Eglė Preikšaitienė

749 total citations
46 papers, 403 citations indexed

About

Eglė Preikšaitienė is a scholar working on Molecular Biology, Genetics and Genetics. According to data from OpenAlex, Eglė Preikšaitienė has authored 46 papers receiving a total of 403 indexed citations (citations by other indexed papers that have themselves been cited), including 28 papers in Molecular Biology, 26 papers in Genetics and 7 papers in Genetics. Recurrent topics in Eglė Preikšaitienė's work include Genomic variations and chromosomal abnormalities (21 papers), Congenital heart defects research (10 papers) and Genetics and Neurodevelopmental Disorders (9 papers). Eglė Preikšaitienė is often cited by papers focused on Genomic variations and chromosomal abnormalities (21 papers), Congenital heart defects research (10 papers) and Genetics and Neurodevelopmental Disorders (9 papers). Eglė Preikšaitienė collaborates with scholars based in Lithuania, Switzerland and Cyprus. Eglė Preikšaitienė's co-authors include Vaidutis Kučinskas, Algirdas Utkus, Jūratė Kasnauskienė, Philippos C. Patsalis, Biruté Tumiene, Loreta Cimbalistienė, Alexandre Reymond, Laima Ambrozaitytė, Aušra Matulevičienė and Norine Voisin and has published in prestigious journals such as SHILAP Revista de lepidopterología, Gene and European Journal of Human Genetics.

In The Last Decade

Eglė Preikšaitienė

43 papers receiving 389 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Eglė Preikšaitienė Lithuania 11 242 194 46 27 25 46 403
Saeed Al Turki Saudi Arabia 7 281 1.2× 276 1.4× 43 0.9× 21 0.8× 39 1.6× 13 526
Sandra Monfort Spain 13 264 1.1× 364 1.9× 94 2.0× 40 1.5× 50 2.0× 41 530
Dirk‐Jan Kleinjan United Kingdom 7 437 1.8× 147 0.8× 18 0.4× 19 0.7× 33 1.3× 9 541
Arnaud Kress France 9 276 1.1× 202 1.0× 18 0.4× 13 0.5× 24 1.0× 17 437
Jean‐François Ouimette France 11 497 2.1× 231 1.2× 22 0.5× 12 0.4× 37 1.5× 15 601
Masahiro Uesaka Japan 12 375 1.5× 124 0.6× 10 0.2× 38 1.4× 22 0.9× 17 508
Zhuozhi Wang Canada 12 355 1.5× 280 1.4× 68 1.5× 32 1.2× 24 1.0× 21 710
Malcolm E Fisher United Kingdom 12 442 1.8× 133 0.7× 25 0.5× 8 0.3× 21 0.8× 17 571
Uirá Souto Melo Brazil 10 261 1.1× 119 0.6× 10 0.2× 35 1.3× 45 1.8× 20 387

Countries citing papers authored by Eglė Preikšaitienė

Since Specialization
Citations

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

Fields of papers citing papers by Eglė Preikšaitienė

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Eglė Preikšaitienė

This figure shows the co-authorship network connecting the top 25 collaborators of Eglė Preikšaitienė. A scholar is included among the top collaborators of Eglė Preikšaitienė 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 Eglė Preikšaitienė. Eglė Preikšaitienė 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.
Utkus, Algirdas, et al.. (2023). A De Novo 8q22.2q22.3 Interstitial Microdeletion in a Girl with Developmental Delay and Congenital Defects. Medicina. 59(6). 1156–1156. 1 indexed citations
2.
Sasnauskienė, Aušra, et al.. (2023). Molecular and Functional Characterisation of a Novel Intragenic 12q24.21 Deletion Resulting in MED13L Haploinsufficiency Syndrome. Medicina. 59(7). 1225–1225. 2 indexed citations
3.
Dapkūnas, Justas, et al.. (2022). PIGN-Related Disease in Two Lithuanian Families: A Report of Two Novel Pathogenic Variants, Molecular and Clinical Characterisation. Medicina. 58(11). 1526–1526. 2 indexed citations
4.
Barysienė, Jūratė, et al.. (2021). Aborted Cardiac Arrest in LQT2 Related to Novel KCNH2 (hERG) Variant Identified in One Lithuanian Family. Medicina. 57(7). 721–721. 1 indexed citations
5.
Preikšaitienė, Eglė, et al.. (2021). Genome Editing in Medicine: Tools and Challenges. SHILAP Revista de lepidopterología. 28(2). 8–8. 4 indexed citations
6.
Glaveckaitė, Sigita, et al.. (2021). Overlapping Phenotype of Cardiomyopathy in a Patient with Double Mutation: A Case Report. SHILAP Revista de lepidopterología. 11(1). 31–38. 1 indexed citations
7.
Preikšaitienė, Eglė, et al.. (2021). Novel In-Frame Deletion in HTRA1 Gene, Responsible for Stroke at a Young Age and Dementia—A Case Study. Genes. 12(12). 1955–1955. 5 indexed citations
8.
9.
Preikšaitienė, Eglė, Norine Voisin, Lucie Gueneau, et al.. (2019). Pathogenic homozygous variant in POMK gene is the cause of prenatally detected severe ventriculomegaly in two Lithuanian families. American Journal of Medical Genetics Part A. 182(3). 536–542. 6 indexed citations
10.
Preikšaitienė, Eglė, et al.. (2019). De Novo Duplication in the CHD7 Gene Associated With Severe CHARGE Syndrome. PubMed. 12. 1799503394–1799503394. 1 indexed citations
11.
Utkus, Algirdas, et al.. (2019). Novel GLI3 variant causes Greig cephalopolysyndactyly syndrome in three generations of a Lithuanian family. Molecular Genetics & Genomic Medicine. 7(9). e878–e878. 2 indexed citations
12.
13.
Jakaitienė, Audronė, Eglė Preikšaitienė, Birutė Burnytė, et al.. (2016). The high frequency of GJB2 gene mutation c.313_326del14 suggests its possible origin in ancestors of Lithuanian population. BMC Genetics. 17(1). 45–45. 18 indexed citations
14.
Preikšaitienė, Eglė, et al.. (2016). Features of KAT6B-related disorders in a patient with 10q22.1q22.3 deletion. Ophthalmic Genetics. 38(4). 383–386. 2 indexed citations
15.
Preikšaitienė, Eglė, et al.. (2016). Recurrent fetal syndromic spina bifida associated with 3q26.1-qter duplication and 5p13.33-pter deletion due to familial balanced rearrangement. Taiwanese Journal of Obstetrics and Gynecology. 55(3). 410–414. 7 indexed citations
16.
Preikšaitienė, Eglė, Alfonso Caro‐Llopis, Silvestre Oltra, et al.. (2015). A novel missense mutation in the NSDHL gene identified in a Lithuanian family by targeted next‐generation sequencing causes CK syndrome. American Journal of Medical Genetics Part A. 167(6). 1342–1348. 7 indexed citations
17.
Preikšaitienė, Eglė, et al.. (2014). R368X mutation in MID1 among recurrent mutations in patients with X-linked Opitz G/BBB syndrome. Clinical Dysmorphology. 24(1). 7–12. 7 indexed citations
18.
Kasnauskienė, Jūratė, et al.. (2012). Two New de novo Interstitial Duplications Covering 2p14–p22.1: Clinical and Molecular Analysis. Cytogenetic and Genome Research. 139(1). 52–58. 2 indexed citations
19.
Kasnauskienė, Jūratė, Loreta Cimbalistienė, Eglė Preikšaitienė, et al.. (2011). De novo 5q35.5 duplication with clinical presentation of Sotos syndrome. American Journal of Medical Genetics Part A. 155(10). 2501–2507. 10 indexed citations
20.
Kasnauskienė, Jūratė, et al.. (2011). Mental retardation and autism associated with recurrent 16p11.2 microdeletion: incomplete penetrance and variable expressivity. Journal of Applied Genetics. 52(4). 443–449. 13 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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