Teresa Costa

5.1k total citations · 1 hit paper
47 papers, 3.3k citations indexed

About

Teresa Costa is a scholar working on Genetics, Molecular Biology and Surgery. According to data from OpenAlex, Teresa Costa has authored 47 papers receiving a total of 3.3k indexed citations (citations by other indexed papers that have themselves been cited), including 30 papers in Genetics, 20 papers in Molecular Biology and 7 papers in Surgery. Recurrent topics in Teresa Costa's work include Connective tissue disorders research (8 papers), Bacterial Genetics and Biotechnology (8 papers) and Genomic variations and chromosomal abnormalities (6 papers). Teresa Costa is often cited by papers focused on Connective tissue disorders research (8 papers), Bacterial Genetics and Biotechnology (8 papers) and Genomic variations and chromosomal abnormalities (6 papers). Teresa Costa collaborates with scholars based in Canada, United States and Portugal. Teresa Costa's co-authors include Adriano O. Henriques, Lı́gia O. Martins, George H. Jones, Miguel Teixeira, Cláudio M. Soares, Manuela M. Pereira, Petros Tsipouras, Linheng Li, L Hood and Yu Deng and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Biological Chemistry and Nature Genetics.

In The Last Decade

Teresa Costa

47 papers receiving 3.2k citations

Hit Papers

align trajectories sort by overperformance

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.

Alagille syndrome is caused by mutations in human Jagged1, which encodes a ligand for Notch1

1997 928 citations Linheng Li, Yu Deng et al. Nature Genetics profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Teresa Costa Canada	27	1.7k	1.3k	666	573	302	47	3.3k
Steven E. Artandi United States	41	5.3k 3.2×	649 0.5×	542 0.8×	349 0.6×	593 2.0×	70	7.9k
William Warren United States	35	3.0k 1.8×	1.3k 1.0×	185 0.3×	642 1.1×	98 0.3×	74	4.7k
Karen Chapman United States	26	2.6k 1.6×	420 0.3×	225 0.3×	552 1.0×	379 1.3×	43	4.0k
Kit Sing Au United States	31	1.2k 0.7×	628 0.5×	358 0.5×	194 0.3×	66 0.2×	85	3.1k
Michel Ouellette Canada	8	2.9k 1.8×	466 0.4×	269 0.4×	283 0.5×	425 1.4×	16	4.9k
Heather Macdonald-Bravo Germany	17	2.8k 1.7×	691 0.5×	379 0.6×	131 0.2×	117 0.4×	21	4.5k
Uwe Karsten Germany	39	3.5k 2.1×	449 0.3×	403 0.6×	80 0.1×	183 0.6×	142	5.1k
Ji‐Fan Hu United States	44	4.6k 2.8×	1.4k 1.1×	292 0.4×	244 0.4×	170 0.6×	145	6.3k
Harmen J.G. van de Werken Netherlands	30	3.4k 2.0×	691 0.5×	229 0.3×	577 1.0×	83 0.3×	84	4.4k
Yue Lu United States	43	4.2k 2.5×	846 0.6×	333 0.5×	304 0.5×	40 0.1×	216	6.8k

Countries citing papers authored by Teresa Costa

Since Specialization

Citations

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

Fields of papers citing papers by Teresa Costa

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Teresa Costa

This figure shows the co-authorship network connecting the top 25 collaborators of Teresa Costa. A scholar is included among the top collaborators of Teresa Costa 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 Teresa Costa. Teresa Costa 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

Costa, Teresa, et al.. (2012). Pneumomediastino espontâneo: relato de um caso. Revista da Associação Médica Brasileira. 58(3). 355–357. 2 indexed citations

Alexander, Roger P., et al.. (2009). RodZ, a component of the bacterial core morphogenic apparatus. Proceedings of the National Academy of Sciences. 106(4). 1239–1244. 132 indexed citations

Perveen, Rahat, Peter Clayton, Catherine M. Hall, et al.. (2009). X-linked isolated growth hormone deficiency: expanding the phenotypic spectrum of SOX3 polyalanine tract expansions. Clinical Dysmorphology. 18(4). 218–221. 28 indexed citations

Buysse, Karen, William Reardon, Lakshmi Mehta, et al.. (2009). The 12q14 microdeletion syndrome: Additional patients and further evidence that HMGA2 is an important genetic determinant for human height. European Journal of Medical Genetics. 52(2-3). 101–107. 43 indexed citations

Chitayat, David, Sarah Keating, Dina J. Zand, et al.. (2008). Chondrodysplasia punctata associated with maternal autoimmune diseases: Expanding the spectrum from systemic lupus erythematosus (SLE) to mixed connective tissue disease (MCTD) and scleroderma report of eight cases. American Journal of Medical Genetics Part A. 146A(23). 3038–3053. 25 indexed citations

Renault, Nisa, Sarah Dyack, Melanie J. Dobson, et al.. (2007). Heritable skewed X-chromosome inactivation leads to haemophilia A expression in heterozygous females. European Journal of Human Genetics. 15(6). 628–637. 61 indexed citations

Menten, Björn, Karen Buysse, Farah Zahir, et al.. (2007). Osteopoikilosis, short stature and mental retardation as key features of a new microdeletion syndrome on 12q14. Journal of Medical Genetics. 44(4). 264–268. 44 indexed citations

Renella, Raffaele, Martine LeMerrer, Yasemin Alanay, et al.. (2006). Spondyloenchondrodysplasia with spasticity, cerebral calcifications, and immune dysregulation: Clinical and radiographic delineation of a pleiotropic disorder. American Journal of Medical Genetics Part A. 140A(6). 541–550. 37 indexed citations

Lachlan, Katherine, Sheila Youings, Teresa Costa, P. A. Jacobs, & N. Simon Thomas. (2005). A clinical and molecular study of 26 females with Xp deletions with special emphasis on inherited deletions. Human Genetics. 118(5). 640–651. 47 indexed citations

10.

Schlade‐Bartusiak, Kamilla, Teresa Costa, Anne Summers, Małgorzata J.M. Nowaczyk, & Diane W. Cox. (2005). FISH‐mapping of telomeric 14q32 deletions: Search for the cause of seizures. American Journal of Medical Genetics Part A. 138A(3). 218–224. 28 indexed citations

11.

Brito, Catarina, et al.. (2003). Importance of Cys, Gln, and Tyr from the Transmembrane Domain of Human α3/4 Fucosyltransferase III for Its Localization and Sorting in the Golgi of Baby Hamster Kidney Cells. Journal of Biological Chemistry. 278(9). 7624–7629. 25 indexed citations

12.

Martins, Lı́gia O., Cláudio M. Soares, Manuela M. Pereira, et al.. (2002). Molecular and Biochemical Characterization of a Highly Stable Bacterial Laccase That Occurs as a Structural Component of the Bacillus subtilis Endospore Coat. Journal of Biological Chemistry. 277(21). 18849–18859. 458 indexed citations

13.

Costa, Teresa, Robert C. Pashby, Marlene J. Huggins, & Ikuko Teshima. (1998). Deletion 3q in Two Patients With Blepharophimosis-ptosis-epicanthus Inversus Syndrome (BPES). Journal of Pediatric Ophthalmology & Strabismus. 35(5). 271–276. 15 indexed citations

14.

Hughes, Helen E., et al.. (1998). Severe prenatal growth retardation, dysmorphic features, pigmentary retinopathy, and generalized absence of subcutaneous tissues: a new entity?. Clinical Dysmorphology. 7(4). 263–268. 3 indexed citations

15.

Costa, Teresa, et al.. (1998). Grebe syndrome: Clinical and radiographic findings in affected individuals and heterozygous carriers. American Journal of Medical Genetics. 75(5). 523–529. 40 indexed citations

16.

Li, Linheng, Yu Deng, Anna Genin, et al.. (1997). Alagille syndrome is caused by mutations in human Jagged1, which encodes a ligand for Notch1. Nature Genetics. 16(3). 243–251. 928 indexed citations breakdown →

17.

Costa, Teresa, Wenda Greer, G Rysiecki, J. Raymond Buncic, & P N Ray. (1997). Monozygotic twins discordant for Aicardi syndrome.. Journal of Medical Genetics. 34(8). 688–691. 17 indexed citations

18.

Thomas, Jack, Michael W. Kilpatrick, Ludwig Erlacher, et al.. (1997). Disruption of human limb morphogenesis by a dominant negative mutation in CDMP1. Nature Genetics. 17(1). 58–64. 278 indexed citations

19.

Osborne, Lucy R., Duane W. Martindale, Stephen W. Scherer, et al.. (1996). Identification of Genes from a 500-kb Region at 7q11.23 That Is Commonly Deleted in Williams Syndrome Patients. Genomics. 36(2). 328–336. 83 indexed citations

20.

Costa, Teresa, et al.. (1985). The Okihiro syndrome of duane anomaly, radial ray abnormalities, and deafness. American Journal of Medical Genetics. 22(2). 273–280. 38 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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