MTHFR c.236+160T>C

Variant ID: 1-11862778-A-G

NM_005957.4(MTHFR):c.236+160T>C

This variant was identified in 84 publications

View GRCh38 version.




Publications:


Genetic Variants Associated with Poor Responsiveness to Sulfonylureas in Filipinos with Type 2 Diabetes Mellitus.

Journal Of The Asean Federation Of Endocrine Societies
Paz-Pacheco, Elizabeth E; Nevado, Jose J; Paz, Eva Maria Cutiongco-De La EMC; Jasul, Gabriel G; Aman, Aimee Yvonne Criselle AYC; Alejandro-Ribaya, Elizabeth Laurize EL; Francisco, Mark David MD; Guanzon, Ma Luz Vicenta MLV; Uyking-Naranjo, May M; Añonuevo-Cruz, Cecille C; Maningat, Maria Patricia Deanna MPD; Jaring, Cristina C; Nacpil-Dominguez, Paulette P; Pala-Mohamad, Aniza A; Uy-Canto, Abigail A; Quisumbing, John Paul JP; Lat, Annabelle Marie AM; Bernardo, Diane Carla DC; Mansibang, Noemie Marie NM; Ribaya, Vincent Sean VS; Calpito, Karell Jo Angelique KJA; Ferrer, Julius Patrick JP; Biwang, Jessica J; Melegrito, Jodelyn J; Deguit, Christian Deo CD; Panerio, Carlos Emmanuel CE
Publication Date: 2023

Variant appearance in text: rs17367504
PubMed Link: 37234931
Variant Present in the following documents:
  • Main text
  • JAFES-38-S1-31.pdf
View BVdb publication page



Multivariate Genome-wide Association Analysis by Iterative Hard Thresholding.

Bioinformatics (Oxford, England)
Chu, Benjamin B BB; Ko, Seyoon S; Zhou, Jin J JJ; Jensen, Aubrey A; Zhou, Hua H; Sinsheimer, Janet S JS; Lange, Kenneth K
Publication Date: 2023-04-17

Variant appearance in text: rs17367504
PubMed Link: 37067496
Variant Present in the following documents:
  • btad193_supplementary_data.pdf
View BVdb publication page



Loss of GLTSCR1 causes congenital heart defects by regulating NPPA transcription.

Angiogenesis
Han, Fengyan F; Yang, Beibei B; Chen, Yan Y; Liu, Lu L; Cheng, Xiaoqing X; Huang, Jiaqi J; Zhou, Ke K; Zhang, Dandan D; Xu, Enping E; Lai, Maode M; Lv, Bingjian B; Cheng, Hongqiang H; Zhang, Honghe H
Publication Date: 2023-02-06

Variant appearance in text: rs17367504
PubMed Link: 36745292
Variant Present in the following documents:
  • Main text
  • 10456_2023_Article_9869.pdf
View BVdb publication page



Systolic blood pressure as the mediator of the effect of early menarche on the risk of coronary artery disease: A Mendelian randomization study.

Frontiers In Cardiovascular Medicine
Fan, Hsien-Yu HY; Huang, Yen-Tsung YT; Chen, Yun-Yu YY; Hsu, Justin BoKai JB; Li, Hung-Yuan HY; Su, Ta-Chen TC; Lin, Hung-Ju HJ; Chien, Kuo-Liong KL; Chen, Yang-Ching YC
Publication Date: 2022

Variant appearance in text: rs17367504
PubMed Link: 36698922
Variant Present in the following documents:
  • Data_Sheet_1.pdf
View BVdb publication page



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: rs17367504
PubMed Link: 36467812
Variant Present in the following documents:
  • JHA2-3-1326-s001.xlsx, sheet 1
View BVdb publication page



Assessing 48 SNPs in Hypertensive Paediatric Patients and Young Adults with Review of Genetic Background of Essential Hypertension.

Children (Basel, Switzerland)
Močnik, Mirjam M; Zagradišnik, Boris B; Marčun Varda, Nataša N
Publication Date: 2022-08-21

Variant appearance in text: rs17367504
PubMed Link: 36010152
Variant Present in the following documents:
  • Main text
  • children-09-01262.pdf
View BVdb publication page



Association Between MTHFR rs17367504 Polymorphism and Major Depressive Disorder in Taiwan: Evidence for Effect Modification by Exercise Habits.

Frontiers In Psychiatry
Hsieh, Ming-Hong MH; Nfor, Oswald Ndi ON; Ho, Chien-Chang CC; Hsu, Shu-Yi SY; Lee, Chun-Te CT; Jan, Cheng-Feng CF; Hsieh, Pao-Chun PC; Liaw, Yung-Po YP
Publication Date: 2022

Variant appearance in text: rs17367504
PubMed Link: 35800018
Variant Present in the following documents:
  • Main text
  • fpsyt-13-821448.pdf
View BVdb publication page



Preeclampsia, Natural History, Genes, and miRNAs Associated with the Syndrome.

Journal Of Pregnancy
Parada-Niño, Laura L; Castillo-León, Luisa Fernanda LF; Morel, Adrien A
Publication Date: 2022

Variant appearance in text: rs17367504
PubMed Link: 35198246
Variant Present in the following documents:
  • JP2022-3851225.pdf
View BVdb publication page



Replication of European hypertension associations in a case-control study of 9,534 African Americans.

Plos One
Kaur, Harpreet H; Crawford, Dana C DC; Liang, Jingjing J; Benchek, Penelope P; , ; Zhu, Xiaofeng X; Kallianpur, Asha R AR; Bush, William S WS
Publication Date: 2021

Variant appearance in text: rs17367504
PubMed Link: 34793544
Variant Present in the following documents:
  • Main text
View BVdb publication page



Replication of European hypertension associations in a case-control study of 9,534 African Americans.

Plos One
Kaur, Harpreet H; Crawford, Dana C DC; Liang, Jingjing J; Benchek, Penelope P; , ; Zhu, Xiaofeng X; Kallianpur, Asha R AR; Bush, William S WS
Publication Date: 2021

Variant appearance in text: rs17367504
PubMed Link: 34793544
Variant Present in the following documents:
  • Main text
View BVdb publication page



Exome-Wide Association Study Identifies East Asian-Specific Missense Variant MTHFR C136T Influencing Homocysteine Levels in Chinese Populations RH: ExWAS of tHCY in a Chinese Population.

Frontiers In Genetics
Liu, Tianzi T; Momin, Mohetaboer M; Zhou, Huiyue H; Zheng, Qiwen Q; Fan, Fangfang F; Jia, Jia J; Liu, Mengyuan M; Bao, Minghui M; Li, Jianping J; Huo, Yong Y; Liu, Jialin J; Zhang, Yaning Y; Mao, Xuemei X; Han, Xiao X; Hu, Zhiyuan Z; Zeng, Changqing C; Liu, Fan F; Zhang, Yan Y
Publication Date: 2021

Variant appearance in text: rs17367504
PubMed Link: 34707639
Variant Present in the following documents:
  • Main text
  • fgene-12-717621.pdf
View BVdb publication page



Coffee and Arterial Hypertension.

Current Hypertension Reports
Surma, Stanisław S; Oparil, Suzanne S
Publication Date: 2021-08-09

Variant appearance in text: rs17367504
PubMed Link: 34370111
Variant Present in the following documents:
  • 11906_2021_Article_1156.pdf
View BVdb publication page



Correction: The genetic risk for hypertension is lower among the Hungarian Roma population compared to the general population.

Plos One
,
Publication Date: 2021

Variant appearance in text: rs17367504
PubMed Link: 34283866
Variant Present in the following documents:
  • pone.0255129.s001.pdf
  • pone.0255129.s002.pdf
View BVdb publication page



Polygenic risk scores predict diabetes complications and their response to intensive blood pressure and glucose control.

Diabetologia
Tremblay, Johanne J; Haloui, Mounsif M; Attaoua, Redha R; Tahir, Ramzan R; Hishmih, Camil C; Harvey, François F; Marois-Blanchet, François-Christophe FC; Long, Carole C; Simon, Paul P; Santucci, Lara L; Hizel, Candan C; Chalmers, John J; Marre, Michel M; Harrap, Stephen S; Cífková, Renata R; Krajčoviechová, Alena A; Matthews, David R DR; Williams, Bryan B; Poulter, Neil N; Zoungas, Sophia S; Colagiuri, Stephen S; Mancia, Giuseppe G; Grobbee, Diederick E DE; Rodgers, Anthony A; Liu, Liusheng L; Agbessi, Mawussé M; Bruat, Vanessa V; Favé, Marie-Julie MJ; Harwood, Michelle P MP; Awadalla, Philip P; Woodward, Mark M; Hussin, Julie G JG; Hamet, Pavel P
Publication Date: 2021-09

Variant appearance in text: rs17367504
PubMed Link: 34226943
Variant Present in the following documents:
  • 125_2021_5491_MOESM1_ESM.pdf
View BVdb publication page



Peripheral Vascular Disease Susceptibility Based on Diabetes Mellitus and rs17367504 Polymorphism of the MTHFR Gene.

Diabetes, Metabolic Syndrome And Obesity : Targets And Therapy
Liu, Yin-Tso YT; Lin, Chuan-Chao CC; Wang, Lee L; Nfor, Oswald Ndi ON; Hsu, Shu-Yi SY; Lung, Chia-Chi CC; Tantoh, Disline Manli DM; Chang, Horng-Rong HR; Liaw, Yung-Po YP
Publication Date: 2021

Variant appearance in text: rs17367504
PubMed Link: 34079316
Variant Present in the following documents:
  • Main text
  • dmso-14-2381.pdf
View BVdb publication page



Genetic associations for two biological age measures point to distinct aging phenotypes.

Aging Cell
Kuo, Chia-Ling CL; Pilling, Luke C LC; Liu, Zuyun Z; Atkins, Janice L JL; Levine, Morgan E ME
Publication Date: 2021-06

Variant appearance in text: rs17367504
PubMed Link: 34038024
Variant Present in the following documents:
  • Main text
  • ACEL-20-e13376.pdf
View BVdb publication page



Exploration of CYP21A2 and CYP17A1 polymorphisms and preeclampsia risk among Chinese Han population: a large-scale case-control study based on 5021 subjects.

Human Genomics
Hou, Bo B; Jia, Xuewen X; Deng, Ziwen Z; Liu, Xin X; Liu, Huitang H; Yu, Haichu H; Liu, Shiguo S
Publication Date: 2020-09-25

Variant appearance in text: rs17367504
PubMed Link: 32977860
Variant Present in the following documents:
  • Main text
  • 40246_2020_Article_286.pdf
View BVdb publication page



Maternal Hypertension-Related Genotypes and Congenital Heart Defects.

American Journal Of Hypertension
Lei, Yunping Y; Ludorf, Katherine L KL; Yu, Xiao X; Benjamin, Renata H RH; Gu, Xue X; Lin, Ying Y; Finnell, Richard H RH; Mitchell, Laura E LE; Musfee, Fadi I FI; Malik, Sadia S; Canfield, Mark A MA; Morrison, Alanna C AC; Hobbs, Charlotte A CA; Van Zutphen, Alissa R AR; Fisher, Sarah S; Agopian, A J AJ
Publication Date: 2021-02-18

Variant appearance in text: rs17367504
PubMed Link: 32710738
Variant Present in the following documents:
  • Main text
View BVdb publication page



The genetic risk for hypertension is lower among the Hungarian Roma population compared to the general population.

Plos One
Soltész, Beáta B; Pikó, Péter P; Sándor, János J; Kósa, Zsigmond Z; Ádány, Róza R; Fiatal, Szilvia S
Publication Date: 2020

Variant appearance in text: rs17367504
PubMed Link: 32555714
Variant Present in the following documents:
  • Main text
View BVdb publication page



Iterative hard thresholding in genome-wide association studies: Generalized linear models, prior weights, and double sparsity.

Gigascience
Chu, Benjamin B BB; Keys, Kevin L KL; German, Christopher A CA; Zhou, Hua H; Zhou, Jin J JJ; Sobel, Eric M EM; Sinsheimer, Janet S JS; Lange, Kenneth K
Publication Date: 2020-06-01

Variant appearance in text: rs17367504
PubMed Link: 32491161
Variant Present in the following documents:
  • Main text
  • giaa044_giga-d-19-00398_original_submission.pdf
  • giaa044_giga-d-19-00398_revision_2.pdf
  • giaa044.pdf
  • giaa044_giga-d-19-00398_revision_1.pdf
View BVdb publication page



A review of omics approaches to study preeclampsia.

Placenta
Benny, Paula A PA; Alakwaa, Fadhl M FM; Schlueter, Ryan J RJ; Lassiter, Cameron B CB; Garmire, Lana X LX
Publication Date: 2020-03

Variant appearance in text: rs17367504
PubMed Link: 32056783
Variant Present in the following documents:
  • Main text
View BVdb publication page



A multiple coefficient of determination-based method for parsing SNPs that correlate with mRNA expression.

Scientific Reports
Song, Fan F; Tao, Yu Y; Sun, Yue Y; Saffen, David D
Publication Date: 2019-12-27

Variant appearance in text: rs17367504
PubMed Link: 31882953
Variant Present in the following documents:
  • 41598_2019_56494_MOESM1_ESM.pdf
View BVdb publication page



Group sparse reduced rank regression for neuroimaging genetic study.

World Wide Web
Zhu, Xiaofeng X; Suk, Heung-Il HI; Shen, Dinggang D
Publication Date: 2019-03

Variant appearance in text: rs17367504
PubMed Link: 31607788
Variant Present in the following documents:
  • Main text
View BVdb publication page



Genome-wide association study of circulating folate one-carbon metabolites.

Genetic Epidemiology
Wang, Jun J; Asante, Isaac I; Baron, John A JA; Figueiredo, Jane C JC; Haile, Robert R; Joan Levine, A A; Newcomb, Polly A PA; Templeton, Allyson S AS; Schumacher, Fredrick R FR; Louie, Stan G SG; Casey, Graham G; Conti, David V DV
Publication Date: 2019-12

Variant appearance in text: rs17367504
PubMed Link: 31502714
Variant Present in the following documents:
  • Main text
View BVdb publication page



A genome-wide association and replication study of blood pressure in Ugandan early adolescents.

Molecular Genetics & Genomic Medicine
Lule, Swaib A SA; Mentzer, Alexander J AJ; Namara, Benigna B; Muwenzi, Allan G AG; Nassanga, Beatrice B; Kizito, Dennison D; Akurut, Helen H; Lubyayi, Lawrence L; Tumusiime, Josephine J; Zziwa, Christopher C; Akello, Florence F; Gurdasani, Deept D; Sandhu, Manjinder M; Smeeth, Liam L; Elliott, Alison M AM; Webb, Emily L EL
Publication Date: 2019-10

Variant appearance in text: rs17367504
PubMed Link: 31469255
Variant Present in the following documents:
  • Main text
  • MGG3-7-e00950.pdf
View BVdb publication page



Causal Factors for Knee, Hip, and Hand Osteoarthritis: A Mendelian Randomization Study in the UK Biobank.

Arthritis & Rheumatology (Hoboken, N.J.)
Funck-Brentano, Thomas T; Nethander, Maria M; Movérare-Skrtic, Sofia S; Richette, Pascal P; Ohlsson, Claes C
Publication Date: 2019-10

Variant appearance in text: rs17367504
PubMed Link: 31099188
Variant Present in the following documents:
  • ART-71-1634-s001.pdf
View BVdb publication page



Genome-Wide Association Studies of Hypertension and Several Other Cardiovascular Diseases.

Pulse (Basel, Switzerland)
Wang, Yan Y; Wang, Ji-Guang JG
Publication Date: 2019-04

Variant appearance in text: rs17367504
PubMed Link: 31049317
Variant Present in the following documents:
  • Main text
View BVdb publication page



Genetics of Hypertension in African Americans and Others of African Descent.

International Journal Of Molecular Sciences
Zilbermint, Mihail M; Hannah-Shmouni, Fady F; Stratakis, Constantine A CA
Publication Date: 2019-03-02

Variant appearance in text: rs17367504
PubMed Link: 30832344
Variant Present in the following documents:
  • Main text
  • ijms-20-01081.pdf
View BVdb publication page



Methylenetetrahydrofolate reductase and psychiatric diseases.

Translational Psychiatry
Wan, Lin L; Li, Yuhong Y; Zhang, Zhengrong Z; Sun, Zuoli Z; He, Yi Y; Li, Rena R
Publication Date: 2018-11-05

Variant appearance in text: rs17367504
PubMed Link: 30397195
Variant Present in the following documents:
  • Main text
  • 41398_2018_Article_276.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: MTHFR: 236+160T>C; rs17367504
PubMed Link: 30319441
Variant Present in the following documents:
  • Table_6.xlsx, sheet 1
View BVdb publication page



Whole genome sequencing identifies high-impact variants in well-known pharmacogenomic genes.

The Pharmacogenomics Journal
Choi, Jihoon J; Tantisira, Kelan G KG; Duan, Qing Ling QL
Publication Date: 2019-04

Variant appearance in text: rs17367504
PubMed Link: 30214008
Variant Present in the following documents:
  • Main text
View BVdb publication page



Hypertension and Cerebral Microangiopathy (Cerebral Small Vessel Disease): Genetic and Epigenetic Aspects of Their Relationship.

Acta Naturae
Dobrynina, L A LA; Zabitova, M R MR; Kalashnikova, L A LA; Gnedovskaya, E V EV; Piradov, M A MA
Publication Date: 2018

Variant appearance in text: rs17367504
PubMed Link: 30116610
Variant Present in the following documents:
  • Main text
  • AN20758251-10-02-004.pdf
View BVdb publication page



Brief Overview of a Decade of Genome-Wide Association Studies on Primary Hypertension.

International Journal Of Endocrinology
Azam, Afifah Binti AB; Azizan, Elena Aisha Binti EAB
Publication Date: 2018

Variant appearance in text: rs17367504
PubMed Link: 29666641
Variant Present in the following documents:
  • Main text
  • IJE2018-7259704.pdf
View BVdb publication page



Advances in the Genetics of Hypertension: The Effect of Rare Variants.

International Journal Of Molecular Sciences
Russo, Alessia A; Di Gaetano, Cornelia C; Cugliari, Giovanni G; Matullo, Giuseppe G
Publication Date: 2018-02-28

Variant appearance in text: rs17367504
PubMed Link: 29495593
Variant Present in the following documents:
  • Main text
View BVdb publication page



Genetic Programming of Hypertension.

Frontiers In Pediatrics
Ahn, Sun-Young SY; Gupta, Charu C
Publication Date: 2017

Variant appearance in text: rs17367504
PubMed Link: 29404309
Variant Present in the following documents:
  • Main text
  • fped-05-00285.pdf
View BVdb publication page



Parental and offspring contribution of genetic markers of adult blood pressure in early life: The FAMILY study.

Plos One
Robiou-du-Pont, Sébastien S; Anand, Sonia S SS; Morrison, Katherine M KM; McDonald, Sarah D SD; Atkinson, Stephanie A SA; Teo, Koon K KK; Meyre, David D
Publication Date: 2017

Variant appearance in text: rs17367504
PubMed Link: 29045471
Variant Present in the following documents:
  • Main text
View BVdb publication page



Towards Precision Medicine for Hypertension: A Review of Genomic, Epigenomic, and Microbiomic Effects on Blood Pressure in Experimental Rat Models and Humans.

Physiological Reviews
Padmanabhan, Sandosh S; Joe, Bina B
Publication Date: 2017-10-01

Variant appearance in text: rs17367504
PubMed Link: 28931564
Variant Present in the following documents:
  • Main text
View BVdb publication page



Genome-Wide Association Study of Blood Pressure Traits by Hispanic/Latino Background: the Hispanic Community Health Study/Study of Latinos.

Scientific Reports
Sofer, Tamar T; Wong, Quenna Q; Hartwig, Fernando P FP; Taylor, Kent K; Warren, Helen R HR; Evangelou, Evangelos E; Cabrera, Claudia P CP; Levy, Daniel D; Kramer, Holly H; Lange, Leslie A LA; Horta, Bernardo L BL; , ; Kerr, Kathleen F KF; Reiner, Alex P AP; Franceschini, Nora N
Publication Date: 2017-09-04

Variant appearance in text: rs17367504
PubMed Link: 28871152
Variant Present in the following documents:
  • 41598_2017_9019_MOESM1_ESM.pdf
View BVdb publication page



Hypertension Susceptibility Loci are Associated with Anthracycline-related Cardiotoxicity in Long-term Childhood Cancer Survivors.

Scientific Reports
Hildebrandt, Michelle A T MAT; Reyes, Monica M; Wu, Xifeng X; Pu, Xia X; Thompson, Kara A KA; Ma, Jianzhong J; Landstrom, Andrew P AP; Morrison, Alanna C AC; Ater, Joann L JL
Publication Date: 2017-08-29

Variant appearance in text: rs17367504
PubMed Link: 28851949
Variant Present in the following documents:
  • Main text
View BVdb publication page



Novel Blood Pressure Locus and Gene Discovery Using Genome-Wide Association Study and Expression Data Sets From Blood and the Kidney.

Hypertension (Dallas, Tex. : 1979)
Wain, Louise V LV; Vaez, Ahmad A; Jansen, Rick R; Joehanes, Roby R; van der Most, Peter J PJ; Erzurumluoglu, A Mesut AM; O'Reilly, Paul F PF; Cabrera, Claudia P CP; Warren, Helen R HR; Rose, Lynda M LM; Verwoert, Germaine C GC; Hottenga, Jouke-Jan JJ; Strawbridge, Rona J RJ; Esko, Tonu T; Arking, Dan E DE; Hwang, Shih-Jen SJ; Guo, Xiuqing X; Kutalik, Zoltan Z; Trompet, Stella S; Shrine, Nick N; Teumer, Alexander A; Ried, Janina S JS; Bis, Joshua C JC; Smith, Albert V AV; Amin, Najaf N; Nolte, Ilja M IM; Lyytikäinen, Leo-Pekka LP; Mahajan, Anubha A; Wareham, Nicholas J NJ; Hofer, Edith E; Joshi, Peter K PK; Kristiansson, Kati K; Traglia, Michela M; Havulinna, Aki S AS; Goel, Anuj A; Nalls, Mike A MA; Sõber, Siim S; Vuckovic, Dragana D; Luan, Jian'an J; Del Greco M, Fabiola F; Ayers, Kristin L KL; Marrugat, Jaume J; Ruggiero, Daniela D; Lopez, Lorna M LM; Niiranen, Teemu T; Enroth, Stefan S; Jackson, Anne U AU; Nelson, Christopher P CP; Huffman, Jennifer E JE; Zhang, Weihua W; Marten, Jonathan J; Gandin, Ilaria I; Harris, Sarah E SE; Zemunik, Tatijana T; Lu, Yingchang Y; Evangelou, Evangelos E; Shah, Nabi N; de Borst, Martin H MH; Mangino, Massimo M; Prins, Bram P BP; Campbell, Archie A; Li-Gao, Ruifang R; Chauhan, Ganesh G; Oldmeadow, Christopher C; Abecasis, Gonçalo G; Abedi, Maryam M; Barbieri, Caterina M CM; Barnes, Michael R MR; Batini, Chiara C; Beilby, John J; Blake, Tineka T; Boehnke, Michael M; Bottinger, Erwin P EP; Braund, Peter S PS; Brown, Morris M; Brumat, Marco M; Campbell, Harry H; Chambers, John C JC; Cocca, Massimiliano M; Collins, Francis F; Connell, John J; Cordell, Heather J HJ; Damman, Jeffrey J JJ; Davies, Gail G; de Geus, Eco J EJ; de Mutsert, Renée R; Deelen, Joris J; Demirkale, Yusuf Y; Doney, Alex S F ASF; Dörr, Marcus M; Farrall, Martin M; Ferreira, Teresa T; Frånberg, Mattias M; Gao, He H; Giedraitis, Vilmantas V; Gieger, Christian C; Giulianini, Franco F; Gow, Alan J AJ; Hamsten, Anders A; Harris, Tamara B TB; Hofman, Albert A; Holliday, Elizabeth G EG; Hui, Jennie J; Jarvelin, Marjo-Riitta MR; Johansson, Åsa Å; Johnson, Andrew D AD; Jousilahti, Pekka P; Jula, Antti A; Kähönen, Mika M; Kathiresan, Sekar S; Khaw, Kay-Tee KT; Kolcic, Ivana I; Koskinen, Seppo S; Langenberg, Claudia C; Larson, Marty M; Launer, Lenore J LJ; Lehne, Benjamin B; Liewald, David C M DCM; Lin, Li L; Lind, Lars L; Mach, François F; Mamasoula, Chrysovalanto C; Menni, Cristina C; Mifsud, Borbala B; Milaneschi, Yuri Y; Morgan, Anna A; Morris, Andrew D AD; Morrison, Alanna C AC; Munson, Peter J PJ; Nandakumar, Priyanka P; Nguyen, Quang Tri QT; Nutile, Teresa T; Oldehinkel, Albertine J AJ; Oostra, Ben A BA; Org, Elin E; Padmanabhan, Sandosh S; Palotie, Aarno A; Paré, Guillaume G; Pattie, Alison A; Penninx, Brenda W J H BWJH; Poulter, Neil N; Pramstaller, Peter P PP; Raitakari, Olli T OT; Ren, Meixia M; Rice, Kenneth K; Ridker, Paul M PM; Riese, Harriëtte H; Ripatti, Samuli S; Robino, Antonietta A; Rotter, Jerome I JI; Rudan, Igor I; Saba, Yasaman Y; Saint Pierre, Aude A; Sala, Cinzia F CF; Sarin, Antti-Pekka AP; Schmidt, Reinhold R; Scott, Rodney R; Seelen, Marc A MA; Shields, Denis C DC; Siscovick, David D; Sorice, Rossella R; Stanton, Alice A; Stott, David J DJ; Sundström, Johan J; Swertz, Morris M; Taylor, Kent D KD; Thom, Simon S; Tzoulaki, Ioanna I; Tzourio, Christophe C; Uitterlinden, André G AG; Völker, Uwe U; Vollenweider, Peter P; Wild, Sarah S; Willemsen, Gonneke G; Wright, Alan F AF; Yao, Jie J; Thériault, Sébastien S; Conen, David D; Attia, John J; Sever, Peter P; Debette, Stéphanie S; Mook-Kanamori, Dennis O DO; Zeggini, Eleftheria E; Spector, Tim D TD; van der Harst, Pim P; Palmer, Colin N A CNA; Vergnaud, Anne-Claire AC; Loos, Ruth J F RJF; Polasek, Ozren O; Starr, John M JM; Girotto, Giorgia G; Hayward, Caroline C; Kooner, Jaspal S JS; Lindgren, Cecila M CM; Vitart, Veronique V; Samani, Nilesh J NJ; Tuomilehto, Jaakko J; Gyllensten, Ulf U; Knekt, Paul P; Deary, Ian J IJ; Ciullo, Marina M; Elosua, Roberto R; Keavney, Bernard D BD; Hicks, Andrew A AA; Scott, Robert A RA; Gasparini, Paolo P; Laan, Maris M; Liu, YongMei Y; Watkins, Hugh H; Hartman, Catharina A CA; Salomaa, Veikko V; Toniolo, Daniela D; Perola, Markus M; Wilson, James F JF; Schmidt, Helena H; Zhao, Jing Hua JH; Lehtimäki, Terho T; van Duijn, Cornelia M CM; Gudnason, Vilmundur V; Psaty, Bruce M BM; Peters, Annette A; Rettig, Rainer R; James, Alan A; Jukema, J Wouter JW; Strachan, David P DP; Palmas, Walter W; Metspalu, Andres A; Ingelsson, Erik E; Boomsma, Dorret I DI; Franco, Oscar H OH; Bochud, Murielle M; Newton-Cheh, Christopher C; Munroe, Patricia B PB; Elliott, Paul P; Chasman, Daniel I DI; Chakravarti, Aravinda A; Knight, Joanne J; Morris, Andrew P AP; Levy, Daniel D; Tobin, Martin D MD; Snieder, Harold H; Caulfield, Mark J MJ; Ehret, Georg B GB
Publication Date: 2017-07-24

Variant appearance in text: rs17367504
PubMed Link: 28739976
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Analysis of Complement C3 Gene Reveals Susceptibility to Severe Preeclampsia.

Frontiers In Immunology
Lokki, A Inkeri AI; Kaartokallio, Tea T; Holmberg, Ville V; Onkamo, Päivi P; Koskinen, Lotta L E LLE; Saavalainen, Päivi P; Heinonen, Seppo S; Kajantie, Eero E; Kere, Juha J; Kivinen, Katja K; Pouta, Anneli A; Villa, Pia M PM; Hiltunen, Leena L; Laivuori, Hannele H; Meri, Seppo S
Publication Date: 2017

Variant appearance in text: rs17367504
PubMed Link: 28611769
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  • fimmu-08-00589.pdf
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Is There a Role for Genomics in the Management of Hypertension?

International Journal Of Molecular Sciences
Burrello, Jacopo J; Monticone, Silvia S; Buffolo, Fabrizio F; Tetti, Martina M; Veglio, Franco F; Williams, Tracy A TA; Mulatero, Paolo P
Publication Date: 2017-05-26

Variant appearance in text: rs17367504
PubMed Link: 28587112
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The genetic overlap between mood disorders and cardiometabolic diseases: a systematic review of genome wide and candidate gene studies.

Translational Psychiatry
Amare, A T AT; Schubert, K O KO; Klingler-Hoffmann, M M; Cohen-Woods, S S; Baune, B T BT
Publication Date: 2017-01-24

Variant appearance in text: rs17367504
PubMed Link: 28117839
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Examination of previously identified associations within the Genetic Analysis Workshop 19 data.

Bmc Proceedings
Howey, Richard A J RA; Eu-Ahsunthornwattana, Jakris J; Darlay, Rebecca R; Cordell, Heather J HJ
Publication Date: 2016

Variant appearance in text: rs17367504
PubMed Link: 27980618
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  • Main text
  • 12919_2016_Article_12.pdf
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The antihypertensive MTHFR gene polymorphism rs17367504-G is a possible novel protective locus for preeclampsia.

Journal Of Hypertension
Thomsen, Liv Cecilie V LC; McCarthy, Nina S NS; Melton, Phillip E PE; Cadby, Gemma G; Austgulen, Rigmor R; Nygård, Ottar K OK; Johnson, Matthew P MP; Brennecke, Shaun S; Moses, Eric K EK; Bjørge, Line L; Iversen, Ann-Charlotte AC
Publication Date: 2017-01

Variant appearance in text: rs17367504
PubMed Link: 27755385
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Variant Discovery and Fine Mapping of Genetic Loci Associated with Blood Pressure Traits in Hispanics and African Americans.

Plos One
Franceschini, Nora N; Carty, Cara L CL; Lu, Yingchang Y; Tao, Ran R; Sung, Yun Ju YJ; Manichaikul, Ani A; Haessler, Jeff J; Fornage, Myriam M; Schwander, Karen K; Zubair, Niha N; Bien, Stephanie S; Hindorff, Lucia A LA; Guo, Xiuqing X; Bielinski, Suzette J SJ; Ehret, Georg G; Kaufman, Joel D JD; Rich, Stephen S SS; Carlson, Christopher S CS; Bottinger, Erwin P EP; North, Kari E KE; Rao, D C DC; Chakravarti, Aravinda A; Barrett, Paula Q PQ; Loos, Ruth J F RJ; Buyske, Steven S; Kooperberg, Charles C
Publication Date: 2016

Variant appearance in text: rs17367504
PubMed Link: 27736895
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Genome Wide Association Study Identifies L3MBTL4 as a Novel Susceptibility Gene for Hypertension.

Scientific Reports
Liu, Xin X; Hu, Cheng C; Bao, Minghui M; Li, Jing J; Liu, Xiaoyan X; Tan, Xuerui X; Zhou, Yong Y; Chen, Yequn Y; Wu, Shouling S; Chen, Shuohua S; Zhang, Rong R; Jiang, Feng F; Jia, Weiping W; Wang, Xingyu X; Yang, Xinchun X; Cai, Jun J
Publication Date: 2016-08-02

Variant appearance in text: rs17367504
PubMed Link: 27480026
Variant Present in the following documents:
  • Main text
  • srep30811.pdf
  • srep30811-s1.pdf
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Utility of blood pressure genetic risk score in admixed Hispanic samples.

Journal Of Human Hypertension
Beecham, A H AH; Wang, L L; Vasudeva, N N; Liu, Z Z; Dong, C C; Goldschmidt-Clermont, P J PJ; Pericak-Vance, M A MA; Rundek, T T; Seo, D D; Blanton, S H SH; Sacco, R L RL; Beecham, G W GW
Publication Date: 2016-12

Variant appearance in text: rs17367504
PubMed Link: 27251080
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Rare Exome Sequence Variants in CLCN6 Reduce Blood Pressure Levels and Hypertension Risk.

Circulation. Cardiovascular Genetics
Yu, Bing B; Pulit, Sara L SL; Hwang, Shih-Jen SJ; Brody, Jennifer A JA; Amin, Najaf N; Auer, Paul L PL; Bis, Joshua C JC; Boerwinkle, Eric E; Burke, Gregory L GL; Chakravarti, Aravinda A; Correa, Adolfo A; Dreisbach, Albert W AW; Franco, Oscar H OH; Ehret, Georg B GB; Franceschini, Nora N; Hofman, Albert A; Lin, Dan-Yu DY; Metcalf, Ginger A GA; Musani, Solomon K SK; Muzny, Donna D; Palmas, Walter W; Raffel, Leslie L; Reiner, Alex A; Rice, Ken K; Rotter, Jerome I JI; Veeraraghavan, Narayanan N; Fox, Ervin E; Guo, Xiuqing X; North, Kari E KE; Gibbs, Richard A RA; van Duijn, Cornelia M CM; Psaty, Bruce M BM; Levy, Daniel D; Newton-Cheh, Christopher C; Morrison, Alanna C AC; ,
Publication Date: 2016-02

Variant appearance in text: rs17367504
PubMed Link: 26658788
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Choline metabolites: gene by diet interactions.

Current Opinion In Lipidology
Smallwood, Tangi T; Allayee, Hooman H; Bennett, Brian J BJ
Publication Date: 2016-02

Variant appearance in text: rs17367504
PubMed Link: 26655287
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Approaches for the identification of genetic modifiers of nutrient dependent phenotypes: examples from folate.

Frontiers In Nutrition
Zinck, John W R JW; MacFarlane, Amanda J AJ
Publication Date: 2014

Variant appearance in text: rs17367504
PubMed Link: 25988111
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Integrative network analysis reveals molecular mechanisms of blood pressure regulation.

Molecular Systems Biology
Huan, Tianxiao T; Meng, Qingying Q; Saleh, Mohamed A MA; Norlander, Allison E AE; Joehanes, Roby R; Zhu, Jun J; Chen, Brian H BH; Zhang, Bin B; Johnson, Andrew D AD; Ying, Saixia S; Courchesne, Paul P; Raghavachari, Nalini N; Wang, Richard R; Liu, Poching P; , ; O'Donnell, Christopher J CJ; Vasan, Ramachandran R; Munson, Peter J PJ; Madhur, Meena S MS; Harrison, David G DG; Yang, Xia X; Levy, Daniel D
Publication Date: 2015-04-16

Variant appearance in text: rs17367504
PubMed Link: 25882670
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Rare genetic variant analysis on blood pressure in related samples.

Bmc Proceedings
Chen, Han H; Choi, Seung Hoan SH; Hong, Jaeyoung J; Lu, Chen C; Milton, Jacqueline N JN; Allard, Catherine C; Lacey, Sean M SM; Lin, Honghuang H; Dupuis, Josée J
Publication Date: 2014

Variant appearance in text: rs17367504
PubMed Link: 25519320
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  • Main text
  • 1753-6561-8-S1-S35.pdf
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Pathogenesis of coronary artery disease: focus on genetic risk factors and identification of genetic variants.

The Application Of Clinical Genetics
Sayols-Baixeras, Sergi S; Lluís-Ganella, Carla C; Lucas, Gavin G; Elosua, Roberto R
Publication Date: 2014

Variant appearance in text: rs17367504
PubMed Link: 24520200
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  • tacg-7-015.pdf
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Identifying common genetic variants in blood pressure due to polygenic pleiotropy with associated phenotypes.

Hypertension (Dallas, Tex. : 1979)
Andreassen, Ole A OA; McEvoy, Linda K LK; Thompson, Wesley K WK; Wang, Yunpeng Y; Reppe, Sjur S; Schork, Andrew J AJ; Zuber, Verena V; Barrett-Connor, Elizabeth E; Gautvik, Kaare K; Aukrust, Pål P; Karlsen, Tom H TH; Djurovic, Srdjan S; Desikan, Rahul S RS; Dale, Anders M AM; ,
Publication Date: 2014-04

Variant appearance in text: rs17367504
PubMed Link: 24396023
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Progress and future aspects in genetics of human hypertension.

Current Hypertension Reports
Zhao, Qi Q; Kelly, Tanika N TN; Li, Changwei C; He, Jiang J
Publication Date: 2013-12

Variant appearance in text: rs17367504
PubMed Link: 24072558
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