ULK4 c.1656+12715C>A

Variant ID: 3-41912651-G-T

NM_017886.2(ULK4):c.1656+12715C>A

This variant was identified in 27 publications

View GRCh38 version.




Publications:


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: rs9815354
PubMed Link: 36467812
Variant Present in the following documents:
  • JHA2-3-1326-s001.xlsx, sheet 1
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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: rs9815354
PubMed Link: 36010152
Variant Present in the following documents:
  • Main text
  • children-09-01262.pdf
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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: rs9815354
PubMed Link: 31049317
Variant Present in the following documents:
  • Main text
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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: rs9815354
PubMed Link: 30116610
Variant Present in the following documents:
  • Main text
  • AN20758251-10-02-004.pdf
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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: rs9815354
PubMed Link: 29666641
Variant Present in the following documents:
  • Main text
  • IJE2018-7259704.pdf
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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: rs9815354
PubMed Link: 28931564
Variant Present in the following documents:
  • Main text
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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: rs9815354
PubMed Link: 28871152
Variant Present in the following documents:
  • 41598_2017_9019_MOESM1_ESM.pdf
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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: rs9815354
PubMed Link: 27980618
Variant Present in the following documents:
  • Main text
  • 12919_2016_Article_12.pdf
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Using a Bayesian latent variable approach to detect pleiotropy in the Genetic Analysis Workshop 18 data.

Bmc Proceedings
Xu, Lizhen L; Craiu, Radu V RV; Derkach, Andriy A; Paterson, Andrew D AD; Sun, Lei L
Publication Date: 2014

Variant appearance in text: rs9815354
PubMed Link: 25519405
Variant Present in the following documents:
  • Main text
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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: rs9815354
PubMed Link: 25519320
Variant Present in the following documents:
  • Main text
  • 1753-6561-8-S1-S35.pdf
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Genome-wide association study in Chinese identifies novel loci for blood pressure and hypertension.

Human Molecular Genetics
Lu, Xiangfeng X; Wang, Laiyuan L; Lin, Xu X; Huang, Jianfeng J; Charles Gu, C C; He, Meian M; Shen, Hongbing H; He, Jiang J; Zhu, Jingwen J; Li, Huaixing H; Hixson, James E JE; Wu, Tangchun T; Dai, Juncheng J; Lu, Ling L; Shen, Chong C; Chen, Shufeng S; He, Lin L; Mo, Zengnan Z; Hao, Yongchen Y; Mo, Xingbo X; Yang, Xueli X; Li, Jianxin J; Cao, Jie J; Chen, Jichun J; Fan, Zhongjie Z; Li, Ying Y; Zhao, Liancheng L; Li, Hongfan H; Lu, Fanghong F; Yao, Cailiang C; Yu, Lin L; Xu, Lihua L; Mu, Jianjun J; Wu, Xianping X; Deng, Ying Y; Hu, Dongsheng D; Zhang, Weidong W; Ji, Xu X; Guo, Dongshuang D; Guo, Zhirong Z; Zhou, Zhengyuan Z; Yang, Zili Z; Wang, Renping R; Yang, Jun J; Zhou, Xiaoyang X; Yan, Weili W; Sun, Ningling N; Gao, Pingjin P; Gu, Dongfeng D
Publication Date: 2015-02-01

Variant appearance in text: rs9815354
PubMed Link: 25249183
Variant Present in the following documents:
  • Main text
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Linking the genetic architecture of cytosine modifications with human complex traits.

Human Molecular Genetics
Zhang, Xu X; Moen, Erika L EL; Liu, Cong C; Mu, Wenbo W; Gamazon, Eric R ER; Delaney, Shannon M SM; Wing, Claudia C; Godley, Lucy A LA; Dolan, M Eileen ME; Zhang, Wei W
Publication Date: 2014-11-15

Variant appearance in text: rs9815354
PubMed Link: 24943591
Variant Present in the following documents:
  • Main text
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Association of cardiovascular and metabolic disease genes with psoriasis.

The Journal Of Investigative Dermatology
Lu, Yingchang Y; Chen, Haoyan H; Nikamo, Pernilla P; Qi Low, Hui H; Helms, Cynthia C; Seielstad, Mark M; Liu, Jianjun J; Bowcock, Anne M AM; Stahle, Mona M; Liao, Wilson W
Publication Date: 2013-03

Variant appearance in text: rs9815354
PubMed Link: 23190900
Variant Present in the following documents:
  • NIHMS404713-supplement-01.pdf
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SNPs and other features as they predispose to complex disease: genome-wide predictive analysis of a quantitative phenotype for hypertension.

Plos One
Won, Joong-Ho JH; Ehret, Georg G; Chakravarti, Aravinda A; Olshen, Richard A RA
Publication Date: 2011

Variant appearance in text: rs9815354
PubMed Link: 22140480
Variant Present in the following documents:
  • Main text
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Genetic variants and blood pressure in a population-based cohort: the Cardiovascular Risk in Young Finns study.

Hypertension (Dallas, Tex. : 1979)
Oikonen, Mervi M; Tikkanen, Emmi E; Juhola, Jonna J; Tuovinen, Tarja T; Seppälä, Ilkka I; Juonala, Markus M; Taittonen, Leena L; Mikkilä, Vera V; Kähönen, Mika M; Ripatti, Samuli S; Viikari, Jorma J; Lehtimäki, Terho T; Havulinna, Aki S AS; Kee, Frank F; Newton-Cheh, Christopher C; Peltonen, Leena L; Schork, Nicholas J NJ; Murray, Sarah S SS; Berenson, Gerald S GS; Chen, Wei W; Srinivasan, Sathanur R SR; Salomaa, Veikko V; Raitakari, Olli T OT
Publication Date: 2011-12

Variant appearance in text: rs9815354
PubMed Link: 22025373
Variant Present in the following documents:
  • Main text
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Implications of discoveries from genome-wide association studies in current cardiovascular practice.

World Journal Of Cardiology
Jeemon, Panniyammakal P; Pettigrew, Kerry K; Sainsbury, Christopher C; Prabhakaran, Dorairaj D; Padmanabhan, Sandosh S
Publication Date: 2011-07-26

Variant appearance in text: rs9815354
PubMed Link: 21860704
Variant Present in the following documents:
  • Main text
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Maps of open chromatin guide the functional follow-up of genome-wide association signals: application to hematological traits.

Plos Genetics
Paul, Dirk S DS; Nisbet, James P JP; Yang, Tsun-Po TP; Meacham, Stuart S; Rendon, Augusto A; Hautaviita, Katta K; Tallila, Jonna J; White, Jacqui J; Tijssen, Marloes R MR; Sivapalaratnam, Suthesh S; Basart, Hanneke H; Trip, Mieke D MD; , ; , ; Göttgens, Berthold B; Soranzo, Nicole N; Ouwehand, Willem H WH; Deloukas, Panos P
Publication Date: 2011-06

Variant appearance in text: rs9815354
PubMed Link: 21738486
Variant Present in the following documents:
  • pgen.1002139.s016.pdf
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Association of genetic variation with systolic and diastolic blood pressure among African Americans: the Candidate Gene Association Resource study.

Human Molecular Genetics
Fox, Ervin R ER; Young, J Hunter JH; Li, Yali Y; Dreisbach, Albert W AW; Keating, Brendan J BJ; Musani, Solomon K SK; Liu, Kiang K; Morrison, Alanna C AC; Ganesh, Santhi S; Kutlar, Abdullah A; Ramachandran, Vasan S VS; Polak, Josef F JF; Fabsitz, Richard R RR; Dries, Daniel L DL; Farlow, Deborah N DN; Redline, Susan S; Adeyemo, Adebowale A; Hirschorn, Joel N JN; Sun, Yan V YV; Wyatt, Sharon B SB; Penman, Alan D AD; Palmas, Walter W; Rotter, Jerome I JI; Townsend, Raymond R RR; Doumatey, Ayo P AP; Tayo, Bamidele O BO; Mosley, Thomas H TH; Lyon, Helen N HN; Kang, Sun J SJ; Rotimi, Charles N CN; Cooper, Richard S RS; Franceschini, Nora N; Curb, J David JD; Martin, Lisa W LW; Eaton, Charles B CB; Kardia, Sharon L R SL; Taylor, Herman A HA; Caulfield, Mark J MJ; Ehret, Georg B GB; Johnson, Toby T; , ; Chakravarti, Aravinda A; Zhu, Xiaofeng X; Levy, Daniel D
Publication Date: 2011-06-01

Variant appearance in text: rs9815354
PubMed Link: 21378095
Variant Present in the following documents:
  • Main text
  • ddr092.pdf
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The genetics of blood pressure and hypertension: the role of rare variation.

Cardiovascular Therapeutics
Doris, Peter A PA
Publication Date: 2011-02

Variant appearance in text: rs9815354
PubMed Link: 21129164
Variant Present in the following documents:
  • Main text
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Discovery and replication of novel blood pressure genetic loci in the Women's Genome Health Study.

Journal Of Hypertension
Ho, Jennifer E JE; Levy, Daniel D; Rose, Lynda L; Johnson, Andrew D AD; Ridker, Paul M PM; Chasman, Daniel I DI
Publication Date: 2011-01

Variant appearance in text: rs9815354
PubMed Link: 21045733
Variant Present in the following documents:
  • Main text
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Recent findings in the genetics of blood pressure and hypertension traits.

American Journal Of Hypertension
Franceschini, Nora N; Reiner, Alexander P AP; Heiss, Gerardo G
Publication Date: 2011-04

Variant appearance in text: rs9815354
PubMed Link: 20948529
Variant Present in the following documents:
  • Main text
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Common variants in the ATP2B1 gene are associated with susceptibility to hypertension: the Japanese Millennium Genome Project.

Hypertension (Dallas, Tex. : 1979)
Tabara, Yasuharu Y; Kohara, Katsuhiko K; Kita, Yoshikuni Y; Hirawa, Nobuhito N; Katsuya, Tomohiro T; Ohkubo, Takayoshi T; Hiura, Yumiko Y; Tajima, Atsushi A; Morisaki, Takayuki T; Miyata, Toshiyuki T; Nakayama, Tomohiro T; Takashima, Naoyuki N; Nakura, Jun J; Kawamoto, Ryuichi R; Takahashi, Norio N; Hata, Akira A; Soma, Masayoshi M; Imai, Yutaka Y; Kokubo, Yoshihiro Y; Okamura, Tomonori T; Tomoike, Hitonobu H; Iwai, Naoharu N; Ogihara, Toshio T; Inoue, Itsuro I; Tokunaga, Katsushi K; Johnson, Toby T; Caulfield, Mark M; Munroe, Patricia P; , ; Umemura, Satoshi S; Ueshima, Hirotsugu H; Miki, Tetsuro T
Publication Date: 2010-11

Variant appearance in text: rs9815354
PubMed Link: 20921432
Variant Present in the following documents:
  • Main text
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Genome-wide association studies: contribution of genomics to understanding blood pressure and essential hypertension.

Current Hypertension Reports
Ehret, Georg B GB
Publication Date: 2010-02

Variant appearance in text: rs9815354
PubMed Link: 20425154
Variant Present in the following documents:
  • Main text
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The genetics of obesity and the metabolic syndrome.

Endocrine, Metabolic & Immune Disorders Drug Targets
Monda, Keri L KL; North, Kari E KE; Hunt, Steven C SC; Rao, D C DC; Province, Michael A MA; Kraja, Aldi T AT
Publication Date: 2010-06

Variant appearance in text: rs9815354
PubMed Link: 20406164
Variant Present in the following documents:
  • Main text
View BVdb publication page



Blood pressure and human genetic variation in the general population.

Current Opinion In Cardiology
Arora, Pankaj P; Newton-Cheh, Christopher C
Publication Date: 2010-05

Variant appearance in text: rs9815354
PubMed Link: 20224392
Variant Present in the following documents:
  • Main text
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Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium.

Nature Genetics
Ganesh, Santhi K SK; Zakai, Neil A NA; van Rooij, Frank J A FJ; Soranzo, Nicole N; Smith, Albert V AV; Nalls, Michael A MA; Chen, Ming-Huei MH; Kottgen, Anna A; Glazer, Nicole L NL; Dehghan, Abbas A; Kuhnel, Brigitte B; Aspelund, Thor T; Yang, Qiong Q; Tanaka, Toshiko T; Jaffe, Andrew A; Bis, Joshua C M JC; Verwoert, Germaine C GC; Teumer, Alexander A; Fox, Caroline S CS; Guralnik, Jack M JM; Ehret, Georg B GB; Rice, Kenneth K; Felix, Janine F JF; Rendon, Augusto A; Eiriksdottir, Gudny G; Levy, Daniel D; Patel, Kushang V KV; Boerwinkle, Eric E; Rotter, Jerome I JI; Hofman, Albert A; Sambrook, Jennifer G JG; Hernandez, Dena G DG; Zheng, Gang G; Bandinelli, Stefania S; Singleton, Andrew B AB; Coresh, Josef J; Lumley, Thomas T; Uitterlinden, André G AG; Vangils, Janine M JM; Launer, Lenore J LJ; Cupples, L Adrienne LA; Oostra, Ben A BA; Zwaginga, Jaap-Jan JJ; Ouwehand, Willem H WH; Thein, Swee-Lay SL; Meisinger, Christa C; Deloukas, Panos P; Nauck, Matthias M; Spector, Tim D TD; Gieger, Christian C; Gudnason, Vilmundur V; van Duijn, Cornelia M CM; Psaty, Bruce M BM; Ferrucci, Luigi L; Chakravarti, Aravinda A; Greinacher, Andreas A; O'Donnell, Christopher J CJ; Witteman, Jacqueline C M JC; Furth, Susan S; Cushman, Mary M; Harris, Tamara B TB; Lin, Jing-Ping JP
Publication Date: 2009-11

Variant appearance in text: rs9815354
PubMed Link: 19862010
Variant Present in the following documents:
  • NIHMS145796-supplement-1.pdf
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Genome-wide association study of blood pressure and hypertension.

Nature Genetics
Levy, Daniel D; Ehret, Georg B GB; Rice, Kenneth K; Verwoert, Germaine C GC; Launer, Lenore J LJ; Dehghan, Abbas A; Glazer, Nicole L NL; Morrison, Alanna C AC; Johnson, Andrew D AD; Aspelund, Thor T; Aulchenko, Yurii Y; Lumley, Thomas T; Köttgen, Anna A; Vasan, Ramachandran S RS; Rivadeneira, Fernando F; Eiriksdottir, Gudny G; Guo, Xiuqing X; Arking, Dan E DE; Mitchell, Gary F GF; Mattace-Raso, Francesco U S FU; Smith, Albert V AV; Taylor, Kent K; Scharpf, Robert B RB; Hwang, Shih-Jen SJ; Sijbrands, Eric J G EJ; Bis, Joshua J; Harris, Tamara B TB; Ganesh, Santhi K SK; O'Donnell, Christopher J CJ; Hofman, Albert A; Rotter, Jerome I JI; Coresh, Josef J; Benjamin, Emelia J EJ; Uitterlinden, André G AG; Heiss, Gerardo G; Fox, Caroline S CS; Witteman, Jacqueline C M JC; Boerwinkle, Eric E; Wang, Thomas J TJ; Gudnason, Vilmundur V; Larson, Martin G MG; Chakravarti, Aravinda A; Psaty, Bruce M BM; van Duijn, Cornelia M CM
Publication Date: 2009-06

Variant appearance in text: rs9815354
PubMed Link: 19430479
Variant Present in the following documents:
  • Main text
View BVdb publication page