Rotem Kadir

Regulation of CHD2 expression by the Chaserr long noncoding RNA gene is essential for viability

Aviv Rom, Liliya Melamed, Noa Gil et al. · Nature Communications · 2019 · 124 citations · Full text

SLC30A9 mutation affecting intracellular zinc homeostasis causes a novel cerebro-renal syndrome

Yonatan Perez, Zamir Shorer, Keren Liani-Leibson et al. · Brain · 2017 · 100 citations · Full text

Glomerular Disease, Genetics, Renal Pathology +28

<i>VPS53</i> mutations cause progressive cerebello-cerebral atrophy type 2 (PCCA2)

Miora Feinstein, Hagit Flusser, Tally Lerman‐Sagie et al. · Journal of Medical Genetics · 2014 · 91 citations

ALFY-Controlled DVL3 Autophagy Regulates Wnt Signaling, Determining Human Brain Size

Rotem Kadir, Tamar Harel, Barak Markus et al. · PLoS Genetics · 2016 · 89 citations · Full text

Mitophagy, Genetics, Molecular Genetics +16

Autosomal recessive Adams–Oliver syndrome caused by homozygous mutation in EOGT, encoding an EGF domain-specific O-GlcNAc transferase

Idan Cohen, Eldad Silberstein, Yonatan Perez et al. · European Journal of Human Genetics · 2013 · 58 citations · Full text

Mendelian Disorder, Genetic Disorder, Genetics +7