H.‐W. Yoo

464 total citations
17 papers, 321 citations indexed

About

H.‐W. Yoo is a scholar working on Molecular Biology, Endocrinology, Diabetes and Metabolism and Clinical Biochemistry. According to data from OpenAlex, H.‐W. Yoo has authored 17 papers receiving a total of 321 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Molecular Biology, 7 papers in Endocrinology, Diabetes and Metabolism and 5 papers in Clinical Biochemistry. Recurrent topics in H.‐W. Yoo's work include Metabolism and Genetic Disorders (5 papers), Neonatal Health and Biochemistry (4 papers) and Genetic Syndromes and Imprinting (3 papers). H.‐W. Yoo is often cited by papers focused on Metabolism and Genetic Disorders (5 papers), Neonatal Health and Biochemistry (4 papers) and Genetic Syndromes and Imprinting (3 papers). H.‐W. Yoo collaborates with scholars based in South Korea, United States and United Kingdom. H.‐W. Yoo's co-authors include Robert J. Desnick, Cecilia A. Warner, Eun Jung Choi, Choong Gon Choi, Jung‐Sun Kim, Jee Ho Choi, Pierre Chatelain, Luciano Tatò, Adam Stevens and Benoit Destenaves and has published in prestigious journals such as Nucleic Acids Research, Journal of Clinical Investigation and Neurology.

In The Last Decade

H.‐W. Yoo

17 papers receiving 318 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
H.‐W. Yoo South Korea	11	166	75	64	62	56	17	321
Rafael Muley Spain	9	166 1.0×	10 0.1×	44 0.7×	27 0.4×	13 0.2×	11	336
Paulina Halat Poland	6	173 1.0×	12 0.2×	19 0.3×	12 0.2×	19 0.3×	8	259
Soledad Kleppe United States	8	153 0.9×	5 0.1×	32 0.5×	57 0.9×	15 0.3×	12	333
Greta Lyons United Kingdom	13	156 0.9×	19 0.3×	21 0.3×	58 0.9×	380 6.8×	30	556
Joanna Taybert Poland	8	118 0.7×	17 0.2×	111 1.7×	35 0.6×	9 0.2×	17	274
Andrew Y. Shuen Canada	11	190 1.1×	13 0.2×	24 0.4×	39 0.6×	12 0.2×	16	412
Shoshi Shpitzen Israel	11	110 0.7×	46 0.6×	108 1.7×	12 0.2×	66 1.2×	15	400
Kevin Larimore United States	8	218 1.3×	13 0.2×	69 1.1×	49 0.8×	37 0.7×	16	452
Letizia Casula Italy	11	229 1.4×	10 0.1×	33 0.5×	27 0.4×	51 0.9×	15	403

Countries citing papers authored by H.‐W. Yoo

Since Specialization

Citations

This map shows the geographic impact of H.‐W. Yoo'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 H.‐W. Yoo with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites H.‐W. Yoo more than expected).

Fields of papers citing papers by H.‐W. Yoo

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by H.‐W. Yoo. 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 H.‐W. Yoo. The network helps show where H.‐W. Yoo may publish in the future.

Co-authorship network of co-authors of H.‐W. Yoo

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

All Works

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17 of 17 papers shown

Suh, Byung‐Kyu, Cheol Woo Ko, Chang Ho Shin, et al.. (2017). Recombinant growth hormone therapy for prepubertal children with idiopathic short stature in Korea: a phase III randomized trial. Journal of Endocrinological Investigation. 41(4). 475–483. 9 indexed citations

Clayton, Peter, Pierre Chatelain, Luciano Tatò, et al.. (2013). A pharmacogenomic approach to the treatment of children with GH deficiency or Turner syndrome. European Journal of Endocrinology. 169(3). 277–289. 25 indexed citations

Stevens, Adam, Peter Clayton, Luciano Tatò, et al.. (2013). Pharmacogenomics of insulin-like growth factor-I generation during GH treatment in children with GH deficiency or Turner syndrome. The Pharmacogenomics Journal. 14(1). 54–62. 27 indexed citations

Yoon, Young-Sil, Chang‐Seok Ki, Hee Jae Huh, et al.. (2013). Clinical Characterization and Molecular Classification of 12 Korean Patients with Pseudohypoparathyroidism and Pseudopseudohypoparathyroidism. Experimental and Clinical Endocrinology & Diabetes. 121(9). 539–545. 11 indexed citations

Choi, Jin‐Ho, Hye Young Jin, Bong‐Ki Lee, et al.. (2011). Clinical Phenotype and Mutation Spectrum of the CYP21A2 Gene in Patients with Steroid 21-Hydroxylase Deficiency. Experimental and Clinical Endocrinology & Diabetes. 120(1). 23–27. 15 indexed citations

Yoo, H.‐W., et al.. (2011). Thyroid Dysfunctions of Prematurity and Impacts on Neurodevelopmental Outcome. Pediatric Research. 70. 626–626. 2 indexed citations

Park, Jeong‐Yeol, et al.. (2008). Identification of a novel human Rad51 variant that promotes DNA strand exchange. Nucleic Acids Research. 36(10). 3226–3234. 15 indexed citations

Choi, Eun Jung, et al.. (2006). Characteristics of CADASIL in Korea. Neurology. 66(10). 1511–1516. 74 indexed citations

Thuluvath, Paul J., Florence Wong, H.‐W. Yoo, et al.. (2006). Oral V₂ receptor antagonist (RWJ‐351647) in patients with cirrhosis and ascites: a randomized, double‐blind, placebo‐controlled, single ascending dose study. Alimentary Pharmacology & Therapeutics. 24(6). 973–982. 18 indexed citations

10.

Choi, Jee Ho, et al.. (2006). Two cases of citrullinaemia presenting with stroke. Journal of Inherited Metabolic Disease. 29(1). 182–183. 14 indexed citations

11.

Yoo, H.‐W., et al.. (2003). A Case of Continuous Venovenous Hemodiafiltration in the Treatment of Neonatal Hyperammonemia Due to Methylmalonic Acidemia.. 7(1). 96–102. 2 indexed citations

12.

Yoon, Hye‐Ran, Arnold W. Strauss, & H.‐W. Yoo. (2001). Sudden death in a Korean infant with very long‐chain acyl‐CoA dehydrogenase deficiency. Journal of Inherited Metabolic Disease. 24(3). 407–408. 3 indexed citations

13.

Yoo, H.‐W., et al.. (2000). Identification of four novel mutations in five unrelated Korean families with Fabry disease. Clinical Genetics. 58(3). 228–233. 13 indexed citations

14.

Yoo, H.‐W., et al.. (1998). Molecular and Clinical Characterization of Korean Patients with Congenital Lipoid Adrenal Hyperplasia. Journal of Pediatric Endocrinology and Metabolism. 11(6). 707–11. 26 indexed citations

15.

Yoo, H.‐W. & Gheun‐Ho Kim. (1998). Prenatal molecular evaluation of six fetuses in four unrelated Korean families with ornithine transcarbamylase deficiency. Journal of Korean Medical Science. 13(2). 179–179. 4 indexed citations

16.

Yoo, H.‐W., Gon‐Ho Kim, & Dong‐Hun Lee. (1995). Identification of new mutations in the ornithine transcarbamylase (OTC) gene in Korean families. Journal of Inherited Metabolic Disease. 19(1). 31–42. 9 indexed citations

17.

Warner, Cecilia A., et al.. (1992). Congenital erythropoietic porphyria: identification and expression of exonic mutations in the uroporphyrinogen III synthase gene.. Journal of Clinical Investigation. 89(2). 693–700. 54 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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