Dzhoy Papingi

First step towards a consensus strategy for multi-locus diagnostic testing of imprinting disorders

Z. Tümer, P. Lapunzina, T. Ogata, 2022, Clinical Epigenetics.

Siblings with Gorlin–Goltz syndrome associated with cardiac tumors: a case report and review of literature

J. Sachweh, D. Biermann, R. Kozlik-Feldmann, 2023, Orphanet Journal of Rare Diseases.

Case Report of a DDX41 Germline Mutation in a Family with Multiple Relatives Suffering from Leukemia

Dzhoy Papingi, Carsten Bokemeyer, Walter Fiedler, 2023, Biomedicines.

A novel TTC26 variant in a patient with hexadactyly, pituitary stalk interruption, hepatopathy, nephropathy, and bilateral lip‐palate cleft: A case report and expansion of the phenotype

T. Bierhals, Theresia Herget, Dzhoy Papingi, 2023, American journal of medical genetics. Part A.