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Top Articles

#TitleJournalYearCitations
1A single ataxia telangiectasia gene with a product similar to PI-3 kinaseScience19952,634
2Philadelphia chromosomal breakpoints are clustered within a limited region, bcr, on chromosome 22Cell19841,552
3Mammalian Cry1 and Cry2 are essential for maintenance of circadian rhythmsNature19991,317
4A cellular oncogene is translocated to the Philadelphia chromosome in chronic myelocytic leukaemiaNature19821,313
5Interacting Molecular Loops in the Mammalian Circadian ClockScience20001,223
6Looping and Interaction between Hypersensitive Sites in the Active β-globin LocusMolecular Cell20021,205
7Chromosomal stability and the DNA double-stranded break connectionNature Reviews Genetics20011,049
8The DNA Double-Strand Break Repair Gene hMRE11 Is Mutated in Individuals with an Ataxia-Telangiectasia-like DisorderCell1999986
9Molecular mechanism of nucleotide excision repairGenes and Development1999978
10Structural organization of the bcr gene and its role in the Ph′ translocationNature1985871
11Localization of the c-abl oncogene adjacent to a translocation break point in chronic myelocytic leukaemiaNature1983848
12Xeroderma Pigmentosum Group C Protein Complex Is the Initiator of Global Genome Nucleotide Excision RepairMolecular Cell1998796
13DNA repair helicase: a component of BTF2 (TFIIH) basic transcription factorScience1993791
14Translocation of c-abl oncogene correlates with the presence of a Philadelphia chromosome in chronic myelocytic leukaemiaNature1983723
15Sequential Assembly of the Nucleotide Excision Repair Factors In VivoMolecular Cell2001712
16ERCC6, a member of a subfamily of putative helicases, is involved in Cockayne's syndrome and preferential repair of active genesCell1992698
17Localization of an ataxia-telangiectasia gene to chromosome 11q22–23Nature1988677
18Nucleotide excision repair and human syndromesCarcinogenesis2000610
19Defective haematopoiesis in fetal liver resulting from inactivation of the EKLF geneNature1995531
20p53 modulation of TFIIH–associated nucleotide excision repair activityNature Genetics1995525
21Runx1 Expression Marks Long-Term Repopulating Hematopoietic Stem Cells in the Midgestation Mouse EmbryoImmunity2002523
22Premature Aging in Mice Deficient in DNA Repair and TranscriptionScience2002509
23Definitive hematopoietic stem cells first develop within the major arterial regions of the mouse embryoEMBO Journal2000507
24Xeroderma Pigmentosum Group F Caused by a Defect in a Structure-Specific DNA Repair EndonucleaseCell1996492
25Repair of DNA interstrand cross-linksMutation Research DNA Repair2001490
26Role of PML in Cell Growth and the Retinoic Acid PathwayScience1998488
27Transcription complex stability and chromatin dynamics in vivoNature1995469
28Human Rad50/Mre11 Is a Flexible Complex that Can Tether DNA EndsMolecular Cell2001437
29Hematopoietic Stem Cells Localize to the Endothelial Cell Layer in the Midgestation Mouse AortaImmunity2002428
30Molecular Mechanisms of the Biological Clock in Cultured FibroblastsScience2001426
31Disruption of Mouse RAD54 Reduces Ionizing Radiation Resistance and Homologous RecombinationCell1997403
32Unique fusion of bcr and c-abl genes in Philadelphia chromosome positive acute lymphoblastic leukemiaCell1987400
33HbVar: A relational database of human hemoglobin variants and thalassemia mutations at the globin gene serverHuman Mutation2002400
34Can, a putative oncogene associated with myeloid leukemogenesis, may be activated by fusion of its 3' half to different genes: characterization of the set gene.Molecular and Cellular Biology1992368
35The transcription factor GATA6 is essential for early extraembryonic developmentDevelopment (Cambridge)1999364
36A temperature-sensitive disorder in basal transcription and DNA repair in humansNature Genetics2001362
37Bicaudal-D regulates COPI-independent Golgi–ER transport by recruiting the dynein–dynactin motor complexNature Cell Biology2002357
38Photic Induction of mPer1 and mPer2 in Cry-Deficient Mice Lacking a Biological ClockScience1999348
39The translocation (6;9), associated with a specific subtype of acute myeloid leukemia, results in the fusion of two genes, dek and can, and the expression of a chimeric, leukemia-specific dek-can mRNA.Molecular and Cellular Biology1992339
40Spatial organization of gene expression: the active chromatin hubChromosome Research2003336
41Disruption of mouse ERCC1 results in a novel repair syndrome with growth failure, nuclear abnormalities and senescenceCurrent Biology1997335
42Molecular characterization of the human excision repair gene : cDNA cloning and amino acid homology with the yeast DNA repair geneCell1986334
43ATP-Dependent Chromatin Remodeling by the Cockayne Syndrome B DNA Repair-Transcription-Coupling FactorMolecular and Cellular Biology2000334
44Intergenic Transcription and Developmental Remodeling of Chromatin Subdomains in the Human β-globin LocusMolecular Cell2000323
45Nucleotide excision repair II: from yeast to mammalsTrends in Genetics1993319
46Absence of Mouse REC8 Cohesin Promotes Synapsis of Sister Chromatids in MeiosisDevelopmental Cell2005310
47Gata3 loss leads to embryonic lethality due to noradrenaline deficiency of the sympathetic nervous systemNature Genetics2000308
48Molecular cloning of a human DNA repair geneNature1984307
49Defective Transcription-Coupled Repair in Cockayne Syndrome B Mice Is Associated with Skin Cancer PredispositionCell1997301
50Crystal Structure of a Human Alkylbase-DNA Repair Enzyme Complexed to DNACell1998284