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Author Details

Hongbo M Xie
Huadong Hospital Affiliated to Fudan University
2007
39
17
PMIDPaper TitleJournal TitlePublished Year
37234260N6-methyladenosine participates in mouse hippocampus neurodegeneration via PD-1/PD-L1 pathway.Front Neurosci2023
37736163Patient-derived Colonoids From Disease-spared Tissue Retain Inflammatory Bowel Disease-specific Transcriptomic Signatures.Gastro Hep Adv2023
37234260N6-methyladenosine participates in mouse hippocampus neurodegeneration via PD-1/PD-L1 pathway.Front Neurosci2023
37492101OpenPBTA: The Open Pediatric Brain Tumor Atlas.Cell Genom2023
37736163Patient-derived Colonoids From Disease-spared Tissue Retain Inflammatory Bowel Disease-specific Transcriptomic Signatures.Gastro Hep Adv2023
37492101OpenPBTA: The Open Pediatric Brain Tumor Atlas.Cell Genom2023
34625796Inducible Sbds deletion impairs bone marrow niche capacity to engraft donor bone marrow after transplantation.Blood Adv2022
36219480Pathogenicity and impact of HLA class I alleles in aplastic anemia patients of different ethnicities.JCI Insight2022
36009018<i>HOXA</i> Amplification Defines a Genetically Distinct Subset of Angiosarcomas.Biomolecules2022
35622075FOCAD Indel in a Family With Juvenile Polyposis Syndrome.J Pediatr Gastroenterol Nutr2022
34625796Inducible Sbds deletion impairs bone marrow niche capacity to engraft donor bone marrow after transplantation.Blood Adv2022
35622075FOCAD Indel in a Family With Juvenile Polyposis Syndrome.J Pediatr Gastroenterol Nutr2022
36009018<i>HOXA</i> Amplification Defines a Genetically Distinct Subset of Angiosarcomas.Biomolecules2022
36219480Pathogenicity and impact of HLA class I alleles in aplastic anemia patients of different ethnicities.JCI Insight2022
34356046Genome-Wide Association Studies of Conotruncal Heart Defects with Normally Related Great Vessels in the United States.Genes (Basel)2021
33542482Menin is necessary for long term maintenance of meningioma-1 driven leukemia.Leukemia2021
34212090The complete chloroplast genome of <i>Atractylodes koreana</i> (Nakai) Kitam and its phylogenetic analysis.Mitochondrial DNA B Resour2021
34356046Genome-Wide Association Studies of Conotruncal Heart Defects with Normally Related Great Vessels in the United States.Genes (Basel)2021
33974912Intrinsically disordered Meningioma-1 stabilizes the BAF complex to cause AML.Mol Cell2021
33542482Menin is necessary for long term maintenance of meningioma-1 driven leukemia.Leukemia2021
34212090The complete chloroplast genome of <i>Atractylodes koreana</i> (Nakai) Kitam and its phylogenetic analysis.Mitochondrial DNA B Resour2021
33974912Intrinsically disordered Meningioma-1 stabilizes the BAF complex to cause AML.Mol Cell2021
32437908Epigenetic regulation of protein translation in KMT2A-rearranged AML.Exp Hematol2020
32437908Epigenetic regulation of protein translation in KMT2A-rearranged AML.Exp Hematol2020
32634241Specific patterns of H3K79 methylation influence genetic interaction of oncogenes in AML.Blood Adv2020
32634241Specific patterns of H3K79 methylation influence genetic interaction of oncogenes in AML.Blood Adv2020
31222980Copy number variations in individuals with conotruncal heart defects reveal some shared developmental pathways irrespective of 22q11.2 deletion status.Birth Defects Res2019
31222980Copy number variations in individuals with conotruncal heart defects reveal some shared developmental pathways irrespective of 22q11.2 deletion status.Birth Defects Res2019
26913981Clonal Replacement Underlies Spontaneous Remission in Paroxysmal Nocturnal Haemoglobinuria.Br J Haematol2017
28971166Somatic HLA Mutations Expose the Role of Class I-Mediated Autoimmunity in Aplastic Anemia and its Clonal Complications.Blood Adv2017
28398664Rare copy number variants in patients with congenital conotruncal heart defects.Birth Defects Res2017
26913981Clonal Replacement Underlies Spontaneous Remission in Paroxysmal Nocturnal Haemoglobinuria.Br J Haematol2017
27735924Copy-number variation is an important contributor to the genetic causality of inherited retinal degenerations.Genet Med2017
28398664Rare copy number variants in patients with congenital conotruncal heart defects.Birth Defects Res2017
28971166Somatic HLA Mutations Expose the Role of Class I-Mediated Autoimmunity in Aplastic Anemia and its Clonal Complications.Blood Adv2017
27735924Copy-number variation is an important contributor to the genetic causality of inherited retinal degenerations.Genet Med2017
26615915Disrupted lymphocyte homeostasis in hepatitis-associated acquired aplastic anemia is associated with short telomeres.Am J Hematol2016
26615915Disrupted lymphocyte homeostasis in hepatitis-associated acquired aplastic anemia is associated with short telomeres.Am J Hematol2016
25800665Emergence of clonal hematopoiesis in the majority of patients with acquired aplastic anemia.Cancer Genet2015
25800665Emergence of clonal hematopoiesis in the majority of patients with acquired aplastic anemia.Cancer Genet2015
23682798The prevalence of 16p12.1 microdeletion in patients with left-sided cardiac lesions.Congenit Heart Dis2014
24116929Single nucleotide polymorphism array analysis of bone marrow failure patients reveals characteristic patterns of genetic changes.Br J Haematol2014
23682798The prevalence of 16p12.1 microdeletion in patients with left-sided cardiac lesions.Congenit Heart Dis2014
25066379Analysis of chromosomal structural variation in patients with congenital left-sided cardiac lesions.Birth Defects Res A Clin Mol Teratol2014
25066379Analysis of chromosomal structural variation in patients with congenital left-sided cardiac lesions.Birth Defects Res A Clin Mol Teratol2014
24116929Single nucleotide polymorphism array analysis of bone marrow failure patients reveals characteristic patterns of genetic changes.Br J Haematol2014
23847141Prevalence of rare mitochondrial DNA mutations in mitochondrial disorders.J Med Genet2013
25489354mtDNA Variation and Analysis Using Mitomap and Mitomaster.Curr Protoc Bioinformatics2013
23847141Prevalence of rare mitochondrial DNA mutations in mitochondrial disorders.J Med Genet2013
24564231Efficient digest of high-throughput sequencing data in a reproducible report.BMC Bioinformatics2013
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Collaborators

Hakon Hakonarson
The Center for Applied Genomics, Children's Hospital of Philadelphia
Co-authored papers 11
Xiaowu Gai
Co-authored papers 9
Zoran Obradovic
Center for Data Analytics and Biomedical Informatics, Temple University
Co-authored papers 7
Elizabeth Goldmuntz
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Tamim H Shaikh
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Slobodan Vucetic
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Vladimir N Uversky
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Co-authored papers 4
Alan Keith Dunker
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Jaclyn A Biegel
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Deanne Taylor
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Joseph T Glessner
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Struan F A Grant
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Cecilia E Kim
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Elaine H Zackai
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Edward C Frackelton
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Gregory P Way
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University Children's Hospital Zurich
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Shannon Robins
Children's Hospital of Philadelphia
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Rishi R Lulla
Hasbro Children's Hospital, Brown University.
Co-authored papers 1
Jonathan P Bradfield
Co-authored papers 1
Nan Zhu
Shanghai General Hospital, Shanghai Jiaotong University
Co-authored papers 1
Daniel P Miller
Center for Data-Driven Discovery in Biomedicine, Children's Hospital of Philadelphia
Co-authored papers 1
Mateusz Koptyra
Children's Hospital of Philadelphia
Co-authored papers 1
Matthew C Dulik
Children's Hospital of Philadelphia, University of Pennsylvania
Co-authored papers 1
Shrivats Kannan
Center for Data-Driven Discovery in Biomedicine, Children's Hospital of Philadelphia
Co-authored papers 1
Jessica Wong
Center for Data-Driven Discovery in Biomedicine, Children's Hospital of Philadelphia
Co-authored papers 1
Bin Xue
University of California at Berkeley
Co-authored papers 1
Adam A Kraya
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