PathoGenetics

Springer Nature

Journal websitePeer review: Peer review
Evaluation status available after sign-in

About the journal

PathoGenetics is a journal published by Springer Nature in United Kingdom. It is listed in PUBMED according to the sources read. Facts are reproduced as recorded at their sources with their capture dates; PublishLens indicators are available after sign-in.

Basic facts

Publisher
Springer Nature
ISSN
1755-8417
Country
United Kingdom
Access
Not open access / not declared
Declared peer-review model
peer_review

Index listings

  • PUBMED · 2008-11-03
Indexing
PUBMED
APC
—
Declared review time (DOAJ)
—
Activity (OpenAlex)
Dormant — no works recorded since 2021
PublishLens list status
Shown after sign-in
Counts for promotion at your university?
Choose your university and rank below ↓

Methodology signals (dated facts from their sources)

Details of the evaluation under the published methodology are shown to signed-in users (free).

Create a free account to view the evaluation

Journal profile

Descriptive metadata from public sources (DOAJ, OpenAlex, PubMed) as of the capture date shown — contains no assessment or judgment.

Works in OpenAlex

18

Last recorded publication year

2021

Reported by OpenAlex in 1 of 3 sources (CC0 flags, not verified indexing)DOAJSciELOOpenAlex Core

h-index

12

i10-index

13

From OpenAlex open data (CC0).

Editorial & policy4
Observed digital preservation (Keepers registry)— snapshot 2026-10-05
Portico
Editorial board
Official page ↗
Open references deposited at Crossref
0%
ORCID iDs in current deposits
0%
Identity & continuity2
Alternate titles
Patho genetics
Source type
journal
Classification(no data)

No data available to the platform for this group

No platform data for: Classification — absence is not a judgment about the journal.

Subject areas

  • Genomics and Rare Diseases
  • Lysosomal Storage Disorders Research
  • Lysosomal Storage Disorders Research
  • Glycogen Storage Diseases and Myoclonus
  • Genetics and Neurodevelopmental Disorders
  • Genetic Syndromes and Imprinting
  • Genomics and Rare Diseases
  • Genetic Syndromes and Imprinting
Show all subjects (75)
  • Genomics and Rare Diseases
  • TGF-β signaling in diseases
  • Genetic and Kidney Cyst Diseases
  • Genetic and Kidney Cyst Diseases
  • Developmental Biology and Gene Regulation
  • Genetic and Kidney Cyst Diseases
  • Lysosomal Storage Disorders Research
  • Pancreatic function and diabetes
  • Epilepsy research and treatment
  • Respiratory viral infections research
  • Ear Surgery and Otitis Media
  • Regulation of Appetite and Obesity
  • Hearing, Cochlea, Tinnitus, Genetics
  • Plant Molecular Biology Research
  • Chromosomal and Genetic Variations
  • Connective tissue disorders research
  • Genomic variations and chromosomal abnormalities
  • CRISPR and Genetic Engineering
  • RNA Research and Splicing
  • Pluripotent Stem Cells Research
  • Microtubule and mitosis dynamics
  • Epigenetics and DNA Methylation
  • MicroRNA in disease regulation
  • Metabolism and Genetic Disorders
  • PI3K/AKT/mTOR signaling in cancer
  • CRISPR and Genetic Engineering
  • RNA Interference and Gene Delivery
  • Cellular transport and secretion
  • Genetic Associations and Epidemiology
  • DNA Repair Mechanisms
  • MicroRNA in disease regulation
  • scientometrics and bibliometrics research
  • Epilepsy research and treatment
  • Pancreatic function and diabetes
  • Pancreatic function and diabetes
  • Cell Adhesion Molecules Research
  • Platelet Disorders and Treatments
  • Platelet Disorders and Treatments
  • Autophagy in Disease and Therapy
  • Asthma and respiratory diseases
  • Cystic Fibrosis Research Advances
  • Ear Surgery and Otitis Media
  • SARS-CoV-2 and COVID-19 Research
  • Down syndrome and intellectual disability research
  • COVID-19 Clinical Research Studies
  • Epilepsy research and treatment
  • Mathematical and Theoretical Epidemiology and Ecology Models
  • COVID-19 Clinical Research Studies
  • Respiratory viral infections research
  • Trypanosoma species research and implications
  • Hearing, Cochlea, Tinnitus, Genetics
  • Chromosomal and Genetic Variations
  • Regulation of Appetite and Obesity
  • MicroRNA in disease regulation
  • Epigenetics and DNA Methylation
  • Microtubule and mitosis dynamics
  • Pluripotent Stem Cells Research
  • RNA Research and Splicing
  • CRISPR and Genetic Engineering
  • Genomic variations and chromosomal abnormalities
  • Connective tissue disorders research
  • scientometrics and bibliometrics research
  • Trypanosoma species research and implications
  • Autophagy in Disease and Therapy
  • Platelet Disorders and Treatments
  • Cell Adhesion Molecules Research
  • COVID-19 Clinical Research Studies

Community confirmations — what users saw in MJL or Scopus Sources; not platform verification and never part of any score.

Loading community confirmations…
How do we evaluate?Publisher of this journal? Appeal a derived assessment or request a factual correction

The journal's record in other sources:Web of Science MJLDOAJ

Everything shown here is produced automatically from named sources (DOAJ, OpenAlex, Crossref, PubMed, the Norwegian register) as of its capture date, with no human editing. Facts appear as recorded at the source; derived scores (PCI, PTD, PublishLens score) follow a published methodology. Not a judgement on the journal, not an official accreditation, not advice.

Wrong items are corrected automatically by re-reading the source (24 h for daily sources, 7 days for weekly ones) with a dated change log, and each item links to its source record. PublishLens-derived assessments are contested through the appeals mechanism (15 working days). Appeals · Indicator guide

Norwegian register data: Kanalregisteret (HK-dir, Norway) — CC BY 4.0 / NLOD — adapted: level extracted per year · OASPA member list — CC BY

Last automated source read: