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82394424

Funded outputs count: 26
Funder award ID: 82394424
OpenAlex ID: G7339082663
Deficiency of NBAS causes immune dysregulation due to hyperactivation of IFN signaling
2026 · Chenlu Liu, Liang Zhang, et al. · Journal of Human Immunity
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Cytotoxic lymphocyte death drives monocyte activation and TNF/IFN-γ synergism in TBK1 deficiency
2026 · Xu Han, Jialin Dai, et al. · Cell Death and Disease
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Labour induction in low-risk women at 39 weeks of gestation: a randomised trial in China (LIRIC) – protocol of an open label, randomised controlled trial
2026 · Huajing Gao, Junhua Shen, et al. · BMJ Open
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RICTOR Prevents Decidualization Disorder in Women With Advanced Maternal Age via Regulating FoxO1 Nuclear Export
2026 · Yifeng Lin, Jiwei Sun, et al. · Aging Cell
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Deciphering complete archaic introgression sequences in modern human genomes
2026 · Mingyu Suo, Aoyue Bi, et al. · bioRxiv (Cold Spring Harbor Laboratory)
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A Multicenter Integrative Cohort Characterizing the Genetic, Clinical, and Transcriptomic Features of ACP5 Deficiency
2026 · Shiling Zhong, Shuangyue Ma, et al. · Arthritis & Rheumatology
Placental invasion mismatch underlines pregnancy disorders and cancers
2026 · Xin Li, Ruixue Chen, et al. · bioRxiv (Cold Spring Harbor Laboratory)
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Immune dysregulation caused by novel gain-of-function UNC93B1 variant with enhanced antigen presentation
2026 · Xu Han, Qintao Wang, et al. · Genes & Diseases · 1
CD8+ T cell loss induces autoinflammation in inborn errors of cell death
2026 · Jialin Dai, Taijie Jin, et al. · Nature Communications
Immune dysregulation caused by novel gain-of-function UNC93B1 variant with enhanced antigen presentation
2026 · Xu Han, Qintao Wang, et al. · medRxiv
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Vitamin D supplementation before in vitro fertilisation in women with polycystic ovary syndrome: multicentre, double blind, placebo controlled, randomised clinical trial
2026 · Kai-Lun Hu, Tingting Liao, et al. · BMJ · 2
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Endogenous retroviruses synthesize heterologous chimeric RNAs to reinforce human early embryo development
2026 · Yangquan Xiang, Yuli Qian, et al. · Science · 18
Multicenter international cohort study of HA20 reveals novel genetic architecture and phenotypic evolution
2026 · Tingyan He, Jun Wang, et al. · medRxiv · 1
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Deficiency of AP1M2 Causes a New Autoinflammatory Disease With Colitis
2025 · Taijie Jin, Jialin Dai, et al. · Arthritis & Rheumatology
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Association between childbearing history and depressive symptoms in postmenopausal women: analysis of data from NHANES 2005-2018
2025 · Linling Zhu, Xinyun Yang, et al. · Psychiatry Research
Novel USP18 mutations lead to severe interferonopathy responsive to JAK inhibitor
2025 · Xiangwei Sun, Ming Li, et al. · Frontiers in Immunology · 6
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Novel pathogenic MAN2B2 variants cause systemic lupus erythematosus and dysregulated glycosylation
2025 · Cheng Gong, Changming Zhang, et al. · Clinical Immunology · 1
Somatic gain-of-function mutation in TLR7 causes early-onset systemic lupus erythematosus
2025 · Yi Zeng, Panfeng Tao, et al. · Annals of the Rheumatic Diseases · 26
Impact of Laser‐Assisted Hatching on Cognitive and Metabolic Development of Singletons Conceived Through Frozen–Thawed Embryo Transfer: A Matched Cohort Study
2025 · Xin‐Yi Liu, Chun‐Xi Zhang, et al. · BJOG An International Journal of Obstetrics & Gynaecology · 2
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Nomogram to predict cumulative live birth rate following in vitro fertilization/intracytoplasmic sperm injection cycles in patients with endometriosis
2025 · Linling Zhu, Tongtong Lin, et al. · BMC Pregnancy and Childbirth · 5
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Ras-MAPK pathway in patients with lupus nephritis
2025 · Changming Zhang, Xiaoman Jing, et al. · Lupus Science & Medicine · 8
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Genetically Determined Plasma Docosahexaenoic Acid Showed a Causal Association with Female Reproductive Longevity-Related Phenotype: A Mendelian Randomization Study
2024 · Huajing Gao, Yuewen Ying, et al. · Nutrients · 1
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Proteome-wide Mendelian randomization and functional studies uncover therapeutic targets for polycystic ovarian syndrome
2024 · Feida Ni, Feixia Wang, et al. · The American Journal of Human Genetics · 16
IRAK2 deficiency causes a new immune dysregulation disorder
2024 · Yudie Fei, Lin Liu, et al. · medRxiv · 1
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Characterization of a Novel Pathogenic PLCG2 Variant Leading to APLAID Syndrome Responsive to a TNF Inhibitor
2024 · Zhaohui Yang, Panfeng Tao, et al. · Arthritis & Rheumatology · 4
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