Xia N. Guo

State Key Laboratory Of Medicinal Chemical Biology, Key Laboratory Of Functional Polymer Materials Of Ministry Of Education
Changhongjie, 300071, China

Last Updated: 09/26/2026

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Found 8 publications

Two Orthogonal Halogen-Bonding Interactions Directed 2D Crystalline Supramolecular J-Dimer Lamellae.

Two Orthogonal Halogen-Bonding Interactions Directed 2D Crystalline Supramolecular J-Dimer Lamellae.

Journal: Chemistry (Weinheim an der Bergstrasse, Germany)

Published: January 27, 2020

A disease-related gene mining method based on weakly supervised learning model.

A disease-related gene mining method based on weakly supervised learning model.

Journal: BMC bioinformatics

Published: December 03, 2019

Ensemble Consensus-Guided Unsupervised Feature Selection to Identify Huntington's Disease-Associated Genes.

Ensemble Consensus-Guided Unsupervised Feature Selection to Identify Huntington's Disease-Associated Genes.

Journal: Genes

Published: May 30, 2018

Identification of a novel loss-of-function C9orf72 splice site mutation in a patient with amyotrophic lateral sclerosis.

Identification of a novel loss-of-function C9orf72 splice site mutation in a patient with amyotrophic lateral sclerosis.

Journal: Neurobiology of aging

Published: March 05, 2016

Mutation spectrum of Chinese patients with familial and sporadic amyotrophic lateral sclerosis.

Mutation spectrum of Chinese patients with familial and sporadic amyotrophic lateral sclerosis.

Journal: Journal of neurology, neurosurgery, and psychiatry

Published: February 15, 2016

Whole-exome sequencing identifies a missense mutation in hnRNPA1 in a family with flail arm ALS.

Whole-exome sequencing identifies a missense mutation in hnRNPA1 in a family with flail arm ALS.

Journal: Neurology

Published: February 06, 2016

Quick genetic screening using targeted next-generation sequencing in patients with tuberous sclerosis.

Quick genetic screening using targeted next-generation sequencing in patients with tuberous sclerosis.

Journal: Journal of child neurology

Published: May 03, 2014

Re-evaluation of PRRT2 mutations in paroxysmal disorders.

Re-evaluation of PRRT2 mutations in paroxysmal disorders.

Journal: Journal of neurology

Published: January 14, 2014

Showing 1-8 of 8

Last Updated: 09/26/2026