Hakutulokset - Rehnström, Karola

Allelic Variants in HTR3C Show Association With Autism Tekijä 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 Tekijä 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 Tekijä 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 Tekijä 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 Tekijä 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 Tekijä 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(†) Tekijä 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 Tekijä 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 Tekijä 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 Tekijä 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 Tekijä 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 Tekijä 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 Tekijä 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 Tekijä 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 Tekijä 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 Tekijä 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 Tekijä 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 Tekijä 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 Tekijä 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 Tekijä 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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