186 related articles for article (PubMed ID: 33859323)
1. The impact of rare and low-frequency genetic variants in common variable immunodeficiency (CVID).
Bisgin A; Sonmezler O; Boga I; Yilmaz M
Sci Rep; 2021 Apr; 11(1):8308. PubMed ID: 33859323
[TBL] [Abstract][Full Text] [Related]
2. Genes associated with common variable immunodeficiency: one diagnosis to rule them all?
Bogaert DJ; Dullaers M; Lambrecht BN; Vermaelen KY; De Baere E; Haerynck F
J Med Genet; 2016 Sep; 53(9):575-90. PubMed ID: 27250108
[TBL] [Abstract][Full Text] [Related]
3. A Novel Targeted Amplicon Next-Generation Sequencing Gene Panel for the Diagnosis of Common Variable Immunodeficiency Has a High Diagnostic Yield: Results from the Perth CVID Cohort Study.
Kermode W; De Santis D; Truong L; Della Mina E; Salman S; Thompson G; Nolan D; Loh R; Mallon D; Mclean-Tooke A; John M; Tangye SG; O'Sullivan M; D'Orsogna LJ
J Mol Diagn; 2022 Jun; 24(6):586-599. PubMed ID: 35570134
[TBL] [Abstract][Full Text] [Related]
4. [Immunological alterations in common variable immunodeficiency].
Berrón-Ruiz L
Rev Alerg Mex; 2017; 64(1):87-108. PubMed ID: 28188716
[TBL] [Abstract][Full Text] [Related]
5. Identification of Novel Genetic Variants in CVID Patients With Autoimmunity, Autoinflammation, or Malignancy.
Christiansen M; Offersen R; Jensen JMB; Petersen MS; Larsen CS; Mogensen TH
Front Immunol; 2019; 10():3022. PubMed ID: 32047491
[TBL] [Abstract][Full Text] [Related]
6. Mutation in IRF2BP2 is responsible for a familial form of common variable immunodeficiency disorder.
Keller MD; Pandey R; Li D; Glessner J; Tian L; Henrickson SE; Chinn IK; Monaco-Shawver L; Heimall J; Hou C; Otieno FG; Jyonouchi S; Calabrese L; van Montfrans J; Orange JS; Hakonarson H
J Allergy Clin Immunol; 2016 Aug; 138(2):544-550.e4. PubMed ID: 27016798
[TBL] [Abstract][Full Text] [Related]
7. Perspective: Application of the American College of Medical Genetics Variant Interpretation Criteria to Common Variable Immunodeficiency Disorders.
Ameratunga R; Allan C; Lehnert K; Woon ST
Clin Rev Allergy Immunol; 2021 Oct; 61(2):226-235. PubMed ID: 33818703
[TBL] [Abstract][Full Text] [Related]
8. Deconstructing common variable immunodeficiency by genetic analysis.
Schäffer AA; Salzer U; Hammarström L; Grimbacher B
Curr Opin Genet Dev; 2007 Jun; 17(3):201-12. PubMed ID: 17467261
[TBL] [Abstract][Full Text] [Related]
9. Evaluation of CARMA1/CARD11 and Bob1 as candidate genes in common variable immunodeficiency.
Tampella G; Baronio M; Vitali M; Soresina A; Badolato R; Giliani S; Plebani A; Lougaris V
J Investig Allergol Clin Immunol; 2011; 21(5):348-53. PubMed ID: 21905497
[TBL] [Abstract][Full Text] [Related]
10. Three different classifications, B lymphocyte subpopulations, TNFRSF13B (TACI), TNFRSF13C (BAFF-R), TNFSF13 (APRIL) gene mutations, CTLA-4 and ICOS gene polymorphisms in Turkish patients with common variable immunodeficiency.
Kutukculer N; Gulez N; Karaca NE; Aksu G; Berdeli A
J Clin Immunol; 2012 Dec; 32(6):1165-79. PubMed ID: 22699762
[TBL] [Abstract][Full Text] [Related]
11. [Genetic basis of common variable immunodeficiency: from common to variable].
Allaoui A; Mokhantar K; Jeddane L; Dehbi H; Ailal F; Bousfiha AA; Elkabli H; Moudatir M
Ann Biol Clin (Paris); 2021 Oct; 79(5):407-413. PubMed ID: 34704938
[TBL] [Abstract][Full Text] [Related]
12. [Common variable immunodeficiency: an update on etiology, pathophysiology, and classification].
Morio T
Nihon Rinsho Meneki Gakkai Kaishi; 2012; 35(1):14-22. PubMed ID: 22374438
[TBL] [Abstract][Full Text] [Related]
13. Review: Diagnosing Common Variable Immunodeficiency Disorder in the Era of Genome Sequencing.
Ameratunga R; Lehnert K; Woon ST; Gillis D; Bryant VL; Slade CA; Steele R
Clin Rev Allergy Immunol; 2018 Apr; 54(2):261-268. PubMed ID: 29030829
[TBL] [Abstract][Full Text] [Related]
14. The role of genomics in common variable immunodeficiency disorders.
Kienzler AK; Hargreaves CE; Patel SY
Clin Exp Immunol; 2017 Jun; 188(3):326-332. PubMed ID: 28236292
[TBL] [Abstract][Full Text] [Related]
15. An evolutionary approach to the medical implications of the tumor necrosis factor receptor superfamily member 13B (TNFRSF13B) gene.
Sazzini M; Zuntini R; Farjadian S; Quinti I; Ricci G; Romeo G; Ferrari S; Calafell F; Luiselli D
Genes Immun; 2009 Sep; 10(6):566-78. PubMed ID: 19494827
[TBL] [Abstract][Full Text] [Related]
16. The Rapidly Expanding Genetic Spectrum of Common Variable Immunodeficiency-Like Disorders.
Ameratunga R; Edwards ESJ; Lehnert K; Leung E; Woon ST; Lea E; Allan C; Chan L; Steele R; Longhurst H; Bryant VL
J Allergy Clin Immunol Pract; 2023 Jun; 11(6):1646-1664. PubMed ID: 36796510
[TBL] [Abstract][Full Text] [Related]
17. How important are rare variants in common disease?
Saint Pierre A; Génin E
Brief Funct Genomics; 2014 Sep; 13(5):353-61. PubMed ID: 25005607
[TBL] [Abstract][Full Text] [Related]
18. Identification of novel NFKB1 and ICOS frameshift variants in patients with CVID.
Liu A; Liu Q; Leng S; Zhang X; Feng Q; Peng J; Feng G
Clin Exp Immunol; 2023 Mar; 211(1):68-77. PubMed ID: 36571238
[TBL] [Abstract][Full Text] [Related]
19. Biochemically deleterious human NFKB1 variants underlie an autosomal dominant form of common variable immunodeficiency.
Li J; Lei WT; Zhang P; Rapaport F; Seeleuthner Y; Lyu B; Asano T; Rosain J; Hammadi B; Zhang Y; Pelham SJ; Spaan AN; Migaud M; Hum D; Bigio B; Chrabieh M; Béziat V; Bustamante J; Zhang SY; Jouanguy E; Boisson-Dupuis S; El Baghdadi J; Aimanianda V; Thoma K; Fliegauf M; Grimbacher B; Korganow AS; Saunders C; Rao VK; Uzel G; Freeman AF; Holland SM; Su HC; Cunningham-Rundles C; Fieschi C; Abel L; Puel A; Cobat A; Casanova JL; Zhang Q; Boisson B
J Exp Med; 2021 Nov; 218(11):. PubMed ID: 34473196
[TBL] [Abstract][Full Text] [Related]
20. Genome-wide association identifies diverse causes of common variable immunodeficiency.
Orange JS; Glessner JT; Resnick E; Sullivan KE; Lucas M; Ferry B; Kim CE; Hou C; Wang F; Chiavacci R; Kugathasan S; Sleasman JW; Baldassano R; Perez EE; Chapel H; Cunningham-Rundles C; Hakonarson H
J Allergy Clin Immunol; 2011 Jun; 127(6):1360-7.e6. PubMed ID: 21497890
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
