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Makale detayı · 2018 · article

Whole Exome Sequencing of Patients with Steroid-Resistant Nephrotic Syndrome

YÖKSİS OpenAlex Açık erişim · green Üst %1
Yıl2018
Atıf239OpenAlex
Atıf211Semantic Scholar · 16 etkili
Yüzdelik%99,3
FWCI11,311,00 = dünya ortalaması
Scopus (SJR)Q1
WoS (JCR)Q1

Veri kaynağı ayrımı

  • YÖKSİSYÖKSİS makale kaydı
  • YÖKSİS dergi adıClinical Journal of the American Society of Nephrology
  • Katalog eşleşmesi (ISSN)Clinical Journal of the American Society of Nephrology
  • OpenAlexOpenAlex zenginleştirmesi (özet, atıf, konular)
  • Semantic Scholaratıf sayısı (OpenAlex ile birleştirilmez)

Özet

OpenAlex İngilizce

Background and objectives Steroid-resistant nephrotic syndrome overwhelmingly progresses to ESRD. More than 30 monogenic genes have been identified to cause steroid-resistant nephrotic syndrome. We previously detected causative mutations using targeted panel sequencing in 30% of patients with steroid-resistant nephrotic syndrome. Panel sequencing has a number of limitations when compared with whole exome sequencing. We employed whole exome sequencing to detect monogenic causes of steroid-resistant nephrotic syndrome in an international cohort of 300 families. Design, setting, participants, & measurements Three hundred thirty-five individuals with steroid-resistant nephrotic syndrome from 300 families were recruited from April of 1998 to June of 2016. Age of onset was restricted to <25 years of age. Exome data were evaluated for 33 known monogenic steroid-resistant nephrotic syndrome genes. Results In 74 of 300 families (25%), we identified a causative mutation in one of 20 genes known to cause steroid-resistant nephrotic syndrome. In 11 families (3.7%), we detected a mutation in a gene that causes a phenocopy of steroid-resistant nephrotic syndrome. This is consistent with our previously published identification of mutations using a panel approach. We detected a causative mutation in a known steroid-resistant nephrotic syndrome gene in 38% of consanguineous families and in 13% of nonconsanguineous families, and 48% of children with congenital nephrotic syndrome. A total of 68 different mutations were detected in 20 of 33 steroid-resistant nephrotic syndrome genes. Fifteen of these mutations were novel. NPHS1 , PLCE1 , NPHS2 , and SMARCAL1 were the most common genes in which we detected a mutation. In another 28% of families, we detected mutations in one or more candidate genes for steroid-resistant nephrotic syndrome. Conclusions Whole exome sequencing is a sensitive approach toward diagnosis of monogenic causes of steroid-resistant nephrotic syndrome. A molecular genetic diagnosis of steroid-resistant nephrotic syndrome may have important consequences for the management of treatment and kidney transplantation in steroid-resistant nephrotic syndrome.

Konular

Atıflar

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Yerel katalogda bu makaleye atıf yapan 26 yayın (OpenAlex referans eşleşmesi; tam dünya listesi değildir).

  1. 2022 Oral Coenzyme Q10 supplementation leads to better preservation of kidney function in steroid-resistant nephrotic syndrome due to primary Coenzyme Q10 deficiencyAtıf 67 · OpenAlex
  2. 2022 Oral Coenzyme Q10 supplementation leads to better preservation of kidney function in steroid-resistant nephrotic syndrome due to primary Coenzyme Q10 deficiencyAtıf 67 · OpenAlex
  3. 2022 Oral Coenzyme Q10 supplementation leads to better preservation of kidney function in steroid-resistant nephrotic syndrome due to primary Coenzyme Q10 deficiencyAtıf 67 · OpenAlex
  4. 2020 Genetic aspects of congenital nephrotic syndrome: a consensus statement from the ERKNet–ESPN inherited glomerulopathy working groupAtıf 41 · OpenAlex
  5. 2020 Genetic aspects of congenital nephrotic syndrome: a consensus statement from the ERKNet–ESPN inherited glomerulopathy working groupAtıf 41 · OpenAlex
  6. 2020 COL4A3 mutation is an independent risk factor for poor prognosis in children with Alport syndromeAtıf 22 · OpenAlex
  7. 2020 COL4A3 mutation is an independent risk factor for poor prognosis in children with Alport syndromeAtıf 22 · OpenAlex
  8. 2020 COL4A3 mutation is an independent risk factor for poor prognosis in children with Alport syndromeAtıf 22 · OpenAlex
  9. 2023 A rare cause of nephrotic syndrome—sphingosine-1-phosphate lyase (SGPL1) deficiency: 6 cases and a review of the literatureAtıf 17 · OpenAlex
  10. 2023 A rare cause of nephrotic syndrome—sphingosine-1-phosphate lyase (SGPL1) deficiency: 6 cases and a review of the literatureAtıf 17 · OpenAlex

Yazarlar

59
  1. Jillian K Warejko 1
  2. Weizhen Tan 2
  3. Ankana Daga 3
  4. David Schapiro 4
  5. Jennifer A Lawson 5
  6. Shirlee Shril 6
  7. Svjetlana Lovric 7
  8. Shazia Ashraf 8
  9. Jia Rao 9
  10. Tobias Hermle 10
  11. Tilman Jobst-Schwan 11
  12. Eugen Widmeier 12
  13. Amar J Majmundar 13
  14. Ronen Schneider 14
  15. Heon Yung Gee 15
  16. J Magdalena Schmidt 16
  17. Asaf Vivante 17
  18. der Ven van 18
  19. Hadas Ityel 19
  20. Jing Chen 20
  21. Stefan Kohl 21
  22. Werner L Pabst 22
  23. Makiko Nakayama 23
  24. Michael JG Somers 24
  25. Nancy M Rodig 25
  26. Ghaleb Daouk 26
  27. Michelle Baum 27
  28. Deborah R Stein 28
  29. Michael A Ferguson 29
  30. Avram Z Traum 30
  31. Neveen A Soliman 31
  32. Jameela A Kari 32
  33. Desoky Sherif El 33
  34. Hanan Fathy 34
  35. Martin Zenker 35
  36. SEVCAN AZİME BAKKALOĞLU EZGÜ GAZİ ÜNİVERSİTESİ 36
  37. Müller Dominik 37
  38. Aytul Noyan 38
  39. Fatih Ozaltin 39
  40. Melissa A Cadnapaphornchai 40
  41. Seema Hashmi 41
  42. Hopcian Jeffrey 42
  43. Jeffrey B Kopp 43
  44. Detlef Bockenhauer 44
  45. Radovan Bogdanovic 45
  46. Nataša Stajić 46
  47. Gil Chernin 47
  48. Robert Ettenger 48
  49. Henry Fehrenbach 49
  50. Markus Kemper 50
  51. Reyner Loza Munarriz 51
  52. Ludmila Podracka 52
  53. Rainer Büscher 53
  54. Erkin Serdaroglu 54
  55. Velibor Tasic 55
  56. Shrikant Mane 56
  57. Richard P Lifton 57
  58. Daniela A Braun 58
  59. Friedhelm Hildebrandt 59