Search Results

Controlling the rate of GWAS false discoveries

by Brzyski, Damian, Peterson, Christine B., Sobczyk, Piotr, Candès, Emmanuel J., Bogdan, Małgorzata, Sabatti, Chiara
Published in Genetics (2017)

Controlling the Rate of GWAS False Discoveries

by Brzyski, Damian, Peterson, Christine B., Sobczyk, Piotr, Candès, Emmanuel J., Bogdan, Malgorzata, Sabatti, Chiara
Published in Genetics (2017)

Controlling the Rate of GWAS False Discoveries

by Brzyski, Damian, Peterson, Christine B, Sobczyk, Piotr, Candès, Emmanuel J, Bogdan, Malgorzata, Sabatti, Chiara
Published in Genetics (2017)

Variance component model to account for sample structure in genome-wide association studies

by Kang, Hyun Min, Sul, Jae Hoon, Service, Susan K, Zaitlen, Noah A, Kong, Sit-yee, Freimer, Nelson B, Sabatti, Chiara, Eskin, Eleazar
Published in Nature Genetics (2010)

Phenotype mining in CNV carriers from a population cohort

by Pietiläinen, Olli P. H., Rehnström, Karola, Jakkula, Eveliina, Service, Susan K., Congdon, Eliza, Tilgmann, Carola, Hartikainen, Anna-Liisa, Taanila, Anja, Heikura, Ulla, Paunio, Tiina, Ripatti, Samuli, Jarvelin, Marjo-Riitta, Isohanni, Matti, Sabatti, Chiara, Palotie, Aarno, Freimer, Nelson B., Peltonen, Leena
Published in Human Molecular Genetics (2011)

Phenotype mining in CNV carriers from a population cohort†

by Pietiläinen, Olli P. H., Rehnström, Karola, Jakkula, Eveliina, Service, Susan K., Congdon, Eliza, Tilgmann, Carola, Hartikainen, Anna-Liisa, Taanila, Anja, Heikura, Ulla, Paunio, Tiina, Ripatti, Samuli, Jarvelin, Marjo-Riitta, Isohanni, Matti, Sabatti, Chiara, Palotie, Aarno, Freimer, Nelson B., Peltonen, Leena
Published in Human Molecular Genetics (2011)

Phenotype mining in CNV carriers from a population cohort

by Pietiläinen, Olli P. H., Rehnström, Karola, Jakkula, Eveliina, Service, Susan K., Congdon, Eliza, Tilgmann, Carola, Hartikainen, Anna-Liisa, Taanila, Anja, Heikura, Ulla, Paunio, Tiina, Ripatti, Samuli, Jarvelin, Marjo-Riitta, Isohanni, Matti, Sabatti, Chiara, Palotie, Aarno, Freimer, Nelson B., Peltonen, Leena
Published in Human Molecular Genetics (2011)

Phenotype mining in CNV carriers from a population cohort

by Pietiläinen, Olli P. H., Rehnström, Karola, Jakkula, Eveliina, Service, Susan K., Congdon, Eliza, Tilgmann, Carola, Hartikainen, Anna-Liisa, Taanila, Anja, Heikura, Ulla, Paunio, Tiina, Ripatti, Samuli, Jarvelin, Marjo-Riitta, Isohanni, Matti, Sabatti, Chiara, Palotie, Aarno, Freimer, Nelson B., Peltonen, Leena
Published in Human Molecular Genetics (2011)

Genome-wide association analysis of metabolic traits in a birth cohort from a founder population.

by Sabatti, Chiara, Service, Susan K, Hartikainen, Anna-Liisa, Pouta, Anneli, Ripatti, Samuli, Brodsky, Jae, Jones, Chris G, Zaitlen, Noah A, Varilo, Teppo, Kaakinen, Marika, Sovio, Ulla, Ruokonen, Aimo, Laitinen, Jaana, Jakkula, Eveliina, Coin, Lachlan, Hoggart, Clive, Collins, Andrew, Turunen, Hannu, Gabriel, Stacey, Elliot, Paul, McCarthy, Mark I, Daly, Mark J, Järvelin, Marjo-Riitta, Freimer, Nelson B, Peltonen, Leena
Published in Nature Genetics (2009)

Genome-wide association analysis of metabolic traits in a birth cohort from a founder population

by Sabatti, Chiara, Service, Susan K, Hartikainen, Anna-Liisa, Pouta, Anneli, Ripatti, Samuli, Brodsky, Jae, Jones, Chris G, Zaitlen, Noah A, Varilo, Teppo, Kaakinen, Marika, Sovio, Ulla, Ruokonen, Aimo, Laitinen, Jaana, Jakkula, Eveliina, Coin, Lachlan, Hoggart, Clive, Collins, Andrew, Turunen, Hannu, Gabriel, Stacey, Elliot, Paul, McCarthy, Mark I, Daly, Mark J, Järvelin, Marjo-Riitta, Freimer, Nelson B, Peltonen, Leena
Published in Nature Genetics (2008)

Genome-wide association analysis of metabolic traits in a birth cohort from a founder population

by Sabatti, Chiara, Service, Susan K., Hartikainen, Anna-Liisa, Pouta, Anneli, Ripatti, Samuli, Brodsky, Jae, Jones, Chris G., Zaitlen, Noah A., Varilo, Teppo, Kaakinen, Marika, Sovio, Ulla, Ruokonen, Aimo, Laitinen, Jaana, Jakkula, Eveliina, Coin, Lachlan, Hoggart, Clive, Collins, Andrew, Turunen, Hannu, Gabriel, Stacey, Elliot, Paul, McCarthy, Mark I., Daly, Mark J., Jarvelin, Marjo-Riitta, Freimer, Nelson B., Peltonen, Leena
Published in Nature Genetics (2009)

Genome-wide association analysis of metabolic traits in a birth cohort from a founder population

by Sabatti, Chiara, Service, Susan K, Hartikainen, Anna-Liisa, Pouta, Anneli, Ripatti, Samuli, Brodsky, Jae, Jones, Chris G., Zaitlen, Noah A, Varilo, Teppo, Kaakinen, Marika, Sovio, Ulla, Ruokonen, Aimo, Laitinen, Jaana, Jakkula, Eveliina, Coin, Lachlan, Hoggart, Clive, Collins, Andrew, Turunen, Hannu, Gabriel, Stacey, Elliot, Paul, McCarthy, Mark I, Daly, Mark J, Jarvelin, Marjo-Riitta, Freimer, Nelson B, Peltonen, Leena
Published in Nature Genetics (2009)

Re-sequencing Expands Our Understanding of the Phenotypic Impact of Variants at GWAS Loci

by Service, Susan K., Teslovich, Tanya M., Fuchsberger, Christian, Ramensky, Vasily, Yajnik, Pranav, Koboldt, Daniel C., Larson, David E., Zhang, Qunyuan, Lin, Ling, Welch, Ryan, Ding, Li, McLellan, Michael D., O'Laughlin, Michele, Fronick, Catrina, Fulton, Lucinda L., Magrini, Vincent, Swift, Amy, Elliott, Paul, Jarvelin, Marjo-Riitta, Kaakinen, Marika, McCarthy, Mark I., Peltonen, Leena, Pouta, Anneli, Bonnycastle, Lori L., Collins, Francis S., Narisu, Narisu, Stringham, Heather M., Tuomilehto, Jaakko, Ripatti, Samuli, Fulton, Robert S., Sabatti, Chiara, Wilson, Richard K., Boehnke, Michael, Freimer, Nelson B.
Published in PLoS Genetics (2014)

Re-sequencing expands our understanding of the phenotypic impact of variants at GWAS loci.

by Service, Susan K, Teslovich, Tanya M, Fuchsberger, Christian, Ramensky, Vasily, Yajnik, Pranav, Koboldt, Daniel C, Larson, David E, Zhang, Qunyuan, Lin, Ling, Welch, Ryan, Ding, Li, McLellan, Michael D, O'Laughlin, Michele, Fronick, Catrina, Fulton, Lucinda L, Magrini, Vincent, Swift, Amy, Elliott, Paul, Jarvelin, Marjo-Riitta, Kaakinen, Marika, McCarthy, Mark I, Peltonen, Leena, Pouta, Anneli, Bonnycastle, Lori L, Collins, Francis S, Narisu, Narisu, Stringham, Heather M, Tuomilehto, Jaakko, Ripatti, Samuli, Fulton, Robert S, Sabatti, Chiara, Wilson, Richard K, Boehnke, Michael, Freimer, Nelson B
Published 2014

Re-sequencing Expands Our Understanding of the Phenotypic Impact of Variants at GWAS Loci

by Service, Susan K, Teslovich, Tanya M, Fuchsberger, Christian, Ramensky, Vasily, Yajnik, Pranav, Koboldt, Daniel C, Larson, David E, Zhang, Qunyuan, Lin, Ling, Welch, Ryan, Ding, Li, McLellan, Michael D, O'Laughlin, Michele, Fronick, Catrina, Fulton, Lucinda L, Magrini, Vincent, Swift, Amy, Elliott, Paul, Jarvelin, Marjo-Riitta, Kaakinen, Marika, McCarthy, Mark I, Peltonen, Leena, Pouta, Anneli, Bonnycastle, Lori L, Collins, Francis S, Narisu, Narisu, Stringham, Heather M, Tuomilehto, Jaakko, Ripatti, Samuli, Fulton, Robert S, Sabatti, Chiara, Wilson, Richard K, Boehnke, Michael, Freimer, Nelson B
Published 2014

Disruption of the neurexin 1 gene is associated with schizophrenia

by Rujescu, Dan, Ingason, Andres, Cichon, Sven, Pietiläinen, Olli P.H., Barnes, Michael R., Toulopoulou, Timothea, Picchioni, Marco, Vassos, Evangelos, Ettinger, Ulrich, Bramon, Elvira, Murray, Robin, Ruggeri, Mirella, Tosato, Sarah, Bonetto, Chiara, Steinberg, Stacy, Sigurdsson, Engilbert, Sigmundsson, Thordur, Petursson, Hannes, Gylfason, Arnaldur, Olason, Pall I., Hardarsson, Gudmundur, Jonsdottir, Gudrun A., Gustafsson, Omar, Fossdal, Ragnheidur, Giegling, Ina, Möller, Hans-Jürgen, Hartmann, Annette M., Hoffmann, Per, Crombie, Caroline, Fraser, Gillian, Walker, Nicholas, Lonnqvist, Jouko, Suvisaari, Jaana, Tuulio-Henriksson, Annamari, Djurovic, Srdjan, Melle, Ingrid, Andreassen, Ole A., Hansen, Thomas, Werge, Thomas, Kiemeney, Lambertus A., Franke, Barbara, Veltman, Joris, Buizer-Voskamp, Jacobine E., Sabatti, Chiara, Ophoff, Roel A., Rietschel, Marcella, Nöthen, Markus M., Stefansson, Kari, Peltonen, Leena, Clair, David St
Published in Human Molecular Genetics (2008)

Disruption of the neurexin 1 gene is associated with schizophrenia

by Rujescu, Dan, Ingason, Andres, Cichon, Sven, Pietilainen, Olli P. H., Barnes, Michael R., Toulopoulou, Timothea, Picchioni, Marco, Vassos, Evangelos, Ettinger, Ulrich, Bramon, Elvira, Murray, Robin, Ruggeri, Mirella, Tosato, Sarah, Bonetto, Chiara, Steinberg, Stacy, Sigurdsson, Engilbert, Sigmundsson, Thordur, Petursson, Hannes, Gylfason, Arnaldur, Olason, Pall I., Hardarsson, Gudmundur, Jonsdottir, Gudrun A., Gustafsson, Omar, Fossdal, Ragnheidur, Giegling, Ina, Moeller, Hans-Jurgen, Hartmann, Annette M., Hoffmann, Per, Crombie, Caroline, Fraser, Gillian, Walker, Nicholas, Lonnqvist, Jouko, Suvisaari, Jaana, Tuulio-Henriksson, Annamari, Djurovic, Srdjan, Melle, Ingrid, Andreassen, Ole A., Hansen, Thomas, Werge, Thomas, Kiemeney, Lambertus A., Franke, Barbara, Veltman, Joris, Buizer-Voskamp, Jacobine E., Sabatti, Chiara, Ophoff, Roel A., Rietschel, Marcella, Noehen, Markus M., Stefansson, Kari, Peltonen, Leena, St Clair, David
Published in Human Molecular Genetics (2009)

Disruption of the neurexin 1 gene is associated with schizophrenia

by Rujescu, Dan, Ingason, Andres, Cichon, Sven, Pietilainen, Olli P. H., Barnes, Michael R., Toulopoulou, Timothea, Picchioni, Marco, Vassos, Evangelos, Ettinger, Ulrich, Bramon, Elvira, Murray, Robin, Ruggeri, Mirella, Tosato, Sarah, Bonetto, Chiara, Steinberg, Stacy, Sigurdsson, Engilbert, Sigmundsson, Thordur, Petursson, Hannes, Gylfason, Arnaldur, Olason, Pall I., Hardarsson, Gudmundur, Jonsdottir, Gudrun A., Gustafsson, Omar, Fossdal, Ragnheidur, Giegling, Ina, Moeller, Hans-Jurgen, Hartmann, Annette M., Hoffmann, Per, Crombie, Caroline, Fraser, Gillian, Walker, Nicholas, Lonnqvist, Jouko, Suvisaari, Jaana, Tuulio-Henriksson, Annamari, Djurovic, Srdjan, Melle, Ingrid, Andreassen, Ole A., Hansen, Thomas, Werge, Thomas, Kiemeney, Lambertus A., Franke, Barbara, Veltman, Joris, Buizer-Voskamp, Jacobine E., Sabatti, Chiara, Ophoff, Roel A., Rietschel, Marcella, Noehen, Markus M., Stefansson, Kari, Peltonen, Leena, St Clair, David
Published in Human Molecular Genetics (2009)

Disruption of the neurexin 1 gene is associated with schizophrenia

by Rujescu, Dan, Ingason, Andres, Cichon, Sven, Pietiläinen, Olli P.H., Barnes, Michael R., Toulopoulou, Timothea, Picchioni, Marco, Vassos, Evangelos, Ettinger, Ulrich, Bramon, Elvira, Murray, Robin, Ruggeri, Mirella, Tosato, Sarah, Bonetto, Chiara, Steinberg, Stacy, Sigurdsson, Engilbert, Sigmundsson, Thordur, Petursson, Hannes, Gylfason, Arnaldur, Olason, Pall I., Hardarsson, Gudmundur, Jonsdottir, Gudrun A., Gustafsson, Omar, Fossdal, Ragnheidur, Giegling, Ina, Möller, Hans-Jürgen, Hartmann, Annette M., Hoffmann, Per, Crombie, Caroline, Fraser, Gillian, Walker, Nicholas, Lonnqvist, Jouko, Suvisaari, Jaana, Tuulio-Henriksson, Annamari, Djurovic, Srdjan, Melle, Ingrid, Andreassen, Ole A., Hansen, Thomas, Werge, Thomas, Kiemeney, Lambertus A., Franke, Barbara, Veltman, Joris, Buizer-Voskamp, Jacobine E., GROUP Investigators, Sabatti, Chiara, Ophoff, Roel A., Rietschel, Marcella, Nöthen, Markus M., Stefansson, Kari, Peltonen, Leena
Published in Human Molecular Genetics (2009)

Disruption of the neurexin 1 gene is associated with schizophrenia

by Rujescu, Dan, Ingason, Andres, Cichon, Sven, Pietiläinen, Olli P H, Barnes, Michael R, Toulopoulou, Timothea, Picchioni, Marco, Vassos, Evangelos, Ettinger, Ulrich, Bramon, Elvira, Murray, Robin, Ruggeri, Mirella, Tosato, Sarah, Bonetto, Chiara, Steinberg, Stacy, Sigurdsson, Engilbert, Sigmundsson, Thordur, Petursson, Hannes, Gylfason, Arnaldur, Olason, Pall I, Hardarsson, Gudmundur, Jonsdottir, Gudrun A, Gustafsson, Omar, Fossdal, Ragnheidur, Giegling, Ina, Möller, Hans-Jürgen, Hartmann, Annette M, Hoffmann, Per, Crombie, Caroline, Fraser, Gillian, Walker, Nicholas, Lonnqvist, Jouko, Suvisaari, Jaana, Tuulio-Henriksson, Annamari, Djurovic, Srdjan, Melle, Ingrid, Andreassen, Ole A, Hansen, Thomas, Werge, Thomas, Kiemeney, Lambertus A, Franke, Barbara, Veltman, Joris, Buizer-Voskamp, Jacobine E, Sabatti, Chiara, Ophoff, Roel A, Rietschel, Marcella, Nöthen, Markus M, Stefansson, Kari, Peltonen, Leena, St Clair, David
Published in Human Molecular Genetics (2011)