TMEM258 c.113+162A>G

Variant ID: 11-61557803-T-C

NM_014206.3(TMEM258):c.113+162A>G

This variant was identified in 81 publications

View GRCh38 version.




Publications:


Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine.

Nature Genetics
Schlosser, Pascal P; Scherer, Nora N; Grundner-Culemann, Franziska F; Monteiro-Martins, Sara S; Haug, Stefan S; Steinbrenner, Inga I; Uluvar, Burulça B; Wuttke, Matthias M; Cheng, Yurong Y; Ekici, Arif B AB; Gyimesi, Gergely G; Karoly, Edward D ED; Kotsis, Fruzsina F; Mielke, Johanna J; Gomez, Maria F MF; Yu, Bing B; Grams, Morgan E ME; Coresh, Josef J; Boerwinkle, Eric E; Köttgen, Michael M; Kronenberg, Florian F; Meiselbach, Heike H; Mohney, Robert P RP; Akilesh, Shreeram S; , ; Schmidts, Miriam M; Hediger, Matthias A MA; Schultheiss, Ulla T UT; Eckardt, Kai-Uwe KU; Oefner, Peter J PJ; Sekula, Peggy P; Li, Yong Y; Köttgen, Anna A
Publication Date: 2023-06-05

Variant appearance in text: rs102275
PubMed Link: 37277652
Variant Present in the following documents:
  • 41588_2023_1409_MOESM4_ESM.pdf
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Comprehensive proteogenomic characterization of early duodenal cancer reveals the carcinogenesis tracks of different subtypes.

Nature Communications
Li, Lingling L; Jiang, Dongxian D; Liu, Hui H; Guo, Chunmei C; Zhao, Rui R; Zhang, Qiao Q; Xu, Chen C; Qin, Zhaoyu Z; Feng, Jinwen J; Liu, Yang Y; Wang, Haixing H; Chen, Weijie W; Zhang, Xue X; Li, Bin B; Bai, Lin L; Tian, Sha S; Tan, Subei S; Yu, Zixiang Z; Chen, Lingli L; Huang, Jie J; Zhao, Jian-Yuan JY; Hou, Yingyong Y; Ding, Chen C
Publication Date: 2023-03-29

Variant appearance in text: rs102275
PubMed Link: 36991000
Variant Present in the following documents:
  • 41467_2023_37221_MOESM5_ESM.xlsx, sheet 3
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Role of the Gut-Brain Axis in the Shared Genetic Etiology Between Gastrointestinal Tract Diseases and Psychiatric Disorders: A Genome-Wide Pleiotropic Analysis.

Jama Psychiatry
Gong, Weiming W; Guo, Ping P; Li, Yuanming Y; Liu, Lu L; Yan, Ran R; Liu, Shuai S; Wang, Shukang S; Xue, Fuzhong F; Zhou, Xiang X; Yuan, Zhongshang Z
Publication Date: 2023-02-08

Variant appearance in text: rs102275
PubMed Link: 36753304
Variant Present in the following documents:
  • jamapsychiatry-e224974-s001.pdf
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JAK-STAT signaling in inflammatory breast cancer enables chemotherapy-resistant cell states.

Cancer Research
Stevens, Laura E LE; Peluffo, Guillermo G; Qiu, Xintao X; Temko, Daniel D; Fassl, Anne A; Li, Zheqi Z; Trinh, Anne A; Seehawer, Marco M; Jovanovic, Bojana B; Aleckovic, Masa M; Wilde, Callahan M CM; Geck, Renee C RC; Shu, Shaokun S; Kingston, Natalie L NL; Harper, Nicholas W NW; Almendro, Vanessa V; Pyke, Alanna L AL; Egri, Shawn B SB; Papanastasiou, Malvina M; Clement, Kendell K; Zhou, Ningxuan N; Walker, Sarah S; Salas, Jacqueline J; Park, So Yeon SY; Frank, David A DA; Meissner, Alexander A; Jaffe, Jacob D JD; Sicinski, Piotr P; Toker, Alex A; Michor, Franziska F; Long, Henry W HW; Overmoyer, Beth A BA; Polyak, Kornelia K
Publication Date: 2022-11-21

Variant appearance in text: TMEM258: 113+162A>G; rs102275
PubMed Link: 36409824
Variant Present in the following documents:
  • can-22-0423_supplementary_table_s3_suppst3.xlsx, sheet 1
View BVdb publication page



miR-1908: a microRNA with diverse functions in cancers and non-malignant conditions.

Cancer Cell International
Ghafouri-Fard, Soudeh S; Khoshbakht, Tayyebeh T; Hussen, Bashdar Mahmud BM; Taheri, Mohammad M; Samsami, Majid M
Publication Date: 2022-09-13

Variant appearance in text: rs102275
PubMed Link: 36100870
Variant Present in the following documents:
  • Main text
  • 12935_2022_Article_2709.pdf
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Role of circulating polyunsaturated fatty acids on cardiovascular diseases risk: analysis using Mendelian randomization and fatty acid genetic association data from over 114,000 UK Biobank participants.

Bmc Medicine
Borges, Maria Carolina MC; Haycock, Philip C PC; Zheng, Jie J; Hemani, Gibran G; Holmes, Michael V MV; Davey Smith, George G; Hingorani, Aroon D AD; Lawlor, Deborah A DA
Publication Date: 2022-06-13

Variant appearance in text: rs102275
PubMed Link: 35692035
Variant Present in the following documents:
  • Main text
  • 12916_2022_Article_2399.pdf
View BVdb publication page



Young-onset diabetes in Asian Indians is associated with lower measured and genetically determined beta cell function.

Diabetologia
Siddiqui, Moneeza K MK; Anjana, Ranjit Mohan RM; Dawed, Adem Y AY; Martoeau, Cyrielle C; Srinivasan, Sundararajan S; Saravanan, Jebarani J; Madanagopal, Sathish K SK; Taylor, Alasdair A; Bell, Samira S; Veluchamy, Abirami A; Pradeepa, Rajendra R; Sattar, Naveed N; Venkatesan, Radha R; Palmer, Colin N A CNA; Pearson, Ewan R ER; Mohan, Viswanathan V
Publication Date: 2022-06

Variant appearance in text: rs102275
PubMed Link: 35247066
Variant Present in the following documents:
  • 125_2022_5671_MOESM1_ESM.pdf
View BVdb publication page



Fatty Acids and Frailty: A Mendelian Randomization Study.

Nutrients
Tomata, Yasutake Y; Wang, Yunzhang Y; Hägg, Sara S; Jylhävä, Juulia J
Publication Date: 2021-10-09

Variant appearance in text: rs102275
PubMed Link: 34684540
Variant Present in the following documents:
  • Main text
  • nutrients-13-03539.pdf
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Using Genetic Variants to Evaluate the Causal Effect of Plasma Phospholipid Fatty Acids on Breast Cancer and Prostate Cancer: A Mendelian Randomization Study.

Frontiers In Genetics
Yang, Ze Z; Li, Jingjia J; Sun, Yandi Y; Qu, Zihao Z; Lin, Yindan Y; Zhang, Lihong L; He, Qian Q; Jia, Xueyao X; Ahmad, Mashaal M; Zhang, Xueyun X; Luo, Yan Y
Publication Date: 2021

Variant appearance in text: rs102275
PubMed Link: 34276774
Variant Present in the following documents:
  • Main text
  • fgene-12-664498.pdf
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Genomic and pleiotropic analyses of resting QT interval identifies novel loci and overlap with atrial electrical disorders.

Human Molecular Genetics
van Duijvenboden, Stefan S; Ramírez, Julia J; Young, William J WJ; Orini, Michele M; Mifsud, Borbala B; Tinker, Andrew A; Lambiase, Pier D PD; Munroe, Patricia B PB
Publication Date: 2021-11-30

Variant appearance in text: rs102275
PubMed Link: 34274964
Variant Present in the following documents:
  • Main text
View BVdb publication page



Plasma Metabolomic Signatures of Chronic Obstructive Pulmonary Disease and the Impact of Genetic Variants on Phenotype-Driven Modules.

Network And Systems Medicine
Gillenwater, Lucas A LA; Pratte, Katherine A KA; Hobbs, Brian D BD; Cho, Michael H MH; Zhuang, Yonghua Y; Halper-Stromberg, Eitan E; Cruickshank-Quinn, Charmion C; Reisdorph, Nichole N; Petrache, Irina I; Labaki, Wassim W WW; O'Neal, Wanda K WK; Ortega, Victor E VE; Jones, Dean P DP; Uppal, Karan K; Jacobson, Sean S; Michelotti, Gregory G; Wendt, Christine H CH; Kechris, Katerina J KJ; Bowler, Russell P RP
Publication Date: 2020-12-01

Variant appearance in text: rs102275
PubMed Link: 33987620
Variant Present in the following documents:
  • Main text
  • nsm.2020.0009.pdf
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A genome-wide meta-analysis yields 46 new loci associating with biomarkers of iron homeostasis.

Communications Biology
Bell, Steven S; Rigas, Andreas S AS; Magnusson, Magnus K MK; Ferkingstad, Egil E; Allara, Elias E; Bjornsdottir, Gyda G; Ramond, Anna A; Sørensen, Erik E; Halldorsson, Gisli H GH; Paul, Dirk S DS; Burgdorf, Kristoffer S KS; Eggertsson, Hannes P HP; Howson, Joanna M M JMM; Thørner, Lise W LW; Kristmundsdottir, Snaedis S; Astle, William J WJ; Erikstrup, Christian C; Sigurdsson, Jon K JK; Vuckovic, Dragana D; Dinh, Khoa M KM; Tragante, Vinicius V; Surendran, Praveen P; Pedersen, Ole B OB; Vidarsson, Brynjar B; Jiang, Tao T; Paarup, Helene M HM; Onundarson, Pall T PT; Akbari, Parsa P; Nielsen, Kaspar R KR; Lund, Sigrun H SH; Juliusson, Kristinn K; Magnusson, Magnus I MI; Frigge, Michael L ML; Oddsson, Asmundur A; Olafsson, Isleifur I; Kaptoge, Stephen S; Hjalgrim, Henrik H; Runarsson, Gudmundur G; Wood, Angela M AM; Jonsdottir, Ingileif I; Hansen, Thomas F TF; Sigurdardottir, Olof O; Stefansson, Hreinn H; Rye, David D; , ; Peters, James E JE; Westergaard, David D; Holm, Hilma H; Soranzo, Nicole N; Banasik, Karina K; Thorleifsson, Gudmar G; Ouwehand, Willem H WH; Thorsteinsdottir, Unnur U; Roberts, David J DJ; Sulem, Patrick P; Butterworth, Adam S AS; Gudbjartsson, Daniel F DF; Danesh, John J; Brunak, Søren S; Di Angelantonio, Emanuele E; Ullum, Henrik H; Stefansson, Kari K
Publication Date: 2021-02-03

Variant appearance in text: rs102275
PubMed Link: 33536631
Variant Present in the following documents:
  • 42003_2020_1575_MOESM4_ESM.xlsx, sheet 10
View BVdb publication page



Maternal and child fatty acid desaturase genotype as determinants of cord blood long-chain PUFA (LCPUFA) concentrations in the Seychelles Child Development Study.

The British Journal Of Nutrition
Conway, Marie C MC; McSorley, Emeir M EM; Mulhern, Maria S MS; Spence, Toni T; Weslowska, Maria M; Strain, J J JJ; van Wijngaarden, Edwin E; Davidson, Phil W PW; Myers, Gary J GJ; Wahlberg, Karin E KE; Shamlaye, Conrad F CF; Cobice, Diego F DF; Hyland, Barry W BW; Pineda, Daniela D; Broberg, Karin K; Yeates, Alison J AJ
Publication Date: 2021-12-14

Variant appearance in text: rs102275
PubMed Link: 33526157
Variant Present in the following documents:
  • Main text
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The Role of Genetically Determined Glycemic Traits in Breast Cancer: A Mendelian Randomization Study.

Frontiers In Genetics
Jung, Su Yon SY; Mancuso, Nicholas N; Han, Sihao S; Zhang, Zuo-Feng ZF
Publication Date: 2020

Variant appearance in text: rs102275
PubMed Link: 33193614
Variant Present in the following documents:
  • Main text
View BVdb publication page



Eicosanoid Inflammatory Mediators Are Robustly Associated With Blood Pressure in the General Population.

Journal Of The American Heart Association
Palmu, Joonatan J; Watrous, Jeramie D JD; Mercader, Kysha K; Havulinna, Aki S AS; Lagerborg, Kim A KA; Salosensaari, Aaro A; Inouye, Mike M; Larson, Martin G MG; Rong, Jian J; Vasan, Ramachandran S RS; Lahti, Leo L; Andres, Allen A; Cheng, Susan S; Jousilahti, Pekka P; Salomaa, Veikko V; Jain, Mohit M; Niiranen, Teemu J TJ
Publication Date: 2020-10-20

Variant appearance in text: rs102275
PubMed Link: 32975162
Variant Present in the following documents:
  • JAH3-9-e017598.pdf
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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: rs102275
PubMed Link: 32879140
Variant Present in the following documents:
  • jciinsight-5-136477-s105.xlsx, sheet 5
View BVdb publication page



A Unifying Framework for Imputing Summary Statistics in Genome-Wide Association Studies.

Journal Of Computational Biology : A Journal Of Computational Molecular Cell Biology
Wu, Yue Y; Eskin, Eleazar E; Sankararaman, Sriram S
Publication Date: 2020-03

Variant appearance in text: rs102275
PubMed Link: 32053016
Variant Present in the following documents:
  • Main text
View BVdb publication page



Genome-Wide Association Study for Serum Omega-3 and Omega-6 Polyunsaturated Fatty Acids: Exploratory Analysis of the Sex-Specific Effects and Dietary Modulation in Mediterranean Subjects with Metabolic Syndrome.

Nutrients
Coltell, Oscar O; Sorlí, Jose V JV; Asensio, Eva M EM; Barragán, Rocío R; González, José I JI; Giménez-Alba, Ignacio M IM; Zanón-Moreno, Vicente V; Estruch, Ramon R; Ramírez-Sabio, Judith B JB; Pascual, Eva C EC; Ortega-Azorín, Carolina C; Ordovas, Jose M JM; Corella, Dolores D
Publication Date: 2020-01-24

Variant appearance in text: rs102275
PubMed Link: 31991592
Variant Present in the following documents:
  • Main text
  • nutrients-12-00310-s001.pdf
  • nutrients-12-00310.pdf
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Influence of fatty acid desaturase (FADS) genotype on maternal and child polyunsaturated fatty acids (PUFA) status and child health outcomes: a systematic review.

Nutrition Reviews
Conway, Marie C MC; McSorley, Emeir M EM; Mulhern, Maria S MS; Strain, J J JJ; van Wijngaarden, Edwin E; Yeates, Alison J AJ
Publication Date: 2020-08-01

Variant appearance in text: rs102275
PubMed Link: 31943072
Variant Present in the following documents:
  • Main text
View BVdb publication page



The Genetics of the Mood Disorder Spectrum: Genome-wide Association Analyses of More Than 185,000 Cases and 439,000 Controls.

Biological Psychiatry
Coleman, Jonathan R I JRI; Gaspar, Héléna A HA; Bryois, Julien J; , ; , ; Breen, Gerome G
Publication Date: 2020-07-15

Variant appearance in text: rs102275
PubMed Link: 31926635
Variant Present in the following documents:
  • Main text
View BVdb publication page



Plasma Phospholipid Fatty Acids, FADS1 and Risk of 15 Cardiovascular Diseases: A Mendelian Randomisation Study.

Nutrients
Yuan, Shuai S; Bäck, Magnus M; Bruzelius, Maria M; Mason, Amy M AM; Burgess, Stephen S; Larsson, Susanna S
Publication Date: 2019-12-07

Variant appearance in text: rs102275
PubMed Link: 31817859
Variant Present in the following documents:
  • Main text
View BVdb publication page



Association of genetic variants related to plasma fatty acids with type 2 diabetes mellitus and glycaemic traits: a Mendelian randomisation study.

Diabetologia
Yuan, Shuai S; Larsson, Susanna C SC
Publication Date: 2020-01

Variant appearance in text: rs102275
PubMed Link: 31690987
Variant Present in the following documents:
  • Main text
  • 125_2019_Article_5019.pdf
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A comprehensive study of metabolite genetics reveals strong pleiotropy and heterogeneity across time and context.

Nature Communications
Gallois, Apolline A; Mefford, Joel J; Ko, Arthur A; Vaysse, Amaury A; Julienne, Hanna H; Ala-Korpela, Mika M; Laakso, Markku M; Zaitlen, Noah N; Pajukanta, Päivi P; Aschard, Hugues H
Publication Date: 2019-10-21

Variant appearance in text: rs102275
PubMed Link: 31636271
Variant Present in the following documents:
  • Main text
  • 41467_2019_Article_12703.pdf
View BVdb publication page



Genome-wide association analysis of 350 000 Caucasians from the UK Biobank identifies novel loci for asthma, hay fever and eczema.

Human Molecular Genetics
Johansson, Åsa Å; Rask-Andersen, Mathias M; Karlsson, Torgny T; Ek, Weronica E WE
Publication Date: 2019-12-01

Variant appearance in text: rs102275
PubMed Link: 31361310
Variant Present in the following documents:
  • Main text
  • ddz175.pdf
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Plasma Phospholipid Fatty Acids and Risk of Atrial Fibrillation: A Mendelian Randomization Study.

Nutrients
Yuan, Shuai S; Larsson, Susanna C SC
Publication Date: 2019-07-19

Variant appearance in text: rs102275
PubMed Link: 31331006
Variant Present in the following documents:
  • Main text
  • nutrients-11-01651.pdf
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Subset-Based Analysis Using Gene-Environment Interactions for Discovery of Genetic Associations across Multiple Studies or Phenotypes.

Human Heredity
Yu, Youfei Y; Xia, Lu L; Lee, Seunggeun S; Zhou, Xiang X; Stringham, Heather M HM; Boehnke, Michael M; Mukherjee, Bhramar B
Publication Date: 2018

Variant appearance in text: rs102275
PubMed Link: 31132756
Variant Present in the following documents:
  • Main text
View BVdb publication page



Mendelian randomisation: A powerful and inexpensive method for identifying and excluding non-genetic risk factors for colorectal cancer.

Molecular Aspects Of Medicine
Cornish, Alex J AJ; Tomlinson, Ian P M IPM; Houlston, Richard S RS
Publication Date: 2019-10

Variant appearance in text: rs102275
PubMed Link: 30710596
Variant Present in the following documents:
  • Main text
  • main.pdf
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Chromatin interactions and expression quantitative trait loci reveal genetic drivers of multimorbidities.

Nature Communications
Fadason, Tayaza T; Schierding, William W; Lumley, Thomas T; O'Sullivan, Justin M JM
Publication Date: 2018-12-05

Variant appearance in text: rs102275
PubMed Link: 30518762
Variant Present in the following documents:
  • 41467_2018_Article_7692.pdf
View BVdb publication page



Genetic Evidence Supporting the Role of the Calcium Channel, CACNA1S, in Tooth Cusp and Root Patterning.

Frontiers In Physiology
Laugel-Haushalter, Virginie V; Morkmued, Supawich S; Stoetzel, Corinne C; Geoffroy, Véronique V; Muller, Jean J; Boland, Anne A; Deleuze, Jean-François JF; Chennen, Kirsley K; Pitiphat, Waranuch W; Dollfus, Hélène H; Niederreither, Karen K; Bloch-Zupan, Agnès A; Pungchanchaikul, Patimaporn P
Publication Date: 2018

Variant appearance in text: rs102275
PubMed Link: 30319441
Variant Present in the following documents:
  • Table_6.xlsx, sheet 1
  • Table_5.xlsx, sheet 1
  • Table_7.xlsx, sheet 1
View BVdb publication page



Improving Imputation Accuracy by Inferring Causal Variants in Genetic Studies.

Journal Of Computational Biology : A Journal Of Computational Molecular Cell Biology
Wu, Yue Y; Hormozdiari, Farhad F; Joo, Jong Wha J JWJ; Eskin, Eleazar E
Publication Date: 2019-11

Variant appearance in text: rs102275
PubMed Link: 30272994
Variant Present in the following documents:
  • Main text
View BVdb publication page



FADS1-FADS2 genetic polymorphisms are associated with fatty acid metabolism through changes in DNA methylation and gene expression.

Clinical Epigenetics
He, Zhen Z; Zhang, Rong R; Jiang, Feng F; Zhang, Hong H; Zhao, Aihua A; Xu, Bo B; Jin, Li L; Wang, Tao T; Jia, Wei W; Jia, Weiping W; Hu, Cheng C
Publication Date: 2018-08-29

Variant appearance in text: rs102275
PubMed Link: 30157936
Variant Present in the following documents:
  • Main text
  • 13148_2018_Article_545.pdf
View BVdb publication page



ExomeChip-Wide Analysis of 95 626 Individuals Identifies 10 Novel Loci Associated With QT and JT Intervals.

Circulation. Genomic And Precision Medicine
Bihlmeyer, Nathan A NA; Brody, Jennifer A JA; Smith, Albert Vernon AV; Warren, Helen R HR; Lin, Honghuang H; Isaacs, Aaron A; Liu, Ching-Ti CT; Marten, Jonathan J; Radmanesh, Farid F; Hall, Leanne M LM; Grarup, Niels N; Mei, Hao H; Müller-Nurasyid, Martina M; Huffman, Jennifer E JE; Verweij, Niek N; Guo, Xiuqing X; Yao, Jie J; Li-Gao, Ruifang R; van den Berg, Marten M; Weiss, Stefan S; Prins, Bram P BP; van Setten, Jessica J; Haessler, Jeffrey J; Lyytikäinen, Leo-Pekka LP; Li, Man M; Alonso, Alvaro A; Soliman, Elsayed Z EZ; Bis, Joshua C JC; Austin, Tom T; Chen, Yii-Der Ida YI; Psaty, Bruce M BM; Harrris, Tamara B TB; Launer, Lenore J LJ; Padmanabhan, Sandosh S; Dominiczak, Anna A; Huang, Paul L PL; Xie, Zhijun Z; Ellinor, Patrick T PT; Kors, Jan A JA; Campbell, Archie A; Murray, Alison D AD; Nelson, Christopher P CP; Tobin, Martin D MD; Bork-Jensen, Jette J; Hansen, Torben T; Pedersen, Oluf O; Linneberg, Allan A; Sinner, Moritz F MF; Peters, Annette A; Waldenberger, Melanie M; Meitinger, Thomas T; Perz, Siegfried S; Kolcic, Ivana I; Rudan, Igor I; de Boer, Rudolf A RA; van der Meer, Peter P; Lin, Henry J HJ; Taylor, Kent D KD; de Mutsert, Renée R; Trompet, Stella S; Jukema, J Wouter JW; Maan, Arie C AC; Stricker, Bruno H C BHC; Rivadeneira, Fernando F; Uitterlinden, André A; Völker, Uwe U; Homuth, Georg G; Völzke, Henry H; Felix, Stephan B SB; Mangino, Massimo M; Spector, Timothy D TD; Bots, Michiel L ML; Perez, Marco M; Raitakari, Olli T OT; Kähönen, Mika M; Mononen, Nina N; Gudnason, Vilmundur V; Munroe, Patricia B PB; Lubitz, Steven A SA; van Duijn, Cornelia M CM; Newton-Cheh, Christopher H CH; Hayward, Caroline C; Rosand, Jonathan J; Samani, Nilesh J NJ; Kanters, Jørgen K JK; Wilson, James G JG; Kääb, Stefan S; Polasek, Ozren O; van der Harst, Pim P; Heckbert, Susan R SR; Rotter, Jerome I JI; Mook-Kanamori, Dennis O DO; Eijgelsheim, Mark M; Dörr, Marcus M; Jamshidi, Yalda Y; Asselbergs, Folkert W FW; Kooperberg, Charles C; Lehtimäki, Terho T; Arking, Dan E DE; Sotoodehnia, Nona N
Publication Date: 2018-01

Variant appearance in text: rs102275
PubMed Link: 29874175
Variant Present in the following documents:
  • hcg-11-e001758-s001.pdf
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Genome-Wide Association Studies of Metabolites in Patients with CKD Identify Multiple Loci and Illuminate Tubular Transport Mechanisms.

Journal Of The American Society Of Nephrology : Jasn
Li, Yong Y; Sekula, Peggy P; Wuttke, Matthias M; Wahrheit, Judith J; Hausknecht, Birgit B; Schultheiss, Ulla T UT; Gronwald, Wolfram W; Schlosser, Pascal P; Tucci, Sara S; Ekici, Arif B AB; Spiekerkoetter, Ute U; Kronenberg, Florian F; Eckardt, Kai-Uwe KU; Oefner, Peter J PJ; Köttgen, Anna A; ,
Publication Date: 2018-05

Variant appearance in text: rs102275
PubMed Link: 29545352
Variant Present in the following documents:
  • Main text
View BVdb publication page



DNA methylation mapping identifies gene regulatory effects in patients with systemic lupus erythematosus.

Annals Of The Rheumatic Diseases
Imgenberg-Kreuz, Juliana J; Carlsson Almlöf, Jonas J; Leonard, Dag D; Alexsson, Andrei A; Nordmark, Gunnel G; Eloranta, Maija-Leena ML; Rantapää-Dahlqvist, Solbritt S; Bengtsson, Anders A AA; Jönsen, Andreas A; Padyukov, Leonid L; Gunnarsson, Iva I; Svenungsson, Elisabet E; Sjöwall, Christopher C; Rönnblom, Lars L; Syvänen, Ann-Christine AC; Sandling, Johanna K JK
Publication Date: 2018-05

Variant appearance in text: rs102275
PubMed Link: 29437559
Variant Present in the following documents:
  • annrheumdis-2017-212379supp016.pdf
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Dietary adaptation of FADS genes in Europe varied across time and geography.

Nature Ecology & Evolution
Ye, Kaixiong K; Gao, Feng F; Wang, David D; Bar-Yosef, Ofer O; Keinan, Alon A
Publication Date: 2017-05-26

Variant appearance in text: rs102275
PubMed Link: 29094686
Variant Present in the following documents:
  • NIHMS869521-supplement-2.pdf
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Pro-inflammatory fatty acid profile and colorectal cancer risk: A Mendelian randomisation analysis.

European Journal Of Cancer (Oxford, England : 1990)
May-Wilson, Sebastian S; Sud, Amit A; Law, Philip J PJ; Palin, Kimmo K; Tuupanen, Sari S; Gylfe, Alexandra A; Hänninen, Ulrika A UA; Cajuso, Tatiana T; Tanskanen, Tomas T; Kondelin, Johanna J; Kaasinen, Eevi E; Sarin, Antti-Pekka AP; Eriksson, Johan G JG; Rissanen, Harri H; Knekt, Paul P; Pukkala, Eero E; Jousilahti, Pekka P; Salomaa, Veikko V; Ripatti, Samuli S; Palotie, Aarno A; Renkonen-Sinisalo, Laura L; Lepistö, Anna A; Böhm, Jan J; Mecklin, Jukka-Pekka JP; Al-Tassan, Nada A NA; Palles, Claire C; Farrington, Susan M SM; Timofeeva, Maria N MN; Meyer, Brian F BF; Wakil, Salma M SM; Campbell, Harry H; Smith, Christopher G CG; Idziaszczyk, Shelley S; Maughan, Timothy S TS; Fisher, David D; Kerr, Rachel R; Kerr, David D; Passarelli, Michael N MN; Figueiredo, Jane C JC; Buchanan, Daniel D DD; Win, Aung K AK; Hopper, John L JL; Jenkins, Mark A MA; Lindor, Noralane M NM; Newcomb, Polly A PA; Gallinger, Steven S; Conti, David D; Schumacher, Fred F; Casey, Graham G; Aaltonen, Lauri A LA; Cheadle, Jeremy P JP; Tomlinson, Ian P IP; Dunlop, Malcolm G MG; Houlston, Richard S RS
Publication Date: 2017-10

Variant appearance in text: rs102275
PubMed Link: 28829991
Variant Present in the following documents:
  • Main text
View BVdb publication page



Genetic variants including markers from the exome chip and metabolite traits of type 2 diabetes.

Scientific Reports
Jäger, Susanne S; Wahl, Simone S; Kröger, Janine J; Sharma, Sapna S; Hoffmann, Per P; Floegel, Anna A; Pischon, Tobias T; Prehn, Cornelia C; Adamski, Jerzy J; Müller-Nurasyid, Martina M; Waldenberger, Melanie M; Strauch, Konstantin K; Peters, Annette A; Gieger, Christian C; Suhre, Karsten K; Grallert, Harald H; Boeing, Heiner H; Schulze, Matthias B MB; Meidtner, Karina K
Publication Date: 2017-07-20

Variant appearance in text: rs102275
PubMed Link: 28729637
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  • 41598_2017_6158_MOESM1_ESM.pdf
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Discovery and fine-mapping of loci associated with MUFAs through trans-ethnic meta-analysis in Chinese and European populations.

Journal Of Lipid Research
Hu, Yao Y; Tanaka, Toshiko T; Zhu, Jingwen J; Guan, Weihua W; Wu, Jason H Y JHY; Psaty, Bruce M BM; McKnight, Barbara B; King, Irena B IB; Sun, Qi Q; Richard, Melissa M; Manichaikul, Ani A; Frazier-Wood, Alexis C AC; Kabagambe, Edmond K EK; Hopkins, Paul N PN; Ordovas, Jose M JM; Ferrucci, Luigi L; Bandinelli, Stefania S; Arnett, Donna K DK; Chen, Yii-Der I YI; Liang, Shuang S; Siscovick, David S DS; Tsai, Michael Y MY; Rich, Stephen S SS; Fornage, Myriam M; Hu, Frank B FB; Rimm, Eric B EB; Jensen, Majken K MK; Lemaitre, Rozenn N RN; Mozaffarian, Dariush D; Steffen, Lyn M LM; Morris, Andrew P AP; Li, Huaixing H; Lin, Xu X
Publication Date: 2017-05

Variant appearance in text: rs102275
PubMed Link: 28298293
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  • Main text
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Integrating molecular QTL data into genome-wide genetic association analysis: Probabilistic assessment of enrichment and colocalization.

Plos Genetics
Wen, Xiaoquan X; Pique-Regi, Roger R; Luca, Francesca F
Publication Date: 2017-03

Variant appearance in text: rs102275
PubMed Link: 28278150
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  • Main text
  • pgen.1006646.pdf
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Epidemiology of colorectal cancer.

International Journal Of Molecular Epidemiology And Genetics
Marley, Andrew R AR; Nan, Hongmei H
Publication Date: 2016

Variant appearance in text: rs102275
PubMed Link: 27766137
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  • Main text
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Blood and Intestine eQTLs from an Anti-TNF-Resistant Crohn's Disease Cohort Inform IBD Genetic Association Loci.

Clinical And Translational Gastroenterology
Di Narzo, Antonio F AF; Peters, Lauren A LA; Argmann, Carmen C; Stojmirovic, Aleksandar A; Perrigoue, Jacqueline J; Li, Katherine K; Telesco, Shannon S; Kidd, Brian B; Walker, Jennifer J; Dudley, Joel J; Cho, Judy J; Schadt, Eric E EE; Kasarskis, Andrew A; Curran, Mark M; Dobrin, Radu R; Hao, Ke K
Publication Date: 2016-06-23

Variant appearance in text: rs102275
PubMed Link: 27336838
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  • Main text
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The 11th NORDIC NUTRITION CONFERENCE NNC2016.

Food & Nutrition Research
Publication Date: 2016

Variant appearance in text: rs102275
PubMed Link: 27317923
Variant Present in the following documents:
  • Main text
  • FNR-60-31961.pdf
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Integrative Multi-omic Analysis of Human Platelet eQTLs Reveals Alternative Start Site in Mitofusin 2.

American Journal Of Human Genetics
Simon, Lukas M LM; Chen, Edward S ES; Edelstein, Leonard C LC; Kong, Xianguo X; Bhatlekar, Seema S; Rigoutsos, Isidore I; Bray, Paul F PF; Shaw, Chad A CA
Publication Date: 2016-05-05

Variant appearance in text: rs102275
PubMed Link: 27132591
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  • Main text
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Insight into Genotype-Phenotype Associations through eQTL Mapping in Multiple Cell Types in Health and Immune-Mediated Disease.

Plos Genetics
Peters, James E JE; Lyons, Paul A PA; Lee, James C JC; Richard, Arianne C AC; Fortune, Mary D MD; Newcombe, Paul J PJ; Richardson, Sylvia S; Smith, Kenneth G C KG
Publication Date: 2016-03

Variant appearance in text: rs102275
PubMed Link: 27015630
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  • Main text
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Meta-analysis of genome-wide association studies identifies three novel loci for saturated fatty acids in East Asians.

European Journal Of Nutrition
Zhu, Jingwen J; Manichaikul, Ani A; Hu, Yao Y; Chen, Yii-Der I YI; Liang, Shuang S; Steffen, Lyn M LM; Rich, Stephen S SS; Tsai, Michael M; Siscovick, David S DS; Lemaitre, Rozenn N RN; Li, Huaixing H; Lin, Xu X
Publication Date: 2017-06

Variant appearance in text: rs102275
PubMed Link: 26932504
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Single Nucleotide Polymorphisms in the FADS Gene Cluster but not the ELOVL2 Gene are Associated with Serum Polyunsaturated Fatty Acid Composition and Development of Allergy (in a Swedish Birth Cohort).

Nutrients
Barman, Malin M; Nilsson, Staffan S; Torinsson Naluai, Åsa Å; Sandin, Anna A; Wold, Agnes E AE; Sandberg, Ann-Sofie AS
Publication Date: 2015-12-03

Variant appearance in text: rs102275
PubMed Link: 26633493
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  • Main text
  • nutrients-07-05521.pdf
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CPAG: software for leveraging pleiotropy in GWAS to reveal similarity between human traits links plasma fatty acids and intestinal inflammation.

Genome Biology
Wang, Liuyang L; Oehlers, Stefan H SH; Espenschied, Scott T ST; Rawls, John F JF; Tobin, David M DM; Ko, Dennis C DC
Publication Date: 2015-09-15

Variant appearance in text: rs102275
PubMed Link: 26374098
Variant Present in the following documents:
  • Main text
  • 13059_2015_Article_722.pdf
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Identification of a common variant with potential pleiotropic effect on risk of inflammatory bowel disease and colorectal cancer.

Carcinogenesis
Khalili, Hamed H; Gong, Jian J; Brenner, Hermann H; Austin, Thomas R TR; Hutter, Carolyn M CM; Baba, Yoshifumi Y; Baron, John A JA; Berndt, Sonja I SI; Bézieau, Stéphane S; Caan, Bette B; Campbell, Peter T PT; Chang-Claude, Jenny J; Chanock, Stephen J SJ; Chen, Constance C; Hsu, Li L; Jiao, Shuo S; Conti, David V DV; Duggan, David D; Fuchs, Charles S CS; Gala, Manish M; Gallinger, Steven S; Haile, Robert W RW; Harrison, Tabitha A TA; Hayes, Richard R; Hazra, Aditi A; Henderson, Brian B; Haiman, Chris C; Hoffmeister, Michael M; Hopper, John L JL; Jenkins, Mark A MA; Kolonel, Laurence N LN; Küry, Sébastien S; LaCroix, Andrea A; Marchand, Loic Le LL; Lemire, Mathieu M; Lindor, Noralane M NM; Ma, Jing J; Manson, JoAnn E JE; Morikawa, Teppei T; Nan, Hongmei H; Ng, Kimmie K; Newcomb, Polly A PA; Nishihara, Reiko R; Potter, John D JD; Qu, Conghui C; Schoen, Robert E RE; Schumacher, Fredrick R FR; Seminara, Daniela D; Taverna, Darin D; Thibodeau, Stephen S; Wactawski-Wende, Jean J; White, Emily E; Wu, Kana K; Zanke, Brent W BW; Casey, Graham G; Hudson, Thomas J TJ; Kraft, Peter P; Peters, Ulrike U; Slattery, Martha L ML; Ogino, Shuji S; Chan, Andrew T AT; ,
Publication Date: 2015-09

Variant appearance in text: rs102275
PubMed Link: 26071399
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Fatty acid desaturase 1 gene polymorphisms control human hepatic lipid composition.

Hepatology (Baltimore, Md.)
Wang, Libo L; Athinarayanan, Shaminie S; Jiang, Guanglong G; Chalasani, Naga N; Zhang, Min M; Liu, Wanqing W
Publication Date: 2015-01

Variant appearance in text: rs102275
PubMed Link: 25123259
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Serum cholesterol and variant in cholesterol-related gene CETP predict white matter microstructure.

Neurobiology Of Aging
Warstadt, Nicholus M NM; Dennis, Emily L EL; Jahanshad, Neda N; Kohannim, Omid O; Nir, Talia M TM; McMahon, Katie L KL; de Zubicaray, Greig I GI; Montgomery, Grant W GW; Henders, Anjali K AK; Martin, Nicholas G NG; Whitfield, John B JB; Jack, Clifford R CR; Bernstein, Matt A MA; Weiner, Michael W MW; Toga, Arthur W AW; Wright, Margaret J MJ; Thompson, Paul M PM; ,
Publication Date: 2014-11

Variant appearance in text: rs102275
PubMed Link: 24997672
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  • Main text
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Large-scale East-Asian eQTL mapping reveals novel candidate genes for LD mapping and the genomic landscape of transcriptional effects of sequence variants.

Plos One
Narahara, Maiko M; Higasa, Koichiro K; Nakamura, Seiji S; Tabara, Yasuharu Y; Kawaguchi, Takahisa T; Ishii, Miho M; Matsubara, Kenichi K; Matsuda, Fumihiko F; Yamada, Ryo R
Publication Date: 2014

Variant appearance in text: rs102275
PubMed Link: 24956270
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  • Main text
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Large-scale genetic study in East Asians identifies six new loci associated with colorectal cancer risk.

Nature Genetics
Zhang, Ben B; Jia, Wei-Hua WH; Matsuda, Koichi K; Kweon, Sun-Seog SS; Matsuo, Keitaro K; Xiang, Yong-Bing YB; Shin, Aesun A; Jee, Sun Ha SH; Kim, Dong-Hyun DH; Cai, Qiuyin Q; Long, Jirong J; Shi, Jiajun J; Wen, Wanqing W; Yang, Gong G; Zhang, Yanfeng Y; Li, Chun C; Li, Bingshan B; Guo, Yan Y; Ren, Zefang Z; Ji, Bu-Tian BT; Pan, Zhi-Zhong ZZ; Takahashi, Atsushi A; Shin, Min-Ho MH; Matsuda, Fumihiko F; Gao, Yu-Tang YT; Oh, Jae Hwan JH; Kim, Soriul S; Ahn, Yoon-Ok YO; , ; Chan, Andrew T AT; Chang-Claude, Jenny J; Slattery, Martha L ML; , ; Gruber, Stephen B SB; Schumacher, Fredrick R FR; Stenzel, Stephanie L SL; , ; Casey, Graham G; Kim, Hyeong-Rok HR; Jeong, Jin-Young JY; Park, Ji Won JW; Li, Hong-Lan HL; Hosono, Satoyo S; Cho, Sang-Hee SH; Kubo, Michiaki M; Shu, Xiao-Ou XO; Zeng, Yi-Xin YX; Zheng, Wei W
Publication Date: 2014-06

Variant appearance in text: rs102275
PubMed Link: 24836286
Variant Present in the following documents:
  • NIHMS588441-supplement-1.pdf
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Genome-wide association study of plasma N6 polyunsaturated fatty acids within the cohorts for heart and aging research in genomic epidemiology consortium.

Circulation. Cardiovascular Genetics
Guan, Weihua W; Steffen, Brian T BT; Lemaitre, Rozenn N RN; Wu, Jason H Y JHY; Tanaka, Toshiko T; Manichaikul, Ani A; Foy, Millennia M; Rich, Stephen S SS; Wang, Lu L; Nettleton, Jennifer A JA; Tang, Weihong W; Gu, Xiangjun X; Bandinelli, Stafania S; King, Irena B IB; McKnight, Barbara B; Psaty, Bruce M BM; Siscovick, David D; Djousse, Luc L; Chen, Yii-Der Ida YI; Ferrucci, Luigi L; Fornage, Myriam M; Mozafarrian, Dariush D; Tsai, Michael Y MY; Steffen, Lyn M LM
Publication Date: 2014-06

Variant appearance in text: rs102275
PubMed Link: 24823311
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GeMes, clusters of DNA methylation under genetic control, can inform genetic and epigenetic analysis of disease.

American Journal Of Human Genetics
Liu, Yun Y; Li, Xin X; Aryee, Martin J MJ; Ekström, Tomas J TJ; Padyukov, Leonid L; Klareskog, Lars L; Vandiver, Amy A; Moore, Ann Zenobia AZ; Tanaka, Toshiko T; Ferrucci, Luigi L; Fallin, M Daniele MD; Feinberg, Andrew P AP
Publication Date: 2014-04-03

Variant appearance in text: rs102275
PubMed Link: 24656863
Variant Present in the following documents:
  • Main text
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Efficient multivariate linear mixed model algorithms for genome-wide association studies.

Nature Methods
Zhou, Xiang X; Stephens, Matthew M
Publication Date: 2014-04

Variant appearance in text: rs102275
PubMed Link: 24531419
Variant Present in the following documents:
  • NIHMS560150-supplement-1.pdf
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Genetic comorbidities in Parkinson's disease.

Human Molecular Genetics
Nalls, Mike A MA; Saad, Mohamad M; Noyce, Alastair J AJ; Keller, Margaux F MF; Schrag, Anette A; Bestwick, Jonathan P JP; Traynor, Bryan J BJ; Gibbs, J Raphael JR; Hernandez, Dena G DG; Cookson, Mark R MR; Morris, Huw R HR; Williams, Nigel N; Gasser, Thomas T; Heutink, Peter P; Wood, Nick N; Hardy, John J; Martinez, Maria M; Singleton, Andrew B AB; , ; , ; , ; ,
Publication Date: 2014-02-01

Variant appearance in text: rs102275
PubMed Link: 24057672
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FADS2 Genetic Variance in Combination with Fatty Acid Intake Might Alter Composition of the Fatty Acids in Brain.

Plos One
Rizzi, Thais S TS; van der Sluis, Sophie S; Derom, Catherine C; Thiery, Evert E; van Kesteren, Ronald E RE; Jacobs, Nele N; Van Gestel, Sofie S; Vlietinck, Robert R; Verhage, Matthijs M; Heutink, Peter P; Posthuma, Danielle D
Publication Date: 2013

Variant appearance in text: rs102275
PubMed Link: 23826354
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  • Main text
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A genome-wide association study of the human metabolome in a community-based cohort.

Cell Metabolism
Rhee, Eugene P EP; Ho, Jennifer E JE; Chen, Ming-Huei MH; Shen, Dongxiao D; Cheng, Susan S; Larson, Martin G MG; Ghorbani, Anahita A; Shi, Xu X; Helenius, Iiro T IT; O'Donnell, Christopher J CJ; Souza, Amanda L AL; Deik, Amy A; Pierce, Kerry A KA; Bullock, Kevin K; Walford, Geoffrey A GA; Vasan, Ramachandran S RS; Florez, Jose C JC; Clish, Clary C; Yeh, J-R Joanna JR; Wang, Thomas J TJ; Gerszten, Robert E RE
Publication Date: 2013-07-02

Variant appearance in text: rs102275
PubMed Link: 23823483
Variant Present in the following documents:
  • Main text
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A novel approach to detect cumulative genetic effects and genetic interactions in Crohn's disease.

Inflammatory Bowel Diseases
Wang, Ming-Hsi MH; Fiocchi, Claudio C; Ripke, Stephan S; Zhu, Xiaofeng X; Duerr, Richard H RH; Achkar, Jean-Paul JP
Publication Date: 2013-08

Variant appearance in text: rs102275
PubMed Link: 23598818
Variant Present in the following documents:
  • Main text
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