Publications:

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Identification of genetic risk loci for depression and migraine comorbidity in Han Chinese residing in Taiwan.

Frontiers In Psychiatry

Tsai, Ming-Chen MC; Tsai, Chia-Lin CL; Liang, Chih-Sung CS; Lin, Yu-Kai YK; Lin, Guan-Yu GY; Tsai, Chia-Kuang CK; Yeh, Po-Kuan PK; Liu, Yi Y; Hung, Kuo-Sheng KS; Yang, Fu-Chi FC

Publication Date: 2022

Variant appearance in text: rs301799

PubMed Link: 36704746

Variant Present in the following documents:

• Main text
• fpsyt-13-1067503.pdf

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Establishment and characterization of a new mantle cell lymphoma cell line with a NOTCH2 mutation, Arbo.

Ejhaem

Safa, Firas F; Rasmussen, Terri T; Lobelle-Rich, Patricia P; Collier, Stephanie S; Milligan, Nicholas N; Schmeig, John J; Schmid, Janet J; Wiewiorowski, Carol C; Totaro, Denise D; Brown, Theresa C TC; Satyavarapu, Ishwarya I; Badoo, Melody M; Ungerleider, Nathan N; Flemington, Erik K EK; Safah, Hana H; Saba, Nakhle S NS

Publication Date: 2022-11

Variant appearance in text: rs301799

PubMed Link: 36467812

Variant Present in the following documents:

• JHA2-3-1326-s001.xlsx, sheet 1

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Genetic evidence suggests that depression increases the risk of erectile dysfunction: A Mendelian randomization study.

Frontiers In Genetics

Ma, Kai K; Song, Pan P; Liu, Zhenghuan Z; Yang, Luchen L; Wang, Linchun L; Zhou, Jing J; Chen, Junhao J; Dong, Qiang Q

Publication Date: 2022

Variant appearance in text: rs301799

PubMed Link: 36313469

Variant Present in the following documents:

• fgene-13-1026227.pdf

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Genetic Pathways Underlying Individual Differences in Regular Physical Activity.

Exercise And Sport Sciences Reviews

de Geus, Eco J C EJC

Publication Date: 2022-09-01

Variant appearance in text: rs301799

PubMed Link: 36044740

Variant Present in the following documents:

• Main text

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Functional Genomics Analysis to Disentangle the Role of Genetic Variants in Major Depression.

Genes

Pérez-Granado, Judith J; Piñero, Janet J; Medina-Rivera, Alejandra A; Furlong, Laura I LI

Publication Date: 2022-07-15

Variant appearance in text: rs301799

PubMed Link: 35886042

Variant Present in the following documents:

• genes-13-01259.pdf

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Major depression disorder may causally associate with the increased breast cancer risk: Evidence from two-sample mendelian randomization analyses.

Cancer Medicine

Ren, Qian Q; Luo, Fangxiu F; Ge, Sheng S; Chen, Peizhan P

Publication Date: 2022-07-19

Variant appearance in text: rs301799

PubMed Link: 35852181

Variant Present in the following documents:

• Main text

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Bidirectional Mendelian Randomization Analysis for Vitamin D and Thyroid Peroxidase Antibody.

International Journal Of Endocrinology

Chen, Yingchao Y; Han, Bing B; Zhu, Chunfang C; Li, Qin Q; Chen, Chi C; Zhai, Hualing H; Wang, Ningjian N; Chen, Yi Y; Lu, Yingli Y

Publication Date: 2022

Variant appearance in text: rs301799

PubMed Link: 35399300

Variant Present in the following documents:

• IJE2022-2260388.pdf

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Depression and Osteoporosis: A Mendelian Randomization Study.

Calcified Tissue International

He, Bin B; Lyu, Qiong Q; Yin, Lifeng L; Zhang, Muzi M; Quan, Zhengxue Z; Ou, Yunsheng Y

Publication Date: 2021-12

Variant appearance in text: rs301799

PubMed Link: 34259888

Variant Present in the following documents:

• Main text
• 223_2021_Article_886.pdf

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Influence of Rapid Urbanization on Thyroid Autoimmune Disease in China.

International Journal Of Endocrinology

Chen, Yingchao Y; Han, Bing B; Yu, Jie J; Chen, Yi Y; Cheng, Jing J; Zhu, Chunfang C; Xia, Fangzhen F; Wang, Ningjian N; Lu, Yingli Y

Publication Date: 2021

Variant appearance in text: rs301799

PubMed Link: 34122544

Variant Present in the following documents:

• Main text
• IJE2021-9967712.pdf

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Relationship between Gene Polymorphisms and Urine Iodine Levels on Susceptibility to Thyroid Peroxidase Antibody Positivity in the Chinese Population.

European Thyroid Journal

Han, Bing B; Chen, Chi C; Chen, Yi Y; Wang, Ningjian N; Yu, Jie J; Cheng, Jing J; Chen, Yingchao Y; Zhu, Chunfang C; Lu, Yingli Y

Publication Date: 2021-03

Variant appearance in text: rs301799

PubMed Link: 33777823

Variant Present in the following documents:

• Main text

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Multiomics dissection of molecular regulatory mechanisms underlying autoimmune-associated noncoding SNPs.

Jci Insight

Chen, Xiao-Feng XF; Guo, Ming-Rui MR; Duan, Yuan-Yuan YY; Jiang, Feng F; Wu, Hao H; Dong, Shan-Shan SS; Zhou, Xiao-Rong XR; Thynn, Hlaing Nwe HN; Liu, Cong-Cong CC; Zhang, Lin L; Guo, Yan Y; Yang, Tie-Lin TL

Publication Date: 2020-09-03

Variant appearance in text: rs301799

PubMed Link: 32879140

Variant Present in the following documents:

• jciinsight-5-136477-s105.xlsx, sheet 5

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meQTL and ncRNA functional analyses of 102 GWAS-SNPs associated with depression implicate HACE1 and SHANK2 genes.

Clinical Epigenetics

Ciuculete, Diana M DM; Voisin, Sarah S; Kular, Lara L; Jonsson, Jörgen J; Rask-Andersen, Mathias M; Mwinyi, Jessica J; Schiöth, Helgi B HB

Publication Date: 2020-07-02

Variant appearance in text: rs301799

PubMed Link: 32616021

Variant Present in the following documents:

• Main text
• 13148_2020_Article_884.pdf

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Conditional GWAS analysis to identify disorder-specific SNPs for psychiatric disorders.

Molecular Psychiatry

Byrne, Enda M EM; Zhu, Zhihong Z; Qi, Ting T; Skene, Nathan G NG; Bryois, Julien J; Pardinas, Antonio F AF; Stahl, Eli E; Smoller, Jordan W JW; Rietschel, Marcella M; , ; , ; Owen, Michael J MJ; Walters, James T R JTR; O'Donovan, Michael C MC; McGrath, John G JG; Hjerling-Leffler, Jens J; Sullivan, Patrick F PF; Goddard, Michael E ME; Visscher, Peter M PM; Yang, Jian J; Wray, Naomi R NR

Publication Date: 2021-06

Variant appearance in text: rs301799

PubMed Link: 32398722

Variant Present in the following documents:

• Main text

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Conditional GWAS analysis to identify disorder-specific SNPs for psychiatric disorders.

Molecular Psychiatry

Byrne, Enda M EM; Zhu, Zhihong Z; Qi, Ting T; Skene, Nathan G NG; Bryois, Julien J; Pardinas, Antonio F AF; Stahl, Eli E; Smoller, Jordan W JW; Rietschel, Marcella M; , ; , ; Owen, Michael J MJ; Walters, James T R JTR; O'Donovan, Michael C MC; McGrath, John G JG; Hjerling-Leffler, Jens J; Sullivan, Patrick F PF; Goddard, Michael E ME; Visscher, Peter M PM; Yang, Jian J; Wray, Naomi R NR

Publication Date: 2021-06

Variant appearance in text: rs301799

PubMed Link: 32398722

Variant Present in the following documents:

• Main text

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Genome-wide association and expression quantitative trait loci studies identify multiple susceptibility loci for thyroid cancer.

Nature Communications

Son, Ho-Young HY; Hwangbo, Yul Y; Yoo, Seong-Keun SK; Im, Sun-Wha SW; Yang, San Duk SD; Kwak, Soo-Jung SJ; Park, Min Seon MS; Kwak, Soo Heon SH; Cho, Sun Wook SW; Ryu, Jun Sun JS; Kim, Jeongseon J; Jung, Yuh-Seog YS; Kim, Tae Hyun TH; Kim, Su-Jin SJ; Lee, Kyu Eun KE; Park, Do Joon DJ; Cho, Nam Han NH; Sung, Joohon J; Seo, Jeong-Sun JS; Lee, Eun Kyung EK; Park, Young Joo YJ; Kim, Jong-Il JI

Publication Date: 2017-07-13

Variant appearance in text: rs301799

PubMed Link: 28703219

Variant Present in the following documents:

• ncomms15966-s2.pdf

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A genetic risk score for thyroid peroxidase antibodies associates with clinical thyroid disease in community-based populations.

The Journal Of Clinical Endocrinology And Metabolism

Schultheiss, Ulla T UT; Teumer, Alexander A; Medici, Marco M; Li, Yong Y; Daya, Natalie N; Chaker, Layal L; Homuth, Georg G; Uitterlinden, Andre G AG; Nauck, Matthias M; Hofman, Albert A; Selvin, Elizabeth E; Völzke, Henry H; Peeters, Robin P RP; Köttgen, Anna A

Publication Date: 2015-05

Variant appearance in text: rs301799

PubMed Link: 25719932

Variant Present in the following documents:

• Main text

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