Gustav Ahlberg

Scopus Author ID ORCID

Publication Activity (10 Years)

Years Active: 2016-2024
Publications (10 Years): 12

Top Venues

Nature genetics

European heart journal

European journal of human genetics : EJHG

Circulation. Genomic and precision medicine

Laboratory for Molecular Cardiology, Copenhagen University Hospital

This page only lists publications with an associated author ORCID identifier.

Affiliation History

Laboratory for Molecular Cardiology, Copenhagen University Hospital Oct 01 2014

Denmark

Phd Student :: Department of Cardiology, Rigshospitalet

Publications

Jonas Ghouse, Gardar Sveinbjörnsson, Marijana Vujkovic, Anne-Sofie Seidelin, Helene Gellert-Kristensen, Gustav Ahlberg, Vinicius Tragante, Søren Albertsen Rand, Joseph Brancale, Silvia Vilarinho, Pia Rengtved Lundegaard, Erik Sørensen, Christian Erikstrup, Mie Topholm Bruun, Bitten Aagaard Jensen, Soren Brunak, Karina Banasik, Henrik Ullum, null null, Niek Verweij, Luca A Lotta, Aris Baras, null null, Tooraj Mirshahi, David J Carey, null null, null null, David E Kaplan, Julie A Lynch, Timothy Morgan, Tae-Hwi Schwantes-An, Daniel R Dochtermann, Saiju Pyarajan, Philip S Tsao, null null, Triin Laisk, Reedik Mägi, Julia Kozlitina, Anne Tybjærg-Hansen, David Jones, Kirk U Knowlton, Lincoln Nadauld, Egil Ferkingstad, Einar S Björnsson, Magnus O Ulfarsson, Árni Sturluson, Patrick Sulem, Ole Birger Vesterager Pedersen, Sisse Rye Ostrowski, Daníel F Guðbjartsson, Kári Stefánsson, Morten Salling Olesen, Kyong-Mi Chang, Hilma Hólm, Henning Bundgaard, Stefan Stender
Integrative common and rare variant analyses provide insights into the genetic architecture of liver cirrhosis. Nature genetics 56 (5) (2024)
Jonas Ghouse, Gardar Sveinbjörnsson, Marijana Vujkovic, Anne-Sofie Seidelin, Helene Gellert-Kristensen, Gustav Ahlberg, Vinicius Tragante, Søren Albertsen Rand, Joseph Brancale, Silvia Vilarinho, Pia Rengtved Lundegaard, Erik Sørensen, Christian Erikstrup, Mie Topholm Bruun, Bitten Aagaard Jensen, Soren Brunak, Karina Banasik, Henrik Ullum, null null, Niek Verweij, Luca A Lotta, Aris Baras, null null, Tooraj Mirshahi, David J Carey, null null, null null, David E Kaplan, Julie A Lynch, Timothy Morgan, Tae-Hwi Schwantes-An, Daniel R Dochtermann, Saiju Pyarajan, Philip S Tsao, null null, Triin Laisk, Reedik Mägi, Julia Kozlitina, Anne Tybjærg-Hansen, David Jones, Kirk U Knowlton, Lincoln Nadauld, Egil Ferkingstad, Einar S Björnsson, Magnus O Ulfarsson, Árni Sturluson, Patrick Sulem, Ole Birger Vesterager Pedersen, Sisse Rye Ostrowski, Daníel F Guðbjartsson, Kári Stefánsson, Morten Salling Olesen, Kyong-Mi Chang, Hilma Hólm, Henning Bundgaard, Stefan Stender
Integrative common and rare variant analyses provide insights into the genetic architecture of liver cirrhosis. Nature genetics (2024)
Jonas Ghouse, Gardar Sveinbjörnsson, Marijana Vujkovic, Anne-Sofie Seidelin, Helene Gellert-Kristensen, Gustav Ahlberg, Vinicius Tragante, Søren Albertsen Rand, Joseph Brancale, Silvia Vilarinho, Pia Rengtved Lundegaard, Erik Sørensen, Christian Erikstrup, Mie Topholm Bruun, Bitten Aagaard Jensen, Soren Brunak, Karina Banasik, Henrik Ullum, null null, Niek Verweij, Luca A Lotta, Aris Baras, null null, Tooraj Mirshahi, David J Carey, null null, null null, David E Kaplan, Julie A Lynch, Timothy Morgan, Tae-Hwi Schwantes-An, Daniel R Dochtermann, Saiju Pyarajan, Philip S Tsao, null null, Triin Laisk, Reedik Mägi, Julia Kozlitina, Anne Tybjærg-Hansen, David Jones, Kirk U Knowlton, Lincoln Nadauld, Egil Ferkingstad, Einar S Björnsson, Magnus O Ulfarsson, Árni Sturluson, Patrick Sulem, Ole Birger Vesterager Pedersen, Sisse Rye Ostrowski, Daníel F Guðbjartsson, Kári Stefánsson, Morten Salling Olesen, Kyong-Mi Chang, Hilma Hólm, Henning Bundgaard, Stefan Stender
Integrative common and rare variant analyses provide insights into the genetic architecture of liver cirrhosis. Nature genetics 56 (5) (2024)
Jonas Ghouse, Gardar Sveinbjörnsson, Marijana Vujkovic, Anne-Sofie Seidelin, Helene Gellert-Kristensen, Gustav Ahlberg, Vinicius Tragante, Søren Albertsen Rand, Joseph Brancale, Silvia Vilarinho, Pia Rengtved Lundegaard, Erik Sørensen, Christian Erikstrup, Mie Topholm Bruun, Bitten Aagaard Jensen, Soren Brunak, Karina Banasik, Henrik Ullum, null null, Niek Verweij, Luca A Lotta, Aris Baras, null null, Tooraj Mirshahi, David J Carey, null null, null null, David E Kaplan, Julie A Lynch, Timothy Morgan, Tae-Hwi Schwantes-An, Daniel R Dochtermann, Saiju Pyarajan, Philip S Tsao, null null, Triin Laisk, Reedik Mägi, Julia Kozlitina, Anne Tybjærg-Hansen, David Jones, Kirk U Knowlton, Lincoln Nadauld, Egil Ferkingstad, Einar S Björnsson, Magnus O Ulfarsson, Árni Sturluson, Patrick Sulem, Ole Birger Vesterager Pedersen, Sisse Rye Ostrowski, Daníel F Guðbjartsson, Kári Stefánsson, Morten Salling Olesen, Kyong-Mi Chang, Hilma Hólm, Henning Bundgaard, Stefan Stender
Integrative common and rare variant analyses provide insights into the genetic architecture of liver cirrhosis. Nature genetics 56 (5) (2024)
Jonas Ghouse, Gardar Sveinbjörnsson, Marijana Vujkovic, Anne-Sofie Seidelin, Helene Gellert-Kristensen, Gustav Ahlberg, Vinicius Tragante, Søren Albertsen Rand, Joseph Brancale, Silvia Vilarinho, Pia Rengtved Lundegaard, Erik Sørensen, Christian Erikstrup, Mie Topholm Bruun, Bitten Aagaard Jensen, Soren Brunak, Karina Banasik, Henrik Ullum, null null, Niek Verweij, Luca A Lotta, Aris Baras, null null, Tooraj Mirshahi, David J Carey, null null, null null, David E Kaplan, Julie A Lynch, Timothy Morgan, Tae-Hwi Schwantes-An, Daniel R Dochtermann, Saiju Pyarajan, Philip S Tsao, null null, Triin Laisk, Reedik Mägi, Julia Kozlitina, Anne Tybjærg-Hansen, David Jones, Kirk U Knowlton, Lincoln Nadauld, Egil Ferkingstad, Einar S Björnsson, Magnus O Ulfarsson, Árni Sturluson, Patrick Sulem, Ole Birger Vesterager Pedersen, Sisse Rye Ostrowski, Daníel F Guðbjartsson, Kári Stefánsson, Morten Salling Olesen, Kyong-Mi Chang, Hilma Hólm, Henning Bundgaard, Stefan Stender
Integrative common and rare variant analyses provide insights into the genetic architecture of liver cirrhosis. Nature genetics 56 (5) (2024)
Christian Zinck Jensen, Jonas Lynggaard Isaksen, Gustav Ahlberg, Morten Salling Olesen, Birte Nygaard, Christina Ellervik, Jørgen Kim Kanters
Association of DIO2 and MCT10 Polymorphisms with Persistent Symptoms in LT4-Treated Patients in UK Biobank. The Journal of clinical endocrinology and metabolism (2023)
Jonas Ghouse, Vinicius Tragante, Ayesha Muhammad, Gustav Ahlberg, Morten W Skov, Dan M Roden, Ingileif Jónsdóttir, Laura Andreasen, Pia Rengtved Lundegaard, Linea C Trudsø, Karina Banasik, Søren Brunak, Sisse Rye Ostrowski, null null, Christian Torp-Pedersen, Ole V Pedersen, Erik Sørensen, Lars Valeur Køber, Kasper Iversen, Unnur Thorsteinsdottir, Gudmundur Thorgeirsson, Henrik Ullum, Daniel F Gudbjartsson, Jonathan D Mosley, Hilma Hólm, Kári Stefánsson, Henning Bundgaard, Morten Salling Olesen
Polygenic risk score for ACE-inhibitor-associated cough based on the discovery of new genetic loci. European heart journal 43 (45) (2022)
Christian Paludan-Müller, Simon Larsen, Gustav Ahlberg, Laura Andreasen, Laia M Monfort, Jesper Hastrup Svendsen, Thomas Jespersen, Henning Bundgaard, Jørgen Kim Kanters, Morten Salling Olesen
Clinical Implications of SCN10A Loss-of-Function Variants in 169 610 Exomes Representing the General Population. Circulation. Genomic and precision medicine 15 (1) (2022)
Gustav Ahlberg, Laura Andreasen, Jonas Ghouse, Litten Bertelsen, Henning Bundgaard, Stig Haunsø, Jesper Hastrup Svendsen, Morten Salling Olesen
Genome-wide association study identifies 18 novel loci associated with left atrial volume and function. European heart journal 42 (44) (2021)
Christian Paludan-Müller, Jonas Ghouse, Oliver Bundgaard Vad, Cecilie B Herfelt, Pia Lundegaard, Gustav Ahlberg, Nicole Schmitt, Jesper H Svendsen, Stig Haunsø, Henning Bundgaard, Torben Hansen, Jørgen K Kanters, Morten S Olesen
Reappraisal of variants previously linked with sudden infant death syndrome: results from three population-based cohorts. European journal of human genetics : EJHG 27 (9) (2019)
Laura Andreasen, Gustav Ahlberg, Chuyi Tang, Charlotte Andreasen, Jacob Peter Hartmann, Jacob Tfelt-Hansen, Elijah R Behr, Steen Pehrson, Stig Haunsø, null LuCamp, Peter E Weeke, Thomas Jespersen, Morten S Olesen, Jesper H Svendsen
Next-generation sequencing of AV nodal reentrant tachycardia patients identifies broad spectrum of variants in ion channel genes. European journal of human genetics : EJHG 26 (5) (2018)
Jonas Ghouse, Christian Theil Have, Morten W Skov, Laura Andreasen, Gustav Ahlberg, Jonas Bille Nielsen, Tea Skaaby, Søren-Peter Olesen, Niels Grarup, Allan Linneberg, Oluf Pedersen, Henrik Vestergaard, Stig Haunsø, Jesper H Svendsen, Torben Hansen, Jørgen Kim Kanters, Morten S Olesen
Numerous Brugada syndrome-associated genetic variants have no effect on J-point elevation, syncope susceptibility, malignant cardiac arrhythmia, and all-cause mortality. Genetics in medicine : official journal of the American College of Medical Genetics 19 (5) (2016)

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Publication Activity (10 Years)

Top Topics

Top Venues

Gustav Ahlberg