Folgen
Ingrid Brænne
Ingrid Brænne
Bestätigte E-Mail-Adresse bei boehringer-ingelheim.com
Titel
Zitiert von
Zitiert von
Jahr
Genomewide association analysis of coronary artery disease
NJ Samani, J Erdmann, AS Hall, C Hengstenberg, M Mangino, B Mayer, ...
New England Journal of Medicine 357 (5), 443-453, 2007
24532007
Hereditary angioedema with a mutation in the plasminogen gene
K Bork, K Wulff, L Steinmüller‐Magin, I Braenne, P Staubach‐Renz, ...
Allergy 73 (2), 442-450, 2018
2952018
Dysfunctional nitric oxide signalling increases risk of myocardial infarction
J Erdmann, K Stark, UB Esslinger, PM Rumpf, D Koesling, C De Wit, ...
Nature 504 (7480), 432-436, 2013
2742013
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
P Linsel-Nitschke, A Götz, J Erdmann, I Braenne, P Braund, ...
PloS one 3 (8), e2986, 2008
1962008
Hereditary angioedema cosegregating with a novel kininogen 1 gene mutation changing the N‐terminal cleavage site of bradykinin
K Bork, K Wulff, H Rossmann, L Steinmüller‐Magin, I Brænne, G Witzke, ...
Allergy 74 (12), 2479-2481, 2019
1762019
Prediction of causal candidate genes in coronary artery disease loci
I Brænne, M Civelek, B Vilne, A Di Narzo, AD Johnson, Y Zhao, B Reiz, ...
Arteriosclerosis, thrombosis, and vascular biology 35 (10), 2207-2217, 2015
1192015
Systematic analysis of variants related to familial hypercholesterolemia in families with premature myocardial infarction
I Brænne, M Kleinecke, B Reiz, E Graf, T Strom, T Wieland, M Fischer, ...
European Journal of Human Genetics 24 (2), 191-197, 2016
962016
New insights into the genetics of X-linked dystonia-parkinsonism (XDP, DYT3)
A Domingo, A Westenberger, LV Lee, I Brænne, T Liu, I Vater, R Rosales, ...
European Journal of Human Genetics 23 (10), 1334-1340, 2015
832015
Expression quantitative trait Loci acting across multiple tissues are enriched in inherited risk for coronary artery disease
H Foroughi Asl, HA Talukdar, ASD Kindt, RK Jain, R Ermel, A Ruusalepp, ...
Circulation: Cardiovascular Genetics 8 (2), 305-315, 2015
492015
Network analysis of coronary artery disease risk genes elucidates disease mechanisms and druggable targets
H Lempiäinen, I Brænne, T Michoel, V Tragante, B Vilne, TR Webb, ...
Scientific reports 8 (1), 3434, 2018
462018
Hidden Mutations in C ornelia de L ange Syndrome Limitations of S anger Sequencing in Molecular Diagnostics
D Braunholz, C Obieglo, I Parenti, J Pozojevic, J Eckhold, B Reiz, ...
Human mutation 36 (1), 26-29, 2015
372015
Old mice have less transcriptional activation but similar periosteal cell proliferation compared to young‐adult mice in response to in vivo mechanical loading
CJ Chermside‐Scabbo, TL Harris, MD Brodt, I Braenne, B Zhang, ...
Journal of Bone and Mineral Research 35 (9), 1751-1764, 2020
302020
On the pathogenicity of the plasminogen K330E mutation for hereditary angioedema
AE Germenis, G Loules, M Zamanakou, F Psarros, T González-Quevedo, ...
Allergy 73 (8), 1751-1753, 2018
302018
Whole-exome sequencing in an extended family with myocardial infarction unmasks familial hypercholesterolemia
I Brænne, B Reiz, A Medack, M Kleinecke, M Fischer, S Tuna, ...
BMC cardiovascular disorders 14, 1-6, 2014
262014
Wellcome Trust Case Control Consortium (WTCCC); Cardiogenics Consortium. Lifelong reduction of LDL-cholesterol related to a common variant in the LDL-receptor gene decreases …
P Linsel-Nitschke, A Götz, J Erdmann, I Braenne, P Braund, ...
PLoS One 3 (8), e2986, 2008
252008
Druggability of coronary artery disease risk loci
V Tragante, D Hemerich, M Alshabeeb, I Brænne, H Lempiäinen, ...
Circulation: Genomic and Precision Medicine 11 (8), e001977, 2018
182018
PLA2G6 mutations and parkinsonism: long-term follow-up of clinical features and neuropathology
C Klein, T Löchte, SM Delamonte, I Brænne, AA Hicks, ...
Movement disorders: official journal of the Movement Disorder Society 31 (12 …, 2016
182016
A familial congenital heart disease with a possible multigenic origin involving a mutation in BMPR1A
TJ Demal, M Heise, B Reiz, D Dogra, I Brænne, H Reichenspurner, ...
Scientific reports 9 (1), 2959, 2019
172019
A genomic exploration identifies mechanisms that may explain adverse cardiovascular effects of COX-2 inhibitors
I Brænne, C Willenborg, V Tragante, T Kessler, L Zeng, B Reiz, ...
Scientific reports 7 (1), 10252, 2017
162017
Seemingly dominant inheritance of a recessive ANO10 mutation in romani families with cerebellar ataxia
ND Mišković, A Domingo, V Dobričić, C Max, I Brænne, I Petrović, K Grütz, ...
Movement disorders: official journal of the Movement Disorder Society 31 (12 …, 2016
122016
Das System kann den Vorgang jetzt nicht ausführen. Versuchen Sie es später erneut.
Artikel 1–20