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Chromatin connectivity maps reveal dynamic promoter-enhancer long-range associations

Nature (London), 2013-12, Vol.504 (7479), p.306-310

2013

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

PLoS genetics, 2016-03, Vol.12 (3), p.e1005919-e1005919

2016

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Coding exons function as tissue-specific enhancers of nearby genes

Genome research, 2012-06, Vol.22 (6), p.1059-1068

2012

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Unraveling the transcriptional regulation of TWIST1 in limb development

PLoS genetics, 2018-10, Vol.14 (10), p.e1007738-e1007738

2018

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ZNF750 is expressed in differentiated keratinocytes and regulates epidermal late differentiation genes

PloS one, 2012-08, Vol.7 (8), p.e42628-e42628

2012

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Uncovering the Role of Hypermethylation by CTG Expansion in Myotonic Dystrophy Type 1 Using Mutant Human Embryonic Stem Cells

Stem cell reports, 2015-08, Vol.5 (2), p.221-231

2015

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Deciphering transcription factors and their corresponding regulatory elements during inhibitory interneuron differentiation using deep neural networks

Frontiers in cell and developmental biology, 2023-02, Vol.11, p.1034604-1034604

2023

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Functional characterization of tissue-specific enhancers in the DLX5/6 locus

Human molecular genetics, 2012-11, Vol.21 (22), p.4930-4938

2012

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Systematic dissection of coding exons at single nucleotide resolution supports an additional role in cell-specific transcriptional regulation

PLoS genetics, 2014-10, Vol.10 (10), p.e1004592-e1004592

2014

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Israel: when reality meets academia

Nature (London), 2023-11, Vol.623 (7986), p.253-253

2023

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IHH enhancer variant within neighboring NHEJ1 intron causes microphthalmia anophthalmia and coloboma

Npj genomic medicine, 2023-08, Vol.8 (1), p.22-22, Article 22

2023

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Mutations in the microtubule-associated protein MAP11 (C7orf43) cause microcephaly in humans and zebrafish

Brain (London, England : 1878), 2019-03, Vol.142 (3), p.574-585

2019

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Functional characterization of the ZEB2 regulatory landscape

Human molecular genetics, 2019-05, Vol.28 (9), p.1487-1497

2019

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Cytokinetic abscission is part of the midblastula transition in early zebrafish embryogenesis

Proceedings of the National Academy of Sciences - PNAS, 2021-04, Vol.118 (15), p.e2021210118

2021

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Control of meiotic chromosomal bouquet and germ cell morphogenesis by the zygotene cilium

Science (American Association for the Advancement of Science), 2022-06, Vol.376 (6599), p.eabh3104-eabh3104

2022

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UNC80 mutation causes a syndrome of hypotonia, severe intellectual disability, dyskinesia and dysmorphism, similar to that caused by mutations in its interacting cation channel NALCN

Journal of medical genetics, 2016-06, Vol.53 (6), p.397-402

2016

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PICOT binding to chromatin-associated EED negatively regulates cyclin D2 expression by increasing H3K27me3 at the CCND2 gene promoter

Cell death & disease, 2019-09, Vol.10 (10), p.685-15, Article 685

2019

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HDAC9 structural variants disrupting TWIST1 transcriptional regulation lead to craniofacial and limb malformations

Genome research, 2022-07, Vol.32 (7), p.1242-1253

2022

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Association analysis identifies ZNF750 regulatory variants in psoriasis

BMC medical genetics, 2011-12, Vol.12 (1), p.167-167, Article 167

2011

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VPS4 is a dynamic component of the centrosome that regulates centrosome localization of γ-tubulin, centriolar satellite stability and ciliogenesis

Scientific reports, 2018-02, Vol.8 (1), p.3353-19, Article 3353

2018

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A neuronal enhancer network upstream of MEF2C is compromised in patients with Rett-like characteristics

Human molecular genetics, 2019-03, Vol.28 (5), p.818-827

2019

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A neuronal enhancer network upstream of MEF2C is compromised in patients with Rett like characteristics

Human molecular genetics, 2020-03, Vol.29 (5), p.879-880

2020

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Dual Function of DNA Sequences: Protein-Coding Sequences Function as Transcriptional Enhancers

Perspectives in biology and medicine, 2015-03, Vol.58 (2), p.182-195

2015

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Seborrhea-like dermatitis with psoriasiform elements caused by a mutation in ZNF750 , encoding a putative C2H2 zinc finger protein

Nature genetics, 2006-07, Vol.38 (7), p.749-751

2006

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Deletion of the first pair of fibronectin type III repeats of the integrin β-4 gene is associated with epidermolysis bullosa, pyloric atresia and aplasia cutis congenita in the original Carmi syndrome patients

American journal of medical genetics. Part A, 2008-04, Vol.146A (8), p.1063-1066

2008

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Chromatin connectivity maps reveal dynamic promoter-enhancer long-range associations

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

Coding exons function as tissue-specific enhancers of nearby genes

Unraveling the transcriptional regulation of TWIST1 in limb development

ZNF750 is expressed in differentiated keratinocytes and regulates epidermal late differentiation genes

Uncovering the Role of Hypermethylation by CTG Expansion in Myotonic Dystrophy Type 1 Using Mutant Human Embryonic Stem Cells

Deciphering transcription factors and their corresponding regulatory elements during inhibitory interneuron differentiation using deep neural networks

Functional characterization of tissue-specific enhancers in the DLX5/6 locus

Systematic dissection of coding exons at single nucleotide resolution supports an additional role in cell-specific transcriptional regulation

Israel: when reality meets academia

IHH enhancer variant within neighboring NHEJ1 intron causes microphthalmia anophthalmia and coloboma

Mutations in the microtubule-associated protein MAP11 (C7orf43) cause microcephaly in humans and zebrafish

Functional characterization of the ZEB2 regulatory landscape

Cytokinetic abscission is part of the midblastula transition in early zebrafish embryogenesis

Control of meiotic chromosomal bouquet and germ cell morphogenesis by the zygotene cilium

UNC80 mutation causes a syndrome of hypotonia, severe intellectual disability, dyskinesia and dysmorphism, similar to that caused by mutations in its interacting cation channel NALCN

PICOT binding to chromatin-associated EED negatively regulates cyclin D2 expression by increasing H3K27me3 at the CCND2 gene promoter

HDAC9 structural variants disrupting TWIST1 transcriptional regulation lead to craniofacial and limb malformations

Association analysis identifies ZNF750 regulatory variants in psoriasis

VPS4 is a dynamic component of the centrosome that regulates centrosome localization of γ-tubulin, centriolar satellite stability and ciliogenesis

A neuronal enhancer network upstream of MEF2C is compromised in patients with Rett-like characteristics

A neuronal enhancer network upstream of MEF2C is compromised in patients with Rett like characteristics

Dual Function of DNA Sequences: Protein-Coding Sequences Function as Transcriptional Enhancers

Seborrhea-like dermatitis with psoriasiform elements caused by a mutation in ZNF750 , encoding a putative C2H2 zinc finger protein

Deletion of the first pair of fibronectin type III repeats of the integrin β-4 gene is associated with epidermolysis bullosa, pyloric atresia and aplasia cutis congenita in the original Carmi syndrome patients

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