Recombination in the human Pseudoautosomal region PAR1 by Hinch, Anjali G, Altemose, Nicolas, Noor, Nudrat, Donnelly, Peter, Myers, Simon R

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The landscape of recombination in African Americans by Hinch, Anjali G., Tandon, Arti, Patterson, Nick, Song, Yunli, Rohland, Nadin, Palmer, Cameron D., Chen, Gary K., Wang, Kai, Buxbaum, Sarah G., Akylbekova, Ermeg L., Aldrich, Melinda C., Ambrosone, Christine B., Amos, Christopher, Bandera, Elisa V., Berndt, Sonja I., Bernstein, Leslie, Blot, William J., Bock, Cathryn H., Boerwinkle, Eric, Cai, Qiuyin, Caporaso, Neil, Casey, Graham, Adrienne Cupples, L., Deming, Sandra L., Ryan Diver, W., Divers, Jasmin, Fornage, Myriam, Gillanders, Elizabeth M., Glessner, Joseph, Harris, Curtis C., Hu, Jennifer J., Ingles, Sue A., Isaacs, William, John, Esther M., Linda Kao, W. H., Keating, Brendan, Kittles, Rick A., Kolonel, Laurence N., Larkin, Emma, Le Marchand, Loic, McNeill, Lorna H., Millikan, Robert C., Murphy, Musani, Solomon, Neslund-Dudas, Christine, Nyante, Sarah, Papanicolaou, George J., Press, Michael F., Psaty, Bruce M., Reiner, Alex P., Rich, Stephen S., Rodriguez-Gil, Jorge L., Rotter, Jerome I., Rybicki, Benjamin A., Schwartz, Ann G., Signorello, Lisa B., Spitz, Margaret, Strom, Sara S., Thun, Michael J., Tucker, Margaret A., Wang, Zhaoming, Wiencke, John K., Witte, John S., Wrensch, Margaret, Wu, Xifeng, Yamamura, Yuko, Zanetti, Krista A., Zheng, Wei, Ziegler, Regina G., Zhu, Xiaofeng, Redline, Susan, Hirschhorn, Joel N., Henderson, Brian E., Taylor Jr, Herman A., Price, Alkes L., Hakonarson, Hakon, Chanock, Stephen J., Haiman, Christopher A., Wilson, James G., Reich, David, Myers, Simon R.

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De novo variants in the RNU4-2 snRNA cause a frequent neurodevelopmental syndrome by Chen, Yuyang, Kim, Hyung Chul, Ljungdahl, Alicia, Stenton, Sarah L., Lord, Jenny, Lemire, Gabrielle, Martin-Geary, Alexandra C., Ganesh, Vijay S., Ma, Jialan, Ellingford, Jamie M., Delage, Erwan, D’Souza, Elston N., Dong, Shan, Adams, David R., Allan, Kirsten, Bakshi, Madhura, Baldwin, Erin E., Berger, Seth I., Brown, Natasha J., Burrage, Lindsay C., Chapman, Kimberly, Coman, David J., Compton, Alison G., Cunningham, Chloe A., D’Souza, Precilla, Danecek, Petr, Délot, Emmanuèle C., Dias, Kerith-Rae, Elias, Ellen R., Elmslie, Frances, Evans, Care-Anne, Ezell, Kimberly, Fraser, Jamie L., Gallacher, Lyndon, Genetti, Casie A., Grant, Christina L., Haack, Tobias, Higgs, Jenny E., Hinch, Anjali G., Hurles, Matthew E., Kuechler, Alma, Lecoquierre, François, Fevre, Anna Le, Leventer, Richard J., Liebelt, Jan E., Lindsay, Sarah, Lockhart, Paul J., Ma, Alan S., Macnamara, Ellen F., Mendez, Hector R., Metcalfe, Kay, Montgomery, Stephen B., Moosajee, Mariya, Nassogne, Marie-Cécile, Neumann, Serena, O’Donoghue, Michael, O’Leary, Melanie, Palmer, Elizabeth E., Pattani, Nikhil, Pitsava, Georgia, Pysar, Ryan, Rehm, Heidi L., Reuter, Chloe M., Revencu, Nicole, Riess, Angelika, Rodan, Lance, Roscioli, Tony, Rosenfeld, Jill A., Sachdev, Rani, Shaw-Smith, Charles J., Simons, Cas, Sisodiya, Sanjay M., Snell, Penny, St Clair, Laura, Stewart, Helen S., Tan, Natalie B., Temple, Suzanna E. L., Thorburn, David R., Tifft, Cynthia J., VanNoy, Grace E., Vilain, Eric, Viskochil, David H., Wedd, Laura, Wheeler, Matthew T., White, Susan M., Wojcik, Monica, Wolfe, Lynne A., Wolfenson, Zoe, Wright, Caroline F., Xiao, Changrui, Zocche, David, Rubenstein, John L., Markenscoff-Papadimitriou, Eirene, Fica, Sebastian M., Baralle, Diana, Depienne, Christel, MacArthur, Daniel G., Sanders, Stephan J., O’Donnell-Luria, Anne, Whiffin, Nicola

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Recombination in the Human Pseudoautosomal Region PAR1: e1004503 by Hinch, Anjali G, Altemose, Nicolas, Noor, Nudrat, Donnelly, Peter, Myers, Simon R

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Re-engineering the zinc fingers of PRDM9 reverses hybrid sterility in mice by Davies, Benjamin, Hatton, Edouard, Altemose, Nicolas, Hussin, Julie G., Pratto, Florencia, Zhang, Gang, Hinch, Anjali Gupta, Moralli, Daniela, Biggs, Daniel, Diaz, Rebeca, Preece, Chris, Li, Ran, Bitoun, Emmanuelle, Brick, Kevin, Green, Catherine M., Camerini-Otero, R. Daniel, Myers, Simon R., Donnelly, Peter

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Integrating sequence and array data to create an improved 1000 Genomes Project haplotype reference panel by Delaneau, Olivier, Marchini, Jonathan

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