Jia-Huan Ding

934 citations

28 papers · 675 indexed · h-index 15

Co-authors: Charles R. Roe Bing-Zhi Yang Ralph V. Shohet Paul Grayburn Christopher B. Newgard Shuyuan Chen Raffi Bekeredjian Hans E. Hohmeier
Topics: Metabolism and Genetic Disorders (11 papers)RNA Research and Splicing (5 papers)Glycogen Storage Diseases and Myoclonus (4 papers)
Cited by: Clinical Biochemistry Rheumatology Molecular Biology
Journals: Proceedings of the National Academy of Sciences Annals of Internal Medicine Annals of Neurology
Partner nations: United States China France

In The Last Decade

Jia-Huan Ding

28 papers receiving 658 citations

Peers

Countries citing papers authored by Jia-Huan Ding

Since Specialization

Citations

This map shows the geographic impact of Jia-Huan Ding's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Jia-Huan Ding with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Jia-Huan Ding more than expected).

Fields of papers citing papers by Jia-Huan Ding

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Jia-Huan Ding. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Jia-Huan Ding. The network helps show where Jia-Huan Ding may publish in the future.

Co-authorship network of co-authors of Jia-Huan Ding

This figure shows the co-authorship network connecting the top 25 collaborators of Jia-Huan Ding. A scholar is included among the top collaborators of Jia-Huan Ding based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Jia-Huan Ding. Jia-Huan Ding is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	Identification of novel mutations including a double mutation in patients with inherited cardiomyopathy by a targeted sequencing approach using the Ion Torrent PGM system 2016 ·International Journal of Molecular Medicine ·(unknown),(unknown),(unknown),Yue Feng,(unknown),Mingjie Pang,(unknown),Hong Zhang,Jia-Huan Ding,Xueshan Xia	7
2	Targeted Next-Generation Sequencing Reveals Hot Spots and Doubly Heterozygous Mutations in Chinese Patients with Familial Cardiomyopathy 2015 ·BioMed Research International ·(unknown),Yue Feng,(unknown),(unknown),Yuzhu Song,A‐Mei Zhang,Li Liu,Hong Zhang,Jia-Huan Ding,Xueshan Xia	13
3	Targeted next-generation sequencing of candidate genes reveals novel mutations in patients with dilated cardiomyopathy 2015 ·International Journal of Molecular Medicine ·(unknown),Yue Feng,(unknown),(unknown),Yuzhu Song,A‐Mei Zhang,Li Liu,Hong Zhang,Jia-Huan Ding,Xueshan Xia	52
4	Silicon multi-nanochannel FETs to improve device uniformity/stability and femtomolar detection of insulin in serum 2013 ·Biosensors and Bioelectronics ·(unknown),Ruhai Tian,Jinming Gao,(unknown),Jia-Huan Ding,Walter Hu	60
5	Free sialic acid storage disease without sialuria 2009 ·Annals of Neurology ·Fanny Mochel,Bing-Zhi Yang,(unknown),Jerry N. Thompson,Udo F. H. Engelke,(unknown),William Benko,Christine R. Kaneski,David R. Adams,Maria Tsokos,Mones Abu‐Asab,Marjan Huizing,F. Seguin,Ron A. Wevers,Jia-Huan Ding,Frans W. Verheijen,Raphael Schiffmann	11
6	Aromatase expression in normal human oral keratinocytes and oral squamous cell carcinoma 2006 ·Archives of Oral Biology ·Yi‐Shing Lisa Cheng,Gabriele Mues,D. Wood,Jia-Huan Ding	8
7	Characterization of the bidirectional promoter region between the human genes encoding VLCAD and PSD-95 2003 ·Genomics ·Li‐Feng Zhang,Jia-Huan Ding,Bing-Zhi Yang,(unknown),Charles R. Roe	16
8	Carnitine/Acylcarnitine Translocase Deficiency (Neonatal Phenotype): Successful Prenatal and Postmortem Diagnosis Associated with a Novel Mutation in a Single Family 2001 ·Molecular Genetics and Metabolism ·Bing-Zhi Yang,(unknown),Diane S. Roe,M. Brivet,Gero Strobel,(unknown),Jia-Huan Ding,Charles R. Roe	27
9	Identification of a Novel Mutation in Patients with Medium-Chain Acyl-CoA Dehydrogenase Deficiency 2000 ·Molecular Genetics and Metabolism ·Bing-Zhi Yang,Jia-Huan Ding,Changcheng Zhou,Mazen M. Dimachkie,Lawrence Sweetman,Majed Dasouki,(unknown),Charles R. Roe	14
10	Identification of Four Novel Mutations in Patients with Carnitine Palmitoyltransferase II (CPT II) Deficiency 1998 ·Molecular Genetics and Metabolism ·Bing-Zhi Yang,Jia-Huan Ding,(unknown),Diane S. Roe,Guocheng He,(unknown),Donald W. Day,France Demaugre,Daniel Rabier,M. Brivet,Charles R. Roe	25
11	A Novel Mutation Identified in Carnitine Palmitoyltransferase II Deficiency 1998 ·Molecular Genetics and Metabolism ·Bing-Zhi Yang,Jia-Huan Ding,Diane S. Roe,(unknown),Donald W. Day,Charles R. Roe	26
12	PRENATAL DIAGNOSIS OF MITOCHONDRIAL FATTY ACID OXIDATION DEFECTS 1996 ·Prenatal Diagnosis ·Mohamed A. Nada,Christine Vianey‐Saban,Charles R. Roe,Jia-Huan Ding,Monique Mathieu,Rebecca S. Wappner,Martin G. Bialer,(unknown),(unknown)	33
13	Improved Detection of the G1528C Mutation in LCHAD Deficiency 1996 ·Biochemical and Molecular Medicine ·Jia-Huan Ding,Bing-Zhi Yang,Mohamed Abu Nada,Charles R. Roe	8
14	The Genes for the α and β Subunits of the Mitochondrial Trifunctional Protein Are Both Located in the Same Region of Human Chromosome 2p23 1996 ·Genomics ·(unknown),Henry H. Heng,Jia-Huan Ding,Charles R. Roe	32
15	Type III glycogen storage disease: An adult case with mild disease but complete absence of debrancher protein 1991 ·Neuromuscular Disorders ·(unknown),C. Neal Stewart,Jia-Huan Ding,(unknown)	2
16	Definitive prenatal diagnosis for type III glycogen storage disease. 1990 ·PubMed ·Bing-Zhi Yang,Jia-Huan Ding,Benjamin Brown,Y T Chen	15
17	Immunoblot analyses of glycogen debranching enzyme in different subtypes of glycogen storage disease type III 1990 ·The Journal of Pediatrics ·Jia-Huan Ding,Th. de Barsy,Barbara I. Brown,Rosalind Coleman,Yuan-Tsong Chen	60
18	Mild Cystic Fibrosis Linked to Chromosome 7q22 Markers with an Uncommon Haplotype 1989 ·Annals of Internal Medicine ·Allyn McConkie‐Rosell,Yuan‐Tsong Chen,David J. Harris,Marcy C. Speer,Margaret A. Pericak‐Vance,Jia-Huan Ding,W. Edward Highsmith,Michael R. Knowles,Stephen G. Kahler	6
19	Glycogen debranching enzyme: purification, antibody characterization, and immunoblot analyses of type III glycogen storage disease. 1987 ·PubMed ·Yuting Chen,(unknown),Jia-Huan Ding,Benjamin Brown	33
20	Identification and quantification of a messenger ribonucleic acid induced by polynuclear aromatic hydrocarbons - using a cloned human cytochrome P-450 gene 1985 ·European Journal of Biochemistry ·Takako Katō,Jia-Huan Ding,(unknown)	7

About Jia-Huan Ding

Jia-Huan Ding is a scholar working on Clinical Biochemistry, Cancer Research and Rheumatology, having authored 28 papers that have together received 675 indexed citations. Recurring topics across this work include Metabolism and Genetic Disorders (11 papers), RNA Research and Splicing (5 papers) and Glycogen Storage Diseases and Myoclonus (4 papers). The work is most often cited by research in Clinical Biochemistry (185 citations), Rheumatology (120 citations) and Molecular Biology (327 citations). Jia-Huan Ding has collaborated with scholars based in United States, China and France. Frequent co-authors include Charles R. Roe, Bing-Zhi Yang, Ralph V. Shohet, Paul Grayburn, Christopher B. Newgard, Shuyuan Chen, Raffi Bekeredjian, Hans E. Hohmeier, Stephen Albert Johnston and Benjamin Brown. Their work appears in journals such as Proceedings of the National Academy of Sciences, Annals of Internal Medicine and Annals of Neurology.

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