Şule Ünal

LAD-1/variant syndrome is caused by mutations in FERMT3

Taco W. Kuijpers, Edith van de Vijver, Marian A. J. Weterman et al. · Blood · 2008 · 221 citations · Full text

Multi‐gene panel testing improves diagnosis and management of patients with hereditary anemias

Roberta Russo, Immacolata Andolfo, Francesco Manna et al. · American Journal of Hematology · 2018 · 155 citations

Comparison of primary human cytotoxic T-cell and natural killer cell responses reveal similar molecular requirements for lytic granule exocytosis but differences in cytokine production

Samuel C. C. Chiang, Jakob Theorell, Miriam Entesarian et al. · Blood · 2013 · 138 citations · Full text

MECOM-associated syndrome: a heterogeneous inherited bone marrow failure syndrome with amegakaryocytic thrombocytopenia

Manuela Germeshausen, Phil Ancliff, Jaime Estrada et al. · Blood Advances · 2018 · 109 citations · Full text

A Monogenic Disease with a Variety of Phenotypes: Deficiency of Adenosine Deaminase 2

Seza Özen, Ezgi Deniz Batu, Ekim Z. Taşkıran et al. · The Journal of Rheumatology · 2019 · 99 citations