| # | Title | Journal | Year | Citations |
|---|
| 1 | Mutations in a member of the ADAMTS gene family cause thrombotic thrombocytopenic purpura | Nature | 2001 | 1,623 |
| 2 | Intertumoral Heterogeneity within Medulloblastoma Subgroups | Cancer Cell | 2017 | 836 |
| 3 | Loss of alleles at loci on human chromosome 11 during genesis of Wilms' tumour | Nature | 1984 | 540 |
| 4 | Loss of heterozygosity in three embryonal tumours suggests a common pathogenetic mechanism | Nature | 1985 | 535 |
| 5 | Recurrence patterns across medulloblastoma subgroups: an integrated clinical and molecular analysis | Lancet Oncology, The | 2013 | 307 |
| 6 | Hemophagocytic lymphohistiocytosis (HLH) and related disorders | Hematology American Society of Hematology Education Program | 2009 | 296 |
| 7 | Sites of Regulated Phosphorylation that Control K-Cl Cotransporter Activity | Cell | 2009 | 269 |
| 8 | Chromosomal localization of the human rhabdomyosarcoma locus by mitotic recombination mapping | Nature | 1987 | 265 |
| 9 | Natural killer cell dysfunction in patients with systemic-onset juvenile rheumatoid arthritis and macrophage activation syndrome | Journal of Pediatrics | 2003 | 257 |
| 10 | Perforin expression in cytotoxic lymphocytes from patients with hemophagocytic lymphohistiocytosis and their family members | Blood | 2002 | 247 |
| 11 | Social, Emotional, and Behavioral Functioning of Children With Cancer | Pediatrics | 1999 | 238 |
| 12 | Clinical relevance of transmembrane drug efflux as a mechanism of multidrug resistance. | Journal of Clinical Oncology | 1998 | 202 |
| 13 | Natural killer cell dysfunction is a distinguishing feature of systemic onset juvenile rheumatoid arthritis and macrophage activation syndrome | Arthritis Research | 2005 | 202 |
| 14 | A Controlled Study of Peer Relationships of Children Surviving Brain Tumors: Teacher, Peer, and Self Ratings | Journal of Pediatric Psychology | 1998 | 194 |
| 15 | TGFβ2 in Corneal Morphogenesis during Mouse Embryonic Development | Developmental Biology | 2001 | 153 |
| 16 | Apparent genotype-phenotype correlation in childhood, adolescent, and adult Chediak-Higashi syndrome | American Journal of Medical Genetics Part A | 2002 | 135 |
| 17 | The current management of hepatoblastoma: A combination of chemotherapy, conventional resection, and liver transplantation | Journal of Pediatrics | 2005 | 134 |
| 18 | A systematic analysis of recombination activity and genotype-phenotype correlation in human recombination-activating gene 1 deficiency | Journal of Allergy and Clinical Immunology | 2014 | 132 |
| 19 | Anti–IL-5 (mepolizumab) therapy reduces eosinophil activation ex vivo and increases IL-5 and IL-5 receptor levels | Journal of Allergy and Clinical Immunology | 2008 | 131 |
| 20 | Signal transducer and activator of transcription 3 activation is required for Asp816 mutant c-Kit–mediated cytokine-independent survival and proliferation in human leukemia cells | Blood | 2001 | 130 |
| 21 | Twenty years of follow‐up among survivors of childhood and young adult acute myeloid leukemia | Cancer | 2008 | 124 |
| 22 | ALLOGRAFT INFLAMMATORY FACTOR-1 | Transplantation | 1996 | 124 |
| 23 | Peer Relationships and Emotional Well-Being of Youngsters with Sickle Cell Disease | Child Development | 1996 | 115 |
| 24 | CONTROVERSIES AND NEW APPROACHES TO TREATMENT OF LANGERHANS CELL HISTIOCYTOSIS | Hematology/Oncology Clinics of North America | 1998 | 104 |
| 25 | Fiber knob modifications overcome low, heterogeneous expression of the coxsackievirus-adenovirus receptor that limits adenovirus gene transfer and oncolysis for human rhabdomyosarcoma cells | Cancer Research | 2001 | 102 |
| 26 | Hemophagocytic Lymphohistiocytosis and Other Hemophagocytic Disorders | Immunology and Allergy Clinics of North America | 2008 | 100 |
| 27 | Diagnosis and manifestations of chronic graft-versus-host disease | Best Practice and Research in Clinical Haematology | 2008 | 96 |
| 28 | Clinical and laboratory variability in a cohort of patients diagnosed with type 1 VWD in the United States | Blood | 2016 | 96 |
| 29 | Twenty years of follow‐up of survivors of childhood osteosarcoma | Cancer | 2011 | 91 |
| 30 | Hereditary cancer risk assessment in a pediatric oncology follow‐up clinic | Pediatric Blood and Cancer | 2012 | 88 |
| 31 | Characterization of T and B cell repertoire diversity in patients with RAG deficiency | Science Immunology | 2016 | 88 |
| 32 | Oncolytic HSV and Erlotinib Inhibit Tumor Growth and Angiogenesis in a Novel Malignant Peripheral Nerve Sheath Tumor Xenograft Model | Molecular Therapy | 2007 | 87 |
| 33 | Mechanisms Linking Tumor Cell–Associated Procoagulant Function to Tumor Dissemination | Seminars in Thrombosis and Hemostasis | 2008 | 87 |
| 34 | Low or absent SPARC expression in acute myeloid leukemia with MLL rearrangements is associated with sensitivity to growth inhibition by exogenous SPARC protein | Leukemia | 2006 | 81 |
| 35 | Targeting Cancer-initiating Cells With Oncolytic Viruses | Molecular Therapy | 2009 | 80 |
| 36 | STAT3 activation is required for Asp816 mutant c-Kit induced tumorigenicity | Oncogene | 2001 | 75 |
| 37 | A Controlled Longitudinal Study of the Social Functioning of Children With Juvenile Rheumatoid Arthritis | Journal of Pediatric Psychology | 2003 | 72 |
| 38 | Allogeneic hematopoietic cell transplantation for primary immune deficiency diseases: Current status and critical needs | Journal of Allergy and Clinical Immunology | 2008 | 70 |
| 39 | Unrelated donor bone marrow transplantation for children with juvenile myelomonocytic leukaemia | British Journal of Haematology | 2002 | 68 |
| 40 | Comparing Parental Distress, Family Functioning, and the Role of Social Support for Caregivers With and Without a Child With Juvenile Rheumatoid Arthritis | Journal of Pediatric Psychology | 2003 | 67 |
| 41 | The pathophysiology of alveolar osteonecrosis of the jaw: Anticardiolipin antibodies, thrombophilia, and hypofibrinolysis | Translational Research | 1996 | 66 |
| 42 | Karyotype Studies in 18 Ependymomas with Literature Review of 107 Cases | Cancer Genetics and Cytogenetics | 1999 | 65 |
| 43 | Primary Immune Deficiency Treatment Consortium (PIDTC) report | Journal of Allergy and Clinical Immunology | 2014 | 65 |
| 44 | Congenital and neonatal leukemia | Seminars in Perinatology | 1999 | 59 |
| 45 | Coordinate regulation of Fanconi anemia gene expression occurs through the Rb/E2F pathway | Oncogene | 2008 | 59 |
| 46 | A Functional Initiator Element in the Human β-Globin Promoter | Journal of Biological Chemistry | 1995 | 58 |
| 47 | Adolescents' Knowledge of Human Papillomavirus and Cervical Dysplasia | Journal of Pediatric and Adolescent Gynecology | 2000 | 57 |
| 48 | Hypoxia modulates early events in T cell receptor-mediated activation in human T lymphocytes via Kv1.3 channels | Journal of Physiology | 2005 | 57 |
| 49 | A rapid flow cytometric screening test for X‐linked lymphoproliferative disease due to XIAP deficiency | Cytometry Part B - Clinical Cytometry | 2009 | 57 |
| 50 | Proliferation-associated SNF2-like gene (PASG): a SNF2 family member altered in leukemia | Cancer Research | 2000 | 57 |
