Publications by authors named "Ingrid Braenne"

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Deep representation learning for clustering longitudinal survival data from electronic health records.
Jiajun Qiu, Yao Hu, Li Li, Abdullah Mesut Erzurumluoglu, Ingrid Braenne

Nat Commun· March 2025

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Dynamic changes in immune gene co-expression networks predict development of type 1 diabetes.
Ingrid Brænne, Suna Onengut-Gumuscu, Ruoxi Chen, Ani W Manichaikul, Stephen S Rich

Sci Rep· November 2021

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Identification of a Functional Variant at the Chromosome 4q27 Coronary Artery Disease Locus in an Extended Myocardial Infarction Family.
Tan An Dang, Thorsten Kessler, Jana Wobst, Michael Wierer, Ingrid Braenne

Circulation· August 2021

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Old Mice Have Less Transcriptional Activation But Similar Periosteal Cell Proliferation Compared to Young-Adult Mice in Response to in vivo Mechanical Loading.
Christopher J Chermside-Scabbo, Taylor L Harris, Michael D Brodt, Ingrid Braenne, Bo Zhang

J Bone Miner Res· September 2020

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Hereditary angioedema cosegregating with a novel kininogen 1 gene mutation changing the N-terminal cleavage site of bradykinin.
Konrad Bork, Karin Wulff, Heidi Rossmann, Lars Steinmüller-Magin, Ingrid Braenne

Allergy· December 2019

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A familial congenital heart disease with a possible multigenic origin involving a mutation in BMPR1A.
Till Joscha Demal, Melina Heise, Benedikt Reiz, Deepika Dogra, Ingrid Brænne

Sci Rep· February 2019

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Druggability of Coronary Artery Disease Risk Loci.
Vinicius Tragante, Daiane Hemerich, Mohammad Alshabeeb, Ingrid Brænne, Harri Lempiäinen

Circ Genom Precis Med· August 2018

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Network analysis of coronary artery disease risk genes elucidates disease mechanisms and druggable targets.
Harri Lempiäinen, Ingrid Brænne, Tom Michoel, Vinicius Tragante, Baiba Vilne

Sci Rep· February 2018

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Genomic correlates of glatiramer acetate adverse cardiovascular effects lead to a novel locus mediating coronary risk.
Ingrid Brænne, Lingyao Zeng, Christina Willenborg, Vinicius Tragante, Thorsten Kessler

PLoS One· October 2017

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Functional Characterization of Rare RAB12 Variants and Their Role in Musician's and Other Dystonias.
Eva Hebert, Friederike Borngräber, Alexander Schmidt, Aleksandar Rakovic, Ingrid Brænne

Genes (Basel)· October 2017

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A genomic exploration identifies mechanisms that may explain adverse cardiovascular effects of COX-2 inhibitors.
Ingrid Brænne, Christina Willenborg, Vinicius Tragante, Thorsten Kessler, Lingyao Zeng

Sci Rep· August 2017

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PLA2G6 mutations and Parkinsonism: Long-term follow-up of clinical features and neuropathology.
Christine Klein, Tobias Löchte, Suzanne M Delamonte, Ingrid Braenne, Andrew A Hicks

Mov Disord· December 2016

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Seemingly dominant inheritance of a recessive ANO10 mutation in romani families with cerebellar ataxia.
Nataša Dragašević Mišković, Aloysius Domingo, Valerija Dobričić, Christoph Max, Ingrid Braenne

Mov Disord· December 2016

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Systematic analysis of variants related to familial hypercholesterolemia in families with premature myocardial infarction.
Ingrid Brænne, Mariana Kleinecke, Benedikt Reiz, Elisabeth Graf, Tim Strom

Eur J Hum Genet· February 2016

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New insights into the genetics of X-linked dystonia-parkinsonism (XDP, DYT3).
Aloysius Domingo, Ana Westenberger, Lillian V Lee, Ingrid Brænne, Tian Liu

Eur J Hum Genet· October 2015

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Prediction of Causal Candidate Genes in Coronary Artery Disease Loci.
Ingrid Brænne, Mete Civelek, Baiba Vilne, Antonio Di Narzo, Andrew D Johnson

Arterioscler Thromb Vasc Biol· October 2015

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Expression quantitative trait Loci acting across multiple tissues are enriched in inherited risk for coronary artery disease.
Hassan Foroughi Asl, Husain A Talukdar, Alida S D Kindt, Rajeev K Jain, Raili Ermel, Ingrid Braenne

Circ Cardiovasc Genet· April 2015

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Hidden mutations in Cornelia de Lange syndrome limitations of sanger sequencing in molecular diagnostics.
Diana Braunholz, Carolin Obieglo, Ilaria Parenti, Jelena Pozojevic, Juliane Eckhold, Ingrid Braenne

Hum Mutat· January 2015

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Genome sequencing identifies a novel mutation in ATP1A3 in a family with dystonia in females only.
Robert Wilcox, Ingrid Brænne, Norbert Brüggemann, Susen Winkler, Karin Wiegers

J Neurol· January 2015

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Whole-exome sequencing in an extended family with myocardial infarction unmasks familial hypercholesterolemia.
Ingrid Brænne, Benedikt Reiz, Anja Medack, Mariana Kleinecke, Marcus Fischer

BMC Cardiovasc Disord· August 2014

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Dysfunctional nitric oxide signalling increases risk of myocardial infarction.
Jeanette Erdmann, Klaus Stark, Ulrike B Esslinger, Philipp Moritz Rumpf, Doris Koesling

Nature· December 2013

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Lifelong reduction of LDL-cholesterol related to a common variant in the LDL-receptor gene decreases the risk of coronary artery disease--a Mendelian Randomisation study.
Patrick Linsel-Nitschke, Anika Götz, Jeanette Erdmann, Ingrid Braenne, Peter Braund

PLoS One· August 2008

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Genomewide association analysis of coronary artery disease.
Nilesh J Samani, Jeanette Erdmann, Alistair S Hall, Christian Hengstenberg, Massimo Mangino, Ingrid Braenne

N Engl J Med· August 2007

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