Mutations in ASPH Cause Facial Dysmorphism, Lens Dislocation, Anterior-Segment Abnormalities, and Spontaneous Filtering Blebs, or Traboulsi Syndrome

ADAMTS10 Mutations in Autosomal Recessive Weill-Marchesani Syndrome

Nathalie Dagoneau, Catherine Benoist-Lasselin, Céline Huber et al. · The American Journal of Human Genetics · 2004 · 281 citations · Full text

Life Sciences, Genetics, Molecular Genetics +8

Homozygous Mutations in ADAMTS10 and ADAMTS17 Cause Lenticular Myopia, Ectopia Lentis, Glaucoma, Spherophakia, and Short Stature

José Morales, Latifa Al-Sharif, Dania S. Khalil et al. · The American Journal of Human Genetics · 2009 · 245 citations · Full text

Life Sciences, Genetics, Molecular Genetics +15

Evolution of distinct EGF domains with specific functions

Merridee A. Wouters, Isidore Rigoutsos, Carmen K. Chu et al. · Protein Science · 2005 · 177 citations · Full text

Life Sciences, Biochemistry, Molecular Biology +17

Absence of Post-translational Aspartyl β-Hydroxylation of Epidermal Growth Factor Domains in Mice Leads to Developmental Defects and an Increased Incidence of Intestinal Neoplasia

Joseph Dinchuk, Richard J. Focht, Jennifer Kelley et al. · Journal of Biological Chemistry · 2002 · 109 citations · Full text

Life Sciences, Developmental Biology, Genetics +13

<i>iSyTE</i>:<u>I</u>ntegrated<u>Sy</u>stems<u>T</u>ool for<u>E</u>ye Gene Discovery

Salil A. Lachke, Joshua W. K. Ho, Gregory V. Kryukov et al. · Investigative Ophthalmology & Visual Science · 2012 · 106 citations · Full text

Medicine, Bioinformatics, Developmental Biology +17