Pain and somatic symptoms are sequelae of sexual assault: Results of a prospective longitudinal study von Ulirsch, J.C., Ballina, L.E., Soward, A.C., Rossi, C., Hauda, W., Holbrook, D., Wheeler, R., Foley, K.A., Batts, J., Collette, R., Goodman, E., McLean, S.A.

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Pain catastrophizing influences pain and itch symptoms within 24 hours of skin autograft von Ballina, L, Ulirsch, J, Nielsen, C, Adasme, R, Thom, N, Pauley, C, Jones, S, Hwang, J, Cairns, B, McLean, S

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Risk factors for persistent pain after motor vehicle collision differ between litigants and non-litigants von Soward, A, Ulirsch, J, Bair, E, Slade, G, Swor, R, Peak, D, Jones, J, Rathlev, N, Lee, D, Domeier, R, Hendry, P, McLean, S

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Interactions between gender and other risk factors are associated with persistent neck pain after motor vehicle collision von Orrey, D, Ulirsch, J, Linnstaedt, S, Swor, R, Peak, D, Jones, J, Rathlev, N, Lee, D, Domeier, R, Hendry, P, McLean, S

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No man is an island: living in a more disadvantaged neighborhood increases the likelihood of developing persistent moderate or severe neck pain 6 weeks after motor vehicle collisio... von Ulirsch, J, Bortsov, A, Soward, A, Swor, R, Peak, D, Jones, J, Rathlev, N, Lee, D, Domeier, R, Hendry, P, McLean, S

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Most sexual assault survivors with new moderate or severe pain do not receive medical care in the initial six weeks after sexual assault von Murray, C, Ulirsch, J, Soward, A, Rossi, C, Rotolo, S, Wheeler, R, Foley, K, Batts, J, Collette, R, Holbrook, D, Goodman, E, Csontos, E, McLean, S

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Author Correction: FinnGen provides genetic insights from a well-phenotyped isolated population von Kurki, Mitja I., Karjalainen, Juha, Palta, Priit, Sipilä, Timo P., Donner, Kati M., Reeve, Mary P., Laivuori, Hannele, Kaunisto, Mari A., Loukola, Anu, Lahtela, Elisa, Mattsson, Hannele, Laiho, Päivi, Della Briotta Parolo, Pietro, Lehisto, Arto A., Kanai, Masahiro, Mars, Nina, Heyne, Henrike O., Veerapen, Kumar, Rüeger, Sina, Lemmelä, Susanna, Zhou, Wei, Ruotsalainen, Sanni, Pärn, Kalle, Hiekkalinna, Tero, Koskelainen, Sami, Llorens, Vincent, Gracia-Tabuenca, Javier, Siirtola, Harri, Reis, Kadri, Elnahas, Abdelrahman G., Aalto-Setälä, Katriina, Biswas, Shameek, Dada, Oluwaseun A., Ding, Zhihao, Ehm, Margaret G., Eklund, Kari, Färkkilä, Martti, Finucane, Hilary, Ganna, Andrea, Ghazal, Awaisa, Hakanen, Antti, Hu, Xinli, Hunkapiller, Julie, Jacob, Howard, Jensen, Jan-Nygaard, Joensuu, Heikki, John, Sally, Junttila, Juhani, Kähönen, Mika, Kallio, Lila, Kaprio, Jaakko, Kettunen, Johannes, Kilpeläinen, Elina, Kosma, Veli-Matti, Kuopio, Teijo, Laisk, Triin, Laukkanen, Jari, Liu, Aoxing, Mägi, Reedik, Mäkitie, Antti, Malarstig, Anders, Maranville, Joseph, Niemi, Mari E. K., Niemi, Marianna, Obeidat, Ma´en, Okafo, George, Palomäki, Antti, Palotie, Tuula, Pitkäranta, Anne, Pulford, David, Raghavan, Neha, Rahimov, Fedik, Riley-Gillis, Bridget, Rodosthenous, Rodosthenis, Salminen, Eveliina, Salomaa, Veikko, Schleutker, Johanna, Serpi, Raisa, Shen, Huei-yi, Siegel, Richard, Sul, Jae Hoon, Tachmazidou, Ioanna, Tienari, Pentti, Tukiainen, Taru, Vaura, Felix, Virolainen, Petri, Waring, Jeffrey, Waterworth, Dawn, Yang, Robert, Nelis, Mari, Metspalu, Andres, Milani, Lili, Fox, Caroline, Havulinna, Aki S., Perola, Markus, Jalanko, Anu, Plenge, Robert, Runz, Heiko, Daly, Mark J., Palotie, Aarno

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Lineage Tracing in Humans Enabled by Mitochondrial Mutations and Single-Cell Genomics von Ludwig, Leif S., Lareau, Caleb A., Ulirsch, Jacob C., Christian, Elena, Muus, Christoph, Li, Lauren H., Pelka, Karin, Ge, Will, Oren, Yaara, Brack, Alison, Law, Travis, Rodman, Christopher, Chen, Jonathan H., Boland, Genevieve M., Hacohen, Nir, Rozenblatt-Rosen, Orit, Aryee, Martin J., Buenrostro, Jason D., Regev, Aviv, Sankaran, Vijay G.

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Tractor uses local ancestry to enable the inclusion of admixed individuals in GWAS and to boost power von Atkinson, Elizabeth G., Maihofer, Adam X., Kanai, Masahiro, Martin, Alicia R., Karczewski, Konrad J., Santoro, Marcos L., Ulirsch, Jacob C., Kamatani, Yoichiro, Okada, Yukinori, Finucane, Hilary K., Koenen, Karestan C., Nievergelt, Caroline M., Daly, Mark J., Neale, Benjamin M.

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The Genetic Landscape of Diamond-Blackfan Anemia von Ulirsch, Jacob C., Verboon, Jeffrey M., Kazerounian, Shideh, Guo, Michael H., Yuan, Daniel, Ludwig, Leif S., Handsaker, Robert E., Abdulhay, Nour J., Fiorini, Claudia, Genovese, Giulio, Lim, Elaine T., Cheng, Aaron, Cummings, Beryl B., Chao, Katherine R., Beggs, Alan H., Genetti, Casie A., Sieff, Colin A., Newburger, Peter E., Niewiadomska, Edyta, Matysiak, Michal, Vlachos, Adrianna, Lipton, Jeffrey M., Atsidaftos, Eva, Glader, Bertil, Narla, Anupama, Gleizes, Pierre-Emmanuel, O’Donohue, Marie-Françoise, Montel-Lehry, Nathalie, Amor, David J., McCarroll, Steven A., O’Donnell-Luria, Anne H., Gupta, Namrata, Gabriel, Stacey B., MacArthur, Daniel G., Lander, Eric S., Lek, Monkol, Da Costa, Lydie, Nathan, David G., Korostelev, Andrei A., Do, Ron, Sankaran, Vijay G., Gazda, Hanna T.

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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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Targeted Application of Human Genetic Variation Can Improve Red Blood Cell Production from Stem Cells von Giani, Felix C., Fiorini, Claudia, Wakabayashi, Aoi, Ludwig, Leif S., Salem, Rany M., Jobaliya, Chintan D., Regan, Stephanie N., Ulirsch, Jacob C., Liang, Ge, Steinberg-Shemer, Orna, Guo, Michael H., Esko, Tõnu, Tong, Wei, Brugnara, Carlo, Hirschhorn, Joel N., Weiss, Mitchell J., Zon, Leonard I., Chou, Stella T., French, Deborah L., Musunuru, Kiran, Sankaran, Vijay G.

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Genetic predisposition to mosaic Y chromosome loss in blood von Thompson, Deborah J., Genovese, Giulio, Halvardson, Jonatan, Ulirsch, Jacob C., Wright, Daniel J., Terao, Chikashi, Davidsson, Olafur B., Day, Felix R., Sulem, Patrick, Jiang, Yunxuan, Danielsson, Marcus, Davies, Hanna, Dennis, Joe, Dunlop, Malcolm G., Easton, Douglas F., Fisher, Victoria A., Zink, Florian, Houlston, Richard S., Ingelsson, Martin, Kar, Siddhartha, Kerrison, Nicola D., Kinnersley, Ben, Kristjansson, Ragnar P., Law, Philip J., Li, Rong, Loveday, Chey, Mattisson, Jonas, McCarroll, Steven A., Murakami, Yoshinori, Murray, Anna, Olszewski, Pawel, Rychlicka-Buniowska, Edyta, Scott, Robert A., Thorsteinsdottir, Unnur, Tomlinson, Ian, Moghadam, Behrooz Torabi, Turnbull, Clare, Wareham, Nicholas J., Gudbjartsson, Daniel F., Kamatani, Yoichiro, Hoffmann, Eva R., Jackson, Steve P., Stefansson, Kari, Auton, Adam, Ong, Ken K., Machiela, Mitchell J., Loh, Po-Ru, Dumanski, Jan P., Chanock, Stephen J., Forsberg, Lars A., Perry, John R. B.

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Functional Selectivity in Cytokine Signaling Revealed Through a Pathogenic EPO Mutation von Kim, Ah Ram, Ulirsch, Jacob C., Wilmes, Stephan, Unal, Ekrem, Moraga, Ignacio, Karakukcu, Musa, Yuan, Daniel, Kazerounian, Shideh, Abdulhay, Nour J., King, David S., Gupta, Namrata, Gabriel, Stacey B., Lander, Eric S., Patiroglu, Turkan, Ozcan, Alper, Ozdemir, Mehmet Akif, Garcia, K. Christopher, Piehler, Jacob, Gazda, Hanna T., Klein, Daryl E., Sankaran, Vijay G.

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Ribosome Levels Selectively Regulate Translation and Lineage Commitment in Human Hematopoiesis von Khajuria, Rajiv K., Munschauer, Mathias, Ulirsch, Jacob C., Fiorini, Claudia, Ludwig, Leif S., McFarland, Sean K., Abdulhay, Nour J., Specht, Harrison, Keshishian, Hasmik, Mani, D.R., Jovanovic, Marko, Ellis, Steven R., Fulco, Charles P., Engreitz, Jesse M., Schütz, Sabina, Lian, John, Gripp, Karen W., Weinberg, Olga K., Pinkus, Geraldine S., Gehrke, Lee, Regev, Aviv, Lander, Eric S., Gazda, Hanna T., Lee, Winston Y., Panse, Vikram G., Carr, Steven A., Sankaran, Vijay G.

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Direct characterization of cis-regulatory elements and functional dissection of complex genetic associations using HCR–FlowFISH von Reilly, Steven K., Gosai, Sager J., Gutierrez, Alan, Mackay-Smith, Ava, Ulirsch, Jacob C., Kanai, Masahiro, Mouri, Kousuke, Berenzy, Daniel, Kales, Susan, Butler, Gina M., Gladden-Young, Adrianne, Bhuiyan, Redwan M., Stitzel, Michael L., Finucane, Hilary K., Sabeti, Pardis C., Tewhey, Ryan

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Leveraging polygenic enrichments of gene features to predict genes underlying complex traits and diseases von Weeks, Elle M., Ulirsch, Jacob C., Cheng, Nathan Y., Trippe, Brian L., Fine, Rebecca S., Miao, Jenkai, Patwardhan, Tejal A., Kanai, Masahiro, Nasser, Joseph, Fulco, Charles P., Tashman, Katherine C., Aguet, Francois, Li, Taibo, Ordovas-Montanes, Jose, Smillie, Christopher S., Biton, Moshe, Shalek, Alex K., Ananthakrishnan, Ashwin N., Xavier, Ramnik J., Regev, Aviv, Gupta, Rajat M., Lage, Kasper, Ardlie, Kristin G., Hirschhorn, Joel N., Lander, Eric S., Engreitz, Jesse M., Finucane, Hilary K.

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Improving fine-mapping by modeling infinitesimal effects von Cui, Ran, Elzur, Roy A., Kanai, Masahiro, Ulirsch, Jacob C., Weissbrod, Omer, Daly, Mark J., Neale, Benjamin M., Fan, Zhou, Finucane, Hilary K.

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Impaired human hematopoiesis due to a cryptic intronic GATA1 splicing mutation von Abdulhay, Nour J, Fiorini, Claudia, Verboon, Jeffrey M, Ludwig, Leif S, Ulirsch, Jacob C, Zieger, Barbara, Lareau, Caleb A, Mi, Xiaoli, Roy, Anindita, Obeng, Esther A, Erlacher, Miriam, Gupta, Namrata, Gabriel, Stacey B, Ebert, Benjamin L, Niemeyer, Charlotte M, Khoriaty, Rami N, Ancliff, Philip, Gazda, Hanna T, Wlodarski, Marcin W, Sankaran, Vijay G

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