A novel approach of homozygous haplotype sharing identifies candidate genes in autism spectrum disorder.
A novel approach of homozygous haplotype sharing identifies candidate genes in autism spectrum disorder. [electronic resource] - Human genetics Apr 2012 - 565-79 p. digital
Publication Type: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
1432-1203
10.1007/s00439-011-1094-6 doi
Adult
Child
Child Development Disorders, Pervasive--genetics
Cluster Analysis
Cohort Studies
DNA Copy Number Variations
Female
Genetic Predisposition to Disease--genetics
Genome-Wide Association Study--methods
Genotype
Haplotypes--genetics
Homozygote
Humans
Linkage Disequilibrium
Male
Middle Aged
Nuclear Family
Polymorphism, Single Nucleotide
A novel approach of homozygous haplotype sharing identifies candidate genes in autism spectrum disorder.
APA
Casey J. P., Magalhaes T., Conroy J. M., Regan R., Shah N., Anney R., Shields D. C., Abrahams B. S., Almeida J., Bacchelli E., Bailey A. J., Baird G., Battaglia A., Berney T., Bolshakova N., Bolton P. F., Bourgeron T., Brennan S., Cali P., Correia C., Corsello C., Coutanche M., Dawson G., de Jonge M., Delorme R., Duketis E., Duque F., Estes A., Farrar P., Fernandez B. A., Folstein S. E., Foley S., Fombonne E., Freitag C. M., Gilbert J., Gillberg C., Glessner J. T., Green J., Guter S. J., Hakonarson H., Holt R., Hughes G., Hus V., Igliozzi R., Kim C., Klauck S. M., Kolevzon A., Lamb J. A., Leboyer M., Le Couteur A., Leventhal B. L., Lord C., Lund S. C., Maestrini E., Mantoulan C., Marshall C. R., McConachie H., McDougle C. J., McGrath J., McMahon W. M., Merikangas A., Miller J., Minopoli F., Mirza G. K., Munson J., Nelson S. F., Nygren G., Oliveira G., Pagnamenta A. T., Papanikolaou K., Parr J. R., Parrini B., Pickles A., Pinto D., Piven J., Posey D. J., Poustka A., Poustka F., Ragoussis J., Roge B., Rutter M. L., Sequeira A. F., Soorya L., Sousa I., Sykes N., Stoppioni V., Tancredi R., Tauber M., Thompson A. P., Thomson S., Tsiantis J., Van Engeland H., Vincent J. B., Volkmar F., Vorstman J. A. S., Wallace S., Wang K., Wassink T. H., White K., Wing K., Wittemeyer K., Yaspan B. L., Zwaigenbaum L., Betancur C., Buxbaum J. D., Cantor R. M., Cook E. H., Coon H., Cuccaro M. L., Geschwind D. H., Haines J. L., Hallmayer J., Monaco A. P., Nurnberger J. I., Pericak-Vance M. A., Schellenberg G. D., Scherer S. W., Sutcliffe J. S., Szatmari P., Vieland V. J., Wijsman E. M., Green A., Gill M., Gallagher L., Vicente A. & Ennis S. (20120514). A novel approach of homozygous haplotype sharing identifies candidate genes in autism spectrum disorder. : Human genetics.
Chicago
Casey Jillian P, Magalhaes Tiago, Conroy Judith M, Regan Regina, Shah Naisha, Anney Richard, Shields Denis C, Abrahams Brett S, Almeida Joana, Bacchelli Elena, Bailey Anthony J, Baird Gillian, Battaglia Agatino, Berney Tom, Bolshakova Nadia, Bolton Patrick F, Bourgeron Thomas, Brennan Sean, Cali Phil, Correia Catarina, Corsello Christina, Coutanche Marc, Dawson Geraldine, de Jonge Maretha, Delorme Richard, Duketis Eftichia, Duque Frederico, Estes Annette, Farrar Penny, Fernandez Bridget A, Folstein Susan E, Foley Suzanne, Fombonne Eric, Freitag Christine M, Gilbert John, Gillberg Christopher, Glessner Joseph T, Green Jonathan, Guter Stephen J, Hakonarson Hakon, Holt Richard, Hughes Gillian, Hus Vanessa, Igliozzi Roberta, Kim Cecilia, Klauck Sabine M, Kolevzon Alexander, Lamb Janine A, Leboyer Marion, Le Couteur Ann, Leventhal Bennett L, Lord Catherine, Lund Sabata C, Maestrini Elena, Mantoulan Carine, Marshall Christian R, McConachie Helen, McDougle Christopher J, McGrath Jane, McMahon William M, Merikangas Alison, Miller Judith, Minopoli Fiorella, Mirza Ghazala K, Munson Jeff, Nelson Stanley F, Nygren Gudrun, Oliveira Guiomar, Pagnamenta Alistair T, Papanikolaou Katerina, Parr Jeremy R, Parrini Barbara, Pickles Andrew, Pinto Dalila, Piven Joseph, Posey David J, Poustka Annemarie, Poustka Fritz, Ragoussis Jiannis, Roge Bernadette, Rutter Michael L, Sequeira Ana F, Soorya Latha, Sousa Inês, Sykes Nuala, Stoppioni Vera, Tancredi Raffaella, Tauber Maïté, Thompson Ann P, Thomson Susanne, Tsiantis John, Van Engeland Herman, Vincent John B, Volkmar Fred, Vorstman Jacob A S, Wallace Simon, Wang Kai, Wassink Thomas H, White Kathy, Wing Kirsty, Wittemeyer Kerstin, Yaspan Brian L, Zwaigenbaum Lonnie, Betancur Catalina, Buxbaum Joseph D, Cantor Rita M, Cook Edwin H, Coon Hilary, Cuccaro Michael L, Geschwind Daniel H, Haines Jonathan L, Hallmayer Joachim, Monaco Anthony P, Nurnberger John I, Pericak-Vance Margaret A, Schellenberg Gerard D, Scherer Stephen W, Sutcliffe James S, Szatmari Peter, Vieland Veronica J, Wijsman Ellen M, Green Andrew, Gill Michael, Gallagher Louise, Vicente Astrid and Ennis Sean. 20120514. A novel approach of homozygous haplotype sharing identifies candidate genes in autism spectrum disorder. : Human genetics.
Harvard
Casey J. P., Magalhaes T., Conroy J. M., Regan R., Shah N., Anney R., Shields D. C., Abrahams B. S., Almeida J., Bacchelli E., Bailey A. J., Baird G., Battaglia A., Berney T., Bolshakova N., Bolton P. F., Bourgeron T., Brennan S., Cali P., Correia C., Corsello C., Coutanche M., Dawson G., de Jonge M., Delorme R., Duketis E., Duque F., Estes A., Farrar P., Fernandez B. A., Folstein S. E., Foley S., Fombonne E., Freitag C. M., Gilbert J., Gillberg C., Glessner J. T., Green J., Guter S. J., Hakonarson H., Holt R., Hughes G., Hus V., Igliozzi R., Kim C., Klauck S. M., Kolevzon A., Lamb J. A., Leboyer M., Le Couteur A., Leventhal B. L., Lord C., Lund S. C., Maestrini E., Mantoulan C., Marshall C. R., McConachie H., McDougle C. J., McGrath J., McMahon W. M., Merikangas A., Miller J., Minopoli F., Mirza G. K., Munson J., Nelson S. F., Nygren G., Oliveira G., Pagnamenta A. T., Papanikolaou K., Parr J. R., Parrini B., Pickles A., Pinto D., Piven J., Posey D. J., Poustka A., Poustka F., Ragoussis J., Roge B., Rutter M. L., Sequeira A. F., Soorya L., Sousa I., Sykes N., Stoppioni V., Tancredi R., Tauber M., Thompson A. P., Thomson S., Tsiantis J., Van Engeland H., Vincent J. B., Volkmar F., Vorstman J. A. S., Wallace S., Wang K., Wassink T. H., White K., Wing K., Wittemeyer K., Yaspan B. L., Zwaigenbaum L., Betancur C., Buxbaum J. D., Cantor R. M., Cook E. H., Coon H., Cuccaro M. L., Geschwind D. H., Haines J. L., Hallmayer J., Monaco A. P., Nurnberger J. I., Pericak-Vance M. A., Schellenberg G. D., Scherer S. W., Sutcliffe J. S., Szatmari P., Vieland V. J., Wijsman E. M., Green A., Gill M., Gallagher L., Vicente A. and Ennis S. (20120514). A novel approach of homozygous haplotype sharing identifies candidate genes in autism spectrum disorder. : Human genetics.
MLA
Casey Jillian P, Magalhaes Tiago, Conroy Judith M, Regan Regina, Shah Naisha, Anney Richard, Shields Denis C, Abrahams Brett S, Almeida Joana, Bacchelli Elena, Bailey Anthony J, Baird Gillian, Battaglia Agatino, Berney Tom, Bolshakova Nadia, Bolton Patrick F, Bourgeron Thomas, Brennan Sean, Cali Phil, Correia Catarina, Corsello Christina, Coutanche Marc, Dawson Geraldine, de Jonge Maretha, Delorme Richard, Duketis Eftichia, Duque Frederico, Estes Annette, Farrar Penny, Fernandez Bridget A, Folstein Susan E, Foley Suzanne, Fombonne Eric, Freitag Christine M, Gilbert John, Gillberg Christopher, Glessner Joseph T, Green Jonathan, Guter Stephen J, Hakonarson Hakon, Holt Richard, Hughes Gillian, Hus Vanessa, Igliozzi Roberta, Kim Cecilia, Klauck Sabine M, Kolevzon Alexander, Lamb Janine A, Leboyer Marion, Le Couteur Ann, Leventhal Bennett L, Lord Catherine, Lund Sabata C, Maestrini Elena, Mantoulan Carine, Marshall Christian R, McConachie Helen, McDougle Christopher J, McGrath Jane, McMahon William M, Merikangas Alison, Miller Judith, Minopoli Fiorella, Mirza Ghazala K, Munson Jeff, Nelson Stanley F, Nygren Gudrun, Oliveira Guiomar, Pagnamenta Alistair T, Papanikolaou Katerina, Parr Jeremy R, Parrini Barbara, Pickles Andrew, Pinto Dalila, Piven Joseph, Posey David J, Poustka Annemarie, Poustka Fritz, Ragoussis Jiannis, Roge Bernadette, Rutter Michael L, Sequeira Ana F, Soorya Latha, Sousa Inês, Sykes Nuala, Stoppioni Vera, Tancredi Raffaella, Tauber Maïté, Thompson Ann P, Thomson Susanne, Tsiantis John, Van Engeland Herman, Vincent John B, Volkmar Fred, Vorstman Jacob A S, Wallace Simon, Wang Kai, Wassink Thomas H, White Kathy, Wing Kirsty, Wittemeyer Kerstin, Yaspan Brian L, Zwaigenbaum Lonnie, Betancur Catalina, Buxbaum Joseph D, Cantor Rita M, Cook Edwin H, Coon Hilary, Cuccaro Michael L, Geschwind Daniel H, Haines Jonathan L, Hallmayer Joachim, Monaco Anthony P, Nurnberger John I, Pericak-Vance Margaret A, Schellenberg Gerard D, Scherer Stephen W, Sutcliffe James S, Szatmari Peter, Vieland Veronica J, Wijsman Ellen M, Green Andrew, Gill Michael, Gallagher Louise, Vicente Astrid and Ennis Sean. A novel approach of homozygous haplotype sharing identifies candidate genes in autism spectrum disorder. : Human genetics. 20120514.