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citing journals

Top Articles

#TitleJournalYearCitations
1Amplification of a gene encoding a p53-associated protein in human sarcomasNature19921,942
2Gene-expression profiles predict survival of patients with lung adenocarcinomaNature Medicine20021,800
3Child development: risk factors for adverse outcomes in developing countriesLancet, The20071,623
4Conjoint Analysis Applications in Health—a Checklist: A Report of the ISPOR Good Research Practices for Conjoint Analysis Task ForceValue in Health20111,429
5Inequality in early childhood: risk and protective factors for early child developmentLancet, The20111,286
6Insights into Autism Spectrum Disorder Genomic Architecture and Biology from 71 Risk LociNeuron20151,264
7Multiple Recurrent De Novo CNVs, Including Duplications of the 7q11.23 Williams Syndrome Region, Are Strongly Associated with AutismNeuron20111,163
8WFH Guidelines for the Management of Hemophilia, 3rd editionHaemophilia20201,074
9Urinary, Circulating, and Tissue Biomonitoring Studies Indicate Widespread Exposure to Bisphenol AEnvironmental Health Perspectives20101,059
10Effective Messages in Vaccine Promotion: A Randomized TrialPediatrics2014973
11Disease proteomicsNature2003968
12Discordant Protein and mRNA Expression in Lung AdenocarcinomasMolecular and Cellular Proteomics2002821
13Integrative clinical genomics of metastatic cancerNature2017729
14Toxicity and management in CAR T-cell therapyMolecular Therapy - Oncolytics2016717
15Isolation of a partial candidate gene for Menkes disease by positional cloningNature Genetics1993692
16The primacy of the gastrointestinal tract as a target organ of acute graft-versus-host disease: rationale for the use of cytokine shields in allogeneic bone marrow transplantationBlood2000646
17Extracorporeal Circulation in Neonatal Respiratory Failure: A Prospective Randomized StudyPediatrics1985634
18The Simons Simplex Collection: A Resource for Identification of Autism Genetic Risk FactorsNeuron2010625
19Membrane Type I Matrix Metalloproteinase Usurps Tumor Growth Control Imposed by the Three-Dimensional Extracellular MatrixCell2003617
20Biobank-driven genomic discovery yields new insight into atrial fibrillation biologyNature Genetics2018612
21The Effect of Weight Loss on the Sensitivity of Blood Pressure to Sodium in Obese AdolescentsNew England Journal of Medicine1989596
22Connexin 43 (GJA1) Mutations Cause the Pleiotropic Phenotype of Oculodentodigital DysplasiaAmerican Journal of Human Genetics2003593
23Mutations in INVS encoding inversin cause nephronophthisis type 2, linking renal cystic disease to the function of primary cilia and left-right axis determinationNature Genetics2003587
24A transition zone complex regulates mammalian ciliogenesis and ciliary membrane compositionNature Genetics2011568
25Association of Hospital-Level Volume of Extracorporeal Membrane Oxygenation Cases and Mortality. Analysis of the Extracorporeal Life Support Organization RegistryAmerican Journal of Respiratory and Critical Care Medicine2015565
26EGFR, p16, HPV Titer, Bcl-xL and p53, Sex, and Smoking As Indicators of Response to Therapy and Survival in Oropharyngeal CancerJournal of Clinical Oncology2008563
27Psychological Status in Childhood Cancer Survivors: A Report From the Childhood Cancer Survivor StudyJournal of Clinical Oncology2009559
28Mutations in FOXC2 (MFH-1), a Forkhead Family Transcription Factor, Are Responsible for the Hereditary Lymphedema-Distichiasis SyndromeAmerican Journal of Human Genetics2000554
29Iron Deficiency and Brain DevelopmentSeminars in Pediatric Neurology2006552
30Mapping the NPHP-JBTS-MKS Protein Network Reveals Ciliopathy Disease Genes and PathwaysCell2011543
31An excitatory paraventricular nucleus to AgRP neuron circuit that drives hungerNature2014542
32Evidence for impaired t cell dna methylation in systemic lupus erythematosus and rheumatoid arthritisArthritis and Rheumatism1990541
33Recurrent reciprocal 1q21.1 deletions and duplications associated with microcephaly or macrocephaly and developmental and behavioral abnormalitiesNature Genetics2008540
34The centrosomal protein nephrocystin-6 is mutated in Joubert syndrome and activates transcription factor ATF4Nature Genetics2006537
35Personalized Oncology Through Integrative High-Throughput Sequencing: A Pilot StudyScience Translational Medicine2011533
36Detectable clonal mosaicism from birth to old age and its relationship to cancerNature Genetics2012525
37A Single-Gene Cause in 29.5% of Cases of Steroid-Resistant Nephrotic SyndromeJournal of the American Society of Nephrology: JASN2015519
38Positional cloning uncovers mutations in PLCE1 responsible for a nephrotic syndrome variant that may be reversibleNature Genetics2006517
39Acute graft-versus-host disease does not require alloantigen expression on host epitheliumNature Medicine2002499
40American College of Critical Care Medicine Clinical Practice Parameters for Hemodynamic Support of Pediatric and Neonatal Septic ShockCritical Care Medicine2017497
41Late mortality after allogeneic hematopoietic cell transplantation and functional status of long-term survivors: report from the Bone Marrow Transplant Survivor StudyBlood2007496
42Inattention, Hyperactivity, and Symptoms of Sleep-Disordered BreathingPediatrics2002477
43Mutation of HOXA13 in hand-foot-genital syndromeNature Genetics1997475
44Global Profiling of the Cell Surface Proteome of Cancer Cells Uncovers an Abundance of Proteins with Chaperone FunctionJournal of Biological Chemistry2003471
45Notch signaling modulates proliferation and differentiation of intestinal crypt base columnar stem cellsDevelopment (Cambridge)2012459
46Epidemiology of Depressive Symptoms in the National Longitudinal Study of Adolescent HealthJournal of the American Academy of Child and Adolescent Psychiatry2002457
47Bisphenol A and Reproductive Health: Update of Experimental and Human Evidence, 2007–2013Environmental Health Perspectives2014453
48A de novo Alu insertion results in neurofibromatosis type 1Nature1991451
49The ciliary gene RPGRIP1L is mutated in cerebello-oculo-renal syndrome (Joubert syndrome type B) and Meckel syndromeNature Genetics2007446
50Mutations in NALP7 cause recurrent hydatidiform moles and reproductive wastage in humansNature Genetics2006429