The genetic relationship between handedness and neurodevelopmental disorders()

द्वारा Brandler, William M., Paracchini, Silvia
प्रकाशित 2014

SV(2): accurate structural variation genotyping and de novo mutation detection from whole genomes

द्वारा Antaki, Danny, Brandler, William M, Sebat, Jonathan
में प्रकाशित Bioinformatics (2018)

PCSK6 is associated with handedness in individuals with dyslexia

द्वारा Scerri, Thomas S., Brandler, William M., Paracchini, Silvia, Morris, Andrew P., Ring, Susan M., Richardson, Alex J., Talcott, Joel B., Stein, John, Monaco, Anthony P.
प्रकाशित 2011

The handedness-associated PCSK6 locus spans an intronic promoter regulating novel transcripts

द्वारा Shore, Robert, Covill, Laura, Pettigrew, Kerry A., Brandler, William M., Diaz, Rebeca, Xu, Yiwang, Tello, Javier A., Talcott, Joel B., Newbury, Dianne F., Stein, John, Monaco, Anthony P., Paracchini, Silvia
में प्रकाशित Hum Mol Genet (2016)

Common Variants in Left/Right Asymmetry Genes and Pathways Are Associated with Relative Hand Skill

द्वारा Brandler, William M., Morris, Andrew P., Evans, David M., Scerri, Thomas S., Kemp, John P., Timpson, Nicholas J., St Pourcain, Beate, Smith, George Davey, Ring, Susan M., Stein, John, Monaco, Anthony P., Talcott, Joel B., Fisher, Simon E., Webber, Caleb, Paracchini, Silvia
प्रकाशित 2013

Increased prevalence of sex chromosome aneuploidies in specific language impairment and dyslexia

द्वारा Simpson, Nuala H, Addis, Laura, Brandler, William M, Slonims, Vicky, Clark, Ann, Watson, Jocelynne, Scerri, Thomas S, Hennessy, Elizabeth R, Bolton, Patrick F, Conti-Ramsden, Gina, Fairfax, Benjamin P, Knight, Julian C, Stein, John, Talcott, Joel B, O'Hare, Anne, Baird, Gillian, Paracchini, Silvia, Fisher, Simon E, Newbury, Dianne F, Consortium, SLI
में प्रकाशित Dev Med Child Neurol (2014)

Autism risk in offspring can be assessed through quantification of male sperm mosaicism

द्वारा Breuss, Martin W., Antaki, Danny, George, Renee D., Kleiber, Morgan, James, Kiely N., Ball, Laurel L., Hong, Oanh, Mitra, Ileena, Yang, Xiaoxu, Wirth, Sara A., Gu, Jing, Garcia, Camila A. B., Gujral, Madhusudan, Brandler, William M., Musaev, Damir, Nguyen, An, McEvoy-Venneri, Jennifer, Knox, Renatta, Sticca, Evan, Botello, Martha Cristina Cancino, Fenner, Javiera Uribe, Pérez, Maria Cárcel, Arranz, Maria, Moffitt, Andrea B., Wang, Zihua, Hervás, Amaia, Devinsky, Orrin, Gymrek, Melissa, Sebat, Jonathan, Gleeson, Joseph G.
में प्रकाशित Nat Med (2019)

Frequency and Complexity of De Novo Structural Mutation in Autism

द्वारा Brandler, William M., Antaki, Danny, Gujral, Madhusudan, Noor, Amina, Rosanio, Gabriel, Chapman, Timothy R., Barrera, Daniel J., Lin, Guan Ning, Malhotra, Dheeraj, Watts, Amanda C., Wong, Lawrence C., Estabillo, Jasper A., Gadomski, Therese E., Hong, Oanh, Fajardo, Karin V. Fuentes, Bhandari, Abhishek, Owen, Renius, Baughn, Michael, Yuan, Jeffrey, Solomon, Terry, Moyzis, Alexandra G., Maile, Michelle S., Sanders, Stephan J., Reiner, Gail E., Vaux, Keith K., Strom, Charles M., Zhang, Kang, Muotri, Alysson R., Akshoomoff, Natacha, Leal, Suzanne M., Pierce, Karen, Courchesne, Eric, Iakoucheva, Lilia M., Corsello, Christina, Sebat, Jonathan
में प्रकाशित Am J Hum Genet (2016)

Paternally inherited cis-regulatory structural variants are associated with autism

द्वारा Brandler, William M, Antaki, Danny, Gujral, Madhusudan, Kleiber, Morgan L, Whitney, Joe, Maile, Michelle S, Hong, Oanh, Chapman, Timothy R, Tan, Shirley, Tandon, Prateek, Pang, Timothy, Tang, Shih C, Vaux, Keith K, Yang, Yan, Harrington, Eoghan, Juul, Sissel, Turner, Daniel J, Thiruvahindrapuram, Bhooma, Kaur, Gaganjot, Wang, Zhuozhi, Kingsmore, Stephen F, Gleeson, Joseph G, Bisson, Denis, Kakaradov, Boyko, Telenti, Amalio, Venter, J Craig, Corominas, Roser, Toma, Claudio, Cormand, Bru, Rueda, Isabel, Guijarro, Silvina, Messer, Karen S, Nievergelt, Caroline M, Arranz, Maria J, Courchesne, Eric, Pierce, Karen, Muotri, Alysson R, Iakoucheva, Lilia M, Hervas, Amaia, Scherer, Stephen W, Corsello, Christina, Sebat, Jonathan
में प्रकाशित Science (2018)

Genome-wide association scan identifies new variants associated with a cognitive predictor of dyslexia

द्वारा Gialluisi, Alessandro, Andlauer, Till F. M., Mirza-Schreiber, Nazanin, Moll, Kristina, Becker, Jessica, Hoffmann, Per, Ludwig, Kerstin U., Czamara, Darina, St Pourcain, Beate, Brandler, William, Honbolygó, Ferenc, Tóth, Dénes, Csépe, Valéria, Huguet, Guillaume, Morris, Andrew P., Hulslander, Jacqueline, Willcutt, Erik G., DeFries, John C., Olson, Richard K., Smith, Shelley D., Pennington, Bruce F., Vaessen, Anniek, Maurer, Urs, Lyytinen, Heikki, Peyrard-Janvid, Myriam, Leppänen, Paavo H. T., Brandeis, Daniel, Bonte, Milene, Stein, John F., Talcott, Joel B., Fauchereau, Fabien, Wilcke, Arndt, Francks, Clyde, Bourgeron, Thomas, Monaco, Anthony P., Ramus, Franck, Landerl, Karin, Kere, Juha, Scerri, Thomas S., Paracchini, Silvia, Fisher, Simon E., Schumacher, Johannes, Nöthen, Markus M., Müller-Myhsok, Bertram, Schulte-Körne, Gerd
में प्रकाशित Transl Psychiatry (2019)

Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects

द्वारा Marshall, Christian R., Howrigan, Daniel P., Merico, Daniele, Thiruvahindrapuram, Bhooma, Wu, Wenting, Greer, Douglas S., Antaki, Danny, Shetty, Aniket, Holmans, Peter A., Pinto, Dalila, Gujral, Madhusudan, Brandler, William M., Malhotra, Dheeraj, Wang, Zhouzhi, Fajarado, Karin V. Fuentes, Maile, Michelle S., Ripke, Stephan, Agartz, Ingrid, Albus, Margot, Alexander, Madeline, Amin, Farooq, Atkins, Joshua, Bacanu, Silviu A., Belliveau, Richard A., Bergen, Sarah E., Bertalan, Marcelo, Bevilacqua, Elizabeth, Bigdeli, Tim B., Black, Donald W., Bruggeman, Richard, Buccola, Nancy G., Buckner, Randy L., Bulik-Sullivan, Brendan, Byerley, William, Cahn, Wiepke, Cai, Guiqing, Cairns, Murray J., Campion, Dominique, Cantor, Rita M., Carr, Vaughan J., Carrera, Noa, Catts, Stanley V., Chambert, Kimberley D., Cheng, Wei, Cloninger, C. Robert, Cohen, David, Cormican, Paul, Craddock, Nick, Crespo-Facorro, Benedicto, Crowley, James J., Curtis, David, Davidson, Michael, Davis, Kenneth L, Degenhardt, Franziska, Del Favero, Jurgen, DeLisi, Lynn E., Dikeos, Dimitris, Dinan, Timothy, Djurovic, Srdjan, Donohoe, Gary, Drapeau, Elodie, Duan, Jubao, Dudbridge, Frank, Eichhammer, Peter, Eriksson, Johan, Escott-Price, Valentina, Essioux, Laurent, Fanous, Ayman H., Farh, Kai-How, Farrell, Martilias S., Frank, Josef, Franke, Lude, Freedman, Robert, Freimer, Nelson B., Friedman, Joseph I., Forstner, Andreas J., Fromer, Menachem, Genovese, Giulio, Georgieva, Lyudmila, Gershon, Elliot S., Giegling, Ina, Giusti-Rodríguez, Paola, Godard, Stephanie, Goldstein, Jacqueline I., Gratten, Jacob, de Haan, Lieuwe, Hamshere, Marian L., Hansen, Mark, Hansen, Thomas, Haroutunian, Vahram, Hartmann, Annette M., Henskens, Frans A., Herms, Stefan, Hirschhorn, Joel N., Hoffmann, Per, Hofman, Andrea, Huang, Hailiang, Ikeda, Masashi, Joa, Inge, Kähler, Anna K, Kahn, René S, Kalaydjieva, Luba, Karjalainen, Juha, Kavanagh, David, Keller, Matthew C., Kelly, Brian J., Kennedy, James L., Kim, Yunjung, Knowles, James A., Konte, Bettina, Laurent, Claudine, Lee, Phil, Lee, S. Hong, Legge, Sophie E., Lerer, Bernard, Levy, Deborah L., Liang, Kung-Yee, Lieberman, Jeffrey, Lönnqvist, Jouko, Loughland, Carmel M., Magnusson, Patrik K.E., Maher, Brion S., Maier, Wolfgang, Mallet, Jacques, Mattheisen, Manuel, Mattingsdal, Morten, McCarley, Robert W, McDonald, Colm, McIntosh, Andrew M., Meier, Sandra, Meijer, Carin J., Melle, Ingrid, Mesholam-Gately, Raquelle I., Metspalu, Andres, Michie, Patricia T., Milani, Lili, Milanova, Vihra, Mokrab, Younes, Morris, Derek W., Müller-Myhsok, Bertram, Murphy, Kieran C., Murray, Robin M., Myin-Germeys, Inez, Nenadic, Igor, Nertney, Deborah A., Nestadt, Gerald, Nicodemus, Kristin K., Nisenbaum, Laura, Nordin, Annelie, O’Callaghan, Eadbhard, O’Dushlaine, Colm, Oh, Sang-Yun, Olincy, Ann, Olsen, Line, O’Neill, F. Anthony, Van Os, Jim, Pantelis, Christos, Papadimitriou, George N., Parkhomenko, Elena, Pato, Michele T., Paunio, Tiina, Perkins, Diana O., Pers, Tune H., Pietiläinen, Olli, Pimm, Jonathan, Pocklington, Andrew J., Powell, John, Price, Alkes, Pulver, Ann E., Purcell, Shaun M., Quested, Digby, Rasmussen, Henrik B., Reichenberg, Abraham, Reimers, Mark A., Richards, Alexander L., Roffman, Joshua L., Roussos, Panos, Ruderfer, Douglas M., Salomaa, Veikko, Sanders, Alan R., Savitz, Adam, Schall, Ulrich, Schulze, Thomas G., Schwab, Sibylle G., Scolnick, Edward M., Scott, Rodney J., Seidman, Larry J., Shi, Jianxin, Silverman, Jeremy M., Smoller, Jordan W., Söderman, Erik, Spencer, Chris C.A., Stahl, Eli A., Strengman, Eric, Strohmaier, Jana, Stroup, T. Scott, Suvisaari, Jaana, Svrakic, Dragan M., Szatkiewicz, Jin P., Thirumalai, Srinivas, Tooney, Paul A., Veijola, Juha, Visscher, Peter M., Waddington, John, Walsh, Dermot, Webb, Bradley T., Weiser, Mark, Wildenauer, Dieter B., Williams, Nigel M., Williams, Stephanie, Witt, Stephanie H., Wolen, Aaron R., Wormley, Brandon K., Wray, Naomi R, Wu, Jing Qin, Zai, Clement C., Adolfsson, Rolf, Andreassen, Ole A., Blackwood, Douglas H.R., Bramon, Elvira, Buxbaum, Joseph D., Cichon, Sven, Collier, David A, Corvin, Aiden, Daly, Mark J., Darvasi, Ariel, Domenici, Enrico, Esko, Tõnu, Gejman, Pablo V., Gill, Michael, Gurling, Hugh, Hultman, Christina M., Iwata, Nakao, Jablensky, Assen V., Jönsson, Erik G, Kendler, Kenneth S, Kirov, George, Knight, Jo, Levinson, Douglas F., Li, Qingqin S, McCarroll, Steven A, McQuillin, Andrew, Moran, Jennifer L., Mowry, Bryan J., Nöthen, Markus M., Ophoff, Roel A., Owen, Michael J., Palotie, Aarno, Pato, Carlos N., Petryshen, Tracey L., Posthuma, Danielle, Rietschel, Marcella, Riley, Brien P., Rujescu, Dan, Sklar, Pamela, St. Clair, David, Walters, James T.R., Werge, Thomas, Sullivan, Patrick F., O’Donovan, Michael C, Scherer, Stephen W., Neale, Benjamin M., Sebat, Jonathan
में प्रकाशित Nat Genet (2016)