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Studies in Documentary Film : Impact Factor & More

eISSN: 1750-3299pISSN: 1750-3280

Key Metrics

CiteScore
1.5
H-Index
14
SJR
Q1Communication
SNIP
0.88
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Studies in Documentary Film Journal Specifications

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  • Web of Science Web of Science
  • Scopus Scopus
  • SJR SJR
Overview
Publisher ROUTLEDGE JOURNALS, TAYLOR & FRANCIS LTD
Language English
Frequency Tri-annual
General Details
LanguageEnglish
FrequencyTri-annual
Publication Start Year2007
Publisher URLVisit website
Website URLVisit website
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Recently Published Papers in Studies in Documentary Film

Total colonic aganglionosis: a bibliometric analysis of trends and themes (1978-2024).
  • 16 May 2026
  • Orphanet journal of rare diseases
Combined omalizumab and desensitization to control IgE-mediated hypersensitivity in enzyme replacement therapy for late-onset Pompe disease.
  • 14 May 2026
  • Orphanet journal of rare diseases
Developing prognostic models that predict onset and progression rates in genetic neurodegenerative diseases: perspectives of healthcare professionals in genetic counselling.
  • 13 May 2026
  • Orphanet journal of rare diseases
Expanding the genetic and clinical landscapes of hereditary spastic paraplegia (HSP): a cohort study of 103 families.
  • 12 May 2026
  • Orphanet journal of rare diseases
Screening for acid sphingomyelinase deficiency in patients with an interstitial lung disease
  • 12 May 2026
  • Orphanet Journal of Rare Diseases
Patient-reported clinical characteristics and healthcare utilization in Spinal Muscular Atrophy (SMA): a cross-sectional study from Iran.
  • 11 May 2026
  • Orphanet journal of rare diseases
Total colonic aganglionosis: a bibliometric analysis of trends and themes (1978-2024).
  • 16 May 2026
  • Orphanet journal of rare diseases
Combined omalizumab and desensitization to control IgE-mediated hypersensitivity in enzyme replacement therapy for late-onset Pompe disease.
  • 14 May 2026
  • Orphanet journal of rare diseases
Developing prognostic models that predict onset and progression rates in genetic neurodegenerative diseases: perspectives of healthcare professionals in genetic counselling.
  • 13 May 2026
  • Orphanet journal of rare diseases
Expanding the genetic and clinical landscapes of hereditary spastic paraplegia (HSP): a cohort study of 103 families.
  • 12 May 2026
  • Orphanet journal of rare diseases
Screening for acid sphingomyelinase deficiency in patients with an interstitial lung disease
  • 12 May 2026
  • Orphanet Journal of Rare Diseases
Patient-reported clinical characteristics and healthcare utilization in Spinal Muscular Atrophy (SMA): a cross-sectional study from Iran.
  • 11 May 2026
  • Orphanet journal of rare diseases

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