Literature DB >> 29367450

A genotype-phenotype correlation for quantitative autistic trait burden in neurofibromatosis 1.

Stephanie M Morris1, David H Gutmann2.   

Abstract

Entities:  

Mesh:

Substances:

Year:  2018        PMID: 29367450     DOI: 10.1212/WNL.0000000000005000

Source DB:  PubMed          Journal:  Neurology        ISSN: 0028-3878            Impact factor:   9.910


× No keyword cloud information.
  9 in total

1.  Neurofibromatosis Type 1 Implicates Ras Pathways in the Genetic Architecture of Neurodevelopmental Disorders.

Authors:  Jessica A Kaczorowski; Taylor F Smith; Amanda M Shrewsbury; Leah R Thomas; Valerie S Knopik; Maria T Acosta
Journal:  Behav Genet       Date:  2020-02-05       Impact factor: 2.805

Review 2.  Insights into optic pathway glioma vision loss from mouse models of neurofibromatosis type 1.

Authors:  Morgan E Freret; David H Gutmann
Journal:  J Neurosci Res       Date:  2018-04-28       Impact factor: 4.164

Review 3.  Optic pathway gliomas in neurofibromatosis-1: controversies and recommendations.

Authors:  Robert Listernick; Rosalie E Ferner; Grant T Liu; David H Gutmann
Journal:  Ann Neurol       Date:  2007-03       Impact factor: 10.422

4.  Examination of the genetic factors underlying the cognitive variability associated with neurofibromatosis type 1.

Authors:  Myrthe J Ottenhoff; André B Rietman; Sabine E Mous; Ellen Plasschaert; Daniela Gawehns; Hilde Brems; Rianne Oostenbrink; Rick van Minkelen; Mark Nellist; Elizabeth Schorry; Eric Legius; Henriette A Moll; Ype Elgersma
Journal:  Genet Med       Date:  2020-02-04       Impact factor: 8.822

5.  Shared developmental gait disruptions across two mouse models of neurodevelopmental disorders.

Authors:  Joseph D Dougherty; Susan E Maloney; Rachel M Rahn; Claire T Weichselbaum; David H Gutmann
Journal:  J Neurodev Disord       Date:  2021-03-20       Impact factor: 4.074

6.  Assessing Psychiatric Comorbidity and Pharmacologic Treatment Patterns Among Patients With Neurofibromatosis Type 1.

Authors:  Alexander C Houpt; Shaina E Schwartz; Robert A Coover
Journal:  Cureus       Date:  2021-12-07

Review 7.  Atypical NF1 Microdeletions: Challenges and Opportunities for Genotype/Phenotype Correlations in Patients with Large NF1 Deletions.

Authors:  Hildegard Kehrer-Sawatzki; Ute Wahlländer; David N Cooper; Victor-Felix Mautner
Journal:  Genes (Basel)       Date:  2021-10-19       Impact factor: 4.096

8.  Human iPSC-Derived Neurons and Cerebral Organoids Establish Differential Effects of Germline NF1 Gene Mutations.

Authors:  Corina Anastasaki; Michelle L Wegscheid; Kelly Hartigan; Jason B Papke; Nathan D Kopp; Jiayang Chen; Olivia Cobb; Joseph D Dougherty; David H Gutmann
Journal:  Stem Cell Reports       Date:  2020-04-02       Impact factor: 7.765

9.  Clinical characterization of children and adolescents with NF1 microdeletions.

Authors:  Hildegard Kehrer-Sawatzki; Lan Kluwe; Johannes Salamon; Lennart Well; Said Farschtschi; Thorsten Rosenbaum; Victor-Felix Mautner
Journal:  Childs Nerv Syst       Date:  2020-06-12       Impact factor: 1.475

  9 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.