Citation Impact
Citing Papers
A Decade of Molecular Studies of Fragile X Syndrome
2002
Genetic Evidence for High-Altitude Adaptation in Tibet
2010 Science
Argonaute2 Is the Catalytic Engine of Mammalian RNAi
2004 StandoutScience
Genomic Variation in Seven Khoe-San Groups Reveals Adaptation and Complex African History
2012 Science
Hunter-gatherer genomic diversity suggests a southern African origin for modern humans
2011
Association of Trypanolytic ApoL1 Variants with Kidney Disease in African Americans
2010 StandoutScience
A genomic region associated with protection against severe COVID-19 is inherited from Neandertals
2021 StandoutNobel
A drug-controllable tag for visualizing newly synthesized proteins in cells and whole animals
2008 StandoutNobel
Origins and Genetic Legacy of Neolithic Farmers and Hunter-Gatherers in Europe
2012 Science
The UK Biobank resource with deep phenotyping and genomic data
2018 StandoutNature
A Novel Function for Fragile X Mental Retardation Protein in Translational Activation
2009
A Distinct FMRP Polysomal Population at an Advanced Stage of Mammalian Erythropoiesis
2000
Fragile X Mental Retardation Protein Targets G Quartet mRNAs Important for Neuronal Function
2001
FMRP targets distinct mRNA sequence elements to regulate protein expression
2012 Nature
Kissing complex RNAs mediate interaction between the Fragile-X mental retardation protein KH2 domain and brain polyribosomes
2005
Dynamic Translational and Proteasomal Regulation of Fragile X Mental Retardation Protein Controls mGluR-Dependent Long-Term Depression
2006
A Mouse Model of the Human Fragile X Syndrome I304N Mutation
2009
Biochemical evidence for the association of fragile X mental retardation protein with brain polyribosomal ribonucleoparticles
2004
The fragile X mental retardation protein inhibits translation via interacting with mRNA
2001
Fragile X Syndrome: Loss of Local mRNA Regulation Alters Synaptic Development and Function
2008
Phosphorylation influences the translation state of FMRP-associated polyribosomes
2003
Discrimination of common and unique RNA-binding activities among Fragile X mental retardation protein paralogs
2009
FMRP RNA targets: identification and validation
2005
Dysregulated Metabotropic Glutamate Receptor-Dependent Translation of AMPA Receptor and Postsynaptic Density-95 mRNAs at Synapses in a Mouse Model of Fragile X Syndrome
2007
An integrated map of genetic variation from 1,092 human genomes
2012 StandoutNature
Evidence that fragile X mental retardation protein is a negative regulator of translation
2001
Microarray Identification of FMRP-Associated Brain mRNAs and Altered mRNA Translational Profiles in Fragile X Syndrome
2001
Hypoxia-Inducible Factors in Physiology and Medicine
2012 StandoutNobel
Ancient Fennoscandian genomes reveal origin and spread of Siberian ancestry in Europe
2018 StandoutNobel
Fragile X Mental Retardation Protein Is Associated with Translating Polyribosomes in Neuronal Cells
2004
Ionotropic Glutamate Receptors & CNS Disorders
2008
Ribosome Profiling of Mouse Embryonic Stem Cells Reveals the Complexity and Dynamics of Mammalian Proteomes
2011 Standout
An Expanded View of Complex Traits: From Polygenic to Omnigenic
2017 Standout
Genetic Variation and Recent Positive Selection in Worldwide Human Populations: Evidence from Nearly 1 Million SNPs
2009
Control of somatic tissue differentiation by the long non-coding RNA TINCR
2012 StandoutNature
The mGluR theory of fragile X mental retardation
2004
Initiation of translation in prokaryotes and eukaryotes
1999
Common Variants in the Trichohyalin Gene Are Associated with Straight Hair in Europeans
2009
MicroRNAs
2004 Standout
Channel opening and gating mechanism in AMPA-subtype glutamate receptors
2017 StandoutNatureNobel
Concurrent versus individual binding of HuR and AUF1 to common labile target mRNAs
2004
A Haplotype at STAT2 Introgressed from Neanderthals and Serves as a Candidate of Positive Selection in Papua New Guinea
2012
The genomic landscape of Neanderthal ancestry in present-day humans
2014 StandoutNatureNobel
Genomic Signatures of Selective Pressures and Introgression from Archaic Hominins at Human Innate Immunity Genes
2016
Identification of mRNA/Protein (mRNP) Complexes Containing Purα, mStaufen, Fragile X Protein, and Myosin Va and their Association with Rough Endoplasmic Reticulum Equipped with a Kinesin Motor
2002
Neandertal Origin of Genetic Variation at the Cluster of OAS Immunity Genes
2013
Genetic Adaptation of Fatty-Acid Metabolism: A Human-Specific Haplotype Increasing the Biosynthesis of Long-Chain Omega-3 and Omega-6 Fatty Acids
2012
Inference of Population Structure using Dense Haplotype Data
2012
RNAi
2000 Standout
TRIBE: Hijacking an RNA-Editing Enzyme to Identify Cell-Specific Targets of RNA-Binding Proteins
2016 StandoutNobel
DNA methylation in health and disease
2000
Natural selection and infectious disease in human populations
2014
Asymmetry in the Assembly of the RNAi Enzyme Complex
2003 Standout
The multilayered complexity of ceRNA crosstalk and competition
2014 StandoutNature
Spatial patterns of variation due to natural selection in humans
2009
Multistep process of FUS aggregation in the cell cytoplasm involves RNA-dependent and RNA-independent mechanisms
2014
Identifying Recent Adaptations in Large-Scale Genomic Data
2013
FMRP Stalls Ribosomal Translocation on mRNAs Linked to Synaptic Function and Autism
2011 Standout
Super-Enhancers in the Control of Cell Identity and Disease
2013 Standout
Interaction of Staufen1 with the 5' end of mRNA facilitates translation of these RNAs
2005
Genetics of human prefrontal function
2003
The Genetic Architecture of Adaptations to High Altitude in Ethiopia
2012
The “All of Us” Research Program
2019 Standout
Fast Principal-Component Analysis Reveals Convergent Evolution of ADH1B in Europe and East Asia
2016
Drosophila Fragile X-Related Gene Regulates the MAP1B Homolog Futsch to Control Synaptic Structure and Function
2001
Genetic Misdiagnoses and the Potential for Health Disparities
2016
Neuroligin-1 Deletion Results in Impaired Spatial Memory and Increased Repetitive Behavior
2010 StandoutNobel
Processing of primary microRNAs by the Microprocessor complex
2004 StandoutNature
The fragile X mental retardation protein binds specifically to its mRNA via a purine quartet motif
2001
Insights into RNA Biology from an Atlas of Mammalian mRNA-Binding Proteins
2012 Standout
Visual Experience Regulates Transient Expression and Dendritic Localization of Fragile X Mental Retardation Protein
2004
Fragile X-related protein and VIG associate with the RNA interference machinery
2002
Stem Cell-derived Neural Stem/Progenitor Cell Supporting Factor Is an Autocrine/Paracrine Survival Factor for Adult Neural Stem/Progenitor Cells
2003 StandoutNobel
RNA-binding proteins in human genetic disease
2020
Identifying Signatures of Natural Selection in Tibetan and Andean Populations Using Dense Genome Scan Data
2010
A Liquid-to-Solid Phase Transition of the ALS Protein FUS Accelerated by Disease Mutation
2015 Standout
Worldwide Distribution of the MYH9 Kidney Disease Susceptibility Alleles and Haplotypes: Evidence of Historical Selection in Africa
2010
A phenotypic and molecular characterization of the fmr1‐tm1Cgr Fragile X mouse
2004
The Role of Geography in Human Adaptation
2009
Ethiopian Genetic Diversity Reveals Linguistic Stratification and Complex Influences on the Ethiopian Gene Pool
2012
Oxygen Sensing, Homeostasis, and Disease
2011 StandoutNobel
How culture shaped the human genome: bringing genetics and the human sciences together
2010 Standout
Structural Bases of Desensitization in AMPA Receptor-Auxiliary Subunit Complexes
2017 StandoutNobel
Evolutionary History and Adaptation from High-Coverage Whole-Genome Sequences of Diverse African Hunter-Gatherers
2012
The Light Skin Allele of SLC24A5 in South Asians and Europeans Shares Identity by Descent
2013
Transcriptome-wide Identification of RNA-Binding Protein and MicroRNA Target Sites by PAR-CLIP
2010 Standout
Mechanisms of gene silencing by double-stranded RNA
2004 StandoutNature
Signals, synapses, and synthesis: how new proteins control plasticity
2009
The Human Condition—A Molecular Approach
2014 StandoutNobel
Structure and function of KH domains
2008
The Genetics of Human Adaptation: Hard Sweeps, Soft Sweeps, and Polygenic Adaptation
2010 Standout
Hepatitis C Virus RNA Functionally Sequesters miR-122
2015 StandoutNobel
Detecting Natural Selection in Genomic Data
2013
Ancient Ethiopian genome reveals extensive Eurasian admixture in Eastern Africa
2015 StandoutScience
Neanderthal ancestry drives evolution of lipid catabolism in contemporary Europeans
2014 StandoutNobel
Clinical iron deficiency disturbs normal human responses to hypoxia
2016 StandoutNobel
Separating endogenous ancient DNA from modern day contamination in a Siberian Neandertal
2014 StandoutNobel
Identification of DNA cleavage- and recombination-specific hnRNP cofactors for activation-induced cytidine deaminase
2015 StandoutNobel
Epigenetic Reprogramming in Mammalian Development
2001 StandoutScience
Excavating Neandertal and Denisovan DNA from the genomes of Melanesian individuals
2016 StandoutScienceNobel
Adaptive and Maladaptive Cardiorespiratory Responses to Continuous and Intermittent Hypoxia Mediated by Hypoxia-Inducible Factors 1 and 2
2012 StandoutNobel
The State of Synapses in Fragile X Syndrome
2009
Pleistocene North African genomes link Near Eastern and sub-Saharan African human populations
2018 StandoutScienceNobel
Genetic legacy of state centralization in the Kuba Kingdom of the Democratic Republic of the Congo
2018 StandoutNobel
Rapid metabolic evolution in human prefrontal cortex
2011 StandoutNobel
Serotonin receptor 1A knockout: An animal model of anxiety-related disorder
1998
Serotonin receptor knockouts: A moody subject
1998 StandoutNobel
Requirement of Hippocampal Neurogenesis for the Behavioral Effects of Antidepressants
2003 StandoutScience
Identification of many microRNAs that copurify with polyribosomes in mammalian neurons
2003 StandoutNobel
Mouse neurexin-1α deletion causes correlated electrophysiological and behavioral changes consistent with cognitive impairments
2009 StandoutNobel
Works of Devin Absher being referenced
Signals of recent positive selection in a worldwide sample of human populations
2009
FMRP Associates with Polyribosomes as an mRNP, and the I304N Mutation of Severe Fragile X Syndrome Abolishes This Association
1997