Parent-of-origin in individuals with familial neurofibromatosis type 1 and optic pathway gliomas (original) (raw)

Children with 5′-end NF1 gene mutations are more likely to have glioma

David Gutmann

Neurology Genetics, 2017

View PDFchevron_right

Childhood neurofibromatosis: Risk factors for malignant disease

Anna Meadows

Cancer Genetics and Cytogenetics, 1986

View PDFchevron_right

Peri-gestational risk factors for pediatric brain tumors in Neurofibromatosis Type 1

David Gutmann

Cancer epidemiology, 2016

View PDFchevron_right

A molecular analysis of individuals with neurofibromatosis type 1 (NF1) and optic pathway gliomas (OPGs), and an assessment of genotype-phenotype correlations

Nalin Thakker

Journal of Medical Genetics, 2011

View PDFchevron_right

Commentary: Identification of Mutation Regions on NF1 Responsible for High- and Low-Risk Development of Optic Pathway Glioma in Neurofibromatosis Type I

David Gutmann

Frontiers in Genetics, 2019

View PDFchevron_right

Molecular genetic analyses in neurofibromatosis type 1 patients with tumors

Yunus Terzi

Cancer genetics and cytogenetics, 2006

View PDFchevron_right

Parental age and Neurofibromatosis Type 1: a report from the NF1 Patient Registry Initiative

Qian Liu

View PDFchevron_right

Clustering of mutations in the 5’ tertile of the NF1 gene in Slovakia patients with optic pathway glioma

Andrea Zatkova

Neoplasma, 2014

View PDFchevron_right

Homozygous inactivation of NF1 gene in a patient with familial NF1 and disseminated neuroblastoma

Paola Origone

American Journal of Medical Genetics, 2003

View PDFchevron_right

Optic pathway gliomas in children with neurofibromatosis 1: Consensus statement from the nf1 optic pathway glioma task force

David Gutmann

Annals of Neurology, 1997

View PDFchevron_right

Unusual clustering of brain tumours in a family with NF1 and variable expression of cutaneous features

Richard Hayward

Journal of medical genetics, 1999

View PDFchevron_right

Exploring the genetic basis for clinical variation in neurofibromatosis type 1

David Gutmann

Expert review of neurotherapeutics, 2016

View PDFchevron_right

Somatic loss of wild typeNF1 allele in neurofibromas: Comparison ofNF1 microdeletion and non-microdeletion patients

Ludwine Messiaen, Eric Legius

Genes, Chromosomes and Cancer, 2006

View PDFchevron_right

Genotype-phenotype associations in neurofibromatosis type 1 (NF1): an increased risk of tumor complications in patients with NF1 splice-site mutations?

Nadia Chuzhanova

2012

View PDFchevron_right

The parental origin of new mutations in neurofibromatosis 2

Kevin Davis

neurogenetics, 2000

View PDFchevron_right

Neurofibromatosis type 1 and malignancy in childhood

Tezer Kutluk

Clinical Genetics, 2015

View PDFchevron_right

Optic glioma and precocious puberty in a girl with neurofibromatosis type 1 carrying an R681X mutation of NF1: case report and review of the literature

Elena Sukarova

BMC Endocrine Disorders, 2015

View PDFchevron_right

Genetic and cellular defects contributing to benign tumor formation in neurofibromatosis type 1

David Gutmann

Human Molecular Genetics, 2000

View PDFchevron_right

Brain tumors in neurofibromatosis type 1

David Gutmann

Neuro-Oncology Advances, 2019

View PDFchevron_right

The mutational spectrum of the NF1 gene in neurofibromatosis type I patients from UAE

Aisha Al-shamsi

Child's Nervous System, 2014

View PDFchevron_right

Clinicopathologic study of glioblastoma in children with neurofibromatosis type 1

Anita Huttner

Pediatric Blood & Cancer, 2010

View PDFchevron_right

Cancer and Central Nervous System Tumor Surveillance in Pediatric Neurofibromatosis 2 and Related Disorders

HECTOR LEONEL PINEDA SALVADOR

Clinical cancer research : an official journal of the American Association for Cancer Research, 2017

View PDFchevron_right

Optic pathway gliomas in neurofibromatosis-1: Controversies and recommendations

David Gutmann

Annals of Neurology, 2007

View PDFchevron_right

Breast cancer risk in neurofibromatosis type 1 is a function of the type of NF1 gene mutation: a new genotype-phenotype correlation

Diana Baralle

Journal of Medical Genetics, 2018

View PDFchevron_right

A prospective study of neurofibromatosis type 1 cancer incidence in the UK

Ian Frayling

2006

View PDFchevron_right

Confirmation of a Double-Hit Model for the NF1Gene in Benign Neurofibromas

David Otero

American Journal of Human Genetics - AMER J HUM GENET, 1997

View PDFchevron_right

Risk of benign tumours of nervous system, and of malignant neoplasms, in people with neurofibromatosis: population-based record-linkage study

Michael Goldacre

British Journal of Cancer, 2012

View PDFchevron_right

Germline and somatic NF1 gene mutations in plexiform neurofibromas

NIck Thomas

Human Mutation, 2008

View PDFchevron_right

Gender as a disease modifier in neurofibromatosis type 1 optic pathway glioma

Darren Hargrave

Annals of Neurology, 2014

View PDFchevron_right

Optic Gliomas in Neurofibromatosis Type 1

Sridevi Abboy

Journal of Pediatric Ophthalmology & Strabismus, 2016

View PDFchevron_right