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DICER1 and Associated Conditions: Identification of At-risk Individuals and Recommended Surveillance Strategies

Clinical cancer research, 2018-05, Vol.24 (10), p.2251-2261

2018

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Revisiting the Threshold for Cancer Genetics Referral in Patients With Wilms Tumor

Journal of clinical oncology, 2022-06, Vol.40 (17), p.JCO2200411-1860

2022

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A Comprehensive Review of Pediatric Tumors and Associated Cancer Predisposition Syndromes

Journal of genetic counseling, 2017-06, Vol.26 (3), p.387-434

2017

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Newly delineated syndrome of congenital lipomatous overgrowth, vascular malformations, and epidermal nevi (CLOVE syndrome) in seven patients

American journal of medical genetics. Part A, 2007-12, Vol.143A (24), p.2944-2958

2007

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Case report: Tisagenlecleucel for treatment of relapsed B- acute lymphoblastic leukemia in a patient with CHEK2 mutation

Frontiers in pediatrics, 2023-03, Vol.11, p.1067131

2023

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P089: POLE and brain tumors: Case report and review of the medical literature

Genetics in Medicine Open, 2024, Vol.2, p.100970, Article 100970

2024

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Atypical Presentations among Older Adults with COVID-19 Disease: A Need for Broadening the Differential Diagnosis

Gerontology and geriatric medicine, 2021, Vol.7, p.2333721421999313

2021

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Reassessment of the Proteus syndrome literature: Application of diagnostic criteria to published cases

American journal of medical genetics. Part A, 2004-10, Vol.130A (2), p.111-122

2004

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Hedgehog Signaling Regulates Sensory Cell Formation and Auditory Function in Mice and Humans

The Journal of neuroscience, 2008-07, Vol.28 (29), p.7350-7358

2008

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Somatic Mosaicism of IDH1 R132H Predisposes to Anaplastic Astrocytoma: A Case of Two Siblings

Frontiers in oncology, 2020-01, Vol.9, p.1507

2020

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Hypothalamic Hamartomas and Seizures: Distinct Natural History of Isolated and Pallister‐Hall Syndrome Cases

Epilepsia (Copenhagen), 2005-01, Vol.46 (1), p.42-47

2005

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The Rev. E. Ethelred Brown and the Harlem Renaissance, 1920–2020

Journal of Caribbean History, 2020, Vol.54 (1), p.30-54

Turner, Joyce Moore

2020

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Evolution of skin lesions in Proteus syndrome

Journal of the American Academy of Dermatology, 2005-05, Vol.52 (5), p.834-838

2005

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An integrated model of care utilizing community health workers to promote safe transitions of care

Journal of the American Geriatrics Society (JAGS), 2021-09, Vol.69 (9), p.2638-2647

2021

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Running With a Trot: Editing a Poem in Russian and Kyrgyz by Turusbek Madilbay

Sic (Zadar), 2011-12 (1.2)

Ellen Turner, Joyce

2011

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A Mosaic Activating Mutation in AKT1 Associated with the Proteus Syndrome

The New England journal of medicine, 2011-08, Vol.365 (7), p.611-619

2011

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72. Kaposiform Lymphangiomatosis as a Cause of Vaginal Bleeding & Discharge: A Case Report & Review of the Literature

Journal of pediatric & adolescent gynecology, 2024-04, Vol.37 (2), p.271-272

2024

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Alex, the Barista

Ploughshares, 2008-09, Vol.34 (2/3), p.169-186

Turner, Joyce E.

2008

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Comfort with Pharmacogenetic Testing Amongst Pediatric Oncology Providers and Their Patients

Journal of pediatric hematology/oncology nursing, 2022-05, Vol.39 (3), p.168-177

2022

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Proteus syndrome: Misdiagnosis with PTEN mutations

American journal of medical genetics. Part A, 2003-11, Vol.122A (4), p.323-324

2003

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Zoom-in comparative genomic hybridisation arrays for the characterisation of variable breakpoint contiguous gene syndromes

Journal of medical genetics, 2007-01, Vol.44 (1), p.e59-e59

2007

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Childhood Rhabdomyosarcoma in Association With a RASopathy Clinical Phenotype and Mosaic Germline SOS1 Duplication

Journal of pediatric hematology/oncology, 2016-11, Vol.38 (8), p.e278-e282

2016

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DICER1-related Sertoli-Leydig cell tumor and gynandroblastoma: Clinical and genetic findings from the International Ovarian and Testicular Stromal Tumor Registry

Gynecologic oncology, 2017-12, Vol.147 (3), p.521-527

2017

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PTEN mutations and Proteus syndrome

The Lancet (British edition), 2001-12, Vol.358 (9298), p.2079-2079

2001

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DICER1 and Associated Conditions: Identification of At-risk Individuals and Recommended Surveillance Strategies

Revisiting the Threshold for Cancer Genetics Referral in Patients With Wilms Tumor

A Comprehensive Review of Pediatric Tumors and Associated Cancer Predisposition Syndromes

Newly delineated syndrome of congenital lipomatous overgrowth, vascular malformations, and epidermal nevi (CLOVE syndrome) in seven patients

Case report: Tisagenlecleucel for treatment of relapsed B- acute lymphoblastic leukemia in a patient with CHEK2 mutation

P089: POLE and brain tumors: Case report and review of the medical literature

Atypical Presentations among Older Adults with COVID-19 Disease: A Need for Broadening the Differential Diagnosis

Reassessment of the Proteus syndrome literature: Application of diagnostic criteria to published cases

Hedgehog Signaling Regulates Sensory Cell Formation and Auditory Function in Mice and Humans

Temporal order of RNase IIIb and loss-of-function mutations during development determines phenotype in pleuropulmonary blastoma / DICER1 syndrome: a unique variant of the two-hit tumor suppression model [version 2; peer review: 2 approved]

Somatic Mosaicism of IDH1 R132H Predisposes to Anaplastic Astrocytoma: A Case of Two Siblings

Hypothalamic Hamartomas and Seizures: Distinct Natural History of Isolated and Pallister‐Hall Syndrome Cases

The Rev. E. Ethelred Brown and the Harlem Renaissance, 1920–2020

Evolution of skin lesions in Proteus syndrome

An integrated model of care utilizing community health workers to promote safe transitions of care

Running With a Trot: Editing a Poem in Russian and Kyrgyz by Turusbek Madilbay

A Mosaic Activating Mutation in AKT1 Associated with the Proteus Syndrome

72. Kaposiform Lymphangiomatosis as a Cause of Vaginal Bleeding & Discharge: A Case Report & Review of the Literature

Alex, the Barista

Comfort with Pharmacogenetic Testing Amongst Pediatric Oncology Providers and Their Patients

Proteus syndrome: Misdiagnosis with PTEN mutations

Zoom-in comparative genomic hybridisation arrays for the characterisation of variable breakpoint contiguous gene syndromes

Childhood Rhabdomyosarcoma in Association With a RASopathy Clinical Phenotype and Mosaic Germline SOS1 Duplication

DICER1-related Sertoli-Leydig cell tumor and gynandroblastoma: Clinical and genetic findings from the International Ovarian and Testicular Stromal Tumor Registry

PTEN mutations and Proteus syndrome

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