Elif Uz
Bursa Uludağ Üni̇versi̇tesi̇(TR)
Publications by Year
Research Areas
Craniofacial Disorders and Treatments, Epigenetics and DNA Methylation, Cancer-related molecular mechanisms research, Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities, Genomic variations and chromosomal abnormalities
Most-Cited Works
- → KIF7 mutations cause fetal hydrolethalus and acrocallosal syndromes(2011)241 cited
- → Disruption of ALX1 Causes Extreme Microphthalmia and Severe Facial Clefting: Expanding the Spectrum of Autosomal-Recessive ALX-Related Frontonasal Dysplasia(2010)152 cited
- → ALX4 dysfunction disrupts craniofacial and epidermal development(2009)123 cited
- → Analysis of skewed X-chromosome inactivation in females with rheumatoid arthritis and autoimmune thyroid diseases(2009)121 cited
- → Evidence from autoimmune thyroiditis of skewed X-chromosome inactivation in female predisposition to autoimmunity(2006)112 cited
- → Mutations in the very low-density lipoprotein receptor VLDLR cause cerebellar hypoplasia and quadrupedal locomotion in humans(2008)105 cited
- → STK4 (MST1) deficiency in two siblings with autoimmune cytopenias: A novel mutation(2015)84 cited
- → Mutations in IRX5 impair craniofacial development and germ cell migration via SDF1(2012)83 cited
- → Mutations in the interleukin receptor IL11RA cause autosomal recessive Crouzon‐like craniosynostosis(2013)75 cited
- → Extreme Clonality in Lymphoblastoid Cell Lines with Implications for Allele Specific Expression Analyses(2008)56 cited