E. Perlman

P. Argani, F. Askin, E. Perlman, 2000, Pediatric and developmental pathology : the official journal of the Society for Pediatric Pathology and the Paediatric Pathology Society.

Pediatric Germ Cell Tumors: Protocol Update for Pathologists

E. Perlman, E. Hawkins, 1998, Pediatric and developmental pathology : the official journal of the Society for Pediatric Pathology and the Paediatric Pathology Society.

The pulmonary vasculature in meconium aspiration.

G. Hutchins, E. Perlman, G. Moore, 1989, Human pathology.

Chromosome analysis of nine osteosarcomas

C. Griffin, E. Perlman, A. Hawkins, 1994, Genes, chromosomes & cancer.

Genetic analysis of mediastinal nonseminomatous germ cell tumors in children and adolescents

M. Fritsch, E. Perlman, D. Harms, 2002, Genes, chromosomes & cancer.

Outcomes of patients with revised stage I clear cell sarcoma of kidney treated in National Wilms Tumor Studies 1-5.

J. Dome, P. Grundy, E. Perlman, 2013, International journal of radiation oncology, biology, physics.

Comparison of diagnostic performance of CT and MRI for abdominal staging of pediatric renal tumors: a report from the Children’s Oncology Group

S. Servaes, A. Naranjo, J. Dome, 2014, Pediatric Radiology.

Bladder wall abnormalities in myelodysplastic bladders: a computer assisted morphometric analysis.

M. Becich, H. Lepor, E. Shapiro, 1991, The Journal of urology.

Detection of the ETV6-NTRK3 Chimeric RNA of Infantile Fibrosarcoma/Cellular Congenital Mesoblastic Nephroma in Paraffin-Embedded Tissue: Application to Challenging Pediatric Renal Stromal Tumors

P. Argani, M. Fritsch, E. Perlman, 2000, Modern Pathology.

Clinical and Pathologic Spectrum of 46,XY Gonadal Dysgenesis: Its Relevance to the Understanding of Sex Differentiation

E. Perlman, C. Migeon, G. Berkovitz, 1991, Medicine.

Surgical protocol violations in children with renal tumors provides an opportunity to improve pediatric cancer care: a report from the Children's Oncology Group

A. Naranjo, J. Dome, E. Perlman, 2016, Pediatric blood & cancer.

DNA content of ovarian immature teratomas and malignant germ cell tumors.

E. Perlman, B. A. Baker, E. Hawkins, 1998, Gynecologic oncology.

Treatment of Stage IV Favorable Histology Wilms Tumor With Lung Metastases: A Report From the Children's Oncology Group AREN0533 Study.

James R. Anderson, J. Gastier-Foster, J. Dome, 2018, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

Pediatric Renal Tumors: Practical Updates for the Pathologist

E. Perlman, 2005, Pediatric and developmental pathology : the official journal of the Society for Pediatric Pathology and the Paediatric Pathology Society.

MIC2 analysis in pediatric lymphomas and leukemias.

M. Link, E. Perlman, P. Dickman, 1994, Human pathology.

Advances in Brief Recurrent Involvement of 2 p 23 in Inflammatory Myofibroblastic Tumors

C. Griffin, E. Perlman, C. Henkle, 1999 .

A prospective study of pediatric and adolescent renal cell carcinoma: A report from the Children's Oncology Group AREN0321 study

J. Dome, E. Perlman, N. Daw, 2020, Cancer.

Bilateral Wilms' tumors with progressive or nonresponsive disease.

P. Argani, D. Green, E. Perlman, 2006, Journal of pediatric surgery.

Deletion mapping of 6q21-26 and frequency of 1p36 deletion in childhood endodermal sinus tumors by microsatellite analysis

M. Fritsch, E. Perlman, Jie Hu, 2001, Oncogene.

Genetic analysis of childhood endodermal sinus tumors by comparative genomic hybridization.

Jie Hu, E. Perlman, R. Castleberry, 2000, Journal of pediatric hematology/oncology.

MIC2 analysis of small cell carcinoma.

F. Askin, J. Lumadue, E. Perlman, 1994, American journal of clinical pathology.

Cytogenetic analysis of childhood endodermal sinus tumors: a Pediatric Oncology Group study.

C. Griffin, E. Perlman, E. Hawkins, 1994, Pediatric pathology.

Apurinic/apyrimidinic endonuclease expression in pediatric yolk sac tumors.

E. Perlman, M. Kelley, M. Davis, 2000, Anticancer research.

Periostin is Upregulated in Coronary Arteriopathy in Kawasaki Disease and is a Potential Diagnostic Biomarker

M. Lingen, E. Perlman, S. Shulman, 2014, The Pediatric infectious disease journal.

The classification of pediatric and young adult renal cell carcinomas registered on the children's oncology group (COG) protocol AREN03B2 after focused genetic testing

D. Kirschmann, J. Dome, E. Perlman, 2018, Cancer.

Congenital disseminated malignant rhabdoid tumor: a distinct clinicopathologic entity demonstrating abnormalities of chromosome 22q11.

J. Biegel, E. Perlman, D. Belchis, 1999, The American journal of surgical pathology.

Infantile Extrarenal Rhabdoid Tumor

C. Griffin, E. Perlman, Syed Z. Ali, 1998, Pediatric and developmental pathology : the official journal of the Society for Pediatric Pathology and the Paediatric Pathology Society.

The Spectrum of Metanephric Adenofibroma and Related Lesions: Clinicopathologic Study of 25 Cases From the National Wilms Tumor Study Group Pathology Center

P. Argani, D. Green, E. Perlman, 2001, The American journal of surgical pathology.

Clinicopathologic findings predictive of relapse in children with stage III favorable-histology Wilms tumor.

N. Breslow, James R. Anderson, D. Green, 2013, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

Impact of the First Generation of Children's Oncology Group Clinical Trials on Clinical Practice for Wilms Tumor.

M. Chintagumpala, J. Dome, P. Grundy, 2021, Journal of the National Comprehensive Cancer Network : JNCCN.

Comparative genomic hybridization of esophageal and gastroesophageal adenocarcinomas shows consensus areas of DNA gain and loss

C. Moskaluk, E. Perlman, Jie Hu, 1998, Genes, chromosomes & cancer.

The Frozen Section Yesterday and Today: Pediatric Solid Tumors—Crucial Issues

P. Burger, C. Paidas, E. Perlman, 2001, Pediatric and developmental pathology : the official journal of the Society for Pediatric Pathology and the Paediatric Pathology Society.

Haplotype-resolved germline and somatic alterations in renal medullary carcinomas

Thomas P. Howard, W. Hahn, M. Meyerson, 2021, Genome medicine.

[Nephrogenic rests and nephroblastomatosis].

E. Perlman, F. Dijoud, L. Boccon-Gibod, 2004, Annales de pathologie.

POU5F1 (OCT3/4) identifies cells with pluripotent potential in human germ cell tumors.

J. Kononen, G. Sauter, C. Bokemeyer, 2003, Cancer research.

Analysis of the SRY gene in gonadal tissue of subjects with 46,XY gonadal dysgenesis.

E. Perlman, J. McLaughlin, G. Berkovitz, 1997, Journal of Clinical Endocrinology and Metabolism.

Combined Leydig cell and Sertoli cell dysfunction in 46,XX males lacking the sex determining region Y gene.

B. Turner, E. Perlman, G. Berkovitz, 1995, American journal of medical genetics.

Insights on neoplastic stem cells from gel‐based proteomics of childhood germ cell tumors

E. Perlman, W. Haskins, S. Eedala, 2012, Pediatric blood & cancer.

Patterns of Congenital Lower Urinary Tract Obstructive Uropathy: Relation to Abnormal Prostate and Bladder Development and the Prune Belly Syndrome

G. Hutchins, M. Fritsch, E. Perlman, 2001, Pediatric and developmental pathology : the official journal of the Society for Pediatric Pathology and the Paediatric Pathology Society.

Genomic Hybridization Genetic Analysis of Ovarian Germ Cell Tumors by Comparative Updated

C. Griffin, E. Perlman, M. Riopel, 2006 .

Genetic analysis of ovarian germ cell tumors by comparative genomic hybridization.

C. Griffin, E. Perlman, M. Riopel, 1998, Cancer research.

Embryonic testicular regression sequence: a part of the clinical spectrum of 46,XY gonadal dysgenesis.

E. Perlman, C. Migeon, G. Berkovitz, 1994, American journal of medical genetics.

Blood Group Antigen Expression in Dysplasia: and Adenocarcinoma of the Prostate

J. Epstein, E. Perlman, 1990, The American journal of surgical pathology.

Randomized comparison of combination chemotherapy with etoposide, bleomycin, and either high-dose or standard-dose cisplatin in children and adolescents with high-risk malignant germ cell tumors: a pediatric intergroup study--Pediatric Oncology Group 9049 and Children's Cancer Group 8882.

W. London, E. Perlman, P. Colombani, 2004, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

Principles and Practice of Pediatric Oncology (Fourth edition)

J. Dome, P. Grundy, E. Perlman, 2004 .

Numerical sex chromosomal abnormalities in pineal teratomas by cytogenetic analysis and fluorescence in situ hybridization.

C. Griffin, E. Perlman, P. Phillips, 1995, Laboratory investigation; a journal of technical methods and pathology.

Patterns of Congenital Lower Urinary Tract Obstructive Uropathy (Reply)

G. Hutchins, M. Fritsch, E. Perlman, 2003 .

Inhibin and Epithelial Membrane Antigen Immunohistochemistry Assist in the Diagnosis of Sex Cord‐Stromal Tumors and Provide Clues to the Histogenesis of Hypercalcemic Small Cell Carcinomas

M. Sherman, R. Kurman, E. Perlman, 1998, International journal of gynecological pathology : official journal of the International Society of Gynecological Pathologists.

Analysis of Smooth Muscle and Collagen Subtypes in the Normal Newborn and Bladder Exstrophy Patient

Benjamin R. Lee, A. Partin, E. Perlman, 1999 .

Evaluation of smooth muscle and collagen subtypes in normal newborns and those with bladder exstrophy.

A. Partin, B. Lee, E. Perlman, 1996, The Journal of urology.

Myogenin is a Specific Marker for Rhabdomyosarcoma: An Immunohistochemical Study in Paraffin-Embedded Tissues

M. Raffeld, E. Perlman, M. Tsokos, 2000, Modern Pathology.

Abnormal gonadal differentiation in two subjects with ambiguous genitalia, Mullerian structures, and normally developed testes: Evidence for a defect in gonadal ridge development

J. Pelletier, E. Perlman, C. Migeon, 1996, Human Genetics.

Clinical and pathologic spectrum of 46, XY gonadal dysgenesis

E. Perlman, C. Migeon, G. Berkovitz, 1991 .

Altered smooth muscle development and innervation in the lower genitourinary and gastrointestinal tract of the male human fetus with myelomeningocele.

G. Hutchins, H. Lepor, E. Shapiro, 1998, The Journal of urology.

Dose-intensified compared with standard chemotherapy for nonmetastatic Ewing sarcoma family of tumors: a Children's Oncology Group Study.

P. Leavey, J. Healey, M. Devidas, 2009, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

Erratum: PGBD5 promotes site-specific oncogenic mutations in human tumors

P. O’Reilly, P. Elliott, D. Levy, 2017, Nature Genetics.

A genome-wide screen for normally methylated human CpG islands that can identify novel imprinted genes.

Andrew P Feinberg, A. Feinberg, E. Perlman, 2002, Genome research.

Genome-Wide Profiles of Extra-cranial Malignant Rhabdoid Tumors Reveal Heterogeneity and Dysregulated Developmental Pathways.

Steven J. M. Jones, Jenny Q. Qian, Richard A. Moore, 2016, Cancer cell.

Pan-cancer genome and transcriptome analyses of 1,699 pediatric leukemias and solid tumors

Xin Zhou, Charles Gawad, Li Dong, 2018, Nature.

TCF21 hypermethylation in genetically quiescent clear cell sarcoma of the kidney

D. Gerhard, J. Khan, J. Gastier-Foster, 2015, Oncotarget.

Genomic alterations in distal bile duct carcinoma by comparative genomic hybridization and karyotype analysis

R. Hruban, S. Kern, C. Yeo, 1999, Genes, chromosomes & cancer.

PGBD5 promotes site-specific oncogenic mutations in human tumors

Z. Weng, D. Torrents, S. Armstrong, 2017, Nature Genetics.

Human PGBD5 DNA transposase promotes site-specific oncogenic mutations in rhabdoid tumors

Z. Weng, D. Torrents, S. Armstrong, 2017, Klinische Pädiatrie.

Recurrent involvement of 2p23 in inflammatory myofibroblastic tumors.

C. Griffin, E. Perlman, C. Henkle, 1999, Cancer research.

Absence of EWS/FLI1 fusion in olfactory neuroblastomas indicates these tumors do not belong to the Ewing's sarcoma family.

P. Meltzer, P. Meltzer, E. Perlman, 1999, Human pathology.

Morphology and DNA content analysis in the evaluation of first trimester placentas for partial hydatidiform mole (PHM).

R. Kurman, E. Perlman, B. Ronnett, 2000, Human pathology.

Rhabdoid Tumor: Gene Expression Clues to Pathogenesis and Potential Therapeutic Targets

Chiang-Ching Huang, S. Gadd, S. Sredni, 2010, Laboratory Investigation.

Treatment of metastatic Ewing sarcoma/primitive neuroectodermal tumor of bone: Evaluation of increasing the dose intensity of chemotherapy—a report from the Children's Oncology Group

Chris L. Fryer, R. Goldsby, S. Donaldson, 2007, Pediatric blood & cancer.

Treatment of anaplastic histology Wilms' tumor: results from the fifth National Wilms' Tumor Study.

N. Breslow, R. Macklis, D. Green, 2006, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

Treatment of metastatic Ewing's sarcoma or primitive neuroectodermal tumor of bone: evaluation of combination ifosfamide and etoposide--a Children's Cancer Group and Pediatric Oncology Group study.

S. Donaldson, N. Tarbell, M. Link, 2004, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

The product of the imprinted H19 gene is an oncofetal RNA.

V. Erdmann, A. Hochberg, N. de Groot, 1997, Molecular pathology : MP.

hTERT gene amplification and increased mRNA expression in central nervous system embryonal tumors.

D. Brat, C. Dang, P. Burger, 2003, The American journal of pathology.

Validation of a prognostic multi‐gene signature in high‐risk neuroblastoma using the high throughput digital NanoString nCounter™ system

Hiroyuki Shimada, Peter Pytel, M John Hicks, 2014, Molecular oncology.

TP53 Mutational Status Is a Potential Marker for Risk Stratification in Wilms Tumour with Diffuse Anaplasia

James R. Anderson, N. Sebire, T. Chagtai, 2014, PloS one.

Molecular profiling reveals frequent gain of MYCN and anaplasia‐specific loss of 4q and 14q in wilms tumor

A. Ashworth, James R. Anderson, T. Chagtai, 2011, Genes, chromosomes & cancer.

Clear Cell Sarcoma of the Kidney: Up-regulation of Neural Markers with Activation of the Sonic Hedgehog and Akt Pathways

Chiang-Ching Huang, Chiang-Ching Huang, Colleen Cutcliffe, 2005, Clinical Cancer Research.

Loss of imprinting of insulin-like growth factor-II (IGF2) gene in distinguishing specific biologic subtypes of Wilms tumor.

A. Feinberg, K. Broman, D. Haber, 2001, Journal of the National Cancer Institute.

Prohibitin is a prognostic marker and therapeutic target to block chemotherapy resistance in Wilms' tumor.

A. Letai, A. Naranjo, H. Steen, 2019, JCI insight.

Prohibitin is a prognostic marker of relapse and therapeutic target to block chemotherapy resistance in Wilms tumor

A. Letai, A. Naranjo, H. Steen, 2018 .

Visceral primitive peripheral neuroectodermal tumors: a clinicopathologic and molecular study.

J. Pfeifer, E. Perlman, L. Dehner, 2001, Human pathology.

Outcome of patients with stage II/favorable histology wilms tumor with and without local tumor spill: A report from the National Wilms Tumor Study Group

N. Breslow, D. Green, A. Evans, 2014, Pediatric blood & cancer.

High telomerase reverse transcriptase (hTERT) messenger RNA level correlates with tumor recurrence in patients with favorable histology Wilms' tumor.

N. Breslow, S. Sukumar, L. Carey, 1999, Cancer research.

Kidney Preservation and Wilms Tumor Development in Children with Diffuse Hyperplastic Perilobar Nephroblastomatosis: A Report from the Children’s Oncology Group Study AREN0534

M. Chintagumpala, J. Dome, E. Perlman, 2022, Annals of Surgical Oncology.

Long-term Outcomes for Infants With Very Low Risk Wilms Tumor Treated With Surgery Alone in National Wilms Tumor Study-5

N. Breslow, James R. Anderson, R. Macklis, 2010, Annals of surgery.

Age distributions, birth weights, nephrogenic rests, and heterogeneity in the pathogenesis of Wilms tumor

N. Breslow, A. Reeve, E. Perlman, 2006, Pediatric blood & cancer.

Micropapillary serous carcinoma of the ovary has distinct patterns of chromosomal imbalances by comparative genomic hybridization compared with atypical proliferative serous tumors and serous carcinomas.

T. Ried, R. Kurman, K. Heselmeyer-Haddad, 2002, Human pathology.

“Large Cell/Anaplastic” Medulloblastomas: A Pediatric Oncology Group Study

P. Burger, H. Friedman, E. Perlman, 2000, Journal of neuropathology and experimental neurology.

DICER1 mutations in childhood cystic nephroma and its relationship to DICER1-renal sarcoma

Gretchen M. Williams, H. Cathro, P. Faria, 2014, Modern Pathology.

Desmoplastic Small Round Cell Tumor of the Kidney in Childhood

F. Barr, T. Collins, A. Perez-Atayde, 2007, The American journal of surgical pathology.

Association of Chromosome 1q Gain With Inferior Survival in Favorable-Histology Wilms Tumor: A Report From the Children's Oncology Group.

James R. Anderson, J. Dome, P. Grundy, 2016, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

International cancer seminars: a focus on kidney cancer.

T. Frayling, S. Chanock, W. Linehan, 2016, Annals of oncology : official journal of the European Society for Medical Oncology.

Clear cell sarcoma of the kidney: a review of 351 cases from the National Wilms Tumor Study Group Pathology Center.

N. Breslow, P. Argani, D. Green, 2000, The American journal of surgical pathology.

Results of the First Prospective Multi-institutional Treatment Study in Children With Bilateral Wilms Tumor (AREN0534): A Report From the Children's Oncology Group

M. Chintagumpala, P. Grundy, E. Perlman, 2017, Annals of surgery.

Outcome analysis of stage I epithelial‐predominant favorable‐histology Wilms tumors: A report from Children's Oncology Group study AREN03B2

J. Dome, E. Perlman, Yeonil Kim, 2020, Cancer.

Children's Oncology Group's 2013 blueprint for research: Renal tumors

James R. Anderson, A. Naranjo, J. Dome, 2013, Pediatric blood & cancer.

Reply to B. Royer-Pokora et al

D. Green, J. Dome, P. Grundy, 2011 .

Treatment with nephrectomy only for small, stage I/favorable histology Wilms' tumor: a report from the National Wilms' Tumor Study Group.

N. Breslow, R. Macklis, D. Green, 2001, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

Detection of preoperative wilms tumor rupture with CT: a report from the Children's Oncology Group.

A. Naranjo, J. Dome, P. Grundy, 2013, Radiology.

Bilateral Wilms' tumor with anaplasia: lessons from the National Wilms' Tumor Study.

P. Argani, D. Green, P. Grundy, 2006, Journal of pediatric surgery.

β-Catenin and K-RAS synergize to form primitive renal epithelial tumors with features of epithelial Wilms' tumors.

H. Moses, P. Clark, M. D. de Caestecker, 2011, The American journal of pathology.

Expression of WT-1, Bcl-2, and CD34 by Primary Renal Spindle Cell Tumors in Children

E. Perlman, D. A. Hill, L. Shao, 2004, Pediatric and developmental pathology : the official journal of the Society for Pediatric Pathology and the Paediatric Pathology Society.

Is esthesioneuroblastoma a peripheral neuroectodermal tumor?

F. Askin, E. Perlman, R. Nelson, 1995, Human pathology.

Devastating sequelae of alloimmune thrombocytopenia: an entity that deserves more attention.

K. Blakemore, E. Perlman, J. Shumway, 1996, The Journal of maternal-fetal medicine.

Ewing Sarcoma/Primitive Neuroectodermal Tumor of the Chest Wall: Impact of Initial Versus Delayed Resection on Tumor Margins, Survival, and Use of Radiation Therapy

N. Tarbell, M. Devidas, M. Gebhardt, 2003, Annals of surgery.

Rhabdoid tumor of the kidney in the National Wilms' Tumor Study: age at diagnosis as a prognostic factor.

N. Breslow, D. Green, G. Tomlinson, 2005, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

Results of Treatment for Patients With Multicentric or Bilaterally Predisposed Unilateral Wilms Tumor (AREN0534): A report from the Children's Oncology Group

M. Chintagumpala, J. Dome, P. Grundy, 2020, Cancer.

Classification of malignant pediatric renal tumors by gene expression

P. Sorensen, Chiang-Ching Huang, Colleen Cutcliffe, 2006, Pediatric blood & cancer.

Anaplastic Sarcoma of the Kidney: A Clinicopathologic Study of 20 Cases of a New Entity With Polyphenotypic Features

A. Kelsey, E. Perlman, G. Vujanić, 2007, The American journal of surgical pathology.

Treatment of stage I anaplastic Wilms' tumour: a report from the Children's Oncology Group AREN0321 study.

J. Dome, P. Grundy, E. Perlman, 2019, European journal of cancer.

Neuroblastoma and peripheral neuroectodermal tumors.

F. Askin, E. Perlman, Frederic B. Askin, 1998, American journal of clinical pathology.

Treatment outcomes in adults with favorable histologic type Wilms tumor-an update from the National Wilms Tumor Study Group.

N. Breslow, B. Nan, D. Green, 2004, International journal of radiation oncology, biology, physics.

The Stuck Twin Phenomenon: Experience with Serial Therapeutic Amniocentesis

K. Blakemore, E. Perlman, J. Wax, 1992 .

MLLT1 YEATS domain mutations in clinically distinctive Favourable Histology Wilms tumours

Richard A. Moore, Daoud M. Meerzaman, D. Wheeler, 2015, Nature Communications.

A prospective study of pediatric renal cell carcinoma: A report from the Children’s Oncology Group study AREN0321.

J. Dome, E. Perlman, N. Daw, 2018 .

Methylation-Associated Silencing of the Heat Shock Protein 47 Gene in Human Neuroblastoma

Qiwei Yang, S. Cohn, E. Perlman, 2004, Cancer Research.

Subsets of Very Low Risk Wilms Tumor Show Distinctive Gene Expression, Histologic, and Clinical Features

Norman Breslow, Chiang-Ching Huang, N. Breslow, 2009, Clinical Cancer Research.

Loss of heterozygosity for chromosomes 1p and 16q is an adverse prognostic factor in favorable-histology Wilms tumor: a report from the National Wilms Tumor Study Group.

N. Breslow, R. Macklis, D. Green, 2005, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

Diagnostic Utility of Pax8, Pax2, and NGFR Immunohistochemical Expression in Pediatric Renal Tumors

N. Arva, E. Perlman, J. Bonadio, 2017, Applied immunohistochemistry & molecular morphology : AIMM.

High telomerase RNA expression level is an adverse prognostic factor for favorable-histology Wilms' tumor.

N. Breslow, D. Green, J. Dome, 2005, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

Clinically relevant subsets identified by gene expression patterns support a revised ontogenic model of Wilms tumor: a Children's Oncology Group Study.

Chiang-Ching Huang, D. Green, S. Gadd, 2012, Neoplasia.

Genetic and Genetic Expression Analyses of Clear Cell Sarcoma of the Kidney

P. Grundy, M. Fritsch, E. Perlman, 2003, Laboratory Investigation.

Erratum to Recurrent DGCR8, DROSHA, and SIX Homeodomain Mutations in Favorable Histology Wilms Tumors [Cancer Cell., 27, 286-297 (2015)] DOI: 10.1016/j.ccell.2015.02.008

Richard A. Moore, D. Wheeler, D. Gerhard, 2015 .

Gain of 1q is associated with inferior event‐free and overall survival in patients with favorable histology Wilms tumor: A report from the Children's Oncology Group

James R. Anderson, J. Dome, P. Grundy, 2013, Cancer.

Pediatric cystic nephromas: distinctive features and frequent DICER1 mutations.

J. Dome, E. Perlman, Lan Gellert, 2016, Human pathology.

Management of adults with Wilms’ tumor: recommendations based on international consensus

G. Gatta, M. Coppes, K. Pritchard-Jones, 2011, Expert review of anticancer therapy.

Impact of cyclophosphamide and etoposide on outcome of clear cell sarcoma of the kidney treated on the National Wilms Tumor Study‐5 (NWTS‐5)

James R. Anderson, D. Green, P. Grundy, 2018, Pediatric blood & cancer.

Expanding the Spectrum of Renal Tumors in Children: Primary Renal Myoepithelial Carcinomas With a Novel EWSR1-KLF15 Fusion

E. Perlman, J. Geller, L. Jennings, 2016, The American journal of surgical pathology.

Mediastinal Germ Cell Tumours (MGCT) in Children and Adolescents: Age Correlates with Histological Differentiation, Genetic Profiles and Clinical Outcome

M. Fritsch, E. Perlman, D. Harms, 2002 .

Imaging Characteristics of Nephrogenic Rests Versus Small Wilms Tumors: A Report From the Children's Oncology Group Study AREN03B2.

J. Sandberg, S. Servaes, J. Dome, 2020, AJR. American journal of roentgenology.

Activity of Vincristine and Irinotecan in Diffuse Anaplastic Wilms Tumor and Therapy Outcomes of Stage II to IV Disease: Results of the Children's Oncology Group AREN0321 Study.

James R. Anderson, J. Dome, P. Grundy, 2020, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

Mucinous Cancers have Fewer Genomic Alterations than More Common Classes of Breast Cancer

E. Gabrielson, E. Garrett, R. Anbazhagan, 2002, Breast Cancer Research and Treatment.

TCF21 hypermethylation regulates renal tumor cell clonogenic proliferation and migration

R. Giles, E. Perlman, H. Gremmels, 2017, Molecular oncology.

Expression of WT-1, Bcl-2, and CD34 by primary renal spindle cell tumors in children

E. Perlman, D. A. Hill, L. Shao, 2004 .

Metanephric stromal tumor: a rare benign pediatric renal mass.

E. Perlman, J. Gearhart, F. Ferrer, 2001, Urology.

Hepatic Metastasis at Diagnosis in Patients With Wilms Tumor is not an Independent Adverse Prognostic Factor for Stage IV Wilms Tumor: A Report From the Children's Oncology Group/National Wilms Tumor Study Group

James R. Anderson, D. Green, J. Dome, 2009, Annals of surgery.

Neural innervation of the newborn exstrophic bladder: an immunohistochemical study.

E. Perlman, R. Mathews, J. Gearhart, 1999, The Journal of urology.

Ewing's sarcoma--routine diagnostic utilization of MIC2 analysis: a Pediatric Oncology Group/Children's Cancer Group Intergroup Study.

F. Askin, M. Link, E. Perlman, 1994, Human pathology.

Three Linked Vasculopathic Processes Characterize Kawasaki Disease: A Light and Transmission Electron Microscopic Study

J. Orenstein, E. Perlman, S. Shulman, 2012, PloS one.

Primary cutaneous neuroendocrine tumors. Diagnostic use of cytogenetic and MIC2 analysis.

C. Griffin, J. Lumadue, E. Perlman, 1995, Cancer genetics and cytogenetics.

Cobalamin C defect associated with hemolytic-uremic syndrome.

D. Valle, E. Perlman, M. Geraghty, 1992, The Journal of pediatrics.

Congenital capillary proliferation of the kidney: a distinctive renal vascular lesion of childhood.

E. Perlman, P. Dickman, P. North, 2017, Human pathology.

Activation of Wnt/β-Catenin Signaling in Distinct Histologic Subtypes of Human Germ Cell Tumors

M. Fritsch, E. Perlman, D. Schneider, 2006 .

Anthropomorphic measurements and event‐free survival in patients with favorable histology Wilms tumor: A report from the Children's Oncology Group

James R. Anderson, D. Green, J. Dome, 2009, Pediatric blood & cancer.

Functional genomic comparison of lineage-related human bladder cancer cell lines with differing tumorigenic and metastatic potentials by spectral karyotyping, comparative genomic hybridization, and a novel method of positional expression profiling.

K. Arden, D. Theodorescu, Michael A. Harding, 2002, Cancer research.

BCOR internal tandem duplications in clear cell sarcoma of the kidney

S. Gadd, E. Perlman, M. M. Heuvel‐Eibrink, 2016, Genes, chromosomes & cancer.

Outcome of clear cell sarcoma of the kidney (CCSK) treated on the National Wilms Tumor Study-5 (NWTS).

N. Breslow, D. Green, M. Coppes, 2006, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

Performance Characteristics of a Reverse Transcriptase–Polymerase Chain Reaction Assay for the Detection of Tumor-specific Fusion Transcripts from Archival Tissue

P. Argani, M. Fritsch, E. Perlman, 2003, Pediatric and developmental pathology : the official journal of the Society for Pediatric Pathology and the Paediatric Pathology Society.

Pathology of Wilms' tumour in International Society of Paediatric Oncology (SIOP) and Children's oncology group (COG) renal tumour studies: Similarities and differences

E. Perlman, G. Vujanić, P. Collini, 2022, Histopathology.

Sexual discordance in monozygotic twins.

G. Hutchins, W. Neuman, K. Blakemore, 1990, American journal of medical genetics.

Integrins alpha4 and alpha M, collagen1A1, and matrix metalloproteinase 7 are upregulated in acute Kawasaki disease vasculopathy

J. Orenstein, M. Lingen, E. Perlman, 2012, Pediatric Research.

A phase 2 study of vincristine and irinotecan in metastatic diffuse anaplastic Wilms tumor: Results from the Children’s Oncology Group AREN0321 study.

James R. Anderson, J. Dome, P. Grundy, 2014 .

Activation of Wnt/beta-catenin signaling in distinct histologic subtypes of human germ cell tumors.

M. Fritsch, E. Perlman, D. Schneider, 2006, Pediatric and developmental pathology : the official journal of the Society for Pediatric Pathology and the Paediatric Pathology Society.

Clinical outcome and biological predictors of relapse following nephrectomy only for very low risk Wilms tumor (VLR WT): A report from Children’s Oncology Group AREN0532.

James R. Anderson, J. Dome, P. Grundy, 2015 .

“Bronchitis” obliterans and prolonged transient hypogammaglobulinemia in a child

G. Loughlin, E. Perlman, G. Taylor, 1993, Pediatric pulmonology.

Comparative genomic hybridization analysis of hepatoblastomas

Jie Hu, E. Perlman, B. A. Baker, 2000, Genes, chromosomes & cancer.

Omission of lung radiation in patients with stage IV favorable histology Wilms Tumor (FHWT) showing complete lung nodule response after chemotherapy: A report from Children's Oncology Group study AREN0533.

James R. Anderson, J. Dome, P. Grundy, 2015 .

Treatment of stage IV favorable histology Wilms tumor with incomplete lung metastasis response after chemotherapy: A report from Children's Oncology Group study AREN0533.

James R. Anderson, J. Dome, P. Grundy, 2014 .

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