Adi Mory

Deleterious Mutations in LRBA Are Associated with a Syndrome of Immune Deficiency and Autoimmunity

Gabriela López‐Herrera, Giacomo Tampella, Qiang Pan‐Hammarström et al. · The American Journal of Human Genetics · 2012 · 513 citations · Full text

Loss of Kindlin-3 in LAD-III eliminates LFA-1 but not VLA-4 adhesiveness developed under shear flow conditions

Eugenia Manevich-Mendelson, Sara W. Feigelson, Ronit Pasvolsky et al. · Blood · 2009 · 101 citations · Full text

Exome sequencing as first‐tier test for fetuses with severe central nervous system structural anomalies

Yuval Yaron, Vered Ofen Glassner, Adi Mory et al. · Ultrasound in Obstetrics and Gynecology · 2022 · 77 citations · Full text

The <i>LRRK2</i> G2019S mutation is associated with Parkinson disease and concomitant non-skin cancers

Rivka Inzelberg, Ohad Cohen, J. Aharon‐Peretz et al. · Neurology · 2012 · 64 citations

Mutations in PIK3C2A cause syndromic short stature, skeletal abnormalities, and cataracts associated with ciliary dysfunction

Dov Tiosano, Hagit Baris, Anlu Chen et al. · PLoS Genetics · 2019 · 64 citations · Full text