MAD1L1 c.1999-40549T>C

Variant ID: 7-1896413-A-G

NM_001013836.1(MAD1L1):c.1999-40549T>C

This variant was identified in 6 publications

View GRCh38 version.




Publications:


Genomic and neuroimaging approaches to bipolar disorder.

Bjpsych Open
Oraki Kohshour, Mojtaba M; Papiol, Sergi S; Ching, Christopher R K CRK; Schulze, Thomas G TG
Publication Date: 2022-02-01

Variant appearance in text: rs4236274
PubMed Link: 35101157
Variant Present in the following documents:
  • Main text
  • S2056472421010826a.pdf
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Genetically predicted bipolar disorder is causally associated with an increased risk of breast cancer: a two-sample Mendelian randomization analysis.

Annals Of Translational Medicine
Peng, Haoxin H; Wu, Xiangrong X; Ge, Fan F; Huo, Zhenyu Z; Wen, Yaokai Y; Li, Caichen C; Lin, Jinsheng J; Liang, Hengrui H; Zhong, Ran R; Liu, Jun J; Wang, Runchen R; He, Jianxing J; Liang, Wenhua W
Publication Date: 2021-03

Variant appearance in text: rs4236274
PubMed Link: 33842622
Variant Present in the following documents:
  • Main text
  • atm-09-05-401.pdf
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Reproducible Genetic Risk Loci for Anxiety: Results From ∼200,000 Participants in the Million Veteran Program.

The American Journal Of Psychiatry
Levey, Daniel F DF; Gelernter, Joel J; Polimanti, Renato R; Zhou, Hang H; Cheng, Zhongshan Z; Aslan, Mihaela M; Quaden, Rachel R; Concato, John J; Radhakrishnan, Krishnan K; Bryois, Julien J; Sullivan, Patrick F PF; , ; Stein, Murray B MB
Publication Date: 2020-03-01

Variant appearance in text: rs4236274
PubMed Link: 31906708
Variant Present in the following documents:
  • Main text
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Replicated associations of FADS1, MAD1L1, and a rare variant at 10q26.13 with bipolar disorder in Chinese population.

Translational Psychiatry
Zhao, Lijuan L; Chang, Hong H; Zhou, Dong-Sheng DS; Cai, Jun J; Fan, Weixing W; Tang, Wei W; Tang, Wenxin W; Li, Xingxing X; Liu, Weiqing W; Liu, Fang F; He, Yuanfang Y; Bai, Yan Y; Sun, Yan Y; Dai, Jiapei J; Li, Lingyi L; Xiao, Xiao X; Zhang, Chen C; Li, Ming M
Publication Date: 2018-12-07

Variant appearance in text: rs4236274
PubMed Link: 30531795
Variant Present in the following documents:
  • Main text
  • 41398_2018_Article_337.pdf
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Genome-wide association study of 40,000 individuals identifies two novel loci associated with bipolar disorder.

Human Molecular Genetics
Hou, Liping L; Bergen, Sarah E SE; Akula, Nirmala N; Song, Jie J; Hultman, Christina M CM; Landén, Mikael M; Adli, Mazda M; Alda, Martin M; Ardau, Raffaella R; Arias, Bárbara B; Aubry, Jean-Michel JM; Backlund, Lena L; Badner, Judith A JA; Barrett, Thomas B TB; Bauer, Michael M; Baune, Bernhard T BT; Bellivier, Frank F; Benabarre, Antonio A; Bengesser, Susanne S; Berrettini, Wade H WH; Bhattacharjee, Abesh Kumar AK; Biernacka, Joanna M JM; Birner, Armin A; Bloss, Cinnamon S CS; Brichant-Petitjean, Clara C; Bui, Elise T ET; Byerley, William W; Cervantes, Pablo P; Chillotti, Caterina C; Cichon, Sven S; Colom, Francesc F; Coryell, William W; Craig, David W DW; Cruceanu, Cristiana C; Czerski, Piotr M PM; Davis, Tony T; Dayer, Alexandre A; Degenhardt, Franziska F; Del Zompo, Maria M; DePaulo, J Raymond JR; Edenberg, Howard J HJ; Étain, Bruno B; Falkai, Peter P; Foroud, Tatiana T; Forstner, Andreas J AJ; Frisén, Louise L; Frye, Mark A MA; Fullerton, Janice M JM; Gard, Sébastien S; Garnham, Julie S JS; Gershon, Elliot S ES; Goes, Fernando S FS; Greenwood, Tiffany A TA; Grigoroiu-Serbanescu, Maria M; Hauser, Joanna J; Heilbronner, Urs U; Heilmann-Heimbach, Stefanie S; Herms, Stefan S; Hipolito, Maria M; Hitturlingappa, Shashi S; Hoffmann, Per P; Hofmann, Andrea A; Jamain, Stephane S; Jiménez, Esther E; Kahn, Jean-Pierre JP; Kassem, Layla L; Kelsoe, John R JR; Kittel-Schneider, Sarah S; Kliwicki, Sebastian S; Koller, Daniel L DL; König, Barbara B; Lackner, Nina N; Laje, Gonzalo G; Lang, Maren M; Lavebratt, Catharina C; Lawson, William B WB; Leboyer, Marion M; Leckband, Susan G SG; Liu, Chunyu C; Maaser, Anna A; Mahon, Pamela B PB; Maier, Wolfgang W; Maj, Mario M; Manchia, Mirko M; Martinsson, Lina L; McCarthy, Michael J MJ; McElroy, Susan L SL; McInnis, Melvin G MG; McKinney, Rebecca R; Mitchell, Philip B PB; Mitjans, Marina M; Mondimore, Francis M FM; Monteleone, Palmiero P; Mühleisen, Thomas W TW; Nievergelt, Caroline M CM; Nöthen, Markus M MM; Novák, Tomas T; Nurnberger, John I JI; Nwulia, Evaristus A EA; Ösby, Urban U; Pfennig, Andrea A; Potash, James B JB; Propping, Peter P; Reif, Andreas A; Reininghaus, Eva E; Rice, John J; Rietschel, Marcella M; Rouleau, Guy A GA; Rybakowski, Janusz K JK; Schalling, Martin M; Scheftner, William A WA; Schofield, Peter R PR; Schork, Nicholas J NJ; Schulze, Thomas G TG; Schumacher, Johannes J; Schweizer, Barbara W BW; Severino, Giovanni G; Shekhtman, Tatyana T; Shilling, Paul D PD; Simhandl, Christian C; Slaney, Claire M CM; Smith, Erin N EN; Squassina, Alessio A; Stamm, Thomas T; Stopkova, Pavla P; Streit, Fabian F; Strohmaier, Jana J; Szelinger, Szabolcs S; Tighe, Sarah K SK; Tortorella, Alfonso A; Turecki, Gustavo G; Vieta, Eduard E; Volkert, Julia J; Witt, Stephanie H SH; Wright, Adam A; Zandi, Peter P PP; Zhang, Peng P; Zollner, Sebastian S; McMahon, Francis J FJ
Publication Date: 2016-08-01

Variant appearance in text: rs4236274
PubMed Link: 27329760
Variant Present in the following documents:
  • Main text
View BVdb publication page