Citation Impact
Citing Papers
Phylogenetic reconstruction and the identification of ancient polymorphism in the Bovini tribe (Bovidae, Bovinae)
2009 Standout
Simple methods for estimating the numbers of synonymous and nonsynonymous nucleotide substitutions.
1986 Standout
Pattern of nucleotide substitution at major histocompatibility complex class I loci reveals overdominant selection
1988 StandoutNature
The Ubiquitin Proteasome System in Neurodegenerative Diseases
2003 StandoutNobel
Maximum likelihood phylogenetic estimation from DNA sequences with variable rates over sites: Approximate methods
1994 Standout
Inherent toxicity of aggregates implies a common mechanism for protein misfolding diseases
2002 StandoutNature
Isolation, Tissue Distribution, and Chromosomal Localization of the Human Activation-Induced Cytidine Deaminase (AID) Gene
2000 StandoutNobel
The β-Thalassemias
1999 Standout
A multilocus phylogeny of the Streptomyces griseus 16S rRNA gene clade: use of multilocus sequence analysis for streptomycete systematics
2008 Standout
Identification and characterization of a spinal muscular atrophy-determining gene
1995 Standout
Early molecular replication of human immunodeficiency virus type 1 in cultured-blood-derived T helper dendritic cells.
1993
The Outcome of Hepatitis C Virus Infection Is Predicted by Escape Mutations in Epitopes Targeted by Cytotoxic T Lymphocytes
2001 StandoutNobel
MEGA3: Integrated software for Molecular Evolutionary Genetics Analysis and sequence alignment
2004 Standout
6 β-Thalassaemia
1993
The muscular dystrophies
2002 Standout
Phylogenetic Analysis of SIV and STLV Type I in Mandrills ( Mandrillus sphinx ): Indications That Intracolony Transmissions Are Predominantly the Result of Male-to-Male Aggressive Contacts
1998 StandoutNobel
Hepatitis C Virus Continuously Escapes From Neutralizing Antibody and T-Cell Responses During Chronic Infection In Vivo
2006 StandoutNobel
Phenotype—genotype relationships in monogenic disease: lessons from the thalassaemias
2001
Protein degradation and protection against misfolded or damaged proteins
2003 StandoutNature
Protein folding and misfolding
2003 StandoutNature
Lineage-Specific Expansions of Retroviral Insertions within the Genomes of African Great Apes but Not Humans and Orangutans
2005 StandoutNobel
Regression of extramedullary haemopoiesis and augmentation of fetal haemoglobin concentration during hydroxyurea therapy in β thalassaemia
1998
MCScanX: a toolkit for detection and evolutionary analysis of gene synteny and collinearity
2012 Standout
A codon-based model of nucleotide substitution for protein-coding DNA sequences.
1994 Standout
Gene Defects in β‐Thalassemia and Their Prenatal Diagnosis
1990
Sickle-cell disease
2010 Standout
Estimation of the number of nucleotide substitutions in the control region of mitochondrial DNA in humans and chimpanzees.
1993 Standout
The ubiquitin system: pathogenesis of human diseases and drug targeting
2004 StandoutNobel
Mutations in CCR5-Coding Sequences Are Not Associated with SIV Carrier Status in African Nonhuman Primates
1999 StandoutNobel
Homology requirements for unequal crossing over in humans.
1991 StandoutNobel
PAML 4: Phylogenetic Analysis by Maximum Likelihood
2007 Standout
A Mild Thalassemia Major Resulting from a Compound Heterozygosity for the IVS-11-1 (G→A) Mutation and the Rare T→C Mutation at the Polyadenylation Site
1991
7 Increased HbF in adult life
1993
Interpreting neural networks for biological sequences by learning stochastic masks
2022 StandoutNobel
TBtools-II: A “one for all, all for one” bioinformatics platform for biological big-data mining
2023 Standout
Cellular Defenses against Unfolded Proteins
2001
Not So Different After All: A Comparison of Methods for Detecting Amino Acid Sites Under Selection
2005 Standout
A rare polyadenylation signal mutation of the FOXP3 gene (AAUAAA→AAUGAA) leads to the IPEX syndrome
2001 StandoutNobel
Parkinson's Disease
2003 Standout
Likelihood Models for Detecting Positively Selected Amino Acid Sites and Applications to the HIV-1 Envelope Gene
1998 Standout
Biochemical activities of T-antigen proteins encoded by simian virus 40 A gene deletion mutants.
1983 Nobel
Genome sequencing and analysis of the model grass Brachypodium distachyon
2010 StandoutNature
Cell Survival Responses to Environmental Stresses Via the Keap1-Nrf2-ARE Pathway
2006 Standout
Molecular characterization of beta-thalassemia intermedia in patients of Italian descent and identification of three novel beta-thalassemia mutations
1991
Dendritic cells and the replication of HIV-1
1996 StandoutNobel
Sequence analysis of the gamma-globin gene locus from a patient with the deletion form of hereditary persistence of fetal hemoglobin
1990
Internalization-defective LDL receptors produced by genes with nonsense and frameshift mutations that truncate the cytoplasmic domain
1985 StandoutNobel
Computational Molecular Evolution
2006 Standout
Molecular basis for dominantly inherited inclusion body beta-thalassemia.
1990
Susceptibility of dendritic cells to HIV-1 infection in vitro
1994 StandoutNobel
A Common Human β Globin Splicing Mutation Modeled in Mice
1998 StandoutNobel
Codon-Substitution Models for Heterogeneous Selection Pressure at Amino Acid Sites
2000 Standout
Lethal thalassemia after insertional disruption of the mouse major adult beta-globin gene.
1993 StandoutNobel
A mouse model for beta 0-thalassemia.
1995 StandoutNobel
beta zero thalassemia in Sardinia is caused by a nonsense mutation.
1981
The Ubiquitin-Proteasome Proteolytic Pathway: Destruction for the Sake of Construction
2002 StandoutNobel
The tortoise and the hare: choosing between noncoding plastome and nuclear Adh sequences for phylogeny reconstruction in a recently diverged plant group
1998 Standout
Neutralizing Monoclonal Antibodies Block Human Immunodeficiency Virus Type 1 Infection of Dendritic Cells and Transmission to T Cells
1998 StandoutNobel
Complete DNA sequence of lymphotropic papovavirus: Prototype of a new species of the polyomavirus genus
1985 StandoutNobel
Immature Dendritic Cells Selectively Replicate Macrophagetropic (M-Tropic) Human Immunodeficiency Virus Type 1, while Mature Cells Efficiently Transmit both M- and T-Tropic Virus to T Cells
1998 StandoutNobel
Observations on the levels of Hb A2 in patients with different beta- thalassemia mutations and a delta chain variant
1990
Works of IS Han being referenced
Clinical and genetic heterogeneity in black patients with homozygous beta-thalassemia from the southeastern United States
1988
Inclusion body beta-thalassemia trait in a Swiss family is caused by an abnormal hemoglobin (Geneva) with an altered and extended beta chain carboxy-terminus due to a modification in codon beta 114
1988
Clinical and genetic heterogeneity in black patients with homozygous beta-thalassemia from the southeastern United States
1988
Nucleotide sequence of the human theta 1-globin gene.
1988
Inclusion body beta-thalassemia trait in a Swiss family is caused by an abnormal hemoglobin (Geneva) with an altered and extended beta chain carboxy-terminus due to a modification in codon beta 114
1988
Identical nucleotide sequences of the 3'A gamma globin gene enhancer elements from four different chromosomes
1989