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Investigating the genetic architecture of noncognitive skills using GWAS-by-subtraction
Investigating the genetic architecture of noncognitive skills using GWAS-by-subtraction
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Investigating the genetic architecture of noncognitive skills using GWAS-by-subtraction

Demange, Perline A ; Malanchini, Margherita ; Mallard, Travis T ; Biroli, Pietro ; Cox, Simon R ; Grotzinger, Andrew D ; Tucker-Drob, Elliot M ; Abdellaoui, Abdel ; Arseneault, Louise ; van Bergen, Elsje ; Boomsma, Dorret I ; Caspi, Avshalom ; Corcoran, David L ; Domingue, Benjamin W ; Harris, Kathleen Mullan ; Ip, Hill F ; Mitchell, Colter ; Moffitt, Terrie E ; Poulton, Richie ; Prinz, Joseph A ; Sugden, Karen ; Wertz, Jasmin ; Williams, Benjamin S ; de Zeeuw, Eveline L ; Belsky, Daniel W ; Harden, K Paige ; Nivard, Michel G

Nature genetics, 2021-01, Vol.53 (1), p.35-44 [Periódico revisado por pares]

United States: Nature Publishing Group

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2
Natural variation in a homolog of Antirrhinum CENTRORADIALIS contributed to spring growth habit and environmental adaptation in cultivated barley
Natural variation in a homolog of Antirrhinum CENTRORADIALIS contributed to spring growth habit and environmental adaptation in cultivated barley
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Natural variation in a homolog of Antirrhinum CENTRORADIALIS contributed to spring growth habit and environmental adaptation in cultivated barley

COMADRAN, Jordi ; KILIAN, Benjamin ; HEDLEY, Pete ; TONDELLI, Alessandro ; PECCHIONI, Nicola ; FRANCIA, Enrico ; KORZUN, Viktor ; WALTHER, Alexander ; WAUGH, Robbie ; RUSSELL, Joanne ; RAMSAY, Luke ; STEIN, Nils ; GANAL, Martin ; SHAWL, Paul ; BAYER, Micha ; THOMAS, William ; MARSHALL, David

Nature genetics, 2012-12, Vol.44 (12), p.1388-1392 [Periódico revisado por pares]

New York, NY: Nature Publishing Group

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3
Germline CBL mutations cause developmental abnormalities and predispose to juvenile myelomonocytic leukemia
Germline CBL mutations cause developmental abnormalities and predispose to juvenile myelomonocytic leukemia
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Germline CBL mutations cause developmental abnormalities and predispose to juvenile myelomonocytic leukemia

Niemeyer, Charlotte M ; Loh, Mignon L ; Kang, Michelle W ; Shin, Danielle H ; Furlan, Ingrid ; Erlacher, Miriam ; Bunin, Nancy J ; Bunda, Severa ; Finklestein, Jerry Z ; Sakamoto, Kathleen M ; Gorr, Thomas A ; Mehta, Parinda ; Schmid, Irene ; Kropshofer, Gabriele ; Corbacioglu, Selim ; Lang, Peter J ; Klein, Christoph ; Schlegel, Paul-Gerhard ; Heinzmann, Andrea ; Schneider, Michaela ; Starý, Jan ; van den Heuvel-Eibrink, Marry M ; Hasle, Henrik ; Locatelli, Franco ; Sakai, Debbie ; Archambeault, Sophie ; Chen, Leslie ; Russell, Ryan C ; Sybingco, Stephanie S ; Ohh, Michael ; Braun, Benjamin S ; Flotho, Christian

Nature genetics, 2010-09, Vol.42 (9), p.794-800 [Periódico revisado por pares]

New York, NY: Nature Publishing Group

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4
Recurrent somatic mutations in ACVR1 in pediatric midline high-grade astrocytoma
Recurrent somatic mutations in ACVR1 in pediatric midline high-grade astrocytoma
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Recurrent somatic mutations in ACVR1 in pediatric midline high-grade astrocytoma

Fontebasso, Adam M ; Papillon-Cavanagh, Simon ; Schwartzentruber, Jeremy ; Nikbakht, Hamid ; Gerges, Noha ; Fiset, Pierre-Olivier ; Bechet, Denise ; Faury, Damien ; De Jay, Nicolas ; Ramkissoon, Lori A ; Corcoran, Aoife ; Jones, David T W ; Sturm, Dominik ; Johann, Pascal ; Tomita, Tadanori ; Goldman, Stewart ; Nagib, Mahmoud ; Bendel, Anne ; Goumnerova, Liliana ; Bowers, Daniel C ; Leonard, Jeffrey R ; Rubin, Joshua B ; Alden, Tord ; Browd, Samuel ; Geyer, J Russell ; Leary, Sarah ; Jallo, George ; Cohen, Kenneth ; Gupta, Nalin ; Prados, Michael D ; Carret, Anne-Sophie ; Ellezam, Benjamin ; Crevier, Louis ; Klekner, Almos ; Bognar, Laszlo ; Hauser, Peter ; Garami, Miklos ; Myseros, John ; Dong, Zhifeng ; Siegel, Peter M ; Malkin, Hayley ; Ligon, Azra H ; Albrecht, Steffen ; Pfister, Stefan M ; Ligon, Keith L ; Majewski, Jacek ; Jabado, Nada ; Kieran, Mark W

Nature genetics, 2014-05, Vol.46 (5), p.462-466 [Periódico revisado por pares]

United States: Nature Publishing Group

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5
Genetic association analyses highlight biological pathways underlying mitral valve prolapse
Genetic association analyses highlight biological pathways underlying mitral valve prolapse
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Genetic association analyses highlight biological pathways underlying mitral valve prolapse

Dina, Christian ; Bouatia-Naji, Nabila ; Tucker, Nathan ; Delling, Francesca N ; Toomer, Katelynn ; Durst, Ronen ; Perrocheau, Maelle ; Fernandez-Friera, Leticia ; Solis, Jorge ; Le Tourneau, Thierry ; Chen, Ming-Huei ; Probst, Vincent ; Bosse, Yohan ; Pibarot, Philippe ; Zelenika, Diana ; Lathrop, Mark ; Hercberg, Serge ; Roussel, Ronan ; Benjamin, Emelia J ; Bonnet, Fabrice ; Lo, Su Hao ; Dolmatova, Elena ; Simonet, Floriane ; Lecointe, Simon ; Kyndt, Florence ; Redon, Richard ; Le Marec, Hervé ; Froguel, Philippe ; Ellinor, Patrick T ; Vasan, Ramachandran S ; Bruneval, Patrick ; Markwald, Roger R ; Norris, Russell A ; Milan, David J ; Slaugenhaupt, Susan A ; Levine, Robert A ; Schott, Jean-Jacques ; Hagege, Albert A ; Jeunemaitre, Xavier

Nature genetics, 2015-10, Vol.47 (10), p.1206-1211 [Periódico revisado por pares]

United States: Nature Publishing Group

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6
Exome sequencing of geographically diverse barley landraces and wild relatives gives insights into environmental adaptation
Exome sequencing of geographically diverse barley landraces and wild relatives gives insights into environmental adaptation
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Exome sequencing of geographically diverse barley landraces and wild relatives gives insights into environmental adaptation

Russell, Joanne ; Mascher, Martin ; Dawson, Ian K ; Kyriakidis, Stylianos ; Calixto, Cristiane ; Freund, Fabian ; Bayer, Micha ; Milne, Iain ; Marshall-Griffiths, Tony ; Heinen, Shane ; Hofstad, Anna ; Sharma, Rajiv ; Himmelbach, Axel ; Knauft, Manuela ; van Zonneveld, Maarten ; Brown, John W S ; Schmid, Karl ; Kilian, Benjamin ; Muehlbauer, Gary J ; Stein, Nils ; Waugh, Robbie

Nature genetics, 2016-09, Vol.48 (9), p.1024-1030 [Periódico revisado por pares]

United States: Nature Publishing Group

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7
Assessing the contribution of rare variants to complex trait heritability from whole-genome sequence data
Assessing the contribution of rare variants to complex trait heritability from whole-genome sequence data
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Assessing the contribution of rare variants to complex trait heritability from whole-genome sequence data

Wainschtein, Pierrick ; Jain, Deepti ; Zheng, Zhili ; Cupples, L Adrienne ; Shadyab, Aladdin H ; McKnight, Barbara ; Shoemaker, Benjamin M ; Mitchell, Braxton D ; Psaty, Bruce M ; Kooperberg, Charles ; Liu, Ching-Ti ; Albert, Christine M ; Roden, Dan ; Chasman, Daniel I ; Darbar, Dawood ; Lloyd-Jones, Donald M ; Arnett, Donna K ; Regan, Elizabeth A ; Boerwinkle, Eric ; Rotter, Jerome I ; O'Connell, Jeffrey R ; Yanek, Lisa R ; de Andrade, Mariza ; Allison, Matthew A ; McDonald, Merry-Lynn N ; Chung, Mina K ; Fornage, Myriam ; Chami, Nathalie ; Smith, Nicholas L ; Ellinor, Patrick T ; Vasan, Ramachandran S ; Mathias, Rasika A ; Loos, Ruth J F ; Rich, Stephen S ; Lubitz, Steven A ; Heckbert, Susan R ; Redline, Susan ; Guo, Xiuqing ; Chen, Y -D Ida ; Laurie, Cecelia A ; Hernandez, Ryan D ; McGarvey, Stephen T ; Goddard, Michael E ; Laurie, Cathy C ; North, Kari E ; Lange, Leslie A ; Weir, Bruce S ; Yengo, Loic ; Yang, Jian ; Visscher, Peter M

Nature genetics, 2022-03, Vol.54 (3), p.263-273 [Periódico revisado por pares]

United States: Nature Publishing Group

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8
Genome-wide association of multiple complex traits in outbred mice by ultra-low-coverage sequencing
Genome-wide association of multiple complex traits in outbred mice by ultra-low-coverage sequencing
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Genome-wide association of multiple complex traits in outbred mice by ultra-low-coverage sequencing

Nicod, Jérôme ; Davies, Robert W ; Cai, Na ; Hassett, Carl ; Goodstadt, Leo ; Cosgrove, Cormac ; Yee, Benjamin K ; Lionikaite, Vikte ; McIntyre, Rebecca E ; Remme, Carol Ann ; Lodder, Elisabeth M ; Gregory, Jennifer S ; Hough, Tertius ; Joynson, Russell ; Phelps, Hayley ; Nell, Barbara ; Rowe, Clare ; Wood, Joe ; Walling, Alison ; Bopp, Nasrin ; Bhomra, Amarjit ; Hernandez-Pliego, Polinka ; Callebert, Jacques ; Aspden, Richard M ; Talbot, Nick P ; Robbins, Peter A ; Harrison, Mark ; Fray, Martin ; Launay, Jean-Marie ; Pinto, Yigal M ; Blizard, David A ; Bezzina, Connie R ; Adams, David J ; Franken, Paul ; Weaver, Tom ; Wells, Sara ; Brown, Steve D M ; Potter, Paul K ; Klenerman, Paul ; Lionikas, Arimantas ; Mott, Richard ; Flint, Jonathan

Nature genetics, 2016-08, Vol.48 (8), p.912-918 [Periódico revisado por pares]

United States: Nature Publishing Group

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9
Dynamic incorporation of multiple in silico functional annotations empowers rare variant association analysis of large whole-genome sequencing studies at scale
Dynamic incorporation of multiple in silico functional annotations empowers rare variant association analysis of large whole-genome sequencing studies at scale
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Dynamic incorporation of multiple in silico functional annotations empowers rare variant association analysis of large whole-genome sequencing studies at scale

Li, Xihao ; Li, Zilin ; Zhou, Hufeng ; Gaynor, Sheila M ; Liu, Yaowu ; Chen, Han ; Sun, Ryan ; Dey, Rounak ; Arnett, Donna K ; Aslibekyan, Stella ; Ballantyne, Christie M ; Bielak, Lawrence F ; Blangero, John ; Boerwinkle, Eric ; Bowden, Donald W ; Broome, Jai G ; Conomos, Matthew P ; Correa, Adolfo ; Cupples, L Adrienne ; Curran, Joanne E ; Freedman, Barry I ; Guo, Xiuqing ; Hindy, George ; Irvin, Marguerite R ; Kardia, Sharon L R ; Kathiresan, Sekar ; Khan, Alyna T ; Kooperberg, Charles L ; Laurie, Cathy C ; Liu, X Shirley ; Mahaney, Michael C ; Manichaikul, Ani W ; Martin, Lisa W ; Mathias, Rasika A ; McGarvey, Stephen T ; Mitchell, Braxton D ; Montasser, May E ; Moore, Jill E ; Morrison, Alanna C ; O'Connell, Jeffrey R ; Palmer, Nicholette D ; Pampana, Akhil ; Peralta, Juan M ; Peyser, Patricia A ; Psaty, Bruce M ; Redline, Susan ; Rice, Kenneth M ; Rich, Stephen S ; Smith, Jennifer A ; Tiwari, Hemant K ; Tsai, Michael Y ; Vasan, Ramachandran S ; Wang, Fei Fei ; Weeks, Daniel E ; Weng, Zhiping ; Wilson, James G ; Yanek, Lisa R ; Neale, Benjamin M ; Sunyaev, Shamil R ; Abecasis, Gonçalo R ; Rotter, Jerome I ; Willer, Cristen J ; Peloso, Gina M ; Natarajan, Pradeep ; Lin, Xihong

Nature genetics, 2020-09, Vol.52 (9), p.969-983 [Periódico revisado por pares]

United States: Nature Publishing Group

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10
Common variants at CD40 and other loci confer risk of rheumatoid arthritis
Common variants at CD40 and other loci confer risk of rheumatoid arthritis
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Common variants at CD40 and other loci confer risk of rheumatoid arthritis

Plenge, Robert M ; Raychaudhuri, Soumya ; Remmers, Elaine F ; Lee, Annette T ; Hackett, Rachel ; Guiducci, Candace ; Burtt, Noël P ; Gianniny, Lauren ; Korman, Benjamin D ; Padyukov, Leonid ; Kurreeman, Fina A S ; Chang, Monica ; Catanese, Joseph J ; Ding, Bo ; Wong, Sandra ; van der Helm-van Mil, Annette H M ; Neale, Benjamin M ; Coblyn, Jonathan ; Cui, Jing ; Tak, Paul P ; Wolbink, Gert Jan ; Crusius, J Bart A ; Horst-Bruinsma, Irene E van der ; Criswell, Lindsey A ; Amos, Christopher I ; Seldin, Michael F ; Kastner, Daniel L ; Ardlie, Kristin G ; Alfredsson, Lars ; Costenbader, Karen H ; Altshuler, David ; Huizinga, Tom W J ; Shadick, Nancy A ; Weinblatt, Michael E ; de Vries, Niek ; Worthington, Jane ; Seielstad, Mark ; Toes, Rene E M ; Karlson, Elizabeth W ; Begovich, Ann B ; Klareskog, Lars ; Gregersen, Peter K ; Daly, Mark J

Nature genetics, 2008-10, Vol.40 (10), p.1216-1223 [Periódico revisado por pares]

London: Nature Publishing Group

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