Rotem Kadir - Concepedia

Author

Rotem Kadir

Ben-Gurion University of the Negev

Also Known As

R. Kadir, Rotem Kadir

Publications

976

Citations

H-Index

Concepts

All Affiliations

Ben-Gurion University of the Negev Soroka Medical Center Clalit Health Services Ariel University Hadassah Medical Center

About

Rotem Kadir is an author at Ben-Gurion University of the Negev specializing in medicine, genetics, and developmental biology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	12	13	577
2	Social Sciences	3	3	146
3	Health Sciences	1	1	45
4	Public Health	1	1	15
5	Biochemistry	1	1	45

Rotem Kadir

Publications

955

Citations

H-Index

Page 1

	Year	Citations
Regulation of CHD2 expression by the Chaserr long noncoding RNA gene is essential for viability Aviv Rom, Liliya Melamed, Noa Gil, Nature Communications	2019	124
SLC30A9 mutation affecting intracellular zinc homeostasis causes a novel cerebro-renal syndrome Yonatan Perez, Zamir Shorer, Keren Liani-Leibson, Brain Glomerular DiseaseGeneticsRenal PathologyGenetic EpidemiologyRenal Inflammation	2017	100
<i>VPS53</i> mutations cause progressive cerebello-cerebral atrophy type 2 (PCCA2) Miora Feinstein, Hagit Flusser, Tally Lerman‐Sagie, Journal of Medical Genetics	2014	91
ALFY-Controlled DVL3 Autophagy Regulates Wnt Signaling, Determining Human Brain Size Rotem Kadir, Tamar Harel, Barak Markus, PLoS Genetics MitophagyGeneticsMolecular GeneticsSocial SciencesCell Autophagy	2016	89
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, European Journal of Human Genetics Mendelian DisorderGenetic DisorderGeneticsInherited Metabolic DiseaseHomozygous Mutation	2013	58
Isolated foveal hypoplasia with secondary nystagmus and low vision is associated with a homozygous SLC38A8 mutation Yonatan Perez, Libe Gradstein, Hagit Flusser, European Journal of Human Genetics Ocular DiseaseSecondary NystagmusRetinaOphthalmologyGlaucoma	2013	53
<i>UNC80</i> mutation causes a syndrome of hypotonia, severe intellectual disability, dyskinesia and dysmorphism, similar to that caused by mutations in its interacting cation channel <i>NALCN</i> Yonatan Perez, Rotem Kadir, Michael Volodarsky, Journal of Medical Genetics	2015	49
SCAPER localizes to primary cilia and its mutation affects cilia length, causing Bardet-Biedl syndrome Ohad Wormser, Libe Gradstein, Yuval Yogev, European Journal of Human Genetics Developmental BiologyMendelian DisorderGenetic DisorderGeneticsPathogenesis	2019	48
<i>SEC31A</i> mutation affects ER homeostasis, causing a neurological syndrome Daniel Halpérin, Rotem Kadir, Yonatan Perez, Journal of Medical Genetics	2018	46
Mutations in the microtubule-associated protein MAP11 (C7orf43) cause microcephaly in humans and zebrafish Yonatan Perez, Reut Bar-Yaacov, Rotem Kadir, Brain Microtubule ExtensionsCytoskeletonMap11 AssociatesCell CycleMicrotubule-associated Protein Map11	2019	45

Page 1