Author details

Full Name

Fengxiang Wang

Affiliation

ORCID

Career Start Year

2009

Papers

H Index

Expertise

CM4AI Collaborator

PMID	Paper Title	Journal Title	Published Year
36672883	Single Cell Transcriptome Analysis of Peripheral Blood Mononuclear Cells in Freshly Isolated versus Stored Blood Samples.	Genes (Basel)	2023
36251323	Metabolomic and lipidomic signatures in autosomal dominant and late-onset Alzheimer's disease brains.	Alzheimers Dement	2023
37264205	Genomic profiling informs diagnoses and treatment in vascular anomalies.	Nat Med	2023
35347896	Identification of Novel Loci Shared by Juvenile Idiopathic Arthritis Subtypes Through Integrative Genetic Analysis.	Arthritis Rheumatol	2022
35246267	Circular RNA detection identifies circPSEN1 alterations in brain specific to autosomal dominant Alzheimer's disease.	Acta Neuropathol Commun	2022
34257703	Construction and Validation of a Lung Cancer Diagnostic Model Based on 6-Gene Methylation Frequency in Blood, Clinical Features, and Serum Tumor Markers.	Computational and Mathematical Methods in Medicine	2021
33591372	Lack of evidence supporting a role for DPP6 sequence variants in Alzheimer's disease in the European American population.	Acta Neuropathol	2021
34239129	Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders.	Nat Neurosci	2021
31456032	The TMEM106B FTLD-protective variant, rs1990621, is also associated with increased neuronal proportion.	Acta Neuropathol	2020
31937769	Rare copy number variants in over 100,000 European ancestry subjects reveal multiple disease associations.	Nat Commun	2020
32894242	Examination of the Effect of Rare Variants in TREM2, ABI3, and PLCG2 in LOAD Through Multiple Phenotypes.	J Alzheimers Dis	2020
30878790	Microduplications at the 15q11.2 BP1-BP2 locus are enriched in patients with anorexia nervosa.	J Psychiatr Res	2019
31591557	An atlas of cortical circular RNA expression in Alzheimer disease brains demonstrates clinical and pathological associations.	Nat Neurosci	2019
30043481	Environmental attitudes in China: The roles of the Dark Triad, future orientation and place attachment.	International Journal of Psychology	2019
29994337	Reconstructible Nonlinear Dimensionality Reduction via Joint Dictionary Learning.	IEEE Transactions on Neural Networks and Learning Systems	2019
31399126	A single-nuclei RNA sequencing study of Mendelian and sporadic AD in the human brain.	Alzheimers Res Ther	2019
28827695	Erratum: A genome-wide association study of anorexia nervosa suggests a risk locus implicated in dysregulated leptin signaling.	Sci Rep	2017
28824517	The Dark Side of Malleability: Incremental Theory Promotes Immoral Behaviors.	Frontiers in Psychology	2017
28630421	A genome-wide association study of anorexia nervosa suggests a risk locus implicated in dysregulated leptin signaling.	Sci Rep	2017
27829420	Association of a rare NOTCH4 coding variant with systemic sclerosis: a family-based whole exome sequencing study.	BMC Musculoskelet Disord	2016
26782110	Erratum to: Copy number variation in CEP57L1 predisposes to congenital absence of bilateral ACL and PCL ligaments.	Hum Genomics	2016
27069701	Early Infantile Epileptic Encephalopathy in an STXBP1 Patient with Lactic Acidemia and Normal Mitochondrial Respiratory Chain Function.	Case Rep Genet	2016
24547928	Advantage of Whole Exome Sequencing over Allele-Specific and Targeted Segment Sequencing in Detection of Novel TULP1 Mutation in Leber Congenital Amaurosis.	Ophthalmic Genet	2015
25927548	An atypical form of AOA2 with myoclonus associated with mutations in SETX and AFG3L2.	BMC Med Genet	2015
25678086	Rare variants at 16p11.2 are associated with common variable immunodeficiency.	J Allergy Clin Immunol	2015
25557462	Delayed diagnosis of congenital myasthenia due to associated mitochondrial enzyme defect.	Neuromuscul Disord	2015
26188062	Copy Number Variations in CTNNA3 and RBFOX1 Associate with Pediatric Food Allergy.	J Immunol	2015
26301688	Meta-analysis of shared genetic architecture across ten pediatric autoimmune diseases.	Nat Med	2015
26450413	Genetic sharing and heritability of paediatric age of onset autoimmune diseases.	Nat Commun	2015
24467814	Identification of rare DNA sequence variants in high-risk autism families and their prevalence in a large case/control population.	Mol Autism	2014
23382853	Copy number variations in alternative splicing gene networks impact lifespan.	PLoS One	2013
23965943	Targeted resequencing identifies defective variants of decoy receptor 3 in pediatric-onset inflammatory bowel disease.	Genes Immun	2013
21497890	Genome-wide association identifies diverse causes of common variable immunodeficiency.	J Allergy Clin Immunol	2011
21429575	The effect of CD47 modified polymer surfaces on inflammatory cell attachment and activation.	Biomaterials	2011
19036723	Eomesodermin requires transforming growth factor-beta/activin signaling and binds Smad2 to activate mesodermal genes.	Journal of Biological Chemistry	2009