364(top 1%)
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61.0K(top 0.1%)
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122(top 0.1%)
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Top Articles

#TitleJournalYearCitations
1Tumour heterogeneity and cancer cell plasticityNature20132,043
2The bone marrow niche for haematopoietic stem cellsNature20141,910
3Requirement for ceramide-initiated SAPK/JNK signalling in stress-induced apoptosisNature19961,789
4Disorders of Iron MetabolismNew England Journal of Medicine19991,693
5Antagonism of Central Melanocortin Receptors in Vitro and in Vivo by Agouti-Related ProteinScience19971,666
6Endothelial and perivascular cells maintain haematopoietic stem cellsNature20121,617
7Losartan, an AT1 Antagonist, Prevents Aortic Aneurysm in a Mouse Model of Marfan SyndromeScience20061,591
8Erythroid differentiation in chimaeric mice blocked by a targeted mutation in the gene for transcription factor GATA-1Nature19911,291
9A Core Complex of BBS Proteins Cooperates with the GTPase Rab8 to Promote Ciliary Membrane BiogenesisCell20071,248
10CiliopathiesNew England Journal of Medicine20111,227
11Pendred syndrome is caused by mutations in a putative sulphate transporter gene (PDS)Nature Genetics19971,081
12Math1: An Essential Gene for the Generation of Inner Ear Hair CellsScience19991,042
13Microarray Identification of FMRP-Associated Brain mRNAs and Altered mRNA Translational Profiles in Fragile X SyndromeCell20011,033
14Interleukin-2 receptor α chain regulates the size and content of the peripheral lymphoid compartmentImmunity19951,017
15Haematopoietic stem cells and early lymphoid progenitors occupy distinct bone marrow nichesNature20131,017
16Cancer Stem Cells: Impact, Heterogeneity, and UncertaintyCancer Cell2012999
17Absence of blood formation in mice lacking the T-cell leukaemia oncoprotein tal-1/SCLNature1995880
18Genetic imprinting suggested by maternal heterodisomy in non-deletion Prader-Willi syndromeNature1989852
19Isolation of a partial candidate gene for Menkes disease by positional cloningNature Genetics1993688
20Genetics of body-weight regulationNature2000682
21Arrested development of embryonic red cell precursors in mouse embryos lacking transcription factor GATA-1.Proceedings of the National Academy of Sciences of the United States of America1996670
22A Critical Role for DNA End-Joining Proteins in Both Lymphogenesis and NeurogenesisCell1998622
23Angiotensin II type 1 receptor blockade attenuates TGF-β–induced failure of muscle regeneration in multiple myopathic statesNature Medicine2007603
24The Pendred syndrome gene encodes a chloride-iodide transport proteinNature Genetics1999524
25Haematopoietic stem cells require a highly regulated protein synthesis rateNature2014522
26Transferrin receptor is necessary for development of erythrocytes and the nervous systemNature Genetics1999510
27Mutation of TRPM6 causes familial hypomagnesemia with secondary hypocalcemiaNature Genetics2002506
28Globin gene regulation and switching: Circa 1990Cell1990497
29Molecular Pathways Underlying Cardiac Remodeling During Pathophysiological StimulationCirculation2010478
30Discovery of five conserved  -defensin gene clusters using a computational search strategyProceedings of the National Academy of Sciences of the United States of America2002464
31Neomorphic agouti mutations in obese yellow miceNature Genetics1994434
32Myelin Gene Regulatory Factor Is a Critical Transcriptional Regulator Required for CNS MyelinationCell2009427
33Signaling effectors underlying pathologic growth and remodeling of the heartJournal of Clinical Investigation2013380
34The Continuing Challenge of Understanding, Preventing, and Treating Neural Tube DefectsScience2013375
35Cryptic and polar variation of the fragile X repeat could result in predisposing normal allelesCell1994371
36Complementary genomic approaches highlight the PI3K/mTOR pathway as a common vulnerability in osteosarcomaProceedings of the National Academy of Sciences of the United States of America2014355
37Iron homeostasis: insights from genetics and animal modelsNature Reviews Genetics2000352
38Exome Capture Reveals ZNF423 and CEP164 Mutations, Linking Renal Ciliopathies to DNA Damage Response SignalingCell2012347
39Early Asymmetry of Gene Transcription in Embryonic Human Left and Right Cerebral CortexScience2005339
40The genetics of pigmentation: from fancy genes to complex traitsTrends in Genetics1996338
41Cyclophilin D controls mitochondrial pore–dependent Ca2+ exchange, metabolic flexibility, and propensity for heart failure in miceJournal of Clinical Investigation2010333
42NephronophthisisJournal of the American Society of Nephrology: JASN2009332
43Identification of the gene (BBS1) most commonly involved in Bardet-Biedl syndrome, a complex human obesity syndromeNature Genetics2002327
44Peripheral myelin protein–22 gene maps in the duplication in chromosome 17p11.2 associated with Charcot–Marie–Tooth 1ANature Genetics1992325
45Obesity, diabetes, and neoplasia in yellow A vy /‐ mice: ectopic expression of the agouti geneFASEB Journal1994323
46Subcellular fractionation of dystrophin to the triads of skeletal muscleNature1987318
47Development of hematopoietic cells lacking transcription factor GATA-1Development (Cambridge)1995317
48Influence of mutation type and X chromosome inactivation on Rett syndrome phenotypesAnnals of Neurology2000314
49Oligodendrocyte-Encoded HIF Function Couples Postnatal Myelination and White Matter AngiogenesisCell2014314
50SCL/Tal-1 transcription factor acts downstream of cloche to specify hematopoietic and vascular progenitors in zebrafishGenes and Development1998312