Publications:

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Maternal genetic polymorphisms in the major mitotic checkpoint genes MAD1L1 and MAD2L1 associated with the risk of survival in abnormal chromosomal fetuses.

Frontiers In Genetics

Chan, Ying Y; Liu, Yize Y; Kong, Yamin Y; Xu, Weiming W; Zeng, Xiaohong X; Li, Haichun H; Guo, Yan Y; Tang, Xinhua X; Zhang, Jinman J; Zhu, Baosheng B

Publication Date: 2023

Variant appearance in text: rs12666575

PubMed Link: 37007941

Variant Present in the following documents:

• fgene-14-1105184.pdf

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Methylation in MAD1L1 is associated with the severity of suicide attempt and phenotypes of depression.

Clinical Epigenetics

Sokolov, Aleksandr V AV; Manu, Diana-Maria DM; Nordberg, Didi O T DOT; Boström, Adrian D E ADE; Jokinen, Jussi J; Schiöth, Helgi B HB

Publication Date: 2023-01-04

Variant appearance in text: rs12666575

PubMed Link: 36600305

Variant Present in the following documents:

• 13148_2022_Article_1394.pdf

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MAD1L1 and TSNARE gene polymorphisms are associated with schizophrenia susceptibility in the Han Chinese population.

Bmc Medical Genomics

Liu, Xianglai X; Xie, Hailing H; Fu, Zejuan Z; Yao, Qiankun Q; Han, Tianming T; Zhan, Dafei D; Lin, Zhan Z; Zhu, Hong H

Publication Date: 2021-09-04

Variant appearance in text: rs12666575

PubMed Link: 34481484

Variant Present in the following documents:

• Main text
• 12920_2021_Article_1070.pdf

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Identification of methylation changes associated with positive and negative growth deviance in Gambian infants using a targeted methyl sequencing approach of genomic DNA.

Faseb Bioadvances

Quilter, Claire R CR; Harvey, Kerry M KM; Bauer, Julien J; Skinner, Benjamin M BM; Gomez, Maria M; Shrivastava, Manu M; Doel, Andrew M AM; Drammeh, Saikou S; Dunger, David B DB; Moore, Sophie E SE; Ong, Ken K KK; Prentice, Andrew M AM; Bernstein, Robin M RM; Sargent, Carole A CA; Affara, Nabeel A NA

Publication Date: 2021-04

Variant appearance in text: rs12666575

PubMed Link: 33842847

Variant Present in the following documents:

• FBA2-3-205-s004.xlsx, sheet 2

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Identification of 34 genes conferring genetic and pharmacological risk for the comorbidity of schizophrenia and smoking behaviors.

Aging

Ma, Yunlong Y; Li, Jingjing J; Xu, Yi Y; Wang, Yan Y; Yao, Yinghao Y; Liu, Qiang Q; Wang, Maiqiu M; Zhao, Xinyi X; Fan, Rongli R; Chen, Jiali J; Zhang, Bin B; Cai, Zhen Z; Han, Haijun H; Yang, Zhongli Z; Yuan, Wenji W; Zhong, Yigang Y; Chen, Xiangning X; Ma, Jennie Z JZ; Payne, Thomas J TJ; Xu, Yizhou Y; Ning, Yuping Y; Cui, Wenyan W; Li, Ming D MD

Publication Date: 2020-02-03

Variant appearance in text: rs12666575

PubMed Link: 32012119

Variant Present in the following documents:

• Main text
• aging-12-102735.pdf

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Progress in genome-wide association studies of schizophrenia in Han Chinese populations.

Npj Schizophrenia

Yue, Weihua W; Yu, Xin X; Zhang, Dai D

Publication Date: 2017-08-10

Variant appearance in text: rs12666575

PubMed Link: 28798405

Variant Present in the following documents:

• Main text
• 41537_2017_Article_29.pdf

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GWAS meta analysis identifies TSNARE1 as a novel Schizophrenia / Bipolar susceptibility locus.

Scientific Reports

Sleiman, Patrick P; Wang, Dai D; Glessner, Joseph J; Hadley, Dexter D; Gur, Raquel E RE; Cohen, Nadine N; Li, Qingqin Q; Hakonarson, Hakon H; ,

Publication Date: 2013-10-29

Variant appearance in text: rs12666575

PubMed Link: 24166486

Variant Present in the following documents:

• Main text

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Genome-wide association study in a Swedish population yields support for greater CNV and MHC involvement in schizophrenia compared with bipolar disorder.

Molecular Psychiatry

Bergen, S E SE; O'Dushlaine, C T CT; Ripke, S S; Lee, P H PH; Ruderfer, D M DM; Akterin, S S; Moran, J L JL; Chambert, K D KD; Handsaker, R E RE; Backlund, L L; Ösby, U U; McCarroll, S S; Landen, M M; Scolnick, E M EM; Magnusson, P K E PK; Lichtenstein, P P; Hultman, C M CM; Purcell, S M SM; Sklar, P P; Sullivan, P F PF

Publication Date: 2012-09

Variant appearance in text: rs12666575

PubMed Link: 22688191

Variant Present in the following documents:

• Main text

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