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
ASPM Is a Novel Marker for Vascular Invasion, Early Recurrence, and Poor Prognosis of Hepatocellular Carcinoma
2008
Cerebral cortex expansion and folding: what have we learned?
2016
The Abnormal Spindle-like, Microcephaly-associated (ASPM) Gene Encodes a Centrosomal Protein
2005
WGCNA: an R package for weighted correlation network analysis
2008 Standout
Sas-4 provides a scaffold for cytoplasmic complexes and tethers them in a centrosome
2011
Microcephaly Syndromes
2007
Hedgehog: functions and mechanisms
2008 Standout
The microcephaly ASPM gene is expressed in proliferating tissues and encodes for a mitotic spindle protein
2005
A Randomized Trial of Prenatal versus Postnatal Repair of Myelomeningocele
2011 Standout
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
Evolution of primary microcephaly genes and the enlargement of primate brains
2005
Forebrain ependymal cells are Notch-dependent and generate neuroblasts and astrocytes after stroke
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
Malignant astrocytic glioma: genetics, biology, and paths to treatment
2007 Standout
Super-resolution microscopy demystified
2018 Standout
Flies without Centrioles
2006
Growth and folding of the mammalian cerebral cortex: from molecules to malformations
2014
Neural-Tube Defects
1999 Standout
Accelerated Evolution of the ASPM Gene Controlling Brain Size Begins Prior to Human Brain Expansion
2004
The molecular landscape of ASPM mutations in primary microcephaly
2008
Axonal Transport: Cargo-Specific Mechanisms of Motility and Regulation
2014
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
ASPM is a major determinant of cerebral cortical size
2002
Human microcephaly
2004
Kinetochore KMN network gene CASC5 mutated in primary microcephaly
2012
The DNA Damage Response: Making It Safe to Play with Knives
2010 Standout
Genetic links between brain development and brain evolution
2005
The cell biology of neurogenesis
2005 Standout
Novel CENPJ mutation causes Seckel syndrome
2010
Microfluidic organs-on-chips
2014 Standout
Nanoparticle-assisted optical tethering of endosomes reveals the cooperative function of dyneins in retrograde axonal transport
2015 StandoutNobel
Metabolic Regulation of Neocortical Expansion in Development and Evolution
2020
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
A Transcriptome Database for Astrocytes, Neurons, and Oligodendrocytes: A New Resource for Understanding Brain Development and Function
2008 Standout
Extension of cortical synaptic development distinguishes humans from chimpanzees and macaques
2012 StandoutNobel
Asymmetric centrosome inheritance maintains neural progenitors in the neocortex
2009 Nature
Alzheimer's Disease
2010 Standout
The mosaic that is our genome
2003 StandoutNatureNobel
A Map of Recent Positive Selection in the Human Genome
2006 Standout
Zika Virus and Birth Defects — Reviewing the Evidence for Causality
2016 Standout
Symmetric versus asymmetric cell division during neurogenesis in the developing vertebrate central nervous system
2005
Identification of Microcephalin, a Protein Implicated in Determining the Size of the Human Brain
2002
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
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
Evolution of primate gene expression
2006 StandoutNobel
The primary cilium: a signalling centre during vertebrate development
2010 Standout
Development and Evolution of the Human Neocortex
2011
Organoid single-cell genomic atlas uncovers human-specific features of brain development
2019 StandoutNatureNobel
Modeling Development and Disease with Organoids
2016 Standout
Molecular genetics of human microcephaly
2001
Genome-wide detection and characterization of positive selection in human populations
2007 StandoutNature
Human disorders of cortical development: from past to present
2006
Ligand-Gated Ion Channels: New Insights into Neurological Disorders and Ligand Recognition
2012
Making bigger brains–the evolution of neural-progenitor-cell division
2008
Expression analysis of the autosomal recessive primary microcephaly genes MCPH1 (microcephalin) and MCPH5 (ASPM, abnormal spindle-like, microcephaly associated) in human malignant gliomas
1994
Letters to the editor
1997
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
Multiple Roles of BRIT1/MCPH1 in DNA Damage Response, DNA Repair, and Cancer Suppression
2010
Analysis of oncogenic signaling networks in glioblastoma identifies ASPM as a molecular target
2006
Topical Review: Cortical Malformation and Pediatric Epilepsy: A Molecular Genetic Approach
2005
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
The Glial Nature of Embryonic and Adult Neural Stem Cells
2009 Standout
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
A Localized Wnt Signal Orients Asymmetric Stem Cell Division in Vitro
2013 StandoutScienceNobel
Emerging Targets in Photopharmacology
2016 StandoutNobel
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
How common are the “common” neurologic disorders?
2007
Works of Peter Corry being referenced
A Third Novel Locus for Primary Autosomal Recessive Microcephaly Maps to Chromosome 9q34
2000
Compound heterozygosity and nonsense mutations in the α1-subunit of the inhibitory glycine receptor in hyperekplexia
2001
Prevalence and type of cerebral palsy in a British ethnic community: the role of consanguinity
1997
Mutation of the Variant α-Tubulin TUBA8 Results in Polymicrogyria with Optic Nerve Hypoplasia
2009
Primary Autosomal Recessive Microcephaly (MCPH1) Maps to Chromosome 8p22-pter
1998
Protein-Truncating Mutations in ASPM Cause Variable Reduction in Brain Size
2003
A centrosomal mechanism involving CDK5RAP2 and CENPJ controls brain size
2005