Effects of apple (Malus×domestica) rootstocks on scion performance and hormone concentration von Lordan, J., Fazio, G., Francescatto, P., Robinson, T.

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Mapping the human genetic architecture of COVID-19 von Niemi, Mari E. K., Karjalainen, Juha, Daly, Mark, Ganna, Andrea, Mehtonen, Juha, Cordioli, Mattia, Kaunisto, Mari, Pigazzini, Sara, Donner, Kati, Kivinen, Katja, Palotie, Aarno, Daly, Mark J., Liao, Rachel G., Kanai, Masahiro, Veerapen, Kumar, Minica, Camelia, Trankiem, Amy, Balaconis, Mary K., Nguyen, Huy, Solomonson, Matthew, Francioli, Laurent, Wang, Qingbo, Green, Robert C., Bryant, Sam, Finucane, Hilary, Martin, Alicia R., Zhou, Wei, Nkambule, Lindokuhle, Karczewski, Konrad J., Atkinson, Elizabeth G., Tsuo, Kristin, Baya, Nikolas, Turley, Patrick, Gupta, Rahul, Walters, Raymond K., Palmer, Duncan S., Sarma, Gopal, Cheng, Nathan, Lu, Wenhan, Churchhouse, Claire, Goldstein, Jacqueline, King, Daniel, Seed, Cotton, Neale, Benjamin M., Satterstrom, F. Kyle, Pathak, Gita A., Wendt, Frank R., Polimanti, Renato, Andrews, Shea J., Sloofman, Laura, Sealfon, Stuart C., Fernandez-Cadenas, Israel, Schulte, Eva C., Protzer, Ulrike, Striano, Pasquale, Coviello, Domenico A., Zara, Federico, Salpietro, Vincenzo, Iacomino, Michele, Scudieri, Paolo, Bocciardi, Renata, Minetti, Carlo, Vari, Maria Stella, Madia, Francesca, Marouli, Eirini, Kanoni, Stavroula, Moutsianas, Loukas, Karim, Mohd Anisul, Ghoussaini, Maya, Schwartzentruber, Jeremy, Dunham, Ian, Savage, Jeanne, Posthuma, Danielle, Tissink, Elleke, Uffelmann, Emil, Butler-Laporte, Guillaume, Richards, J. Brent, Nakanishi, Tomoko, Morrison, David R., Forgetta, Vincenzo, Ghosh, Biswarup, Laurent, Laetitia, Henry, Danielle, Abdullah, Tala, Adeleye, Olumide, Mamlouk, Noor, Kimchi, Nofar, Afrasiabi, Zaman, Rezk, Nardin, Vulesevic, Branka, Bouab, Meriem, Guzman, Charlotte, Petitjean, Louis, Tselios, Chris, Xue, Xiaoqing, Afilalo, Jonathan, Adra, Darin, Kim, Han-Na, Okada, Yukinori, Byun, Jinyoung

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Missense mutations in TENM4, a regulator of axon guidance and central myelination, cause essential tremor von Hor, Hyun, Francescatto, Ludmila, Bartesaghi, Luca, Ortega-Cubero, Sara, Kousi, Maria, Lorenzo-Betancor, Oswaldo, Jiménez-Jiménez, Felix J, Gironell, Alexandre, Clarimón, Jordi, Drechsel, Oliver, Agúndez, José A G, Kenzelmann Broz, Daniela, Chiquet-Ehrismann, Ruth, Lleó, Alberto, Coria, Francisco, García-Martin, Elena, Alonso-Navarro, Hortensia, Martí, Maria J, Kulisevsky, Jaume, Hor, Charlotte N, Ossowski, Stephan, Chrast, Roman, Katsanis, Nicholas, Pastor, Pau, Estivill, Xavier

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An atlas of active enhancers across human cell types and tissues von Andersson, Robin, Gebhard, Claudia, Miguel-Escalada, Irene, Hoof, Ilka, Bornholdt, Jette, Boyd, Mette, Chen, Yun, Zhao, Xiaobei, Schmidl, Christian, Suzuki, Takahiro, Ntini, Evgenia, Arner, Erik, Valen, Eivind, Li, Kang, Schwarzfischer, Lucia, Glatz, Dagmar, Raithel, Johanna, Lilje, Berit, Rapin, Nicolas, Bagger, Frederik Otzen, Jørgensen, Mette, Andersen, Peter Refsing, Bertin, Nicolas, Rackham, Owen, Burroughs, A. Maxwell, Baillie, J. Kenneth, Ishizu, Yuri, Shimizu, Yuri, Furuhata, Erina, Maeda, Shiori, Negishi, Yutaka, Mungall, Christopher J., Meehan, Terrence F., Lassmann, Timo, Itoh, Masayoshi, Kawaji, Hideya, Kondo, Naoto, Kawai, Jun, Lennartsson, Andreas, Daub, Carsten O., Heutink, Peter, Hume, David A., Jensen, Torben Heick, Suzuki, Harukazu, Hayashizaki, Yoshihide, Müller, Ferenc, Forrest, Alistair R. R., Carninci, Piero, Rehli, Michael, Sandelin, Albin

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Disruptive CHD8 Mutations Define a Subtype of Autism Early in Development von Bernier, Raphael, Golzio, Christelle, Xiong, Bo, Stessman, Holly A., Coe, Bradley P., Penn, Osnat, Witherspoon, Kali, Gerdts, Jennifer, Baker, Carl, Vulto-van Silfhout, Anneke T., Schuurs-Hoeijmakers, Janneke H., Fichera, Marco, Bosco, Paolo, Buono, Serafino, Alberti, Antonino, Failla, Pinella, Peeters, Hilde, Steyaert, Jean, Vissers, Lisenka E.L.M., Francescatto, Ludmila, Mefford, Heather C., Rosenfeld, Jill A., Bakken, Trygve, O’Roak, Brian J., Pawlus, Matthew, Moon, Randall, Shendure, Jay, Amaral, David G., Lein, Ed, Rankin, Julia, Romano, Corrado, de Vries, Bert B.A., Katsanis, Nicholas, Eichler, Evan E.

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Achievements of recent research on severe accidents at CEA/IRESNE in support of future nuclear fission technology von Seiler, N., Bachrata, A., Bigot, B., Bouyer, V., Brayer, C., Charollais, F., Chauvin, R., Clavier, R., Denoix, A., Delacroix, J., Dufour, E., Francescatto, J., Gubernatis, P., Johnson, M., Journeau, C., Lecoanet, A., Le Tellier, R., Piluso, P., Pons, K., Saas, L., Trotignon, L.

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Functionally compromised CHD7 alleles in patients with isolated GnRH deficiency von Balasubramanian, Ravikumar, Choi, Jin-Ho, Francescatto, Ludmila, Willer, Jason, Horton, Edward R., Asimacopoulos, Eleni P., Stankovic, Konstantina M., Plummer, Lacey, Buck, Cassandra L., Quinton, Richard, Nebesio, Todd D., Mericq, Veronica, Merino, Paulina M., Meyer, Brian F., Monies, Dorota, Gusella, James F., Tassan, Nada Al, Katsanis, Nicholas, Crowley, William F.

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Application of a proposed additive manufacturing performance measurement system in a Brazilian industry von Neuenfeldt, A, Nogueiraa, P, Francescattoa, M, Siluka, J, De Parisa, S, Mandlhatea, M

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Differential roles of epigenetic changes and Foxp3 expression in regulatory T cell-specific transcriptional regulation von Morikawa, Hiromasa, Ohkura, Naganari, Vandenbon, Alexis, Itoh, Masayoshi, Nagao-Sato, Sayaka, Kawaji, Hideya, Lassmann, Timo, Carninci, Piero, Hayashizaki, Yoshihide, Forrest, Alistair R. R., Standley, Daron M., Date, Hiroshi, Sakaguchi, Shimon

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A verified genomic reference sample for assessing performance of cancer panels detecting small variants of low allele frequency von Jones, Wendell, Gong, Binsheng, Novoradovskaya, Natalia, Li, Dan, Kusko, Rebecca, Richmond, Todd A., Johann, Donald J., Bisgin, Halil, Sahraeian, Sayed Mohammad Ebrahim, Bushel, Pierre R., Pirooznia, Mehdi, Wilkins, Katherine, Chierici, Marco, Bao, Wenjun, Basehore, Lee Scott, Lucas, Anne Bergstrom, Burgess, Daniel, Butler, Daniel J., Cawley, Simon, Chang, Chia-Jung, Chen, Guangchun, Chen, Tao, Chen, Yun-Ching, Craig, Daniel J., Del Pozo, Angela, Foox, Jonathan, Francescatto, Margherita, Fu, Yutao, Furlanello, Cesare, Giorda, Kristina, Grist, Kira P., Guan, Meijian, Hao, Yingyi, Happe, Scott, Hariani, Gunjan, Haseley, Nathan, Jasper, Jeff, Jurman, Giuseppe, Kreil, David Philip, Labaj, Pawel, Lai, Kevin, Li, Jianying, Li, Quan-Zhen, Li, Yulong, Li, Zhiguang, Liu, Zhichao, Lopez, Mario Solis, Miclaus, Kelci, Miller, Raymond, Mittal, Vinay K., Mohiyuddin, Marghoob, Pabon-Pena, Carlos, Parsons, Barbara L., Qiu, Fujun, Scherer, Andreas, Shi, Tieliu, Stiegelmeyer, Suzy, Suo, Chen, Tom, Nikola, Wang, Dong, Wen, Zhining, Wu, Leihong, Xiao, Wenzhong, Xu, Chang, Yu, Ying, Zhang, Jiyang, Zhang, Yifan, Zhang, Zhihong, Zheng, Yuanting, Mason, Christopher E., Willey, James C., Tong, Weida, Shi, Leming, Xu, Joshua

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Regional differences in gene expression and promoter usage in aged human brains von Pardo, Luba M, Rizzu, Patrizia, Francescatto, Margherita, Vitezic, Morana, Leday, Gwenaël G.R, Sanchez, Javier Simon, Khamis, Abdullah, Takahashi, Hazuki, van de Berg, Wilma D.J, Medvedeva, Yulia A, van de Wiel, Mark A, Daub, Carsten O, Carninci, Piero, Heutink, Peter

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Ceruloplasmin is a novel adipokine which is overexpressed in adipose tissue of obese subjects and in obesity-associated cancer cells von Arner, Erik, Forrest, Alistair R R, Ehrlund, Anna, Mejhert, Niklas, Itoh, Masayoshi, Kawaji, Hideya, Lassmann, Timo, Laurencikiene, Jurga, Rydén, Mikael, Arner, Peter

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The statistical geometry of transcriptome divergence in cell-type evolution and cancer von Liang, Cong, Forrest, Alistair R.R., Wagner, Günter P.

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GWAS Meta-Analysis of Glomerular Filtration Rate in Three Cohorts of Sickle Cell Disease Patients and In Vivo Functional Analysis Reveals Potential Nephropathy Candidate Genes von Anderson, Blair R., Garrett, Melanie E., Soldano, Karen L., Orringer, Eugene P., Eckman, James R., Francescatto, Ludmila, Davis, Erica E., Gladwin, Mark T., Gordeuk, Victor R., Telen, Marilyn J., Ashley-Koch, Allison E.

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Description Osteo-Oto-Hepato-Enteric (O2HE) syndrome, a new recessive autosomal syndrome secondary to loss of function mutations in the UNC45A gene von Faivre, L., Esteve, Clothilde, Francescatto, L., Tan, P. L., Bourchany, A., Delafoulhouze, C., Marinier, E., Bourgeois, Patrice, Brochier-Armanet, C., Bruel, A., Delarue, A., Duffourd, Y., Ecochard-Dugelay, E., Goulet, O., Gauchez, P., Gonzales, E., Guettier-Bouttier, C., Huet, F., Komutora, M., Hery, G., Lacoste, Caroline, Maudinas, R., Mazodier, K., Rimet, Y., Rivière, Jérôme, Roquelaure, B., Sarles, J., Sigaudy, Sabine, Savajols, E., Stephenne, X., Thauvin-Robinet, C., Thevenon, J., Levy, Nicolas, Badens, Catherine, Hugot, J., Katsanis, N., Fabre, Alexandre

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Profiling transcription initiation in human aged brain using deep-CAGE von Francescatto, Margherita, Pardo, Luba, Rizzu, Patrizia, Vitezic, Morana, Simón-Sánchez, Javier, Takahashi, Hazuki, Daub, Carsten, Carninci, Piero, Heutink, Peter

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Differential and shared genetic effects on kidney function between diabetic and non-diabetic individuals von Thomas, LF, Tin, A, Chu, AY, Cusi, D, Li, M, Scholz, M, Van der Most, PJ, Yang, Q, Guenther, F, Correa, A, Zonderman, AB, De Grandi, A, Rosenkranz, AR, Teren, A, Hicks, AA, Mahajan, A, Brumpton, B, Asvold, BO, Smith, BH, Hayward, C, Hartman, CA, Wang, C, Khor, C-C, Gieger, C, Shaffer, CM, Willer, CJ, Ruggiero, D, Mascalzoni, D, Mook-Kanamori, DO, Reilly, DF, Hofer, E, Salvi, E, Tai, E-S, Rivadeneira, F, Ehret, G, Pistis, G, Nadkarni, GN, Montgomery, GW, Schmidt, H, Tzoulaki, I, Wilson, JF, Halbritter, J, O'Connell, J, Liu, J, Xu, J, Whitfield, JB, Marten, J, Jonas, JB, Eckardt, K-U, Ho, K, Matsuda, K, Raffield, LM, Klaric, L, Ikram, MA, Ciullo, M, Gogele, M, La Bianca, M, Lukas, MA, Kavousi, M, Akiyama, M, Yasuda, M, Nauck, M, Chee, M-L, Preuss, MH, Stumvoll, M, O'Donoghue, ML, Kubo, M, Martin, NG, Tan, NYQ, Palmer, ND, Mononen, N, Raitakari, OT, Manunta, P, Sulem, P, Magnusson, PKE, Hamet, P, Joshi, PK, Pramstaller, PP, Rossing, P, Vollenweider, P, Dorajoo, R, Burkhardt, R, Schmidt, R, Rueedi, R, Gansevoort, RT, Graham, SE, Ahluwalia, TS, Salomaa, V, Vitart, V, Huang, W, Kiess, W, Lieb, W, Gao, X, Wang, YX, Friedlander, Y, Kamatani, Y, Stark, KJ, Stefansson, K, Hung, AM, Kronenberg, F

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Application of Gene Expression Trajectories Initiated from ErbB Receptor Activation Highlights the Dynamics of Divergent Promoter Usage von Carbajo, Daniel, Magi, Shigeyuki, Itoh, Masayoshi, Kawaji, Hideya, Lassmann, Timo, Arner, Erik, Forrest, Alistair R R, Carninci, Piero, Hayashizaki, Yoshihide, Daub, Carsten O, Okada-Hatakeyama, Mariko, Mar, Jessica C

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Disruptive CHD8 Mutations Define a Subtype of Autism Early in Development von Bernier, Raphael, Golzio, Christelle, Xiong, Bo, Stessman, Holly A, Coe, Bradley P, Penn, Osnat, Witherspoon, Kali, Gerdts, Jennifer, Baker, Carl, Vulto-van Silfhout, Anneke T, Schuurs-Hoeijmakers, Janneke H, Fichera, Marco, Bosco, Paolo, Buono, Serafino, Alberti, Antonino, Failla, Pinella, Peeters, Hilde, Steyaert, Jean, Vissers, Lisenka E.L.M, Francescatto, Ludmila, Mefford, Heather C, Rosenfeld, Jill A, Bakken, Trygve, O'Roak, Brian J, Pawlus, Matthew, Moon, Randall, Shendure, Jay, Amaral, David G, Lein, Ed, Rankin, Julia, Romano, Corrado, de Vries, Bert B.A, Katsanis, Nicholas, Eichler, Evan E

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A second update on mapping the human genetic architecture of COVID-19 von Kanai, M, Andrews, SJ, Cordioli, M, Stevens, C, Neale, BM, Daly, M, Ganna, A, Pathak, GA, Iwasaki, A, Karjalainen, J, Mehtonen, J, Pirinen, M, Chwialkowska, K, Trankiem, A, Balaconis, MK, Veerapen, K, Wolford, BN, Ahmad, HF, Andrews, S, von Hohenstaufen Puoti, KA, Boer, C, Boua, PR, Butler-Laporte, G, Cadilla, CL, Colombo, F, Douillard, V, Dueker, N, Dutta, AK, El-Sherbiny, YM, Eltoukhy, MM, Esmaeeli, S, Faucon, A, Fave, MJ, Cadenas, IF, Francescatto, M, Francioli, L, Franke, L, Fuentes, M, Durán, RG, Cabrero, DG, Harry, EN, Jansen, P, Szentpéteri, JL, Kaja, E, Kirk, C, Kousathanas, A, Krieger, JE, Patel, SK, Lemaçon, A, Limou, S, Lió, P, Marouli, E, Marttila, MM, Medina-Gómez, C, Michaeli, Y, Migeotte, I, Mondal, S, Moreno-Estrada, A, Moya, L, Nakanishi, T, Nasir, J, Pasko, D, Pearson, NM, Pereira, AC, Priest, J, Prijatelj, V, Prokić, I, Teumer, A, Várnai, R, Romero-Gómez, M, Roos, C, Rosenfeld, J, Ruolin, L, Schulte, EC, Schurmann, C, Sedaghati-Khayat, B, Shaheen, D, Shivanathan, I, Sipeky, C, Sirui, Z, Striano, P, Tanigawa, Y, Remesal, AU, Vadgama, N, Vallerga, CL, van der Laan, S, Verdugo, RA, Wang, QS, Wei, Z, Zainulabid, UA, Zárate, RN, Auton, A, Shelton, JF, Shastri, AJ, Weldon, CH, Filshtein-Sonmez, T, Coker, D, Symons, A, Aslibekyan, S, O’Connell, J

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