Author

Huafang Jiang

Observed names: H F Jiang, Hua-Fang Jiang, Jiang, Huafang

Institutions: Capital Medical University, Hainan Maternal and Child Health Hospital, Beijing Children’s Hospital, Weifang Maternity and Child Care Hospital

Observed institutions: South Central Minzu University, Capital Medical University, Chinese Center For Disease Control and Prevention, Peking University, Hainan Maternal and Child Health Hospital, National Institute for Viral Disease Control and Prevention, Beijing Children’s Hospital, Weifang Maternity and Child Care Hospital

ORCID: 0000-0002-6632-1793

Observed ORCID: 0000-0002-6632-1793

OpenAlex ID: A5000915499

Transmission of Human Enterovirus 85 Recombinants Containing New Unknown Serotype HEV-B Donor Sequences in Xinjiang Uighur Autonomous Region, China

2013 · Qiang Sun, Yong Zhang, et al. · PLoS ONE · 22

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TRIT1 defect leads to a recognizable phenotype of myoclonic epilepsy, speech delay, strabismus, progressive spasticity, and normal lactate levels

2022 · Ewout Muylle, Huafang Jiang, et al. · Journal of Inherited Metabolic Disease · 19

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Identification and characterization of novel MPC1 gene variants causing mitochondrial pyruvate carrier deficiency

2021 · Huafang Jiang, Ahmad Alahmad, et al. · Journal of Inherited Metabolic Disease · 17

Dominant KPNA3 Mutations Cause Infantile‐Onset Hereditary Spastic Paraplegia

2021 · Claudia Schob, Maja Hempel, et al. · Annals of Neurology · 11

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Complete Genome Sequence of Two Coxsackievirus A1 Strains That Were Cytotoxic to Human Rhabdomyosarcoma Cells

2012 · Qiang Sun, Yong Zhang, et al. · Journal of Virology · 8

Thiamine pyrophosphokinase deficiency: report of two Chinese cases and a literature review

2023 · Dan Zhao, Ming Liu, et al. · Frontiers in Pediatrics · 7

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[Reliability and validity of the Chinese version of adverse childhood experiences international questionnaire in parents of preschool children].

2023 · X Y Mi, S S Hou, et al. · PubMed · 6

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The genotypic and phenotypic landscape of PDHA1 -related pyruvate dehydrogenase complex deficiency

2025 · Kajus Merkevicius, Dmitrii Smirnov, et al. · Brain · 5

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Clinical characteristics and long-term prognosis of 150 children with MELAS syndrome in China

2025 · Chaolong Xu, Sisi Dai, et al. · Journal of Neurology · 4

Novel mutations in MTERF3: First report of a new genetic cause in two Chinese patients with developmental delay, intermittent hypoglycemia and metabolic acidosis

2025 · Ruoyu Duan, Refiloe Laurentinah Mahlatsi, et al. · Mitochondrion · 3

Deficiency of the NAD(P)HX metabolic repair system: a treatable mitochondrial disease

2026 · Chaolong Xu, Hong Jin, et al. · Orphanet Journal of Rare Diseases · 1

Case Report: Biallelic variants in MRPS36, encoding a component of the 2-oxoglutarate dehydrogenase complex, cause leigh syndrome

2025 · Huafang Jiang, Chaolong Xu, et al. · Frontiers in Pediatrics · 1

Establishment of an iPSC line (BCHNDi001-A) from a patient with nicotinamide nucleotide repair system deficiency caused by biallelic NAXD mutations

2024 · Chaolong Xu, Ling Zhou, et al. · Stem Cell Research · 1

Analysis of respiratory viruses in children with acute respiratory tract infection in Weifang

2018 · Huafang Jiang, Jinliang Li, et al. · Chinese Journal of Clinical Hepatology · 1

[Analysis of genetic characteristics of type II non-wild poliovirus in mainland China, 2010].

2012 · Hua-Fang Jiang, Dong-Mei Yan, et al. · PubMed · 1

Clinical Spectrum, Heteroplasmy‐Phenotype Correlation, and Prognosis of the MT‐ND3 m.10191 T > C Mutation

2026 · Zimeng He, Huafang Jiang, et al. · CNS Neuroscience & Therapeutics

Additional file 2 of Deficiency of the NAD(P)HX metabolic repair system: a treatable mitochondrial disease

2026 · Xu, Chaolong, Jin, Hong, et al. · Figshare

Additional file 1 of Deficiency of the NAD(P)HX metabolic repair system: a treatable mitochondrial disease

2026 · Xu, Chaolong, Jin, Hong, et al. · Figshare

Deficiency of the NAD(P)HX metabolic repair system: a treatable mitochondrial disease

2026 · Xu, Chaolong, Jin, Hong, et al. · Figshare

Additional file 3 of Deficiency of the NAD(P)HX metabolic repair system: a treatable mitochondrial disease

2026 · Xu, Chaolong, Jin, Hong, et al. · Figshare

[Long-term efficacy observation of nicotinamide in the treatment of early-onset progressive encephalopathy with brain edema and (or) leukoencephalopathy-2 caused by NAXD gene variation].

2025 · C L Xu, F Fang, et al. · PubMed

Preliminary investigation on the economic cost of mitochondrial disease in Chinese children

2025 · Chaolong Xu, Dan Zhao, et al. · Orphanet Journal of Rare Diseases

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[Clinical characteristics of children with MT-TK gene m.8344A>G variation].

2024 · M Z Wang, H F Jiang, et al. · PubMed

Phenotypic spectrum of iron-sulfur cluster assembly gene IBA57 mutations: c.286 T > C identified as a hotspot mutation in Chinese patients with a stable natural history

2024 · Huafang Jiang, Chaolong Xu, et al. · Journal of Human Genetics

Phenotypic spectrum of iron-sulfur cluster assembly gene IBA57 mutations: c.286T>C identified as a hotspot mutation in Chinese patients with a stable natural history

2024 · Huafang Jiang, Chaolong Xu, et al. · Research Square

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Works count: 29

Citation count: 107

H-index: 6

I10-index: 4