Citation Impact
Citing Papers
Role of the CLOCK Protein in the Mammalian Circadian Mechanism
1998 StandoutScience
The DNA mismatch repair genes Msh3 and Msh6 cooperate in intestinal tumor suppression.
2000
Mechanisms in Eukaryotic Mismatch Repair
2006 StandoutNobel
Finishing the euchromatic sequence of the human genome
2004 StandoutNature
T-Brain-1: A homolog of Brachyury whose expression defines molecularly distinct domains within the cerebral cortex
1995
A Whole-Genome Radiation Hybrid Map of the Dog Genome
1998
The Ubiquitin Proteasome System in Neurodegenerative Diseases
2003 StandoutNobel
NFAT dysregulation by increased dosage of DSCR1 and DYRK1A on chromosome 21
2006 StandoutNature
Molecular Bases for Circadian Clocks
1999 Standout
Mutation of the novel gene Tmie results in sensory cell defects in the inner ear of spinner, a mouse model of human hearing loss DFNB6
2002
Identification and expression cloning of a leptin receptor, OB-R
1995 Standout
Strand-specific Mismatch Repair in Mammalian Cells
1997 StandoutNobel
A microsatellite genetic linkage map for zebrafish (Danio rerio)
1998
Eomesodermin, a Key Early Gene in Xenopus Mesoderm Differentiation
1996 StandoutNobel
The genomic landscape of Neanderthal ancestry in present-day humans
2014 StandoutNatureNobel
Hyperproinsulinaemia in obese fat/fat mice associated with a carboxypeptidase E mutation which reduces enzyme activity
1995
A Mutant Drosophila Homolog of Mammalian Clock Disrupts Circadian Rhythms and Transcription of period and timeless
1998 StandoutNobel
A comprehensive genetic map of the human genome based on 5,264 microsatellites
1996 StandoutNature
A Complex Genetic Basis to X-Linked Hybrid Male Sterility Between Two Species of House Mice
2008
Interactions of Human Mismatch Repair Proteins MutSα and MutLα with Proteins of the ATR-Chk1 Pathway
2009 StandoutNobel
Chromosomal deletion complexes in mice by radiation of embryonic stem cells
1997
Mutations in a member of the ADAMTS gene family cause thrombotic thrombocytopenic purpura
2001 StandoutNature
Targeted Disruption of the Melanocortin-4 Receptor Results in Obesity in Mice
1997 Standout
Intragenic deletion in the gene encoding ubiquitin carboxy-terminal hydrolase in gad mice
1999
Mechanically Activated Ion Channels
2015 StandoutNobel
Polygenic control of Caenorhabditis elegans fat storage
2006 StandoutNobel
DNA Polymerase δ Is Required for Human Mismatch Repair in Vitro
1997 StandoutNobel
Central nervous system control of food intake
2000 StandoutNature
CCR7 Coordinates the Primary Immune Response by Establishing Functional Microenvironments in Secondary Lymphoid Organs
1999 Standout
A mouse model for Down syndrome exhibits learning and behaviour deficits
1995 Standout
Genome-wide RNAi analysis of Caenorhabditis elegans fat regulatory genes
2003 StandoutNatureNobel
Demographic history and linkage disequilibrium in human populations
1997 StandoutNobel
The tyrosine kinase c-Abl regulates p73 in apoptotic response to cisplatin-induced DNA damage
1999 StandoutNatureNobel
The Sleep Disorder Canine Narcolepsy Is Caused by a Mutation in the Hypocretin (Orexin) Receptor 2 Gene
1999 Standout
DNA hypomethylation leads to elevated mutation rates
1998 Nature
Positional cloning of zebrafish ferroportin1 identifies a conserved vertebrate iron exporter
2000 StandoutNature
Abnormal splicing of the leptin receptor in diabetic mice
1996 StandoutNature
Inactivation of the mouse Msh2 gene results in mismatch repair deficiency, methylation tolerance, hyperrecombination, and predisposition to cancer
1995
An Olfactory Sensory Map Develops in the Absence of Normal Projection Neurons or GABAergic Interneurons
1998 StandoutNobel
A Simple Genetic Basis for a Complex Psychological Trait in Laboratory Mice
1995 Science
Isolation of MutSβ from Human Cells and Comparison of the Mismatch Repair Specificities of MutSβ and MutSα
1998 StandoutNobel
A mutation in the human leptin receptor gene causes obesity and pituitary dysfunction
1998 StandoutNature
Truncating mutations of hSNF5/INI1 in aggressive paediatric cancer
1998 StandoutNature
A candidate gene for the mouse mutation tubby
1996 Nature
Meiotic Pachytene Arrest in MLH1-Deficient Mice
1996
Leptin and the regulation of body weight in mammals
1998 StandoutNature
Mutation in the Mismatch Repair Gene Msh6 Causes Cancer Susceptibility
1997
Role of leptin in the neuroendocrine response to fasting
1996 StandoutNature
Leptin Inhibits Bone Formation through a Hypothalamic Relay
2000 Standout
Evidence That the Diabetes Gene Encodes the Leptin Receptor: Identification of a Mutation in the Leptin Receptor Gene in db/db Mice
1996 Standout
Simple sequences
1994
Genetics of Mouse Behavior: Interactions with Laboratory Environment
1999 StandoutScience
Epigenetic Reprogramming in Mammalian Development
2001 StandoutScience
DNA Mismatch Repair: Functions and Mechanisms
2005 StandoutNobel
Tumorigenesis in Mlh1 and Mlh1/Apc1638N mutant mice.
1999
PMS2 endonuclease activity has distinct biological functions and is essential for genome maintenance
2010 StandoutNobel
Population genetics of dinucleotide (dC-dA)n.(dG-dT)n polymorphisms in world populations.
1995
Global Patterns of Linkage Disequilibrium at the CD4 Locus and Modern Human Origins
1996 StandoutScienceNobel
Constitutive Expression of AID Leads to Tumorigenesis
2003 StandoutNobel
The Mouse Clock Mutation Behaves as an Antimorph and Maps Within the W19H Deletion, Distal of Kit
1997
Antagonism of Central Melanocortin Receptors in Vitro and in Vivo by Agouti-Related Protein
1997 StandoutScience
High rate of CAD gene amplification in human cells deficient in MLH1 or MSH6
2001 StandoutNobel
A Novel Mutant Gene Involved in T-Lymphocyte–Specific Homing Into Peripheral Lymphoid Organs on Mouse Chromosome 4
1998
The Ubiquitin-Proteasome Proteolytic Pathway: Destruction for the Sake of Construction
2002 StandoutNobel
Association of Anxiety-Related Traits with a Polymorphism in the Serotonin Transporter Gene Regulatory Region
1996 StandoutScience
hMutSα- and hMutLα-dependent phosphorylation of p53 in response to DNA methylator damage
1999 StandoutNobel
The Human Genome Project: Reaching the Finish Line
1998 StandoutScienceNobel
Impairment of the Ubiquitin-Proteasome System by Protein Aggregation
2001 StandoutScience
SMART, a simple modular architecture research tool: Identification of signaling domains
1998 Standout
Mutation of the E6-AP Ubiquitin Ligase Reduces Nuclear Inclusion Frequency While Accelerating Polyglutamine-Induced Pathology in SCA1 Mice
1999 StandoutNobel
Works of Michael Wessel being referenced
A genetic map of the mouse with 4,006 simple sequence length polymorphisms
1994