Concepedia

Ann Haskins Olney

AH

27

Publications

2.3K

Citations

25

H-Index

1985

Active since

Affiliations

University of Nebraska Medical Center(Current)

Nebraska Medical Center

Center for Human Genetics

University of Washington

Johns Hopkins University

Ann Haskins Olney is an author at University of Nebraska Medical Center specializing in medicine, genetics, and pathology.

Top concepts

Publications per year

1985–2016

27

Publications

27

GLI3 frameshift mutations cause autosomal dominant Pallister-Hall syndrome

Seongman Kang, John M. Graham, Ann Haskins Olney et al. · Nature Genetics · 1997 · 506 citations

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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 · 281 citations · Full text

, , +8

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 · 266 citations

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 · 163 citations · Full text

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 · 144 citations · Full text

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