Citation Impact
Citing Papers
Human cerebral organoids recapitulate gene expression programs of fetal neocortex development
2015 StandoutNobel
Potential etiologic and functional implications of genome-wide association loci for human diseases and traits
2009 Standout
Association of Trypanolytic ApoL1 Variants with Kidney Disease in African Americans
2010 StandoutScience
Microcephalin , a Gene Regulating Brain Size, Continues to Evolve Adaptively in Humans
2005 Science
Human-specific gene ARHGAP11B promotes basal progenitor amplification and neocortex expansion
2015 StandoutScienceNobel
Cerebral cortex expansion and folding: what have we learned?
2016
The Abnormal Spindle-like, Microcephaly-associated (ASPM) Gene Encodes a Centrosomal Protein
2005
The Gene Ontology of eukaryotic cilia and flagella
2017
Ror2 signaling regulates Golgi structure and transport through IFT20 for tumor invasiveness
2017 Standout
Superresolution Pattern Recognition Reveals the Architectural Map of the Ciliary Transition Zone
2015
Small molecule inhibitors of Smoothened ciliary localization and ciliogenesis
2012
Sas-4 provides a scaffold for cytoplasmic complexes and tethers them in a centrosome
2011
Engineering precision nanoparticles for drug delivery
2020 Standout
The Gene Ontology Resource: 20 years and still GOing strong
2018 Standout
Hedgehog: functions and mechanisms
2008 Standout
The mechanisms of Hedgehog signalling and its roles in development and disease
2013 Standout
The microcephaly ASPM gene is expressed in proliferating tissues and encodes for a mitotic spindle protein
2005
Regulation and function of the cGAS–STING pathway of cytosolic DNA sensing
2016 Standout
MKS1, encoding a component of the flagellar apparatus basal body proteome, is mutated in Meckel syndrome
2006
STED Microscopy with Optimized Labeling Density Reveals 9-Fold Arrangement of a Centriole Protein
2012 StandoutNobel
The microenvironment of the embryonic neural stem cell: Lessons from adult niches?
2007
CDK5RAP2 Regulates Centriole Engagement and Cohesion in Mice
2010
ALFY-Controlled DVL3 Autophagy Regulates Wnt Signaling, Determining Human Brain Size
2016
Cdk5rap2 exposes the centrosomal root of microcephaly syndromes
2011
Mammalian phosphoinositide kinases and phosphatases
2009 StandoutNobel
What primary microcephaly can tell us about brain growth
2006
Spindle orientation in mammalian cerebral cortical development
2012
Compound heterozygous ASPM mutations associated with microcephaly and simplified cortical gyration in a consanguineous Algerian family
2009
Organoid Models and Applications in Biomedical Research
2015 Standout
Super-resolution microscopy demystified
2018 Standout
Footprints of selection in the ancestral admixture of a New World Creole cattle breed
2011 Standout
Flies without Centrioles
2006
Polycystic kidney disease
2018
Growth and folding of the mammalian cerebral cortex: from molecules to malformations
2014
The molecular landscape of ASPM mutations in primary microcephaly
2008
Insulinoma-Associated 1 Has a Panneurogenic Role and Promotes the Generation and Expansion of Basal Progenitors in the Developing Mouse Neocortex
2008 StandoutNobel
Autosomal Recessive Primary Microcephaly (MCPH): A Review of Clinical, Molecular, and Evolutionary Findings
2005
Biological Functions of Autophagy Genes: A Disease Perspective
2019 Standout
Genetic Changes Shaping the Human Brain
2015
Aberrant splicing is a common mutational mechanism inMKS1, a key player in Meckel-Gruber syndrome
2007
CEP162 is an axoneme-recognition protein promoting ciliary transition zone assembly at the cilia base
2013
Kinetochore KMN network gene CASC5 mutated in primary microcephaly
2012
Human Splicing Finder: an online bioinformatics tool to predict splicing signals
2009 Standout
Novel CENPJ mutation causes Seckel syndrome
2010
Microfluidic organs-on-chips
2014 Standout
Unraveling the therapeutic potential of the Hedgehog pathway in cancer
2013 Standout
Leber congenital amaurosis: Genes, proteins and disease mechanisms
2008 Standout
Mutations in STIL, Encoding a Pericentriolar and Centrosomal Protein, Cause Primary Microcephaly
2009
NOVEL PROTEIN-TRUNCATING MUTATIONS IN THEASPMGENE IN FAMILIES WITH AUTOSOMAL RECESSIVE PRIMARY MICROCEPHALY
2007
Transmembrane Pickets Connect Cyto- and Pericellular Skeletons Forming Barriers to Receptor Engagement
2018 StandoutNobel
Asymmetric centrosome inheritance maintains neural progenitors in the neocortex
2009 Nature
Fluorescence nanoscopy in cell biology
2017 StandoutNobel
Classic Selective Sweeps Revealed by Massive Sequencing in Cattle
2014 Standout
Stages of ciliogenesis and regulation of ciliary length
2011
A Smoothened-Evc2 Complex Transduces the Hedgehog Signal at Primary Cilia
2012
A ciliopathy complex at the transition zone protects the cilia as a privileged membrane domain
2011
A Map of Recent Positive Selection in the Human Genome
2006 Standout
Symmetric versus asymmetric cell division during neurogenesis in the developing vertebrate central nervous system
2005
Cerebral organoids model human brain development and microcephaly
2013 StandoutNature
Haploinsufficiency of DNA Damage Response Genes and their Potential Influence in Human Genomic Disorders
2008
Genomic instability — an evolving hallmark of cancer
2010 Standout
A novel nonsense CDK5RAP2 mutation in a Somali child with primary microcephaly and sensorineural hearing loss
2012
How culture shaped the human genome: bringing genetics and the human sciences together
2010 Standout
Trafficking in and to the primary cilium
2012
A primary microcephaly protein complex forms a ring around parental centrioles
2011
The Human Condition—A Molecular Approach
2014 StandoutNobel
Cytoskeletal genes regulating brain size
2005
Centrioles, Centrosomes, and Cilia in Health and Disease
2009
Acute Versus Chronic Loss of Mammalian Azi1/Cep131 Results in Distinct Ciliary Phenotypes
2013
Evolution of primate gene expression
2006 StandoutNobel
The Genetics of Human Adaptation: Hard Sweeps, Soft Sweeps, and Polygenic Adaptation
2010 Standout
The primary cilium: a signalling centre during vertebrate development
2010 Standout
Development and Evolution of the Human Neocortex
2011
A Wnt/beta-Catenin Pathway Antagonist Chibby Binds Cenexin at the Distal End of Mother Centrioles and Functions in Primary Cilia Formation
2012
Organoid single-cell genomic atlas uncovers human-specific features of brain development
2019 StandoutNatureNobel
Modeling Development and Disease with Organoids
2016 Standout
Genome-wide detection and characterization of positive selection in human populations
2007 StandoutNature
Human disorders of cortical development: from past to present
2006
Mutations of the CEP290 gene encoding a centrosomal protein cause Meckel-Gruber syndrome
2007
Making bigger brains–the evolution of neural-progenitor-cell division
2008
Modulation of the cGAS-STING DNA sensing pathway by gammaherpesviruses
2015
Chronic Kidney Disease Diagnosis and Management
2019 Standout
Casein kinase 1δ functions at the centrosome and Golgi to promote ciliogenesis
2014
The Genetics of Primary Microcephaly
2018
A Genome-Scan Method to Identify Selected Loci Appropriate for Both Dominant and Codominant Markers: A Bayesian Perspective
2008 Standout
The Cell Biology of Neurogenesis: Toward an Understanding of the Development and Evolution of the Neocortex
2014
The Rilp-like proteins Rilpl1 and Rilpl2 regulate ciliary membrane content
2012
Longer metaphase and fewer chromosome segregation errors in modern human than Neanderthal brain development
2022 StandoutNobel
Organogenesis in a dish: Modeling development and disease using organoid technologies
2014 StandoutScience
Cdk5rap2 regulates centrosome function and chromosome segregation in neuronal progenitors
2010
Human TKTL1 implies greater neurogenesis in frontal neocortex of modern humans than Neanderthals
2022 StandoutScienceNobel
The Joint Allele-Frequency Spectrum in Closely Related Species
2007 StandoutNobel
Aspm specifically maintains symmetric proliferative divisions of neuroepithelial cells
2006 StandoutNobel
A novel domain suggests a ciliary function for ASPM, a brain size determining gene
2006
Cby1 promotes Ahi1 recruitment to a ring-shaped domain at the centriole–cilium interface and facilitates proper cilium formation and function
2014 StandoutNobel
A molecular mechanism of mitotic centrosome assembly in Drosophila
2014
Mutations in mouse Aspm (abnormal spindle-like microcephaly associated) cause not only microcephaly but also major defects in the germline
2010 StandoutNobel
Barriers to the free diffusion of proteins and lipids in the plasma membrane
2015
A Localized Wnt Signal Orients Asymmetric Stem Cell Division in Vitro
2013 StandoutScienceNobel
A single splice site mutation in human-specific ARHGAP11B causes basal progenitor amplification
2016 StandoutNobel
Transcriptomes of germinal zones of human and mouse fetal neocortex suggest a role of extracellular matrix in progenitor self-renewal
2012 StandoutNobel
ASPM and Citron Kinase Co-Localize to the Midbody Ring during Cytokinesis
2007
Differences and similarities between human and chimpanzee neural progenitors during cerebral cortex development
2016 StandoutNobel
The base of the cilium: roles for transition fibres and the transition zone in ciliary formation, maintenance and compartmentalization
2012
Works of Christopher Bennett being referenced
A novel locus for Meckel-Gruber syndrome, MKS3 , maps to chromosome 8q24
2002
A transition zone complex regulates mammalian ciliogenesis and ciliary membrane composition
2011
Human ASPM participates in spindle organisation, spindle orientation and cytokinesis
2010
A centrosomal mechanism involving CDK5RAP2 and CENPJ controls brain size
2005
The Viral Interferon Regulatory Factors of Kaposi's Sarcoma-Associated Herpesvirus Differ in Their Inhibition of Interferon Activation Mediated by Toll-Like Receptor 3
2012