Parker B. Antin

7.2k total citations
70 papers, 3.9k citations indexed

About

Parker B. Antin is a scholar working on Molecular Biology, Genetics and Cardiology and Cardiovascular Medicine. According to data from OpenAlex, Parker B. Antin has authored 70 papers receiving a total of 3.9k indexed citations (citations by other indexed papers that have themselves been cited), including 58 papers in Molecular Biology, 17 papers in Genetics and 12 papers in Cardiology and Cardiovascular Medicine. Recurrent topics in Parker B. Antin's work include Congenital heart defects research (20 papers), Animal Genetics and Reproduction (13 papers) and Cardiomyopathy and Myosin Studies (10 papers). Parker B. Antin is often cited by papers focused on Congenital heart defects research (20 papers), Animal Genetics and Reproduction (13 papers) and Cardiomyopathy and Myosin Studies (10 papers). Parker B. Antin collaborates with scholars based in United States, Italy and Germany. Parker B. Antin's co-authors include Tatiana A. Yatskievych, Howard Holtzer, Diana K. Darnell, Charles P. Ordahl, Carol C. Gregorio, Andrea N. Ladd, V T Nachmias, Andrzej A. Dlugosz, Simran Kaur and Stephen Dalton and has published in prestigious journals such as Science, Proceedings of the National Academy of Sciences and Nucleic Acids Research.

In The Last Decade

Parker B. Antin

70 papers receiving 3.8k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Parker B. Antin United States 34 3.0k 745 682 567 542 70 3.9k
Denise Paulin France 35 3.0k 1.0× 483 0.6× 1.4k 2.0× 229 0.4× 466 0.9× 86 4.3k
David M. Bader United States 38 3.9k 1.3× 1.0k 1.4× 621 0.9× 355 0.6× 734 1.4× 94 5.3k
Didier Montarras France 35 4.9k 1.7× 472 0.6× 580 0.9× 571 1.0× 676 1.2× 82 5.7k
Frank L. Conlon United States 33 5.4k 1.8× 349 0.5× 591 0.9× 1.8k 3.1× 690 1.3× 87 6.2k
Cecilia W. Lo United States 36 3.3k 1.1× 343 0.5× 359 0.5× 161 0.3× 723 1.3× 67 3.9k
Mario Looso Germany 31 2.2k 0.8× 392 0.5× 307 0.5× 369 0.7× 216 0.4× 84 3.0k
Masanori Taira Japan 42 5.0k 1.7× 232 0.3× 728 1.1× 307 0.5× 957 1.8× 133 6.0k
Juan Carlos Izpisúa‐Belmonte United States 32 4.4k 1.5× 248 0.3× 463 0.7× 773 1.4× 1.3k 2.3× 41 5.5k
Karen A. Knudsen United States 36 3.5k 1.2× 314 0.4× 1.2k 1.7× 392 0.7× 431 0.8× 68 4.7k
Charles P. Ordahl United States 41 5.4k 1.8× 1.3k 1.7× 566 0.8× 158 0.3× 941 1.7× 80 6.2k

Countries citing papers authored by Parker B. Antin

Since Specialization
Citations

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

Fields of papers citing papers by Parker B. Antin

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Parker B. Antin. 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 Parker B. Antin. The network helps show where Parker B. Antin may publish in the future.

Co-authorship network of co-authors of Parker B. Antin

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

All Works

20 of 20 papers shown
1.
Ronda, Luca, Soi Bui, Mitla Garcia‐Maya, et al.. (2023). Cysteine Enrichment Mediates Co-Option of Uricase in Reptilian Skin and Transition to Uricotelism. Molecular Biology and Evolution. 40(9). 4 indexed citations
2.
Antin, Parker B., et al.. (2012). Olfactomedin-1 activity identifies a cell invasion checkpoint during epithelial-mesenchymal transition in the embryonic heart. Disease Models & Mechanisms. 6(3). 632–42. 18 indexed citations
3.
Darnell, Diana K., et al.. (2011). Accelerated evolution of 3'avian FOXE1 genes, and thyroid and feather specific expression of chicken FoxE1. BMC Evolutionary Biology. 11(1). 302–302. 2 indexed citations
4.
Darnell, Diana K., Stacey Stanislaw, Simran Kaur, & Parker B. Antin. (2010). Whole mount in situ hybridization detection of mRNAs using short LNA containing DNA oligonucleotide probes. RNA. 16(3). 632–637. 30 indexed citations
5.
Tsukada, Takehiro, Christopher T. Pappas, Natalia Moroz, et al.. (2010). Leiomodin-2 is an antagonist of tropomodulin-1 at the pointed end of the thin filaments in cardiac muscle. Journal of Cell Science. 123(18). 3136–3145. 86 indexed citations
6.
Konieczka, Jay H., et al.. (2010). Arsenic Exposure Perturbs Epithelial-Mesenchymal Cell Transition and Gene Expression In a Collagen Gel Assay. Toxicological Sciences. 116(1). 273–285. 17 indexed citations
7.
Burt, David W., Wilfrid Carré, Mark Fell, et al.. (2009). The chicken gene nomenclature committee report. BMC Genomics. 10(Suppl 2). S5–S5. 45 indexed citations
8.
Hardy, Katharine M., Robert J. Garriock, Tatiana A. Yatskievych, et al.. (2008). Non-canonical Wnt signaling through Wnt5a/b and a novel Wnt11 gene, Wnt11b, regulates cell migration during avian gastrulation. Developmental Biology. 320(2). 391–401. 68 indexed citations
9.
Darnell, Diana K., et al.. (2006). MicroRNA expression during chick embryo development. Developmental Dynamics. 235(11). 3156–3165. 204 indexed citations
10.
Antin, Parker B. & Jay H. Konieczka. (2005). Genomic resources for chicken. Developmental Dynamics. 232(4). 877–882. 12 indexed citations
11.
Vokes, Steven A., Tatiana A. Yatskievych, Ronald L. Heimark, et al.. (2004). Hedgehog signaling is essential for endothelial tube formation during vasculogenesis. Development. 131(17). 4371–4380. 160 indexed citations
12.
Baker, Robert K. & Parker B. Antin. (2003). Ephs and ephrins during early stages of chick embryogenesis. Developmental Dynamics. 228(1). 128–142. 38 indexed citations
13.
Antin, Parker B., et al.. (2002). Precocious expression of cardiac troponin T in early chick embryos is independent of bone morphogenetic protein signaling. Developmental Dynamics. 225(3). 376–376. 2 indexed citations
14.
Baker, Robert K., et al.. (2001). Expression of the receptor tyrosine kinase gene EphB3 during early stages of chick embryo development. Mechanisms of Development. 104(1-2). 129–132. 21 indexed citations
15.
Gregorio, Carol C., et al.. (2000). To the heart of myofibril assembly. Trends in Cell Biology. 10(9). 355–362. 119 indexed citations
16.
Yatskievych, Tatiana A., et al.. (1999). The RNA-binding protein gene, hermes, is expressed at high levels in the developing heart. Mechanisms of Development. 80(1). 77–86. 59 indexed citations
17.
Ladd, Andrea N., Tatiana A. Yatskievych, & Parker B. Antin. (1998). Regulation of Avian Cardiac Myogenesis by Activin/TGFβ and Bone Morphogenetic Proteins. Developmental Biology. 204(2). 407–419. 141 indexed citations
18.
Antin, Parker B., et al.. (1996). Expression of avian glypican is developmentally regulated. Developmental Dynamics. 207(1). 25–34. 15 indexed citations
19.
Antin, Parker B., et al.. (1996). Cloning and sequencing of a developmentally regulated avian mRNA containing the LEA motif found in plant seed proteins. Gene. 175(1-2). 187–191. 14 indexed citations
20.
Antin, Parker B., J H Mar, & Charles P. Ordahl. (1990). Single cell analysis of transfected gene expression in primary heart cultures containing multiple cell types.. PubMed. 6(7). 640–2, 645. 21 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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