Nara Sobreira

2.1k total citations
27 papers, 550 citations indexed

About

Nara Sobreira is a scholar working on Molecular Biology, Genetics and Pathology and Forensic Medicine. According to data from OpenAlex, Nara Sobreira has authored 27 papers receiving a total of 550 indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Molecular Biology, 15 papers in Genetics and 3 papers in Pathology and Forensic Medicine. Recurrent topics in Nara Sobreira's work include Genomics and Rare Diseases (9 papers), Congenital heart defects research (5 papers) and Genomic variations and chromosomal abnormalities (4 papers). Nara Sobreira is often cited by papers focused on Genomics and Rare Diseases (9 papers), Congenital heart defects research (5 papers) and Genomic variations and chromosomal abnormalities (4 papers). Nara Sobreira collaborates with scholars based in United States, Brazil and Pakistan. Nara Sobreira's co-authors include David Valle, Julie Hoover‐Fong, Elizabeth Wohler, David Valle‐García, David J. Cutler, John A. McGrath, Ann E. Pulver, Stephen T. Warren, Adele A. Mitchell and Jennifer G. Mullé and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Blood and Scientific Reports.

In The Last Decade

Nara Sobreira

26 papers receiving 540 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Nara Sobreira United States 10 325 323 63 42 36 27 550
Andrea M. Oza United States 8 294 0.9× 271 0.8× 58 0.9× 24 0.6× 38 1.1× 13 593
Dustin Baldridge United States 13 312 1.0× 386 1.2× 68 1.1× 38 0.9× 28 0.8× 26 617
Joanna Wiszniewska United States 12 348 1.1× 360 1.1× 38 0.6× 28 0.7× 15 0.4× 22 607
Katrina Tatton‐Brown United Kingdom 14 704 2.2× 696 2.2× 38 0.6× 27 0.6× 43 1.2× 32 1.0k
Julia Parrish United States 13 414 1.3× 348 1.1× 55 0.9× 39 0.9× 54 1.5× 19 695
James Colley United Kingdom 8 241 0.7× 383 1.2× 48 0.8× 31 0.7× 61 1.7× 13 539
Kenji Naritomi Japan 17 400 1.2× 463 1.4× 22 0.3× 40 1.0× 26 0.7× 58 689
Davor Lessel Germany 17 523 1.6× 181 0.6× 50 0.8× 34 0.8× 39 1.1× 44 733
Sérgio B. Sousa Portugal 12 351 1.1× 359 1.1× 21 0.3× 18 0.4× 26 0.7× 37 594
Sanne M. C. Savelberg Netherlands 10 246 0.8× 257 0.8× 24 0.4× 16 0.4× 35 1.0× 11 443

Countries citing papers authored by Nara Sobreira

Since Specialization
Citations

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

Fields of papers citing papers by Nara Sobreira

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Nara Sobreira

This figure shows the co-authorship network connecting the top 25 collaborators of Nara Sobreira. A scholar is included among the top collaborators of Nara Sobreira 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 Nara Sobreira. Nara Sobreira 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.
Ashbrook, Liza, Maya Yamazaki, Elizabeth Wohler, et al.. (2025). CACNA1D is a circadian gene and causes familial advanced sleep phase. Proceedings of the National Academy of Sciences. 122(23). e2424387122–e2424387122.
2.
Naz, Sadaf, Asma Mushtaq, Elizabeth Wohler, et al.. (2023). Exome Sequencing Reveals SLC4A11 Variant Underlying Congenital Hereditary Endothelial Dystrophy (CHED2) Misdiagnosed as Congenital Glaucoma. Genes. 14(2). 310–310. 4 indexed citations
3.
Wohler, Elizabeth, Sen Zhao, Steven W. Hwang, et al.. (2023). COL11A2 as a candidate gene for vertebral malformations and congenital scoliosis. Human Molecular Genetics. 32(19). 2913–2928. 7 indexed citations
4.
Hatzimanolis, Alexandros, Elizabeth Wohler, Xue Yang, et al.. (2023). A Missense Variant in CASKIN1’s Proline-Rich Region Segregates with Psychosis in a Three-Generation Family. Genes. 14(1). 177–177. 2 indexed citations
5.
Rodgers, Kristen, Christine Kim, Jinny S. Ha, et al.. (2023). Anxiety and dysautonomia symptoms in patients with a NaV1.7 mutation and the potential benefits of low-dose short-acting guanfacine. Clinical Autonomic Research. 34(1). 191–201. 2 indexed citations
6.
Gowans, Lord Jephthah Joojo, Mary Li, Tamara Busch, et al.. (2021). Co‐occurrence of orofacial clefts and clubfoot phenotypes in a sub‐Saharan African cohort: Whole‐exome sequencing implicates multiple syndromes and genes. Molecular Genetics & Genomic Medicine. 9(4). e1655–e1655. 4 indexed citations
7.
Ramzan, Memoona, Rasheeda Bashir, Ghulam Mujtaba, et al.. (2020). Spectrum of genetic variants in moderate to severe sporadic hearing loss in Pakistan. Scientific Reports. 10(1). 11902–11902. 10 indexed citations
8.
Giorgio, Elisa, Fabio Sirchia, Martino Bosco, et al.. (2018). A novel case of Greenberg dysplasia and genotype–phenotype correlation analysis for LBR pathogenic variants: An instructive example of one gene‐multiple phenotypes. American Journal of Medical Genetics Part A. 179(2). 306–311. 9 indexed citations
9.
Sobreira, Nara, Harindra Arachchi, Orion J. Buske, et al.. (2017). Matchmaker Exchange. Current Protocols in Human Genetics. 95(1). 9.31.1–9.31.15. 32 indexed citations
10.
Zhulin, Igor B., et al.. (2017). A novel PRRT2 pathogenic variant in a family with paroxysmal kinesigenic dyskinesia and benign familial infantile seizures. Molecular Case Studies. 4(1). a002287–a002287. 9 indexed citations
11.
Sobreira, Nara, Lisa G. Riley, Wendy Gold, et al.. (2017). Mutations in RARS cause a hypomyelination disorder akin to Pelizaeus–Merzbacher disease. European Journal of Human Genetics. 25(10). 1134–1141. 33 indexed citations
12.
Chacón‐Camacho, Oscar F., et al.. (2016). Exome sequencing identifies a de novo frameshift mutation in the imprinted gene ZDBF2 in a sporadic patient with Nasopalpebral Lipoma‐coloboma syndrome. American Journal of Medical Genetics Part A. 170(7). 1934–1937. 2 indexed citations
13.
Ben‐Salem, Salma, Nara Sobreira, Nadia Akawi, et al.. (2015). Gonadal mosaicism in ARID1B gene causes intellectual disability and dysmorphic features in three siblings. American Journal of Medical Genetics Part A. 170(1). 156–161. 11 indexed citations
14.
Shahzad, Mohsin, Cecilia Herráiz, Rizwan Yousaf, et al.. (2015). Identification and functional characterization of natural human melanocortin 1 receptor mutant alleles in Pakistani population. Pigment Cell & Melanoma Research. 28(6). 730–735. 3 indexed citations
15.
Braunstein, Evan M., Ruijuan Li, Nara Sobreira, et al.. (2015). A Germline Mutation in ERBB3 Predisposes to Inherited Erythroid Myelodysplasia/Erythroleukemia. Blood. 126(23). 4105–4105. 1 indexed citations
16.
Meloni, Vera Ayres, Roberta Santos Guilherme, Mariana Moysés‐Oliveira, et al.. (2014). Cytogenomic delineation and clinical follow‐up of two siblings with an 8.5 Mb 6q24.2‐q25.2 deletion inherited from a paternal insertion. American Journal of Medical Genetics Part A. 164(9). 2378–2384. 5 indexed citations
17.
Hamosh, Ada, Nara Sobreira, Julie Hoover‐Fong, et al.. (2013). P heno DB : A New Web‐Based Tool for the Collection, Storage, and Analysis of Phenotypic Features. Human Mutation. 34(4). 566–571. 48 indexed citations
18.
Sobreira, Nara, Elizabeth T. Cirulli, Dimitrios Avramopoulos, et al.. (2010). Whole-Genome Sequencing of a Single Proband Together with Linkage Analysis Identifies a Mendelian Disease Gene. PLoS Genetics. 6(6). e1000991–e1000991. 161 indexed citations
19.
Mullé, Jennifer G., Anne Dodd, John A. McGrath, et al.. (2010). Microdeletions of 3q29 Confer High Risk for Schizophrenia. The American Journal of Human Genetics. 87(2). 229–236. 152 indexed citations
20.
Sobreira, Nara, Mirlene Cecília Soares Pinho Cernach, Décio Brunoni, & Ana Beatriz Alvarez Pérez. (2008). Complex toe syndactyly with characteristic facial phenotype: A new syndrome?. American Journal of Medical Genetics Part A. 146A(13). 1725–1728. 3 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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