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Malignant rhabdoid tumors originating within and outside the central nervous system are clinically and molecularly heterogeneous

Acta neuropathologica, 2018-08, Vol.136 (2), p.315-326

2018

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Forty-five patient-derived xenografts capture the clinical and biological heterogeneity of Wilms tumor

Nature communications, 2019-12, Vol.10 (1), p.5806-13, Article 5806

2019

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TERT Expression in Wilms Tumor Is Regulated by Promoter Mutation or Hypermethylation, WT1, and N-MYC

Cancers, 2022-03, Vol.14 (7), p.1655

2022

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Establishment and Characterization of the First Pediatric Adrenocortical Carcinoma Xenograft Model Identifies Topotecan as a Potential Chemotherapeutic Agent

Clinical cancer research, 2013-04, Vol.19 (7), p.1740-1747

2013

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The E180splice mutation in the GHR gene causing Laron syndrome: Witness of a Sephardic Jewish exodus from the Iberian Peninsula to the New World?

American journal of medical genetics. Part A, 2014-05, Vol.164A (5), p.1204-1208

2014

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Multiple TP53 p.R337H haplotypes and implications for tumor susceptibility

HGG advances, 2024-01, Vol.5 (1), p.100244-100244, Article 100244

2024

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Pathological and Genetic Stratification for Management of Adrenocortical Carcinoma

The journal of clinical endocrinology and metabolism, 2022-03, Vol.107 (4), p.1159-1169

2022

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An update on the central nervous system manifestations of Li–Fraumeni syndrome

Acta neuropathologica, 2020-04, Vol.139 (4), p.669-687

2020

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Acromegaly: correlation between expression of somatostatin receptor subtypes and response to octreotide-lar treatment

Pituitary, 2009, Vol.12 (4), p.297-303

2009

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Treatment of Pediatric Adrenocortical Carcinoma With Surgery, Retroperitoneal Lymph Node Dissection, and Chemotherapy: The Children's Oncology Group ARAR0332 Protocol

Journal of clinical oncology, 2021-08, Vol.39 (22), p.2463-2473

2021

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Familial predisposition to adrenocortical tumors: Clinical and biological features and management strategies

Baillière's best practice & research. Clinical endocrinology & metabolism, 2010-06, Vol.24 (3), p.477-490

2010

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Genomic landscape of paediatric adrenocortical tumours

Nature communications, 2015-03, Vol.6 (1), p.6302-6302, Article 6302

2015

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The International Pediatric Adrenocortical Tumor Registry initiative: Contributions to clinical, biological, and treatment advances in pediatric adrenocortical tumors

Molecular and cellular endocrinology, 2012-03, Vol.351 (1), p.37-43

2012

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The degree of external genitalia virilization in girls with 21-hydroxylase deficiency appears to be influenced by the CAG repeats in the androgen receptor gene

Clinical endocrinology (Oxford), 2008-02, Vol.68 (2), p.226-232

2008

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The Common Germline TP53-R337H Mutation Is Hypomorphic and Confers Incomplete Penetrance and Late Tumor Onset in a Mouse Model

Cancer research (Chicago, Ill.), 2021-05, Vol.81 (9), p.2442-2456

2021

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Clinical and Functional Significance of TP53 Exon 4-Intron 4 Splice Junction Variants

Molecular cancer research, 2022-02, Vol.20 (2), p.207-216

2022

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A common polymorphism in the retinoic acid pathway modifies adrenocortical carcinoma age-dependent incidence

British journal of cancer, 2020-04, Vol.122 (8), p.1231-1241

2020

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Insulin-like growth factor 1 gene (CA)n repeats and a variable number of tandem repeats of the insulin gene in Brazilian children born small for gestational age

Clinics (São Paulo, Brazil), 2013-06, Vol.68 (6), p.785-791

2013

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XAF1 as a modifier of p53 function and cancer susceptibility

Science advances, 2020-06, Vol.6 (26), p.eaba3231-eaba3231

2020

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TP53-Associated Pediatric Malignancies

Genes & cancer, 2011-04, Vol.2 (4), p.485-490

2011

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From uncertainty to pathogenicity: clinical and functional interrogation of a rare TP53 in-frame deletion

Cold Spring Harbor molecular case studies, 2019-08, Vol.5 (4), p.a003921

2019

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Differential elemental distribution of retained particles along the respiratory tract

Inhalation toxicology, 2011-07, Vol.23 (8), p.459-467

2011

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Genetic and epigenetic features of bilateral Wilms tumor predisposition in patients from the Children's Oncology Group AREN18B5-Q

Malignant rhabdoid tumors originating within and outside the central nervous system are clinically and molecularly heterogeneous

Forty-five patient-derived xenografts capture the clinical and biological heterogeneity of Wilms tumor

TERT Expression in Wilms Tumor Is Regulated by Promoter Mutation or Hypermethylation, WT1, and N-MYC

Establishment and Characterization of the First Pediatric Adrenocortical Carcinoma Xenograft Model Identifies Topotecan as a Potential Chemotherapeutic Agent

The E180splice mutation in the GHR gene causing Laron syndrome: Witness of a Sephardic Jewish exodus from the Iberian Peninsula to the New World?

Multiple TP53 p.R337H haplotypes and implications for tumor susceptibility

Pathological and Genetic Stratification for Management of Adrenocortical Carcinoma

An update on the central nervous system manifestations of Li–Fraumeni syndrome

Acromegaly: correlation between expression of somatostatin receptor subtypes and response to octreotide-lar treatment

Treatment of Pediatric Adrenocortical Carcinoma With Surgery, Retroperitoneal Lymph Node Dissection, and Chemotherapy: The Children's Oncology Group ARAR0332 Protocol

Familial predisposition to adrenocortical tumors: Clinical and biological features and management strategies

Genomic landscape of paediatric adrenocortical tumours

The International Pediatric Adrenocortical Tumor Registry initiative: Contributions to clinical, biological, and treatment advances in pediatric adrenocortical tumors

The degree of external genitalia virilization in girls with 21-hydroxylase deficiency appears to be influenced by the CAG repeats in the androgen receptor gene

The Common Germline TP53-R337H Mutation Is Hypomorphic and Confers Incomplete Penetrance and Late Tumor Onset in a Mouse Model

A Rare TP53 Mutation Predominant in Ashkenazi Jews Confers Risk of Multiple Cancers

Clinical and Functional Significance of TP53 Exon 4-Intron 4 Splice Junction Variants

A common polymorphism in the retinoic acid pathway modifies adrenocortical carcinoma age-dependent incidence

Insulin-like growth factor 1 gene (CA)n repeats and a variable number of tandem repeats of the insulin gene in Brazilian children born small for gestational age

XAF1 as a modifier of p53 function and cancer susceptibility

Environmental Contaminants Modulate Breast Cancer Development and Outcome in TP53 p.R337H Carriers and Noncarriers

TP53-Associated Pediatric Malignancies

From uncertainty to pathogenicity: clinical and functional interrogation of a rare TP53 in-frame deletion

Differential elemental distribution of retained particles along the respiratory tract

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