Journal of Endocrinological Investigation Template
Write in a clean editor, then format for Journal of Endocrinological Investigation in one click — DocuGuru applies the official Springer Nature template with numbered references and exports a submission-ready PDF plus the editable LaTeX source. Free to start.
About the Journal of Endocrinological Investigation format
Journal of Endocrinological Investigation is a peer-reviewed journal published by Springer Nature, covering Thyroid Disorders and Treatments, Pituitary Gland Disorders and Treatments, Growth Hormone and Insulin-like Growth Factors.
| Publisher | Springer Nature |
|---|---|
| Reference style | Numbered (Springer Basic) Numbered — [1], [2] in the text 1. Smith A, Jones B, Lee C (2023) A representative article title. Journal of Endocrinological Investigation 12:45–58
Formats any DOI in Journal of Endocrinological Investigation style. No sign-up. |
| Publishes research in | Thyroid Disorders and Treatments Pituitary Gland Disorders and Treatments Growth Hormone and Insulin-like Growth Factors Thyroid Cancer Diagnosis and Treatment Adrenal Hormones and Disorders |
| ISSN | 0391-4097 |
| Citation impact (2-yr) | 3.22 |
| h-index | 126 |
| i10-index | 4,252 |
| Total citations | 164,003 |
| Article processing charge | $4,390 |
| Top institutions publishing here | University of Pisa |
| Journal website | link.springer.com |
| You get | A submission-ready PDF and the editable LaTeX source — ready to submit. |
Papers published in Journal of Endocrinological Investigation per year
Citation impact of Journal of Endocrinological Investigation by publication year
Citations each year’s papers have accumulated so far — the most recent years are still building up.
Most-cited papers in Journal of Endocrinological Investigation
INTRODUCTION: Prader-Willi syndrome (PWS) is a multisystemic complex genetic disorder caused by lack of expression of genes on the paternally inherited chromosome 15q11.2-q13 region. There are three main genetic subtypes in PWS: paternal 15q11-q13 deletion (65-75 % of cases), maternal uniparental disomy 15 (20-30 % of cases), and imprinting defect (1-3 %). DNA methylation analysis…