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List of works by Nan Wu

A multi-ethnic meta-analysis confirms the association of rs6570507 with adolescent idiopathic scoliosis

scientific article published in Scientific Reports

A novel COMP mutation in a Chinese family with multiple epiphyseal dysplasia

scientific article published on 27 May 2020

Author Correction: The copy number variation landscape of congenital anomalies of the kidney and urinary tract

scientific article published on 01 April 2019

Cover Image, Volume 118, Number 10, October 2017.

scientific article published in October 2017

Diagnostic yield and clinical impact of exome sequencing in early-onset scoliosis (EOS)

scientific article published on 07 May 2020

Downregulation of stathmin 1 in human gallbladder carcinoma inhibits tumor growth in vitro and in vivo

scientific article published on 28 June 2016

Endovascular aneurysm repair in emergent ruptured abdominal aortic aneurysm with a 'real' hostile neck and severely tortuous iliac artery of an elderly patient

scientific article

Evaluation of a novel poly(amidoamine) with pendant aminobutyl group on the cellular properties of transfected bone marrow mesenchymal stem cells

scientific article published on 7 October 2017

Exome sequencing reveals a novel variant in NFX1 causing intracranial aneurysm in a Chinese family

scientific article published on 10 August 2019

Full-thickness excision using transanal endoscopic microsurgery for treatment of rectal neuroendocrine tumors

scientific article

Genetic and molecular mechanism for distinct clinical phenotypes conveyed by allelic truncating mutations implicated in FBN1

scientific article published on 27 November 2019

Genetic polymorphisms of GPR126 are functionally associated with PUMC classifications of adolescent idiopathic scoliosis in a Northern Han population ⬇️

scientific article

Identification of likely pathogenic and known variants in TSPEAR, LAMB3, BCOR, and WNT10A in four Turkish families with tooth agenesis

scientific article published on 26 July 2018

Identification of novel FBN1 variations implicated in congenital scoliosis

scientific article published on 11 December 2019

Identification of two novel null variants in CLN8 by targeted next-generation sequencing: first report of a Chinese patient with neuronal ceroid lipofuscinosis due to CLN8 variants.

scientific article published on 8 February 2018

Increased TBX6 gene dosages induce congenital cervical vertebral malformations in humans and mice

scientific article published on 30 December 2019

Mechanical sensing protein PIEZO1 regulates bone homeostasis via osteoblast-osteoclast crosstalk

scientific article published on 15 January 2020

Molecular therapeutic strategies for FGFR3 gene-related skeletal dysplasia

scientific article

Mutational burden and potential oligogenic model of TBX6-mediated genes in congenital scoliosis

scientific article published on 20 August 2020

Novel NTRK1 Frameshift Mutation in Congenital Insensitivity to Pain With Anhidrosis

scientific article published on 14 October 2014

Perturbations of BMP/TGF-β and VEGF/VEGFR signalling pathways in non-syndromic sporadic brain arteriovenous malformations (BAVM)

scientific article published on 17 August 2018

Phenotypic and genetic spectrum of isolated macrodactyly: somatic mosaicism of PIK3CA and AKT1 oncogenic variants

scientific article published on 14 October 2020

Piezo1/2 mediate mechanotransduction essential for bone formation through concerted activation of NFAT-YAP1-ß-catenin

scientific article published on 18 March 2020

Possible single-nucleotide polymorphism loci associated with systemic sclerosis susceptibility: a genetic association study in a Chinese Han population

scientific article

Progress and Application of CRISPR/Cas Technology in Biological and Biomedical Investigation

scientific article

Progress and perspective of TBX6 gene in congenital vertebral malformations

scientific article published on 15 July 2016

Prolonged Hoarseness Caused by Arytenoid Dislocation After Anterior Cervical Corpectomy and Fusion

scientific article

Recurrence-Associated Long Non-coding RNA Signature for Determining the Risk of Recurrence in Patients with Colon Cancer

scientific article published on 26 June 2018

TBX6 missense variants expand the mutational spectrum in a non-Mendelian inheritance disease

scientific article published on 26 September 2019

TBX6 null variants and a common hypomorphic allele in congenital scoliosis

scientific article

The Regulatory Roles of MicroRNAs in Bone Remodeling and Perspectives as Biomarkers in Osteoporosis

scientific article

The Role of Semaphorin 3A in Bone Remodeling.

scientific article published on 28 February 2017

The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease

scientific article published on 17 July 2018

The copy number variation landscape of congenital anomalies of the kidney and urinary tract

scientific article published on 21 December 2018

Whole-exome sequencing reveals known and novel variants in a cohort of intracranial vertebral–basilar artery dissection (IVAD)

scientific article published on 16 August 2018

Whole-spine Computed Tomography Findings in SAPHO Syndrome

scientific article published in March 2017

ceRNA in cancer: possible functions and clinical implications.

scientific article published on 10 September 2015

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