Genetic Evaluation and Application of Posterior Cranial Fossa Traits as Endophenotypes for Chiari Type I Malformation

Chiari Malformation Type I: A Case-Control Association Study of 58 Developmental Genes

(2013) Aintzane Urbizu et al.   PLoS One

Stratified Whole Genome Linkage Analysis of Chiari Type I Malformation Implicates Known Klippel-Feil Syndrome Genes as Putative Disease Candidates

(2013) Christina A. Markunas et al.   PLoS One

Clinical, radiological, and genetic similarities between patients with Chiari Type I and Type 0 malformations

(2012) Christina A. Markunas et al.   Journal of Neurosurgery-Pediatrics

Transcriptional Regulatory Cascades in Runx2-Dependent Bone Development

(2012) Tong Ming Liu et al.   TISSUE ENGINEERING PART B-REVIEWS

Identical twin sisters with Rubinstein-Taybi syndrome associated with Chiari malformations and syrinx

(2011) Lea Parsley et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Institutional experience with 500 cases of surgically treated pediatric Chiari malformation Type I

(2011) R. Shane Tubbs et al.   Journal of Neurosurgery-Pediatrics

Mechanisms of cerebellar tonsil herniation in patients with Chiari malformations as guide to clinical management

(2010) Thomas H. Milhorat et al.   ACTA NEUROCHIRURGICA

Rubinstein-Taybi syndrome associated with Chiari type I malformation caused by a large 16p13.3 microdeletion: A contiguous gene syndrome?

(2010) Cezary Wójcik et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Incidence of basioccipital hypoplasia in Chiari malformation Type I: comparative morphometric study of the posterior cranial fossa

(2009) Rémy Noudel et al.   JOURNAL OF NEUROSURGERY

High heritability of metabolomic profiles in families burdened with premature cardiovascular disease

(2009) Svati H Shah et al.   Molecular Systems Biology