Genetics articles for Australia

Time frame: 1 June 2025 - 30 May 2026

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Count: 60

Article ‘Count’ for Genetics.

Journal Count Share
1 0.03
De novo variants in KDM2A cause a syndromic neurodevelopmental disorder 0.03
2 1.12
The impact of sex on the immune system explored at the single-cell level 1.00
Palindrome-mediated 16p13.3 triplications cause a recognizable neurodegenerative disorder with ataxia 0.12
1 0.07
Alternative Translation Initiation in PRKN Delays the Onset of Parkinson's Disease and Offers a Therapeutic Target 0.07
3 1.10
Epilepsy concordance in monozygotic twins: the role of common genetic variants 1.00
Loss of DOT1L disrupts neuronal transcription and leads to a neurodevelopmental disorder 0.02
The genetic and phenotypic spectrum of iGABRB1/i-related disorders 0.08
1 0.08
Dynamic and Ongoing De Novo L1 Retrotransposition Contributes to Genome Plasticity and Intrapatient Heterogeneity in Ovarian Cancer. 0.08
1 1.00
Peptide-directed folding of the elusive RNA i-motif 1.00
1 0.40
The B-class auxin response factor MpARF2 is essential for meristem organization in free-living plant gametophytes 0.40
1 0.01
Deletion of METTL14, a key methylation regulator, attenuates vascular ageing 0.01
1 0.11
Dominant-negative effects of Weaver syndrome-associated EZH2 variants 0.11
1 0.11
Landscape of microRNA and target expression variation and covariation in single mouse embryonic stem cells 0.11
2 1.02
Genome-wide analysis highlights epigenetic link to age at menarche 0.94
SWS1-complex in premature ovarian insufficiency: iSWSAP1/i as a new POI gene 0.08
1 0.24
Functional consequence of pathogenic GABRA3 variants determines whether X-linked inheritance is dominant or recessive 0.24
1 0.17
Higher Promoter Methylation of the Ubiquitin-Associated and SH3 Domain Containing A (UBASH3A) Gene Is Associated With T-Lymphocyte Ontogeny and Reduced Susceptibility to Early-Onset Sepsis 0.17
1 0.17
Hmx2 and Dmrt2 Coordinate the Differentiation of Intercalated Cell Subtypes in Kidney. 0.17
2 1.11
Accessory subunits of PRC2 mimic H3K27me3 to restrict the spread of Polycomb domains 1.00
CRAMP1 drives linker histone expression to enable Polycomb repression 0.11
4 1.20
Gut microbiome alterations are sex-dependently associated with brain abnormalities in a mouse model of Neurofibromatosis type I 1.00
Genome-wide tandem repeat expansions modify schizophrenia risk in the presence of a 22q11.2 deletion 0.03
Splitting schizophrenia: divergent cognitive and educational outcomes revealed by genomic structural equation modelling 0.03
Association between polygenic risk for Major Depression and brain structure in a mega-analysis of 50,975 participants across 11 studies 0.14
3 0.19
An X-linked long non-coding RNA, PTCHD1-AS, and the core features of autism 0.03
Expanding the human proteome with microproteins and peptideins 0.02
Developmental organization of sensory and sympathetic ganglia 0.14
1 0.90
DOT1L provides transcriptional memory through PRC1.1 antagonism 0.90
13 5.70
Quantitative live imaging reveals PRICKLE1 controls junctional neural tube morphogenesis independent of Planar Cell Polarity 1.00
Retinoic acid drives cell fate specification, maturation and retinal regionality in human retinal organoids 1.00
Genetic nurture in intergenerational transmission of substance use 0.13
AMR-GNN: a multi-representation graph neural network framework to enable genomic antimicrobial resistance prediction 0.93
Arms races between selfish genetic elements and their host defence in termites 0.17
Immunological surveillance against cancer across mammals 0.07
Serum Proteomics Reveals Diagnostic Biomarkers and Molecular Pathways in Cerebral Palsy 0.05
Paternal SARS-CoV-2 infection impacts sperm small noncoding RNAs and increases anxiety in offspring in a sex-dependent manner 1.00
SETBP1 variants outside the degron disrupt DNA-binding, transcription and neuronal differentiation capacity to cause a heterogeneous neurodevelopmental disorder 0.27
Sex-stratified genome-wide association meta-analysis of major depressive disorder 0.46
Transposable element expression and sub-cellular dynamics during hPSC differentiation to endoderm, mesoderm, and ectoderm lineages 0.04
Removal of promoter CpG methylation by epigenome editing reverses silencing 0.38
Somites are a source of nephron progenitors in zebrafish 0.22
4 0.21
Biallelic variants in cause a remarkably frequent developmental and epileptic encephalopathy 0.11
Genome-wide association analyses highlight the role of the intestinal molecular environment in human gut microbiota variation 0.03
Pathogenic variants cause a neurodevelopmental syndrome by impairing synaptic function 0.05
Bryophytes hold a larger gene family space than vascular plants 0.02
1 0.15
APOE ε4 carriers share immune-related proteomic changes across neurodegenerative diseases 0.15
1 1.00
KAT6A is essential for developmental control gene expression in neural stem and progenitor cells 1.00
5 2.30
Chinmo defines the region-specific oncogenic competence in the Drosophila central nervous system 0.83
MHC-I diversity enables rapid adaptation during a viral pandemic in wild rabbit populations 0.10
Gas-sensing neurons prime mitochondrial fitness to offset metabolic stress 1.00
A sterility-associated long noncoding RNA involved in honey bee caste determination and adult queen and worker fertility 0.17
Cell-type-informed genotyping of mosaic focal epilepsies reveals cell-autonomous and non-cell-autonomous disease-associated transcriptional programs 0.20
1 0.25
Diversification of pre-mating behaviours through temporal reordering of components 0.25
1 0.04
Nutritional specialization and social evolution in woodroaches and termites 0.04
4 3.10
Deep-sea fish reveal an alternative developmental trajectory for vertebrate vision 0.44
An epidermal membrane-associated periodic skeleton restricts endocytosis to stabilize neuron-epidermal attachment and preserve axons 1.00
Isoform-level profiling of m6A epitranscriptomic signatures in human brain 1.00
Nonchromatin regulatory functions of the histone variant H2A.B in SWI/SNF genomic deposition 0.67
1 0.97
Combined inhibition of FACT and BET disrupts transcription to suppress tumor growth in mouse models of diffuse midline glioma 0.97
1 0.34
Auto-inhibition of PRC2 by the broadly expressed long isoform of AEBP2 0.34

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