Personal information

Other IDs

Scopus Author ID: 20734773800

Biography

Dr. Xiao-Fei Kong is a renowned gastroenterologist and physician-scientist dedicated to advancing the understanding of complex clinical conditions. His pioneering research integrates human genetics and immunology to tackle challenges in celiac disease, inflammatory bowel disease, inflammation-related cancers, and neurological disorders, with a steadfast commitment to discovering innovative cures.

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Education and qualifications (3)

Rockefeller University: New York, NY, US

2008-09-28 to 2015-06-30
Education
Source: Self-asserted source
Xiao-Fei Kong

Université Pierre et Marie Curie: Paris, Île-de-France, FR

2007-10-01 to 2010-10-01 | Ph.D
Education
Source: Self-asserted source
Xiao-Fei Kong

Shanghai Jiao Tong University School of Medicine: Shanghai, CN

2001-09-01 to 2007-09-30 | Master degree/Residency
Education
Source: Self-asserted source
Xiao-Fei Kong

Works (50 of 54)

Items per page:
Page 1 of 2

Impact of population screening for Lynch syndrome insights from the All of Us data

Nature Communications
2025-01-09 | Journal article
DOI: 10.1038/s41467-024-52562-5
Contributors: Jiheum Park; Hemanth Karnati; Sheila D. Rustgi; Chin Hur; Xiao-Fei Kong; Fay Kastrinos
Source: check_circle
Crossref

Epidermodysplasia Verruciformis and Vδ2 γδ T-cell Expansion in STK4 Deficiency.

Journal of clinical immunology
2024-08-07 | Journal article
DOI: 10.1007/s10875-024-01780-z
PMID: 39110273
PMC: PMC11306306
Contributors: Ying W; Long X; Vandergriff T; Karnati H; Heberton M; Chen M; Wang X; Wysocki C; Kong XF
Source: Self-asserted source
Xiao-Fei Kong

The diagnostic yield of exome sequencing in liver diseases from a curated gene panel

Scientific Reports
2023-12-06 | Journal article
DOI: 10.1038/s41598-023-42202-1
Part of ISSN: 2045-2322
Contributors: Xiao-Fei Kong; Kelsie Bogyo; Sheena Kapoor; Patrick R. Shea; Emily E. Groopman; Amanda Thomas-Wilson; Enrico Cocchi; Hila Milo Rasouly; Beishi Zheng; Siming Sun et al.
Source: Self-asserted source
Xiao-Fei Kong

Serological Investigation of Persistent Villous Atrophy in Celiac Disease

Clinical and Translational Gastroenterology
2023-09-27 | Journal article | Author
DOI: 10.14309/ctg.0000000000000639
Part of ISSN: 2155-384X
Contributors: Changlin Gong; Claudia Saborit; Xin Long; Ao Wang; Beishi Zheng; Howard Chung; Suzanne K Lewis; Suneeta Krishnareddy; Govind Bhagat; Peter H R Green et al.
Source: Self-asserted source
Xiao-Fei Kong

Challenges associated with diagnostic exome sequencing in liver diseases

2022-06-25 | Preprint
DOI: 10.1101/2022.06.21.22276400
Contributors: Xiao-Fei Kong; Kelsie Bogyo; Sheena Kapoor; Emily E. Groopman; Amanda Thomas-Wilson; Enrico Cocchi; Hila Milo Rasouly; Beishi Zheng; Siming Sun; Junying Zhang et al.
Source: check_circle
Crossref

Immunogenetics of Gastrointestinal Cancers: A Systematic Review of Inborn Errors of Immunity in Humans

2022-01-25 | Preprint
DOI: 10.1101/2022.01.25.22269823
Contributors: Beishi Zheng; Howard Chung; Chen Bing; Siming Sun; Peter H.R. Green; Timothy C. Wang; Xiao-Fei Kong
Source: check_circle
Crossref

Interferon-Driven Immune Dysregulation in Down Syndrome: A Review of the Evidence

Journal of Inflammation Research
2021-10 | Journal article
DOI: 10.2147/JIR.S280953
Contributors: Howard Chung; Peter HR Green; Timothy C Wang; Xiao-Fei Kong
Source: check_circle
Crossref

Anesthesia Assistance in Screening Colonoscopy and Adenoma Detection Rate Among Trainees

Digestive Diseases and Sciences
2020 | Journal article
DOI: 10.1007/s10620-019-05820-2
EID:

2-s2.0-85071740882
Contributors: Krigel, A.; Patel, A.; Kaplan, J.; Kong, X.-F.; Garcia-Carrasquillo, R.; Lebwohl, B.; Krishnareddy, S.
Source: Self-asserted source
Xiao-Fei Kong via Scopus - Elsevier

Individuals with Down syndrome hospitalized with COVID-19 have more severe disease

Genetics in Medicine
2020 | Journal article
DOI: 10.1038/s41436-020-01004-w
EID:

2-s2.0-85092652997

Part of ISBN:

15300366 10983600
Contributors: Malle, L.; Gao, C.; Hur, C.; Truong, H.Q.; Bouvier, N.M.; Percha, B.; Kong, X.-F.; Bogunovic, D.
Source: Self-asserted source
Xiao-Fei Kong via Scopus - Elsevier

Three Copies of Four Interferon Receptor Genes Underlie a Mild Type I Interferonopathy in Down Syndrome

Journal of Clinical Immunology
2020-08-22 | Journal article
DOI: 10.1007/s10875-020-00803-9
Contributors: Xiao-Fei Kong; Lisa Worley; Darawan Rinchai; Vincent Bondet; Puthen Veettil Jithesh; Marie Goulet; Emilie Nonnotte; Anne Sophie Rebillat; Martine Conte; Clotilde Mircher et al.
Source: check_circle
Crossref
grade
Preferred source (of 2)‎

A deep intronic splice mutation of STAT3 underlies hyper IgE syndrome by negative dominance

Proceedings of the National Academy of Sciences of the United States of America
2019 | Journal article
DOI: 10.1073/pnas.1901409116
EID:

2-s2.0-85071353049
Contributors: Khourieh, J.; Rao, G.; Habib, T.; Avery, D.T.; Lefèvre-Utile, A.; Chandesris, M.-O.; Belkadi, A.; Chrabieh, M.; Alwaseem, H.; Grandin, V. et al.
Source: Self-asserted source
Xiao-Fei Kong via Scopus - Elsevier

Erratum: A purely quantitative form of partial recessive IFN-γR2 deficiency caused by mutations of the initiation or second codon (Human Molecular Genetics (2018) DOI:10.1093/hmg/ddy275)

Human Molecular Genetics
2019 | Journal article
DOI: 10.1093/hmg/ddy357
EID:

2-s2.0-85060146306
Contributors: Oleaga-Quintas, C.; Deswarte, C.; Moncada-Vélez, M.; Metin, A.; Rao, I.K.; Kanık-Yüksek, S.; Nieto-Patlán, A.; Guérin, A.; Gülhan, B.; Murthy, S. et al.
Source: Self-asserted source
Xiao-Fei Kong via Scopus - Elsevier

Mendelian susceptibility to mycobacterial disease: 2014–2018 update

Immunology and Cell Biology
2019 | Journal article
DOI: 10.1111/imcb.12210
EID:

2-s2.0-85055711153
Contributors: Rosain, J.; Kong, X.-F.; Martinez-Barricarte, R.; Oleaga-Quintas, C.; Ramirez-Alejo, N.; Markle, J.; Okada, S.; Boisson-Dupuis, S.; Casanova, J.-L.; Bustamante, J.
Source: Self-asserted source
Xiao-Fei Kong via Scopus - Elsevier

The Light at the End of the Tunnel

Gastroenterology
2019 | Journal article
DOI: 10.1053/j.gastro.2018.11.072
EID:

2-s2.0-85063357658
Contributors: Krigel, A.; Kong, X.-F.; Freedberg, D.E.
Source: Self-asserted source
Xiao-Fei Kong via Scopus - Elsevier

A purely quantitative form of partial recessive IFN-γR2 deficiency caused by mutations of the initiation or second codon

Human Molecular Genetics
2018 | Journal article
DOI: 10.1093/hmg/ddy275
EID:

2-s2.0-85055698414
Contributors: Oleaga-Quintas, C.; Deswarte, C.; Moncada-Vélez, M.; Metin, A.; Rao, I.K.; Kanık-Yüksek, S.; Nieto-Patlán, A.; Guérin, A.; Gülhan, B.; Murthy, S. et al.
Source: Self-asserted source
Xiao-Fei Kong via Scopus - Elsevier

Disruption of an antimycobacterial circuit between dendritic and helper T cells in human SPPL2a deficiency

Nature Immunology
2018 | Journal article
DOI: 10.1038/s41590-018-0178-z
EID:

2-s2.0-85051985294
Contributors: Kong, X.-F.; Martinez-Barricarte, R.; Kennedy, J.; Mele, F.; Lazarov, T.; Deenick, E.K.; Ma, C.S.; Breton, G.; Lucero, K.B.; Langlais, D. et al.
Source: Self-asserted source
Xiao-Fei Kong via Scopus - Elsevier

Human IFN- immunity to mycobacteria is governed by both IL-12 and IL-23

Science Immunology
2018 | Journal article
DOI: 10.1126/sciimmunol.aau6759
EID:

2-s2.0-85057006182
Contributors: Martínez-Barricarte, R.; Markle, J.G.; Ma, C.S.; Deenick, E.K.; Ramírez-Alejo, N.; Mele, F.; Latorre, D.; Mahdaviani, S.A.; Aytekin, C.; Mansouri, D. et al.
Source: Self-asserted source
Xiao-Fei Kong via Scopus - Elsevier

Alanine-scanning mutagenesis of human signal transducer and activator of transcription 1 to estimate loss- or gain-of-function variants

Journal of Allergy and Clinical Immunology
2017 | Journal article
DOI: 10.1016/j.jaci.2016.09.035
EID:

2-s2.0-85008185826
Contributors: Kagawa, R.; Fujiki, R.; Tsumura, M.; Sakata, S.; Nishimura, S.; Itan, Y.; Kong, X.-F.; Kato, Z.; Ohnishi, H.; Hirata, O. et al.
Source: Self-asserted source
Xiao-Fei Kong via Scopus - Elsevier

Human genetics of tuberculosis of the nervous system

Tuberculosis of the Central Nervous System: Pathogenesis, Imaging, and Management
2017 | Book
Part of DOI: 10.1007/978-3-319-50712-5_2
EID:

2-s2.0-85038945959
Contributors: El Baghdadi, J.; El Azbaoui, S.; Ailal, F.; Akhaddar, A.; Sabri, A.; Kong, X.-F.; Bousfiha, A.A.; Casanova, J.L.; Abel, L.; Boisson-Dupuis, S.
Source: Self-asserted source
Xiao-Fei Kong via Scopus - Elsevier

Anti-IFN-γ autoantibodies are strongly associated with HLA-DR∗15:02/16:02 and HLA-DQ∗05:01/05:02 across Southeast Asia

Journal of Allergy and Clinical Immunology
2016 | Journal article
DOI: 10.1016/j.jaci.2015.09.018
EID:

2-s2.0-84951310291
Contributors: Ku, C.-L.; Lin, C.-H.; Chang, S.-W.; Chu, C.-C.; Chan, J.F.W.; Kong, X.-F.; Lee, C.-H.; Rosen, E.A.; Ding, J.-Y.; Lee, W.-I. et al.
Source: Self-asserted source
Xiao-Fei Kong via Scopus - Elsevier

Interferon-γ autoantibodies as predisposing factor for nontuberculous mycobacterial infection

Emerging Infectious Diseases
2016 | Journal article
DOI: 10.3201/eid2206.151860
EID:

2-s2.0-84969263696
Contributors: Valour, F.; Perpoint, T.; Sénéchal, A.; Kong, X.-F.; Bustamante, J.; Ferry, T.; Chidiac, C.; Ader, F.
Source: Self-asserted source
Xiao-Fei Kong via Scopus - Elsevier

Human TYK2 deficiency: Mycobacterial and viral infections without hyper-IgE syndrome

Journal of Experimental Medicine
2015 | Journal article
DOI: 10.1084/jem.20140280
EID:

2-s2.0-84944807941
Contributors: Kreins, A.Y.; Ciancanelli, M.J.; Okada, S.; Kong, X.-F.; Ramírez-Alejo, N.; Kilic, S.S.; El Baghdadi, J.; Nonoyama, S.; Mahdaviani, S.A.; Ailal, F. et al.
Source: Self-asserted source
Xiao-Fei Kong via Scopus - Elsevier

The human gene damage index as a gene-level approach to prioritizing exome variants

Proceedings of the National Academy of Sciences of the United States of America
2015 | Journal article
DOI: 10.1073/pnas.1518646112
EID:

2-s2.0-84946595515
Contributors: Itan, Y.; Shang, L.; Boisson, B.; Patin, E.; Bolze, A.; Moncada-Vélez, M.; Scott, E.; Ciancanelli, M.J.; Lafaille, F.G.; Markle, J.G. et al.
Source: Self-asserted source
Xiao-Fei Kong via Scopus - Elsevier

Inherent lipid metabolic dysfunction in glycogen storage disease IIIa

Biochemical and Biophysical Research Communications
2014 | Journal article
DOI: 10.1016/j.bbrc.2014.10.096
EID:

2-s2.0-84912114305
Contributors: Li, X.-H.; Gong, Q.-M.; Ling, Y.; Huang, C.; Yu, D.-M.; Gu, L.-L.; Liao, X.-W.; Zhang, D.-H.; Hu, X.-Q.; Han, Y. et al.
Source: Self-asserted source
Xiao-Fei Kong via Scopus - Elsevier

Mycobacterium simiae Infection in Two Unrelated Patients with Different Forms of Inherited IFN-γR2 Deficiency

Journal of Clinical Immunology
2014 | Journal article
DOI: 10.1007/s10875-014-0085-5
EID:

2-s2.0-84912001917
Contributors: Martínez-Barricarte, R.; Megged, O.; Stepensky, P.; Casimir, P.; Moncada-Velez, M.; Averbuch, D.; Assous, M.V.; Abuzaitoun, O.; Kong, X.-F.; Pedergnana, V. et al.
Source: Self-asserted source
Xiao-Fei Kong via Scopus - Elsevier

Simple diagnosis of STAT1 gain-of-function alleles in patients with chronic mucocutaneous candidiasis

Journal of Leukocyte Biology
2014 | Journal article
DOI: 10.1189/jlb.0513250
EID:

2-s2.0-84899791876
Contributors: Mizoguchi, Y.; Tsumura, M.; Okada, S.; Hirata, O.; Minegishi, S.; Imai, K.; Hyakuna, N.; Muramatsu, H.; Kojima, S.; Ozaki, Y. et al.
Source: Self-asserted source
Xiao-Fei Kong via Scopus - Elsevier

A Novel Homozygous p.R1105X Mutation of the AP4E1 Gene in Twins with Hereditary Spastic Paraplegia and Mycobacterial Disease

PLoS ONE
2013 | Journal article
DOI: 10.1371/journal.pone.0058286
EID:

2-s2.0-84874629660
Contributors: Kong, X.-F.; Bousfiha, A.; Rouissi, A.; Itan, Y.; Abhyankar, A.; Bryant, V.; Okada, S.; Ailal, F.; Bustamante, J.; Casanova, J.-L. et al.
Source: Self-asserted source
Xiao-Fei Kong via Scopus - Elsevier

Haploinsufficiency at the human IFNGR2 locus contributes to mycobacterial disease

Human Molecular Genetics
2013 | Journal article
DOI: 10.1093/hmg/dds484
EID:

2-s2.0-84873025890
Contributors: Kong, X.-F.; Vogt, G.; Itan, Y.; Macura-Biegun, A.; Szaflarska, A.; Kowalczyk, D.; Chapgier, A.; Abhyankar, A.; Furthner, D.; Djambas Khayat, C. et al.
Source: Self-asserted source
Xiao-Fei Kong via Scopus - Elsevier

Partial IFN-γR2 deficiency is due to protein misfolding and can be rescued by inhibitors of glycosylation

Blood
2013 | Journal article
DOI: 10.1182/blood-2013-01-480814
EID:

2-s2.0-84887670038
Contributors: Moncada-Vélez, M.; Martinez-Barricarte, R.; Bogunovic, D.; Kong, X.-F.; Blancas-Galicia, L.; Tirpan, C.; Aksu, G.; Vincent, Q.B.; Boisson, B.; Itan, Y. et al.
Source: Self-asserted source
Xiao-Fei Kong via Scopus - Elsevier

Recurrent porphyria attacks in a Chinese patient with a heterozygous PBGD mutation

Gene
2013 | Journal article
DOI: 10.1016/j.gene.2013.03.130
EID:

2-s2.0-84878650177
Contributors: Kong, X.-F.; Han, Y.; Li, X.-H.; Gao, D.-Y.; Zhang, X.-X.; Gong, Q.-M.
Source: Self-asserted source
Xiao-Fei Kong via Scopus - Elsevier

Dominant-negative STAT1 SH2 domain mutations in unrelated patients with mendelian susceptibility to mycobacterial disease

Human Mutation
2012 | Journal article
DOI: 10.1002/humu.22113
EID:

2-s2.0-84865174263
Contributors: Tsumura, M.; Okada, S.; Sakai, H.; Yasunaga, S.; Ohtsubo, M.; Murata, T.; Obata, H.; Yasumi, T.; Kong, X.-F.; Abhyankar, A. et al.
Source: Self-asserted source
Xiao-Fei Kong via Scopus - Elsevier

Inborn errors of human STAT1: Allelic heterogeneity governs the diversity of immunological and infectious phenotypes

Current Opinion in Immunology
2012 | Journal article
DOI: 10.1016/j.coi.2012.04.011
EID:

2-s2.0-84865308028
Contributors: Boisson-Dupuis, S.; Kong, X.-F.; Okada, S.; Cypowyj, S.; Puel, A.; Abel, L.; Casanova, J.-L.
Source: Self-asserted source
Xiao-Fei Kong via Scopus - Elsevier

Mendelian susceptibility to mycobacterial disease in Egyptian children

Mediterranean Journal of Hematology and Infectious Diseases
2012 | Journal article
DOI: 10.4084/MJHID.2012.033
EID:

2-s2.0-84875980193
Contributors: Galal, N.; Boutros, J.; Marsafy, A.; Kong, X.-F.; Feinberg, J.; Casanova, J.-L.; Boisson-Dupuis, S.; Bustamante, J.
Source: Self-asserted source
Xiao-Fei Kong via Scopus - Elsevier

Mycobacterial disease and impaired IFN-γ immunity in humans with inherited ISG15 deficiency

Science
2012 | Journal article
DOI: 10.1126/science.1224026
EID:

2-s2.0-84866748115
Contributors: Bogunovic, D.; Byun, M.; Durfee, L.A.; Abhyankar, A.; Sanal, O.; Mansouri, D.; Salem, S.; Radovanovic, I.; Grant, A.V.; Adimi, P. et al.
Source: Self-asserted source
Xiao-Fei Kong via Scopus - Elsevier

Clinical and molecular characterization of Wilson's disease in China: Identification of 14 novel mutations

BMC Medical Genetics
2011 | Journal article
DOI: 10.1186/1471-2350-12-6
EID:

2-s2.0-78651074120
Contributors: Li, X.-H.; Lu, Y.; Ling, Y.; Fu, Q.-C.; Xu, J.; Zang, G.-Q.; Zhou, F.; De-Min, Y.; Han, Y.; Zhang, D.-H. et al.
Source: Self-asserted source
Xiao-Fei Kong via Scopus - Elsevier

Gain-of-function human STAT1 mutations impair IL-17 immunity and underlie chronic mucocutaneous candidiasis

Journal of Experimental Medicine
2011 | Journal article
DOI: 10.1084/jem.20110958
EID:

2-s2.0-79961154447
Contributors: Liu, L.; Okada, S.; Kong, X.-F.; Kreins, A.Y.; Cypowyj, S.; Abhyankar, A.; Toubiana, J.; Itan, Y.; Audry, M.; Nitschke, P. et al.
Source: Self-asserted source
Xiao-Fei Kong via Scopus - Elsevier

IRF8 mutations and human dendritic-cell immunodeficiency

New England Journal of Medicine
2011 | Journal article
DOI: 10.1056/NEJMoa1100066
EID:

2-s2.0-79960219807
Contributors: Hambleton, S.; Salem, S.; Bustamante, J.; Bigley, V.; Boisson-Dupuis, S.; Azevedo, J.; Fortin, A.; Haniffa, M.; Ceron-Gutierrez, L.; Bacon, C.M. et al.
Source: Self-asserted source
Xiao-Fei Kong via Scopus - Elsevier

Partial recessive IFN-γR1 deficiency: Genetic, immunological and clinical features of 14 patients from 11 kindreds

Human Molecular Genetics
2011 | Journal article
DOI: 10.1093/hmg/ddr029
EID:

2-s2.0-79953072406
Contributors: Sologuren, I.; Boisson-Dupuis, S.; Pestano, J.; Vincent, Q.B.; Fernández-Pérez, L.; Chapgier, A.; Cárdenes, M.; Feinberg, J.; García-Laorden, M.I.; Picard, C. et al.
Source: Self-asserted source
Xiao-Fei Kong via Scopus - Elsevier

A novel form of human STAT1 deficiency impairing early but not late responses to interferons

Blood
2010 | Journal article
DOI: 10.1182/blood-2010-04-280586.
EID:

2-s2.0-78650633201
Contributors: Kong, X.-F.; Ciancanelli, M.; Al-Hajjar, S.; Alsina, L.; Zumwalt, T.; Bustamante, J.; Feinberg, J.; Audry, M.; Prando, C.; Bryant, V. et al.
Source: Self-asserted source
Xiao-Fei Kong via Scopus - Elsevier

Paternal uniparental isodisomy of chromosome 6 causing a complex syndrome including complete IFN-γ receptor 1 deficiency

American Journal of Medical Genetics, Part A
2010 | Journal article
DOI: 10.1002/ajmg.a.33291
EID:

2-s2.0-77649229733
Contributors: Prando, C.; Boisson-Dupuis, S.; Grant, A.V.; Kong, X.-F.; Bustamante, J.; Feinberg, J.; Chapgier, A.; Rose, Y.; Jannière, L.; Rizzardi, E. et al.
Source: Self-asserted source
Xiao-Fei Kong via Scopus - Elsevier

Revisiting human IL-12Rβ1 deficiency: A survey of 141 patients from 30 countries

Medicine
2010 | Journal article
DOI: 10.1097/MD.0b013e3181fdd832
EID:

2-s2.0-78649351360
Contributors: De Beaucoudrey, L.; Samarina, A.; Bustamante, J.; Cobat, A.; Boisson-Dupuis, S.; Feinberg, J.; Al-Muhsen, S.; Jannière, L.; Rose, Y.; De Suremain, M. et al.
Source: Self-asserted source
Xiao-Fei Kong via Scopus - Elsevier

A novel form of cell type-specific partial IFN-γR1 deficiency caused by a germ line mutation of the IFNGR1 initiation codon

Human Molecular Genetics
2009 | Journal article
DOI: 10.1093/hmg/ddp507
EID:

2-s2.0-77949902855
Contributors: Kong, X.-F.; Vogt, G.; Chapgier, A.; Lamaze, C.; Bustamante, J.; Prando, C.; Fortin, A.; Puel, A.; Feinberg, J.; Zhang, X.-X. et al.
Source: Self-asserted source
Xiao-Fei Kong via Scopus - Elsevier

A partial form of recessive STAT1 deficiency in humans

Journal of Clinical Investigation
2009 | Journal article
DOI: 10.1172/JCI37083
EID:

2-s2.0-67651007827
Contributors: Chapgier, A.; Kong, X.-F.; Boisson-Dupuis, S.; Jouanguy, E.; Averbuch, D.; Feinberg, J.; Zhang, S.-Y.; Bustamante, J.; Vogt, G.; Lejeune, J. et al.
Source: Self-asserted source
Xiao-Fei Kong via Scopus - Elsevier

Association study of IFNAR2 and IL10RB genes with the susceptibility and interferon response in HBV infection

Journal of Viral Hepatitis
2009 | Journal article
DOI: 10.1111/j.1365-2893.2009.01130.x
EID:

2-s2.0-68949203817
Contributors: Gong, Q.-M.; Kong, X.-F.; Yang, Z.-T.; Xu, J.; Wang, L.; Li, X.-H.; Jin, G.-D.; Gao, J.; Zhang, D.-H.; Jiang, J.-H. et al.
Source: Self-asserted source
Xiao-Fei Kong via Scopus - Elsevier

Characterization of hepatitis B virus reverse transcriptase sequences in Chinese treatment naive patients

Journal of Gastroenterology and Hepatology (Australia)
2009 | Journal article
DOI: 10.1111/j.1440-1746.2009.05864.x
EID:

2-s2.0-69049086720
Contributors: Han, Y.; Huang, L.H.; Liu, C.M.; Yang, S.; Li, J.; Lin, Z.M.; Kong, X.F.; Yu, D.M.; Zhang, D.H.; Jin, G.D. et al.
Source: Self-asserted source
Xiao-Fei Kong via Scopus - Elsevier

Successful hematopoietic stem cell transplantation from an unrelated donor in a child with interferon gamma receptor deficiency

Pediatric Infectious Disease Journal
2009 | Journal article
DOI: 10.1097/INF.0b013e318195092e
EID:

2-s2.0-77449137359
Contributors: Moilanen, P.; Korppi, M.; Hovi, L.; Chapgier, A.; Feinberg, J.; Kong, X.-F.; Boisson-Dupuis, S.; Arola, M.; Casanova, J.-L.; Saarinen-Pihkala, U.M.
Source: Self-asserted source
Xiao-Fei Kong via Scopus - Elsevier

[Primary immunodeficiency complicated with Bacillus Calmette-Guerin infection: identification and clinical phenotype of a case of novel interleukin-12Rbeta1 gene mutation].

Zhonghua er ke za zhi. Chinese journal of pediatrics
2008 | Journal article
EID:

2-s2.0-84879789374
Contributors: Xie, N.; Jiang, L.P.; Kong, X.F.; Zhu, C.M.; Liu, Z.Y.; Liu, W.; Zhang, X.X.; Yang, X.Q.
Source: Self-asserted source
Xiao-Fei Kong via Scopus - Elsevier

Assessment of specific antibodies to F protein in serum samples from Chinese hepatitis C patients treated with interferon plus ribavarin

Journal of Clinical Microbiology
2008 | Journal article
DOI: 10.1128/JCM.00612-08
EID:

2-s2.0-55849100318
Contributors: Gao, D.-Y.; Zhang, X.-X.; Hou, G.; Jin, G.-D.; Deng, Q.; Kong, X.-F.; Zhang, D.-H.; Ling, Y.; Yu, D.-M.; Gong, Q.-M. et al.
Source: Self-asserted source
Xiao-Fei Kong via Scopus - Elsevier

Identification of a ferrochelatase mutation in a Chinese family with erythropoietic protoporphyria

Journal of Hepatology
2008 | Journal article
DOI: 10.1016/j.jhep.2007.09.013
EID:

2-s2.0-37849001329
Contributors: Kong, X.-F.; Ye, J.; Gao, D.-Y.; Gong, Q.-M.; Zhang, D.-H.; Lu, Z.-M.; Lu, Y.-M.; Zhang, X.-X.
Source: Self-asserted source
Xiao-Fei Kong via Scopus - Elsevier

Polymorphisms of microsomal triglyceride transfer protein in different hepatitis B virus-infected patients

World Journal of Gastroenterology
2008 | Journal article
DOI: 10.3748/wjg.14.5454
EID:

2-s2.0-64849092043
Contributors: Yang, Z.-T.; Zhang, X.-X.; Kong, X.-F.; Zhang, D.-H.; Zhang, S.-Y.; Jiang, J.-H.; Gong, Q.-M.; Jin, G.-D.; Lu, Z.-M.
Source: Self-asserted source
Xiao-Fei Kong via Scopus - Elsevier
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Peer review (9 reviews for 3 publications/grants)

Review activity for BMC infectious diseases (1)
Review activity for European journal of medical genetics. (1)
Review activity for Journal of clinical immunology. (7)
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