CELSR2 is a candidate susceptibility gene in idiopathic scoliosis von Einarsdottir, Elisabet, Grauers, Anna, Wang, Jingwen, Jiao, Hong, Escher, Stefan A, Danielsson, Aina, Simony, Ane, Andersen, Mikkel, Christensen, Steen Bach, Åkesson, Kristina, Kou, Ikuyo, Khanshour, Anas M, Ohlin, Acke, Wise, Carol, Ikegawa, Shiro, Kere, Juha, Gerdhem, Paul

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Genetic determinants of long-term changes in blood lipid concentrations: 10-year follow-up of the GLACIER study von Varga, Tibor V, Sonestedt, Emily, Shungin, Dmitry, Koivula, Robert W, Hallmans, Göran, Escher, Stefan A, Barroso, Inês, Nilsson, Peter, Melander, Olle, Orho-Melander, Marju, Renström, Frida, Franks, Paul W

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Diabetes mellitus, high BMI and low education level predict sudden cardiac death within 24 hours of incident myocardial infarction von Andersson, Jonas, Wennberg, Patrik, Lundblad, Dan, Escher, Stefan A, Jansson, Jan-Håkan

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A Novel Mutation in the LIM Homeobox 3 Gene Is Responsible for Combined Pituitary Hormone Deficiency, Hearing Impairment, and Vertebral Malformations von Kriström, Berit, Zdunek, Anna-Maija, Rydh, Anders, Jonsson, Håkan, Sehlin, Petra, Escher, Stefan A.

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A genealogical and clinical study of the phenotypical variation within the Swedish transthyretin His88Arg ( p. His108Arg ) amyloidosis family von Hellman, Urban, Lundgren, Hans-Erik, Westermark, Per, Stafberg, Christina, Nahi, Hareth, Tachlinski, Sascha, Guggi, Michael, Flogegård, Max, Hamid, Mehmet, Escher, Stefan A, Suhr, Ole B

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Linkage of ischemic stroke to the PDE4D region on 5q in a Swedish population von NILSSON-ARDNOR, Sofie, WIKLUND, Per-Gunnar, LINDGREN, Petter, NILSSON, Anna Karin, JANUNGER, Tomas, ESCHER, Stefan A, HALLBECK, Björn, STEGMAYR, Birgitta, ASPLUND, Kjell, HOLMBERG, Dan

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The genetic population structure of northern Sweden and its implications for mapping genetic diseases von Einarsdottir, Elisabet, Egerbladh, Inez, Beckman, Lars, Holmberg, Dan, A. Escher, Stefan

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Genome-wide linkage scan of common stroke in families from northern Sweden von NILSSON-ARDNOR, Sofie, JANUNGER, Tomas, WIKLUND, Per-Gunnar, LACKOVIC, Kurt, KARIN NILSSON, Anna, LINDGREN, Petter, ESCHER, Stefan A, STEGMAYR, Birgitta, ASPLUND, Kjell, HOLMBERG, Dan

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Linkage but Not Association of Calpain-10 to Type 2 Diabetes Replicated in Northern Sweden von EINARSDOTTIR, Elisabet, MAYANS, Sofia, RUIKKA, Karin, ESCHER, Stefan A, LINDGREN, Petter, AGREN, Asa, ELIASSON, Mats, HOLMBERG, Dan

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Coding Variation in ANGPTL4, LPL, and SVEP1 and the Risk of Coronary Disease von Stitziel, Nathan O, Stirrups, Kathleen E, Masca, Nicholas G D, Erdmann, Jeanette, Ferrario, Paola G, König, Inke R, Weeke, Peter E, Webb, Thomas R, Auer, Paul L, Schick, Ursula M, Lu, Yingchang, Zhang, He, Dube, Marie-Pierre, Goel, Anuj, Farrall, Martin, Peloso, Gina M, Won, Hong-Hee, Do, Ron, van Iperen, Erik, Kanoni, Stavroula, Kruppa, Jochen, Mahajan, Anubha, Scott, Robert A, Willenberg, Christina, Braund, Peter S, van Capelleveen, Julian C, Doney, Alex S F, Donnelly, Louise A, Asselta, Rosanna, Merlini, Piera A, Duga, Stefano, Marziliano, Nicola, Denny, Josh C, Shaffer, Christian M, El-Mokhtari, Nour Eddine, Franke, Andre, Gottesman, Omri, Heilmann, Stefanie, Hengstenberg, Christian, Hoffman, Per, Holmen, Oddgeir L, Hveem, Kristian, Jansson, Jan-Håkan, Jöckel, Karl-Heinz, Kessler, Thorsten, Kriebel, Jennifer, Laugwitz, Karl L, Marouli, Eirini, Martinelli, Nicola, McCarthy, Mark I, Van Zuydam, Natalie R, Meisinger, Christa, Esko, Tõnu, Mihailov, Evelin, Escher, Stefan A, Alver, Maris, Moebus, Susanne, Morris, Andrew D, Müller-Nurasyid, Martina, Nikpay, Majid, Olivieri, Oliviero, Lemieux Perreault, Louis-Philippe, AlQarawi, Alaa, Robertson, Neil R, Akinsanya, Karen O, Reilly, Dermot F, Vogt, Thomas F, Yin, Wu, Asselbergs, Folkert W, Kooperberg, Charles, Jackson, Rebecca D, Stahl, Eli, Strauch, Konstantin, Varga, Tibor V, Waldenberger, Melanie, Zeng, Lingyao, Kraja, Aldi T, Liu, Chunyu, Ehret, George B, Newton-Cheh, Christopher, Chasman, Daniel I, Chowdhury, Rajiv, Ferrario, Marco, Ford, Ian, Jukema, J Wouter, Kee, Frank, Kuulasmaa, Kari, Nordestgaard, Børge G, Perola, Markus, Saleheen, Danish, Sattar, Naveed, Surendran, Praveen, Tregouet, David, Young, Robin, Howson, Joanna M M, Butterworth, Adam S, Danesh, John, Ardissino, Diego, Bottinger, Erwin P, Erbel, Raimund

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A Novel Mutation in the LHX3 Gene is Responsible for Combined Pituitary Hormone Deficiency, Hearing Impairment, and Vertebral Malformations von Kriström, Berit, Zdunek, Anna-Maija, Rydh, Anders, Jonsson, Håkan, Sehlin, Petra, Escher, Stefan A

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Loss-of-Function Mutations in APOC3, Triglycerides, and Coronary Disease von Crosby, Jacy, Peloso, Gina M, Auer, Paul L, Crosslin, David R, Stitziel, Nathan O, Lange, Leslie A, Lu, Yingchang, Tang, Zheng-zheng, Zhang, He, Hindy, George, Masca, Nicholas, Stirrups, Kathleen, Kanoni, Stavroula, Do, Ron, Jun, Goo, Hu, Youna, Kang, Hyun Min, Xue, Chenyi, Goel, Anuj, Farrall, Martin, Duga, Stefano, Merlini, Pier Angelica, Asselta, Rosanna, Girelli, Domenico, Olivieri, Oliviero, Martinelli, Nicola, Yin, Wu, Reilly, Dermot, Speliotes, Elizabeth, Fox, Caroline S, Hveem, Kristian, Holmen, Oddgeir L, Nikpay, Majid, Farlow, Deborah N, Assimes, Themistocles L, Franceschini, Nora, Robinson, Jennifer, North, Kari E, Martin, Lisa W, DePristo, Mark, Gupta, Namrata, Escher, Stefan A, Jansson, Jan-Håkan, Van Zuydam, Natalie, Palmer, Colin N A, Wareham, Nicholas, Koch, Werner, Meitinger, Thomas, Peters, Annette, Lieb, Wolfgang, Erbel, Raimund, Konig, Inke R, Kruppa, Jochen, Degenhardt, Franziska, Gottesman, Omri, Bottinger, Erwin P, O'Donnell, Christopher J, Psaty, Bruce M, Ballantyne, Christie M, Abecasis, Goncalo, Ordovas, Jose M, Melander, Olle, Watkins, Hugh, Orho-Melander, Marju, Ardissino, Diego, Loos, Ruth J F, McPherson, Ruth, Willer, Cristen J, Erdmann, Jeanette, Hall, Alistair S, Samani, Nilesh J, Deloukas, Panos, Schunkert, Heribert, Wilson, James G, Kooperberg, Charles, Rich, Stephen S, Tracy, Russell P, Lin, Dan-Yu, Altshuler, David, Gabriel, Stacey, Nickerson, Deborah A, Jarvik, Gail P, Cupples, L Adrienne, Reiner, Alex P, Boerwinkle, Eric, Kathiresan, Sekar

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A Novel Mutation in The LHX3 Gene is Responsible for Combined Pituitary Hormone Deficiency, Hearing Impairment, and Vertebral Malformations von Kriström, Berit, Zdunek, Anna-Maija, Rydh, Anders, Jonsson, Håkan, Sehlin, Petra, Escher, Stefan A

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Systematic Evaluation of Pleiotropy Identifies 6 Further Loci Associated With Coronary Artery Disease von Webb, Thomas R., PhD, Stirrups, Kathleen E., PhD, Stitziel, Nathan O., MD, PhD, Masca, Nicholas G.D., PhD, Kanoni, Stavroula, PhD, Nelson, Christopher P., PhD, Ferrario, Paola G., PhD, Eicher, John D., PhD, Hamby, Stephen E., PhD, Ruusalepp, Arno, MD, PhD, Franzén, Oscar, PhD, Björkegren, Johan L.M., MD, PhD, Schick, Ursula M., PhD, Zhang, He, PhD, Dube, Marie-Pierre, PhD, Goel, Anuj, MSc, Farrall, Martin, MD, Peloso, Gina M., PhD, Do, Ron, PhD, van Iperen, Erik, MSc, Kruppa, Jochen, PhD, Mahajan, Anubha, PhD, Scott, Robert A., PhD, Willenborg, Christina, PhD, Braund, Peter S., PhD, Doney, Alex S.F., MD, PhD, Donnelly, Louise A., PhD, Merlini, Pier A., MD, Duga, Stefano, PhD, Marziliano, Nicola, PhD, Denny, Josh C., MD, MS, El-Mokhtari, Nour Eddine, MD, Franke, Andre, PhD, Heilmann, Stefanie, PhD, Hengstenberg, Christian, MD, Hveem, Kristian, MD, PhD, Jöckel, Karl-Heinz, PhD, Kriebel, Jennifer, PhD, Laugwitz, Karl L., MD, Marouli, Eirini, MSc, Martinelli, Nicola, MD, PhD, McCarthy, Mark I., MD, Van Zuydam, Natalie R., PhD, Meisinger, Christa, MD, MPH, Esko, Tõnu, PhD, Moebus, Susanne, PhD, Morris, Andrew D., MD, Virtamo, Jarma, MD, PhD, Nikpay, Majid, PhD, Provost, Sylvie, MSc, AlQarawi, Alaa, BSc, Robertson, Neil R., MSc, Akinsansya, Karen O., PhD, Reilly, Dermot F., PhD, Vogt, Thomas F., PhD, Kooperberg, Charles, PhD, Jackson, Rebecca D., MD, Stahl, Eli, PhD, Müller-Nurasyid, Martina, PhD, Strauch, Konstantin, PhD, Varga, Tibor V., PhD, Waldenberger, Melanie, PhD, Zeng, Lingyao, MSc, Chowdhury, Rajiv, MD, PhD, Ford, Ian, PhD, Amouyel, Philippe, MD, PhD, Kontto, Jukka, MSSc, Nordestgaard, Børge G., MD, DMSc, Ferrières, Jean, MD, Saleheen, Danish, MBBS, PhD, Surendran, Praveen, PhD, Young, Robin, PhD, Howson, Joanna M.M., PhD, Butterworth, Adam S., PhD, Danesh, John, DPhil, Ardissino, Diego, MD, Bottinger, Erwin P., MD, Erbel, Raimund, MD, Franks, Paul W., PhD, Girelli, Domenico, MD, PhD, Hall, Alistair S., MD, PhD, Hovingh, G. Kees, MD, PhD, Kastrati, Adnan, MD, Lieb, Wolfgang, MD, MSc, Meitinger, Thomas, MD, Melander, Olle, MD, PhD, Metspalu, Andres, MD, PhD, Palmer, Colin N.A., PhD, Peters, Annette, PhD, Rader, Daniel J., MD, Loos, Ruth J.F., PhD, Reiner, Alex P., MD, MSc, Tardif, Jean-Claude, MD, Wareham, Nicholas J., MB, BS, PhD, Watkins, Hugh, MD, PhD, Willer, Cristen J., PhD, Samani, Nilesh J., MD, Schunkert, Heribert, MD, Deloukas, Panos, PhD, Kathiresan, Sekar, MD

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SOS2 and ACP1 Loci Identified through Large-Scale Exome Chip Analysis Regulate Kidney Development and Function von Li, Man, Li, Yong, Weeks, Olivia, Mijatovic, Vladan, Teumer, Alexander, Huffman, Jennifer E, Tromp, Gerard, Fuchsberger, Christian, Gorski, Mathias, Lyytikäinen, Leo-Pekka, Nutile, Teresa, Sedaghat, Sanaz, Sorice, Rossella, Tin, Adrienne, Yang, Qiong, Ahluwalia, Tarunveer S, Arking, Dan E, Bihlmeyer, Nathan A, Böger, Carsten A, Carroll, Robert J, Chasman, Daniel I, Cornelis, Marilyn C, Dehghan, Abbas, Faul, Jessica D, Feitosa, Mary F, Gambaro, Giovanni, Gasparini, Paolo, Giulianini, Franco, Heid, Iris, Huang, Jinyan, Imboden, Medea, Jackson, Anne U, Jeff, Janina, Jhun, Min A, Katz, Ronit, Kifley, Annette, Kilpeläinen, Tuomas O, Kumar, Ashish, Laakso, Markku, Li-Gao, Ruifang, Lohman, Kurt, Lu, Yingchang, Mägi, Reedik, Malerba, Giovanni, Mihailov, Evelin, Mohlke, Karen L, Mook-Kanamori, Dennis O, Robino, Antonietta, Ruderfer, Douglas, Salvi, Erika, Schick, Ursula M, Schulz, Christina-Alexandra, Smith, Albert V, Smith, Jennifer A, Traglia, Michela, Yerges-Armstrong, Laura M, Zhao, Wei, Goodarzi, Mark O, Kraja, Aldi T, Liu, Chunyu, Wessel, Jennifer, Boerwinkle, Eric, Borecki, Ingrid B, Bork-Jensen, Jette, Bottinger, Erwin P, Braga, Daniele, Brandslund, Ivan, Brody, Jennifer A, Campbell, Archie, Carey, David J, Christensen, Cramer, Coresh, Josef, Crook, Errol, Curhan, Gary C, Cusi, Daniele, de Boer, Ian H, de Vries, Aiko P J, Denny, Joshua C, Devuyst, Olivier, Dreisbach, Albert W, Endlich, Karlhans, Esko, Tõnu, Franco, Oscar H, Fulop, Tibor, Gerhard, Glenn S, Glümer, Charlotte, Gottesman, Omri, Grarup, Niels, Gudnason, Vilmundur, Hansen, Torben, Harris, Tamara B, Hayward, Caroline, Hocking, Lynne, Hofman, Albert, Hu, Frank B, Husemoen, Lise Lotte N, Jackson, Rebecca D, Jørgensen, Torben, Jørgensen, Marit E, Kähönen, Mika

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A mutation in Drosophila simulans that lengthens the circadian period of locomotor activity von Rogers, A S, Escher, Stefan A, Pasetto, C, Rosato, E, Costa, R, Kyriacou, C P

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The Drosophila Glucose Transporter Gene: cDNA Sequence, Phylogenetic Comparisons, Analysis of Functional Sites and Secondary Structures von Escher, Stefan Andersson, Rasmuson‐Lestander, Åsa

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The Drosophilidae (Diptera) of Estonia von Escher, Stefan, Ekenstedt, Johan, Elberg, Kaupo, Saura, Anssi

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Genetic Determinants of Long-Term Changes in Blood Lipid Concentrations: 10-Year Follow-Up of the GLACIER Study: e1004388 von Varga, Tibor V, Sonestedt, Emily, Shungin, Dmitry, Koivula, Robert W, Hallmans, Göran, Escher, Stefan A, Barroso, Inês, Nilsson, Peter, Melander, Olle, Orho-Melander, Marju, Renström, Frida, Franks, Paul W

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Genetic Determinants of Long-Term Changes in Blood Lipid Concentrations: 10-Year Follow-Up of the GLACIER Study von Varga, Tibor V, Sonestedt, Emily, Shungin, Dmitry, Koivula, Robert W, Hallmans, Göran, Escher, Stefan A, Barroso, Inês, Nilsson, Peter, Melander, Olle, Orho-Melander, Marju, Renström, Frida, Franks, Paul W

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