Natália D. Linhares

579 total citations
21 papers, 350 citations indexed

About

Natália D. Linhares is a scholar working on Genetics, Molecular Biology and Surgery. According to data from OpenAlex, Natália D. Linhares has authored 21 papers receiving a total of 350 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Genetics, 8 papers in Molecular Biology and 3 papers in Surgery. Recurrent topics in Natália D. Linhares's work include Genomic variations and chromosomal abnormalities (4 papers), Genetics and Neurodevelopmental Disorders (4 papers) and Genomics and Rare Diseases (3 papers). Natália D. Linhares is often cited by papers focused on Genomic variations and chromosomal abnormalities (4 papers), Genetics and Neurodevelopmental Disorders (4 papers) and Genomics and Rare Diseases (3 papers). Natália D. Linhares collaborates with scholars based in Brazil, Germany and United States. Natália D. Linhares's co-authors include Sérgio D.J. Pena, Eugênia Ribeiro Valadares, Stanley de Almeida Araújo, Marta Svartman, Carla Rosenberg, Christoph Walz, Christoph Klein, Uta Behrends, Josef Mautner and Gundula Jaeger and has published in prestigious journals such as Nature Communications, Blood and BMC Bioinformatics.

In The Last Decade

Natália D. Linhares

21 papers receiving 338 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Natália D. Linhares Brazil 10 168 102 89 43 34 21 350
K Matsushita Japan 13 175 1.0× 60 0.6× 82 0.9× 20 0.5× 23 0.7× 28 544
Wolfram Heinritz Germany 12 175 1.0× 104 1.0× 33 0.4× 30 0.7× 16 0.5× 28 380
Shazia Micheal Pakistan 18 274 1.6× 124 1.2× 38 0.4× 89 2.1× 56 1.6× 36 655
Jürgen Groet United Kingdom 12 213 1.3× 98 1.0× 59 0.7× 29 0.7× 29 0.9× 15 502
Cinzia Mazzanti Italy 9 189 1.1× 193 1.9× 120 1.3× 21 0.5× 25 0.7× 13 403
Natalia V. Voronova Russia 9 137 0.8× 78 0.8× 82 0.9× 26 0.6× 19 0.6× 12 322
L. Alexander Liggett United States 7 193 1.1× 92 0.9× 110 1.2× 32 0.7× 16 0.5× 7 446
Keiya Ozawa Japan 13 186 1.1× 126 1.2× 60 0.7× 57 1.3× 15 0.4× 38 443
Patrick Maschmeyer Germany 14 130 0.8× 56 0.5× 195 2.2× 44 1.0× 11 0.3× 21 469
Sonja Smith United States 10 206 1.2× 25 0.2× 117 1.3× 23 0.5× 16 0.5× 19 399

Countries citing papers authored by Natália D. Linhares

Since Specialization
Citations

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

Fields of papers citing papers by Natália D. Linhares

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Natália D. Linhares. 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 Natália D. Linhares. The network helps show where Natália D. Linhares may publish in the future.

Co-authorship network of co-authors of Natália D. Linhares

This figure shows the co-authorship network connecting the top 25 collaborators of Natália D. Linhares. A scholar is included among the top collaborators of Natália D. Linhares 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 Natália D. Linhares. Natália D. Linhares 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.
Linhares, Natália D., et al.. (2022). Uniparental disomy screen of Irish rare disorder cohort unmasks homozygous variants of clinical significance in the TMCO1 and PRKRA genes. Frontiers in Genetics. 13. 945296–945296. 6 indexed citations
2.
Linhares, Natália D., et al.. (2022). Mild Phenotype of Arthrogryposis, Renal Dysfunction, and Cholestasis Syndrome 1 Caused by a Novel VPS33B Variant. Frontiers in Genetics. 13. 796759–796759. 2 indexed citations
3.
Li, Dong, Alanna Strong, David Cassiman, et al.. (2020). De novo loss-of-function variants in X-linked MED12 are associated with Hardikar syndrome in females. Genetics in Medicine. 23(4). 637–644. 22 indexed citations
4.
Linhares, Natália D., et al.. (2020). Noncoding SNPs Associated with Increased GDF15 Levels Located in a Metformin-Activated Enhancer Region Upstream of GDF15. Pharmacogenomics. 21(8). 509–520. 9 indexed citations
5.
Oliveira, Aline C., Marcos Barrouin Melo, Daisy Motta‐Santos, et al.. (2018). Genetic deletion of the alamandine receptor MRGD leads to dilated cardiomyopathy in mice. American Journal of Physiology-Heart and Circulatory Physiology. 316(1). H123–H133. 34 indexed citations
6.
Tuwaijri, Abeer Al, Sanny Moussette, Francisco Martı́nez, et al.. (2018). X chromosome dosage and presence of SRY shape sex-specific differences in DNA methylation at an autosomal region in human cells. Biology of Sex Differences. 9(1). 10–10. 16 indexed citations
7.
Soardi, Fernanda Caroline, Alice Machado-Silva, Natália D. Linhares, et al.. (2017). Familial STAG2 germline mutation defines a new human cohesinopathy. npj Genomic Medicine. 2(1). 7–7. 48 indexed citations
8.
Schober, Tilmann, Thomas Magg, Melanie Laschinger, et al.. (2017). A human immunodeficiency syndrome caused by mutations in CARMIL2. Nature Communications. 8(1). 14209–14209. 83 indexed citations
9.
Linhares, Natália D., et al.. (2017). Mendel,MD: A user-friendly open-source web tool for analyzing WES and WGS in the diagnosis of patients with Mendelian disorders. PLoS Computational Biology. 13(6). e1005520–e1005520. 9 indexed citations
10.
Linhares, Natália D., et al.. (2017). Nephrotic syndrome and adrenal insufficiency caused by a variant in SGPL1. Clinical Kidney Journal. 11(4). 462–467. 34 indexed citations
11.
Gurgel‐Giannetti, Juliana, et al.. (2017). Rare phenotypes related to novel autosomal recessive TTN truncating mutations: Escobar syndrome and congenital heart defect in two Brazilian patients. Neuromuscular Disorders. 27. S238–S238. 1 indexed citations
12.
Linhares, Natália D., Eugênia Ribeiro Valadares, Silvia Souza da Costa, et al.. (2016). Inherited Xq13.2-q21.31 duplication in a boy with recurrent seizures and pubertal gynecomastia: Clinical, chromosomal and aCGH characterization. Meta Gene. 9. 185–190. 10 indexed citations
13.
Schober, Tilmann, Thomas Magg, Melanie Laschinger, et al.. (2016). Rltpr Is a Central Scaffold Protein Regulating Human TCR Co-Signaling and Cytoskeletal Dynamics. Blood. 128(22). 131–131. 1 indexed citations
14.
Linhares, Natália D., Katherine Lachlan, Bruno Dallapiccola, et al.. (2016). 1p13.2 deletion displays clinical features overlapping Noonan syndrome, likely related to NRAS gene haploinsufficiency. Genetics and Molecular Biology. 39(3). 349–357. 3 indexed citations
15.
Linhares, Natália D., et al.. (2015). Subtelomeric 6p25 deletion/duplication: Report of a patient with new clinical findings and genotype–phenotype correlations. European Journal of Medical Genetics. 58(5). 310–318. 20 indexed citations
16.
Linhares, Natália D., et al.. (2015). Mendel,MD: a user-friendly online program for clinical exome analysis. BMC Bioinformatics. 16(S8). 7 indexed citations
17.
Linhares, Natália D., et al.. (2014). Exome sequencing identifies a novel homozygous variant in NDRG4 in a family with infantile myofibromatosis. European Journal of Medical Genetics. 57(11-12). 643–648. 9 indexed citations
18.
Linhares, Natália D., et al.. (2014). Short Communication Modulation of expressivity in PDGFRB-related infantile myofibromatosis: a role for PTPRG?. Genetics and Molecular Research. 13(3). 6287–6292. 18 indexed citations
19.
20.
Linhares, Natália D., Marta Svartman, & Eugênia Ribeiro Valadares. (2012). Diagnóstico citogenético de pacientes com retardo mental idiopático. Jornal Brasileiro de Patologia e Medicina Laboratorial. 48(1). 33–39. 2 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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