Nevin Yalman

Spectrum of Perforin Gene Mutations in Familial Hemophagocytic Lymphohistiocytosis

Kim Göransdotter Ericson, Bengt Fadeel, Sofie Nilsson-Ardnor et al. · The American Journal of Human Genetics · 2001 · 251 citations · Full text

Life Sciences, Genetics, Molecular Genetics +11

Rab27a

Philippe Bahadoran, Édith Aberdam, F. Mantoux et al. · The Journal of Cell Biology · 2001 · 219 citations · Full text

Medicine, Dermatology, Genetics +14

Two Genes Are Responsible for Griscelli Syndrome at the Same 15q21 Locus

Élodie Pastural, Fügen Ersoy, Nevin Yalman et al. · Genomics · 2000 · 120 citations

Life Sciences, Genetics, Molecular Genetics +8

Characterization of <i>PRF1</i>, <i>STX11</i> and <i>UNC13D</i> genotype‐phenotype correlations in familial hemophagocytic lymphohistiocytosis

AnnaCarin Horne, Kim Ramme, Eva Rudd et al. · British Journal of Haematology · 2008 · 92 citations

Life Sciences, Genetics, Molecular Genetics +17

A male-specific increase in the HLA-DRB4 (DR53) frequency in high-risk and relapsed childhood ALL

M. Tevfik Dorak, Fatma Savran Oğuz, Nevin Yalman et al. · Leukemia Research · 2002 · 49 citations

Life Sciences, Genetics, Oncology +4