Citation Impact
Citing Papers
Nuclear Lamin-A Scales with Tissue Stiffness and Enhances Matrix-Directed Differentiation
2013 StandoutScience
Lymphatic function is required prenatally for lung inflation at birth
2014
Nucleoside-modified VEGFC mRNA induces organ-specific lymphatic growth and reverses experimental lymphedema
2021 StandoutNobel
Cell type-specific binding patterns reveal that TCF7L2 can be tethered to the genome by association with GATA3
2012
Association between TCF7L2gene polymorphisms and susceptibility to Type 2 Diabetes Mellitus: a large Human Genome Epidemiology (HuGE) review and meta-analysis
2009
Administration of nucleoside-modified mRNA encoding broadly neutralizing antibody protects humanized mice from HIV-1 challenge
2017 StandoutNobel
An integrated encyclopedia of DNA elements in the human genome
2012 StandoutNature
Strategy for mutation analysis in the autosomal recessive limb-girdle muscular dystrophies
2001
Cancer chemoprevention with dietary phytochemicals
2003 Standout
Integrated analysis of somatic mutations and focal copy-number changes identifies key genes and pathways in hepatocellular carcinoma
2012 Standout
Linkage of a commoner form of recessive amyotrophic lateral sclerosis to chromosome 15q15-q22 markers
1998
β-Catenin—A Linchpin in Colorectal Carcinogenesis?
2002
Forces in Tissue Morphogenesis and Patterning
2013 Standout
RNAi screen identifies Brd4 as a therapeutic target in acute myeloid leukaemia
2011 StandoutNature
Mutations in the glutamate transporter EAAT2 gene do not cause abnormal EAAT2 transcripts in amyotrophic lateral sclerosis
1998 StandoutNobel
Identification and characterization of a spinal muscular atrophy-determining gene
1995 Standout
hEST2, the Putative Human Telomerase Catalytic Subunit Gene, Is Up-Regulated in Tumor Cells and during Immortalization
1997 Standout
Campomelic dysplasia and autosomal sex reversal caused by mutations in an SRY-related gene
1994 StandoutNature
A molecular basis for cardiac arrhythmia: HERG mutations cause long QT syndrome
1995 Standout
Hepatocellular adenoma: Classification, variants and clinical relevance
2016
A first-generation physical map of the human genome
1993 Nature
A comprehensive genetic map of the human genome based on 5,264 microsatellites
1996 StandoutNature
High-resolution structure of the Shigella type-III secretion needle by solid-state NMR and cryo-electron microscopy
2014 StandoutNobel
The muscular dystrophies
2002 Standout
A Physical Map of Human Chromosome 7: An Integrated YAC Contig Map with Average STS Spacing of 79 kb
1997
The FHIT Gene, Spanning the Chromosome 3p14.2 Fragile Site and Renal Carcinoma–Associated t(3;8) Breakpoint, Is Abnormal in Digestive Tract Cancers
1996 Standout
A Bivalent Chromatin Structure Marks Key Developmental Genes in Embryonic Stem Cells
2006 Standout
A Detailed Physical and Transcriptional Map of the Region of Chromosome 20 That Is Deleted in Myeloproliferative Disorders and Refinement of the Common Deleted Region
1998
The 1993–94 Généthon human genetic linkage map
1994 Standout
Colorectal cancer
2013 Standout
Translocation breakpoints in three patients with campomelic dysplasia and autosomal sex reversal map more than 130 kb from SOX9
1996
Exon sequencing and association analysis of polymorphisms in TCF7L2 with type 2 diabetes in a Chinese population
2008
Miltefosine for New World Cutaneous Leishmaniasis
2004
High resolution analysis of DNA copy number variation using comparative genomic hybridization to microarrays
1998 Standout
Viral hepatitis and liver cancer: the case of hepatitis C
2006
Telomerase RNA structure and function: implications for dyskeratosis congenita
2004 StandoutNobel
The Molecular Basis of Leukemia
2004
On the involvement of calpains in the degradation of the tumor suppressor protein p53
1997 StandoutNobel
Diabetes in Asia
2009 Standout
Linking actin dynamics and gene transcription to drive cellular motile functions
2010
TCF Transcription Factors, Mediators of Wnt-Signaling in Development and Cancer
2002
The human interferon ? species and receptors
2000
Wnt/β-Catenin Signaling and Disease
2012 Standout
DNA mismatch repair defects: role in colorectal carcinogenesis
2002
Transcriptome classification of HCC is related to gene alterations and to new therapeutic targets
2006
Integrated YAC contig containing the 3pl4.2 hereditary renal carcinoma 3;8 translocation breakpoint and the fragile site FRA3B
1994
A Wnt kinase network alters nuclear localization of TCF-1 in colon cancer
2009 StandoutNobel
STATs in cancer inflammation and immunity: a leading role for STAT3
2009 Standout
Diversity of LEF/TCF action in development and disease
2006
Genetic Landscape and Biomarkers of Hepatocellular Carcinoma
2015
A human chromosome 7 yeast artificial chromosome (YAC) resource: construction, characterization, and screening
1995
Frequent in-frame somatic deletions activate gp130 in inflammatory hepatocellular tumours
2008 Nature
5-Fluorouracil: mechanisms of action and clinical strategies
2003 Standout
Complementation Cloning of , a Gene Encoding a Putative Metalloprotease Required for Intramembrane Cleavage of SREBPs
1997 Nobel
Recurrent AAV2-related insertional mutagenesis in human hepatocellular carcinomas
2015
A census of human cancer genes
2004 Standout
From head to toes: the multiple facets of Sox proteins
1999 Standout
MLL-mediated transcriptional gene regulation investigated by gene expression profiling
2003
Matrix Crosslinking Forces Tumor Progression by Enhancing Integrin Signaling
2009 Standout
Colorectal cancer and genetic alterations in the Wnt pathway
2006
Two transmembrane aspartates in presenilin-1 required for presenilin endoproteolysis and γ-secretase activity
1999 StandoutNature
Amyotrophic Lateral Sclerosis
2001 Standout
European Gene Mapping Project(EUROGEM): Genetic Maps basedon the CEPH reference families
1994 Nobel
Role of YAP/TAZ in mechanotransduction
2011 StandoutNature
Hepatocellular carcinoma
2022 Standout
A presenilin-1-dependent γ-secretase-like protease mediates release of Notch intracellular domain
1999 StandoutNature
Human Telomerase and Its Regulation
2002
The mouse and human genes encoding the recognition component of the N-end rule pathway
1998 StandoutNobel
Hepatocellular Carcinoma
2019 Standout
Molecular Pathogenesis ofShigellaspp.: Controlling Host Cell Signaling, Invasion, and Death by Type III Secretion
2008
Life with 6000 Genes
1996 StandoutScience
Mutations at coding repeat sequences in mismatch repair-deficient human cancers: toward a new concept of target genes for instability.
2002
PKD2 , a Gene for Polycystic Kidney Disease That Encodes an Integral Membrane Protein
1996 StandoutScience
TYPE I INTERFERONS (α/β) IN IMMUNITY AND AUTOIMMUNITY
2004 StandoutNobel
The Calpain System
2003 Standout
Advances in leishmaniasis
2005 Standout
De Novo and Inherited Deletions of the 5q13 Region in Spinal Muscular Atrophies
1994 Science
Dynamic Molecular Combing: Stretching the Whole Human Genome for High-Resolution Studies
1997 Science
EASL Clinical Practice Guidelines: Management of hepatocellular carcinoma
2018 Standout
Association Study of the Genetic Polymorphisms of the Transcription Factor 7-Like 2 (TCF7L2) Gene and Type 2 Diabetes in the Chinese Population
2007
Recombinant expression and isolation of human l -arginine:glycine amidinotransferase and identification of its active-site cysteine residue
1997 Nobel
Turmeric curcumin inhibits entry of all hepatitis C virus genotypes into human liver cells
2013 StandoutNobel
Mutations in the proteolytic enzyme calpain 3 cause limb-girdle muscular dystrophy type 2A
1995
The Human Genome Project: Reaching the Finish Line
1998 StandoutScienceNobel
Creatine and Creatinine Metabolism
2000 Standout
DPC4 , A Candidate Tumor Suppressor Gene at Human Chromosome 18q21.1
1996 StandoutScience
Works of Hung Bui being referenced
Bi-allelic inactivation of TCF1 in hepatic adenomas
2002
A Specific Genetic Background Is Required for Acquisition and Expression of Virulence Factors in Escherichia coli
2004
The human telomerase gene: complete genomic sequence and analysis of tandem repeat polymorphisms in intronic regions
2002
Mapping of a chromosome 15 region involved in limb girdle muscular dystrophy
1994
Germline hepatocyte nuclear factor 1α and 1β mutations in renal cell carcinomas
2005
Isolation of chromosome 21–specific yeast artificial chromosomes from a total human genome library
1992
Recurrence of OTT–MAL fusion in t(1;22) of infant AML‐M7
2001
Proteolytic activation defines distinct lymphangiogenic mechanisms for VEGFC and VEGFD
2016
Prospective Value of PCR Amplification and Sequencing for Diagnosis and Typing of Old World Leishmania Infections in an Area of Nonendemicity
2003
The secreted lymphangiogenic factor CCBE1 is essential for fetal liver erythropoiesis
2013
The human T-cell transcription factor-4 gene: structure, extensive characterization of alternative splicings, and mutational analysis in colorectal cancer cell lines.
2000