Probabilistic Machine Learning Could Eliminate No Fault Found von Teixeira, Rodrigo E., Morris, Kari E., Sautter, F. Christian

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Genome Analyses of >200,000 Individuals Identify 58 Loci for Chronic Inflammation and Highlight Pathways that Link Inflammation and Complex Disorders von Võsa, Urmo, Stathopoulou, Maria G., de Vries, Paul S., Tanaka, Toshiko, Wu, Ying, Karlsson, Robert, Pool, René, Kemp, John P., Verweij, Niek, Smith, Albert V., Huq, Mahmudul, Deelen, Joris, Alizadeh, Behrooz Z., van der Harst, Pim, Navis, Gerjan, Snieder, Harold, Chasman, Daniel I., Meigs, James, Ligthart, Symen, Bis, Josh, Gross, Myron, Koenig, Wolfgang, Uher, Rudolf, Ward-Caviness, Cavin, Boerwinkle, Eric, Stacey, David, Eriksson, Johan, Lahti, Jari, Schraut, Katharina E., Suktitipat, Bhoom, Nutile, Teresa, Schork, Nicholas, Thiering, Elisabeth, Mahajan, Anubha, Aslibekyan, Stella, Yengo, Loïc, Rajan, Kumar B., Timpson, Nicholas, Huang, Hongyan, Uh, Hae-Won, Yanek, Lisa R., Verbanck, Marie, Magnusson, Patrik K.E., Ballantyne, Christie M., Montgomery, Grant W., Rueedi, Rico, Steri, Maristella, Stott, David J., Felix, Stephan B., Kraft, Peter, Seppälä, Ilkka, Williams, Stephen R., Moed, Matthijs, Langenberg, Claudia, Räikkönen, Katri, Sale, Michele M., Chen, Yii-Der I., James, Alan L., Soranzo, Nicole, Berenson, Gerald S., Liewald, David, Beilby, John, Ryan, Kathleen A., Balkau, Beverly, Paternoster, Lavinia, Kähönen, Mika, Sattar, Naveed, van Heemst, Diana, Gambaro, Giovanni, Ferrucci, Luigi, Karlsson, Magnus, Lind, Lars, Mori, Trevor A., Buckley, Brendan M., de Craen, Anton J.M., Scott, Rodney J., Strachan, David P., Jarvelin, Marjo-Riitta, Jukema, J. Wouter, Hamsten, Anders, Gudnason, Vilmundur, Qi, Lu, März, Winfried, Penninx, Brenda W.J.H., Worrall, Bradford B., Gibson, Greg, Oldehinkel, Albertine J., Murray, Sarah S., Pramstaller, Peter P., Deary, Ian J., Desch, Karl C., Hayward, Caroline, Arnett, Donna K., Jess, Tine, Psaty, Bruce M., Tracy, Russell P., Nolte, Ilja M., Visvikis-Siest, Sophie, Franke, Lude, Franco, Oscar H.

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Survival of children with rare structural congenital anomalies: a multi-registry cohort study von Coi, Alessio, Santoro, Michele, Pierini, Anna, Rankin, Judith, Glinianaia, Svetlana V, Tan, Joachim, Reid, Abigail-Kate, Garne, Ester, Loane, Maria, Given, Joanne, Ballardini, Elisa, Cavero-Carbonell, Clara, de Walle, Hermien E K, Gatt, Miriam, García-Villodre, Laura, Gissler, Mika, Jordan, Sue, Kiuru-Kuhlefelt, Sonja, Kjaer Urhoj, Stine, Klungsøyr, Kari, Lelong, Nathalie, Lutke, L Renée, Neville, Amanda J, Rahshenas, Makan, Scanlon, Ieuan, Wellesley, Diana, Morris, Joan K

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Meta-analysis identifies five novel loci associated with endometriosis highlighting key genes involved in hormone metabolism von Sapkota, Yadav, Steinthorsdottir, Valgerdur, Morris, Andrew P., Fassbender, Amelie, Rahmioglu, Nilufer, De Vivo, Immaculata, Buring, Julie E., Zhang, Futao, Edwards, Todd L., Jones, Sarah, O, Dorien, Peterse, Daniëlle, Rexrode, Kathryn M., Ridker, Paul M., Schork, Andrew J., MacGregor, Stuart, Martin, Nicholas G., Becker, Christian M., Adachi, Sosuke, Yoshihara, Kosuke, Enomoto, Takayuki, Takahashi, Atsushi, Kamatani, Yoichiro, Matsuda, Koichi, Kubo, Michiaki, Thorleifsson, Gudmar, Geirsson, Reynir T., Thorsteinsdottir, Unnur, Wallace, Leanne M., Yang, Jian, Velez Edwards, Digna R., Nyegaard, Mette, Low, Siew-Kee, Zondervan, Krina T., Missmer, Stacey A., D'Hooghe, Thomas, Montgomery, Grant W., Chasman, Daniel I., Stefansson, Kari, Tung, Joyce Y., Nyholt, Dale R.

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Dostarlimab for Primary Advanced or Recurrent Endometrial Cancer von Mirza, Mansoor R., Chase, Dana M., Slomovitz, Brian M., dePont Christensen, René, Novák, Zoltán, Black, Destin, Gilbert, Lucy, Sharma, Sudarshan, Valabrega, Giorgio, Landrum, Lisa M., Hanker, Lars C., Stuckey, Ashley, Boere, Ingrid, Gold, Michael A., Auranen, Annika, Pothuri, Bhavana, Cibula, David, McCourt, Carolyn, Raspagliesi, Francesco, Shahin, Mark S., Gill, Sarah E., Monk, Bradley J., Buscema, Joseph, Herzog, Thomas J., Copeland, Larry J., Tian, Min, He, Zangdong, Stevens, Shadi, Zografos, Eleftherios, Coleman, Robert L., Powell, Matthew A.

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A reference panel of 64,976 haplotypes for genotype imputation von McCarthy, Shane, Das, Sayantan, Kretzschmar, Warren, Delaneau, Olivier, Wood, Andrew R, Teumer, Alexander, Kang, Hyun Min, Fuchsberger, Christian, Danecek, Petr, Sharp, Kevin, Luo, Yang, Sidore, Carlo, Kwong, Alan, Timpson, Nicholas, Koskinen, Seppo, Vrieze, Scott, Scott, Laura J, Zhang, He, Mahajan, Anubha, Veldink, Jan, Peters, Ulrike, Pato, Carlos, van Duijn, Cornelia M, Gillies, Christopher E, Gandin, Ilaria, Mezzavilla, Massimo, Gilly, Arthur, Cocca, Massimiliano, Traglia, Michela, Angius, Andrea, Barrett, Jeffrey C, Boomsma, Dorrett, Branham, Kari, Breen, Gerome, Brummett, Chad M, Busonero, Fabio, Campbell, Harry, Chan, Andrew, Chen, Sai, Chew, Emily, Collins, Francis S, Corbin, Laura J, Smith, George Davey, Dedoussis, George, Dorr, Marcus, Farmaki, Aliki-Eleni, Ferrucci, Luigi, Forer, Lukas, Fraser, Ross M, Gabriel, Stacey, Levy, Shawn, Groop, Leif, Harrison, Tabitha, Hattersley, Andrew, Holmen, Oddgeir L, Hveem, Kristian, Kretzler, Matthias, Lee, James C, McGue, Matt, Meitinger, Thomas, Melzer, David, Min, Josine L, Mohlke, Karen L, Vincent, John B, Nauck, Matthias, Nickerson, Deborah, Palotie, Aarno, Pato, Michele, Pirastu, Nicola, McInnis, Melvin, Richards, J Brent, Sala, Cinzia, Salomaa, Veikko, Schlessinger, David, Schoenherr, Sebastian, Slagboom, P Eline, Small, Kerrin, Spector, Timothy, Stambolian, Dwight, Tuke, Marcus, Tuomilehto, Jaakko, Van den Berg, Leonard H, Van Rheenen, Wouter, Volker, Uwe, Wijmenga, Cisca, Toniolo, Daniela, Zeggini, Eleftheria, Gasparini, Paolo, Sampson, Matthew G, Wilson, James F, Frayling, Timothy, de Bakker, Paul I W, Swertz, Morris A, McCarroll, Steven, Kooperberg, Charles, Dekker, Annelot, Altshuler, David, Willer, Cristen, Iacono, William, Ripatti, Samuli

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Survival, hospitalisation and surgery in children born with Pierre Robin sequence: a European population-based cohort study von Santoro, M, Garne, E, Coi, A, Tan, J, Loane, M, Ballardini, E, Cavero-Carbonell, C, de Walle, HE, Gatt, M, Gissler, M, Jordan, S, Klungsoyr, K, Lelong, N, Urhoj, SK, Wellesley, DG, Morris, JK

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Population-based trends in pregnancy hypertension and pre-eclampsia: an international comparative study von Roberts, Christine L, Ford, Jane B, Algert, Charles S, Antonsen, Sussie, Chalmers, James, Cnattingius, Sven, Gokhale, Manjusha, Kotelchuck, Milton, Melve, Kari K, Langridge, Amanda, Morris, Carole, Morris, Jonathan M, Nassar, Natasha, Norman, Jane E, Norrie, John, Sørensen, Henrik Toft, Walker, Robin, Weir, Christopher J

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Trends in congenital anomalies in Europe from 1980 to 2012 von Morris, Joan K, Springett, Anna L, Greenlees, Ruth, Loane, Maria, Addor, Marie-Claude, Arriola, Larraitz, Barisic, Ingeborg, Bergman, Jorieke E H, Csaky-Szunyogh, Melinda, Dias, Carlos, Draper, Elizabeth S, Garne, Ester, Gatt, Miriam, Khoshnood, Babak, Klungsoyr, Kari, Lynch, Catherine, McDonnell, Robert, Nelen, Vera, Neville, Amanda J, O'Mahony, Mary, Pierini, Anna, Queisser-Luft, Annette, Randrianaivo, Hanitra, Rankin, Judith, Rissmann, Anke, Kurinczuk, Jennifer, Tucker, David, Verellen-Dumoulin, Christine, Wellesley, Diana, Dolk, Helen

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Ten-Year Survival of Children With Congenital Anomalies: A European Cohort Study von Glinianaia, Svetlana V, Rankin, Judith, Pierini, Anna, Coi, Alessio, Santoro, Michele, Tan, Joachim, Reid, Abigail, Garne, Ester, Loane, Maria, Given, Joanne, Cavero-Carbonell, Clara, de Walle, Hermien E K, Gatt, Miriam, Gissler, Mika, Heino, Anna, Khoshnood, Babak, Klungsøyr, Kari, Lelong, Nathalie, Neville, Amanda J, Thayer, Daniel S, Tucker, David, Urhøj, Stine K, Wellesley, Diana, Zurriaga, Oscar, Morris, Joan K

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Post-Transcriptional Genetic Silencing of BCL11A to Treat Sickle Cell Disease von Esrick, Erica B, Lehmann, Leslie E, Biffi, Alessandra, Achebe, Maureen, Brendel, Christian, Ciuculescu, Marioara F, Daley, Heather, MacKinnon, Brenda, Morris, Emily, Federico, Amy, Abriss, Daniela, Boardman, Kari, Khelladi, Radia, Shaw, Kit, Negre, Helene, Negre, Olivier, Nikiforow, Sarah, Ritz, Jerome, Pai, Sung-Yun, London, Wendy B, Dansereau, Colleen, Heeney, Matthew M, Armant, Myriam, Manis, John P, Williams, David A

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Prevalence of microcephaly in Europe: population based study von Morris, Joan K, Rankin, Judith, Garne, Ester, Loane, Maria, Greenlees, Ruth, Addor, Marie-Claude, Arriola, Larraitz, Barisic, Ingeborg, Bergman, Jorieke E H, Csaky-Szunyogh, Melinda, Dias, Carlos, Draper, Elizabeth S, Gatt, Miriam, Khoshnood, Babak, Klungsoyr, Kari, Kurinczuk, Jennifer J, Lynch, Catherine, McDonnell, Robert, Nelen, Vera, Neville, Amanda J, O’Mahony, Mary T, Pierini, Anna, Randrianaivo, Hanitra, Rissmann, Anke, Tucker, David, Verellen-Dumoulin, Christine, de Walle, Hermien E K, Wellesley, Diana, Wiesel, Awi, Dolk, Helen

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Ten-year survival of children with trisomy 13 or trisomy 18: a multi-registry European cohort study von Glinianaia, SV, Rankin, J, Tan, JC, Loane, M, Garne, E, Cavero-Carbonell, C, de Walle, HEK, Gatt, M, Gissler, M, Klungsoyr, K, Lelong, N, Neville, A, Pierini, A, Tucker, DF, Urhoj, SK, Wellesley, DG, Morris, JK

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Mendelian randomization of blood lipids for coronary heart disease von Holmes, Michael V, Asselbergs, Folkert W, Palmer, Tom M, Drenos, Fotios, Lanktree, Matthew B, Nelson, Christopher P, Dale, Caroline E, Padmanabhan, Sandosh, Finan, Chris, Swerdlow, Daniel I, Tragante, Vinicius, van Iperen, Erik P A, Sivapalaratnam, Suthesh, Shah, Sonia, Elbers, Clara C, Shah, Tina, Engmann, Jorgen, Giambartolomei, Claudia, White, Jon, Zabaneh, Delilah, Sofat, Reecha, McLachlan, Stela, Doevendans, Pieter A, Balmforth, Anthony J, Hall, Alistair S, North, Kari E, Almoguera, Berta, Hoogeveen, Ron C, Cushman, Mary, Fornage, Myriam, Patel, Sanjay R, Redline, Susan, Siscovick, David S, Tsai, Michael Y, Karczewski, Konrad J, Hofker, Marten H, Verschuren, W Monique, Bots, Michiel L, van der Schouw, Yvonne T, Melander, Olle, Dominiczak, Anna F, Morris, Richard, Ben-Shlomo, Yoav, Price, Jackie, Kumari, Meena, Baumert, Jens, Peters, Annette, Thorand, Barbara, Koenig, Wolfgang, Gaunt, Tom R, Humphries, Steve E, Clarke, Robert, Watkins, Hugh, Farrall, Martin, Wilson, James G, Rich, Stephen S, de Bakker, Paul I W, Lange, Leslie A, Davey Smith, George, Reiner, Alex P, Talmud, Philippa J, Kivimäki, Mika, Lawlor, Debbie A, Dudbridge, Frank, Samani, Nilesh J, Keating, Brendan J, Hingorani, Aroon D, Casas, Juan P

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Mice with an adipocyte-specific lipin 1 separation-of-function allele reveal unexpected roles for phosphatidic acid in metabolic regulation von Mitra, Mayurranjan S., Chen, Zhouji, Ren, Hongmei, Harris, Thurl E., Chambers, Kari T., Hall, Angela M., Nadra, Karim, Klein, Samuel, Chrast, Roman, Su, Xiong, Morris, Andrew J., Finck, Brian N.

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Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection von Pardiñas, Antonio F., Holmans, Peter, Pocklington, Andrew J., Escott-Price, Valentina, Ripke, Stephan, Carrera, Noa, Legge, Sophie E., Bishop, Sophie, Cameron, Darren, Hamshere, Marian L., Han, Jun, Hubbard, Leon, Lynham, Amy, Mantripragada, Kiran, Rees, Elliott, MacCabe, James H., McCarroll, Steven A., Baune, Bernhard T., Breen, Gerome, Byrne, Enda M., Dannlowski, Udo, Eley, Thalia C., Hayward, Caroline, Martin, Nicholas G., McIntosh, Andrew M., Plomin, Robert, Porteous, David J., Wray, Naomi R., Caballero, Armando, Geschwind, Daniel H., Huckins, Laura M., Ruderfer, Douglas M., Santiago, Enrique, Sklar, Pamela, Stahl, Eli A., Won, Hyejung, Agerbo, Esben, Als, Thomas D., Andreassen, Ole A., Bækvad-Hansen, Marie, Mortensen, Preben Bo, Pedersen, Carsten Bøcker, Børglum, Anders D., Bybjerg-Grauholm, Jonas, Djurovic, Srdjan, Durmishi, Naser, Pedersen, Marianne Giørtz, Golimbet, Vera, Grove, Jakob, Hougaard, David M., Mattheisen, Manuel, Molden, Espen, Mors, Ole, Nordentoft, Merete, Pejovic-Milovancevic, Milica, Sigurdsson, Engilbert, Silagadze, Teimuraz, Hansen, Christine Søholm, Stefansson, Kari, Stefansson, Hreinn, Steinberg, Stacy, Tosato, Sarah, Werge, Thomas, Collier, David A., Rujescu, Dan, Kirov, George, Owen, Michael J., O’Donovan, Michael C., Walters, James T. R.

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Surveillance of multiple congenital anomalies; searching for new associations von Morris, Joan K, Bergman, Jorieke E H, Barisic, Ingeborg, Wellesley, Diana, Tucker, David, Limb, Elizabeth, Addor, Marie-Claude, Cavero-Carbonell, Clara, Matias Dias, Carlos, Draper, Elisabeth S, Echevarría-González-de-Garibay, Luis Javier, Gatt, Miriam, Klungsøyr, Kari, Lelong, Nathalie, Luyt, Karen, Materna-Kiryluk, Anna, Nelen, Vera, Neville, Amanda, Perthus, Isabelle, Pierini, Anna, Randrianaivo-Ranjatoelina, Hanitra, Rankin, Judith, Rissmann, Anke, Rouget, Florence, Sayers, Geraldine, Wertelecki, Wladimir, Kinsner-Ovaskainen, Agnieszka, Garne, Ester

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Exome-wide association study of plasma lipids in >300,000 individuals von Peloso, Gina M, Wang, Xiao, Alam, Dewan, Arveiler, Dominique, Ballantyne, Christie M, Bis, Joshua C, Boerwinkle, Eric, Bork-Jensen, Jette, Brandslund, Ivan, Busonero, Fabio, Caulfield, Mark J, Chasman, Daniel I, Chen, Yii-Der Ida, Christensen, Cramer, Cucca, Francesco, Cupples, L Adrienne, Davies, Gail, Deary, Ian J, Dubé, Marie-Pierre, Ford, Ian, Fornage, Myriam, Fuster, Valentin, Ganesh, Santhi K, Giulianini, Franco, Grarup, Niels, Groop, Leif, Hansen, Torben, Harris, Tamara B, Hayward, Caroline, Hveem, Kristian, Jabeen, Sehrish, Jackson, Anne U, Jensen, Gorm B, Jørgensen, Marit E, Kamstrup, Pia R, Kanoni, Stavroula, Khera, Amit V, Koistinen, Heikki A, Kooperberg, Charles, Kuusisto, Johanna, Laakso, Markku, Langsted, Anne, Linneberg, Allan, Loos, Ruth J F, Lu, Yingchang, Malarstig, Anders, Manichaikul, Ani, Manning, Alisa K, Marouli, Eirini, Maschio, Andrea, Melander, Olle, Morrison, Alanna C, Mulas, Antonella, Neville, Matt J, Nielsen, Jonas B, Nordestgaard, Børge G, Mehran, Roxana, O'Donnell, Christoper J, Molony, Cliona M, Palmer, Colin N A, Pasko, Dorota, Peters, Annette, Pisinger, Charlotta, Polasek, Ozren, Poulter, Neil, Psaty, Bruce M, Rasheed, Asif, Reiner, Alex P, Robertson, Neil R, Rudan, Igor, Salomaa, Veikko, Sanna, Serena, Schmidt, Ellen M, Sever, Peter, Sevilla, Raquel S, Smith, Blair H, Speliotes, Elizabeth K, Stirrups, Kathleen E, Stitziel, Nathan, Surendran, Praveen, Tall, Alan R, Tsao, Philip S, van Zuydam, Natalie R, Varbo, Anette, Waldenberger, Melanie, Wareham, Nick J, Weeke, Peter E, Wessel, Jennifer, Wilson, James G, Wilson, Peter W F, Yaghootkar, Hanieh, Young, Robin, Zeggini, Eleftheria, Zhang, Weihua, Zhou, Wei, Howson, Joanna M M, McCarthy, Mark I, Cowan, Chad A, Deloukas, Panos, Kathiresan, Sekar

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Large-scale meta-analysis of genome-wide association data identifies six new risk loci for Parkinson's disease von Nalls, Mike A, Pankratz, Nathan, Lill, Christina M, Do, Chuong B, Hernandez, Dena G, Saad, Mohamad, DeStefano, Anita L, Kara, Eleanna, Bras, Jose, Sharma, Manu, Schulte, Claudia, Keller, Margaux F, Arepalli, Sampath, Letson, Christopher, Edsall, Connor, Stefansson, Hreinn, Liu, Xinmin, Pliner, Hannah, Lee, Joseph H, Cheng, Rong, Ikram, M Arfan, Ioannidis, John P A, Hadjigeorgiou, Georgios M, Bis, Joshua C, Martinez, Maria, Perlmutter, Joel S, Goate, Alison, Marder, Karen, Fiske, Brian, Sutherland, Margaret, Xiromerisiou, Georgia, Myers, Richard H, Clark, Lorraine N, Stefansson, Kari, Hardy, John A, Heutink, Peter, Chen, Honglei, Wood, Nicholas W, Houlden, Henry, Payami, Haydeh, Brice, Alexis, Scott, William K, Gasser, Thomas, Bertram, Lars, Eriksson, Nicholas, Foroud, Tatiana, Singleton, Andrew B

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Rare SLC13A1 variants associate with intervertebral disc disorder highlighting role of sulfate in disc pathology von Bjornsdottir, Gyda, Stefansdottir, Lilja, Thorleifsson, Gudmar, Sulem, Patrick, Norland, Kristjan, Ferkingstad, Egil, Oddsson, Asmundur, Zink, Florian, Lund, Sigrun H., Nawaz, Muhammad S., Bragi Walters, G., Skuladottir, Astros Th, Gudjonsson, Sigurjon A., Einarsson, Gudmundur, Halldorsson, Gisli H., Bjarnadottir, Valgerdur, Sveinbjornsson, Gardar, Helgadottir, Anna, Styrkarsdottir, Unnur, Gudmundsson, Larus J., Pedersen, Ole B., Hansen, Thomas Folkmann, Werge, Thomas, Banasik, Karina, Troelsen, Anders, Skou, Soren T., Thørner, Lise Wegner, Erikstrup, Christian, Nielsen, Kaspar Rene, Mikkelsen, Susan, Jonsdottir, Ingileif, Bjornsson, Aron, Olafsson, Ingvar H., Ulfarsson, Elfar, Blondal, Josep, Vikingsson, Arnor, Brunak, Soren, Ostrowski, Sisse R., Ullum, Henrik, Thorsteinsdottir, Unnur, Stefansson, Hreinn, Gudbjartsson, Daniel F., Thorgeirsson, Thorgeir E., Stefansson, Kari

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