Daniel R. Carvalho

2.1k total citations
31 papers, 343 citations indexed

About

Daniel R. Carvalho is a scholar working on Molecular Biology, Genetics and Rheumatology. According to data from OpenAlex, Daniel R. Carvalho has authored 31 papers receiving a total of 343 indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Molecular Biology, 9 papers in Genetics and 5 papers in Rheumatology. Recurrent topics in Daniel R. Carvalho's work include Metabolism and Genetic Disorders (4 papers), Genomic variations and chromosomal abnormalities (4 papers) and Oropharyngeal Anatomy and Pathologies (4 papers). Daniel R. Carvalho is often cited by papers focused on Metabolism and Genetic Disorders (4 papers), Genomic variations and chromosomal abnormalities (4 papers) and Oropharyngeal Anatomy and Pathologies (4 papers). Daniel R. Carvalho collaborates with scholars based in Brazil, United States and Denmark. Daniel R. Carvalho's co-authors include Carlos E. Speck‐Martins, Jaime Moritz Brum, Riccardo Pratesi, Luciano Farage, Pedro Madureira, Céu Figueiredo, Nuno Guimarães, Nuno F. Azevedo, Nara Sobreira and Guilherme D. Brand and has published in prestigious journals such as Applied Microbiology and Biotechnology, Gene and Biochemical Engineering Journal.

In The Last Decade

Daniel R. Carvalho

28 papers receiving 325 citations

Peers

Daniel R. Carvalho
Deborah L. Renaud United States
C R Müller Germany
Joan E. Pellegrino United States
Sue Forrest Australia
Cristina Dias United Kingdom
Lisa Worgan Australia
Bird Td United States
Daniel R. Carvalho
Citations per year, relative to Daniel R. Carvalho Daniel R. Carvalho (= 1×) peers Rocío Sánchez-Alcudia

Countries citing papers authored by Daniel R. Carvalho

Since Specialization
Citations

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

Fields of papers citing papers by Daniel R. Carvalho

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Daniel R. Carvalho. 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 Daniel R. Carvalho. The network helps show where Daniel R. Carvalho may publish in the future.

Co-authorship network of co-authors of Daniel R. Carvalho

This figure shows the co-authorship network connecting the top 25 collaborators of Daniel R. Carvalho. A scholar is included among the top collaborators of Daniel R. Carvalho 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 Daniel R. Carvalho. Daniel R. Carvalho 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.
Scott, Alexandra J., Thi Tuyet Mai Nguyen, Klaas J. Wierenga, et al.. (2024). Exploring the phenotypic spectrum and osteopenia mechanisms in Yunis-Varón syndrome. Genetics in Medicine Open. 2. 101837–101837.
2.
Wongkittichote, Parith, Daniel R. Carvalho, Claudio M. de Gusmão, et al.. (2023). Phenotypic, molecular, and functional characterization of COQ7-related primary CoQ10 deficiency: Hypomorphic variants and two distinct disease entities. Molecular Genetics and Metabolism. 139(4). 107630–107630. 5 indexed citations
3.
Carvalho, Daniel R., et al.. (2023). Czech dysplasia mimicking rheumatoid arthritis: Case series and literature review. Modern Rheumatology. 34(4). 705–710.
4.
Carvalho, Daniel R., et al.. (2021). Clinical Features of de novo Pure 16q21q24.1 Chromosome Duplication. Cytogenetic and Genome Research. 161(3-4). 160–166. 1 indexed citations
5.
Carvalho, Daniel R., et al.. (2021). Charcot‐Marie‐Tooth disease: Genetic profile of patients from a large Brazilian neuromuscular reference center. Journal of the Peripheral Nervous System. 26(3). 290–297. 8 indexed citations
6.
Leon, Eyby, Jullianne Diaz, Hanne Hove, et al.. (2020). Unique skeletal manifestations in patients with Primrose syndrome. European Journal of Medical Genetics. 63(8). 103967–103967. 6 indexed citations
7.
Carvalho, Daniel R., et al.. (2018). Femoral‐facial syndrome: A review of the literature and 14 additional patients including a monozygotic discordant twin pair. American Journal of Medical Genetics Part A. 176(9). 1917–1928. 7 indexed citations
8.
Carvalho, Daniel R., et al.. (2018). 19q13.11 microdeletion: Clinical features overlapping ectrodactyly ectodermal dysplasia‐clefting syndrome phenotype. Clinical Case Reports. 6(7). 1300–1307. 8 indexed citations
9.
Carvalho, Daniel R., et al.. (2017). Additional features of Gillespie syndrome in two Brazilian siblings with a novel ITPR1 homozygous pathogenic variant. European Journal of Medical Genetics. 61(3). 134–138. 13 indexed citations
10.
Carvalho, Daniel R., Nuno Guimarães, Pedro Madureira, et al.. (2016). Application of locked nucleic acid-based probes in fluorescence in situ hybridization. Applied Microbiology and Biotechnology. 100(13). 5897–5906. 15 indexed citations
11.
Carvalho, Daniel R., et al.. (2016). Serological prevalence of celiac disease in Brazilian population of multiple sclerosis, neuromyelitis optica and myelitis. Multiple Sclerosis and Related Disorders. 9. 125–128. 5 indexed citations
12.
Carvalho, Daniel R., et al.. (2012). Clinical Features and Neurologic Progression of Hyperargininemia. Pediatric Neurology. 46(6). 369–374. 42 indexed citations
13.
Carvalho, Daniel R., Guilherme D. Brand, Jaime Moritz Brum, et al.. (2012). Analysis of novel ARG1 mutations causing hyperargininemia and correlation with arginase I activity in erythrocytes. Gene. 509(1). 124–130. 25 indexed citations
14.
Simon, Marleen, Belinda Campos‐Xavier, Eugênia Ribeiro Valadares, et al.. (2012). Severe neurologic manifestations from cervical spine instability in spondylo‐megaepiphyseal‐metaphyseal dysplasia. American Journal of Medical Genetics Part C Seminars in Medical Genetics. 160C(3). 230–237. 7 indexed citations
15.
Carvalho, Daniel R. & Carlos E. Speck‐Martins. (2011). Additional features of unique Primrose syndrome phenotype. American Journal of Medical Genetics Part A. 155(6). 1379–1383. 10 indexed citations
16.
Vieira, Gustavo Henrique Apolinário, et al.. (2011). Smith-Magenis syndrome: clinical evaluation in seven Brazilian patients. Genetics and Molecular Research. 10(4). 2664–2670. 10 indexed citations
17.
Carvalho, Daniel R., et al.. (2011). Tibial hemimelia in Langer–Giedion syndrome with 8q23.1‐q24.12 interstitial deletion. American Journal of Medical Genetics Part A. 155(11). 2784–2787. 8 indexed citations
18.
Carvalho, Daniel R., et al.. (2011). Craniofacial findings in fibrodysplasia ossificans progressiva: computerized tomography evaluation. Oral Surgery Oral Medicine Oral Pathology Oral Radiology and Endodontology. 111(4). 499–502. 15 indexed citations
19.
Carvalho, Daniel R., Natalia Freitas Rossi, Silvana Artioli Schellini, Danilo Moretti‐Ferreira, & Antônio Richieri‐Costa. (2008). Schilbach–Rott/blepharofacioskeletal syndrome in a Brazilian patient. American Journal of Medical Genetics Part A. 146A(16). 2134–2137. 3 indexed citations
20.
Carvalho, Daniel R., et al.. (2006). Autosomal dominant atretic cephalocele with phenotype variability: Report of a Brazilian family with six affected in four generations. American Journal of Medical Genetics Part A. 140A(13). 1458–1462. 16 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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