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European Journal of Human Genetics : EJHG|December 11, 2008
A paternal deletion of MKRN3, MAGEL2 and NDN does not result in Prader-Willi syndromeDeniz Kanber, Jacques Giltay, Dagmar Wieczorek, et al.Molecular Cytogenetics|August 8, 2020
13q deletion syndrome resulting from balanced chromosomal rearrangement in father: the significance of parental karyotypingSabine Dittner-Moormann, Madlen Reschke, Eva Biewald, et al.American Journal of Medical Genetics. Part A|July 6, 2010
Segmental paternal uniparental disomy (patUPD) of 14q32 with abnormal methylation elicits the characteristic features of complete patUPD14Melita D Irving, Karin Buiting, Deniz Kanber, et al.Hypertension in Pregnancy|October 9, 2018
Maternal levels of growth differentiation factor-15 in patients with preeclampsiaIlkbal Temel Yuksel, Begum Aydogan Mathyk, Berna Aslan Cetin, et al.Cancers|May 14, 2022
RB1-Negative Retinal Organoids Display Proliferation of Cone Photoreceptors and Loss of Retinal DifferentiationDeniz Kanber, Julia Woestefeld, Hannah Döpper, et al.Molecular Genetics & Genomic Medicine|November 28, 2017
The maternal uniparental disomy of chromosome 6 (upd(6)mat) "phenotype": result of placental trisomy 6 mosaicism?Thomas Eggermann, Barbara Oehl-Jaschkowitz, Severin Dicks, et al.The Journal of Maternal-Fetal & Neonatal Medicine : the Official Journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians|December 14, 2017
Increased levels of the novel hepatokine fetuin B in patients with intrahepatic cholestasis of pregnancyNadiye Koroglu, Ahmet Tayyar, Esra Nur Tola, et al.European Journal of Human Genetics : EJHG|December 27, 2007
IGF2/H19 hypomethylation in Silver-Russell syndrome and isolated hemihypoplasiaMichael Zeschnigk, Beate Albrecht, Karin Buiting, et al.Pediatric Blood & Cancer|April 2, 2026
MYCN Amplification in RB1-Inactivated Retinoblastoma: Association With High-Risk FeaturesKyriaki Papaioannou, Regina Kubica, Karen Fischhuber, et al.BMC Medical Genetics|May 7, 2015
A novel large deletion of the ICR1 region including H19 and putative enhancer elementsHelen Fryssira, Stella Amenta, Deniz Kanber, et al.Pageof 5