Interrogation of human hematopoiesis at single-cell and single-variant resolution von Ulirsch, Jacob C., Lareau, Caleb A., Bao, Erik L., Ludwig, Leif S., Guo, Michael H., Benner, Christian, Satpathy, Ansuman T., Kartha, Vinay K., Salem, Rany M., Hirschhorn, Joel N., Finucane, Hilary K., Aryee, Martin J., Buenrostro, Jason D., Sankaran, Vijay G.

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Transcriptional States and Chromatin Accessibility Underlying Human Erythropoiesis von Ludwig, Leif S, Lareau, Caleb A, Bao, Erik L, Nandakumar, Satish K, Muus, Christoph, Ulirsch, Jacob C, Chowdhary, Kaitavjeet, Buenrostro, Jason D, Mohandas, Narla, An, Xiuli, Aryee, Martin J, Regev, Aviv, Sankaran, Vijay G

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The genetics of human hematopoiesis and its disruption in disease von Bao, Erik L, Cheng, Aaron N, Sankaran, Vijay G

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Shared and distinct genetic etiologies for different types of clonal hematopoiesis von Brown, Derek W., Cato, Liam D., Zhao, Yajie, Nandakumar, Satish K., Bao, Erik L., Gardner, Eugene J., Hubbard, Aubrey K., DePaulis, Alexander, Rehling, Thomas, Song, Lei, Yu, Kai, Chanock, Stephen J., Perry, John R. B., Sankaran, Vijay G., Machiela, Mitchell J.

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A genome-wide association study of blood cell morphology identifies cellular proteins implicated in disease aetiology von Akbari, Parsa, Vuckovic, Dragana, Stefanucci, Luca, Jiang, Tao, Kundu, Kousik, Kreuzhuber, Roman, Bao, Erik L., Collins, Janine H., Downes, Kate, Grassi, Luigi, Guerrero, Jose A., Kaptoge, Stephen, Knight, Julian C., Meacham, Stuart, Sambrook, Jennifer, Seyres, Denis, Stegle, Oliver, Verboon, Jeffrey M., Walter, Klaudia, Watkins, Nicholas A., Danesh, John, Roberts, David J., Di Angelantonio, Emanuele, Sankaran, Vijay G., Frontini, Mattia, Burgess, Stephen, Kuijpers, Taco, Peters, James E., Butterworth, Adam S., Ouwehand, Willem H., Soranzo, Nicole, Astle, William J.

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Author Correction: Functional dissection of inherited non-coding variation influencing multiple myeloma risk von Ajore, Ram, Niroula, Abhishek, Pertesi, Maroulio, Cafaro, Caterina, Thodberg, Malte, Went, Molly, Bao, Erik L., Duran-Lozano, Laura, Lopez de Lapuente Portilla, Aitzkoa, Olafsdottir, Thorunn, Ugidos-Damboriena, Nerea, Magnusson, Olafur, Samur, Mehmet, Lareau, Caleb A., Halldorsson, Gisli H., Thorleifsson, Gudmar, Norddahl, Gudmundur L., Gunnarsdottir, Kristbjorg, Försti, Asta, Goldschmidt, Hartmut, Hemminki, Kari, van Rhee, Frits, Kimber, Scott, Sperling, Adam S., Kaiser, Martin, Anderson, Kenneth, Jonsdottir, Ingileif, Munshi, Nikhil, Rafnar, Thorunn, Waage, Anders, Weinhold, Niels, Thorsteinsdottir, Unnur, Sankaran, Vijay G., Stefansson, Kari, Houlston, Richard, Nilsson, Björn

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SLICE: determining cell differentiation and lineage based on single cell entropy von Guo, Minzhe, Bao, Erik L, Wagner, Michael, Whitsett, Jeffrey A, Xu, Yan

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Persistence of LPS-induced lung inflammation in surfactant protein-C-deficient mice von Glasser, Stephan W, Maxfield, Melissa D, Ruetschilling, Teah L, Akinbi, Henry T, Baatz, John E, Kitzmiller, Joseph A, Page, Kristen, Xu, Yan, Bao, Erik L, Korfhagen, Thomas R

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From GWAS variant to function: A study of ∼148,000 variants for blood cell traits von Sun, Quan, Crowley, Cheynna A., Huang, Le, Wen, Jia, Chen, Jiawen, Bao, Erik L., Auer, Paul L., Lettre, Guillaume, Reiner, Alexander P., Sankaran, Vijay G., Raffield, Laura M., Li, Yun

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The Polygenic and Monogenic Basis of Blood Traits and Diseases von Vuckovic, Dragana, Bao, Erik L., Akbari, Parsa, Mousas, Abdou, Jiang, Tao, Chen, Ming-Huei, Raffield, Laura M., Huffman, Jennifer E., Ritchie, Scott C., Megy, Karyn, Ponstingl, Hannes, Penkett, Christopher J., Albers, Patrick K., Wigdor, Emilie M., Sakaue, Saori, Moscati, Arden, Manansala, Regina, Lo, Ken Sin, Qian, Huijun, Akiyama, Masato, Bartz, Traci M., Beswick, Andrew, Bork-Jensen, Jette, Bottinger, Erwin P., van Rooij, Frank J.A., Chitrala, Kumaraswamy N., Wilson, Peter W.F., Choquet, Hélène, Danesh, John, Di Angelantonio, Emanuele, Dimou, Niki, Ding, Jingzhong, Elliott, Paul, Esko, Tõnu, Evans, Michele K., Felix, Stephan B., Floyd, James S., Grarup, Niels, Guo, Michael H., Guo, Qi, Greinacher, Andreas, Haessler, Jeff, Howson, Joanna M.M., Huang, Wei, Kacprowski, Tim, Kähönen, Mika, Kamatani, Yoichiro, Kanai, Masahiro, Karthikeyan, Savita, Koskeridis, Fotios, Lange, Leslie A., Lehtimäki, Terho, Linneberg, Allan, Liu, Yongmei, Lyytikäinen, Leo-Pekka, Manichaikul, Ani, Matsuda, Koichi, Mohlke, Karen L., Mononen, Nina, Murakami, Yoshinori, Nikus, Kjell, Pankratz, Nathan, Pedersen, Oluf, Preuss, Michael, Psaty, Bruce M., Rich, Stephen S., Rodriguez, Benjamin A.T., Rosen, Jonathan D., Rotter, Jerome I., Spracklen, Cassandra N., Surendran, Praveen, Tang, Hua, Tardif, Jean-Claude, Ghanbari, Mohsen, Völzke, Henry, Watkins, Nicholas A., Cai, Na, Kundu, Kousik, Watt, Stephen B., Walter, Klaudia, Zonderman, Alan B., Cho, Kelly, Li, Yun, Loos, Ruth J.F., Knight, Julian C., Georges, Michel, Stegle, Oliver, Evangelou, Evangelos, Okada, Yukinori, Roberts, David J., Inouye, Michael, Johnson, Andrew D., Auer, Paul L., Astle, William J., Reiner, Alexander P., Butterworth, Adam S., Ouwehand, Willem H., Lettre, Guillaume, Sankaran, Vijay G., Soranzo, Nicole

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Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations von Chen, Ming-Huei, Raffield, Laura M., Mousas, Abdou, Sakaue, Saori, Huffman, Jennifer E., Moscati, Arden, Trivedi, Bhavi, Jiang, Tao, Akbari, Parsa, Vuckovic, Dragana, Bao, Erik L., Zhong, Xue, Manansala, Regina, Laplante, Véronique, Chen, Minhui, Lo, Ken Sin, Qian, Huijun, Lareau, Caleb A., Beaudoin, Mélissa, Akiyama, Masato, Ben-Shlomo, Yoav, Beswick, Andrew, Bottinger, Erwin P., Brody, Jennifer A., van Rooij, Frank J.A., Cho, Kelly, Choquet, Hélène, Correa, Adolfo, Di Angelantonio, Emanuele, Dimou, Niki, Ding, Jingzhong, Elliott, Paul, Esko, Tõnu, Evans, Michele K., Floyd, James S., Broer, Linda, Grarup, Niels, Guo, Michael H., Greinacher, Andreas, Haessler, Jeff, Hansen, Torben, Howson, Joanna M.M., Huang, Qin Qin, Huang, Wei, Jorgenson, Eric, Kacprowski, Tim, Kanai, Masahiro, Karthikeyan, Savita, Koskeridis, Fotis, Lange, Leslie A., Lerch, Markus M., Linneberg, Allan, Liu, Yongmei, Lyytikäinen, Leo-Pekka, Manichaikul, Ani, Martin, Hilary C., Matsuda, Koichi, Mohlke, Karen L., Mononen, Nina, Murakami, Yoshinori, Nadkarni, Girish N., Nauck, Matthias, Nikus, Kjell, Ouwehand, Willem H., Pankratz, Nathan, Pedersen, Oluf, Preuss, Michael, Psaty, Bruce M., Raitakari, Olli T., Roberts, David J., Rich, Stephen S., Rodriguez, Benjamin A.T., Rosen, Jonathan D., Rotter, Jerome I., Schubert, Petra, Spracklen, Cassandra N., Surendran, Praveen, Tang, Hua, Tardif, Jean-Claude, Trembath, Richard C., Ghanbari, Mohsen, Völker, Uwe, Völzke, Henry, Watkins, Nicholas A., Zonderman, Alan B., Wilson, Peter W.F., Li, Yun, Butterworth, Adam S., Gauchat, Jean-François, Chiang, Charleston W.K., Li, Bingshan, Loos, Ruth J.F., Astle, William J., Evangelou, Evangelos, van Heel, David A., Sankaran, Vijay G., Okada, Yukinori, Johnson, Andrew D., Reiner, Alexander P., Auer, Paul L.

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Inherited blood cancer predisposition through altered transcription elongation von Zhao, Jiawei, Cato, Liam D., Arora, Uma P., Bao, Erik L., Bryant, Samuel C., Williams, Nicholas, Jia, Yuemeng, Goldman, Seth R., Nangalia, Jyoti, Erb, Michael A., Vos, Seychelle M., Armstrong, Scott A., Sankaran, Vijay G.

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Macrothrombocytopenia associated with a rare GFI1B missense variant confounding the presentation of immune thrombocytopenia von Cheng, Aaron N., Bao, Erik L., Fiorini, Claudia, Sankaran, Vijay G.

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Congenital anemia reveals distinct targeting mechanisms for master transcription factor GATA1 von Ludwig, Leif S., Lareau, Caleb A., Bao, Erik L., Liu, Nan, Utsugisawa, Taiju, Tseng, Alex M., Myers, Samuel A., Verboon, Jeffrey M., Ulirsch, Jacob C., Luo, Wendy, Muus, Christoph, Fiorini, Claudia, Olive, Meagan E., Vockley, Christopher M., Munschauer, Mathias, Hunter, Abigail, Ogura, Hiromi, Yamamoto, Toshiyuki, Inada, Hiroko, Nakagawa, Shinichiro, Ohzono, Shuichi, Subramanian, Vidya, Chiarle, Roberto, Glader, Bertil, Carr, Steven A., Aryee, Martin J., Kundaje, Anshul, Orkin, Stuart H., Regev, Aviv, McCavit, Timothy L., Kanno, Hitoshi, Sankaran, Vijay G.

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Antiepileptic drug treatment after an unprovoked first seizure: A decision analysis von Bao, Erik L, Chao, Ling-Ya, Ni, Peiyun, Moura, Lidia M.V.R, Cole, Andrew J, Cash, Sydney S, Hoch, Daniel B, Bianchi, Matt T, Westover, M Brandon

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Common α-globin variants modify hematologic and other clinical phenotypes in sickle cell trait and disease von Raffield, Laura M, Ulirsch, Jacob C, Naik, Rakhi P, Lessard, Samuel, Handsaker, Robert E, Jain, Deepti, Kang, Hyun M, Pankratz, Nathan, Auer, Paul L, Bao, Erik L, Smith, Joshua D, Lange, Leslie A, Lange, Ethan M, Li, Yun, Thornton, Timothy A, Young, Bessie A, Abecasis, Goncalo R, Laurie, Cathy C, Nickerson, Deborah A, McCarroll, Steven A, Correa, Adolfo, Wilson, James G, Lettre, Guillaume, Sankaran, Vijay G, Reiner, Alex P

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Bronchopulmonary dysplasia impairs L-type amino acid transporter-1 expression in human and baboon lung von Bao, Erik L., Chystsiakova, Anastasiya, Brahmajothi, Mulugu V., Sunday, Mary E., Pavlisko, Elizabeth N., Wempe, Michael F., Auten, Richard L.

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Heritability of fetal hemoglobin, white cell count, and other clinical traits from a sickle cell disease family cohort von Bao, Erik L., Lareau, Caleb A., Brugnara, Carlo, Fulcher, Isabel R., Barau, Caroline, Moutereau, Stephane, Habibi, Anoosha, Badaoui, Bouchra, Berkenou, Jugurtha, Bartolucci, Pablo, Galactéros, Frédéric, Platt, Orah S., Mahaney, Michael, Sankaran, Vijay G.

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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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Inherited myeloproliferative neoplasm risk affects haematopoietic stem cells von Bao, Erik L., Nandakumar, Satish K., Liao, Xiaotian, Bick, Alexander G., Karjalainen, Juha, Tabaka, Marcin, Gan, Olga I., Havulinna, Aki S., Kiiskinen, Tuomo T. J., Lareau, Caleb A., de Lapuente Portilla, Aitzkoa L., Li, Bo, Emdin, Connor, Codd, Veryan, Nelson, Christopher P., Walker, Christopher J., Churchhouse, Claire, de la Chapelle, Albert, Klein, Daryl E., Nilsson, Björn, Wilson, Peter W. F., Cho, Kelly, Pyarajan, Saiju, Gaziano, J. Michael, Samani, Nilesh J., Regev, Aviv, Palotie, Aarno, Neale, Benjamin M., Dick, John E., Natarajan, Pradeep, O’Donnell, Christopher J., Daly, Mark J., Milyavsky, Michael, Kathiresan, Sekar, Sankaran, Vijay G.

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