Asymmetric synthesis of unnatural α-amino acids through photoredox-mediated C-O bond activation of aliphatic alcohols by Alvey, Gregory R, Stepanova, Elena V, Shatskiy, Andrey, Lantz, Josefin, Willemsen, Rachel, Munoz, Alix, Dinér, Peter, Kärkäs, Markus D

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Blood pressure tracking during pregnancy and the risk of gestational hypertensive disorders: The Generation R Study by Gaillard, Romy, Bakker, Rachel, Willemsen, Sten P., Hofman, Albert, Steegers, Eric A.P., Jaddoe, Vincent W.V.

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Progressive cerebellar atrophy and polyneuropathy: expanding the spectrum of PNKP mutations by Poulton, Cathryn, Oegema, Renske, Heijsman, Daphne, Hoogeboom, Jeannette, Schot, Rachel, Stroink, Hans, Willemsen, Michèl A., Verheijen, Frans W., van de Spek, Peter, Kremer, Andreas, Mancini, Grazia M. S.

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Expanding the phenotype of ASXL3‐related syndrome: A comprehensive description of 45 unpublished individuals with inherited and de novo pathogenic variants in ASXL3 by Schirwani, Schaida, Albaba, Shadi, Carere, Deanna Alexis, Guillen Sacoto, Maria J., Milan Zamora, Francisca, Si, Yue, Rabin, Rachel, Pappas, John, Renaud, Deborah L., Hauser, Natalie, Reid, Evan, Blanchet, Patricia, Foulds, Nichola, Dixit, Abhijit, Fisher, Richard, Armstrong, Ruth, Isidor, Bertrand, Cogne, Benjamin, Schrier Vergano, Samantha, Demirdas, Serwet, Dykzeul, Natalie, Cohen, Julie S., Grand, Katheryn, Morel, Dayna, Slavotinek, Anne, Albassam, Hessa F., Naik, Swati, Dean, John, Ragge, Nicola, Cinzia, Costa, Tedesco, Maria Giovanna, Harrison, Rachel E., Bouman, Arjan, Palen, Emily, Challman, Thomas D., Willemsen, Marjolein H., Vogt, Julie, Cunniff, Christopher, Bergstrom, Katherine, Walia, Jagdeep S., Bruel, Ange‐Line, Kini, Usha, Alkuraya, Fowzan S., Slegesky, Valerie, Meeks, Naomi, Girotto, Paula, Johnson, Diana, Newbury‐Ecob, Ruth, Ockeloen, Charlotte W., Prontera, Paolo, Lynch, Sally Ann, Li, Dong, Graham, John M., Balasubramanian, Meena

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Clinical features and genotype–phenotype correlations in epilepsy patients with de novo DYNC1H1 variants by Cuccurullo, Claudia, Cerulli Irelli, Emanuele, Ugga, Lorenzo, Riva, Antonella, D'Amico, Alessandra, Cabet, Sara, Lesca, Gaetan, Bilo, Leonilda, Zara, Federico, Iliescu, Catrinel, Barca, Diana, Fung, France, Helbig, Katherine, Ortiz‐Gonzalez, Xilma, Schelhaas, Helenius J., Willemsen, Marjolein H., Linden, Inge, Canafoglia, Laura, Courage, Carolina, Gommaraschi, Samuele, Gonzalez‐Alegre, Pedro, Bardakjian, Tanya, Syrbe, Steffen, Schuler, Elisabeth, Lemke, Johannes R., Vari, Stella, Roende, Gitte, Bak, Mads, Huq, Mahbulul, Powis, Zoe, Johannesen, Katrine M., Hammer, Trine Bjørg, Møller, Rikke S., Rabin, Rachel, Pappas, John, Zupanc, Mary L., Zadeh, Neda, Cohen, Julie, Naidu, Sakkubai, Krey, Ilona, Saneto, Russell, Thies, Jenny, Licchetta, Laura, Tinuper, Paolo, Bisulli, Francesca, Minardi, Raffaella, Bayat, Allan, Villeneuve, Nathalie, Molinari, Florence, Salimi Dafsari, Hormos, Moller, Birk, Le Roux, Marie, Houdayer, Clara, Vecchi, Marilena, Mammi, Isabella, Fiorini, Elena, Proietti, Jacopo, Ferri, Sofia, Cantalupo, Gaetano, Battaglia, Domenica Immacolata, Gambardella, Maria Luigia, Contaldo, Ilaria, Brogna, Claudia, Trivisano, Marina, De Dominicis, Angela, Bova, Stefania Maria, Gardella, Elena, Striano, Pasquale, Coppola, Antonietta

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Association between overweight and obesity with coronary artery bypass graft failure: an individual patient data analysis of clinical trials by An, Kevin R, Sandner, Sigrid, Redfors, Björn, Alexander, John H, Alzghari, Talal, Caldonazo, Tulio, Cancelli, Gianmarco, Dell’Aquila, Michele, Dimagli, Arnaldo, Gibson, C Michael, Harik, Lamia, Heise, Rachel, Kulik, Alexander, Lamy, Andre, Leith, Jordan, Peper, Joyce, Perezgrovas-Olaria, Roberto, Rossi, Camilla S, Ruel, Marc, Soletti, Giovanni Jr, Ten Berg, Jurrien M, Willemsen, Laura M, Wojdyla, Daniel M, Zhao, Qiang, Zhu, Yunpeng, Verma, Subodh, Gaudino, Mario F L

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Mutation in the AP4M1 Gene Provides a Model for Neuroaxonal Injury in Cerebral Palsy by Verkerk, Annemieke J.M.H., Schot, Rachel, Dumee, Belinda, Schellekens, Karlijn, Swagemakers, Sigrid, Bertoli-Avella, Aida M., Lequin, Maarten H., Dudink, Jeroen, Govaert, Paul, van Zwol, A.L., Hirst, Jennifer, Wessels, Marja W., Catsman-Berrevoets, Coriene, Verheijen, Frans W., de Graaff, Esther, de Coo, Irenaeus F.M., Kros, Johan M., Willemsen, Rob, Willems, Patrick J., van der Spek, Peter J., Mancini, Grazia M.S.

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Germline AGO2 mutations impair RNA interference and human neurological development by Lessel, Davor, Zeitler, Daniela M., Reijnders, Margot R. F., Kazantsev, Andriy, Hassani Nia, Fatemeh, Bartholomäus, Alexander, Martens, Victoria, Bruckmann, Astrid, Graus, Veronika, McConkie-Rosell, Allyn, McDonald, Marie, Lozic, Bernarda, Tan, Ee-Shien, Gerkes, Erica, Johannsen, Jessika, Denecke, Jonas, Telegrafi, Aida, Zonneveld-Huijssoon, Evelien, Lemmink, Henny H., Cham, Breana W. M., Kovacevic, Tanja, Ramsdell, Linda, Foss, Kimberly, Le Duc, Diana, Mitter, Diana, Syrbe, Steffen, Merkenschlager, Andreas, Sinnema, Margje, Panis, Bianca, Lazier, Joanna, Osmond, Matthew, Hartley, Taila, Mortreux, Jeremie, Busa, Tiffany, Missirian, Chantal, Prasun, Pankaj, Lüttgen, Sabine, Mannucci, Ilaria, Lessel, Ivana, Schob, Claudia, Kindler, Stefan, Pappas, John, Rabin, Rachel, Willemsen, Marjolein, Gardeitchik, Thatjana, Löhner, Katharina, Rump, Patrick, Dias, Kerith-Rae, Evans, Carey-Anne, Andrews, Peter Ian, Roscioli, Tony, Brunner, Han G., Chijiwa, Chieko, Lewis, M. E. Suzanne, Jamra, Rami Abou, Dyment, David A., Boycott, Kym M., Stegmann, Alexander P. A., Kubisch, Christian, Tan, Ene-Choo, Mirzaa, Ghayda M., McWalter, Kirsty, Kleefstra, Tjitske, Pfundt, Rolph, Ignatova, Zoya, Meister, Gunter, Kreienkamp, Hans-Jürgen

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Loss of Gap Junction Delta-2 (GJD2) gene orthologs leads to refractive error in zebrafish by Quint, Wim H., Tadema, Kirke C. D., de Vrieze, Erik, Lukowicz, Rachel M., Broekman, Sanne, Winkelman, Beerend H. J., Hoevenaars, Melanie, de Gruiter, H. Martijn, van Wijk, Erwin, Schaeffel, Frank, Meester-Smoor, Magda, Miller, Adam C., Willemsen, Rob, Klaver, Caroline C. W., Iglesias, Adriana I.

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Genetic Relationship between Schizophrenia and Nicotine Dependence by Chen, Jingchun, Bacanu, Silviu-Alin, Yu, Hui, Zhao, Zhongming, Jia, Peilin, Kendler, Kenneth S., Kranzler, Henry R., Gelernter, Joel, Farrer, Lindsay, Minica, Camelia, Pool, Rene, Milaneschi, Yuri, Boomsma, Dorret I., Penninx, Brenda W. J. H., Tyndale, Rachel F., Ware, Jennifer J., Vink, Jacqueline M., Kaprio, Jaakko, Munafò, Marcus, Chen, Xiangning

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De Novo Truncating Mutations in the Last and Penultimate Exons of PPM1D Cause an Intellectual Disability Syndrome by Jansen, Sandra, Geuer, Sinje, Pfundt, Rolph, Brough, Rachel, Ghongane, Priyanka, Herkert, Johanna C., Marco, Elysa J., Willemsen, Marjolein H., Kleefstra, Tjitske, Hannibal, Mark, Shieh, Joseph T., Lynch, Sally Ann, Flinter, Frances, FitzPatrick, David R., Gardham, Alice, Bernhard, Birgitta, Ragge, Nicola, Newbury-Ecob, Ruth, Bernier, Raphael, Kvarnung, Malin, Magnusson, E.A. Helena, Wessels, Marja W., van Slegtenhorst, Marjon A., Monaghan, Kristin G., de Vries, Petra, Veltman, Joris A., Lord, Christopher J., Vissers, Lisenka E.L.M., de Vries, Bert B.A.

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Genome-Wide Meta-Analysis of Cotinine Levels in Cigarette Smokers Identifies Locus at 4q13.2 by Ware, Jennifer J., Chen, Xiangning, Vink, Jacqueline, Loukola, Anu, Minica, Camelia, Pool, Rene, Milaneschi, Yuri, Mangino, Massimo, Menni, Cristina, Chen, Jingchun, Peterson, Roseann E., Auro, Kirsi, Lyytikäinen, Leo-Pekka, Wedenoja, Juho, Stiby, Alexander I., Hemani, Gibran, Willemsen, Gonneke, Hottenga, Jouke Jan, Korhonen, Tellervo, Heliövaara, Markku, Perola, Markus, Rose, Richard J., Paternoster, Lavinia, Timpson, Nic, Wassenaar, Catherine A., Zhu, Andy Z. X., Davey Smith, George, T. Raitakari, Olli, Lehtimäki, Terho, Kähönen, Mika, Koskinen, Seppo, Spector, Timothy, Penninx, Brenda W. J. H., Salomaa, Veikko, Boomsma, Dorret I., Tyndale, Rachel F., Kaprio, Jaakko, Munafò, Marcus R.

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Spatiotemporal processing deficits in female CGG KI mice modeling the fragile X premutation by Borthwell, Rachel M., Hunsaker, Michael R., Willemsen, Rob, Berman, Robert F.

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Progressive cerebellar atrophy and polyneuropathy: expanding the spectrum of PNKP mutations by Poulton, Cathryn, Oegema, Renske, Heijsman, Daphne, Hoogeboom, Jeannette, Schot, Rachel, Stroink, Hans, Willemsen, Michèl A., Verheijen, Frans W., van de Spek, Peter, Kremer, Andreas, Mancini, Grazia M. S.

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Genome-Wide Meta-Analyses of FTND and TTFC Phenotypes by Chen, Jingchun, Loukola, Anu, Gillespie, Nathan A, Peterson, Roseann, Jia, Peilin, Riley, Brien, Maes, Hermine, Dick, Daniella M, Kendler, Kenneth S, Damaj, M Imad, Miles, Michael F, Zhao, Zhongming, Li, Ming D, Vink, Jacqueline M, Minica, Camelia C, Willemsen, Gonneke, Boomsma, Dorret I, Qaiser, Beenish, Madden, Pamela A F, Korhonen, Tellervo, Jousilahti, Pekka, Hällfors, Jenni, Gelernter, Joel, Kranzler, Henry R, Sherva, Richard, Farrer, Lindsay, Maher, Brion, Vanyukov, Michael, Taylor, Michelle, Ware, Jenifer J, Munafò, Marcus R, Lutz, Sharon M, Hokanson, John E, Gu, Fangyi, Landi, Maria T, Caporaso, Neil E, Hancock, Dana B, Gaddis, Nathan C, Baker, Timothy B, Bierut, Laura J, Johnson, Eric O, Chenoweth, Meghan, Lerman, Caryn, Tyndale, Rachel, Kaprio, Jaakko, Chen, Xiangning

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Human USP18 deficiency underlies type 1 interferonopathy leading to severe pseudo-TORCH syndrome by Meuwissen, Marije E C, Schot, Rachel, Buta, Sofija, Oudesluijs, Grétel, Tinschert, Sigrid, Speer, Scott D, Li, Zhi, van Unen, Leontine, Heijsman, Daphne, Goldmann, Tobias, Lequin, Maarten H, Kros, Johan M, Stam, Wendy, Hermann, Mark, Willemsen, Rob, Brouwer, Rutger W W, Van IJcken, Wilfred F J, Martin-Fernandez, Marta, de Coo, Irenaeus, Dudink, Jeroen, de Vries, Femke A T, Bertoli Avella, Aida, Prinz, Marco, Crow, Yanick J, Verheijen, Frans W, Pellegrini, Sandra, Bogunovic, Dusan, Mancini, Grazia M S

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Obesity-susceptibility loci have a limited influence on birth weight: a meta-analysis of up to 28,219 individuals by Kilpeläinen, Tuomas O, den Hoed, Marcel, Ong, Ken K, Grøntved, Anders, Brage, Soren, Consortium, Early Growth Genetics, Jameson, Karen, Cooper, Cyrus, Khaw, Kay-Tee, Ekelund, Ulf, Wareham, Nicholas J, Loos, Ruth JF

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NPHP4 Variants Are Associated With Pleiotropic Heart Malformations by French, Vanessa M, van de Laar, Ingrid M.B.H, Wessels, Marja W, Rohe, Christan, Roos-Hesselink, Jolien W, Wang, Guangliang, Frohn-Mulder, Ingrid M.E, Severijnen, Lies-Anne, de Graaf, Bianca M, Schot, Rachel, Breedveld, Guido, Mientjes, Edwin, van Tienhoven, Marianne, Jadot, Elodie, Jiang, Zhengxin, Verkerk, Annemieke, Swagemakers, Sigrid, Venselaar, Hanka, Rahimi, Zohreh, Najmabadi, Hossein, Meijers-Heijboer, Hanne, de Graaff, Esther, Helbing, Wim A, Willemsen, Rob, Devriendt, Koen, Belmont, John W, Oostra, Ben A, Amack, Jeffrey D, Bertoli-Avella, Aida M

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Genome-wide association study of offspring birth weight in 86 577 women identifies five novel loci and highlights maternal genetic effects that are independent of fetal genetics by Beaumont, Robin N, Warrington, Nicole M, Cavadino, Alana, Tyrrell, Jessica, Nodzenski, Michael, Horikoshi, Momoko, Geller, Frank, Myhre, Ronny, Richmond, Rebecca C, Paternoster, Lavinia, Bradfield, Jonathan P, Kreiner-Møller, Eskil, Huikari, Ville, Metrustry, Sarah, Lunetta, Kathryn L, Painter, Jodie N, Hottenga, Jouke-Jan, Allard, Catherine, Barton, Sheila J, Espinosa, Ana, Marsh, Julie A, Potter, Catherine, Zhang, Ge, Ang, Wei, Berry, Diane J, Bouchard, Luigi, Das, Shikta, Hakonarson, Hakon, Heikkinen, Jani, Helgeland, Øyvind, Hocher, Berthold, Hofman, Albert, Inskip, Hazel M, Jones, Samuel E, Kogevinas, Manolis, Lind, Penelope A, Marullo, Letizia, Medland, Sarah E, Murray, Anna, Murray, Jeffrey C, Njølstad, Pål Rasmus, Nohr, Ellen A, Reichetzeder, Christoph, Ring, Susan M, Ruth, Katherine S, Santa-Marina, Loreto, Scholtens, Denise M, Sebert, Sylvain, Sengpiel, Verena, Tuke, Marcus A, Vaudel, Marc, Weedon, Michael N, Willemsen, Gonneke, Wood, Andrew R, Yaghootkar, Hanieh, Muglia, Louis J, Bartels, Meike, Relton, Caroline L, Pennell, Craig E, Chatzi, Leda, Estivill, Xavier, Holloway, John W, Boomsma, Dorret I, Montgomery, Grant W, Murabito, Joanne M, Spector, Tim D, Power, Christine, Järvelin, Marjo-Riitta, Bisgaard, Hans, Grant, Struan F.A, Sørensen, Thorkild I.A, Jaddoe, Vincent W, Jacobsson, Bo, Melbye, Mads, McCarthy, Mark I, Hattersley, Andrew T, Hayes, M. Geoffrey, Hivert, Marie-France, Frayling, Timothy M, Felix, Janine F, Hyppönen, Elina, Lowe, William L, Evans, David M, Lawlor, Debbie A, Feenstra, Bjarke, Freathy, Rachel M

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Genome-wide association study of offspring birth weight in 86 577 women identifies five novel loci and highlights maternal genetic effects that are independent of fetal genetics by Beaumont, Robin N, Warrington, Nicole M, Cavadino, Alana, Tyrrell, Jessica, Nodzenski, Michael, Horikoshi, Momoko, Geller, Frank, Myhre, Ronny, Richmond, Rebecca C, Paternoster, Lavinia, Bradfield, Jonathan P, Kreiner-Møller, Eskil, Huikari, Ville, Metrustry, Sarah, Lunetta, Kathryn L, Painter, Jodie N, Hottenga, Jouke-Jan, Allard, Catherine, Barton, Sheila J, Espinosa, Ana, Marsh, Julie A, Potter, Catherine, Zhang, Ge, Ang, Wei, Berry, Diane J, Bouchard, Luigi, Das, Shikta, Hakonarson, Hakon, Heikkinen, Jani, Helgeland, Øyvind, Hocher, Berthold, Hofman, Albert, Inskip, Hazel M, Jones, Samuel E, Kogevinas, Manolis, Lind, Penelope A, Marullo, Letizia, Medland, Sarah E, Murray, Anna, Murray, Jeffrey C, Njølstad, Pål Rasmus, Nohr, Ellen A, Reichetzeder, Christoph, Ring, Susan M, Ruth, Katherine S, Santa-Marina, Loreto, Scholtens, Denise M, Sebert, Sylvain, Sengpiel, Verena, Tuke, Marcus A, Vaudel, Marc, Weedon, Michael N, Willemsen, Gonneke, Wood, Andrew R, Yaghootkar, Hanieh, Muglia, Louis J, Bartels, Meike, Relton, Caroline L, Pennell, Craig E, Chatzi, Leda, Estivill, Xavier, Holloway, John W, Boomsma, Dorret I, Montgomery, Grant W, Murabito, Joanne M, Spector, Tim D, Power, Christine, Järvelin, Marjo-Riitta, Bisgaard, Hans, Grant, Struan F.A, Sørensen, Thorkild I.A, Jaddoe, Vincent W, Jacobsson, Bo, Melbye, Mads, McCarthy, Mark I, Hattersley, Andrew T, Hayes, M. Geoffrey, Hivert, Marie-France, Frayling, Timothy M, Felix, Janine F, Hyppönen, Elina, Lowe, William L, Evans, David M, Lawlor, Debbie A, Feenstra, Bjarke, Freathy, Rachel M

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