The anti-tubercular drug delamanid as a potential oral treatment for visceral leishmaniasis von Patterson, Stephen, Wyllie, Susan, Norval, Suzanne, Stojanovski, Laste, Simeons, Frederick Rc, Auer, Jennifer L, Osuna-Cabello, Maria, Read, Kevin D, Fairlamb, Alan H

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DNA sequence-selective G-A cross-linking ADC payloads for use in solid tumour therapies von Procopiou, George, Jackson, Paul J. M., di Mascio, Daniella, Auer, Jennifer L., Pepper, Chris, Rahman, Khondaker Miraz, Fox, Keith R., Thurston, David E.

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Novel pyridyl nitrofuranyl isoxazolines show antibacterial activity against multiple drug resistant Staphylococcus species von Picconi, Pietro, Prabaharan, Priya, Auer, Jennifer L., Sandiford, Stephanie, Cascio, Francesco, Chowdhury, Madiha, Hind, Charlotte, Wand, Matthew E., Sutton, J. Mark, Rahman, Khondaker M.

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Evaluating the level of nitroreductase activity in clinical Klebsiella pneumoniae isolates to support strategies for nitro drug and prodrug development von Wand, Matthew E., Taylor, Holly V., Auer, Jennifer L., Bock, Lucy J., Hind, Charlotte K., Jamshidi, Shirin, Rahman, Khondaker Miraz, Sutton, J. Mark

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Abstract 1749: A new class of DNA sequence-selective G-A cross-linking antibody-drug conjugate (ADC) payloads von Procopiou, George, Jackson, Paul J., di Mascio, Daniella M., Auer, Jennifer L., Andriollo, Paolo, Pysz, Ilona, Rahman, Khondaker M., Fox, Keith R., Thurston, David E.

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Genome-wide Association and Population Genetic Analysis of C-Reactive Protein in African American and Hispanic American Women von Reiner, Alex P., Beleza, Sandra, Franceschini, Nora, Auer, Paul L., Robinson, Jennifer G., Kooperberg, Charles, Peters, Ulrike, Tang, Hua

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Rare coding variants pinpoint genes that control human hematological traits von Mousas, Abdou, Ntritsos, Georgios, Chen, Ming-Huei, Song, Ci, Huffman, Jennifer E, Tzoulaki, Ioanna, Elliott, Paul, Psaty, Bruce M, Auer, Paul L, Johnson, Andrew D, Evangelou, Evangelos, Lettre, Guillaume, Reiner, Alexander P

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All your data (effectively) belong to us: data practices among direct-to-consumer genetic testing firms von Laestadius, Linnea I., Rich, Jennifer R., Auer, Paul L.

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Prenatal Socioeconomic Disadvantage and Epigenetic Alterations at Birth Among Children Born to White British and Pakistani Mothers in the Born in Bradford Study von Simanek, Amanda M., Manansala, Regina, Woo, Jennifer M.P., Meier, Helen C. S., Needham, Belinda L., Auer, Paul L.

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Pathogenic Variants for Mendelian and Complex Traits in Exomes of 6,517 European and African Americans: Implications for the Return of Incidental Results von Tabor, Holly K., Auer, Paul L., Jamal, Seema M., Chong, Jessica X., Yu, Joon-Ho, Gordon, Adam S., Graubert, Timothy A., O’Donnell, Christopher J., Rich, Stephen S., Nickerson, Deborah A., Bamshad, Michael J.

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Whole-exome sequencing of 14 389 individuals from the ESP and CHARGE consortia identifies novel rare variation associated with hemostatic factors von Pankratz, Nathan, Wei, Peng, Brody, Jennifer A, Chen, Ming-Huei, de Vries, Paul S, Huffman, Jennifer E, Stimson, Mary Rachel, Auer, Paul L, Boerwinkle, Eric, Cushman, Mary, de Maat, Moniek P M, Folsom, Aaron R, Franco, Oscar H, Gibbs, Richard A, Haagenson, Kelly K, Hofman, Albert, Johnsen, Jill M, Kovar, Christie L, Kraaij, Robert, McKnight, Barbara, Metcalf, Ginger A, Muzny, Donna, Psaty, Bruce M, Tang, Weihong, Uitterlinden, André G, van Rooij, Jeroen G J, Dehghan, Abbas, O'Donnell, Christopher J, Reiner, Alex P, Morrison, Alanna C, Smith, Nicholas L

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Use of >100,000 NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium whole genome sequences improves imputation quality and detection of rare variant associations in admixe... von Kowalski, Madeline H, Qian, Huijun, Hou, Ziyi, Rosen, Jonathan D, Tapia, Amanda L, Shan, Yue, Jain, Deepti, Argos, Maria, Arnett, Donna K, Avery, Christy, Barnes, Kathleen C, Becker, Lewis C, Bien, Stephanie A, Bis, Joshua C, Blangero, John, Boerwinkle, Eric, Bowden, Donald W, Buyske, Steve, Cai, Jianwen, Cho, Michael H, Choi, Seung Hoan, Choquet, Hélène, Cupples, L Adrienne, Cushman, Mary, Daya, Michelle, de Vries, Paul S, Ellinor, Patrick T, Faraday, Nauder, Fornage, Myriam, Gabriel, Stacey, Ganesh, Santhi K, Graff, Misa, Gupta, Namrata, He, Jiang, Heckbert, Susan R, Hidalgo, Bertha, Hodonsky, Chani J, Irvin, Marguerite R, Johnson, Andrew D, Jorgenson, Eric, Kaplan, Robert, Kardia, Sharon L R, Kelly, Tanika N, Kooperberg, Charles, Lasky-Su, Jessica A, Loos, Ruth J F, Lubitz, Steven A, Mathias, Rasika A, McHugh, Caitlin P, Montgomery, Courtney, Moon, Jee-Young, Morrison, Alanna C, Palmer, Nicholette D, Pankratz, Nathan, Papanicolaou, George J, Peralta, Juan M, Peyser, Patricia A, Rich, Stephen S, Rotter, Jerome I, Silverman, Edwin K, Smith, Jennifer A, Smith, Nicholas L, Taylor, Kent D, Thornton, Timothy A, Tiwari, Hemant K, Tracy, Russell P, Wang, Tao, Weiss, Scott T, Weng, Lu-Chen, Wiggins, Kerri L, Wilson, James G, Yanek, Lisa R, Zöllner, Sebastian, North, Kari E, Auer, Paul L, Raffield, Laura M, Reiner, Alexander P, Li, Yun

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Early life trauma and adult leucocyte telomere length von Woo, Jennifer M.P., Parks, Christine G., Hyde, Emily E., Auer, Paul L., Simanek, Amanda M., Konkel, Rebecca H., Taylor, Jack, Sandler, Dale P., Meier, Helen C.S.

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FAHN/SPG35: a narrow phenotypic spectrum across disease classifications von Rattay, Tim W, Lindig, Tobias, Baets, Jonathan, Smets, Katrien, Deconinck, Tine, Söhn, Anne S, Hörtnagel, Konstanze, Eckstein, Kathrin N, Wiethoff, Sarah, Reichbauer, Jennifer, Döbler-Neumann, Marion, Krägeloh-Mann, Ingeborg, Auer-Grumbach, Michaela, Plecko, Barbara, Münchau, Alexander, Wilken, Bernd, Janauschek, Marc, Giese, Anne-Katrin, De Bleecker, Jan L, Ortibus, Els, Debyser, Martine, Lopez de Munain, Adolfo, Pujol, Aurora, Bassi, Maria Teresa, D'Angelo, Maria Grazia, De Jonghe, Peter, Züchner, Stephan, Bauer, Peter, Schöls, Ludger, Schüle, Rebecca

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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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Quantifying rare, deleterious variation in 12 human cytochrome P450 drug-metabolism genes in a large-scale exome dataset von Gordon, Adam S, Tabor, Holly K, Johnson, Andrew D, Snively, Beverly M, Assimes, Themistocles L, Auer, Paul L, Ioannidis, John P A, Peters, Ulrike, Robinson, Jennifer G, Sucheston, Lara E, Wang, Danxin, Sotoodehnia, Nona, Rotter, Jerome I, Psaty, Bruce M, Jackson, Rebecca D, Herrington, David M, O'Donnell, Christopher J, Reiner, Alexander P, Rich, Stephen S, Rieder, Mark J, Bamshad, Michael J, Nickerson, Deborah A

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Characterization of the Phenotypic Consequences of the Duffy-Null Genotype von Hysong, Micah R, Shuey, Megan, Huffman, Jennifer E, Auer, Paul L, Reiner, Alexander P, Raffield, Laura M

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Exome sequencing identifies rare LDLR and APOA5 alleles conferring risk for myocardial infarction von Do, Ron, Stitziel, Nathan O., Won, Hong-Hee, Jørgensen, Anders Berg, Duga, Stefano, Angelica Merlini, Pier, Kiezun, Adam, Farrall, Martin, Goel, Anuj, Zuk, Or, Guella, Illaria, Asselta, Rosanna, Lange, Leslie A., Peloso, Gina M., Auer, Paul L., Girelli, Domenico, Martinelli, Nicola, Farlow, Deborah N., DePristo, Mark A., Roberts, Robert, Stewart, Alexander F. R., Saleheen, Danish, Danesh, John, Epstein, Stephen E., Sivapalaratnam, Suthesh, Kees Hovingh, G., Kastelein, John J., Samani, Nilesh J., Schunkert, Heribert, Erdmann, Jeanette, Shah, Svati H., Kraus, William E., Davies, Robert, Nikpay, Majid, Johansen, Christopher T., Wang, Jian, Hegele, Robert A., Hechter, Eliana, Marz, Winfried, Kleber, Marcus E., Huang, Jie, Johnson, Andrew D., Li, Mingyao, Burke, Greg L., Gross, Myron, Liu, Yongmei, Assimes, Themistocles L., Heiss, Gerardo, Lange, Ethan M., Folsom, Aaron R., Taylor, Herman A., Olivieri, Oliviero, Hamsten, Anders, Clarke, Robert, Reilly, Dermot F., Yin, Wu, Rivas, Manuel A., Donnelly, Peter, Rossouw, Jacques E., Psaty, Bruce M., Herrington, David M., Wilson, James G., Rich, Stephen S., Bamshad, Michael J., Tracy, Russell P., Adrienne Cupples, L., Rader, Daniel J., Reilly, Muredach P., Spertus, John A., Cresci, Sharon, Hartiala, Jaana, Wilson Tang, W. H., Hazen, Stanley L., Allayee, Hooman, Reiner, Alex P., Carlson, Christopher S., Kooperberg, Charles, Jackson, Rebecca D., Boerwinkle, Eric, Lander, Eric S., Schwartz, Stephen M., Siscovick, David S., McPherson, Ruth, Tybjaerg-Hansen, Anne, Abecasis, Goncalo R., Watkins, Hugh, Nickerson, Deborah A., Ardissino, Diego, Sunyaev, Shamil R., O'Donnell, Christopher J., Altshuler, David, Gabriel, Stacey, Kathiresan, Sekar

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Communication and social interaction anxiety enhance interleukin-1 beta and cortisol reactivity during high-stakes public speaking von Auer, Brandon J., Calvi, Jessica L., Jordan, Nicolas M., Schrader, David, Byrd-Craven, Jennifer

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Collagen-Specific Molecular Magnetic Resonance Imaging of Prostate Cancer von Kader, Avan, Kaufmann, Jan O, Mangarova, Dilyana B, Moeckel, Jana, Adams, Lisa C, Brangsch, Julia, Heyl, Jennifer L, Zhao, Jing, Verlemann, Christine, Karst, Uwe, Collettini, Federico, Auer, Timo A, Hamm, Bernd, Makowski, Marcus R

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