Kala F. Schilter

PITX2 and FOXC1 spectrum of mutations in ocular syndromes

Linda M. Reis, Rebecca C. Tyler, Bethany A. Kloss et al. · European Journal of Human Genetics · 2012 · 146 citations · Full text

Ocular Disease, Ophthalmology, Genetic Disorder +4

BMP4 loss-of-function mutations in developmental eye disorders including SHORT syndrome

Linda M. Reis, Rebecca C. Tyler, Kala F. Schilter et al. · Human Genetics · 2011 · 118 citations · Full text

Analyzing the Genetic Spectrum of Vascular Anomalies with Overgrowth via Cancer Genomics

Dawn H. Siegel, Catherine E. Cottrell, Jenna L. Streicher et al. · Journal of Investigative Dermatology · 2017 · 74 citations · Full text

Angiogenesis, Somatic Variant, Tumor Heterogeneity +10

Prostate cancer risk locus at 8q24 as a regulatory hub by physical interactions with multiple genomic loci across the genome

Meijun Du, Tiezheng Yuan, Kala F. Schilter et al. · Human Molecular Genetics · 2014 · 61 citations · Full text

Genetics, Genetic Epidemiology, Genomic Mechanism +22

Potential Novel Mechanism for Axenfeld-Rieger Syndrome: Deletion of a Distant Region Containing Regulatory Elements of<i>PITX2</i>

B. A. Volkmann, Natalya S. Zinkevich, Aki Mustonen et al. · Investigative Ophthalmology & Visual Science · 2010 · 51 citations · Full text