Chozhavendan Rathinam

HAX1 deficiency causes autosomal recessive severe congenital neutropenia (Kostmann disease)

Christoph Klein, Magda Grudzien, Giridharan Appaswamy et al. · Nature Genetics · 2006 · 501 citations

Hax1 Deficiency, Mendelian Disorder, Genetic Disorder +7

Telomere dysfunction induces environmental alterations limiting hematopoietic stem cell function and engraftment

Zhenyu Ju, Hong Jiang, Maike Jaworski et al. · Nature Medicine · 2007 · 284 citations

Cell Therapy, Marrow Transplantation, Medicine +9

Transgenic expression of human signal regulatory protein alpha in Rag2^−/−γ_c^−/−mice improves engraftment of human hematopoietic cells in humanized mice

Till Strowig, Anthony Rongvaux, Chozhavendan Rathinam et al. · Proceedings of the National Academy of Sciences · 2011 · 221 citations · Full text

A novel human primary immunodeficiency syndrome caused by deficiency of the endosomal adaptor protein p14

Georg Bohn, Anna Allroth, Gudrun Brandes et al. · Nature Medicine · 2006 · 209 citations

Primary Immunodeficiency, Autoimmune Disease, Immunodeficiencies +8

Memory/effector (CD45RBlo) CD4 T cells are controlled directly by IL-10 and cause IL-22–dependent intestinal pathology

Masahito Kamanaka, Samuel Huber, Lauren A. Zenewicz et al. · The Journal of Experimental Medicine · 2011 · 189 citations · Full text