Transfer learning for ECG classification von Weimann, Kuba, Conrad, Tim O. F.

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Prediction of Covid-19 spreading and optimal coordination of counter-measures: From microscopic to macroscopic models to Pareto fronts von Wulkow, Hanna, Conrad, Tim O F, Djurdjevac Conrad, Nataša, Müller, Sebastian A, Nagel, Kai, Schütte, Christof

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The impact of structural variation on human gene expression von Chiang, Colby, Scott, Alexandra J, Davis, Joe R, Tsang, Emily K, Li, Xin, Kim, Yungil, Hadzic, Tarik, Damani, Farhan N, Ganel, Liron, Montgomery, Stephen B, Battle, Alexis, Conrad, Donald F, Hall, Ira M

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Genetic intersection of male infertility and cancer von Nagirnaja, Liina, Aston, Kenneth I., Conrad, Donald F.

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Understanding microbiome dynamics via interpretable graph representation learning von Melnyk, Kateryna, Weimann, Kuba, Conrad, Tim O. F.

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Economic Valuation of Ecosystem Services Provided by Oyster Reefs von Grabowski, Jonathan H, Brumbaugh, Robert D, Conrad, Robert F, Keeler, Andrew G, Opaluch, James J, Peterson, Charles H, Piehler, Michael F, Powers, Sean P, Smyth, Ashley R

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The natural history of medically managed acute type B aortic dissection von Durham, Christopher A., MD, Cambria, Richard P., MD, Wang, Linda J., MD, Ergul, Emel A., MS, Aranson, Nathan J., MD, Patel, Virendra I., MD, MPH, Conrad, Mark F., MD, MSSc

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Mutation of CFAP57, a protein required for the asymmetric targeting of a subset of inner dynein arms in Chlamydomonas, causes primary ciliary dyskinesia von Bustamante-Marin, Ximena M, Horani, Amjad, Stoyanova, Mihaela, Charng, Wu-Lin, Bottier, Mathieu, Sears, Patrick R, Yin, Wei-Ning, Daniels, Leigh Anne, Bowen, Hailey, Conrad, Donald F, Knowles, Michael R, Ostrowski, Lawrence E, Zariwala, Maimoona A, Dutcher, Susan K

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Cis and trans effects of human genomic variants on gene expression von Bryois, Julien, Buil, Alfonso, Evans, David M, Kemp, John P, Montgomery, Stephen B, Conrad, Donald F, Ho, Karen M, Ring, Susan, Hurles, Matthew, Deloukas, Panos, Davey Smith, George, Dermitzakis, Emmanouil T

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Bi-allelic Recessive Loss-of-Function Variants in FANCM Cause Non-obstructive Azoospermia von Kasak, Laura, Punab, Margus, Nagirnaja, Liina, Grigorova, Marina, Minajeva, Ave, Lopes, Alexandra M., Punab, Anna Maria, Aston, Kenneth I., Carvalho, Filipa, Laasik, Eve, Smith, Lee B., Conrad, Donald F., Laan, Maris

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Clonal architecture of secondary acute myeloid leukemia defined by single-cell sequencing von Hughes, Andrew E O, Magrini, Vincent, Demeter, Ryan, Miller, Christopher A, Fulton, Robert, Fulton, Lucinda L, Eades, William C, Elliott, Kevin, Heath, Sharon, Westervelt, Peter, Ding, Li, Conrad, Donald F, White, Brian S, Shao, Jin, Link, Daniel C, DiPersio, John F, Mardis, Elaine R, Wilson, Richard K, Ley, Timothy J, Walter, Matthew J, Graubert, Timothy A

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A Systematic Survey of Loss-of-Function Variants in Human Protein-Coding Genes von MacArthur, Daniel G., Balasubramanian, Suganthi, Frankish, Adam, Huang, Ni, Morris, James, Walter, Klaudia, Jostins, Luke, Habegger, Lukas, Pickrell, Joseph K., Montgomery, Stephen B., Albers, Cornelis A., Zhang, Zhengdong D., Conrad, Donald F., Lunter, Gerton, Zheng, Hancheng, Ayub, Qasim, DePristo, Mark A., Banks, Eric, Hu, Min, Handsaker, Robert E., Rosenfeld, Jeffrey A., Fromer, Menachem, Jin, Mike, Mu, Xinmeng Jasmine, Khurana, Ekta, Ye, Kai, Kay, Mike, Saunders, Gary Ian, Suner, Marie-Marthe, Hunt, Toby, Barnes, H. A., Amid, Clara, Carvalho-Silva, Denise R., Bignell, Alexandra H., Snow, Catherine, Yngvadottir, Bryndis, Bumpstead, Suzannah, Cooper, David N., Xue, Yali, Romero, Irene Gallego, Wang, Jun, Li, Yingrui, Gibbs, Richard A., McCarroll, Steven A., Dermitzakis, Emmanouil T., Pritchard, Jonathan K., Barrett, Jeffrey C., Harrow, Jennifer, Hurles, Matthew E., Gerstein, Mark B., Tyler-Smith, Chris

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Evaluation of the modified Pittsburgh classification for predicting the disease‐free survival outcome of squamous cell carcinoma of the external auditory canal von Nabuurs, Cindy H., Kievit, Wietske, Labbé, Nilou, Leemans, C. René, Smit, Conrad F. G. M., Brekel, Michiel W. M., Pauw, Robert J., Laan, Bernard F. A. M., Jansen, Jeroen C., Lacko, Martin, Braunius, Weibel W., Morita, Shinya, Wierzbicka, Małgorzata, Matoba, Takuma, Hanai, Nobuhiro, Takes, Robert P., Kunst, Henricus P. M.

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Unified single-cell analysis of testis gene regulation and pathology in five mouse strains von Jung, Min, Wells, Daniel, Rusch, Jannette, Ahmad, Suhaira, Marchini, Jonathan, Myers, Simon R, Conrad, Donald F

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Human spermatogenic failure purges deleterious mutation load from the autosomes and both sex chromosomes, including the gene DMRT1 von Lopes, Alexandra M, Aston, Kenneth I, Thompson, Emma, Carvalho, Filipa, Gonçalves, João, Huang, Ni, Matthiesen, Rune, Noordam, Michiel J, Quintela, Inés, Ramu, Avinash, Seabra, Catarina, Wilfert, Amy B, Dai, Juncheng, Downie, Jonathan M, Fernandes, Susana, Guo, Xuejiang, Sha, Jiahao, Amorim, António, Barros, Alberto, Carracedo, Angel, Hu, Zhibin, Hurles, Matthew E, Moskovtsev, Sergey, Ober, Carole, Paduch, Darius A, Schiffman, Joshua D, Schlegel, Peter N, Sousa, Mário, Carrell, Douglas T, Conrad, Donald F

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TAD evolutionary and functional characterization reveals diversity in mammalian TAD boundary properties and function von Okhovat, Mariam, VanCampen, Jake, Nevonen, Kimberly A., Harshman, Lana, Li, Weiyu, Layman, Cora E., Ward, Samantha, Herrera, Jarod, Wells, Jackson, Sheng, Rory R., Mao, Yafei, Ndjamen, Blaise, Lima, Ana C., Vigh-Conrad, Katinka A., Stendahl, Alexandra M., Yang, Ran, Fedorov, Lev, Matthews, Ian R., Easow, Sarah A., Chan, Dylan K., Jan, Taha A., Eichler, Evan E., Rugonyi, Sandra, Conrad, Donald F., Ahituv, Nadav, Carbone, Lucia

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Origins and functional impact of copy number variation in the human genome von Scherer, Stephen W, Hurles, Matthew E, Conrad, Donald F, Pinto, Dalila, Redon, Richard, Feuk, Lars, Gokcumen, Omer, Zhang, Yujun, Aerts, Jan, Andrews, T. Daniel, Barnes, Chris, Campbell, Peter, Fitzgerald, Tomas, Hu, Min, Ihm, Chun Hwa, Kristiansson, Kati, MacArthur, Daniel G, MacDonald, Jeffrey R, Onyiah, Ifejinelo, Pang, Andy Wing Chun, Robson, Sam, Stirrups, Kathy, Valsesia, Armand, Walter, Klaudia, Wei, John, Tyler-Smith, Chris, Carter, Nigel P, Lee, Charles

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Recurrent 16p11.2 microdeletions in autism von Kumar, Ravinesh A., KaraMohamed, Samer, Sudi, Jyotsna, Conrad, Donald F., Brune, Camille, Badner, Judith A., Gilliam, T. Conrad, Nowak, Norma J., Cook, Edwin H., Dobyns, William B., Christian, Susan L.

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A high-resolution survey of deletion polymorphism in the human genome von Pritchard, Jonathan K, Conrad, Donald F, Andrews, T Daniel, Carter, Nigel P, Hurles, Matthew E

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An Interpretable Deep Learning Approach for Biomarker Detection in LC-MS Proteomics Data von Iravani, Sahar, Conrad, Tim O.F.

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