Teresa Costa

5.1k citations

47 papers · 3.3k indexed · 1 hit paper · h-index 27

Molecular Biology top 5%
Genetics top 1%
Surgery top 5%
Plant Science top 5%
Biotechnology top 2%

Co-authors: Adriano O. Henriques Lı́gia O. Martins Manuela M. Pereira Cláudio M. Soares George H. Jones Miguel Teixeira Petros Tsipouras Linheng Li
Topics: Connective tissue disorders research (8 papers)Bacterial Genetics and Biotechnology (8 papers)Genomic variations and chromosomal abnormalities (6 papers)
Cited by: Genetics Developmental Neuroscience Biotechnology
Journals: Proceedings of the National Academy of Sciences Journal of Biological Chemistry Nature Genetics
Partner nations: Canada United States Portugal

In The Last Decade

Teresa Costa

47 papers receiving 3.2k 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.

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

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

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20 of 20 papers shown

#	Work	Indexed citations
1	Pneumomediastino espontâneo: relato de um caso 2012 ·Revista da Associação Médica Brasileira ·(unknown),(unknown),(unknown),(unknown),Teresa Costa,(unknown),Amélia Pereira	2
2	RodZ, a component of the bacterial core morphogenic apparatus 2009 ·Proceedings of the National Academy of Sciences ·(unknown),Roger P. Alexander,Teresa Costa,Adriano O. Henriques,Thierry Emonet,Christine Jacobs‐Wagner	132
3	The 12q14 microdeletion syndrome: Additional patients and further evidence that HMGA2 is an important genetic determinant for human height 2009 ·European Journal of Medical Genetics ·Karen Buysse,William Reardon,Lakshmi Mehta,Teresa Costa,(unknown),D. Kingsbury,(unknown),Barbara McGillivray,Jan Hellemans,Nicole de Leeuw,Bert B.A. de Vries,Frank Speleman,Björn Menten,Geert Mortier	43
4	X-linked isolated growth hormone deficiency: expanding the phenotypic spectrum of SOX3 polyalanine tract expansions 2009 ·Clinical Dysmorphology ·(unknown),Rahat Perveen,Peter Clayton,Catherine M. Hall,Teresa Costa,Annie Procter,(unknown),Dian Donnai,Graeme C. Black	28
5	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 2008 ·American Journal of Medical Genetics Part A ·David Chitayat,Sarah Keating,Dina J. Zand,Teresa Costa,Elaine H. Zackai,Earl D. Silverman,George E. Tiller,Sheila Unger,Stephen F. Miller,John Kingdom,Ants Toi,Cynthia J. Curry	25
6	Heritable skewed X-chromosome inactivation leads to haemophilia A expression in heterozygous females 2007 ·European Journal of Human Genetics ·Nisa Renault,Sarah Dyack,Melanie J. Dobson,Teresa Costa,Wan L. Lam,Wenda Greer	61
7	Osteopoikilosis, short stature and mental retardation as key features of a new microdeletion syndrome on 12q14 2007 ·Journal of Medical Genetics ·Björn Menten,Karen Buysse,Farah Zahir,Jan Hellemans,Sara Hamilton,Teresa Costa,Cecilia Fagerström,(unknown),D. Kingsbury,Barbara McGillivray,Marco A. Marra,Jan M. Friedman,Frank Speleman,Geert Mortier	44
8	Spondyloenchondrodysplasia with spasticity, cerebral calcifications, and immune dysregulation: Clinical and radiographic delineation of a pleiotropic disorder 2006 ·American Journal of Medical Genetics Part A ·Raffaele Renella,(unknown),Martine LeMerrer,Yasemin Alanay,Nurgün Kandemir,Georg Eich,Teresa Costa,Diana Ballhausen,Eugen Boltshauser,Luisa Bonafé,A Giedion,Sheila Unger,Andrea Superti‐Furga	37
9	FISH‐mapping of telomeric 14q32 deletions: Search for the cause of seizures 2005 ·American Journal of Medical Genetics Part A ·Kamilla Schlade‐Bartusiak,Teresa Costa,Anne Summers,Małgorzata J.M. Nowaczyk,Diane W. Cox	28
10	A clinical and molecular study of 26 females with Xp deletions with special emphasis on inherited deletions 2005 ·Human Genetics ·Katherine Lachlan,Sheila Youings,Teresa Costa,P. A. Jacobs,N. Simon Thomas	47
11	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 2003 ·Journal of Biological Chemistry ·(unknown),Catarina Brito,Teresa Costa,Joël Lanoix,Tommy Nilsson,Júlia Costa	25
12	Molecular and Biochemical Characterization of a Highly Stable Bacterial Laccase That Occurs as a Structural Component of the Bacillus subtilis Endospore Coat 2002 ·Journal of Biological Chemistry ·Lı́gia O. Martins,Cláudio M. Soares,Manuela M. Pereira,Miguel Teixeira,Teresa Costa,George H. Jones,Adriano O. Henriques	458
13	A new syndrome with craniofacial and skeletal dysmorphisms and developmental delay 2001 ·Clinical Dysmorphology ·Vazken M. Der Kaloustian,M. Pelletier,Teresa Costa,(unknown),Kamaldine Oudjhane	11
14	Expression and characterization of recombinant human α-3/4-fucosyltransferase III from Spodoptera frugiperda (Sf9) and Trichoplusia ni (Tn) cells using the baculovirus expression system 2001 ·Biochemical Journal ·Vanessa A. Morais,Jacinta Serpa,Angelina S. Palma,Teresa Costa,Luis Maranga,Júlia Costa	28
15	Severe prenatal growth retardation, dysmorphic features, pigmentary retinopathy, and generalized absence of subcutaneous tissues: a new entity? 1998 ·Clinical Dysmorphology ·(unknown),Helen E. Hughes,Teresa Costa,Joe T.R. Clarke	3
16	Deletion 3q in Two Patients With Blepharophimosis-ptosis-epicanthus Inversus Syndrome (BPES) 1998 ·Journal of Pediatric Ophthalmology & Strabismus ·Teresa Costa,Robert C. Pashby,Marlene J. Huggins,Ikuko Teshima	15
17	Alagille syndrome is caused by mutations in human Jagged1, which encodes a ligand for Notch1breakdown → 1997 ·Nature Genetics ·Linheng Li,(unknown),Yu Deng,Anna Genin,Amy B. Banta,Colin C. Collins,Ming Qi,Barbara J. Trask,Wen Lin Kuo,(unknown),Teresa Costa,Mary Ella Pierpont,Elizabeth B. Rand,(unknown),L Hood,Nancy B. Spinner	928
18	Disruption of human limb morphogenesis by a dominant negative mutation in CDMP1 1997 ·Nature Genetics ·Jack Thomas,Michael W. Kilpatrick,(unknown),Ludwig Erlacher,Peter Lembessis,Teresa Costa,Petros Tsipouras,Frank P. Luyten	278
19	Identification of Genes from a 500-kb Region at 7q11.23 That Is Commonly Deleted in Williams Syndrome Patients 1996 ·Genomics ·Lucy R. Osborne,Duane W. Martindale,Stephen W. Scherer,Xiaomei Shi,Jack J. Huizenga,Henry H. Heng,Teresa Costa,Barbara R. Pober,(unknown),(unknown),Johanna M. Rommens,Ben F. Koop,Lap‐Chee Tsui	83
20	A common FGFR3 gene mutation in hypochondroplasia 1995 ·Human Molecular Genetics ·Panagiotis Prinos,Teresa Costa,Annemarie Sommer,M W Kilpatrick,Petros Tsipouras	95

About Teresa Costa

Teresa Costa is a scholar working on Genetics, Developmental Neuroscience and Developmental Biology, having authored 47 papers that have together received 3.3k indexed citations. Recurring topics across this work include Connective tissue disorders research (8 papers), Bacterial Genetics and Biotechnology (8 papers) and Genomic variations and chromosomal abnormalities (6 papers). The work is most often cited by research in Genetics (1.3k citations), Developmental Neuroscience (153 citations) and Biotechnology (302 citations). Teresa Costa has collaborated with scholars based in Canada, United States and Portugal. Frequent co-authors include Adriano O. Henriques, Lı́gia O. Martins, Manuela M. Pereira, Cláudio M. Soares, George H. Jones, Miguel Teixeira, Petros Tsipouras, Linheng Li, Mary Ella Pierpont and Wen Lin Kuo. Their work appears in journals such as Proceedings of the National Academy of Sciences, Journal of Biological Chemistry and Nature Genetics.

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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