Citation Impact
Citing Papers
Visualizing enveloping layer glycans during zebrafish early embryogenesis
2010 StandoutNobel
Probing mucin-type O-linked glycosylation in living animals
2006 StandoutNobel
C2c2 is a single-component programmable RNA-guided RNA-targeting CRISPR effector
2016 StandoutScience
Gene essentiality and synthetic lethality in haploid human cells
2015 Science
The mucin-selective protease StcE enables molecular and functional analysis of human cancer-associated mucins
2019 StandoutNobel
Modulation of immune cell reactivity with cis -binding Siglec agonists
2021 StandoutNobel
SGK196 Is a Glycosylation-Specific O -Mannose Kinase Required for Dystroglycan Function
2013 Science
A metabolic labeling approach toward proteomic analysis of mucin-type O-linked glycosylation
2003 StandoutNobel
Accelerated Evolution of Conserved Noncoding Sequences in Humans
2006 StandoutScienceNobel
PIEZOs mediate neuronal sensing of blood pressure and the baroreceptor reflex
2018 StandoutScienceNobel
ER Tubules Mark Sites of Mitochondrial Division
2011 StandoutScience
Copper-free click chemistry in living animals
2010 StandoutNobel
PIEZO ion channel is required for root mechanotransduction in Arabidopsis thaliana
2021 StandoutNobel
The functional O-mannose glycan on α-dystroglycan contains a phospho-ribitol primed for matriglycan addition
2016
Cerebral cortex expansion and folding: what have we learned?
2016
Monkeypox Virus Host Factor Screen Using Haploid Cells Identifies Essential Role of GARP Complex in Extracellular Virus Formation
2017
Discovery and functional interrogation of SARS-CoV-2 RNA-host protein interactions
2021 StandoutNobel
Binding of the G domains of laminin α1 and α2 chains and perlecan to heparin, sulfatides, α-dystroglycan and several extracellular matrix proteins
1999
Discoveries in structure and physiology of mechanically activated ion channels
2020 StandoutNatureNobel
Biological functions of fucose in mammals
2017
Deletion of brain dystroglycan recapitulates aspects of congenital muscular dystrophy
2002 Nature
Physical Principles of Membrane Shape Regulation by the Glycocalyx
2019 StandoutNobel
The cytoplasmic body component TRIM5α restricts HIV-1 infection in Old World monkeys
2004 StandoutNature
Chemical Technologies for Probing Glycans
2006 StandoutNobel
Genome-wide detection of tissue-specific alternative splicing in the human transcriptome
2002
Alternative isoform regulation in human tissue transcriptomes
2008 StandoutNature
The cancer glycocalyx mechanically primes integrin-mediated growth and survival
2014 StandoutNatureNobel
Mitotic Spindle Regulation by Nde1 Controls Cerebral Cortical Size
2004
A bit of give and take: the relationship between the extracellular matrix and the developing chondrocyte
2003
Guillain-Barré syndrome
2016 Standout
Glycosylation in Cellular Mechanisms of Health and Disease
2006 Standout
The Muscular Dystrophy Gene TMEM5 Encodes a Ribitol β1,4-Xylosyltransferase Required for the Functional Glycosylation of Dystroglycan
2016
A CRISPR toolbox to study virus–host interactions
2017
The KLHL12–Cullin-3 ubiquitin ligase negatively regulates the Wnt–β-catenin pathway by targeting Dishevelled for degradation
2006
A Strategy for O-Glycoproteomics of Enveloped Viruses—the O-Glycoproteome of Herpes Simplex Virus Type 1
2015
Regulation of endoplasmic reticulum turnover by selective autophagy
2015 Nature
Genetic defects in the human glycome
2006
Dmdmdx-βgeo: A new allele for the mouse dystrophin gene
1998
Piezos thrive under pressure: mechanically activated ion channels in health and disease
2017 StandoutNobel
Immunotherapy for Guillain-Barre syndrome: a systematic review
2007
Ubiquitin-dependent regulation of COPII coat size and function
2012 StandoutNatureNobel
Extracellular matrix structure
2015 Standout
Intrinsic Immunity Shapes Viral Resistance of Stem Cells
2017 StandoutNobel
Mammalian Mechanoelectrical Transduction: Structure and Function of Force-Gated Ion Channels
2019
Structure of the mechanically activated ion channel Piezo1
2017 StandoutNatureNobel
Diverse Viruses Require the Calcium Transporter SPCA1 for Maturation and Spread
2017 StandoutNobel
Probing the gating mechanism of the mechanosensitive channel Piezo1 with the small molecule Yoda1
2018
Regulation of LNS Domain Function by Alternative Splicing: The Structure of the Ligand-Binding Domain of Neurexin Iβ
1999 StandoutNobel
Extracellular Matrix: Functions in the Nervous System
2010
Intravenous immunoglobulin in the treatment of autoimmune neuromuscular diseases: Present status and practical therapeutic guidelines
1999
Genome-Scale Identification of SARS-CoV-2 and Pan-coronavirus Host Factor Networks
2020 StandoutNobel
Autophagy is defective in collagen VI muscular dystrophies, and its reactivation rescues myofiber degeneration
2010
Transcriptional co-activator PGC-1α drives the formation of slow-twitch muscle fibres
2002 StandoutNature
Receptor-mediated selective autophagy degrades the endoplasmic reticulum and the nucleus
2015 StandoutNatureNobel
PIEZO2 in sensory neurons and urothelial cells coordinates urination
2020 StandoutNatureNobel
Agrin Is a High-affinity Binding Protein of Dystroglycan in Non-muscle Tissue
1998
Muscular dystrophies: genes to pathogenesis
2003
BTBD1 and BTBD2 colocalize to cytoplasmic bodies with the RBCC/tripartite motif protein, TRIM5δ
2003
Disease mutations in CMP-sialic acid transporter SLC35A1 result in abnormal -dystroglycan O-mannosylation, independent from sialic acid
2014
Dyssegmental dysplasia, Silverman-Handmaker type, is caused by functional null mutations of the perlecan gene
2001
Protein Sequence Editing of SKN-1A/Nrf1 by Peptide:N-Glycanase Controls Proteasome Gene Expression
2019 StandoutNobel
TMEM41B Is a Pan-flavivirus Host Factor
2020 StandoutNobel
The BTB protein MEL-26 is a substrate-specific adaptor of the CUL-3 ubiquitin-ligase
2003 Nature
Structural Basis of Defects in the Sacsin HEPN Domain Responsible for Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay (ARSACS)
2011
Small RNAs are modified with N-glycans and displayed on the surface of living cells
2021 StandoutNobel
α-Neurexins couple Ca2+ channels to synaptic vesicle exocytosis
2003 StandoutNatureNobel
Genome-wide detection and characterization of positive selection in human populations
2007 StandoutNature
Human disorders of cortical development: from past to present
2006
Mitochondrial Dynamics in Diabetes
2010
A Genetic Approach to Mammalian Glycan Function
2003
Haploid Genetic Screen Reveals a Profound and Direct Dependence on Cholesterol for Hantavirus Membrane Fusion
2015
In Vivo Imaging of Membrane-Associated Glycans in Developing Zebrafish
2008 StandoutScienceNobel
Lassa virus entry requires a trigger-induced receptor switch
2014 Science
An α-syntrophin-dependent pool of AQP4 in astroglial end-feet confers bidirectional water flow between blood and brain
2003 StandoutNobel
Muscular Dystrophies—Diseases of the Dystrophin-Glycoprotein Complex
1995 Science
Intravenous immunoglobulin for Guillain-Barré syndrome
2014
B4GAT1 is the priming enzyme for the LARGE-dependent functional glycosylation of α-dystroglycan
2014
Intravenously Administered Immunoglobulin in the Treatment of Childhood Guillain-Barre Syndrome: A Randomized Trial
2005
New concepts in basement membrane biology
2015
Sialic Acid Glycoengineering Using an Unnatural Sialic Acid for the Detection of Sialoglycan Biosynthesis Defects and On-Cell Synthesis of Siglec Ligands
2015
A Haploid Genetic Screen Identifies Heparan Sulfate Proteoglycans Supporting Rift Valley Fever Virus Infection
2015
Mechanisms of action of IVIg and therapeutic considerations in the treatment of acute and chronic demyelinating neuropathies
2002
Mitochondrial Fission, Fusion, and Stress
2012 StandoutScience
Calcium Ion in Skeletal Muscle: Its Crucial Role for Muscle Function, Plasticity, and Disease
2000
Exploring and Engineering the Cell Surface Interface
2005 StandoutScience
Hunting Viral Receptors Using Haploid Cells
2015
Human TKTL1 implies greater neurogenesis in frontal neocortex of modern humans than Neanderthals
2022 StandoutScienceNobel
Role of Glycosylation in Development
2004
Aspm specifically maintains symmetric proliferative divisions of neuroepithelial cells
2006 StandoutNobel
Posttranslational Modification of α-Dystroglycan, the Cellular Receptor for Arenaviruses, by the Glycosyltransferase LARGE Is Critical for Virus Binding
2005
Mechanically activated ion channel PIEZO1 is required for lymphatic valve formation
2018 StandoutNobel
Mining the O-mannose glycoproteome reveals cadherins as major O-mannosylated glycoproteins
2013
Imaging the glycome
2008 StandoutNobel
Syntrophin-dependent expression and localization of Aquaporin-4 water channel protein
2001 StandoutNobel
Specific ablation of the nidogen-binding site in the laminin γ1 chain interferes with kidney and lung development
2002
Neurological Aspects of Human Glycosylation Disorders
2015
Transcriptomes of germinal zones of human and mouse fetal neocortex suggest a role of extracellular matrix in progenitor self-renewal
2012 StandoutNobel
Delayed onset of brain edema and mislocalization of aquaporin-4 in dystrophin-null transgenic mice
2002 StandoutNobel
PIEZO2 mediates injury-induced tactile pain in mice and humans
2018
Structure and Function of Basement Membranes
2007
Mechanisms in Protein O-Glycan Biosynthesis and Clinical and Molecular Aspects of Protein O-Glycan Biosynthesis Defects: A Review
2006
E3 ubiquitin ligase Mindbomb 1 facilitates nuclear delivery of adenovirus genomes
2020 StandoutNobel
Accurate proteome-wide missense variant effect prediction with AlphaMissense
2023 StandoutScienceNobel
Genetic Dissection of the Host Tropism of Human-Tropic Pathogens
2015
Chemical Glycoproteomics
2016 StandoutNobel
The glucuronyltransferase B4GAT1 is required for initiation of LARGE-mediated α-dystroglycan functional glycosylation
2014
Works of Haluk Topaloğlu being referenced
Bethlem myopathy (BETHLEM) and Ullrich scleroatonic muscular dystrophy: 100th ENMC International Workshop, 23–24 November 2001, Naarden, The Netherlands
2002
The human CDC42 gene: genomic organization, evidence for the existence of a putative pseudogene and exclusion as a SJS1 candidate gene
1999
Mutations in FAM134B, encoding a newly identified Golgi protein, cause severe sensory and autonomic neuropathy
2009
Muscular Dystrophy and Neuronal Migration Disorder Caused by Mutations in a Glycosyltransferase, POMGnT1
2001
Private SACS mutations in autosomal recessive spastic ataxia of Charlevoix-Saguenay (ARSACS) families from Turkey
2004
Perlecan, the major proteoglycan of basement membranes, is altered in patients with Schwartz-Jampel syndrome (chondrodystrophic myotonia)
2000
A Dystroglycan Mutation Associated with Limb-Girdle Muscular Dystrophy
2011
A novel form of recessive limb girdle muscular dystrophy with mental retardation and abnormal expression of α-dystroglycan
2003
Deficiency of α-Dystroglycan in Muscle–Eye–Brain Disease
2002
Spectrum of Brain Changes in Patients With Congenital Muscular Dystrophy and FKRP Gene Mutations
2006
Recessive PIEZO2 stop mutation causes distal arthrogryposis with distal muscle weakness, scoliosis and proprioception defects
2016
Mutations in the laminin α2–chain gene (LAMA2) cause merosin–deficient congenital muscular dystrophy
1995
Enzymatic diagnostic test for Muscle-Eye-Brain type congenital muscular dystrophy using commercially available reagents
2003
Mutations in SEPN1 cause congenital muscular dystrophy with spinal rigidity and restrictive respiratory syndrome
2001
An autosomal recessive limb girdle muscular dystrophy (LGMD2) with mild mental retardation is allelic to Walker–Warburg syndrome (WWS) caused by a mutation in the POMT1 gene
2005
The gene encoding gigaxonin, a new member of the cytoskeletal BTB/kelch repeat family, is mutated in giant axonal neuropathy
2000
FKRP gene mutations cause congenital muscular dystrophy, mental retardation, and cerebellar cysts
2003
Intravenous immunoglobulin treatment in children with Guillain-Barré syndrome
1997
A homozygous nonsense mutation in the Fukutin gene causes a Walker-Warburg syndrome phenotype
2003
Mutations in GDAP1
2002
Readjusting the localization of merosin (laminin alpha 2-chain) deficient congenital muscular dystrophy locus on chromosome 6q2.
1995
Clinical and genetic distinction between Walker–Warburg syndrome and muscle–eye–brain disease
2001
Deciphering the Glycosylome of Dystroglycanopathies Using Haploid Screens for Lassa Virus Entry
2013 Science