Green Journals

Functional C1q deficiency in a systemic lupus erythematosus patient with a concurrent somatic TNFAIP3 variant

Siming Peng, Yu Zhou, Zhongxun Yu et al.

2026-11-13

DOI: 10.1186/s12920-026-02509-0

A novel ultra-rare nonsense variant linked to PCDHGC4-related neurodevelopmental disorder in an Iranian patient

Teymoor Khosravi, Ali Kowsari, Morteza Oladnabi

2026-11-13

DOI: 10.1186/s12920-026-02511-6

Trio-based segregation analysis of type 1 3-methylcrotonyl-CoA carboxylase deficiency associated with rare compound heterozygous MCCC1 variants

Jincheng Dai, Zhanqi Hu, Xiangsheng Cai

2026-11-13

DOI: 10.1186/s12920-026-02523-2

Family-based reclassification of COL1A1 NM_000088.4:c.4123G > A (p.Ala1375Thr) in a four-generation pedigree with osteogenesis imperfecta

Shurong Hong, Yajun Su, Junyan Wu et al.

2026-11-13

DOI: 10.1186/s12920-026-02510-7

Beyond the classic triad: three novel AAAS variants expand the genetic spectrum of triple A syndrome and reveal marked phenotypic heterogeneity in five families

Solmaz Jabbarzadeh, Fatemeh Ghermezcheshmeh, Aida Ghasemi et al.

2026-11-11

DOI: 10.1186/s12920-026-02515-2

Whole-exome sequencing revealed co-segregating variants in a multigenerational family with schizophrenia

Indu Priya, Amrit Sudershan, Monika Jaithal et al.

2026-11-7

DOI: 10.1186/s12920-026-02477-5

ALPACA: a visual data mining system for subcellular location-specific knowledge mining from multi-omics data in cancer

Minwoo Pak, Dabin Jeong, Sungjoon Park et al.

2026-11-6 Vol. 16 Issue S1

DOI: 10.1186/s12920-026-02440-4

Single-cell transcriptome analysis reveals aberrant low-density neutrophil differentiation and immune signaling dysregulation in myasthenia gravis

Yuxuan Yong, Zainafuguli Maimaiti, Mengdie Hao et al.

2026-11-5

DOI: 10.1186/s12920-026-02465-9

A de novo SEMA3E frameshift variant in a child with CHARGE-like phenotype

Yaqian Xiao, Yang Gao, Jing Chen et al.

2026-11-4

DOI: 10.1186/s12920-026-02494-4

Selection of endoplasmic reticulum stress-related feature genes in hypertrophic cardiomyopathy based on bioinformatics analysis and experimental verification

Zhizhengrong Tian, Fengyun Zhao, Hongmei Mou et al.

2026-11-4

DOI: 10.1186/s12920-026-02507-2

Year	A	B
2026
2025
2024
2023
2021/2022	✓	✓
2020		✓
2019	✓	✓
2018	✓

Journal Report

Journal Information

Classification History

Recent Articles

Functional C1q deficiency in a systemic lupus erythematosus patient with a concurrent somatic TNFAIP3 variant

A novel ultra-rare nonsense variant linked to PCDHGC4-related neurodevelopmental disorder in an Iranian patient

Trio-based segregation analysis of type 1 3-methylcrotonyl-CoA carboxylase deficiency associated with rare compound heterozygous MCCC1 variants

Family-based reclassification of COL1A1 NM_000088.4:c.4123G > A (p.Ala1375Thr) in a four-generation pedigree with osteogenesis imperfecta

Beyond the classic triad: three novel AAAS variants expand the genetic spectrum of triple A syndrome and reveal marked phenotypic heterogeneity in five families

Whole-exome sequencing revealed co-segregating variants in a multigenerational family with schizophrenia

ALPACA: a visual data mining system for subcellular location-specific knowledge mining from multi-omics data in cancer

Single-cell transcriptome analysis reveals aberrant low-density neutrophil differentiation and immune signaling dysregulation in myasthenia gravis

A de novo SEMA3E frameshift variant in a child with CHARGE-like phenotype

Selection of endoplasmic reticulum stress-related feature genes in hypertrophic cardiomyopathy based on bioinformatics analysis and experimental verification