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Matteo Bianchi

Uppsala University
H指数:24
被引数:2,483

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Unraveling the Genetics of Shared Clinical and Serological Manifestations in Patients With Systemic Inflammatory Autoimmune Diseases

揭示系统性炎症性自身免疫性疾病患者共有临床和血清学表现的遗传学

2024-10-254
OAAI
A survey of ficolin-3 activity in Systemic Lupus Erythematosus reveals a link to hematological disease manifestations and autoantibody profile
2024-02-010
OA
Genome sequencing of 2000 canids by the Dog10K consortium advances the understanding of demography, genome function and architecture (vol 24, 187, 2023)
2023-11-070
OAAI
Genome sequencing of 2000 canids by the Dog10K consortium advances the understanding of demography, genome function and architecture
2023-08-1523
OAAI
Leveraging base-pair mammalian constraint to understand genetic variation and human disease
Science
IF45.8
2023-01-010
OAAI
Evolutionary constraint and innovation across hundreds of placental mammals

数百种胎盘哺乳动物的进化限制和创新

Science
IF45.8
2023-01-010
OAAI
Mer-tyrosine kinase: a novel susceptibility gene for SLE related end-stage renal disease
2022-11-047
OAAI
Strong Association of Combined Genetic Deficiencies in the Classical Complement Pathway With Risk of Systemic Lupus Erythematosus and Primary Sjogren's Syndrome

经典补体途径中的联合遗传缺陷与系统性红斑狼疮和原发性干燥综合征的风险密切相关

2022-10-0717
OAAI
Complement C4 Copy Number Variation is Linked to SSA/Ro and SSB/La Autoantibodies in Systemic Inflammatory Autoimmune Diseases

系统性炎症性自身免疫性疾病中补体C4拷贝数变异与SSA/Ro和SSB/La自身抗体相关

2022-06-2723
OA
Contribution of Rare Genetic Variation to Disease Susceptibility in a Large Scandinavian Myositis Cohort

斯堪的纳维亚大型肌炎队列中罕见遗传变异对疾病易感性的贡献

2021-12-2311
OAAI
Whole-genome genotyping and resequencing reveal the association of a deletion in the complex interferon alpha gene cluster with hypothyroidism in dogs

全基因组基因分型和重测序揭示了复杂干扰素 α 基因簇的缺失与犬甲状腺功能减退的关联

2020-04-168
OAAI
Common genetic variation in the autoimmune regulator (AIRE) locus is associated with autoimmune Addison's disease in Sweden
2018-05-3023
OAAI
Cytokine Autoantibody Screening in the Swedish Addison Registry Identifies Patients With Undiagnosed APS1
2017-10-206
OAAI
Extended exome sequencing identifies BACH2 as a novel major risk locus for Addison's disease
2016-11-0241
OAAI