TRIM65 c.511-91A>C

Variant ID: 17-73888672-T-G

NM_173547.3(TRIM65):c.511-91A>C

This variant was identified in 21 publications

View GRCh38 version.




Publications:


Dissecting Polygenic Etiology of Ischemic Stroke in the Era of Precision Medicine.

Journal Of Clinical Medicine
Li, Jiang J; Abedi, Vida V; Zand, Ramin R
Publication Date: 2022-10-11

Variant appearance in text: rs3744028
PubMed Link: 36294301
Variant Present in the following documents:
  • Main text
  • jcm-11-05980.pdf
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Gene-mapping study of extremes of cerebral small vessel disease reveals TRIM47 as a strong candidate.

Brain : A Journal Of Neurology
Mishra, Aniket A; Duplaà, Cécile C; Vojinovic, Dina D; Suzuki, Hideaki H; Sargurupremraj, Muralidharan M; Zilhão, Nuno R NR; Li, Shuo S; Bartz, Traci M TM; Jian, Xueqiu X; Zhao, Wei W; Hofer, Edith E; Wittfeld, Katharina K; Harris, Sarah E SE; van der Auwera-Palitschka, Sandra S; Luciano, Michelle M; Bis, Joshua C JC; Adams, Hieab H H HHH; Satizabal, Claudia L CL; Gottesman, Rebecca F RF; Gampawar, Piyush G PG; Bülow, Robin R; Weiss, Stefan S; Yu, Miao M; Bastin, Mark E ME; Lopez, Oscar L OL; Vernooij, Meike W MW; Beiser, Alexa S AS; Völker, Uwe U; Kacprowski, Tim T; Soumare, Aicha A; Smith, Jennifer A JA; Knopman, David S DS; Morris, Zoe Z; Zhu, Yicheng Y; Rotter, Jerome I JI; Dufouil, Carole C; Valdés Hernández, Maria M; Muñoz Maniega, Susana S; Lathrop, Mark M; Boerwinkle, Erik E; Schmidt, Reinhold R; Ihara, Masafumi M; Mazoyer, Bernard B; Yang, Qiong Q; Joutel, Anne A; Tournier-Lasserve, Elizabeth E; Launer, Lenore J LJ; Deary, Ian J IJ; Mosley, Thomas H TH; Amouyel, Philippe P; DeCarli, Charles S CS; Psaty, Bruce M BM; Tzourio, Christophe C; Kardia, Sharon L R SLR; Grabe, Hans J HJ; Teumer, Alexander A; van Duijn, Cornelia M CM; Schmidt, Helena H; Wardlaw, Joanna M JM; Ikram, M Arfan MA; Fornage, Myriam M; Gudnason, Vilmundur V; Seshadri, Sudha S; Matthews, Paul M PM; Longstreth, William T WT; Couffinhal, Thierry T; Debette, Stephanie S
Publication Date: 2022-06-30

Variant appearance in text: rs3744028
PubMed Link: 35511193
Variant Present in the following documents:
  • awab432_supplementary_data.pdf
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Novel germline TRAF3IP3 mutation in a dyad with familial acute B lymphoblastic leukemia.

Cancer Reports (Hoboken, N.J.)
Pommert, Lauren L; Burns, Robert R; Furumo, Quinlan Q; Pulakanti, Kirthi K; Brandt, Jon J; Burke, Michael J MJ; Rao, Sridhar S
Publication Date: 2021-06

Variant appearance in text: rs3744028
PubMed Link: 33503336
Variant Present in the following documents:
  • CNR2-4-e1335-s003.xlsx, sheet 1
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Replication of Top Loci From COL4A1/2 Associated With White Matter Hyperintensity Burden in Patients With Ischemic Stroke.

Stroke
Li, Jiang J; Abedi, Vida V; , ; Zand, Ramin R; Griessenauer, Christoph J CJ
Publication Date: 2020-12

Variant appearance in text: rs3744028
PubMed Link: 33148145
Variant Present in the following documents:
  • Main text
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Common Genetic Variation Indicates Separate Causes for Periventricular and Deep White Matter Hyperintensities.

Stroke
Armstrong, Nicola J NJ; Mather, Karen A KA; Sargurupremraj, Muralidharan M; Knol, Maria J MJ; Malik, Rainer R; Satizabal, Claudia L CL; Yanek, Lisa R LR; Wen, Wei W; Gudnason, Vilmundur G VG; Dueker, Nicole D ND; Elliott, Lloyd T LT; Hofer, Edith E; Bis, Joshua J; Jahanshad, Neda N; Li, Shuo S; Logue, Mark A MA; Luciano, Michelle M; Scholz, Markus M; Smith, Albert V AV; Trompet, Stella S; Vojinovic, Dina D; Xia, Rui R; Alfaro-Almagro, Fidel F; Ames, David D; Amin, Najaf N; Amouyel, Philippe P; Beiser, Alexa S AS; Brodaty, Henry H; Deary, Ian J IJ; Fennema-Notestine, Christine C; Gampawar, Piyush G PG; Gottesman, Rebecca R; Griffanti, Ludovica L; Jack, Clifford R CR; Jenkinson, Mark M; Jiang, Jiyang J; Kral, Brian G BG; Kwok, John B JB; Lampe, Leonie L; C M Liewald, David D; Maillard, Pauline P; Marchini, Jonathan J; Bastin, Mark E ME; Mazoyer, Bernard B; Pirpamer, Lukas L; Rafael Romero, José J; Roshchupkin, Gennady V GV; Schofield, Peter R PR; Schroeter, Matthias L ML; Stott, David J DJ; Thalamuthu, Anbupalam A; Trollor, Julian J; Tzourio, Christophe C; van der Grond, Jeroen J; Vernooij, Meike W MW; Witte, Veronica A VA; Wright, Margaret J MJ; Yang, Qiong Q; Morris, Zoe Z; Siggurdsson, Siggi S; Psaty, Bruce B; Villringer, Arno A; Schmidt, Helena H; Haberg, Asta K AK; van Duijn, Cornelia M CM; Jukema, J Wouter JW; Dichgans, Martin M; Sacco, Ralph L RL; Wright, Clinton B CB; Kremen, William S WS; Becker, Lewis C LC; Thompson, Paul M PM; Mosley, Thomas H TH; Wardlaw, Joanna M JM; Ikram, M Arfan MA; Adams, Hieab H H HHH; Seshadri, Sudha S; Sachdev, Perminder S PS; Smith, Stephen M SM; Launer, Lenore L; Longstreth, William W; DeCarli, Charles C; Schmidt, Reinhold R; Fornage, Myriam M; Debette, Stephanie S; Nyquist, Paul A PA
Publication Date: 2020-07

Variant appearance in text: rs3744028
PubMed Link: 32517579
Variant Present in the following documents:
  • Main text
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The Associations of PMF1, ICAM1, AGT, TRIM65, FBF1, and ACOX1 Variants With Leukoaraiosis in Chinese Population.

Frontiers In Genetics
Huang, Wen-Qing WQ; Ye, Hui-Ming HM; Cai, Liang-Liang LL; Ma, Qi-Lin QL; Lu, Cong-Xia CX; Tong, Sui-Jun SJ; Tzeng, Chi-Meng CM; Lin, Qing Q
Publication Date: 2019

Variant appearance in text: rs3744028
PubMed Link: 31396257
Variant Present in the following documents:
  • Main text
  • fgene-10-00615.pdf
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Advances in Understanding the Pathophysiology of Lacunar Stroke: A Review.

Jama Neurology
Regenhardt, Robert W RW; Das, Alvin S AS; Lo, Eng H EH; Caplan, Louis R LR
Publication Date: 2018-10-01

Variant appearance in text: rs3744028
PubMed Link: 30167649
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: rs3744028
PubMed Link: 30116610
Variant Present in the following documents:
  • Main text
  • AN20758251-10-02-004.pdf
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A Comprehensive Atlas of E3 Ubiquitin Ligase Mutations in Neurological Disorders.

Frontiers In Genetics
George, Arlene J AJ; Hoffiz, Yarely C YC; Charles, Antoinette J AJ; Zhu, Ying Y; Mabb, Angela M AM
Publication Date: 2018

Variant appearance in text: rs3744028
PubMed Link: 29491882
Variant Present in the following documents:
  • Table1.xlsx, sheet 1
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Analysis of genetic polymorphisms associated with leukoaraiosis in the southern Chinese population: A case-control study.

Medicine
Huang, Wen-Qing WQ; Ye, Hui-Ming HM; Li, Fang-Fang FF; Yi, Ke-Hui KH; Zhang, Ya Y; Cai, Liang-Liang LL; Lin, Hui-Nuan HN; Lin, Qing Q; Tzeng, Chi-Meng CM
Publication Date: 2016-08

Variant appearance in text: rs3744028
PubMed Link: 27583843
Variant Present in the following documents:
  • Main text
  • medi-95-e3857.pdf
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Comprehensive promoter level expression quantitative trait loci analysis of the human frontal lobe.

Genome Medicine
Blauwendraat, Cornelis C; Francescatto, Margherita M; Gibbs, J Raphael JR; Jansen, Iris E IE; Simón-Sánchez, Javier J; Hernandez, Dena G DG; Dillman, Allissa A AA; Singleton, Andrew B AB; Cookson, Mark R MR; Rizzu, Patrizia P; Heutink, Peter P
Publication Date: 2016-06-10

Variant appearance in text: rs3744028
PubMed Link: 27287230
Variant Present in the following documents:
  • Main text
  • 13073_2016_Article_320.pdf
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White Matter Lesion Progression: Genome-Wide Search for Genetic Influences.

Stroke
Hofer, Edith E; Cavalieri, Margherita M; Bis, Joshua C JC; DeCarli, Charles C; Fornage, Myriam M; Sigurdsson, Sigurdur S; Srikanth, Velandai V; Trompet, Stella S; Verhaaren, Benjamin F J BF; Wolf, Christiane C; Yang, Qiong Q; Adams, Hieab H H HH; Amouyel, Philippe P; Beiser, Alexa A; Buckley, Brendan M BM; Callisaya, Michele M; Chauhan, Ganesh G; de Craen, Anton J M AJ; Dufouil, Carole C; van Duijn, Cornelia M CM; Ford, Ian I; Freudenberger, Paul P; Gottesman, Rebecca F RF; Gudnason, Vilmundur V; Heiss, Gerardo G; Hofman, Albert A; Lumley, Thomas T; Martinez, Oliver O; Mazoyer, Bernard B; Moran, Chris C; Niessen, Wiro J WJ; Phan, Thanh T; Psaty, Bruce M BM; Satizabal, Claudia L CL; Sattar, Naveed N; Schilling, Sabrina S; Shibata, Dean K DK; Slagboom, P Eline PE; Smith, Albert A; Stott, David J DJ; Taylor, Kent D KD; Thomson, Russell R; Töglhofer, Anna M AM; Tzourio, Christophe C; van Buchem, Mark M; Wang, Jing J; Westendorp, Rudi G J RG; Windham, B Gwen BG; Vernooij, Meike W MW; Zijdenbos, Alex A; Beare, Richard R; Debette, Stéphanie S; Ikram, M Arfan MA; Jukema, J Wouter JW; Launer, Lenore J LJ; Longstreth, W T WT; Mosley, Thomas H TH; Seshadri, Sudha S; Schmidt, Helena H; Schmidt, Reinhold R; ,
Publication Date: 2015-11

Variant appearance in text: rs3744028
PubMed Link: 26451028
Variant Present in the following documents:
  • Main text
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Candidate-gene analysis of white matter hyperintensities on neuroimaging.

Journal Of Neurology, Neurosurgery, And Psychiatry
Tran, Theresa T; Cotlarciuc, Ioana I; Yadav, Sunaina S; Hasan, Nazeeha N; Bentley, Paul P; Levi, Christopher C; Worrall, Bradford B BB; Meschia, James F JF; Rost, Natalia N; Sharma, Pankaj P
Publication Date: 2016-03

Variant appearance in text: rs3744028
PubMed Link: 25835038
Variant Present in the following documents:
  • Main text
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Genetics of cerebral small vessel disease.

Journal Of Stroke
Choi, Jay Chol JC
Publication Date: 2015-01

Variant appearance in text: rs3744028
PubMed Link: 25692103
Variant Present in the following documents:
  • Main text
  • jos-17-7.pdf
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Multiethnic genome-wide association study of cerebral white matter hyperintensities on MRI.

Circulation. Cardiovascular Genetics
Verhaaren, Benjamin F J BF; Debette, Stéphanie S; Bis, Joshua C JC; Smith, Jennifer A JA; Ikram, M Kamran MK; Adams, Hieab H HH; Beecham, Ashley H AH; Rajan, Kumar B KB; Lopez, Lorna M LM; Barral, Sandra S; van Buchem, Mark A MA; van der Grond, Jeroen J; Smith, Albert V AV; Hegenscheid, Katrin K; Aggarwal, Neelum T NT; de Andrade, Mariza M; Atkinson, Elizabeth J EJ; Beekman, Marian M; Beiser, Alexa S AS; Blanton, Susan H SH; Boerwinkle, Eric E; Brickman, Adam M AM; Bryan, R Nick RN; Chauhan, Ganesh G; Chen, Christopher P L H CP; Chouraki, Vincent V; de Craen, Anton J M AJ; Crivello, Fabrice F; Deary, Ian J IJ; Deelen, Joris J; De Jager, Philip L PL; Dufouil, Carole C; Elkind, Mitchell S V MS; Evans, Denis A DA; Freudenberger, Paul P; Gottesman, Rebecca F RF; Guðnason, Vilmundur V; Habes, Mohamad M; Heckbert, Susan R SR; Heiss, Gerardo G; Hilal, Saima S; Hofer, Edith E; Hofman, Albert A; Ibrahim-Verbaas, Carla A CA; Knopman, David S DS; Lewis, Cora E CE; Liao, Jiemin J; Liewald, David C M DC; Luciano, Michelle M; van der Lugt, Aad A; Martinez, Oliver O OO; Mayeux, Richard R; Mazoyer, Bernard B; Nalls, Mike M; Nauck, Matthias M; Niessen, Wiro J WJ; Oostra, Ben A BA; Psaty, Bruce M BM; Rice, Kenneth M KM; Rotter, Jerome I JI; von Sarnowski, Bettina B; Schmidt, Helena H; Schreiner, Pamela J PJ; Schuur, Maaike M; Sidney, Stephen S SS; Sigurdsson, Sigurdur S; Slagboom, P Eline PE; Stott, David J M DJ; van Swieten, John C JC; Teumer, Alexander A; Töglhofer, Anna Maria AM; Traylor, Matthew M; Trompet, Stella S; Turner, Stephen T ST; Tzourio, Christophe C; Uh, Hae-Won HW; Uitterlinden, André G AG; Vernooij, Meike W MW; Wang, Jing J JJ; Wong, Tien Y TY; Wardlaw, Joanna M JM; Windham, B Gwen BG; Wittfeld, Katharina K; Wolf, Christiane C; Wright, Clinton B CB; Yang, Qiong Q; Zhao, Wei W; Zijdenbos, Alex A; Jukema, J Wouter JW; Sacco, Ralph L RL; Kardia, Sharon L R SL; Amouyel, Philippe P; Mosley, Thomas H TH; Longstreth, W T WT; DeCarli, Charles C CC; van Duijn, Cornelia M CM; Schmidt, Reinhold R; Launer, Lenore J LJ; Grabe, Hans J HJ; Seshadri, Sudha S SS; Ikram, M Arfan MA; Fornage, Myriam M
Publication Date: 2015-04

Variant appearance in text: rs3744028
PubMed Link: 25663218
Variant Present in the following documents:
  • Main text
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Genes from a translational analysis support a multifactorial nature of white matter hyperintensities.

Stroke
Lopez, Lorna M LM; Hill, W David WD; Harris, Sarah E SE; Valdes Hernandez, Maria M; Munoz Maniega, Susana S; Bastin, Mark E ME; Bailey, Emma E; Smith, Colin C; McBride, Martin M; McClure, John J; Graham, Delyth D; Dominiczak, Anna A; Yang, Qiong Q; Fornage, Myriam M; Ikram, M Arfan MA; Debette, Stephanie S; Launer, Lenore L; Bis, Joshua C JC; Schmidt, Reinhold R; Seshadri, Sudha S; Porteous, David J DJ; Starr, John J; Deary, Ian J IJ; Wardlaw, Joanna M JM
Publication Date: 2015-02

Variant appearance in text: rs3744028
PubMed Link: 25586835
Variant Present in the following documents:
  • Main text
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Clinical neurogenetics: stroke.

Neurologic Clinics
Rost, Natalia S NS
Publication Date: 2013-11

Variant appearance in text: rs3744028
PubMed Link: 24176416
Variant Present in the following documents:
  • Main text
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17q25 Locus is associated with white matter hyperintensity volume in ischemic stroke, but not with lacunar stroke status.

Stroke
Adib-Samii, Poneh P; Rost, Natalia N; Traylor, Matthew M; Devan, William W; Biffi, Alessandro A; Lanfranconi, Silvia S; Fitzpatrick, Kaitlin K; Bevan, Steve S; Kanakis, Allison A; Valant, Valerie V; Gschwendtner, Andreas A; Malik, Rainer R; Richie, Alexa A; Gamble, Dale D; Segal, Helen H; Parati, Eugenio A EA; Ciusani, Emilio E; Holliday, Elizabeth G EG; Maguire, Jane J; Wardlaw, Joanna J; Worrall, Bradford B; Bis, Joshua J; Wiggins, Kerri L KL; Longstreth, Will W; Kittner, Steve J SJ; Cheng, Yu-Ching YC; Mosley, Thomas T; Falcone, Guido J GJ; Furie, Karen L KL; Leiva-Salinas, Carlos C; Lau, Benison C BC; Saleem Khan, Muhammed M; , ; , ; , ; Sharma, Pankaj P; Fornage, Myriam M; Mitchell, Braxton D BD; Psaty, Bruce M BM; Sudlow, Cathie C; Levi, Christopher C; Boncoraglio, Giorgio B GB; Rothwell, Peter M PM; Meschia, James J; Dichgans, Martin M; Rosand, Jonathan J; Markus, Hugh S HS; ,
Publication Date: 2013-06

Variant appearance in text: rs3744028
PubMed Link: 23674528
Variant Present in the following documents:
  • Main text
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Overlap between common genetic polymorphisms underpinning kidney traits and cardiovascular disease phenotypes: the CKDGen consortium.

American Journal Of Kidney Diseases : The Official Journal Of The National Kidney Foundation
Olden, Matthias M; Teumer, Alexander A; Bochud, Murielle M; Pattaro, Cristian C; Köttgen, Anna A; Turner, Stephen T ST; Rettig, Rainer R; Chen, Ming-Huei MH; Dehghan, Abbas A; Bastardot, Francois F; Schmidt, Reinhold R; Vollenweider, Peter P; Schunkert, Heribert H; Reilly, Muredach P MP; Fornage, Myriam M; Launer, Lenore J LJ; Verwoert, Germaine C GC; Mitchell, Gary F GF; Bis, Joshua C JC; O'Donnell, Christopher J CJ; Cheng, Ching-Yu CY; Sim, Xueling X; Siscovick, David S DS; Coresh, Josef J; Kao, W H Linda WH; Fox, Caroline S CS; O'Seaghdha, Conall M CM; ,
Publication Date: 2013-06

Variant appearance in text: rs3744028
PubMed Link: 23474010
Variant Present in the following documents:
  • Main text
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Genetics of subcortical vascular dementia.

Experimental Gerontology
Schmidt, Helena H; Freudenberger, Paul P; Seiler, Stephan S; Schmidt, Reinhold R
Publication Date: 2012-11

Variant appearance in text: rs3744028
PubMed Link: 22735669
Variant Present in the following documents:
  • Main text
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Genome-wide association studies of cerebral white matter lesion burden: the CHARGE consortium.

Annals Of Neurology
Fornage, Myriam M; Debette, Stephanie S; Bis, Joshua C JC; Schmidt, Helena H; Ikram, M Arfan MA; Dufouil, Carole C; Sigurdsson, Sigurdur S; Lumley, Thomas T; DeStefano, Anita L AL; Fazekas, Franz F; Vrooman, Henri A HA; Shibata, Dean K DK; Maillard, Pauline P; Zijdenbos, Alex A; Smith, Albert V AV; Gudnason, Haukur H; de Boer, Renske R; Cushman, Mary M; Mazoyer, Bernard B; Heiss, Gerardo G; Vernooij, Meike W MW; Enzinger, Christian C; Glazer, Nicole L NL; Beiser, Alexa A; Knopman, David S DS; Cavalieri, Margherita M; Niessen, Wiro J WJ; Harris, Tamara B TB; Petrovic, Katja K; Lopez, Oscar L OL; Au, Rhoda R; Lambert, Jean-Charles JC; Hofman, Albert A; Gottesman, Rebecca F RF; Garcia, Melissa M; Heckbert, Susan R SR; Atwood, Larry D LD; Catellier, Diane J DJ; Uitterlinden, Andre G AG; Yang, Qiong Q; Smith, Nicholas L NL; Aspelund, Thor T; Romero, Jose R JR; Rice, Kenneth K; Taylor, Kent D KD; Nalls, Michael A MA; Rotter, Jerome I JI; Sharrett, Richey R; van Duijn, Cornelia M CM; Amouyel, Philippe P; Wolf, Philip A PA; Gudnason, Vilmundur V; van der Lugt, Aad A; Boerwinkle, Eric E; Psaty, Bruce M BM; Seshadri, Sudha S; Tzourio, Christophe C; Breteler, Monique M B MM; Mosley, Thomas H TH; Schmidt, Reinhold R; Longstreth, W T WT; DeCarli, Charles C; Launer, Lenore J LJ
Publication Date: 2011-06

Variant appearance in text: rs3744028
PubMed Link: 21681796
Variant Present in the following documents:
  • Main text
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