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Iranian Journal of Pediatrics|February 23, 2013
First genetic screening for maternal uniparental disomy of chromosome 7 in Turkish silver-russell syndrome patientsEmin Karaca, Beyhan Tuysuz, Sacide Pehlivan, et al.Molecular Syndromology|February 28, 2022
Spondylometaepiphyseal Dysplasia Short Limb-Abnormal Calcification Type in Turkish Patients Reveals a Novel Mutation and New FeaturesElif Yilmaz Gulec, Bassam R Ali, Anne John, et al.Cerebellum (London, England)|May 9, 2026
Prenatal Diagnosis of Poretti-Boltshauser Syndrome: A Case of Live Birth with Confirmed LAMA1 VariantsIsmail Yilmaz, Gorkem Arica, Beyhan Tuysuz, et al.AJNR. American Journal of Neuroradiology|April 16, 2003
Abnormalities in the cerebral arterial system in osteogenesis imperfectaSait Albayram, Osman Kizilkilic, Halit Yilmaz, et al.Turkish Archives of Pediatrics|February 3, 2022
Effects of Long-Term Pamidronate Treatment on Bone Density and Fracture Rate in 65 Osteogenesis Imperfecta PatientsHakan Yazan, Nilay Güneş, Evren Akpınar, et al.European Journal of Human Genetics : EJHG|November 6, 2008
A novel matrix metalloproteinase 2 (MMP2) terminal hemopexin domain mutation in a family with multicentric osteolysis with nodulosis and arthritis with cardiac defectsBeyhan Tuysuz, Rebecca Mosig, Gürkan Altun, et al.Cerebellum (London, England)|October 23, 2010
Unilateral cerebellar hypoplasia with different clinical featuresGulcin Benbir, Simay Kara, Beyza Citci Yalcinkaya, et al.Journal of Human Genetics|March 20, 2015
A novel mutation in EED associated with overgrowthAna S A Cohen, Beyhan Tuysuz, Yaoqing Shen, et al.Journal of Child Neurology|March 28, 2012
Macrocephaly-capillary malformation syndrome in a newborn with tetralogy of fallot and sagittal sinus thrombosisTugba Erener Ercan, Funda Oztunc, Tiraje Celkan, et al.Journal of Human Genetics|March 26, 2022
Biallelic BICD2 variant is a novel candidate for Cohen-like syndromeAhmet Okay Caglayan, Beyhan Tuysuz, Ece Gül, et al.Pageof 5