Sing-Ping Huang

2.9k total citations
14 papers, 2.3k citations indexed

About

Sing-Ping Huang is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Sing-Ping Huang has authored 14 papers receiving a total of 2.3k indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Molecular Biology, 7 papers in Genetics and 3 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Sing-Ping Huang's work include Congenital heart defects research (4 papers), Genetic Syndromes and Imprinting (3 papers) and Epigenetics and DNA Methylation (3 papers). Sing-Ping Huang is often cited by papers focused on Congenital heart defects research (4 papers), Genetic Syndromes and Imprinting (3 papers) and Epigenetics and DNA Methylation (3 papers). Sing-Ping Huang collaborates with scholars based in United States, Australia and Japan. Sing-Ping Huang's co-authors include Alexander Grinberg, Heiner Westphal, John Drago, Yangu Zhao, Forbes D. Porter, Christopher A. Wassif, Hui Z. Sheng, Eric J. Lee, Eric Lee and Karl Pfeifer and has published in prestigious journals such as Nature, Science and Proceedings of the National Academy of Sciences.

In The Last Decade

Sing-Ping Huang

13 papers receiving 2.2k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Sing-Ping Huang United States	12	1.7k	864	385	258	221	14	2.3k
A. Paula Monaghan United States	30	4.0k 2.4×	1.2k 1.3×	484 1.3×	352 1.4×	172 0.8×	42	5.4k
Tayfun Özçelık Türkiye	30	1.5k 0.9×	859 1.0×	541 1.4×	317 1.2×	255 1.2×	59	3.1k
Hui Z. Sheng China	21	2.6k 1.5×	744 0.9×	797 2.1×	246 1.0×	137 0.6×	39	3.6k
C. Beldjord France	22	1.0k 0.6×	887 1.0×	213 0.6×	267 1.0×	336 1.5×	54	2.5k
Patrick Calvas France	31	2.1k 1.3×	1.4k 1.6×	346 0.9×	348 1.3×	207 0.9×	104	3.9k
Brian G. Condie United States	30	2.4k 1.4×	618 0.7×	632 1.6×	299 1.2×	203 0.9×	46	3.3k
Montserrat Milà Spain	34	2.2k 1.3×	1.8k 2.1×	511 1.3×	238 0.9×	138 0.6×	140	4.0k
Angeliki Louvi United States	31	2.4k 1.4×	1.1k 1.3×	520 1.4×	378 1.5×	200 0.9×	43	4.0k
Chijen R. Lin United States	16	2.2k 1.3×	834 1.0×	337 0.9×	166 0.6×	206 0.9×	19	3.8k
G. Giacomo Consalez Italy	35	2.0k 1.2×	667 0.8×	723 1.9×	371 1.4×	155 0.7×	93	3.3k

Countries citing papers authored by Sing-Ping Huang

Since Specialization

Citations

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

Fields of papers citing papers by Sing-Ping Huang

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Sing-Ping Huang

This figure shows the co-authorship network connecting the top 25 collaborators of Sing-Ping Huang. A scholar is included among the top collaborators of Sing-Ping 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 Sing-Ping Huang. Sing-Ping 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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14 of 14 papers shown

Huang, Sing-Ping, et al.. (2015). HOXC8 (homeobox C8). Atlas of Genetics and Cytogenetics in Oncology and Haematology.

Fu, Xi, et al.. (2012). Mutations in NR5A1 and PIN1 associated with idiopathic hypogonadotropic hypogonadism. Genetics and Molecular Research. 11(4). 4575–4584. 6 indexed citations

Park, Kyeyoon, Elizabeth A. Sellars, Alexander Grinberg, Sing-Ping Huang, & Karl Pfeifer. (2004). TheH19Differentially Methylated Region Marks the Parental Origin of a Heterologous Locus without Gametic DNA Methylation. Molecular and Cellular Biology. 24(9). 3588–3595. 36 indexed citations

Grinberg, Alex, et al.. (2003). Vasopressin receptor 1a-mediated negative regulation of B cell receptor signaling. Journal of Neuroimmunology. 135(1-2). 72–81. 39 indexed citations

Mukhopadhyay, Mahua, Andreas Teufel, Tsuyoshi Yamashita, et al.. (2003). Functional ablation of the mouseLdb1gene results in severe patterning defects during gastrulation. Development. 130(3). 495–505. 129 indexed citations

Srivastava, M. P., et al.. (2000). H19 and Igf2 monoallelic expression is regulated in two distinct ways by a shared cis acting regulatory region upstream of H19. Genes & Development. 14(10). 1186–1195. 123 indexed citations

Birk, Ohad S., Christopher A. Wassif, Tiziana Cogliati, et al.. (2000). The LIM homeobox gene Lhx9 is essential for mouse gonad formation. Nature. 403(6772). 909–913. 281 indexed citations

Srivastava, M. P., Kyeyoon Park, Elizabeth Ives, et al.. (2000). A transcriptional insulator at the imprinted H19/Igf2 locus. Genes & Development. 14(15). 1908–1919. 131 indexed citations

Zhao, Yangu, Hui Z. Sheng, Alexander Grinberg, et al.. (1999). Control of Hippocampal Morphogenesis and Neuronal Differentiation by the LIM Homeobox Gene Lhx5. Science. 284(5417). 1155–1158. 139 indexed citations

10.

Zhao, Yangu, Andreas C. Tomac, Alexander Grinberg, et al.. (1999). Isolated cleft palate in mice with a targeted mutation of the LIM homeobox gene Lhx8. Proceedings of the National Academy of Sciences. 96(26). 15002–15006. 134 indexed citations

11.

Porter, Forbes D., John Drago, Yang Xu, et al.. (1997). Lhx2, a LIM homeobox gene, is required for eye, forebrain, and definitive erythrocyte development. Development. 124(15). 2935–2944. 390 indexed citations

12.

Sheng, Hui Z., Alexander B. Zhadanov, B Mosinger, et al.. (1996). Specification of Pituitary Cell Lineages by the LIM Homeobox Gene Lhx3 . Science. 272(5264). 1004–1007. 353 indexed citations

13.

Drago, John, C R Gerfen, Jean E. Lachowicz, et al.. (1994). Altered striatal function in a mutant mouse lacking D1A dopamine receptors.. Proceedings of the National Academy of Sciences. 91(26). 12564–12568. 282 indexed citations

14.

Tybulewicz, Victor L. J., Michel L. Tremblay, Rob Willemsen, et al.. (1992). Animal model of Gaucher's disease from targeted disruption of the mouse glucocerebrosidase gene. Nature. 357(6377). 407–410. 245 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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