Resultats de la cerca - Katrin Männik

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  1. 1
    The 16p11.2 locus modulates brain structures common to autism, schizophrenia and obesity

    The 16p11.2 locus modulates brain structures common to autism, schizophrenia and obesity per Anne Maillard, Anne Ruef, Fabrizio Pizzagalli, Eugenia Migliavacca, Loyse Hippolyte, Stanisław Adaszewski, Juergen Dukart, Carlotta Ferrari, Philippe Conus, Katrin Männik, Marianna Zazhytska, Vanessa Siffredi, Philippe Maeder, Zoltán Kutalik, Ferath Kherif, Nouchine Hadjikhani, J. Beckmann, Alexandre Reymond, Bogdan Draganski, Sébastien Jacquemont

    Publicat 2014
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  2. 2
    The Human-Specific BOLA2 Duplication Modifies Iron Homeostasis and Anemia Predisposition in Chromosome 16p11.2 Autism Individuals

    The Human-Specific BOLA2 Duplication Modifies Iron Homeostasis and Anemia Predisposition in Chromosome 16p11.2 Autism Individuals per Giuliana Giannuzzi, Paul J. Schmidt, Eleonora Porcu, Gilles Willemin, Katherine M. Munson, Xander Nuttle, Rachel K. Earl, Jacqueline Chrast, Kendra Hoekzema, Davide Risso, Katrin Männik, Pasquelena De Nittis, Ethan Baratz, Yann Hérault, Xiang Gao, Caroline C. Philpott, Raphael Bernier, Zoltán Kutalik, Mark D. Fleming, Evan E. Eichler, Alexandre Reymond

    Publicat 2019
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  3. 3
    Copy Number Variations and Cognitive Phenotypes in Unselected Populations

    Copy Number Variations and Cognitive Phenotypes in Unselected Populations per Katrin Männik, Reedik Mägi, Aurélien Mace, Ben Cole, Anna L. Guyatt, Hashem A. Shihab, Anne Maillard, Helene Alavere, Anneli Kolk, Anu Reigo, Evelin Mihailov, Liis Leitsalu, Anne-Maud Ferreira, Margit Nõukas, Alexander Teumer, Erika Salvi, Daniele Cusi, Matt McGue, William G. Iacono, Tom R. Gaunt, J. Beckmann, Sébastien Jacquemont, Zoltán Kutalik, Nathan Pankratz, Nicholas J. Timpson, Andres Metspalu, Alexandre Reymond

    Publicat 2015
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  4. 4
    The Number of Genomic Copies at the 16p11.2 Locus Modulates Language, Verbal Memory, and Inhibition

    The Number of Genomic Copies at the 16p11.2 Locus Modulates Language, Verbal Memory, and Inhibition per Loyse Hippolyte, Anne Maillard, Borja Rodríguez‐Herreros, Aurélie Pain, Sandra Martin-Brevet, Carina Ferrari, Philippe Conus, Aurélien Mace, Nouchine Hadjikhani, Andres Metspalu, Anu Reigo, Anneli Kolk, Katrin Männik, Mandy Barker, Bertrand Isidor, Cédric Le Caignec, Cyril Mignot, Laurence Schneider, Laurent Mottron, Boris Keren, Albert David, Martine Doco‐Fenzy, Marion Gérard, Raphael Bernier, Robin P. Goin‐Kochel, Ellen Hanson, LeeAnne Green Snyder, Franck Ramus, J. Beckmann, Bogdan Draganski, Alexandre Reymond, Sébastien Jacquemont

    Publicat 2015
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  5. 5
    Chromosomal contacts connect loci associated with autism, BMI and head circumference phenotypes

    Chromosomal contacts connect loci associated with autism, BMI and head circumference phenotypes per Maria Nicla Loviglio, Marion Leleu, Katrin Männik, Marzia Passeggeri, Giuliana Giannuzzi, Inge van der Werf, Sebastian M. Waszak, Marianna Zazhytska, I Roberts-Caldeira, Nele Gheldof, Eugenia Migliavacca, Ali Abdullah Alfaiz, Loyse Hippolyte, Anne Maillard, Anke Van Dijck, R. Frank Kooy, Damien Sanlaville, Jill A. Rosenfeld, Lisa G. Shaffer, Joris Andrieux, C. Marshall, Stephen W. Scherer, Yiping Shen, James F. Gusella, U. Thorsteinsdottir, Guðmar Þorleifsson, Emmanouil T. Dermitzakis, Bart Deplancke, J. Beckmann, Jacques Rougemont, Sébastien Jacquemont, Alexandre Reymond

    Publicat 2016
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  6. 6
    A Potential Contributory Role for Ciliary Dysfunction in the 16p11.2 600 kb BP4-BP5 Pathology

    A Potential Contributory Role for Ciliary Dysfunction in the 16p11.2 600 kb BP4-BP5 Pathology per Eugenia Migliavacca, Christelle Golzio, Katrin Männik, Ian Blumenthal, Edwin C. Oh, Louise Harewood, Jack A. Kosmicki, Maria Nicla Loviglio, Giuliana Giannuzzi, Loyse Hippolyte, Anne Maillard, Ali Abdullah Alfaiz, Mieke M. van Haelst, Joris Andrieux, James F. Gusella, Mark J. Daly, J. Beckmann, Sébastien Jacquemont, Michael E. Talkowski, Nicholas Katsanis, Alexandre Reymond, Eugenia Migliavacca, Katrin Männik, Louise Harewood, Maria Nicla Loviglio, Robert M. Witwicki, Gérard Didelot, Ilse van der Werf, Ali Abdullah Alfaiz, Marianna Zazhytska, Giuliana Giannuzzi, Jacqueline Chrast, Aurélien Macé, Sven Bergmann, Zoltán Kutalik, Loyse Hippolyte, Anne Maillard, Vanessa Siffredi, Flore Zufferey, Danielle Martinet, Frédérique Béna, Anita Rauch, Sonia Bouquillon, Joris Andrieux, Bruno Delobel, Odile Boute, Bénédicte Duban‐Bedu, Cédric Le Caignec, Bertrand Isidor, Jean Chiésa, Boris Keren, Brigitte Gilbert‐Dussardier, Renaud Touraine, Dominique Campion, Caroline Rooryck, Michèle Mathieu‐Dramard, Ghislaine Plessis, R. Frank Kooy, Hilde Peeters, Katrin Õunap, Anneke T. Vulto‐van Silfhout, Bert Ba de Vries, Ellen van Binsbergen, Mieke M. van Haelst, Ann Nordgren, Mafalda Mucciolo, Alessandra Renieri, Evica Rajcan‐Separovic, John A. Philipps, Richard J. Ellis, J. Beckmann, Sébastien Jacquemont, Alexandre Reymond

    Publicat 2015
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  7. 7
    A 600 kb deletion syndrome at 16p11.2 leads to energy imbalance and neuropsychiatric disorders

    A 600 kb deletion syndrome at 16p11.2 leads to energy imbalance and neuropsychiatric disorders per Flore Zufferey, Elliott H. Sherr, Noam D. Beckmann, Ellen Hanson, Anne Maillard, Loyse Hippolyte, Aurélien Mace, Carina Ferrari, Zoltán Kutalik, Joris Andrieux, Elizabeth Aylward, Mandy Barker, Raphael Bernier, Sonia Bouquillon, Philippe Conus, Bruno Delobel, W. Andrew Faucett, Robin P. Goin‐Kochel, P. Ellen Grant, Louise Harewood, Jill V. Hunter, Sébastien Lebon, David H. Ledbetter, Alastair J. Martin, Katrin Männik, Danielle Martinet, Pratik Mukherjee, Melissa B. Ramocki, Sarah Spence, Kyle J. Steinman, Jennifer Tjernagel, John E. Spiro, Alexandre Reymond, J. Beckmann, Wendy K. Chung, Sébastien Jacquemont

    Publicat 2012
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  8. 8
    Rare variants in the genetic background modulate cognitive and developmental phenotypes in individuals carrying disease-associated variants

    Rare variants in the genetic background modulate cognitive and developmental phenotypes in individuals carrying disease-associated variants per Lucilla Pizzo, Matthew Jensen, Andrew Polyak, Jill A. Rosenfeld, Katrin Männik, Arjun Krishnan, M. Elizabeth McCready, Olivier Pichon, Cédric Le Caignec, Anke Van Dijck, Kate Pope, Els Voorhoeve, Jieun Yoon, Paweł Stankiewicz, Sau Wai Cheung, Damian Pazuchanics, Emily Huber, Vijay Kumar, Rachel L. Kember, Francesca Mari, Aurora Currò, Lucia Castiglia, Ornella Galesi, Emanuela Avola, Teresa Mattina, Marco Fichera, Luana Mandarà, Marie Vincent, Mathilde Nizon, Sandra Mercier, Claire Bénéteau, Sophie Blesson, Dominique Martin–Coignard, Anne-Laure Mosca-Boidron, Jean-Hubert Caberg, Maja Bućan, Susan Zeesman, Małgorzata J.M. Nowaczyk, Mathilde Lefebvre, Laurence Faivre, Patrick Callier, Cindy Skinner, Boris Keren, Perrine Charles, Paolo Prontera, Nathalie Marle, Alessandra Renieri, Alexandre Reymond, R. Frank Kooy, Bertrand Isidor, Charles E. Schwartz, Corrado Romano, Erik A. Sistermans, David J. Amor, Joris Andrieux, Santhosh Girirajan

    Publicat 2018
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  9. 9
    Defining the Effect of the 16p11.2 Duplication on Cognition, Behavior, and Medical Comorbidities

    Defining the Effect of the 16p11.2 Duplication on Cognition, Behavior, and Medical Comorbidities per Debra D’Angelo, Sébastien Lebon, Qixuan Chen, Sandra Martin-Brevet, LeeAnne Green Snyder, Loyse Hippolyte, Ellen Hanson, Anne Maillard, W. Andrew Faucett, Aurélien Mace, Aurélie Pain, Raphael Bernier, Samuel J. R. A. Chawner, Albert David, Joris Andrieux, Elizabeth Aylward, Geneviève Baujat, Inês Caldeira, Philippe Conus, Carrina Ferrari, Francesca Forzano, Marion Gérard, Robin P. Goin‐Kochel, P. Ellen Grant, Jill V. Hunter, Bertrand Isidor, Aurélia Jacquette, Aia Elise Jønch, Boris Keren, Didier Lacombe, Cédric Le Caignec, Alastair J. Martin, Katrin Männik, Andres Metspalu, Cyril Mignot, Pratik Mukherjee, Michael J. Owen, Marzia Passeggeri, Caroline Rooryck, Jill A. Rosenfeld, Sarah Spence, Kyle J. Steinman, Jennifer Tjernagel, Mieke M. van Haelst, Yiping Shen, Bogdan Draganski, Elliott H. Sherr, David H. Ledbetter, Marianne B. M. van den Bree, J. Beckmann, John E. Spiro, Alexandre Reymond, Sébastien Jacquemont, Wendy K. Chung

    Publicat 2015
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  10. 10
    A new highly penetrant form of obesity due to deletions on chromosome 16p11.2

    A new highly penetrant form of obesity due to deletions on chromosome 16p11.2 per Robin Walters, Sébastien Jacquemont, Armand Valsesia, Adam J. de Smith, Danielle Martinet, Johanna C. Andersson‐Assarsson, Mario Falchi, Fei Chen, Joris Andrieux, Stéphane Lobbens, B Delobel, Fanny Stutzmann, Julia S. El-Sayed Moustafa, Jean-Claude Chèvre, Cécile Lecœur, Vincent Vatin, Sonia Bouquillon, Jessica L. Buxton, Odile Boute, Muriel Holder‐Espinasse, Jean‐Marie Cuisset, M. Lemaître, Anne‐Emmanuelle Ambresin, Andrea Brioschi, Muriel Gaillard, Vittorio Giusti, Florence Fellmann, Alessandra Ferrarini, Nouchine Hadjikhani, Dominique Campion, Audrey Guilmatre, Anna Goldenberg, Nadège Calmels, Jean‐Louis Mandel, Cédric Le Caignec, A. David, Bertrand Isidor, Marie‐Pierre Cordier, Sophie Dupuis‐Girod, Audrey Labalme, Damien Sanlaville, Mylène Béri‐Dexheimer, Philippe Jonveaux, Bruno Leheup, Katrin Õunap, Elena G. Bochukova, Elana Henning, Julia M. Keogh, Richard J. Ellis, K D MacDermot, Mieke M. van Haelst, C. Vincent‐Delorme, Ghislaine Plessis, Renaud Touraine, Anne Philippe, Valérie Malan, M. Mathieu‐Dramard, Jean Chiésa, Bettina Blaumeiser, R. Frank Kooy, Robert Caïazzo, Marie Pigeyre, Beverley Balkau, Robert Sladek, Sven Bergmann, Vincent Mooser, Dawn Waterworth, Alexandre Reymond, Péter Vollenweider, Gérard Waeber, Ants Kurg, Priit Palta, Tõnu Esko, Andres Metspalu, Mari Nelis, Paul Elliott, Anna‐Liisa Hartikainen, Mark I. McCarthy, L. Peltonen, Lena Carlsson, Peter Jacobson, Lars Sjöström, Ni Huang, Matthew E. Hurles, Stephen O’Rahilly, I. Sadaf Farooqi, Katrin Männik, Marjo‐Riitta Järvelin, François Pattou, Stephen Eyre, Andrew J. Walley, Lachlan Coin, Alexandra I. F. Blakemore, Philippe Froguel, J. Beckmann

    Publicat 2010
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  11. 11
    Mirror extreme BMI phenotypes associated with gene dosage at the chromosome 16p11.2 locus

    Mirror extreme BMI phenotypes associated with gene dosage at the chromosome 16p11.2 locus per Sébastien Jacquemont, Alexandre Reymond, Flore Zufferey, Louise Harewood, Robin Walters, Zoltán Kutalik, Danielle Martinet, Yiping Shen, Armand Valsesia, Noam D. Beckmann, Guðmar Þorleifsson, Marco Belfiore, Sonia Bouquillon, Dominique Campion, Nicole de Leeuw, Bert B.A. de Vries, Tõnu Esko, Bridget A. Fernandez, Fernando Fernández‐Aranda, José Manuel Fernández‐Real, Mónica Gratacòs, Audrey Guilmatre, Juliane Hoyer, Marjo‐Riitta Järvelin, R. Frank Kooy, Ants Kurg, Cédric Le Caignec, Katrin Männik, Orah S. Platt, Damien Sanlaville, Mieke M. van Haelst, Sergi Villatoro, Faida Walha, Bai-Lin Wu, Yongguo Yu, Azzedine Aboura, Marie‐Claude Addor, Yves Alembik, Stylianos E. Antonarakis, Benoı̂t Arveiler, Magalie Barth, Nathalie Bednarek, Frédérique Béna, Sven Bergmann, Mylène Béri, Laura Bernardini, Bettina Blaumeiser, Dominique Bonneau, Armand Bottani, Odile Boute, Han G. Brunner, Dorothée Cailley, Patrick Callier, Jean Chiésa, Jacqueline Chrast, Lachlan Coin, Charles Coutton, Jean‐Marie Cuisset, J. Cuvellier, Albert David, Bénédicte de Fréminville, Bruno Delobel, Marie‐Ange Delrue, Bénédicte Demeer, Dominique Descamps, Gérard Didelot, Klaus Dieterich, Vittoria Disciglio, Martine Doco‐Fenzy, Séverine Drunat, Bénédicte Duban‐Bedu, Christèle Dubourg, Julia S. El-Sayed Moustafa, Paul Elliott, Brigitte H. W. Faas, Laurence Faivre, Anne Faudet, Florence Fellmann, Alessandra Ferrarini, Richard Fisher, Elisabeth Flori, Lukas Forer, Dominique Gaillard, Marion Gérard, Christian Gieger, Stefania Gimelli, Giorgio Gimelli, Hans J. Grabe, Agnès Guichet, Olivier Guillin, Anna‐Liisa Hartikainen, Delphine Héron, Loyse Hippolyte, Muriel Holder, Georg Homuth, Bertrand Isidor, Sylvie Jaillard, Zdenek Jaros, Susana Jiménez‐Múrcia, Géraldine Joly Helas

    Publicat 2011
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  12. 12
    A genome-wide association study of anorexia nervosa

    A genome-wide association study of anorexia nervosa per Vesna Boraska Perica, Christopher S. Franklin, J A B Floyd, Laura M. Thornton, Laura M. Huckins, Lorraine Southam, Nigel W. Rayner, Ioanna Tachmazidou, Kelly L. Klump, Janet Treasure, Cathryn M. Lewis, Ulrike Schmidt, Federica Tozzi, Kirsty Kiezebrink, Johannes Hebebrand, Philip Gorwood, R A H Adan, Martien J. Kas, Angela Favaro, Paolo Santonastaso, Fernando Fernández‐Aranda, Mónica Gratacòs, Filip Rybakowski, Monika Dmitrzak‐Węglarz, Jaakko Kaprio, Anna Keski‐Rahkonen, Anu Raevuori, Eric F. van Furth, M Landt, James I. Hudson, Ted Reichborn‐Kjennerud, G P S Knudsen, Palmiero Monteleone, A S Kaplan, Andreas Karwautz, Hákon Hákonarson, Wade H. Berrettini, Yirin Guo, D Li, Nicholas J. Schork, Gen Komaki, Tetsuya Ando, Hidetoshi Inoko, Tõnu Esko, Krista Fischer, Katrin Männik, Andres Metspalu, Jessica H. Baker, Roger D. Cone, Jennifer Dackor, Janiece E. DeSocio, Christopher Hilliard, Julie K. O’Toole, Jacques Pantel, Jin P. Szatkiewicz, Chrysecolla Taico, Stephanie Zerwas, Sara E. Trace, Oliver S. P. Davis, Sietske G. Helder, Katharina Bühren, Roland Burghardt, Martina de Zwaan, Karin Egberts, Stefan Ehrlich, B Herpertz‐Dahlmann, Wolfgang Herzog, Hartmut Imgart, André Scherag, Susann Scherag, Stephan Zipfel, Claudette Boni, Nicolás Ramoz, Audrey Versini, Marek K. Brandys, Unna N. Danner, Carolien G. F. de Kovel, Judith Hendriks, Bobby P.C. Koeleman, Roel A. Ophoff, E Strengman, Annemarie Elburg, Alice Bruson, Massimo Clementi, Daniela Degortes, Monica Forzan, Elena Tenconi, Elisa Docampo, Geòrgia Escaramís, Susana Jiménez‐Múrcia, Jolanta Lissowska, Andrzej Rajewski, Neonila Szeszenia‐Dąbrowska, Agnieszka Slopien, Joanna Hauser, Leila Karhunen, Ingrid Meulenbelt, P. Eline Slagboom, Alfonso Tortorella, Mario Maj

    Publicat 2014
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  13. 13
    16p11.2 600 kb Duplications confer risk for typical and atypical Rolandic epilepsy

    16p11.2 600 kb Duplications confer risk for typical and atypical Rolandic epilepsy per Eva M. Reinthaler, Dennis Lal, Sébastien Lebon, Michael S. Hildebrand, Hans‐Henrik M. Dahl, Brigid M. Regan, Martha Feucht, Hannelore Steinböck, Birgit Neophytou, Gabriel M. Ronen, Laurian Roche, U Gruber‐Sedlmayr, Julia Geldner, Edda Haberlandt, Per Hoffmann, Stefan Herms, Christian Gieger, Mélanie Waldenberger, André Franke, Michael Wittig, Susanne Schoch, Albert J. Becker, Andreas Hahn, Katrin Männik, Mohammad R. Toliat, Georg Winterer, Holger Lerche, Peter Nürnberg, Heather C. Mefford, Ingrid E. Scheffer, Samuel F. Berkovic, J. Beckmann, Thomas Sander, Sébastien Jacquemont, Alexandre Reymond, Fritz Zimprich, Bernd A. Neubauer, Eva M. Reinthaler, Fritz Zimprich, Martha Feucht, Hannelore Steinböck, Birgit Neophytou, Julia Geldner, U Gruber‐Sedlmayr, Edda Haberlandt, Gabriel M. Ronen, Laurian Roche, Dennis Lal, Peter Nürnberg, Thomas Sander, Holger Lerche, Bernd A. Neubauer, Fritz Zimprich, Martina Mörzinger, Martha Feucht, Arvid Suls, Sarah Weckhuysen, Lieve Claes, Liesbet Deprez, Katrien Smets, Tine Van Dyck, Tine Deconinck, Peter De Jonghe, Rikke S. Møller, Laura L. Klitten, Helle Hjalgrim, Rikke S. Møller, Kiel Campus, Ingo Helbig, Hiltrud Muhle, P Ostertag, Sarah von Spiczak, Ulrich Stephani, Peter Nürnberg, Thomas Sander, Holger Trucks, Christian E. Elger, Ailing A. Kleefuß‐Lie, Wolfram S. Kunz, Rainer Surges, Verena Gaus, Diéter Janz, Thomas Sander, Bettina Schmitz, Felix Rosenow, Karl Martin Klein, Philipp S. Reif, Wolfgang H. Oertel, Hajo M. Hamer, Felicitas Becker, Yvonne G. Weber, Holger Lerche, Bobby P.C. Koeleman, Carolien G. F. de Kovel, Dick Lindhout, Dick Lindhout, Agnès Ameil, Joris Andrieux, Sonia Bouquillon, Odile Boute

    Publicat 2014
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  14. 14
    Evidence for three genetic loci involved in both anorexia nervosa risk and variation of body mass index

    Evidence for three genetic loci involved in both anorexia nervosa risk and variation of body mass index per Anke Hinney, Miriam Kesselmeier, Sigrid Jall, A-L Volckmar, Manuel Föcker, Jochen Antel, Vesna Boraska Perica, C. Franklin, James Floyd, Laura M. Thornton, Laura M. Huckins, Lorraine Southam, N. William Rayner, Ioanna Tachmazidou, Kelly L. Klump, Janet Treasure, Cathryn M. Lewis, Ulrike Schmidt, Federica Tozzi, Kirsty iezebrink, Johannes Hebebrand, Philip Gorwood, Roger A.H. Adan, Martien J. Kas, Angela Favaro, Paolo Santonastaso, Fernando Fernández‐Aranda, Mónica Gratacòs, Filip Rybakowski, Monika Dmitrzak‐Węglarz, Jaakko Kaprio, Anna Keski‐Rahkonen, Anu Raevuori, Eric F. van Furth, M Landt, James I. Hudson, Ted Reichborn‐Kjennerud, Gun Peggy Knudsen, Palmiero Monteleone, Allan S. Kaplan, Andreas Karwautz, Hákon Hákonarson, Wade H. Berrettini, Yiran Guo, Dong Li, Nicholas J. Schork, Gen Komaki, Tetsuya Ando, Hidetoshi Inoko, Tõnu Esko, Krista Fischer, Katrin Männik, Andres Metspalu, Jessica H. Baker, Roger D. Cone, Jennifer Dackor, Janiece E. DeSocio, Christopher Hilliard, Julie K. O’Toole, Jacques Pantel, Jin P. Szatkiewicz, Chrysecolla Taico, Stephanie Zerwas, Sara E. Trace, Oliver S. P. Davis, Sietske G. Helder, Katharina Bühren, Roland Burghardt, Martina de Zwaan, Karin Egberts, Stefan Ehrlich, Beate Herpertz‐Dahlmann, Wolfgang Herzog, Hartmut Imgart, André Scherag, Susann Scherag, Stephan Zipfel, Claudette Boni, Nicolás Ramoz, Audrey Versini, Marek K. Brandys, Unna N. Danner, Carolien de Kove, Judith Hendriks, Bobby P.C. Koeleman, Roel A. Ophoff, Eric Strengman, Annemarie Elburg, Alice Bruson, Maurizio Clementi, Daniela Degortes, Monica Forzan, Elena Tenconi, Elisa Docampo, Geòrgia Escaramí, Susana Jiménez‐Múrcia, Jolanta Lissowska, Andrzej Rajewski, Neonila Szeszenia‐Dąbrowska, Agnieszka Slopien

    Publicat 2016
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  15. 15
    CNV-association meta-analysis in 191,161 European adults reveals new loci associated with anthropometric traits

    CNV-association meta-analysis in 191,161 European adults reveals new loci associated with anthropometric traits per Aurélien Macé, Marcus A. Tuke, Patrick Deelen, Kati Kristiansson, Hannele Mattsson, Margit Nõukas, Yadav Sapkota, Ursula M. Schick, Eleonora Porcu, Sina Rüeger, Aaron F. McDaid, David J. Porteous, Thomas W. Winkler, Erika Salvi, Nick Shrine, Xueping Liu, Wei Ang, Weihua Zhang, Mary F. Feitosa, Cristina Venturini, Peter J. van der Most, Anders Rosengren, Andrew R. Wood, Robin N. Beaumont, Samuel E. Jones, Katherine S. Ruth, Hanieh Yaghootkar, Jessica Tyrrell, Aki S. Havulinna, Harmen Boers, Reedik Mägi, Jennifer Kriebel, Martina Müller‐Nurasyid, Markus Perola, Markku S. Nieminen, Marja‐Liisa Lokki, Mika Kähönen, Jorma Viikari, Frank Geller, Jari Lahti, Aarno Palotie, Päivikki Koponen, Annamari Lundqvist, Harri Rissanen, Erwin P. Böttinger, Saima Afaq, Mary K. Wojczynski, Petra Lenzini, Ilja M. Nolte, Thomas Sparsø, Nicole Schupf, Kaare Christensen, Thomas T. Perls, Anne B. Newman, Thomas Werge, Harold Snieder, Timothy D. Spector, John C. Chambers, Seppo Koskinen, Mads Melbye, Olli T. Raitakari, Terho Lehtimäki, Martin D. Tobin, Louise V. Wain, Juha Sinisalo, Annette Peters, Thomas Meitinger, Nicholas G. Martin, Naomi R. Wray, Grant W. Montgomery, Sarah E. Medland, Morris A. Swertz, Erkki Vartiainen, Katja Borodulin, Satu Männistö, Anna Murray, Murielle Bochud, Sébastien Jacquemont, Fernando Rivadeneira, Thomas Hansen, Albertine J. Oldehinkel, Massimo Mangino, Michael A. Province, Panos Deloukas, Jaspal S. Kooner, Rachel M. Freathy, Craig E. Pennell, Bjarke Feenstra, David P. Strachan, Guillaume Lettre, Joel N. Hirschhorn, Daniele Cusi, Iris M. Heid, Caroline Hayward, Katrin Männik, J. Beckmann, Ruth J. F. Loos, Dale R. Nyholt, Andres Metspalu, Johan G. Eriksson

    Publicat 2017
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