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Binner, Priska
19
results:
Search for persons
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Format
Online (19)
Mediatypes
Articles (Online) (12)
OpenAccess-fulltext (7)
Languages
english (18)
german (1)
Sorted by: Year
Sorted by: Relevance
?
1
Clinical characterization and mutation spectrum of patients..:
Bardey, Frieda
;
Rieck, Lorenz
;
Spira, Dominik
...
Journal of Lipid Research. , 2024
Link:
https://doi.org/10.1016/..
?
2
FH ALERT: efficacy of a novel approach to identify patients..:
Fath, Felix
;
Bengeser, Andreas
;
Barresi, Mathias
...
Scientific Reports. 11 (2021) 1 - p. , 2021
Link:
https://doi.org/10.1038/..
?
3
FH ALERT: efficacy of a novel approach to identify patients..:
Felix Fath
;
Andreas Bengeser
;
Mathias Barresi
...
https://doi.org/10.1038/s41598-021-99961-y. , 2021
Link:
https://doi.org/10.1038/..
?
4
Clinical characterization and mutation spectrum of German p..:
Grenkowitz, Thomas
;
Kassner, Ursula
;
Wühle-Demuth, Marion
...
Atherosclerosis. 253 (2016) - p. 88-93 , 2016
Link:
https://doi.org/10.1016/..
?
5
High-density oligonucleotide-based resequencing assay for m..:
Kathiravel, Ushanthine
;
Keyser, Britta
;
Hoffjan, Sabine
...
Molecular and Cellular Probes. 27 (2013) 2 - p. 103-108 , 2013
Link:
https://doi.org/10.1016/..
?
6
Six sequence variants on chromosome 9p21.3 are associated w..:
Forschungsverbund Herz-Kreislauf in NRW (Research Consortium Heart and Circulation in North Rhine-Westphalia)
;
Scheffold, Thomas
;
Kullmann, Silke
...
BMC Cardiovascular Disorders. 11 (2011) 1 - p. , 2011
Link:
https://doi.org/10.1186/..
?
7
Novel correlations between the genotype and the phenotype o..:
Waldmüller, Stephan
;
Erdmann, Jeanette
;
Binner, Priska
...
European Journal of Heart Failure. 13 (2011) 11 - p. 1185-1192 , 2011
Link:
https://doi.org/10.1093/..
?
8
Three novel mutations in the ACTA2 gene in German patients ..:
Hoffjan, Sabine
;
Waldmüller, Stephan
;
Blankenfeldt, Wulf
...
info:eu-repo/semantics/altIdentifier/doi/10.1038/ejhg.2010.239. , 2011
Link:
https://hal.archives-ouv..
?
9
Six sequence variants on chromosome 9p21.3 are associated w..:
Stellbrink Christoph
;
Hegge Franz
;
Motz Wolfgang
...
http://www.biomedcentral.com/1471-2261/11/9. , 2011
Link:
https://doi.org/10.1186/..
?
10
Six sequence variants on chromosome 9p21.3 are associated w..:
Scheffold, Thomas
;
Kullmann, Silke
;
Huge, Andreas
...
http://www.biomedcentral.com/1471-2261/11/9. , 2011
Link:
http://www.biomedcentral..
?
11
Variation in the human soluble epoxide hydrolase gene and r..:
Kullmann, Silke
;
Binner, Priska
;
Rackebrandt, Kirsten
...
BMC Cardiovascular Disorders. 9 (2009) 1 - p. , 2009
Link:
https://doi.org/10.1186/..
?
12
Variation in the human soluble epoxide hydrolase gene and r..:
Lankisch Mark
;
Haltern Georg
;
Huge Andreas
...
http://www.biomedcentral.com/1471-2261/9/48. , 2009
Link:
https://doi.org/10.1186/..
?
13
Variation in the human soluble epoxide hydrolase gene and r..:
Kullmann, Silke
;
Binner, Priska
;
Rackebrandt, Kirsten
...
http://www.biomedcentral.com/1471-2261/9/48. , 2009
Link:
http://www.biomedcentral..
?
14
Array-Based Resequencing Assay for Mutations Causing Hypert..:
Scheffold, Thomas
;
Bonin, Michael
;
Poths, Sven
...
Clinical Chemistry. 54 (2008) 4 - p. 682-687 , 2008
Link:
https://doi.org/10.1373/..
?
15
Noncompaction of the Ventricular Myocardium Is Associated w..:
Budde, Birgit S.
;
Binner, Priska
;
Waldmüller, Stephan
...
PLoS ONE. 2 (2007) 12 - p. e1362 , 2007
Link:
https://doi.org/10.1371/..
1-15