Sahan V. Rannan‐Eliya

Genomic Screening of Fibroblast Growth-Factor Receptor 2 Reveals a Wide Spectrum of Mutations in Patients with Syndromic Craniosynostosis

Shih‐hsin Kan, Navaratnam Elanko, David Johnson et al. · The American Journal of Human Genetics · 2002 · 266 citations · Full text

Dentistry, Genetics, Molecular Genetics +16

Paternal origin of FGFR3 mutations in Muenke-type craniosynostosis

Sahan V. Rannan‐Eliya, Indira B. Taylor, Inge Marieke de Heer et al. · Human Genetics · 2004 · 74 citations

Dentistry, Genetics, Molecular Genetics +16

Experience of an Orthoplastic Limb Salvage Team after the Haiti Earthquake: Analysis of Caseload and Early Outcomes

A. James P. Clover, Sahan V. Rannan‐Eliya, Waseem Saeed et al. · Plastic & Reconstructive Surgery · 2011 · 63 citations

Medicine, Orthopedic Surgery, Surgery +12

Parietal foramina with cleidocranial dysplasia is caused by mutation in MSX2

Sixto García‐Miñaúr, Lampros A. Mavrogiannis, Sahan V. Rannan‐Eliya et al. · European Journal of Human Genetics · 2003 · 50 citations · Full text

Medicine, Craniofacial Biology, Neurology +14

Surgical interventions for the treatment of radiation‐induced alopecia in pediatric practice

Yi Fan Rannan‐Eliya, Sahan V. Rannan‐Eliya, Kenneth E. Graham et al. · Pediatric Blood & Cancer · 2006 · 18 citations · Full text

Medicine, Dermatology, Surgery +17