Publications:

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Systematic Review and Bioinformatic Analysis of microRNA Expression in Autism Spectrum Disorder Identifies Pathways Associated With Cancer, Metabolism, Cell Signaling, and Cell Adhesion.

Frontiers In Psychiatry

Huang, Zhi-Xiong ZX; Chen, Yanhui Y; Guo, Hong-Ru HR; Chen, Guo-Feng GF

Publication Date: 2021

Variant appearance in text: rs1495099

PubMed Link: 34744804

Variant Present in the following documents:

• Table_4.xlsx, sheet 2

View BVdb publication page

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Prioritizing natural-selection signals from the deep-sequencing genomic data suggests multi-variant adaptation in Tibetan highlanders.

National Science Review

Deng, Lian L; Zhang, Chao C; Yuan, Kai K; Gao, Yang Y; Pan, Yuwen Y; Ge, Xueling X; He, Yaoxi Y; Yuan, Yuan Y; Lu, Yan Y; Zhang, Xiaoxi X; Chen, Hao H; Lou, Haiyi H; Wang, Xiaoji X; Lu, Dongsheng D; Liu, Jiaojiao J; Tian, Lei L; Feng, Qidi Q; Khan, Asifullah A; Yang, Yajun Y; Jin, Zi-Bing ZB; Yang, Jian J; Lu, Fan F; Qu, Jia J; Kang, Longli L; Su, Bing B; Xu, Shuhua S

Publication Date: 2019-11

Variant appearance in text: rs1495099

PubMed Link: 34691999

Variant Present in the following documents:

• Main text
• nwz108.pdf

View BVdb publication page

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Pathological priming causes developmental gene network heterochronicity in autistic subject-derived neurons.

Nature Neuroscience

Schafer, Simon T ST; Paquola, Apua C M ACM; Stern, Shani S; Gosselin, David D; Ku, Manching M; Pena, Monique M; Kuret, Thomas J M TJM; Liyanage, Marvin M; Mansour, Abed AlFatah AA; Jaeger, Baptiste N BN; Marchetto, Maria C MC; Glass, Christopher K CK; Mertens, Jerome J; Gage, Fred H FH

Publication Date: 2019-02

Variant appearance in text: rs1495099

PubMed Link: 30617258

Variant Present in the following documents:

• NIHMS1512664-supplement-Sup_Table_5.xlsx, sheet 1

View BVdb publication page

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The evolution of a series of behavioral traits is associated with autism-risk genes in cavefish.

Bmc Evolutionary Biology

Yoshizawa, Masato M; Settle, Alexander A; Hermosura, Meredith C MC; Tuttle, Lillian J LJ; Cetraro, Nicolas N; Passow, Courtney N CN; McGaugh, Suzanne E SE

Publication Date: 2018-06-18

Variant appearance in text: rs1495099

PubMed Link: 29909776

Variant Present in the following documents:

• 12862_2018_1199_MOESM1_ESM.xlsx, sheet 6

View BVdb publication page

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Burden of de novo mutations and inherited rare single nucleotide variants in children with sensory processing dysfunction.

Bmc Medical Genomics

Marco, Elysa Jill EJ; Aitken, Anne Brandes AB; Nair, Vishnu Prakas VP; da Gente, Gilberto G; Gerdes, Molly Rae MR; Bologlu, Leyla L; Thomas, Sean S; Sherr, Elliott H EH

Publication Date: 2018-05-25

Variant appearance in text: rs1495099

PubMed Link: 29801487

Variant Present in the following documents:

• 12920_2018_362_MOESM2_ESM.xls, sheet 1

View BVdb publication page

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Allele-specific expression in a family quartet with autism reveals mono-to-biallelic switch and novel transcriptional processes of autism susceptibility genes.

Scientific Reports

Lin, Chun-Yen CY; Chang, Kai-Wei KW; Lin, Chia-Yi CY; Wu, Jia-Ying JY; Coon, Hilary H; Huang, Pei-Hsin PH; Ho, Hong-Nerng HN; Akbarian, Schahram S; Gau, Susan Shur-Fen SS; Huang, Hsien-Sung HS

Publication Date: 2018-03-09

Variant appearance in text: rs1495099

PubMed Link: 29523860

Variant Present in the following documents:

• 41598_2018_22753_MOESM11_ESM.xlsx, sheet 1

View BVdb publication page

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Pathway Network Analyses for Autism Reveal Multisystem Involvement, Major Overlaps with Other Diseases and Convergence upon MAPK and Calcium Signaling.

Plos One

Wen, Ya Y; Alshikho, Mohamad J MJ; Herbert, Martha R MR

Publication Date: 2016

Variant appearance in text: rs1495099

PubMed Link: 27055244

Variant Present in the following documents:

• pone.0153329.s001.xls, sheet 1

View BVdb publication page

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Mining the 3'UTR of autism-implicated genes for SNPs perturbing microRNA regulation.

Genomics, Proteomics & Bioinformatics

Vaishnavi, Varadharajan V; Manikandan, Mayakannan M; Munirajan, Arasambattu Kannan AK

Publication Date: 2014-04

Variant appearance in text: rs1495099

PubMed Link: 24747189

Variant Present in the following documents:

• mmc3.xlsx, sheet 1

View BVdb publication page

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DRD2 and PPP1R1B (DARPP-32) polymorphisms independently confer increased risk for autism spectrum disorders and additively predict affected status in male-only affected sib-pair families.

Behavioral And Brain Functions : Bbf

Hettinger, Joe A JA; Liu, Xudong X; Hudson, Melissa L ML; Lee, Alana A; Cohen, Ira L IL; Michaelis, Ron C RC; Schwartz, Charles E CE; Lewis, Suzanne M E SM; Holden, Jeanette J A JJ

Publication Date: 2012-05-04

Variant appearance in text: rs1495099

PubMed Link: 22559203

Variant Present in the following documents:

• Main text

View BVdb publication page

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Gender-stratified gene and gene-treatment interactions in smoking cessation.

The Pharmacogenomics Journal

Lee, W W; Bergen, A W AW; Swan, G E GE; Li, D D; Liu, J J; Thomas, P P; Tyndale, R F RF; Benowitz, N L NL; Lerman, C C; Conti, D V DV

Publication Date: 2012-12

Variant appearance in text: rs1495099

PubMed Link: 21808284

Variant Present in the following documents:

• NIHMS305090-supplement-3.pdf

View BVdb publication page

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