Deficit of homozygosity among 1.52 million individuals and genetic causes of recessive lethality (vol 14, 3453, 2023) von Oddsson, AR, Sulem, P, Sveinbjornsson, G, Arnadottir, G, Steinthorsdottir, VM, Halldorsson, G, Atlason, B, Oskarsson, GO, Helgason, H, Nielsen, HS

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The Relationship Between Birth Weight and Blood Pressure in Childhood: A Population-Based Study von Steinthorsdottir, Sandra D., Eliasdottir, Sigridur B., Indridason, Olafur S., Palsson, Runolfur, Edvardsson, Vidar O.

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Genome-wide association scan meta-analysis identifies three Loci influencing adiposity and fat distribution von Lindgren, Cecilia M, Heid, Iris M, Randall, Joshua C, Lamina, Claudia, Steinthorsdottir, Valgerdur, Qi, Lu, Speliotes, Elizabeth K, Thorleifsson, Gudmar, Willer, Cristen J, Herrera, Blanca M, Jackson, Anne U, Lim, Noha, Scheet, Paul, Soranzo, Nicole, Amin, Najaf, Aulchenko, Yurii S, Chambers, John C, Drong, Alexander, Luan, Jian'an, Lyon, Helen N, Rivadeneira, Fernando, Sanna, Serena, Timpson, Nicholas J, Zillikens, M Carola, Zhao, Jing Hua, Almgren, Peter, Bandinelli, Stefania, Bennett, Amanda J, Bergman, Richard N, Bonnycastle, Lori L, Bumpstead, Suzannah J, Chanock, Stephen J, Cherkas, Lynn, Chines, Peter, Coin, Lachlan, Cooper, Cyrus, Crawford, Gabriel, Doering, Angela, Dominiczak, Anna, Doney, Alex S F, Ebrahim, Shah, Elliott, Paul, Erdos, Michael R, Estrada, Karol, Ferrucci, Luigi, Fischer, Guido, Forouhi, Nita G, Gieger, Christian, Grallert, Harald, Groves, Christopher J, Grundy, Scott, Guiducci, Candace, Hadley, David, Hamsten, Anders, Havulinna, Aki S, Hofman, Albert, Holle, Rolf, Holloway, John W, Illig, Thomas, Isomaa, Bo, Jacobs, Leonie C, Jameson, Karen, Jousilahti, Pekka, Karpe, Fredrik, Kuusisto, Johanna, Laitinen, Jaana, Lathrop, G Mark, Lawlor, Debbie A, Mangino, Massimo, McArdle, Wendy L, Meitinger, Thomas, Morken, Mario A, Morris, Andrew P, Munroe, Patricia, Narisu, Narisu, Nordström, Anna, Nordström, Peter, Oostra, Ben A, Palmer, Colin N A, Payne, Felicity, Peden, John F, Prokopenko, Inga, Renström, Frida, Ruokonen, Aimo, Salomaa, Veikko, Sandhu, Manjinder S, Scott, Laura J, Scuteri, Angelo, Silander, Kaisa, Song, Kijoung, Yuan, Xin, Stringham, Heather M, Swift, Amy J, Tuomi, Tiinamaija, Uda, Manuela, Vollenweider, Peter, Waeber, Gerard, Wallace, Chris, Walters, G Bragi, Weedon, Michael N

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Deficit of homozygosity among 1.52 million individuals and genetic causes of recessive lethality von Oddsson, Asmundur, Sulem, Patrick, Sveinbjornsson, Gardar, Arnadottir, Gudny A., Steinthorsdottir, Valgerdur, Halldorsson, Gisli H., Atlason, Bjarni A., Oskarsson, Gudjon R., Helgason, Hannes, Nielsen, Henriette Svarre, Westergaard, David, Karjalainen, Juha M., Katrinardottir, Hildigunnur, Fridriksdottir, Run, Jensson, Brynjar O., Tragante, Vinicius, Ferkingstad, Egil, Jonsson, Hakon, Gudjonsson, Sigurjon A., Beyter, Doruk, Moore, Kristjan H. S., Thordardottir, Helga B., Kristmundsdottir, Snaedis, Stefansson, Olafur A., Rantapää-Dahlqvist, Solbritt, Sonderby, Ida Elken, Didriksen, Maria, Stridh, Pernilla, Haavik, Jan, Tryggvadottir, Laufey, Frei, Oleksandr, Walters, G. Bragi, Kockum, Ingrid, Hjalgrim, Henrik, Olafsdottir, Thorunn A., Selbaek, Geir, Nyegaard, Mette, Erikstrup, Christian, Brodersen, Thorsten, Saevarsdottir, Saedis, Olsson, Tomas, Nielsen, Kaspar Rene, Haraldsson, Asgeir, Bruun, Mie Topholm, Hansen, Thomas Folkmann, Steingrimsdottir, Thora, Jacobsen, Rikke Louise, Lie, Rolv T., Djurovic, Srdjan, Alfredsson, Lars, Lopez de Lapuente Portilla, Aitzkoa, Brunak, Soren, Melsted, Pall, Halldorsson, Bjarni V., Saemundsdottir, Jona, Magnusson, Olafur Th, Padyukov, Leonid, Banasik, Karina, Rafnar, Thorunn, Askling, Johan, Klareskog, Lars, Pedersen, Ole Birger, Masson, Gisli, Havdahl, Alexandra, Nilsson, Bjorn, Andreassen, Ole A., Daly, Mark, Ostrowski, Sisse Rye, Jonsdottir, Ingileif, Stefansson, Hreinn, Holm, Hilma, Helgason, Agnar, Thorsteinsdottir, Unnur, Stefansson, Kari, Gudbjartsson, Daniel F.

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The impact of rare and low-frequency genetic variants in common disease von Bomba, Lorenzo, Walter, Klaudia, Soranzo, Nicole

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Neuregulin-1 polymorphism in late onset Alzheimer's disease families with psychoses von Go, Rodney C. P., Perry, Rodney T., Wiener, Howard, Bassett, Susan S., Blacker, Deborah, Devlin, Bernie, Sweet, Robert A.

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Assessing the Combined Impact of 18 Common Genetic Variants of Modest Effect Sizes on Type 2 Diabetes Risk von Lango, Hana, Palmer, Colin N A, Morris, Andrew D, Zeggini, Eleftheria, Hattersley, Andrew T, McCarthy, Mark I, Frayling, Timothy M, Weedon, Michael N

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Dominant PDX1 deficiency causes highly penetrant diabetes at different ages, associated with obesity and exocrine pancreatic deficiency: Lessons for precision medicine von Kouidrat, Youssef, Le Collen, Lauriane, Vaxillaire, Martine, Dechaume, Aurélie, Toussaint, Bénédicte, Vaillant, Emmanuel, Amanzougarene, Souhila, Derhourhi, Mehdi, Delemer, Brigitte, Azahaf, Mustapha, Froguel, Philippe, Bonnefond, Amélie

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Isolated populations and complex disease gene identification von Kristiansson, Kati, Naukkarinen, Jussi, Peltonen, Leena

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Genetics of murine type 2 diabetes and comorbidities von Lone, Iqbal M., Iraqi, Fuad A.

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Using Genomic Structural Equation Modeling to Partition the Genetic Covariance Between Birthweight and Cardiometabolic Risk Factors into Maternal and Offspring Components in the No... von Moen, Gunn-Helen, Nivard, Michel, Bhatta, Laxmi, Warrington, Nicole M, Willer, Cristen, Åsvold, Bjørn Olav, Brumpton, Ben, Evans, David M.

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Genetic Contributions to Risk of Adverse Pregnancy Outcomes von Hughes, Zachary H., Hughes, Lydia M., Khan, Sadiya S.

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Genome-wide association analysis identifies variants associated with nonalcoholic fatty liver disease that have distinct effects on metabolic traits von Speliotes, Elizabeth K, Yerges-Armstrong, Laura M, Wu, Jun, Hernaez, Ruben, Kim, Lauren J, Palmer, Cameron D, Gudnason, Vilmundur, Eiriksdottir, Gudny, Garcia, Melissa E, Launer, Lenore J, Nalls, Michael A, Clark, Jeanne M, Mitchell, Braxton D, Shuldiner, Alan R, Butler, Johannah L, Tomas, Marta, Hoffmann, Udo, Hwang, Shih-Jen, Massaro, Joseph M, O'Donnell, Christopher J, Sahani, Dushyant V, Salomaa, Veikko, Schadt, Eric E, Schwartz, Stephen M, Siscovick, David S, Voight, Benjamin F, Carr, J Jeffrey, Feitosa, Mary F, Harris, Tamara B, Fox, Caroline S, Smith, Albert V, Kao, W H Linda, Hirschhorn, Joel N, Borecki, Ingrid B

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Cisplatin-induced increase in heregulin 1 and its attenuation by the monoclonal ErbB3 antibody seribantumab in bladder cancer von Steele, Thomas M., Tsamouri, Maria Malvina, Siddiqui, Salma, Lucchesi, Christopher A., Vasilatis, Demitria, Mooso, Benjamin A., Durbin-Johnson, Blythe P., Ma, Ai-Hong, Hejazi, Nazila, Parikh, Mamta, Mudryj, Maria, Pan, Chong-xian, Ghosh, Paramita M.

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Latent autoimmune diabetes of the adult: current knowledge and uncertainty von Laugesen, E., Østergaard, J. A., Leslie, R. D. G.

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Candidate genes for age at menarche are associated with endometrial hyperplasia von Ponomarenko, Irina, Reshetnikov, Evgeny, Polonikov, Alexey, Sorokina, Inna, Yermachenko, Anna, Dvornyk, Volodymyr, Churnosov, Mikhail

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Endometriosis von Giudice, Linda C, Kao, Lee C

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Tau: From research to clinical development von Holtzman, David M, Carrillo, Maria C, Hendrix, James A, Bain, Lisa J, Catafau, Ana M, Gault, Laura M, Goedert, Michel, Mandelkow, Eckhard, Mandelkow, Eva-Maria, Miller, David S, Ostrowitzki, Susanne, Polydoro, Manuela, Smith, Sean, Wittmann, Marion, Hutton, Michael

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Propagation of Tau Aggregates and Neurodegeneration von Goedert, Michel, Eisenberg, David S, Crowther, R. Anthony

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Messenger RNA and MicroRNA transcriptomic signatures of cardiometabolic risk factors von McManus, David D, Rong, Jian, Huan, Tianxiao, Lacey, Sean, Tanriverdi, Kahraman, Munson, Peter J, Larson, Martin G, Joehanes, Roby, Murthy, Venkatesh, Shah, Ravi, Freedman, Jane E, Levy, Daniel

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