Search Results - Rehnström, Karola

Allelic Variants in HTR3C Show Association With Autism by Rehnström, Karola, Ylisaukko-oja, Tero, Nummela, Ilona, Ellonen, Pekka, Kempas, Elli, Vanhala, Raija, von Wendt, Lennart, Järvelä, Irma, Peltonen, Leena

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Linkage and Linkage Disequilibrium Scan for Autism Loci in an Extended Pedigree from Finland by Kilpinen, Helena, Ylisaukko-oja, Tero, Rehnström, Karola, Gaál, Emilia, Turunen, Joni A., Kempas, Elli, von Wendt, Lennart, Varilo, Teppo, Peltonen, Leena

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A Genome Wide Association Study of Mathematical Ability Reveals an Association at Chromosome 3q29, a Locus Associated with Autism and Learning Difficulties: A Preliminary Study by Baron-Cohen, Simon, Murphy, Laura, Chakrabarti, Bhismadev, Craig, Ian, Mallya, Uma, Lakatošová, Silvia, Rehnstrom, Karola, Peltonen, Leena, Wheelwright, Sally, Allison, Carrie, Fisher, Simon E., Warrier, Varun

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A Pooled Genome-Wide Association Study of Asperger Syndrome by Warrier, Varun, Chakrabarti, Bhismadev, Murphy, Laura, Chan, Allen, Craig, Ian, Mallya, Uma, Lakatošová, Silvia, Rehnstrom, Karola, Peltonen, Leena, Wheelwright, Sally, Allison, Carrie, Fisher, Simon E., Baron-Cohen, Simon

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Identification of Small Exonic CNV from Whole-Exome Sequence Data and Application to Autism Spectrum Disorder by Poultney, Christopher S., Goldberg, Arthur P., Drapeau, Elodie, Kou, Yan, Harony-Nicolas, Hala, Kajiwara, Yuji, De Rubeis, Silvia, Durand, Simon, Stevens, Christine, Rehnström, Karola, Palotie, Aarno, Daly, Mark J., Ma’ayan, Avi, Fromer, Menachem, Buxbaum, Joseph D.

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The Genome-wide Patterns of Variation Expose Significant Substructure in a Founder Population by Jakkula, Eveliina, Rehnström, Karola, Varilo, Teppo, Pietiläinen, Olli P.H., Paunio, Tiina, Pedersen, Nancy L., deFaire, Ulf, Järvelin, Marjo-Riitta, Saharinen, Juha, Freimer, Nelson, Ripatti, Samuli, Purcell, Shaun, Collins, Andrew, Daly, Mark J., Palotie, Aarno, Peltonen, Leena

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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

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Platelet surface receptor glycoprotein VI-dimer is overexpressed in stroke: The Glycoprotein VI in Stroke (GYPSIE) study results by Induruwa, Isuru, McKinney, Harriet, Kempster, Carly, Thomas, Patrick, Batista, Joana, Malcor, Jean-Daniel, Bonna, Arkadiusz, McGee, Joanne, Bumanlag-Amis, Elaine, Rehnstrom, Karola, Ashford, Sophie, Soejima, Kenji, Ouwehand, Willem, Farndale, Richard, Downes, Kate, Warburton, Elizabeth, Moroi, Masaaki, Jung, Stephanie

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A Genome-Wide Analysis of Populations from European Russia Reveals a New Pole of Genetic Diversity in Northern Europe by Khrunin, Andrey V., Khokhrin, Denis V., Filippova, Irina N., Esko, Tõnu, Nelis, Mari, Bebyakova, Natalia A., Bolotova, Natalia L., Klovins, Janis, Nikitina-Zake, Liene, Rehnström, Karola, Ripatti, Samuli, Schreiber, Stefan, Franke, Andre, Macek, Milan, Krulišová, Veronika, Lubinski, Jan, Metspalu, Andres, Limborska, Svetlana A.

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The Genetic Structure of the Swedish Population by Humphreys, Keith, Grankvist, Alexander, Leu, Monica, Hall, Per, Liu, Jianjun, Ripatti, Samuli, Rehnström, Karola, Groop, Leif, Klareskog, Lars, Ding, Bo, Grönberg, Henrik, Xu, Jianfeng, Pedersen, Nancy L., Lichtenstein, Paul, Mattingsdal, Morten, Andreassen, Ole A., O'Dushlaine, Colm, Purcell, Shaun M., Sklar, Pamela, Sullivan, Patrick F., Hultman, Christina M., Palmgren, Juni, Magnusson, Patrik K. E.

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Intracranial Aneurysm Risk Locus 5q23.2 Is Associated with Elevated Systolic Blood Pressure by Gaál, Emília Ilona, Salo, Perttu, Kristiansson, Kati, Rehnström, Karola, Kettunen, Johannes, Sarin, Antti-Pekka, Niemelä, Mika, Jula, Antti, Raitakari, Olli T., Lehtimäki, Terho, Eriksson, Johan G., Widen, Elisabeth, Günel, Murat, Kurki, Mitja, von und zu Fraunberg, Mikael, Jääskeläinen, Juha E., Hernesniemi, Juha, Järvelin, Marjo-Riitta, Pouta, Anneli, Newton-Cheh, Christopher, Salomaa, Veikko, Palotie, Aarno, Perola, Markus

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Lineage-Specific Genome Architecture Links Enhancers and Non-coding Disease Variants to Target Gene Promoters by Javierre, Biola M., Burren, Oliver S., Wilder, Steven P., Kreuzhuber, Roman, Hill, Steven M., Sewitz, Sven, Cairns, Jonathan, Wingett, Steven W., Várnai, Csilla, Thiecke, Michiel J., Burden, Frances, Farrow, Samantha, Cutler, Antony J., Rehnström, Karola, Downes, Kate, Grassi, Luigi, Kostadima, Myrto, Freire-Pritchett, Paula, Wang, Fan, Stunnenberg, Hendrik G., Todd, John A., Zerbino, Daniel R., Stegle, Oliver, Ouwehand, Willem H., Frontini, Mattia, Wallace, Chris, Spivakov, Mikhail, Fraser, Peter

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A framework for the interpretation of de novo mutation in human disease by Samocha, Kaitlin E., Robinson, Elise B., Sanders, Stephan J., Stevens, Christine, Sabo, Aniko, McGrath, Lauren M., Kosmicki, Jack A., Rehnström, Karola, Mallick, Swapan, Kirby, Andrew, Wall, Dennis P., MacArthur, Daniel G., Gabriel, Stacey B., dePristo, Mark, Purcell, Shaun M., Palotie, Aarno, Boerwinkle, Eric, Buxbaum, Joseph D., Cook, Edwin H., Gibbs, Richard A., Schellenberg, Gerard D., Sutcliffe, James S., Devlin, Bernie, Roeder, Kathryn, Neale, Benjamin M., Daly, Mark J.

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Deletion of TOP3β, a component of FMRP-containing mRNPs, contributes to neurodevelopmental disorders by Stoll, Georg, Pietiläinen, Olli P. H., Linder, Bastian, Suvisaari, Jaana, Brosi, Cornelia, Hennah, William, Leppä, Virpi, Torniainen, Minna, Ripatti, Samuli, Ala-Mello, Sirpa, Plöttner, Oliver, Rehnström, Karola, Tuulio-Henriksson, Annamari, Varilo, Teppo, Tallila, Jonna, Kristiansson, Kati, Isohanni, Matti, Kaprio, Jaakko, Eriksson, Johan G., Raitakari, Olli T., Lehtimäki, Terho, Jarvelin, Marjo-Riitta, Salomaa, Veikko, Hurles, Matthew, Stefansson, Hreinn, Peltonen, Leena, Sullivan, Patrick F., Paunio, Tiina, Lönnqvist, Jouko, Daly, Mark J., Fischer, Utz, Freimer, Nelson B., Palotie, Aarno

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Transcriptional, epigenetic and metabolic signatures in cardiometabolic syndrome defined by extreme phenotypes by Seyres, Denis, Cabassi, Alessandra, Lambourne, John J., Burden, Frances, Farrow, Samantha, McKinney, Harriet, Batista, Joana, Kempster, Carly, Pietzner, Maik, Slingsby, Oliver, Cao, Thong Huy, Quinn, Paulene A., Stefanucci, Luca, Sims, Matthew C., Rehnstrom, Karola, Adams, Claire L., Frary, Amy, Ergüener, Bekir, Kreuzhuber, Roman, Mocciaro, Gabriele, D’Amore, Simona, Koulman, Albert, Grassi, Luigi, Griffin, Julian L., Ng, Leong Loke, Park, Adrian, Savage, David B., Langenberg, Claudia, Bock, Christoph, Downes, Kate, Wareham, Nicholas J., Allison, Michael, Vacca, Michele, Kirk, Paul D. W., Frontini, Mattia

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Genetic characterization of northeastern Italian population isolates in the context of broader European genetic diversity by Esko, Tõnu, Mezzavilla, Massimo, Nelis, Mari, Borel, Christelle, Debniak, Tadeusz, Jakkula, Eveliina, Julia, Antonio, Karachanak, Sena, Khrunin, Andrey, Kisfali, Peter, Krulisova, Veronika, Aušrelé Kučinskiené, Zita, Rehnström, Karola, Traglia, Michela, Nikitina-Zake, Liene, Zimprich, Fritz, Antonarakis, Stylianos E, Estivill, Xavier, Glavač, Damjan, Gut, Ivo, Klovins, Janis, Krawczak, Michael, Kučinskas, Vaidutis, Lathrop, Mark, Macek, Milan, Marsal, Sara, Meitinger, Thomas, Melegh, Béla, Limborska, Svetlana, Lubinski, Jan, Paolotie, Aarno, Schreiber, Stefan, Toncheva, Draga, Toniolo, Daniela, Wichmann, H-Erich, Zimprich, Alexander, Metspalu, Mait, Gasparini, Paolo, Metspalu, Andres, D'Adamo, Pio

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Genetic Structure of Europeans: A View from the North–East by Nelis, Mari, Esko, Tõnu, Mägi, Reedik, Zimprich, Fritz, Zimprich, Alexander, Toncheva, Draga, Karachanak, Sena, Piskáčková, Tereza, Balaščák, Ivan, Peltonen, Leena, Jakkula, Eveliina, Rehnström, Karola, Lathrop, Mark, Heath, Simon, Galan, Pilar, Schreiber, Stefan, Meitinger, Thomas, Pfeufer, Arne, Wichmann, H-Erich, Melegh, Béla, Polgár, Noémi, Toniolo, Daniela, Gasparini, Paolo, D'Adamo, Pio, Klovins, Janis, Nikitina-Zake, Liene, Kučinskas, Vaidutis, Kasnauskienė, Jūratė, Lubinski, Jan, Debniak, Tadeusz, Limborska, Svetlana, Khrunin, Andrey, Estivill, Xavier, Rabionet, Raquel, Marsal, Sara, Julià, Antonio, Antonarakis, Stylianos E., Deutsch, Samuel, Borel, Christelle, Attar, Homa, Gagnebin, Maryline, Macek, Milan, Krawczak, Michael, Remm, Maido, Metspalu, Andres

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Correction: Genetic Structure of Europeans: A View from the North–East by Nelis, Mari, Esko, Tõnu, Mägi, Reedik, Zimprich, Fritz, Zimprich, Alexander, Toncheva, Draga, Karachanak, Sena, Piskáčková, Tereza, Balaščák, Ivan, Peltonen, Leena, Jakkula, Eveliina, Rehnström, Karola, Lathrop, Mark, Heath, Simon, Galan, Pilar, Schreiber, Stefan, Meitinger, Thomas, Pfeufer, Arne, Wichmann, H-Erich, Melegh, Béla, Polgár, Noémi, Toniolo, Daniela, Gasparini, Paolo, D'Adamo, Pio, Klovins, Janis, Nikitina-Zake, Liene, Kučinskas, Vaidutis, Kasnauskienė, Jūratė, Lubinski, Jan, Debniak, Tadeusz, Limborska, Svetlana, Khrunin, Andrey, Estivill, Xavier, Rabionet, Raquel, Marsal, Sara, Julià, Antonio, Antonarakis, Stylianos E., Deutsch, Samuel, Borel, Christelle, Attar, Homa, Gagnebin, Maryline, Macek, Milan, Krawczak, Michael, Remm, Maido, Metspalu, Andres

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Increased DNA methylation variability in type 1 diabetes across three immune effector cell types by Paul, Dirk S., Teschendorff, Andrew E., Dang, Mary A.N., Lowe, Robert, Hawa, Mohammed I., Ecker, Simone, Beyan, Huriya, Cunningham, Stephanie, Fouts, Alexandra R., Ramelius, Anita, Burden, Frances, Farrow, Samantha, Rowlston, Sophia, Rehnstrom, Karola, Frontini, Mattia, Downes, Kate, Busche, Stephan, Cheung, Warren A., Ge, Bing, Simon, Marie-Michelle, Bujold, David, Kwan, Tony, Bourque, Guillaume, Datta, Avik, Lowy, Ernesto, Clarke, Laura, Flicek, Paul, Libertini, Emanuele, Heath, Simon, Gut, Marta, Gut, Ivo G, Ouwehand, Willem H., Pastinen, Tomi, Soranzo, Nicole, Hofer, Sabine E., Karges, Beate, Meissner, Thomas, Boehm, Bernhard O., Cilio, Corrado, Elding Larsson, Helena, Lernmark, Åke, Steck, Andrea K., Rakyan, Vardhman K., Beck, Stephan, Leslie, R. David

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Distribution and Medical Impact of Loss-of-Function Variants in the Finnish Founder Population by Lim, Elaine T., Würtz, Peter, Havulinna, Aki S., Palta, Priit, Tukiainen, Taru, Rehnström, Karola, Esko, Tõnu, Mägi, Reedik, Inouye, Michael, Lappalainen, Tuuli, Chan, Yingleong, Salem, Rany M., Lek, Monkol, Flannick, Jason, Sim, Xueling, Manning, Alisa, Ladenvall, Claes, Bumpstead, Suzannah, Hämäläinen, Eija, Aalto, Kristiina, Maksimow, Mikael, Salmi, Marko, Blankenberg, Stefan, Ardissino, Diego, Shah, Svati, Horne, Benjamin, McPherson, Ruth, Hovingh, Gerald K., Reilly, Muredach P., Watkins, Hugh, Goel, Anuj, Farrall, Martin, Girelli, Domenico, Reiner, Alex P., Stitziel, Nathan O., Kathiresan, Sekar, Gabriel, Stacey, Barrett, Jeffrey C., Lehtimäki, Terho, Laakso, Markku, Groop, Leif, Kaprio, Jaakko, Perola, Markus, McCarthy, Mark I., Boehnke, Michael, Altshuler, David M., Lindgren, Cecilia M., Hirschhorn, Joel N., Metspalu, Andres, Freimer, Nelson B., Zeller, Tanja, Jalkanen, Sirpa, Koskinen, Seppo, Raitakari, Olli, Durbin, Richard, MacArthur, Daniel G., Salomaa, Veikko, Ripatti, Samuli, Daly, Mark J., Palotie, Aarno

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