A. Richieri‐Costa

1.5k total citations
75 papers, 1.0k citations indexed

About

A. Richieri‐Costa is a scholar working on Genetics, Molecular Biology and Genetics. According to data from OpenAlex, A. Richieri‐Costa has authored 75 papers receiving a total of 1.0k indexed citations (citations by other indexed papers that have themselves been cited), including 51 papers in Genetics, 22 papers in Molecular Biology and 18 papers in Genetics. Recurrent topics in A. Richieri‐Costa's work include Craniofacial Disorders and Treatments (22 papers), Cleft Lip and Palate Research (20 papers) and Connective tissue disorders research (16 papers). A. Richieri‐Costa is often cited by papers focused on Craniofacial Disorders and Treatments (22 papers), Cleft Lip and Palate Research (20 papers) and Connective tissue disorders research (16 papers). A. Richieri‐Costa collaborates with scholars based in Brazil, Uruguay and United States. A. Richieri‐Costa's co-authors include M. L. Guion‐Almeida, John M. Opitz, James F. Reynolds, Lucilene Arilho Ribeiro, Maria Rita Passos‐Bueno, Thomaz Rafael Gollop, Angela Maria Vianna‐Morgante, Yolande van Bever, Nivaldo Alonso and Luís Garcia Alonso and has published in prestigious journals such as Journal of Medical Genetics, Human Mutation and American Journal of Medical Genetics.

In The Last Decade

A. Richieri‐Costa

72 papers receiving 965 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
A. Richieri‐Costa Brazil 19 658 432 197 167 138 75 1.0k
Frank Majewski Germany 16 755 1.1× 579 1.3× 200 1.0× 157 0.9× 118 0.9× 26 1.3k
Fahed Halal Canada 18 564 0.9× 462 1.1× 332 1.7× 98 0.6× 82 0.6× 50 1.2k
Naomi Fitch Canada 22 585 0.9× 479 1.1× 262 1.3× 95 0.6× 87 0.6× 44 1.1k
M. Michael Cohen Canada 21 713 1.1× 422 1.0× 279 1.4× 70 0.4× 42 0.3× 50 1.2k
Louise Brueton United Kingdom 24 604 0.9× 908 2.1× 154 0.8× 198 1.2× 59 0.4× 34 1.5k
M. Preus Canada 19 443 0.7× 412 1.0× 102 0.5× 66 0.4× 71 0.5× 44 966
Eric A. Wulfsberg United States 23 768 1.2× 462 1.1× 241 1.2× 81 0.5× 44 0.3× 47 1.2k
Florence Petit France 20 461 0.7× 610 1.4× 107 0.5× 91 0.5× 92 0.7× 61 1.0k
Yves Lacassie United States 18 425 0.6× 475 1.1× 174 0.9× 77 0.5× 29 0.2× 70 952
Laurence Taine France 21 398 0.6× 428 1.0× 147 0.7× 43 0.3× 86 0.6× 46 924

Countries citing papers authored by A. Richieri‐Costa

Since Specialization
Citations

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

Fields of papers citing papers by A. Richieri‐Costa

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of A. Richieri‐Costa

This figure shows the co-authorship network connecting the top 25 collaborators of A. Richieri‐Costa. A scholar is included among the top collaborators of A. Richieri‐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 A. Richieri‐Costa. A. Richieri‐Costa 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.
Petrin, Aline, et al.. (2010). Clinical findings in patients with GLI2 mutations – phenotypic variability. Clinical Genetics. 81(1). 70–75. 48 indexed citations
2.
Lamônica, Dionísia Aparecida Cusin, et al.. (2009). Possible new syndrome: Left ventricular noncompaction, partial agenesis of the corpus callosum, and developmental delay in a Brazilian child. American Journal of Medical Genetics Part A. 149A(5). 1041–1045. 3 indexed citations
3.
Dalben, Gisele da Silva, et al.. (2008). Tooth abnormalities and soft tissue alterations in patients with G/BBB syndrome. Oral Diseases. 14(8). 747–753. 9 indexed citations
4.
Lamônica, Dionísia Aparecida Cusin, et al.. (2007). Evolução de habilidades comunicativas na Síndrome de Williams – Processo terapêutico de um caso clínico. Distúrbios da Comunicação. ISSN 2176-2724. 19(2). 203–211. 1 indexed citations
5.
Guion‐Almeida, Maria Leine & A. Richieri‐Costa. (2006). Frontonasal malformation, first branchial arch anomalies, congenital heart defect, and severe central nervous system involvement: A possible “new” autosomal recessive syndrome?. American Journal of Medical Genetics Part A. 140A(22). 2478–2481. 5 indexed citations
6.
Richieri‐Costa, A., et al.. (1993). Carpenter syndrome with normal intelligence: Brazilian girl born to consanguineous parents. American Journal of Medical Genetics. 47(2). 281–283. 9 indexed citations
7.
Bever, Yolande van, et al.. (1993). The oav - spectrum and associated anomalies in 77 patients. Revista brasileira de genetica. 16(3). 811–817. 1 indexed citations
8.
Richieri‐Costa, A., et al.. (1993). Mandibulofacial dysostosis: Report on two Brazilian families suggesting autosomal recessive inheritance. American Journal of Medical Genetics. 46(6). 659–664. 9 indexed citations
9.
Richieri‐Costa, A., M. L. Guion‐Almeida, & Nina A. B. Pagnan. (1992). Acro‐fronto‐facio‐nasal dysostosis: Report of a new brazilian family. American Journal of Medical Genetics. 44(6). 800–802. 8 indexed citations
10.
Bever, Yolande van, et al.. (1992). Marden‐Walker‐like syndrome without psychomotor retardation: Report of a Brazilian girl born to consanguineous parents. American Journal of Medical Genetics. 42(4). 467–469. 18 indexed citations
11.
Richieri‐Costa, A., M. L. Guion‐Almeida, & Jenneke van den Ende. (1991). Sporadic, idiopathic MCA syndrome with mandibulofacial dysostosis and tibial hemimelia. American Journal of Medical Genetics. 41(3). 330–332. 1 indexed citations
12.
Richieri‐Costa, A., et al.. (1990). Rapp‐Hodgkin syndrome: Report of a Brazilian family. American Journal of Medical Genetics. 36(4). 463–466. 13 indexed citations
13.
Richieri‐Costa, A. & M. L. Guion‐Almeida. (1989). Postaxial acrofacial dysostosis: Report of a Brazilian patient. American Journal of Medical Genetics. 33(4). 447–449. 8 indexed citations
14.
Richieri‐Costa, A., et al.. (1989). Autosomal recessive acro‐fronto‐facio‐nasal dysostosis associated with genitourinary anomalies. American Journal of Medical Genetics. 33(1). 121–124. 17 indexed citations
15.
Richieri‐Costa, A.. (1987). Profound limb deficiency, thoracic anomalies, unusual facies and normal intelligence - the al - awadi syndrome - report of a brazilian patient. Revista brasileira de genetica. 10(3). 611–616. 8 indexed citations
16.
Richieri‐Costa, A., John M. Opitz, & James F. Reynolds. (1986). FG syndrome in a Brazilian child with additional previously unreported signs. American Journal of Medical Genetics. 25(S2). 247–254. 8 indexed citations
17.
Richieri‐Costa, A., et al.. (1986). Coffin-Siris syndrome in a brazilian child with consanguineous parents. Revista brasileira de genetica. 9(1). 169–177. 3 indexed citations
18.
Richieri‐Costa, A., John M. Opitz, & James F. Reynolds. (1986). Ulnar ray A/hypoplasia. Evidence for a developmental field defect on the basis of genetic heterogeneity. Report of three Brazilian families. American Journal of Medical Genetics. 25(S2). 195–206. 19 indexed citations
19.
Mustacchi, Zan, et al.. (1983). Schwartz syndrome associated with dental and cardiac involvement. UNIFESP Institutional Repository (Universidade Federal de São Paulo). 6(1). 93–99. 2 indexed citations
20.
Richieri‐Costa, A. & Oswaldo Frota‐Pessoa. (1979). Atrichia, Abnormal EEG, Epilepsy and Mental Retardation in Two Sisters. Human Heredity. 29(5). 293–297. 6 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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