Anja A. T. Geisterfer-Lowrance

Author

Also Known As

A A Geisterfer-Lowrance, A Geisterfer-Lowrance, Anja A. T. Geisterfer-Lowrance, Anja A.T. Geisterfer-Lowrance, Anja Geisterfer-Lowrance, Ted W. Love

Publications

2.9K

Citations

H-Index

Concepts

All Affiliations

Brigham and Women's Hospital Howard Hughes Medical Institute Harvard University

About

Anja A. T. Geisterfer-Lowrance is an author at Brigham and Women's Hospital specializing in medicine, genetics, and genetic engineering.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	4	4	2.1K
2	Cell Biology	2	2	551
3	Pathology	2	2	1.5K
4	Cardiovascular Genetics	2	2	1.5K
5	Public Health	1	1	149

Anja A. T. Geisterfer-Lowrance

Publications

2.9K

Citations

H-Index

Page 1

	Year	Citations
A molecular basis for familial hypertrophic cardiomyopathy: A β cardiac myosin heavy chain gene missense mutation Anja A. T. Geisterfer-Lowrance, Susan Kass, G Tanigawa, Cell Cardiac MuscleCardiomyopathyFamilial Hypertrophic CardiomyopathyCardiovascular DiseaseGenetics	1990	1.4K
A Mouse Model of Familial Hypertrophic Cardiomyopathy Anja A. T. Geisterfer-Lowrance, Michael E. Christe, David A. Conner, Science	1996	556
Production of homozygous mutant ES cells with a single targeting construct. Richard M. Mortensen, David A. Conner, Stephen Chao, Molecular and Cellular Biology GeneticsEmbryonic StemCell CultureCell SpecializationSingle Targeting Construct	1992	413
Familial hypertrophic cardiomyopathy is a genetically heterogeneous disease. Scott D. Solomon, J A Jarcho, William J. McKenna, Journal of Clinical Investigation CardiomyopathyMendelian DisorderFamilial Hypertrophic CardiomyopathyCardiovascular DiseaseFamily Members	1990	149
Production of Homozygous Mutant ES Cells with a Single Targeting Construct Richard M. Mortensen, David A. Conner, Stephen Chao, Molecular and Cellular Biology GeneticsEmbryonic StemCell CultureCell SpecializationSingle Targeting Construct	1992	138
Targeted Ablation of the Murine α-Tropomyosin Gene E. M. Blanchard, Kenji Iizuka, Michael E. Christe, Circulation Research	1997	104
A locus for familial hypertrophic cardiomyopathy is closely linked to the cardiac myosin heavy chain genes, CRI-L436, and CRI-L329 on chromosome 14 at q11-q12. Scott D. Solomon, Anja A. T. Geisterfer-Lowrance, Hans-Peter Vosberg, PubMed	1990	70
Functional analysis of myosin missense mutations in familial hypertrophic cardiomyopathy. Anthony J. Straceski, Anja A. T. Geisterfer-Lowrance, Christine E. Seidman, Proceedings of the National Academy of Sciences	1994	42

Page 1