Kayserili, Hülya
Koç University · Istanbul University
6 papers on CoChatORCID 0000-0003-0376-499X
Most cited papers
- Verified
Disruptions of Topological Chromatin Domains Cause Pathogenic Rewiring of Gene-Enhancer Interactions
Lupiáñez, D. G., Kraft, K., Heinrich, V., Krawitz, P., Brancati, F., Klopocki, E., Horn, D., Kayserili, H., Opitz, J. M., Laxova, R., et al. (2015) · Cell
Genomics and Chromatin DynamicsGenomic variations and chromosomal abnormalities
Cited by 2,132
- Verified
RSPO2 inhibition of RNF43 and ZNRF3 governs limb development independently of LGR4/5/6
Szenker-Ravi, E., Altunoglu, U., Leushacke, M., Bosso-Lefèvre, C., Khatoo, M., Thi Tran, H., Naert, T., Noelanders, R., Hajamohideen, A., Beneteau, C., et al. (2018) · Nature
Wnt/β-catenin signaling in development and cancerCongenital limb and hand anomalies
Cited by 190
- Verified
LRP4 mutations alter Wnt/β-catenin signaling and cause limb and kidney malformations in Cenani–Lenz syndrome
Li, Y., Pawlik, B., Elcioglu, N., Aglan, M., Kayserili, H., Yigit, G., Percin, F., Goodman, F., Nürnberg, G., Cenani, A., et al. (2010) · The American Journal of Human Genetics
Congenital limb and hand anomaliesWnt/β-catenin signaling in development and cancer
Cited by 171
- Verified
Frequency of renal malformations in Turner syndrome: analysis of 82 Turkish children
Bilge, I., Kayserili, H., Emre, S., Nayir, A., Sirin, A., Tukel, T., Bas, F., Kilic, G., Basaran, S., Gunoz, H., et al. (2000) · Pediatric Nephrology
Genetic and Clinical Aspects of Sex Determination and Chromosomal AbnormalitiesPediatric Urology and Nephrology Studies
Cited by 77
- Verified
DOCK6 Mutations Are Responsible for a Distinct Autosomal-Recessive Variant of Adams-Oliver Syndrome Associated with Brain and Eye Anomalies
Sukalo, M., Tilsen, F., Kayserili, H., Müller, D., Tüysüz, B., Ruddy, D. M., Wakeling, E., Ørstavik, K. H., Snape, K. M., Trembath, R., et al. (2015) · Human Mutation
Congenital limb and hand anomaliesGenomics and Rare Diseases
Cited by 50
- Verified
Mild nasal clefting may be predictive for ALX4 heterozygotes
Altunoglu, U., Satkın, B., Uyguner, Z. O., & Kayserili, H. (2014) · American Journal of Medical Genetics Part A
Craniofacial Disorders and TreatmentsCleft Lip and Palate Research
Cited by 18
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