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DOKTOR ÖĞRETİM ÜYESİ

SELÇUK ÜNİVERSİTESİ TIP FAKÜLTESİ DAHİLİ TIP BİLİMLERİ BÖLÜMÜ

  • Ana Dal Sağlık Bilimleri Temel Alanı
  • Yan Dal Çocuk Endokrinolojisi (Çocuk Sağlığı ve Hastalıkları)

Kayıtlı çıktılara kısa bakış — ayrıntılar aşağıda.

  • Makale 53
  • Proje 0
  • Kitap 0
  • Bildiri 0
  • Patent 0
  • Sanatsal 0
Scopus (SJR) Q1 4 Q2 7 Q3 7 Q4 3
WoS (JCR) Q1 1 Q2 5 Q3 5 Q4 10
TR Index 10 makale

Alan+yıl+tür normalize OpenAlex yüzdelik — Clarivate ESI / SciVal değildir.

Üst %1 makale 0
Üst %10 makale 0
Ort. yüzdelik 42.1%
Üst %1 payı 0.0%
Üst %10 payı 0.0%

Makaleler

YÖKSİS ve OpenAlex kaynak ayrımıyla makaleler; quartile ve TR Index ile daraltabilirsiniz.

Dizin filtreleri

Toplam 53 yayın

Makale listesi

OpenAlex zenginleştirme görünümü — 33 kayıt.

  1. 2026 Pharmacogenetic hypersensitivity to somatropin in a child with severe growth hormone deficiency and MC4R p.V166I variant Journal of Pediatric Endocrinology and Metabolism DOI 10.1515/jpem-2026-0165 OpenAlex 82.9%
  2. 2022 POU6F2 mutation identified in humans with pubertal failure shifts isoform formation and alters GnRH transcript expression bioRxiv (Cold Spring Harbor Laboratory) DOI 10.1101/2022.10.12.511883
  3. 2021 Adrenocortical hormone profiles do not predict the molecular etiology in non-CAH primary adrenal insufficiency OpenAlex 16.0%
  4. 2021 Supplemental Table 5. Adrenal steroid hormones of non-CAH PAI patients with identified molecular etiologies compared to control group Figshare DOI 10.6084/m9.figshare.16641544.v2
  5. 2021 Supplemental Table 2. Figshare DOI 10.6084/m9.figshare.16641520.v1
  6. 2021 Supplemental Table 1. Characteristics of patients with SGPL1 mutations Figshare DOI 10.6084/m9.figshare.16641505.v3
  7. 2021 Supplemental Material: Case summaries according to molecular etiologies Figshare DOI 10.6084/m9.figshare.16641463.v6
  8. 2021 Supplemental Table 3. Comparison of clinical and biochemical characteristics of PAI patients with solved or unsolved etiology Figshare DOI 10.6084/m9.figshare.16641523
  9. 2021 Supplemental Material: Case summaries according to molecular etiologies Figshare DOI 10.6084/m9.figshare.16641463.v3
  10. 2021 Supplemental Table 4. Comparison of adrenal steroids of non-CAH PAI patients with identified molecular etiologies causing isolated glucocorticoid (patients with MC2R, MRAP and NNT mutations) vs glucocorticoid+mineralocorticoid+sex steroid deficiency (patients with StAR, CYP11A1, SGPL1, ABCD1, AAAS, NR0B1/DAX1, AIRE mutations). Figshare DOI 10.6084/m9.figshare.16641535.v2
  11. 2021 Supplemental Table 5. Figshare DOI 10.6084/m9.figshare.16641544.v1
  12. 2021 Supplemental Table 2. Characteristics of PAI patients with unknown molecular etiology Figshare DOI 10.6084/m9.figshare.16641520.v2
  13. 2021 Supplemental Table 1. Figshare DOI 10.6084/m9.figshare.16641505.v1
  14. 2021 Supplemental Table 3. Figshare DOI 10.6084/m9.figshare.16641523.v1
  15. 2021 Supplemental Table 3. Comparison of clinical and biochemical characteristics of PAI patients with solved or unsolved etiology Figshare DOI 10.6084/m9.figshare.16641523.v2
  16. 2021 Supplemental Table 4. Figshare DOI 10.6084/m9.figshare.16641535.v1
  17. 2021 Supplemental Table 1. Characteristics of patients with SGPL1 mutations Figshare DOI 10.6084/m9.figshare.16641505.v2
  18. 2021 Supplemental Material: Case summaries according to molecular etiologies Figshare DOI 10.6084/m9.figshare.16641463.v4
  19. 2021 Supplemental Material: Case summaries according to molecular etiologies Figshare DOI 10.6084/m9.figshare.16641463.v2
  20. 2021 Supplemental Material: Case summaries according to molecular etiologies Figshare DOI 10.6084/m9.figshare.16641463.v5

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