézieau, Stéphane, Kang, Hyun M, Huyghe, Jeroen, Brenner, Hermann, Casey, Graham, Chan, Andrew T, Hopper, John L, Banbury, Barbara L, Chang-Claude, Jenny, Chanock, Stephen J, Haile, Robert W, Hoffmeister, Michael, Fuchsberger, Christian, Jenkins, Mark A, Leal, Suzanne M, Lemire, Mathieu, Newcomb, Polly A, Gallinger, Steven, Potter, John D, Schoen, Robert E, Slattery, Martha L, Smith, Joshua D, Le Marchand, Loic, White, Emily, Zanke, Brent W, Abeçasis, Goncalo R, Carlson, Christopher S, Peters, Ulrike, Nickerson, Deborah A, Kundaje, Anshul, Hsu, Li

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Fine-Mapping of Common Genetic Variants Associated with Colorectal Tumor Risk Identified Potential Functional Variants von Du, Mengmeng, Jiao, Shuo, Bien, Stephanie A, Gala, Manish, Abecasis, Goncalo, Bezieau, Stephane, Brenner, Hermann, Butterbach, Katja, Caan, Bette J, Carlson, Christopher S, Casey, Graham, Chang-Claude, Jenny, Conti, David V, Curtis, Keith R, Duggan, David, Gallinger, Steven, Haile, Robert W, Harrison, Tabitha A, Hayes, Richard B, Hoffmeister, Michael, Hopper, John L, Hudson, Thomas J, Jenkins, Mark A, Küry, Sébastien, Le Marchand, Loic, Leal, Suzanne M, Newcomb, Polly A, Nickerson, Deborah A, Potter, John D, Schoen, Robert E, Schumacher, Fredrick R, Seminara, Daniela, Slattery, Martha L, Hsu, Li, Chan, Andrew T, White, Emily, Berndt, Sonja I, Peters, Ulrike

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Whole-Exome Capture and Sequencing Identifies HEATR2 Mutation as a Cause of Primary Ciliary Dyskinesia von HORANI, Amjad, DRULEY, Todd E, TURNER, Emily H, NICKERSON, Deborah A, SHENDURE, Jay, BAYLY, Philip V, LEIGH, Margaret W, KNOWLES, Michael R, BRODY, Steven L, DUTCHER, Susan K, FERKOL, Thomas W, ZARIWALA, Maimoona A, PATEL, Anand C, LEVINSON, Benjamin T, VAN ARENDONK, Laura G, THORNTON, Katherine C, GIACALONE, Joe C, ALBEE, Alison J, WILSON, Kate S

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Targeted Capture and Massively Parallel Sequencing of Twelve Human Exomes von Ng, Sarah B., Turner, Emily H., Robertson, Peggy D., Flygare, Steven D., Bigham, Abigail W., Lee, Choli, Shaffer, Tristan, Wong, Michelle, Bhattacharjee, Arindam, Eichler, Evan E., Bamshad, Michael, Nickerson, Deborah A., Shendure, Jay

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An association study of angiotensinogen polymorphisms with serum level and hypertension in an African-American population. Commentary von XIAODONG WU, LUKE, Amy, MACCIARDI, Fabio, BARLASSINA, Cristina, RIEDER, Mark, LEE, Kwok, TOTH, Emily J, NICKERSON, Deborah, XIAOFENG ZHU, DONGHUI KAN, COOPER, Richard S, CUSI, Daniele

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The science of voter mobilization von Green, Donald P, Gerber, Alan S, Nickerson, David W, Cardy, Emily Arthur, McNulty, John E, Ramírez, Ricardo, Michelson, Melissa R, Wong, Janelle S, Trivedi, Neema, Bennion, Elizabeth A, Mann, Christopher B, Arceneaux, Kevin, Levine, Peter, Lopez, Mark Hugo

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Enrichment of colorectal cancer associations in functional regions: Insight for using epigenomics data in the analysis of whole genome sequence-imputed GWAS data von Bien, Stephanie A, Auer, Paul L, Harrison, Tabitha A, Qu, Conghui, Connolly, Charles M, Greenside, Peyton G, Chen, Sai, Berndt, Sonja I, Bézieau, Stéphane, Kang, Hyun M, Huyghe, Jeroen, Brenner, Hermann, Casey, Graham, Chan, Andrew T, Hopper, John L, Banbury, Barbara L, Chang-Claude, Jenny, Chanock, Stephen J, Haile, Robert W, Hoffmeister, Michael, Fuchsberger, Christian, Jenkins, Mark A, Leal, Suzanne M, Lemire, Mathieu, Newcomb, Polly A, Gallinger, Steven, Potter, John D, Schoen, Robert E, Slattery, Martha L, Smith, Joshua D, Le Marchand, Loic, White, Emily, Zanke, Brent W, Abeçasis, Goncalo R, Carlson, Christopher S, Peters, Ulrike, Nickerson, Deborah A, Kundaje, Anshul, Hsu, Li

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