E. Gökpınar İli

Hereditary Breast-Ovarian Cancer and BRCA1 / BRCA2 variants: a single center experience

A. Gezdirici, E. Gökpınar İli, B. Değirmenci, 2021, Acta Oncologica Turcica.

Association of pyrin mutations and autoinflammation with complex phenotype hidradenitis suppurativa: a case–control study

L. Holdt, C. Durmaz, K. Giehl, 2019, The British journal of dermatology.

Phenotypic and molecular characterization of five patients with PIK3CA‐related overgrowth spectrum (PROS)

C. Durmaz, H. Karabulut, S. Vural, 2022, American journal of medical genetics. Part A.

Cytogenetic, Molecular, and Phenotypic Characterization of a Patient with de novo Derivative Chromosome 18 and Review of the Literature

H. Karabulut, E. Gökpınar İli, Şule Altıner, 2019, Cytogenetic and Genome Research.

Promising effect of intravenous immunoglobulin therapy for epidermolysis bullosa pruriginosa

J. McGrath, C. Durmaz, A. Heper, 2020, International journal of dermatology.

New Homozygous Missense MSMO1 Mutation in Two Siblings with SC4MOL Deficiency Presenting with Psoriasiform Dermatitis

M. Simpson, J. McGrath, A. Onoufriadis, 2020, Cytogenetic and Genome Research.