New generation genetic testing entering the clinic-Reference-Cited by-同舟云学术

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New generation genetic testing entering the clinic

Published:2020-04 Issue: Volume:73 Page:72-84
ISSN:1353-8020
Container-title:Parkinsonism & Related Disorders
language:en
Short-container-title:Parkinsonism & Related Disorders

Author:

Gorcenco Sorina,Ilinca Andreea,Almasoudi Wejdan,Kafantari Efthymia,Lindgren Arne G.,Puschmann Andreas

Funder

ALF

Lund University

Bayer

BMS

Pfizer

Parkinson Foundation

Parkinsonfonden

Publisher

Elsevier BV

Subject

Clinical Neurology,Geriatrics and Gerontology,Neurology

Reference99 articles.

1. Genetics of movement disorders in the next-generation sequencing era;Olgiati;Mov. Disord.,2016

2. Next-generation sequencing to diagnose suspected genetic disorders;Adams;N. Engl. J. Med.,2018

3. Clinical application of next-generation sequencing to the practice of neurology;Rexach;Lancet Neurol.,2019

4. Genetics of movement disorders and the practicing clinician; who and what to test for?;Di Fonzo;Curr. Neurol. Neurosci. Rep.,2018

5. International Parkinson's disease movement disorders society task force on rare movement disorders, treatable inherited rare movement disorders;Jinnah;Mov. Disord.,2018

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1. The yield of genetic workup for middle-aged and elderly patients with neurological disorders in a real-world setting;Journal of the Neurological Sciences;2024-08

2. A systematic review to assess the utility of genomic autopsy using exome or genome sequencing in cases of congenital anomalies and perinatal death;Genetics in Medicine;2024-07

3. The Use of Genetic Testing in Nephrolithiasis Evaluation: A Retrospective Review From a Multidisciplinary Kidney Stone Clinic;Urology;2024-07

4. Large‐Scale Screening: Phenotypic and Mutational Spectrum in Isolated and Combined Dystonia Genes;Movement Disorders;2024-01-12

5. Next-generation sequencing and bioinformatics in rare movement disorders;Nature Reviews Neurology;2024-01-03

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