Citation Impact
Citing Papers
Argonaute2 Is the Catalytic Engine of Mammalian RNAi
2004 StandoutScience
Widespread Parallel Evolution in Sticklebacks by Repeated Fixation of Ectodysplasin Alleles
2005 StandoutScience
Suppression of Aging in Mice by the Hormone Klotho
2005 StandoutScience
Rapid Identification of a Disease Allele in Mouse Through Whole Genome Sequencing and Bulk Segregation Analysis
2010 StandoutNobel
The 22q11.2 Deletion Syndrome
2001
A GATA-dependent right ventricular enhancer controls dHAND transcription in the developing heart
2000
Cell mechanics and the cytoskeleton
2010 StandoutNature
Relationship between asymmetric nodal expression and the direction of embryonic turning
1996 Nature
Common fragile sites
2003
Radiation hybrid map spanning the huntington disease gene region of chromosome 4
1992
Growth Hormone Treatment of Non–Growth Hormone-Deficient Growth Disorders
2007
Maintenance of functional equivalence during paralogous Hox gene evolution
2000 StandoutNatureNobel
Natural engineering principles of electron tunnelling in biological oxidation–reduction
1999 StandoutNature
Telomerase Mutations in Families with Idiopathic Pulmonary Fibrosis
2007 StandoutNobel
Epithelial-Mesenchymal Transitions in Development and Disease
2009 Standout
extradenticle, a regulator of homeotic gene activity, is a homolog of the homeobox-containing human proto-oncogene pbx1
1993 StandoutNobel
Functional Characterization of the Human Interleukin-15 Receptor αChain and Close Linkage of IL15RA and IL2RA Genes
1995
Campomelic dysplasia and autosomal sex reversal caused by mutations in an SRY-related gene
1994 StandoutNature
Hedgehog signalling in the mouse requires intraflagellar transport proteins
2003 StandoutNature
Mendelian cytogenetics. Chromosome rearrangements associated with mendelian disorders.
1993
Association of klotho gene polymorphism with bone density and spondylosis of the lumbar spine in postmenopausal women
2002
Chromosome Break-Induced DNA Replication Leads to Nonreciprocal Translocations and Telomere Capture
1998
Regional mapping panel for human chromosome 17: Application to neurofibromatosis type 1
1987
Morphogenesis of the murine node and notochordal plate
1994
Molecular Mechanism of Liver Development and Regeneration
2007
Sinistral Snails and Gentlemen Scientists
2005 StandoutNobel
When Checkpoints Fail
1997 StandoutNobel
Full-term development of mice from enucleated oocytes injected with cumulus cell nuclei
1998 StandoutNature
Vertebrate Smoothened functions at the primary cilium
2005 StandoutNature
Telomere Dysfunction Increases Mutation Rate and Genomic Instability
2001 StandoutNobel
Mammalian karyotype evolution
2007
Left–right asymmetry in embryonic development: a comprehensive review
2004
Short Telomeres, even in the Presence of Telomerase, Limit Tissue Renewal Capacity
2005 StandoutNobel
What cardiovascular defect does my prenatal mouse mutant have, and why?
2002
Deoxyribonucleoside triphosphate levels: A critical factor in the maintenance of genetic stability
1994
A gene expression atlas of the central nervous system based on bacterial artificial chromosomes
2003 StandoutNature
Osteoclast differentiation and activation
2003 StandoutNature
Dyskeratosis congenita in all its forms
2000
Centriole Age Underlies Asynchronous Primary Cilium Growth in Mammalian Cells
2009
Developmental defects of the ear, cranial nerves and hindbrain resulting from targeted disruption of the mouse homeobox geneHox-#150;1.6
1992 StandoutNatureNobel
Involvement of a novel Tnf receptor homologue in hair follicle induction
1999
An integrated metric physical map of human chromosome 19
1995
GATA4 mutations cause human congenital heart defects and reveal an interaction with TBX5
2003 StandoutNature
Mice with targeted disruptions in the paralogous genes hoxa-3 and hoxd-3 reveal synergistic interactions
1994 StandoutNatureNobel
Activation of the DNA damage checkpoint and genomic instability in human precancerous lesions
2005 StandoutNature
Are Complex Behaviors Specified by Dedicated Regulatory Genes? Reasoning from Drosophila
2001 StandoutNobel
Ectodysplasin-A1 is sufficient to rescue both hair growth and sweat glands in Tabby mice
2001
The consequences of chromosome imbalance
2005
Dyskeratosis congenita: its link to telomerase and aplastic anaemia
2003
Mouse gastrulation: the formation of a mammalian body plan
1997
Localization of transcription factor GATA-4 to regions of the mouse embryo involved in cardiac development
1994
A homologue of the TNF receptor and its ligand enhance T-cell growth and dendritic-cell function
1997 StandoutNature
A molecular pathway determining left-right asymmetry in chick embryogenesis
1995
Notch3 mutations in CADASIL, a hereditary adult-onset condition causing stroke and dementia
1996 StandoutNature
Regionally restricted developmental defects resulting from targeted disruption of the mouse homeobox gene hox-1.5
1991 Nature
Eomesodermin is required for mouse trophoblast development and mesoderm formation
2000 StandoutNatureNobel
Crystal structure of photosystem II from Synechococcus elongatus at 3.8 Å resolution
2001 StandoutNature
A mutation of Ikbkg causes immune deficiency without impairing degradation of IκBα
2010 StandoutNobel
THE GREEN FLUORESCENT PROTEIN
1998 StandoutNobel
The left-right determinant Inversin is a component of node monocilia and other 9+0 cilia
2003
De novo assembly of the Aedes aegypti genome using Hi-C yields chromosome-length scaffolds
2017 StandoutScience
Patched1 Regulates Hedgehog Signaling at the Primary Cilium
2007 StandoutScience
SQV-7, a protein involved in Caenorhabditis elegans epithelial invagination and early embryogenesis, transports UDP-glucuronic acid, UDP- N - acetylgalactosamine, and UDP-galactose
2001 StandoutNobel
The Primary Cilium as the Cell's Antenna: Signaling at a Sensory Organelle
2006 Science
Mechanism of Cis-Dihydroxylation and Epoxidation of Alkenes by Highly H2O2 Efficient Dinuclear Manganese Catalysts
2007 StandoutNobel
G Protein-Coupled Receptors: Functional and Mechanistic Insights Through Altered Gene Expression
1998 StandoutNobel
A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosomes
1993 Standout
Clusters of Master Control Genes Regulate the Development of Higher Organisms
1992 StandoutNobel
Piezo1, a mechanically activated ion channel, is required for vascular development in mice
2014 StandoutNobel
Manganese Cluster in Photosynthesis: Where Plants Oxidize Water to Dioxygen
1996
A novel domain suggests a ciliary function for ASPM, a brain size determining gene
2006
Molecular detection of microscopic and submicroscopic deletions associated with Miller-Dieker syndrome.
1988
Type 1 Neurofibromatosis Gene: Identification of a Large Transcript Disrupted in Three NF1 Patients
1990 StandoutScience
Mutations in mouse Aspm (abnormal spindle-like microcephaly associated) cause not only microcephaly but also major defects in the germline
2010 StandoutNobel
Complex asparagine-linked oligosaccharides are required for morphogenic events during post-implantation development.
1994
Genetic Control of Branching Morphogenesis
1999 Science
Protein Radicals in Enzyme Catalysis
1998 Standout
MATRIX PROTEOGLYCANS: From Molecular Design to Cellular Function
1998 Standout
Protein Glycoengineering Enabled by the Versatile Synthesis of Aminooxy Glycans and the Genetically Encoded Aldehyde Tag
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
Mouse models of abnormal skeletal development and homeostasis
2001
The Oak Ridge Polycystic Kidney (orpk) disease gene is required for left-right axis determination
2000
THE UBIQUITIN SYSTEM
1998 StandoutNobel
Regulation of Rate of Cartilage Differentiation by Indian Hedgehog and PTH-Related Protein
1996 StandoutScience
Chromosome 17 Deletions and p53 Gene Mutations in Colorectal Carcinomas
1989 StandoutScience
Recombination signal sequence-binding protein Jκ alters mesodermal cell fate decisions by suppressing cardiomyogenesis
2003 StandoutNobel
Works of F.F.B. Elder being referenced
Insertional Mutation of the Collagen Genes Col4a3 and Col4a4 in a Mouse Model of Alport Syndrome
1999
Characterization of Human DSPG3, a Small Dermatan Sulfate Proteoglycan
1996
Genetic mapping of an insertional hydrocephalus-inducing mutation allelic to hy3
2002
Multiple common fragile sites are expressed in the genome of the laboratory rat
1987
Abnormality of platelet size and T‐lymphocyte proliferation in an autosomal recessive form of dyskeratosis congenita
1987
Rodent common fragile sites: Are they conserved? Evidence from mouse and rat
1989
Mutations in exon 17B of cartilage oligomeric matrix protein (COMP) cause pseudoachondroplasia
1995
YAC rescue of downless locus mutations in mice
1998
Inversin, a novel gene in the vertebrate left-right axis pathway, is partially deleted in the inv mouse
1998
The Phenotype of Short Stature Homeobox Gene (SHOX) Deficiency in Childhood: Contrasting Children with Leri-Weill Dyschondrosteosis and Turner Syndrome
2005
Chromosome painting among Proboscidea, Hyracoidea and Sirenia: support for Paenungulata (Afrotheria, Mammalia) but not Tethytheria
2007
Familial Miller‐Dieker syndrome associated with pericentric inversion of chromosome 17
1986
Cytogenetic findings in a prospective series of patients with DiGeorge anomaly.
1988
Molecular confirmation of Wolf-Hirschhorn syndrome with a subtle translocation of chromosome 4.
1991
Reversal of Left-Right Asymmetry: a Situs Inversus Mutation
1993 Science
Identical twins with deletion 16q syndrome: Evidence that 16q12.2-q13 is the critical band region
1984
Unbalanced translocation (15;17)(q13;p13.3) with apparent Prader‐Willi syndrome but without Miller‐Dieker syndrome
1985