Collective philanthropy: describing and modeling the ecology of giving von Gottesman, William L, Reagan, Andrew James, Dodds, Peter Sheridan

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Collective Philanthropy: Describing and Modeling the Ecology of Giving von Gottesman, William L, Reagan, Andrew James, Peter Sheridan Dodds

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Mycobacterium tuberculosis Rv0991c Is a Redox-Regulated Molecular Chaperone von Becker, Samuel H., Ulrich, Kathrin, Dhabaria, Avantika, Ueberheide, Beatrix, Beavers, William, Skaar, Eric P., Iyer, Lakshminarayan M., Aravind, L., Jakob, Ursula, Darwin, K. Heran

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Delirium after coronary artery bypass graft surgery and late mortality von Gottesman, Rebecca F., Grega, Maura A., Bailey, Maryanne M., Pham, Luu D., Zeger, Scott L., Baumgartner, William A., Selnes, Ola A., McKhann, Guy M.

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Cognitive and Neurologic Outcomes after Coronary-Artery Bypass Surgery von Selnes, Ola A, Gottesman, Rebecca F, Grega, Maura A, Baumgartner, William A, Zeger, Scott L, McKhann, Guy M

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Severe skeletal toxicity from protracted etidronate therapy for generalized arterial calcification of infancy von Otero, Jesse E, Gottesman, Gary S, McAlister, William H, Mumm, Steven, Madson, Katherine L, Kiffer‐Moreira, Tina, Sheen, Campbell, Millán, José Luis, Ericson, Karen L, Whyte, Michael P

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Stroke genetics informs drug discovery and risk prediction across ancestries von Jürgenson, Tuuli, Namba, Shinichi, Posner, Daniel C., Kamanu, Frederick K., Koido, Masaru, He, Yunye, Caro, Ilana, Krebs, Kristi, Liaw, Yi-Ching, Parodi, Livia, Bae, Hee-Joon, Chong, Michael R., Tomppo, Liisa, Akinyemi, Rufus, Roshchupkin, Gennady V., Habib, Naomi, Jee, Yon Ho, Thomassen, Jesper Qvist, Abedi, Vida, Cárcel-Márquez, Jara, Nygaard, Marianne, Yonova-Doing, Ekaterina, Knol, Maria J., Lewis, Adam J., Judy, Renae L., Amouyel, Philippe, Bakker, Mark K., Bennett, David A., Bis, Joshua C., Bordes, Constance, Børte, Sigrid, Cain, Anael, Ridker, Paul M., Cho, Kelly, Chen, Zhengming, Cruchaga, Carlos, Cole, John W., de Cid, Rafael, Ferreira, Leslie E., He, Jing, Jeon, Christina E., Jern, Christina, Kamouchi, Masahiro, Keene, Keith L., Konuma, Takahiro, Kumar, Amit, Launer, Lenore J., Lee, Keon-Joo, Li, Jiang, Li, Liming, Manichaikul, Ani, Markus, Hugh S., Meitinger, Thomas, Mitchell, Braxton D., Morisaki, Takayuki, O’Donnell, Martin J., Onland-Moret, N. Charlotte, Ovbiagele, Bruce, Peters, Annette, Rosand, Jonathan, Sabatine, Marc S., Sacco, Ralph L., Saleheen, Danish, Schmidt, Carsten O., Smith, Nicholas L., Sloane, Kelly L., Sutoh, Yoichi, Tiwari, Hemant K., Wennberg, Patrik, Wilson, Peter W. F., Yang, Qiong, Yoon, Kyungheon, Gieger, Christian, Ninomiya, Toshiharu, Grabe, Hans J., Jukema, J. Wouter, Kim, Young Jin, Chen, Pei-Hsin, Mayerhofer, Ernst, Ikram, Mohammad A., Worrall, Bradford B., Lathrop, G. Mark, Riaz, Moeen, Simonsick, Eleanor M., Kõrv, Janika, Zand, Ramin, Prasad, Kameshwar, Frikke-Schmidt, Ruth, Liman, Thomas, Ruigrok, Ynte M., Bastarache, Lisa, Damrauer, Scott M., Rotter, Jerome I., Niiranen, Teemu J., Walters, Robin G., Owolabi, Mayowa O., Huffman, Jennifer E., Kamatani, Yoichiro, Dichgans, Martin, Debette, Stephanie

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New explanation for autosomal dominant high bone mass: Mutation of low-density lipoprotein receptor-related protein 6 von Whyte, Michael P., McAlister, William H., Zhang, Fan, Bijanki, Vinieth N., Nenninger, Angela, Gottesman, Gary S., Lin, Elizabeth L., Huskey, Margaret, Duan, Shenghui, Dahir, Kathryn, Mumm, Steven

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Abcg2a is the functional homolog of human ABCG2 expressed at the zebrafish blood-brain barrier von Thomas, Joanna R, Frye, William J E, Robey, Robert W, Warner, Andrew C, Butcher, Donna, Matta, Jennifer L, Morgan, Tamara C, Edmondson, Elijah F, Salazar, Paula B, Ambudkar, Suresh V, Gottesman, Michael M

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Coalescing expansile skeletal disease: Delineation of an extraordinary osteopathy involving the IFITM5 mutation of osteogenesis imperfecta type V von Whyte, Michael P., Aronson, James, McAlister, William H., Weinstein, Robert S., Wenkert, Deborah, Clements, Karen L., Gottesman, Gary S., Madson, Katherine L., Stolina, Marina, Bijanki, Vinieth N., Plotkin, Horacio, Huskey, Margaret, Duan, Shenghui, Mumm, Steven

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QT effects of bedaquiline, delamanid, or both in patients with rifampicin-resistant tuberculosis: a phase 2, open-label, randomised, controlled trial von Dooley, Kelly E, Rosenkranz, Susan L, Conradie, Francesca, Moran, Laura, Hafner, Richard, von Groote-Bidlingmaier, Florian, Lama, Javier R., Shenje, Justin, De Los Rios, Jorge, Comins, Kyla, Morganroth, Joel, Diacon, Andreas H, Cramer, Yoninah S, Donahue, Kathleen, Maartens, Gary, Alli, Oladapo, Gottesman, Joan, Guevara, Maria, Hikuam, Chris, Hovind, Laura, Karlsson, Mats, McClaren, Jennifer, McIlleron, Helen, Murtaugh, William, Rolls, Barbara, Shahkolahi, Akbar, Stone, Lynnett, Tegha, Gerald, Tenai, Jacob, Upton, Caryn, Wimbish, Chanelle

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Different effects of cardiometabolic syndrome on brain age in relation to gender and ethnicity von Kang, Sung Hoon, Liu, Mengting, Park, Gilsoon, Kim, Sharon Y, Lee, Hyejoo, Matloff, William, Zhao, Lu, Yoo, Heejin, Kim, Jun Pyo, Jang, Hyemin, Kim, Hee Jin, Jahanshad, Neda, Oh, Kyumgmi, Koh, Seong-Beom, Na, Duk L, Gallacher, John, Gottesman, Rebecca F, Seo, Sang Won, Kim, Hosung

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Vitamin B6 deficiency with normal plasma levels of pyridoxal 5′-phosphate in perinatal hypophosphatasia von Whyte, Michael P., May, Jennifer D., McAlister, William H., Burgener, Katherine, Cortez, Samuel R., Kreienkamp, Raymond, Castro, Olivia, Verzola, Rachel, Zavala, Ana Solis, McPherson, Christopher C., Gottesman, Gary S., Ericson, Karen L., Coburn, Stephen P., Arbelaez, Ana Maria

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Vitamin B 6 deficiency with normal plasma levels of pyridoxal 5'-phosphate in perinatal hypophosphatasia von Whyte, Michael P, May, Jennifer D, McAlister, William H, Burgener, Katherine, Cortez, Samuel R, Kreienkamp, Raymond, Castro, Olivia, Verzola, Rachel, Zavala, Ana Solis, McPherson, Christopher C, Gottesman, Gary S, Ericson, Karen L, Coburn, Stephen P, Arbelaez, Ana Maria

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Melorheostosis: Exome sequencing of an associated dermatosis implicates postzygotic mosaicism of mutated KRAS von Whyte, Michael P, Griffith, Malachi, Trani, Lee, Mumm, Steven, Gottesman, Gary S, McAlister, William H, Krysiak, Kilannin, Lesurf, Robert, Skidmore, Zachary L, Campbell, Katie M, Rosman, Ilana S, Bayliss, Susan, Bijanki, Vinieth N, Nenninger, Angela, Van Tine, Brian A, Griffith, Obi L, Mardis, Elaine R

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Epigenetic and integrative cross-omics analyses of cerebral white matter hyperintensities on MRI von Yang, Yunju, Knol, Maria J, Wang, Ruiqi, Mishra, Aniket, Liu, Dan, Luciano, Michelle, Teumer, Alexander, Armstrong, Nicola, Bis, Joshua C, Jhun, Min A, Li, Shuo, Adams, Hieab H H, Aziz, Nasir Ahmad, Bastin, Mark E, Bourgey, Mathieu, Brody, Jennifer A, Frenzel, Stefan, Gottesman, Rebecca F, Hosten, Norbert, Hou, Lifang, Kardia, Sharon L R, Lohner, Valerie, Marquis, Pascale, Maniega, Susana Muñoz, Satizabal, Claudia L, Sorond, Farzaneh A, Valdés Hernández, Maria C, van Duijn, Cornelia M, Vernooij, Meike W, Wittfeld, Katharina, Yang, Qiong, Zhao, Wei, Boerwinkle, Eric, Levy, Daniel, Deary, Ian J, Jiang, Jiyang, Mather, Karen A, Mosley, Thomas H, Psaty, Bruce M, Sachdev, Perminder S, Smith, Jennifer A, Sotoodehnia, Nona, DeCarli, Charles S, Breteler, Monique M B, Ikram, M Arfan, Grabe, Hans J, Wardlaw, Joanna, Longstreth, W T, Launer, Lenore J, Seshadri, Sudha, Debette, Stephanie, Fornage, Myriam

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Marrow Cell Transplantation for Infantile Hypophosphatasia von Whyte, Michael P, Kurtzberg, Joanne, McALISTER, William H, Mumm, Steven, Podgornik, Michelle N, Coburn, Stephen P, Ryan, Lawrence M, Miller, Cindy R, Gottesman, Gary S, Smith, Alan K, Douville, Judy, Waters‐Pick, Barbara, Armstrong, R Douglas, Martin, Paul L

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Healing of vitamin D deficiency rickets complicating hypophosphatasia suggests a role beyond circulating mineral sufficiency for vitamin D in musculoskeletal health von Lin, Elizabeth L., Gottesman, Gary S., McAlister, William H., Bijanki, Vinieth N., Mack, Karen E., Griffin, Donna M., Mumm, Steven, Whyte, Michael P.

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Auricular ossification: A newly recognized feature of osteoprotegerin-deficiency juvenile Paget disease von Gottesman, Gary S., Madson, Katherine L., McAlister, William H., Nenninger, Angela, Wenkert, Deborah, Mumm, Steven, Whyte, Michael P.

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Persistent idiopathic hyperphosphatasemia from bone alkaline phosphatase in a healthy boy von Whyte, Michael P., Ma, Nina S., Mumm, Steven, Gottesman, Gary S., McAlister, William H., Nenninger, Angela R., Bijanki, Vinieth N., Ericson, Karen L., Magnusson, Per

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