Şükrü Öztürk

WRN mutations in Werner syndrome patients: genomic rearrangements, unusual intronic mutations and ethnic-specific alterations

Katrin Friedrich, Lin Lee, Dru F. Leistritz et al. · Human Genetics · 2010 · 101 citations · Full text

Life Sciences, Genetics, Molecular Genetics +11

Mutations in RAD21 Disrupt Regulation of APOB in Patients With Chronic Intestinal Pseudo-Obstruction

Elena Bonora, Francesca Bianco, Lina Cordeddu et al. · Gastroenterology · 2015 · 81 citations · Full text

Life Sciences, Genetics, Molecular Genetics +11

Initial maternal meiotic I error leading to the formation of a maternal i(2q) and a paternal i(2p) in a healthy male

Alessandra Baumer, Malgorzata Taralczak, Kıvanç Çefle et al. · Cytogenetic and Genome Research · 2007 · 79 citations · Full text

Life Sciences, Biology, Genetics +15

REST Final-Exon-Truncating Mutations Cause Hereditary Gingival Fibromatosis

Yavuz Bayram, Janson J. White, Nursel Elçioğlu et al. · The American Journal of Human Genetics · 2017 · 59 citations · Full text

Life Sciences, Genetics, Molecular Genetics +10

Multidisciplinary treatment of non-syndromic oligodontia

Canan Bural, Evren Öztaş, Şükrü Öztürk et al. · European Journal of Dentistry · 2012 · 44 citations · Full text

Dentistry, Orthodontics, Pediatric Dentistry +17