Ai-Chu Huang

1.3k total citations
15 papers, 940 citations indexed

About

Ai-Chu Huang is a scholar working on Clinical Biochemistry, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Ai-Chu Huang has authored 15 papers receiving a total of 940 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Clinical Biochemistry, 6 papers in Molecular Biology and 6 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Ai-Chu Huang's work include Metabolism and Genetic Disorders (9 papers), Neonatal Health and Biochemistry (6 papers) and Mitochondrial Function and Pathology (5 papers). Ai-Chu Huang is often cited by papers focused on Metabolism and Genetic Disorders (9 papers), Neonatal Health and Biochemistry (6 papers) and Mitochondrial Function and Pathology (5 papers). Ai-Chu Huang collaborates with scholars based in Taiwan, United States and Germany. Ai-Chu Huang's co-authors include Wuh‐Liang Hwu, Yin‐Hsiu Chien, Ni‐Chung Lee, Shu‐Chuan Chiang, Shu-Chuan Chiang, Pei‐Hsin Huang, Yuan-Tsong Chen, Joan Keutzer, Mei‐Hwan Wu and Chun‐An Chen and has published in prestigious journals such as PEDIATRICS, Archives of Disease in Childhood and Oncotarget.

In The Last Decade

Ai-Chu Huang

15 papers receiving 922 citations

Peers

Ai-Chu Huang

PHYSI

RHEUM

EPIDE

Clare Beesley United Kingdom

María Josep Coll Spain

I Maire France

Ting‐Rong Hsu Taiwan

Esmée Oussoren Netherlands

Alexander Broomfield United Kingdom

F. A. Beemer Netherlands

Deyanira Corzo United States

Rosanna Gatti Italy

Ana Cristina Puga United States

Clare Beesley United Kingdom

Ai-Chu Huang

607 ×1.0

PHYSI

241 ×0.7

RHEUM

288 ×1.0

189 ×0.7

262 ×1.3

EPIDE

Citations per year, relative to Ai-Chu Huang Ai-Chu Huang (= 1×) peers Clare Beesley

Countries citing papers authored by Ai-Chu Huang

Since Specialization

Citations

This map shows the geographic impact of Ai-Chu Huang'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 Ai-Chu Huang with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Ai-Chu Huang more than expected).

Fields of papers citing papers by Ai-Chu Huang

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Ai-Chu Huang. 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 Ai-Chu Huang. The network helps show where Ai-Chu Huang may publish in the future.

Co-authorship network of co-authors of Ai-Chu Huang

This figure shows the co-authorship network connecting the top 25 collaborators of Ai-Chu Huang. A scholar is included among the top collaborators of Ai-Chu Huang 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 Ai-Chu Huang. Ai-Chu Huang is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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15 of 15 papers shown

Hwu, Wuh‐Liang, Yin‐Hsiu Chien, Shieh‐Yueh Yang, et al.. (2019). Composite Scores of Plasma Tau and β-Amyloids Correlate with Dementia in Down Syndrome. ACS Chemical Neuroscience. 11(2). 191–196. 5 indexed citations

Lin, Po‐Han, Wen‐Hung Kuo, Ai-Chu Huang, et al.. (2016). Multiple gene sequencing for risk assessment in patients with early-onset or familial breast cancer. Oncotarget. 7(7). 8310–8320. 69 indexed citations

Roter, Debra, et al.. (2013). Parental discussion of G6PD deficiency and child health: implications for clinical practice. Archives of Disease in Childhood. 99(3). 251–255. 1 indexed citations

Chien, Yin‐Hsiu, et al.. (2012). Promising outcomes in glutaric aciduria type I patients detected by newborn screening. Metabolic Brain Disease. 28(1). 61–67. 28 indexed citations

Hwu, Wuh‐Liang, Yin‐Hsiu Chien, Ni‐Chung Lee, et al.. (2009). Newborn screening for Fabry disease in Taiwan reveals a high incidence of the later-onsetGLAmutation c.936+919G>A (IVS4+919G>A). Human Mutation. 30(10). 1397–1405. 263 indexed citations

Lee, Ni‐Chung, Nelson L.S. Tang, Yin‐Hsiu Chien, et al.. (2009). Diagnoses of newborns and mothers with carnitine uptake defects through newborn screening. Molecular Genetics and Metabolism. 100(1). 46–50. 78 indexed citations

Chien, Yin‐Hsiu, Ni‐Chung Lee, Beth L. Thurberg, et al.. (2009). Pompe Disease in Infants: Improving the Prognosis by Newborn Screening and Early Treatment. PEDIATRICS. 124(6). e1116–e1125. 166 indexed citations

Hwu, Wuh‐Liang, et al.. (2008). Early Detection of Glutaric Aciduria Type I by Newborn Screening in Taiwan. Journal of the Formosan Medical Association. 107(2). 139–144. 15 indexed citations

Lee, Ni‐Chung, Yin‐Hsiu Chien, Steven Shinn‐Forng Peng, et al.. (2008). Brain Damage by Mild Metabolic Derangements in Methylmalonic Acidemia. Pediatric Neurology. 39(5). 325–329. 21 indexed citations

10.

Chien, Yin‐Hsiu, Shu‐Chuan Chiang, Joan Keutzer, et al.. (2008). Early Detection of Pompe Disease by Newborn Screening Is Feasible: Results From the Taiwan Screening Program. PEDIATRICS. 122(1). e39–e45. 190 indexed citations

11.

Chien, Yin‐Hsiu, Shu-Chuan Chiang, Ai-Chu Huang, et al.. (2005). Phenylalanine hydroxylase deficiency: intelligence of patients after early dietary treatment.. PubMed. 45(6). 320–3. 4 indexed citations

12.

Chien, Yin‐Hsiu, Shu-Chuan Chiang, Ai-Chu Huang, & Wuh‐Liang Hwu. (2004). Spectrum of hypermethioninemia in neonatal screening. Early Human Development. 81(6). 529–533. 30 indexed citations

13.

Chien, Yin‐Hsiu, Chia‐Chi Hsu, Ai-Chu Huang, et al.. (2004). Poor Outcome for Neonatal-Type Nonketotic Hyperglycinemia Treated With High-Dose Sodium Benzoate and Dextromethorphan. Journal of Child Neurology. 19(1). 39–42. 33 indexed citations

14.

Chien, Yin‐Hsiu, et al.. (2004). Mutation spectrum in Taiwanese patients with phenylalanine hydroxylase deficiency and a founder effect for the R241C mutation. Human Mutation. 23(2). 206–206. 28 indexed citations

15.

Hwu, Wuh‐Liang, et al.. (2003). Neonatal screening and monitoring system in Taiwan.. PubMed. 34 Suppl 3. 91–3. 9 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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