TEK c.1327+1589C>T

Variant ID: 9-27187216-C-T

NM_000459.3(TEK):c.1327+1589C>T

This variant was identified in 10 publications

View GRCh38 version.




Publications:


Does TGFBR3 Polymorphism Increase the Risk of Silent Cerebral Infarction in Egyptian Children with Sickle Cell Disease?

Indian Journal Of Pediatrics
Hassab, Hoda H; Hanafi, Marwa M; Elbeheiry, Ahmed A; Hassan, Mona M; Chazli, Yasmine El YE
Publication Date: 2022-07-04

Variant appearance in text: rs489347
PubMed Link: 35781614
Variant Present in the following documents:
  • Main text
  • 12098_2022_Article_4181.pdf
View BVdb publication page



Genetic, laboratory and clinical risk factors in the development of overt ischemic stroke in children with sickle cell disease.

Hematology, Transfusion And Cell Therapy
Belisário, André Rolim AR; Silva, Célia Maria CM; Velloso-Rodrigues, Cibele C; Viana, Marcos Borato MB
Publication Date: 2018

Variant appearance in text: rs489347
PubMed Link: 30057991
Variant Present in the following documents:
  • Main text
  • main.pdf
View BVdb publication page



Genetics of Sickle Cell-Associated Cardiovascular Disease: An Expert Review with Lessons Learned in Africa.

Omics : A Journal Of Integrative Biology
Geard, Amy A; Pule, Gift D GD; Chelo, David D; Bitoungui, Valentina Josiane Ngo VJ; Wonkam, Ambroise A
Publication Date: 2016-10

Variant appearance in text: rs489347
PubMed Link: 27726639
Variant Present in the following documents:
  • Main text
View BVdb publication page



Stroke genomics in people of African ancestry: charting new paths.

Cardiovascular Journal Of Africa
Akinyemi, R O RO; Ovbiagele, B B; Akpalu, A A; Jenkins, C C; Sagoe, K K; Owolabi, L L; Sarfo, F F; Obiako, R R; Gebreziabher, M M; Melikam, E E; Warth, S S; Arulogun, O O; Lackland, D D; Ogunniyi, A A; Tiwari, H H; Kalaria, R N RN; Arnett, D D; Owolabi, M O MO; ,
Publication Date: 2015

Variant appearance in text: rs489347
PubMed Link: 25962947
Variant Present in the following documents:
  • Main text
  • cvja-26-s39.pdf
View BVdb publication page



Genetic mapping and exome sequencing identify 2 mutations associated with stroke protection in pediatric patients with sickle cell anemia.

Blood
Flanagan, Jonathan M JM; Sheehan, Vivien V; Linder, Heidi H; Howard, Thad A TA; Wang, Yong-Dong YD; Hoppe, Carolyn C CC; Aygun, Banu B; Adams, Robert J RJ; Neale, Geoffrey A GA; Ware, Russell E RE
Publication Date: 2013-04-18

Variant appearance in text: rs489347
PubMed Link: 23422753
Variant Present in the following documents:
  • Main text
View BVdb publication page



The search for genetic modifiers of disease severity in the β-hemoglobinopathies.

Cold Spring Harbor Perspectives In Medicine
Lettre, Guillaume G
Publication Date: 2012-10-01

Variant appearance in text: rs489347
PubMed Link: 23028136
Variant Present in the following documents:
  • Main text
View BVdb publication page



Genetic modifiers of sickle cell disease.

American Journal Of Hematology
Steinberg, Martin H MH; Sebastiani, Paola P
Publication Date: 2012-08

Variant appearance in text: rs489347
PubMed Link: 22641398
Variant Present in the following documents:
  • Main text
View BVdb publication page



Genetic predictors for stroke in children with sickle cell anemia.

Blood
Flanagan, Jonathan M JM; Frohlich, Denise M DM; Howard, Thad A TA; Schultz, William H WH; Driscoll, Catherine C; Nagasubramanian, Ramamoorthy R; Mortier, Nicole A NA; Kimble, Amy C AC; Aygun, Banu B; Adams, Robert J RJ; Helms, Ronald W RW; Ware, Russell E RE
Publication Date: 2011-06-16

Variant appearance in text: rs489347
PubMed Link: 21515823
Variant Present in the following documents:
  • Main text
View BVdb publication page



Sickle Cell Disease in the Post Genomic Era: A Monogenic Disease with a Polygenic Phenotype.

Genomics Insights
Driss, A A; Asare, K O KO; Hibbert, J M JM; Gee, B E BE; Adamkiewicz, T V TV; Stiles, J K JK
Publication Date: 2009-07-30

Variant appearance in text: rs489347
PubMed Link: 20401335
Variant Present in the following documents:
  • Main text
  • gei-2-2009-023.pdf
View BVdb publication page



Genetic dissection and prognostic modeling of overt stroke in sickle cell anemia.

Nature Genetics
Sebastiani, Paola P; Ramoni, Marco F MF; Nolan, Vikki V; Baldwin, Clinton T CT; Steinberg, Martin H MH
Publication Date: 2005-04

Variant appearance in text: rs489347
PubMed Link: 15778708
Variant Present in the following documents:
  • Main text
View BVdb publication page