High prevalence of genetic variants previously associated with LQT syndrome in new exome data

por Refsgaard, Lena, Holst, Anders G, Sadjadieh, Golnaz, Haunsø, Stig, Nielsen, Jonas B, Olesen, Morten S
Publicado 2012

New population-based exome data are questioning the pathogenicity of previously cardiomyopathy-associated genetic variants

por Andreasen, Charlotte, Nielsen, Jonas B, Refsgaard, Lena, Holst, Anders G, Christensen, Alex H, Andreasen, Laura, Sajadieh, Ahmad, Haunsø, Stig, Svendsen, Jesper H, Olesen, Morten S
Publicado 2013

Mutations in the potassium channel subunit KCNE1 are associated with early-onset familial atrial fibrillation

por Olesen, Morten S, Bentzen, Bo H, Nielsen, Jonas B, Steffensen, Annette B, David, Jens-Peter, Jabbari, Javad, Jensen, Henrik K, Haunsø, Stig, Svendsen, Jesper H, Schmitt, Nicole
Publicado 2012

New population-based exome data question the pathogenicity of some genetic variants previously associated with Marfan syndrome

por Yang, Ren-Qiang, Jabbari, Javad, Cheng, Xiao-Shu, Jabbari, Reza, Nielsen, Jonas B, Risgaard, Bjarke, Chen, Xu, Sajadieh, Ahmad, Haunsø, Stig, Svendsen, Jesper Hastrup, Olesen, Morten S, Tfelt-Hansen, Jacob
Publicado 2014

Risk prediction of cardiovascular death based on the QTc interval: evaluating age and gender differences in a large primary care population

por Nielsen, Jonas B., Graff, Claus, Rasmussen, Peter V., Pietersen, Adrian, Lind, Bent, Olesen, Morten S., Struijk, Johannes J., Haunsø, Stig, Svendsen, Jesper H., Køber, Lars, Gerds, Thomas A., Holst, Anders G.
Publicado 2014

Association Between ECG Abnormalities and Fatal Cardiovascular Disease Among Patients With and Without Severe Mental Illness

por Polcwiartek, Christoffer, Atwater, Brett D., Kragholm, Kristian, Friedman, Daniel J., Barcella, Carlo A., Attar, Rubina, Graff, Claus, Nielsen, Jonas B., Pietersen, Adrian, Søgaard, Peter, Torp‐Pedersen, Christian, Jensen, Svend E.
Publicado 2021

Ventricular rate in atrial fibrillation and the risk of heart failure and death

por Westergaard, Lucas Malta, Alhakak, Amna, Rørth, Rasmus, Fosbøl, Emil L, Kristensen, Søren L, Svendsen, Jesper H, Graff, Claus, Nielsen, Jonas B, Gislason, Gunnar H, Køber, Lars, Torp-Pedersen, Christian, Lee, Christina J Y, Weeke, Peter E
Publicado 2023

Rare truncating variants in the sarcomeric protein titin associate with familial and early-onset atrial fibrillation

por Ahlberg, Gustav, Refsgaard, Lena, Lundegaard, Pia R., Andreasen, Laura, Ranthe, Mattis F., Linscheid, Nora, Nielsen, Jonas B., Melbye, Mads, Haunsø, Stig, Sajadieh, Ahmad, Camp, Lu, Olesen, Søren-Peter, Rasmussen, Simon, Lundby, Alicia, Ellinor, Patrick T., Holst, Anders G., Svendsen, Jesper H., Olesen, Morten S.
Publicado 2018

Risk Prediction of Atrial Fibrillation Based on Electrocardiographic Interatrial Block

por Skov, Morten W., Ghouse, Jonas, Kühl, Jørgen T., Platonov, Pyotr G., Graff, Claus, Fuchs, Andreas, Rasmussen, Peter V., Pietersen, Adrian, Nordestgaard, Børge G., Torp‐Pedersen, Christian, Hansen, Steen M., Olesen, Morten S., Haunsø, Stig, Køber, Lars, Gerds, Thomas A., Kofoed, Klaus F., Svendsen, Jesper H., Holst, Anders G., Nielsen, Jonas B.
Publicado 2018

Mitochondrial genome-wide association study of migraine – the HUNT Study

por Børte, Sigrid, Zwart, John-Anker, Skogholt, Anne Heidi, Gabrielsen, Maiken Elvestad, Thomas, Laurent F, Fritsche, Lars G, Surakka, Ida, Nielsen, Jonas B, Zhou, Wei, Wolford, Brooke N, Vigeland, Magnus D, Hagen, Knut, Kristoffersen, Espen Saxhaug, Nyholt, Dale R, Chasman, Daniel I, Brumpton, Ben M, Willer, Cristen J, Winsvold, Bendik S
Publicado 2020

Efficiently controlling for case-control imbalance and sample relatedness in large-scale genetic association studies

por Zhou, Wei, Nielsen, Jonas B., Fritsche, Lars G., Dey, Rounak, Gabrielsen, Maiken E., Wolford, Brooke N., LeFaive, Jonathon, VandeHaar, Peter, Gagliano, Sarah A., Gifford, Aliya, Bastarache, Lisa A., Wei, Wei-Qi, Denny, Joshua C., Lin, Maoxuan, Hveem, Kristian, Kang, Hyun Min, Abecasis, Goncalo R., Willer, Cristen J., Lee, Seunggeun
Publicado 2018

Genome-wide meta-analysis of iron status biomarkers and the effect of iron on all-cause mortality in HUNT

por Moksnes, Marta R., Graham, Sarah E., Wu, Kuan-Han, Hansen, Ailin Falkmo, Gagliano Taliun, Sarah A., Zhou, Wei, Thorstensen, Ketil, Fritsche, Lars G., Gill, Dipender, Mason, Amy, Cucca, Francesco, Schlessinger, David, Abecasis, Gonçalo R., Burgess, Stephen, Åsvold, Bjørn Olav, Nielsen, Jonas B., Hveem, Kristian, Willer, Cristen J., Brumpton, Ben M.
Publicado 2022

Sex-specific and pleiotropic effects underlying kidney function identified from GWAS meta-analysis

por Graham, Sarah E., Nielsen, Jonas B., Zawistowski, Matthew, Zhou, Wei, Fritsche, Lars G., Gabrielsen, Maiken E., Skogholt, Anne Heidi, Surakka, Ida, Hornsby, Whitney E., Fermin, Damian, Larach, Daniel B., Kheterpal, Sachin, Brummett, Chad M., Lee, Seunggeun, Kang, Hyun Min, Abecasis, Goncalo R., Romundstad, Solfrid, Hallan, Stein, Sampson, Matthew G., Hveem, Kristian, Willer, Cristen J.
Publicado 2019

Type 2 diabetes sex-specific effects associated with E167K coding variant in TM6SF2

por Fan, Yanbo, Wolford, Brooke N., Lu, Haocheng, Liang, Wenying, Sun, Jinjian, Zhou, Wei, Rom, Oren, Mahajan, Anubha, Surakka, Ida, Graham, Sarah E., Liu, Zhipeng, Kim, Hyunbae, Ramdas, Shweta, Fritsche, Lars G., Nielsen, Jonas B., Gabrielsen, Maiken Elvestad, Hveem, Kristian, Yang, Dongshan, Song, Jun, Garcia-Barrio, Minerva T., Zhang, Jifeng, Liu, Wanqing, Zhang, Kezhong, Willer, Cristen J., Chen, Y. Eugene
Publicado 2021

MEPE loss-of-function variant associates with decreased bone mineral density and increased fracture risk

por Surakka, Ida, Fritsche, Lars G., Zhou, Wei, Backman, Joshua, Kosmicki, Jack A., Lu, Haocheng, Brumpton, Ben, Nielsen, Jonas B., Gabrielsen, Maiken E., Skogholt, Anne Heidi, Wolford, Brooke, Graham, Sarah E., Chen, Y. Eugene, Lee, Seunggeun, Kang, Hyun Min, Langhammer, Arnulf, Forsmo, Siri, Åsvold, Bjørn O., Styrkarsdottir, Unnur, Holm, Hilma, Gudbjartsson, Daniel, Stefansson, Kari, Baras, Aris, Abecasis, Goncalo R., Hveem, Kristian, Willer, Cristen J.
Publicado 2020

Is disrupted sleep a risk factor for Alzheimer’s disease? Evidence from a two-sample Mendelian randomization analysis

por Anderson, Emma L, Richmond, Rebecca C, Jones, Samuel E, Hemani, Gibran, Wade, Kaitlin H, Dashti, Hassan S, Lane, Jacqueline M, Wang, Heming, Saxena, Richa, Brumpton, Ben, Korologou-Linden, Roxanna, Nielsen, Jonas B, Åsvold, Bjørn Olav, Abecasis, Gonçalo, Coulthard, Elizabeth, Kyle, Simon D, Beaumont, Robin N, Tyrrell, Jessica, Frayling, Timothy M, Munafò, Marcus R, Wood, Andrew R, Ben-Shlomo, Yoav, Howe, Laura D, Lawlor, Deborah A, Weedon, Michael N, Davey Smith, George
Publicado 2020

Genome-wide association study of cardiac troponin I in the general population

por Moksnes, Marta R, Røsjø, Helge, Richmond, Anne, Lyngbakken, Magnus N, Graham, Sarah E, Hansen, Ailin Falkmo, Wolford, Brooke N, Gagliano Taliun, Sarah A, LeFaive, Jonathon, Rasheed, Humaira, Thomas, Laurent F, Zhou, Wei, Aung, Nay, Surakka, Ida, Douville, Nicholas J, Campbell, Archie, Porteous, David J, Petersen, Steffen E, Munroe, Patricia B, Welsh, Paul, Sattar, Naveed, Smith, George Davey, Fritsche, Lars G, Nielsen, Jonas B, Åsvold, Bjørn Olav, Hveem, Kristian, Hayward, Caroline, Willer, Cristen J, Brumpton, Ben M, Omland, Torbjørn
Publicado 2021

Coding variants in RPL3L and MYZAP increase risk of atrial fibrillation

por Thorolfsdottir, Rosa B., Sveinbjornsson, Gardar, Sulem, Patrick, Nielsen, Jonas B., Jonsson, Stefan, Halldorsson, Gisli H., Melsted, Pall, Ivarsdottir, Erna V., Davidsson, Olafur B., Kristjansson, Ragnar P., Thorleifsson, Gudmar, Helgadottir, Anna, Gretarsdottir, Solveig, Norddahl, Gudmundur, Rajamani, Sridharan, Torfason, Bjarni, Valgardsson, Atli S., Sverrisson, Jon T., Tragante, Vinicius, Holmen, Oddgeir L., Asselbergs, Folkert W., Roden, Dan M., Darbar, Dawood, Pedersen, Terje R., Sabatine, Marc S., Willer, Cristen J., Løchen, Maja-Lisa, Halldorsson, Bjarni V., Jonsdottir, Ingileif, Hveem, Kristian, Arnar, David O., Thorsteinsdottir, Unnur, Gudbjartsson, Daniel F., Holm, Hilma, Stefansson, Kari
Publicado 2018

Genome-wide analysis yields new loci associating with aortic valve stenosis

por Helgadottir, Anna, Thorleifsson, Gudmar, Gretarsdottir, Solveig, Stefansson, Olafur A., Tragante, Vinicius, Thorolfsdottir, Rosa B., Jonsdottir, Ingileif, Bjornsson, Thorsteinn, Steinthorsdottir, Valgerdur, Verweij, Niek, Nielsen, Jonas B., Zhou, Wei, Folkersen, Lasse, Martinsson, Andreas, Heydarpour, Mahyar, Prakash, Siddharth, Oskarsson, Gylfi, Gudbjartsson, Tomas, Geirsson, Arnar, Olafsson, Isleifur, Sigurdsson, Emil L., Almgren, Peter, Melander, Olle, Franco-Cereceda, Anders, Hamsten, Anders, Fritsche, Lars, Lin, Maoxuan, Yang, Bo, Hornsby, Whitney, Guo, Dongchuan, Brummett, Chad M., Abecasis, Gonçalo, Mathis, Michael, Milewicz, Dianna, Body, Simon C., Eriksson, Per, Willer, Cristen J., Hveem, Kristian, Newton-Cheh, Christopher, Smith, J. Gustav, Danielsen, Ragnar, Thorgeirsson, Gudmundur, Thorsteinsdottir, Unnur, Gudbjartsson, Daniel F., Holm, Hilma, Stefansson, Kari
Publicado 2018

Age-of-onset information helps identify 76 genetic variants associated with allergic disease

por Ferreira, Manuel A. R., Vonk, Judith M., Baurecht, Hansjörg, Marenholz, Ingo, Tian, Chao, Hoffman, Joshua D., Helmer, Quinta, Tillander, Annika, Ullemar, Vilhelmina, Lu, Yi, Grosche, Sarah, Rüschendorf, Franz, Granell, Raquel, Brumpton, Ben M., Fritsche, Lars G., Bhatta, Laxmi, Gabrielsen, Maiken E., Nielsen, Jonas B., Zhou, Wei, Hveem, Kristian, Langhammer, Arnulf, Holmen, Oddgeir L., Løset, Mari, Abecasis, Gonçalo R., Willer, Cristen J., Emami, Nima C., Cavazos, Taylor B., Witte, John S., Szwajda, Agnieszka, Hinds, David A., Hübner, Norbert, Weidinger, Stephan, Magnusson, Patrik KE, Jorgenson, Eric, Karlsson, Robert, Paternoster, Lavinia, Boomsma, Dorret I., Almqvist, Catarina, Lee, Young-Ae, Koppelman, Gerard H.
Publicado 2020