Impact Factor
2.33
Journal Citation Impact
Estimated influence, citation density, publishing volume, and citation integrity from the analytics table.
Citation rate
1.46
45 total citations
h5-index
13
h5 depth signal
Cited share
43.2%
16 of 37
Total citations
45
Citation footprint
Metric signal
0.90
External metric anchor
Self-citation
0.0%
0 self-citations
Citations Trend
Monthly Publications Cadence
Citing Geographic Demographics
United States
141
Canada
33
China
24
Japan
23
Germany
21
Citing Fields of Research
Cell Biology
126
Genetics & Genomics
58
Entomology
44
Cell Differentiation & Development
40
Neurodegenerative Disorders
40
Publishing Activity & Reach
Volume, recency, access pattern, and citing-community signals from the journal analytics record.
All-time article footprint
957
Articles tracked across the journal lifetime
Indexed publication set
37
16 cited publications
Last 12 months
16
2.3 publications/month
Open access share
12.5%
2 OA publications in the last year
Leading citing country
United States
141 citing publications
Leading citing field
Cell Biology
126 citing publications
Latest tracked publication
17 September 2026
10 recent records available
Coverage & Indexing History
v1n1, 1983-
v1n1, 1983-
Active Coverage
Research Focus & Classification
Indexed Subjects
Cell Biology
Neurodegenerative Disorders
Animal Biology
Genetics & Genomics
Brain Neurological Disorders
Nervous System Disorders
Broad Categories
Genetics, Medical
Neurology
Neurodegenerative Disorders
Cancer & Development
Mitochondria
Nervous System Disorders
Smell & Taste Science
Brain Neurological Disorders
MeSH Descriptors
Genetics
Neurology
Latest Publications
Recent article records with DOI-first linking and condensed abstracts.
01
DOI 10.1080/01677063.2026.2730920
Open DOI
Extra-synaptic localization of Bruchpilot in association with neurite outgrowth and cell motility in dissociated Drosophila embryonic cell cultures
Neurite outgrowth and cell motility are closely linked processes essential to nervous system development and repair. Both processes are regulated by shared mechanisms driven by the contractile dyna...
02
DOI 10.1080/01677063.2026.2696088
Open DOI
Fine mapping of a putative genomic element that mediates the induction of a male-specific muscle in Drosophila.
The muscle of Lawrence (MOL) is a pair of male-specific longitudinal muscles located below the tergite of the fifth abdominal segment in adult Drosophila melanogaster. For the MOL to form, the innervating motor neuron (MOL-inducing neuro...
03
DOI 10.1080/01677063.2026.2695462
Open DOI
Psilocybin-induced behavioral and cellular effects
After decades of limited scientific attention, psychedelic compounds are now gaining renewed interest for their profound affective effects and, more importantly, their therapeutic potential in trea...
04
DOI 10.1080/01677063.2026.2687566
Open DOI
Novel Variants in PLPBP, SCN1A, and SLC6A1: Genetics, Bioinformatics, and clinical Elucidation of Three Distinct Cases of Developmental and Epileptic Encephalopathy.
Developmental and epileptic encephalopathies (DEEs) are severe early-onset disorders featuring refractory seizures, abnormal EEGs, and developmental delays. Clinically and etiologically heterogeneous, they include subtypes such as Dravet...
05
DOI 10.1080/01677063.2026.2658577
Open DOI
D-ribose-L-cysteine protects against rotenone-induced neurotoxicity in Drosophila via redox, neurotransmitter, and DDC gene regulation
1. Parkinson’s disease (PD) is a neurodegenerative condition owing to multifactorial alterations in the brain, triggering progressive cell death. Clinically, PD first presents with various motor im...
06
DOI 10.1080/01677063.2026.2671912
Open DOI
Genetic architecture of hereditary spastic paraplegia: from monogenic to oligogenic models
Hereditary spastic paraplegia (HSP) encompasses a clinically and genetically heterogeneous group of neurodegenerative disorders, characterized by progressive lower limb spasticity due to corticospinal tract degeneration. While traditiona...
07
DOI 10.1080/01677063.2026.2649162
Open DOI
Expression of sulfate pathway genes in human neurodevelopment
Sulfate is a vital nutrient for healthy brain development. More than 90 sulfate-related genes are highly conserved across mammalian species, with 16 of these genes being clinically reportable for adverse brain conditions. To determine th...
08
DOI 10.1080/01677063.2026.2655158
Open DOI
Nckx30c , a Drosophila K + -dependent Na + /Ca 2+ exchanger, regulates temperature-sensitive convulsions and age-related neurodegeneration
Calcium (Ca2+) homeostasis is fundamental to neuronal physiology, including in the regulation of membrane excitability and synaptic transmission. Disruptions in the ion transporters regulating Ca2+ influx and efflux are clearly linked to...
09
DOI 10.1080/01677063.2026.2636893
Open DOI
A zinc finger MYM-type containing 3 (ZMYM3) allele is associated with autism spectrum disorder in Iranian people
1. Autism spectrum disorder (ASD) is a complex neurodevelopmental disorder with a global prevalence of approxiamtely 1% worldwide, with recent studies estimating a prevalence of 1 in 54 children an...
10
Bibliographical & Catalog Notes
Title from cover.
Imprint varies.
Print issues ceased with v. 26 (2012).
Also issued online.
Vol. 1, no. 1 (SEP 1983)19920825 Notice not published Printed on acid-free paper