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Binner, Priska
19  results:
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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/..
 
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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/..
 
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3

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/..
 
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4

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/..
 
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5

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/..
 
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6

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/..
 
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7

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/..
 
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8

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/..
 
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9

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/..
 
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10

Hypertrophe Kardiomyopathie:

Scheffold, Thomas ; Binner, Priska ; Erdmann, Jeanette..
Herz Kardiovaskuläre Erkrankungen.  30 (2005)  6 - p. 550-557 , 2005
Link: https://doi.org/10.1007/..
 
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11

Mutations in the Human Muscle LIM Protein Gene in Families ..:

Geier, Christian ; Perrot, Andreas ; Özcelik, Cemil...
Circulation.  107 (2003)  10 - p. 1390-1395 , 2003
Link: https://doi.org/10.1161/..
 
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12

MHC class I antigen processing pathway defects, ras mutatio..:

Atkins, Derek ; Breuckmann, Aldona ; Schmahl, Gerd E....
International Journal of Cancer.  109 (2003)  2 - p. 265-273 , 2003
Link: https://doi.org/10.1002/..
 
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13

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/..
 
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14

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..
 
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15

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..
 
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