Sini Ezer

X–linked anhidrotic (hypohidrotic) ectodermal dysplasia is caused by mutation in a novel transmembrane protein

Juha Kere, Anand Srivastava, Outi Montonen et al. · Nature Genetics · 1996 · 753 citations

Developmental Biology, Mendelian Disorder, Genetic Disorder +10

The Tabby phenotype is caused by mutation in a mouse homologue of the<i>EDA</i>gene that reveals novel mouse and human exons and encodes a protein (ectodysplasin-A) with collagenous domains

Anand K. Srivastava, Johanna Pispa, Andrew J. Hartung et al. · Proceedings of the National Academy of Sciences · 1997 · 312 citations · Full text

The Anhidrotic Ectodermal Dysplasia Gene (EDA) Undergoes Alternative Splicing and Encodes Ectodysplasin-A with Deletion Mutations in Collagenous Repeats

Mónica Bayés, Andrew J. Hartung, Sini Ezer et al. · Human Molecular Genetics · 1998 · 229 citations · Full text

Ectodysplasin is a collagenous trimeric type II membrane protein with a tumor necrosis factor-like domain and co-localizes with cytoskeletal structures at lateral and apical surfaces of cells

Sini Ezer · Human Molecular Genetics · 1999 · 147 citations · Full text

Assessment of the Neuropeptide S System in Anxiety Disorders

Jonas Donner, Rita Haapakoski, Sini Ezer et al. · Biological Psychiatry · 2010 · 93 citations

Psychiatry, Neuroanatomy, Psychopharmacology +9