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Author Details
Full Name
Fanggeng Zou
Affiliation
Cincinnati Children's Hospital Medical Center
ORCID
Career Start Year
2002
Papers
43
H Index
27
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
34321324
Delineating the genotypic and phenotypic spectrum of <i>HECW2</i>-related neurodevelopmental disorders.
J Med Genet
2022
35675510
Phenotypic and genetic spectrum of ATP6V1A encephalopathy: a disorder of lysosomal homeostasis.
Brain
2022
36182950
The phenotypic spectrum and genotype-phenotype correlations in 106 patients with variants in major autism gene CHD8.
Transl Psychiatry
2022
35104249
High-throughput evaluation of epilepsy-associated KCNQ2 variants reveals functional and pharmacological heterogeneity.
JCI Insight
2022
34748075
MYT1L-associated neurodevelopmental disorder: description of 40 new cases and literature review of clinical and molecular aspects.
Hum Genet
2022
33909990
Truncating SRCAP variants outside the Floating-Harbor syndrome locus cause a distinct neurodevelopmental disorder with a specific DNA methylation signature.
Am J Hum Genet
2021
28460589
Expanding the phenotypic spectrum of GABRG2 variants: a recurrent GABRG2 missense variant associated with a severe phenotype.
J Neurogenet
2017
27030769
ABCA7 Deficiency Accelerates Amyloid-β Generation and Alzheimer's Neuronal Pathology.
J Neurosci
2016
26603840
The genetic fingerprint of susceptibility for transplant-associated thrombotic microangiopathy.
Blood
2016
27727239
Human whole genome genotype and transcriptome data for Alzheimer's and other neurodegenerative diseases.
Sci Data
2016
25881291
Genetically-controlled Vesicle-Associated Membrane Protein 1 expression may contribute to Alzheimer's pathophysiology and susceptibility.
Mol Neurodegener
2015
26399695
Erratum to: Genetically-controlled Vesicle-Associated Membrane Protein 1 expression may contribute to Alzheimer's pathophysiology and susceptibility.
Mol Neurodegener
2015
26284228
Clinical Impact and Cost-Effectiveness of Whole Exome Sequencing as a Diagnostic Tool: A Pediatric Center's Experience.
Front Pediatr
2015
27066552
Late-onset Alzheimer disease risk variants mark brain regulatory loci.
Neurol Genet
2015
24607147
ApoE variant p.V236E is associated with markedly reduced risk of Alzheimer's disease.
Mol Neurodegener
2014
25324900
Association of MAPT haplotypes with Alzheimer's disease risk and MAPT brain gene expression levels.
Alzheimers Res Ther
2014
25129075
Alzheimer's disease: early alterations in brain DNA methylation at ANK1, BIN1, RHBDF2 and other loci.
Nat Neurosci
2014
24922517
Gene-wide analysis detects two new susceptibility genes for Alzheimer's disease.
PLoS One
2014
23750206
LRRTM3 interacts with APP and BACE1 and has variants associating with late-onset Alzheimer's disease (LOAD).
PLoS One
2013
24162737
Meta-analysis of 74,046 individuals identifies 11 new susceptibility loci for Alzheimer's disease.
Nat Genet
2013
23724096
Linking protective GAB2 variants, increased cortical GAB2 expression and decreased Alzheimer's disease pathology.
PLoS One
2013
22494505
Glutathione S-transferase omega genes in Alzheimer and Parkinson disease risk, age-at-diagnosis and brain gene expression: an association study with mechanistic implications.
Mol Neurodegener
2012
22722634
Novel late-onset Alzheimer disease loci variants associate with brain gene expression.
Neurology
2012
22685416
Brain expression genome-wide association study (eGWAS) identifies human disease-associated variants.
PLoS Genet
2012
21185624
Association of common KIBRA variants with episodic memory and AD risk.
Neurobiol Aging
2011
21867541
Evaluation of the global association between cholesterol-associated polymorphisms and Alzheimer's disease suggests a role for rs3846662 and HMGCR splicing in disease risk.
Mol Neurodegener
2011
21798052
Replication of EPHA1 and CD33 associations with late-onset Alzheimer's disease: a multi-centre case-control study.
Mol Neurodegener
2011
21595938
Rheumatoid arthritis-associated polymorphisms are not protective against Alzheimer's disease.
Mol Neurodegener
2011
21321396
Replication of BIN1 association with Alzheimer's disease and evaluation of genetic interactions.
J Alzheimers Dis
2011
21132329
Investigation of 15 of the top candidate genes for late-onset Alzheimer's disease.
Hum Genet
2011
21220680
Meta-analysis of the association between variants in SORL1 and Alzheimer disease.
Arch Neurol
2011
20098734
Concordant association of insulin degrading enzyme gene (IDE) variants with IDE mRNA, Abeta, and Alzheimer's disease.
PLoS One
2010
20554627
Replication of CLU, CR1, and PICALM associations with alzheimer disease.
Arch Neurol
2010
20142614
Gene expression levels as endophenotypes in genome-wide association studies of Alzheimer disease.
Neurology
2010
19136949
Genetic variation in PCDH11X is associated with susceptibility to late-onset Alzheimer's disease.
Nat Genet
2009
18065781
Sex-dependent association of a common low-density lipoprotein receptor polymorphism with RNA splicing efficiency in the brain and Alzheimer's disease.
Hum Mol Genet
2008
18524908
BRI2 (ITM2b) inhibits Abeta deposition in vivo.
J Neurosci
2008
17220890
The neuronal sortilin-related receptor SORL1 is genetically associated with Alzheimer disease.
Nat Genet
2007
16402132
Further evidence for the association between G72/G30 genes and schizophrenia in two ethnically distinct populations.
Mol Psychiatry
2006
16510121
A two-stage linkage analysis of Chinese schizophrenia pedigrees in 10 target chromosomes.
Biochem Biophys Res Commun
2006
15653269
A family-based study of the association between the G72/G30 genes and schizophrenia in the Chinese population.
Schizophr Res
2005
12624728
A locus for congenital preauricular fistula maps to chromosome 8q11.1-q13.3.
J Hum Genet
2003
11803454
A family-based and case-control association study of the NOTCH4 gene and schizophrenia.
Mol Psychiatry
2002
1 - 43 of 43
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