Genome-Wide Association Study to Find Modifiers for Tetralogy of Fallot in the 22q11.2 Deletion Syndrome Identifies Variants in the GPR98 Locus on 5q14.3-Reference-Cited by-同舟云学术

Genome-Wide Association Study to Find Modifiers for Tetralogy of Fallot in the 22q11.2 Deletion Syndrome Identifies Variants in the GPR98 Locus on 5q14.3

Published:2017-10 Issue:5 Volume:10 Page:
ISSN:1942-325X
Container-title:Circulation: Cardiovascular Genetics
language:en
Short-container-title:Circ Cardiovasc Genet

Author:

Guo Tingwei¹,Repetto Gabriela M.¹,McDonald McGinn Donna M.¹,Chung Jonathan H.¹,Nomaru Hiroko¹,Campbell Christopher L.¹,Blonska Anna¹,Bassett Anne S.¹,Chow Eva W.C.¹,Mlynarski Elisabeth E.¹,Swillen Ann¹,Vermeesch Joris¹,Devriendt Koen¹,Gothelf Doron¹,Carmel Miri¹,Michaelovsky Elena¹,Schneider Maude¹,Eliez Stephan¹,Antonarakis Stylianos E.¹,Coleman Karlene¹,Tomita-Mitchell Aoy¹,Mitchell Michael E.¹,Digilio M. Cristina¹,Dallapiccola Bruno¹,Marino Bruno¹,Philip Nicole¹,Busa Tiffany¹,Kushan-Wells Leila¹,Bearden Carrie E.¹,Piotrowicz Małgorzata¹,Hawuła Wanda¹,Roberts Amy E.¹,Tassone Flora¹,Simon Tony J.¹,van Duin Esther D.A.¹,van Amelsvoort Thérèse A.¹,Kates Wendy R.¹,Zackai Elaine¹,Johnston H. Richard¹,Cutler David J.¹,Agopian A.J.¹,Goldmuntz Elizabeth¹,Mitchell Laura E.¹,Wang Tao¹,Emanuel Beverly S.¹,Morrow Bernice E.¹

Affiliation:

1. From the Department of Genetics (T.G., J.H.C., H.N., C.L.C., T.W., B.E.M.) and Department of Epidemiology and Population Health (T.W.), Albert Einstein College of Medicine, Bronx, NY; Center for Human Genetics, Facultad de Medicina Clinica Alemana Universidad del Desarrollo, Santiago, Chile (G.M.R.); Division of Human Genetics (D.M.M.M., E.E.M., E.Z., B.S.E.), Division of Cardiology (E.G.), and Department of Pediatrics (E.G.), Children’s Hospital of Philadelphia, Perelman School of Medicine,...

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Genetics (clinical),Cardiology and Cardiovascular Medicine,Genetics

Reference53 articles.

1. 22q11.2 deletion syndrome

2. Submicroscopic deletions at 22q11.2: Variability of the clinical picture and delineation of a commonly deleted region

3. Velo-cardio-facial syndrome: Frequency and extent of 22q1l deletions

4. Molecular definition of the 22q11 deletions in velo-cardio-facial syndrome.;Morrow B;Am J Hum Genet,1995

5. Developmental genetics of the heart

Cited by 21 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Understanding the Variability of 22q11.2 Deletion Syndrome: The Role of Epigenetic Factors;Genes;2024-02-29

2. Clinically Relevant Genetic Considerations for Patients With Tetralogy of Fallot;CJC Pediatric and Congenital Heart Disease;2023-12

3. Chromatin regulators in the TBX1 network confer risk for conotruncal heart defects in 22q11.2DS;npj Genomic Medicine;2023-07-18

4. Abnormalities of hsa-mir-16 and hsa-mir-124 Affect Mitochondrial Function and Fatty Acid Metabolism in Tetralogy of Fallot;Combinatorial Chemistry & High Throughput Screening;2023-02

5. Chromatin regulators in the TBX1 network confer risk for conotruncal heart defects in 22q11.2DS and sporadic congenital heart disease;2022-10-03