| Single-cell genomics identifies cell type–specific molecular changes in autism D Velmeshev, L Schirmer, D Jung, M Haeussler, Y Perez, S Mayer, ... Science 364 (6441), 685-689, 2019 | 722 | 2019 |
| Tropism of SARS-CoV-2 for human cortical astrocytes MG Andrews, T Mukhtar, UC Eze, CR Simoneau, J Ross, N Parikshak, ... Proceedings of the National Academy of Sciences 119 (30), e2122236119, 2022 | 92 | 2022 |
| SLC30A9 mutation affecting intracellular zinc homeostasis causes a novel cerebro-renal syndrome Y Perez, Z Shorer, K Liani-Leibson, P Chabosseau, R Kadir, ... Brain 140 (4), 928-939, 2017 | 91 | 2017 |
| ALFY-controlled DVL3 autophagy regulates Wnt signaling, determining human brain size R Kadir, T Harel, B Markus, Y Perez, A Bakhrat, I Cohen, M Volodarsky, ... PLoS genetics 12 (3), e1005919, 2016 | 90 | 2016 |
| Autosomal recessive Adams–Oliver syndrome caused by homozygous mutation in EOGT, encoding an EGF domain-specific O-GlcNAc transferase I Cohen, E Silberstein, Y Perez, D Landau, K Elbedour, Y Langer, R Kadir, ... European Journal of Human Genetics 22 (3), 374-378, 2014 | 70 | 2014 |
| UNC80 mutation causes a syndrome of hypotonia, severe intellectual disability, dyskinesia and dysmorphism, similar to that caused by mutations in its interacting cation channel … Y Perez, R Kadir, M Volodarsky, I Noyman, H Flusser, Z Shorer, ... Journal of medical genetics 53 (6), 397-402, 2016 | 59 | 2016 |
| Isolated foveal hypoplasia with secondary nystagmus and low vision is associated with a homozygous SLC38A8 mutation Y Perez, L Gradstein, H Flusser, B Markus, I Cohen, Y Langer, M Marcus, ... European Journal of Human Genetics 22 (5), 703-706, 2014 | 52 | 2014 |
| Tropism of SARS-CoV-2 for developing human cortical astrocytes MG Andrews, T Mukhtar, UC Eze, CR Simoneau, Y Perez, ... BioRxiv, 2021 | 46 | 2021 |
| SCAPER localizes to primary cilia and its mutation affects cilia length, causing Bardet-Biedl syndrome O Wormser, L Gradstein, Y Yogev, Y Perez, R Kadir, I Goliand, Y Sadka, ... European Journal of Human Genetics 27 (6), 928-940, 2019 | 45 | 2019 |
| Mutations in the microtubule-associated protein MAP11 (C7orf43) cause microcephaly in humans and zebrafish Y Perez, R Bar-Yaacov, R Kadir, O Wormser, I Shelef, OS Birk, H Flusser, ... Brain 142 (3), 574-585, 2019 | 41 | 2019 |
| SEC31A mutation affects ER homeostasis, causing a neurological syndrome D Halperin, R Kadir, Y Perez, M Drabkin, Y Yogev, O Wormser, ... Journal of medical genetics 56 (3), 139-148, 2019 | 36 | 2019 |
| Hyperuricemia and gout caused by missense mutation in d-lactate dehydrogenase M Drabkin, Y Yogev, L Zeller, R Zarivach, R Zalk, D Halperin, O Wormser, ... The Journal of clinical investigation 129 (12), 5163-5168, 2019 | 35 | 2019 |
| Single-cell analysis of prenatal and postnatal human cortical development D Velmeshev, Y Perez, Z Yan, JE Valencia, DR Castaneda-Castellanos, ... Science 382 (6667), eadf0834, 2023 | 33 | 2023 |
| RSRC1 mutation affects intellect and behaviour through aberrant splicing and transcription, downregulating IGFBP3 Y Perez, S Menascu, I Cohen, R Kadir, O Basha, Z Shorer, H Romi, ... Brain 141 (4), 961-970, 2018 | 29 | 2018 |
| Progressive hereditary spastic paraplegia caused by a homozygous KY mutation Y Yogev, Y Perez, I Noyman, AA Madegem, H Flusser, Z Shorer, E Cohen, ... European Journal of Human Genetics 25 (8), 966-972, 2017 | 26 | 2017 |
| CDH2 mutation affecting N-cadherin function causes attention-deficit hyperactivity disorder in humans and mice D Halperin, A Stavsky, R Kadir, M Drabkin, O Wormser, Y Yogev, V Dolgin, ... Nature Communications 12 (1), 6187, 2021 | 23 | 2021 |
| Nocturnal Atrial Fibrillation Caused by Mutation in KCND2, Encoding Pore-Forming (α) Subunit of the Cardiac Kv4.2 Potassium Channel M Drabkin, N Zilberberg, S Menahem, W Mulla, D Halperin, Y Yogev, ... Circulation: Genomic and Precision Medicine 11 (11), e002293, 2018 | 22 | 2018 |
| A cross-species proteomic map reveals neoteny of human synapse development L Wang, K Pang, L Zhou, A Cebrián-Silla, S González-Granero, S Wang, ... Nature 622 (7981), 112-119, 2023 | 20 | 2023 |
| Novel GUCY2D mutation causes phenotypic variability of Leber congenital amaurosis in a large kindred L Gradstein, J Zolotushko, YV Sergeev, I Lavy, G Narkis, Y Perez, ... BMC Medical Genetics 17, 1-6, 2016 | 20 | 2016 |
| A novel homozygous SLC25A1 mutation with impaired mitochondrial complex V: Possible phenotypic expansion I Cohen, O Staretz‐Chacham, O Wormser, Y Perez, A Saada, R Kadir, ... American Journal of Medical Genetics Part A 176 (2), 330-336, 2018 | 18 | 2018 |
rotem kadir在 post.bgu.ac.il 的电子邮件经过验证
