Iván K. Chinn

Primary immunodeficiency diseases: Genomic approaches delineate heterogeneous Mendelian disorders

Asbjørg Stray‐Pedersen, Hanne Sørmo Sorte, Pubudu Samarakoon et al. · Journal of Allergy and Clinical Immunology · 2016 · 269 citations · Full text

Primary Immunodeficiency, Mendelian Disorder, Autoimmune Disease +9

Identifying Genes Whose Mutant Transcripts Cause Dominant Disease Traits by Potential Gain-of-Function Alleles

Zeynep Coban‐Akdemir, Janson J. White, Xiaofei Song et al. · The American Journal of Human Genetics · 2018 · 228 citations · Full text

Genetic Analysis, Allelic Variant, Systems Biology +7

Review of 54 patients with complete DiGeorge anomaly enrolled in protocols for thymus transplantation: outcome of 44 consecutive transplants

M. Louise Markert, Blythe H. Devlin, Marilyn J. Alexieff et al. · Blood · 2007 · 212 citations · Full text

Genetic and mechanistic diversity in pediatric hemophagocytic lymphohistiocytosis

Iván K. Chinn, Olive S. Eckstein, Erin C. Peckham‐Gregory et al. · Blood · 2018 · 192 citations · Full text

A novel disorder involving dyshematopoiesis, inflammation, and HLH due to aberrant CDC42 function

Michael T. Lam, Simona Coppola, Oliver H.F. Krumbach et al. · The Journal of Experimental Medicine · 2019 · 191 citations · Full text