Kerstin Uhl

Statistics

Publications

Citations

235

H-Index

Active since

1998

Affiliations

Max Planck Institute for Heart and Lung Research(Current)

Kerstin Uhl is an author at Max Planck Institute for Heart and Lung Research specializing in genetics, human genetics, and inherited cardiomyopathies.

Publications per year

1998–2000

Publications

A Newly Created Splice Donor Site in Exon 25 of the MyBP-C Gene Is Responsible for Inherited Hypertrophic Cardiomyopathy With Incomplete Disease Penetrance

Johannes Moolman, Sebastian Reith, Kerstin Uhl et al. · Circulation · 2000 · 127 citations · Full text

Life Sciences, Genetics, Molecular Genetics +14

A high risk phenotype of hypertrophic cardiomyopathy associated with a compound genotype of two mutated β-myosin heavy chain genes

Brigitte Jeschke, Kerstin Uhl, Bernd Weist et al. · Human Genetics · 1998 · 71 citations

Medicine, Cardiology, Genetics +12

Genomic structure and fine mapping of the two human filamin gene paralogues FLNB and FLNC and comparative analysis of the filamin gene family

Christina Chakarova, Manfred Wehnert, Kerstin Uhl et al. · Human Genetics · 2000 · 37 citations

Life Sciences, Genetics, Molecular Genetics +7

1–3 of 3