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Mingyan Fang

Karolinska University Hospital

16

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493

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T Cell Repertoire Abnormality in Immunodeficiency Patients with DNA Repair and Methylation Defects.

2021 Journal of Clinical Immunology
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Clinical implications of experimental analyses of AID function on predictive computational tools: Challenge of missense variants.

2020 Clinical Genetics
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Noncoding RNA transcription alters chromosomal topology to promote isotype-specific class switch recombination

2020 Science immunology
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Homozygous Recessive Versican Missense Variation Is Associated With Early Teeth Loss in a Pakistani Family

2019 Frontiers in Genetics
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Molecular genetic analysis using targeted NGS analysis of 677 individuals with retinal dystrophy

2019 Scientific Reports
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Compound Heterozygous Mutations of IL2-Inducible T cell Kinase in a Swedish Patient: the Importance of Early Genetic Diagnosis

2019 Journal of Clinical Immunology
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The novel HLA-C*08:80 allele identified by full-length sequencing of the HLA region

2019
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Clinical implications of systematic phenotyping and exome sequencing in patients with primary antibody deficiency

2019 Genetics in Medicine
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SMYD1 is the underlying gene for the AnWj-negative blood group phenotype

2018 European Journal of Haematology
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Combined immunodeficiency and Epstein-Barr virus?induced B cell malignancy in humans with inherited CD70 deficiency

2017 Journal of Experimental Medicine
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Citations (97)