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β-Catenin Activation in a Novel Liver Progenitor Cell Type Is Sufficient to Cause Hepatocellular Carcinoma and Hepatoblastoma

Cancer research (Chicago, Ill.), 2014-08, Vol.74 (16), p.4515-4525

2014

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Mediators of receptor tyrosine kinase activation in infantile fibrosarcoma: a Children's Oncology Group study

The Journal of pathology, 2012-09, Vol.228 (1), p.119-130

2012

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WT1 Mutation and 11P15 Loss of Heterozygosity Predict Relapse in Very Low-Risk Wilms Tumors Treated With Surgery Alone: A Children's Oncology Group Study

Journal of clinical oncology, 2011-02, Vol.29 (6), p.698-703

2011

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

Annals of surgery, 2010-03, Vol.251 (3), p.555-558

2010

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Loss of Heterozygosity at 2q37 in Sporadic Wilms' Tumor: Putative Role for miR-562

Clinical cancer research, 2009-10, Vol.15 (19), p.5985-5992

2009

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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: Molecular oncology: genomics

Journal of clinical oncology, 2005, Vol.23 (29), p.7312-7321

2005

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Twenty-four new cases of WT1 germline mutations and review of the literature: Genotype/phenotype correlations for Wilms tumor development

American journal of medical genetics, 2004-06, Vol.127A (3), p.249-257

2004

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Familial Wilms tumor: Inherited Cancer Predisposition

American journal of medical genetics, 2004, Vol.129C (1), p.29-34

2004

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Upregulation of c-MYC in WT1-mutant tumors: assessment of WT1 putative transcriptional targets using cDNA microarray expression profiling of genetically defined Wilms' tumors

Oncogene, 2003-06, Vol.22 (24), p.3821-3826

2003

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Treatment With Nephrectomy Only for Small, Stage I/Favorable Histology Wilms’ Tumor: A Report From the National Wilms’ Tumor Study Group

Journal of clinical oncology, 2001-09, Vol.19 (17), p.3719-3724

2001

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Pulmonary dysplasia, Denys-Drash syndrome and wilms tumor 1 gene mutation in twins

Pediatric nephrology (Berlin, West), 2001-03, Vol.16 (3), p.227-231

2001

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Frequent association of β-catenin and WT1 mutations in Wilms tumors

Cancer research (Chicago, Ill.), 2000-11, Vol.60 (22), p.6288-6292

2000

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Wilms tumor genetics

American journal of medical genetics, 1998-10, Vol.79 (4), p.260-267

Huff, Vicki

1998

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Linkage of familial Wilms' tumor predisposition to chromosome 19 and a two-locus model for the etiology of familial tumors

Cancer research (Chicago, Ill.), 1998-04, Vol.58 (7), p.1387-1390

1998

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Evidence for genetic heterogeneity in familial wilms' tumor

Cancer research (Chicago, Ill.), 1997-05, Vol.57 (10), p.1859-1862

1997

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Microsatellite instability in preinvasive and invasive head and neck squamous carcinoma

The American journal of pathology, 1996-06, Vol.148 (6), p.2067-2072

1996

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Allelic loss and replication errors at microsatellite loci on chromosome 11p in head and neck squamous carcinoma: association with aggressive biological features

Clinical cancer research, 1996-05, Vol.2 (5), p.903-907

1996

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Pleuropulmonary blastoma: A marker for familial disease

The Journal of pediatrics, 1996-02, Vol.128 (2), p.220-224

1996

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Sequential loss of heterozygosity at microsatellite motifs in preinvasive and invasive head and neck squamous carcinoma

Cancer research (Chicago, Ill.), 1995-06, Vol.55 (12), p.2656-2659

1995

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Hereditary hyperparathyroidism-jaw tumor syndrome : the endocrine tumor gene HRPT2 maps to chromosome 1q21-q31

American journal of human genetics, 1995-04, Vol.56 (4), p.944-950

1995

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Loss of heterozygosity for chromosomes 16q and 1p in Wilms' tumors predicts an adverse outcome

Cancer research (Chicago, Ill.), 1994-05, Vol.54 (9), p.2331-2333

1994

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Denys-Drash syndrome: Relating a clinical disorder to genetic alterations in the tumor suppressor gene WT1

The Journal of pediatrics, 1993-11, Vol.123 (5), p.673-678

1993

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Nonlinkage of 16q markers to familial predisposition to wilms tumor

Cancer research (Chicago, Ill.), 1992-11, Vol.52 (21), p.6117-6120

1992

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RNA Expression of the WT1 Gene in Wilms' Tumors in Relation to Histology

JNCI : Journal of the National Cancer Institute, 1992-02, Vol.84 (3), p.181-187

1992

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Smallest region of overlap in Wilms tumor deletions uniquely implicates an 11p13 zinc finger gene as the disease locus

Genomics (San Diego, Calif.), 1991-05, Vol.10 (1), p.293-297

1991

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β-Catenin Activation in a Novel Liver Progenitor Cell Type Is Sufficient to Cause Hepatocellular Carcinoma and Hepatoblastoma

Mediators of receptor tyrosine kinase activation in infantile fibrosarcoma: a Children's Oncology Group study

WT1 Mutation and 11P15 Loss of Heterozygosity Predict Relapse in Very Low-Risk Wilms Tumors Treated With Surgery Alone: A Children's Oncology Group Study

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

Loss of Heterozygosity at 2q37 in Sporadic Wilms' Tumor: Putative Role for miR-562

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: Molecular oncology: genomics

Twenty-four new cases of WT1 germline mutations and review of the literature: Genotype/phenotype correlations for Wilms tumor development

Familial Wilms tumor: Inherited Cancer Predisposition

Upregulation of c-MYC in WT1-mutant tumors: assessment of WT1 putative transcriptional targets using cDNA microarray expression profiling of genetically defined Wilms' tumors

Treatment With Nephrectomy Only for Small, Stage I/Favorable Histology Wilms’ Tumor: A Report From the National Wilms’ Tumor Study Group

Pulmonary dysplasia, Denys-Drash syndrome and wilms tumor 1 gene mutation in twins

Frequent association of β-catenin and WT1 mutations in Wilms tumors

Wilms tumor genetics

Linkage of familial Wilms' tumor predisposition to chromosome 19 and a two-locus model for the etiology of familial tumors

Evidence for genetic heterogeneity in familial wilms' tumor

Microsatellite instability in preinvasive and invasive head and neck squamous carcinoma

Allelic loss and replication errors at microsatellite loci on chromosome 11p in head and neck squamous carcinoma: association with aggressive biological features

Pleuropulmonary blastoma: A marker for familial disease

Sequential loss of heterozygosity at microsatellite motifs in preinvasive and invasive head and neck squamous carcinoma

Hereditary hyperparathyroidism-jaw tumor syndrome : the endocrine tumor gene HRPT2 maps to chromosome 1q21-q31

Loss of heterozygosity for chromosomes 16q and 1p in Wilms' tumors predicts an adverse outcome

Denys-Drash syndrome: Relating a clinical disorder to genetic alterations in the tumor suppressor gene WT1

Nonlinkage of 16q markers to familial predisposition to wilms tumor

RNA Expression of the WT1 Gene in Wilms' Tumors in Relation to Histology

Smallest region of overlap in Wilms tumor deletions uniquely implicates an 11p13 zinc finger gene as the disease locus

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