Concepedia

Ann Haskins Olney

AH

Statistics

Publications

28

Citations

2.5K

H-Index

25

Active since

1985

Affiliations

University of Nebraska Medical Center(Current)

Nebraska Medical Center

Center for Human Genetics

University of British Columbia

University of Washington

Ann Haskins Olney is an author at University of Nebraska Medical Center specializing in life sciences, molecular genetics, and genetics.

Publications per year

1985–2018

28

Publications

28

GLI3 frameshift mutations cause autosomal dominant Pallister-Hall syndrome

Seongman Kang, John M. Graham, Ann Haskins Olney et al. · Nature Genetics · 1997 · 510 citations

, , +8

Refinement of a 400-kb Critical Region Allows Genotypic Differentiation between Isolated Lissencephaly, Miller-Dieker Syndrome, and Other Phenotypes Secondary to Deletions of 17p13.3

Carlos Cardoso, Richard J. Leventer, Heather L. Ward et al. · The American Journal of Human Genetics · 2003 · 283 citations · Full text

, , +5

De novo <i>ACTA2</i> mutation causes a novel syndrome of multisystemic smooth muscle dysfunction

Dianna M. Milewicz, John R. Østergaard, Leena Ala‐Kokko et al. · American Journal of Medical Genetics Part A · 2010 · 269 citations

, , +13

Genotype-Phenotype Analysis in Congenital Adrenal Hyperplasia due to P450 Oxidoreductase Deficiency

Nils Krone, Nicole Reisch, Jan Idkowiak et al. · The Journal of Clinical Endocrinology & Metabolism · 2011 · 166 citations · Full text

, , +17

Diamond–Blackfan anemia with mandibulofacial dystostosis is heterogeneous, including the novel DBA genes <i>TSR2</i> and <i>RPS28</i>

Karen W. Gripp, Cynthia J. Curry, Ann Haskins Olney et al. · American Journal of Medical Genetics Part A · 2014 · 148 citations · Full text

, , +17

1–5 of 28