Antonio Baldini

14.6k total citations · 3 hit papers
191 papers, 10.8k citations indexed

About

Antonio Baldini is a scholar working on Molecular Biology, Genetics and Plant Science. According to data from OpenAlex, Antonio Baldini has authored 191 papers receiving a total of 10.8k indexed citations (citations by other indexed papers that have themselves been cited), including 160 papers in Molecular Biology, 74 papers in Genetics and 36 papers in Plant Science. Recurrent topics in Antonio Baldini's work include Congenital heart defects research (92 papers), Genomic variations and chromosomal abnormalities (45 papers) and Chromosomal and Genetic Variations (34 papers). Antonio Baldini is often cited by papers focused on Congenital heart defects research (92 papers), Genomic variations and chromosomal abnormalities (45 papers) and Chromosomal and Genetic Variations (34 papers). Antonio Baldini collaborates with scholars based in United States, Italy and United Kingdom. Antonio Baldini's co-authors include Elizabeth A. Lindsay, Richard A. Wells, Jacob W. IJdo, Stephen T. Reeders, David C. Ward, Masae Morishima, Tuong Huynh, Vesna Jurecic, Peter Scambler and Zhen Zhang and has published in prestigious journals such as Nature, Proceedings of the National Academy of Sciences and Nucleic Acids Research.

In The Last Decade

Antonio Baldini

186 papers receiving 10.6k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

p57KIP2, a structurally distinct member of the p21CIP1 Cdk inhibitor family, is a candidate tumor suppressor gene.

1995 801 citations Antonio Baldini et al. profile →
Tbx1 haploinsufficiency in the DiGeorge syndrome region causes aortic arch defects in mice

2001 747 citations Tuong Huynh, Vesna Jurecic et al. profile →
Improved telomere detection using a telomere repeat probe (TTAGGG)_ngenerated by PCR

1991 517 citations Antonio Baldini et al. profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Antonio Baldini United States	50	8.5k	3.4k	1.9k	1.4k	1.2k	191	10.8k
Virginia E. Papaioannou United States	62	12.6k 1.5×	4.0k 1.2×	1.4k 0.8×	429 0.3×	937 0.8×	176	17.8k
Helen Donis-Keller United States	38	4.8k 0.6×	2.4k 0.7×	979 0.5×	721 0.5×	682 0.6×	105	8.6k
Thomas W. Glover United States	60	10.3k 1.2×	4.5k 1.3×	722 0.4×	1.2k 0.8×	1.2k 1.0×	159	15.8k
Manfred Gessler Germany	53	8.6k 1.0×	1.7k 0.5×	609 0.3×	535 0.4×	1.4k 1.2×	165	10.8k
Bruce A.J. Ponder United Kingdom	45	5.0k 0.6×	3.8k 1.1×	866 0.5×	932 0.6×	464 0.4×	88	9.4k
Nicholas D. Hastie United Kingdom	54	9.7k 1.1×	3.0k 0.9×	386 0.2×	560 0.4×	1.4k 1.2×	128	12.1k
Brian L. Black United States	49	8.5k 1.0×	1.7k 0.5×	1.3k 0.7×	324 0.2×	581 0.5×	103	10.0k
Toru Nakano Japan	68	12.9k 1.5×	2.7k 0.8×	608 0.3×	2.5k 1.7×	479 0.4×	208	18.9k
James C. Cross Canada	65	7.6k 0.9×	2.4k 0.7×	579 0.3×	321 0.2×	640 0.5×	142	14.8k
S. Steven Potter United States	60	9.2k 1.1×	3.0k 0.9×	284 0.2×	741 0.5×	1.3k 1.1×	166	12.4k

Countries citing papers authored by Antonio Baldini

Since Specialization

Citations

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

Fields of papers citing papers by Antonio Baldini

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Antonio Baldini. 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 Antonio Baldini. The network helps show where Antonio Baldini may publish in the future.

Co-authorship network of co-authors of Antonio Baldini

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

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

Bilio, Marchesa, Johannes Liebig, Katharina Jechow, et al.. (2025). Tbx1 stabilizes differentiation of the cardiopharyngeal mesoderm and drives morphogenesis in the pharyngeal apparatus. Development. 152(12).

Caterino, Marianna, Debora Paris, Giulia Torromino, et al.. (2024). Brain and behavioural anomalies caused byTbx1haploinsufficiency are corrected by vitamin B12. Life Science Alliance. 8(2). e202403075–e202403075. 2 indexed citations

Lania, Gabriella, Monica Franzese, Noritaka Adachi, et al.. (2022). A phenotypic rescue approach identifies lineage regionalization defects in a mouse model of DiGeorge syndrome. Disease Models & Mechanisms. 15(9). 4 indexed citations

Du, Qiumei, Ashwani Kumar, Chao Xing, et al.. (2022). Mesenchymal cell replacement corrects thymic hypoplasia in murine models of 22q11.2 deletion syndrome. Journal of Clinical Investigation. 132(22). 7 indexed citations

Nomaru, Hiroko, Yang Liu, Christopher De Bono, et al.. (2021). Single cell multi-omic analysis identifies a Tbx1-dependent multilineage primed population in murine cardiopharyngeal mesoderm. Nature Communications. 12(1). 6645–6645. 32 indexed citations

Lü, Wei, Wenfeng Wang, Junjie Yang, et al.. (2020). Pharyngeal epithelial deletion of Tbx1 causes caudal pharyngeal arch defect but not cardiac conotruncal anomaly. Biochemical and Biophysical Research Communications. 533(4). 1315–1322. 2 indexed citations

Alfano, Daniela, et al.. (2019). Tbx1 regulates extracellular matrix-cell interactions in the second heart field. Human Molecular Genetics. 28(14). 2295–2308. 23 indexed citations

Moreau, Julie, Scott Kesteven, Ella MMA Martin, et al.. (2019). Gene-environment interaction impacts on heart development and embryo survival. Development. 146(4). 49 indexed citations

Baldini, Antonio, et al.. (2016). Tbx1. Current topics in developmental biology. 122. 223–243. 49 indexed citations

10.

Gao, Song, María Moreno, Steve Eliason, et al.. (2015). TBX1 protein interactions and microRNA-96-5p regulation controls cell proliferation during craniofacial and dental development: implications for 22q11.2 deletion syndrome. Human Molecular Genetics. 24(8). 2330–2348. 47 indexed citations

11.

Chen, Li, Annalisa Mupo, Tuong Huynh, et al.. (2010). Tbx1 regulates Vegfr3 and is required for lymphatic vessel development. The Journal of Cell Biology. 189(3). 417–424. 61 indexed citations

12.

Zhang, Zhen, Tuong Huynh, & Antonio Baldini. (2006). Mesodermal expression of Tbx1 is necessary and sufficient for pharyngeal arch and cardiac outflow tract development. Development. 133(18). 3587–3595. 152 indexed citations

13.

Xu, Huansheng, et al.. (2006). Tbx1 regulates population, proliferation and cell fate determination of otic epithelial cells. Developmental Biology. 302(2). 670–682. 47 indexed citations

14.

Xu, Huansheng, Fabiana Cerrato, & Antonio Baldini. (2005). Timed mutation and cell-fate mapping reveal reiterated roles of Tbx1 during embryogenesis, and a crucial function during segmentation of the pharyngeal system via regulation of endoderm expansion. Development. 132(19). 4387–4395. 102 indexed citations

15.

Vincentz, Joshua W., John R. McWhirter, Cornelis Murre, Antonio Baldini, & Yasuhide Furuta. (2005). Fgf15 is required for proper morphogenesis of the mouse cardiac outflow tract. genesis. 41(4). 192–201. 52 indexed citations

16.

Baldini, Antonio. (1999). Is the genetic basis of DiGeorge syndrome in HAND?. Nature Genetics. 21(3). 246–247. 10 indexed citations

17.

Wang, Mei, So Hee Dho, Jun R. Huh, et al.. (1999). A 12-Mb Complete Coverage BAC Contig Map in Human Chromosome 16p13.1–p11.2. Genome Research. 9(8). 763–774. 15 indexed citations

18.

Rizzu, Patrizia, et al.. (1996). Cloning and comparative mapping of a gene deleted in DiGeorge and velocardiofacial syndromes conserved in the C.elegans genome.. UCL Discovery (University College London). 1 indexed citations

19.

Halford, Stephanie, et al.. (1993). Low-copy-number repeat sequences flank the DiGeorge/velo-cardio-facial syndrome loci at 22q11. Human Molecular Genetics. 2(2). 191–196. 66 indexed citations

20.

Ginzinger, David G., Viji Shridhar, Antonio Baldini, et al.. (1992). The human loci DNF15S2 and D3S94 have a high degree of sequence similarity to acyl-peptide hydrolase and are located at 3p21.3.. PubMed. 50(4). 826–33. 8 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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