David Ginsburg

Analysis of the relationship of von Willebrand disease (vWD) and hereditary hemorrhagic telangiectasia and identification of a potential type IIA vWD mutation (IIe865 to Thr).

F. Collins, M. Boehnke, M. Iannuzzi, 1991, American journal of human genetics.

von Willebrand disease and quantitative variation in von Willebrand factor.

K. Mohlke, D. Ginsburg, David Ginsburg, 1997, The Journal of laboratory and clinical medicine.

The molecular basis of von Willebrand disease

K. Mohlke, D. Ginsburg, W. Nichols, 1999, International journal of clinical & laboratory research.

The molecular biology of von Willebrand disease

D. Ginsburg, David Ginsburg, 1999, Haemophilia : the official journal of the World Federation of Hemophilia.

Genetic regulation of plasma von Willebrand factor levels: quantitative trait loci analysis in a mouse model

J. Shavit, David Ginsburg, Heidi L. Lemmerhirt, 2007, Journal of thrombosis and haemostasis : JTH.

Comparative mapping of distal murine chromosome 11 and human 17q21.3 in a region containing a modifying locus for murine plasma von Willebrand factor level.

K. Mohlke, R. Westrick, D. Ginsburg, 1998, Genomics.

von Willebrand disease.

David Ginsburg, William C. Nichols, 1997, Medicine.

Characterization of Leu777Pro and Ile865Thr type IIA von Willebrand disease mutations.

K. Cooney, D. Ginsburg, P. Bockenstedt, 1994, Blood.

Cloning and expression of human deoxycytidine kinase cDNA.

B. Mitchell, D. Gribbin, D. Ginsburg, 1991, Proceedings of the National Academy of Sciences of the United States of America.