Author details

Full Name

Guiqing Cai

Affiliation

ORCID

Career Start Year

1997

Papers

H Index

Expertise

CM4AI Collaborator

PMID	Paper Title	Journal Title	Published Year
34900526	Personalized medicine of non-gene-specific chemotherapies for non-small cell lung cancer.	Acta Pharmaceutica Sinica B	2021
31880409	Lessons learned from expanded reproductive carrier screening in self-reported Ashkenazi, Sephardi, and Mizrahi Jewish patients.	Mol Genet Genomic Med	2020
30109178	Personalized medicine in non-small cell lung cancer: a review from a pharmacogenomics perspective.	Acta Pharmaceutica Sinica B	2018
27869829	Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects.	Nat Genet	2017
25882707	Two knockdown models of the autism genes SYNGAP1 and SHANK3 in zebrafish produce similar behavioral phenotypes associated with embryonic disruptions of brain morphogenesis.	Hum Mol Genet	2015
24650168	De novo SCN2A splice site mutation in a boy with Autism spectrum disorder.	BMC Med Genet	2014
24768552	Convergence of genes and cellular pathways dysregulated in autism spectrum disorders.	Am J Hum Genet	2014
24574008	Vascular endothelial growth factor coordinates islet innervation via vascular scaffolding.	Development	2014
25114262	Expression profiling associates blood and brain glucocorticoid receptor signaling with trauma-related individual differences in both sexes.	Proc Natl Acad Sci U S A	2014
23743231	Whole exome sequencing reveals minimal differences between cell line and whole blood derived DNA.	Genomics	2013
22966069	Estrogen treatment after ovariectomy protects against fatty liver and may improve pathway-selective insulin resistance.		2013
23990902	Characterization of SLITRK1 variation in obsessive-compulsive disorder.	PLoS One	2013
23758760	Prospective investigation of autism and genotype-phenotype correlations in 22q13 deletion syndrome and SHANK3 deficiency.	Mol Autism	2013
23884891	Vascular endothelial growth factor-a and islet vascularization are necessary in developing, but not adult, pancreatic islets.		2013
22257670	AnnTools: a comprehensive and versatile annotation toolkit for genomic variants.	Bioinformatics	2012
22546694	Enhanced expression of VEGF-A in Î² cells increases endothelial cell number but impairs islet morphogenesis and Î² cell proliferation.	Developmental Biology	2012
22495311	Patterns and rates of exonic de novo mutations in autism spectrum disorders.	Nature	2012
22566635	A common X-linked inborn error of carnitine biosynthesis may be a risk factor for nondysmorphic autism.	Proc Natl Acad Sci U S A	2012
20381196	Evidence against a role for rare ADAM10 mutations in sporadic Alzheimer disease.	Neurobiol Aging	2012
21491612	No evidence for IL1RAPL1 involvement in selected high-risk autism pedigrees from the AGRE data set.	Autism Res	2011
21295283	Whole-exome sequencing links a variant in DHDDS to retinitis pigmentosa.	Am J Hum Genet	2011
21062623	Analysis of a purported SHANK3 mutation in a boy with autism: clinical impact of rare variant research in neurodevelopmental disabilities.	Brain Res	2011
21508514	Genetic markers for PTSD risk and resilience among survivors of the World Trade Center attacks.	Dis Markers	2011
20885792	Dementia revealed: novel chromosome 6 locus for late-onset Alzheimer disease provides genetic evidence for folate-pathway abnormalities.	PLoS Genet	2010
19746410	Association between methylenetetrahydrofolate reductase (MTHFR) C677T polymorphism and age of onset in schizophrenia.	Am J Med Genet B Neuropsychiatr Genet	2010
19401682	High-density SNP association study and copy number variation analysis of the AUTS1 and AUTS5 loci implicate the IMMP2L-DOCK4 gene region in autism susceptibility.	Mol Psychiatry	2010
19393990	Gene expression patterns associated with posttraumatic stress disorder following exposure to the World Trade Center attacks.	Biol Psychiatry	2009
19404257	Autism genome-wide copy number variation reveals ubiquitin and neuronal genes.	Nature	2009
18827292	Correlation and familial aggregation of dimensions of psychosis in affected sibling pairs from China.	Br J Psychiatry	2008
19360675	A large-scale screen for coding variants in SERT/SLC6A4 in autism spectrum disorders.	Autism Res	2008
18348195	An analysis of candidate autism loci on chromosome 2q24-q33: evidence for association to the STK39 gene.	Am J Med Genet B Neuropsychiatr Genet	2008
18925931	Multiplex ligation-dependent probe amplification for genetic screening in autism spectrum disorders: efficient identification of known microduplications and identification of a novel microduplication in ASMT.	BMC Med Genomics	2008
18001468	Mutation analysis of the NSD1 gene in patients with autism spectrum disorders and macrocephaly.	BMC Med Genet	2007
17427195	Mutation screening of the PTEN gene in patients with autism spectrum disorders and macrocephaly.	Am J Med Genet B Neuropsychiatr Genet	2007
16958027	Family-based association study of TPH1 and TPH2 polymorphisms in autism.	Am J Med Genet B Neuropsychiatr Genet	2006
16215936	Mutations of 15 short tandem repeat loci in Chinese population.	Chinese Journal of Medical Genetics	2005
15003824	Rapid detection of six common Chinese G6PD mutations by MALDI-TOF MS.	Blood Cells, Molecules, and Diseases	2004
15626662	[The characteristics of polymorphism and gene structure of DYF155S1 locus in Y-specific minisatellite from Chinese Uygur population].	Yi chuan = Hereditas / Zhongguo yi chuan xue hui bian ji	2004
15007393	Identification of a novel neuregulin 1 at-risk haplotype in Han schizophrenia Chinese patients, but no association with the Icelandic/Scottish risk haplotype.	Mol Psychiatry	2004
14682249	[Sequence variation of D12S391 and D11S554 loci in Guangzhou han population].		2003
14671796	[DNA analysis of a 500 year mummy sample].	Fa yi xue za zhi	2003
12812070	[Studying the polymorphism at DYF155S1 locus in Chinese Han population by MVR-PCR marked with fluorescence].		2003
12048677	[A linkage disequilibrium study of methylenetetrahydrofolate reductase C677T and schizophrenia].	Chinese Journal of Medical Genetics	2002
12170462	[A linkage analysis of quantitative trait loci for familial schizophrenia on chromosome 1].	Zhonghua Yi Xue Yi Chuan Xue Za Zhi	2002
11836676	[Linkage disequilibrium study of microsatellite markers on chromosome 6 and schizophrenia].	Chinese Journal of Medical Genetics	2002
12476422	[Linkage analysis of susceptibility genes for familial schizophrenia on chromosome 1 in Chinese population].	Zhonghua Yi Xue Yi Chuan Xue Za Zhi	2002
11378844	Affected sibling pair linkage analysis of qualitative and quantitative traits for schizophrenia on chromosome 22 in a Chinese population.	Am J Med Genet	2001
11592037	[Linkage disequilibrium analysis of chromosome 22 and schizophrenia in a Chinese population].	Zhonghua Yi Xue Yi Chuan Xue Za Zhi	2001
10482338	Association analysis between dopamine receptor genes and bipolar affective disorder.	Psychiatry Res	1999
9352569	Catechol-O-methyltransferase Val158Met polymorphism: frequency analysis in Han Chinese subjects and allelic association of the low activity allele with bipolar affective disorder.	Pharmacogenetics	1997