APA

Anney R., Klei L., Pinto D., Regan R., Conroy J., Magalhaes T. R., Correia C., Abrahams B. S., Sykes N., Pagnamenta A. T., Almeida J., Bacchelli E., Bailey A. J., Baird G., Battaglia A., Berney T., Bolshakova N., Bölte S., Bolton P. F., Bourgeron T., Brennan S., Brian J., Carson A. R., Casallo G., Casey J., Chu S. H., Cochrane L., Corsello C., Crawford E. L., Crossett A., Dawson G., de Jonge M., Delorme R., Drmic I., Duketis E., Duque F., Estes A., Farrar P., Fernandez B. A., Folstein S. E., Fombonne E., Freitag C. M., Gilbert J., Gillberg C., Glessner J. T., Goldberg J., Green J., Guter S. J., Hakonarson H., Heron E. A., Hill M., Holt R., Howe J. L., Hughes G., Hus V., Igliozzi R., Kim C., Klauck S. M., Kolevzon A., Korvatska O., Kustanovich V., Lajonchere C. M., Lamb J. A., Laskawiec M., Leboyer M., Le Couteur A., Leventhal B. L., Lionel A. C., Liu X., Lord C., Lotspeich L., Lund S. C., Maestrini E., Mahoney W., Mantoulan C., Marshall C. R., McConachie H., McDougle C. J., McGrath J., McMahon W. M., Melhem N. M., Merikangas A., Migita O., Minshew N. J., Mirza G. K., Munson J., Nelson S. F., Noakes C., Noor A., Nygren G., Oliveira G., Papanikolaou K., Parr J. R., Parrini B., Paton T., Pickles A., Piven J., Posey D. J., Poustka A., Poustka F., Prasad A., Ragoussis J., Renshaw K., Rickaby J., Roberts W., Roeder K., Roge B., Rutter M. L., Bierut L. J., Rice J. P., Salt J., Sansom K., Sato D., Segurado R., Senman L., Shah N., Sheffield V. C., Soorya L., Sousa I., Stoppioni V., Strawbridge C., Tancredi R., Tansey K., Thiruvahindrapduram B., Thompson A. P., Thomson S., Tryfon A., Tsiantis J., Van Engeland H., Vincent J. B., Volkmar F., Wallace S., Wang K., Wang Z., Wassink T. H., Wing K., Wittemeyer K., Wood S., Yaspan B. L., Zurawiecki D., Zwaigenbaum L., Betancur C., Buxbaum J. D., Cantor R. M., Cook E. H., Coon H., Cuccaro M. L., Gallagher L., Geschwind D. H., Gill M., Haines J. L., Miller J., Monaco A. P., Nurnberger J. I., Paterson A. D., Pericak-Vance M. A., Schellenberg G. D., Scherer S. W., Sutcliffe J. S., Szatmari P., Vicente A. M., Vieland V. J., Wijsman E. M., Devlin B., Ennis S. & Hallmayer J. (20110301). A genome-wide scan for common alleles affecting risk for autism. : Human molecular genetics.

Chicago

Anney Richard, Klei Lambertus, Pinto Dalila, Regan Regina, Conroy Judith, Magalhaes Tiago R, Correia Catarina, Abrahams Brett S, Sykes Nuala, Pagnamenta Alistair T, Almeida Joana, Bacchelli Elena, Bailey Anthony J, Baird Gillian, Battaglia Agatino, Berney Tom, Bolshakova Nadia, Bölte Sven, Bolton Patrick F, Bourgeron Thomas, Brennan Sean, Brian Jessica, Carson Andrew R, Casallo Guillermo, Casey Jillian, Chu Su H, Cochrane Lynne, Corsello Christina, Crawford Emily L, Crossett Andrew, Dawson Geraldine, de Jonge Maretha, Delorme Richard, Drmic Irene, Duketis Eftichia, Duque Frederico, Estes Annette, Farrar Penny, Fernandez Bridget A, Folstein Susan E, Fombonne Eric, Freitag Christine M, Gilbert John, Gillberg Christopher, Glessner Joseph T, Goldberg Jeremy, Green Jonathan, Guter Stephen J, Hakonarson Hakon, Heron Elizabeth A, Hill Matthew, Holt Richard, Howe Jennifer L, Hughes Gillian, Hus Vanessa, Igliozzi Roberta, Kim Cecilia, Klauck Sabine M, Kolevzon Alexander, Korvatska Olena, Kustanovich Vlad, Lajonchere Clara M, Lamb Janine A, Laskawiec Magdalena, Leboyer Marion, Le Couteur Ann, Leventhal Bennett L, Lionel Anath C, Liu Xiao-Qing, Lord Catherine, Lotspeich Linda, Lund Sabata C, Maestrini Elena, Mahoney William, Mantoulan Carine, Marshall Christian R, McConachie Helen, McDougle Christopher J, McGrath Jane, McMahon William M, Melhem Nadine M, Merikangas Alison, Migita Ohsuke, Minshew Nancy J, Mirza Ghazala K, Munson Jeff, Nelson Stanley F, Noakes Carolyn, Noor Abdul, Nygren Gudrun, Oliveira Guiomar, Papanikolaou Katerina, Parr Jeremy R, Parrini Barbara, Paton Tara, Pickles Andrew, Piven Joseph, Posey David J, Poustka Annemarie, Poustka Fritz, Prasad Aparna, Ragoussis Jiannis, Renshaw Katy, Rickaby Jessica, Roberts Wendy, Roeder Kathryn, Roge Bernadette, Rutter Michael L, Bierut Laura J, Rice John P, Salt Jeff, Sansom Katherine, Sato Daisuke, Segurado Ricardo, Senman Lili, Shah Naisha, Sheffield Val C, Soorya Latha, Sousa Inês, Stoppioni Vera, Strawbridge Christina, Tancredi Raffaella, Tansey Katherine, Thiruvahindrapduram Bhooma, Thompson Ann P, Thomson Susanne, Tryfon Ana, Tsiantis John, Van Engeland Herman, Vincent John B, Volkmar Fred, Wallace Simon, Wang Kai, Wang Zhouzhi, Wassink Thomas H, Wing Kirsty, Wittemeyer Kerstin, Wood Shawn, Yaspan Brian L, Zurawiecki Danielle, Zwaigenbaum Lonnie, Betancur Catalina, Buxbaum Joseph D, Cantor Rita M, Cook Edwin H, Coon Hilary, Cuccaro Michael L, Gallagher Louise, Geschwind Daniel H, Gill Michael, Haines Jonathan L, Miller Judith, Monaco Anthony P, Nurnberger John I, Paterson Andrew D, Pericak-Vance Margaret A, Schellenberg Gerard D, Scherer Stephen W, Sutcliffe James S, Szatmari Peter, Vicente Astrid M, Vieland Veronica J, Wijsman Ellen M, Devlin Bernie, Ennis Sean and Hallmayer Joachim. 20110301. A genome-wide scan for common alleles affecting risk for autism. : Human molecular genetics.

Harvard

Anney R., Klei L., Pinto D., Regan R., Conroy J., Magalhaes T. R., Correia C., Abrahams B. S., Sykes N., Pagnamenta A. T., Almeida J., Bacchelli E., Bailey A. J., Baird G., Battaglia A., Berney T., Bolshakova N., Bölte S., Bolton P. F., Bourgeron T., Brennan S., Brian J., Carson A. R., Casallo G., Casey J., Chu S. H., Cochrane L., Corsello C., Crawford E. L., Crossett A., Dawson G., de Jonge M., Delorme R., Drmic I., Duketis E., Duque F., Estes A., Farrar P., Fernandez B. A., Folstein S. E., Fombonne E., Freitag C. M., Gilbert J., Gillberg C., Glessner J. T., Goldberg J., Green J., Guter S. J., Hakonarson H., Heron E. A., Hill M., Holt R., Howe J. L., Hughes G., Hus V., Igliozzi R., Kim C., Klauck S. M., Kolevzon A., Korvatska O., Kustanovich V., Lajonchere C. M., Lamb J. A., Laskawiec M., Leboyer M., Le Couteur A., Leventhal B. L., Lionel A. C., Liu X., Lord C., Lotspeich L., Lund S. C., Maestrini E., Mahoney W., Mantoulan C., Marshall C. R., McConachie H., McDougle C. J., McGrath J., McMahon W. M., Melhem N. M., Merikangas A., Migita O., Minshew N. J., Mirza G. K., Munson J., Nelson S. F., Noakes C., Noor A., Nygren G., Oliveira G., Papanikolaou K., Parr J. R., Parrini B., Paton T., Pickles A., Piven J., Posey D. J., Poustka A., Poustka F., Prasad A., Ragoussis J., Renshaw K., Rickaby J., Roberts W., Roeder K., Roge B., Rutter M. L., Bierut L. J., Rice J. P., Salt J., Sansom K., Sato D., Segurado R., Senman L., Shah N., Sheffield V. C., Soorya L., Sousa I., Stoppioni V., Strawbridge C., Tancredi R., Tansey K., Thiruvahindrapduram B., Thompson A. P., Thomson S., Tryfon A., Tsiantis J., Van Engeland H., Vincent J. B., Volkmar F., Wallace S., Wang K., Wang Z., Wassink T. H., Wing K., Wittemeyer K., Wood S., Yaspan B. L., Zurawiecki D., Zwaigenbaum L., Betancur C., Buxbaum J. D., Cantor R. M., Cook E. H., Coon H., Cuccaro M. L., Gallagher L., Geschwind D. H., Gill M., Haines J. L., Miller J., Monaco A. P., Nurnberger J. I., Paterson A. D., Pericak-Vance M. A., Schellenberg G. D., Scherer S. W., Sutcliffe J. S., Szatmari P., Vicente A. M., Vieland V. J., Wijsman E. M., Devlin B., Ennis S. and Hallmayer J. (20110301). A genome-wide scan for common alleles affecting risk for autism. : Human molecular genetics.

MLA

Anney Richard, Klei Lambertus, Pinto Dalila, Regan Regina, Conroy Judith, Magalhaes Tiago R, Correia Catarina, Abrahams Brett S, Sykes Nuala, Pagnamenta Alistair T, Almeida Joana, Bacchelli Elena, Bailey Anthony J, Baird Gillian, Battaglia Agatino, Berney Tom, Bolshakova Nadia, Bölte Sven, Bolton Patrick F, Bourgeron Thomas, Brennan Sean, Brian Jessica, Carson Andrew R, Casallo Guillermo, Casey Jillian, Chu Su H, Cochrane Lynne, Corsello Christina, Crawford Emily L, Crossett Andrew, Dawson Geraldine, de Jonge Maretha, Delorme Richard, Drmic Irene, Duketis Eftichia, Duque Frederico, Estes Annette, Farrar Penny, Fernandez Bridget A, Folstein Susan E, Fombonne Eric, Freitag Christine M, Gilbert John, Gillberg Christopher, Glessner Joseph T, Goldberg Jeremy, Green Jonathan, Guter Stephen J, Hakonarson Hakon, Heron Elizabeth A, Hill Matthew, Holt Richard, Howe Jennifer L, Hughes Gillian, Hus Vanessa, Igliozzi Roberta, Kim Cecilia, Klauck Sabine M, Kolevzon Alexander, Korvatska Olena, Kustanovich Vlad, Lajonchere Clara M, Lamb Janine A, Laskawiec Magdalena, Leboyer Marion, Le Couteur Ann, Leventhal Bennett L, Lionel Anath C, Liu Xiao-Qing, Lord Catherine, Lotspeich Linda, Lund Sabata C, Maestrini Elena, Mahoney William, Mantoulan Carine, Marshall Christian R, McConachie Helen, McDougle Christopher J, McGrath Jane, McMahon William M, Melhem Nadine M, Merikangas Alison, Migita Ohsuke, Minshew Nancy J, Mirza Ghazala K, Munson Jeff, Nelson Stanley F, Noakes Carolyn, Noor Abdul, Nygren Gudrun, Oliveira Guiomar, Papanikolaou Katerina, Parr Jeremy R, Parrini Barbara, Paton Tara, Pickles Andrew, Piven Joseph, Posey David J, Poustka Annemarie, Poustka Fritz, Prasad Aparna, Ragoussis Jiannis, Renshaw Katy, Rickaby Jessica, Roberts Wendy, Roeder Kathryn, Roge Bernadette, Rutter Michael L, Bierut Laura J, Rice John P, Salt Jeff, Sansom Katherine, Sato Daisuke, Segurado Ricardo, Senman Lili, Shah Naisha, Sheffield Val C, Soorya Latha, Sousa Inês, Stoppioni Vera, Strawbridge Christina, Tancredi Raffaella, Tansey Katherine, Thiruvahindrapduram Bhooma, Thompson Ann P, Thomson Susanne, Tryfon Ana, Tsiantis John, Van Engeland Herman, Vincent John B, Volkmar Fred, Wallace Simon, Wang Kai, Wang Zhouzhi, Wassink Thomas H, Wing Kirsty, Wittemeyer Kerstin, Wood Shawn, Yaspan Brian L, Zurawiecki Danielle, Zwaigenbaum Lonnie, Betancur Catalina, Buxbaum Joseph D, Cantor Rita M, Cook Edwin H, Coon Hilary, Cuccaro Michael L, Gallagher Louise, Geschwind Daniel H, Gill Michael, Haines Jonathan L, Miller Judith, Monaco Anthony P, Nurnberger John I, Paterson Andrew D, Pericak-Vance Margaret A, Schellenberg Gerard D, Scherer Stephen W, Sutcliffe James S, Szatmari Peter, Vicente Astrid M, Vieland Veronica J, Wijsman Ellen M, Devlin Bernie, Ennis Sean and Hallmayer Joachim. A genome-wide scan for common alleles affecting risk for autism. : Human molecular genetics. 20110301.