Lorida Llaci

466 total citations
12 papers, 170 citations indexed

About

Lorida Llaci is a scholar working on Molecular Biology, Sensory Systems and Surgery. According to data from OpenAlex, Lorida Llaci has authored 12 papers receiving a total of 170 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Molecular Biology, 4 papers in Sensory Systems and 3 papers in Surgery. Recurrent topics in Lorida Llaci's work include Hearing, Cochlea, Tinnitus, Genetics (4 papers), RNA regulation and disease (3 papers) and Head and Neck Anomalies (3 papers). Lorida Llaci is often cited by papers focused on Hearing, Cochlea, Tinnitus, Genetics (4 papers), RNA regulation and disease (3 papers) and Head and Neck Anomalies (3 papers). Lorida Llaci collaborates with scholars based in United States, Australia and Austria. Lorida Llaci's co-authors include Johanna K. DiStefano, Ivana Malenica, Matthew J. Huentelman, Isabelle Schrauwen, Marcus Naymik, Sampathkumar Rangasamy, Glenn S. Gerhard, Xin Chu, James A. Knowles and Christopher D. Still and has published in prestigious journals such as Journal of Clinical Investigation, Nature Communications and Experimental Eye Research.

In The Last Decade

Lorida Llaci

11 papers receiving 168 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Lorida Llaci United States	8	95	25	22	20	17	12	170
Ryan Lu United States	10	112 1.2×	35 1.4×	15 0.7×	6 0.3×	6 0.4×	17	326
Amjad Khan Pakistan	12	170 1.8×	124 5.0×	18 0.8×	11 0.6×	3 0.2×	40	291
Nada Abdelmagid Sweden	8	62 0.7×	9 0.4×	20 0.9×	3 0.1×	8 0.5×	9	207
Piotr Gasperowicz Poland	12	191 2.0×	74 3.0×	8 0.4×	4 0.2×	7 0.4×	23	312
Emily Bonkowski United States	4	118 1.2×	72 2.9×	32 1.5×	5 0.3×	2 0.1×	11	277
Yvan Herenger France	5	135 1.4×	136 5.4×	8 0.4×	9 0.5×	6 0.4×	6	251
Zixi Sun China	11	224 2.4×	67 2.7×	18 0.8×	12 0.6×	110 6.5×	37	304
Xinzhang Cai China	10	140 1.5×	23 0.9×	13 0.6×	112 5.6×	13 0.8×	28	235
Akiko Hikoya Japan	10	114 1.2×	45 1.8×	33 1.5×	7 0.3×	109 6.4×	31	222
Birutė Burnytė Lithuania	7	103 1.1×	70 2.8×	12 0.5×	15 0.8×		28	194

Countries citing papers authored by Lorida Llaci

Since Specialization

Citations

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

Fields of papers citing papers by Lorida Llaci

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Lorida Llaci

This figure shows the co-authorship network connecting the top 25 collaborators of Lorida Llaci. A scholar is included among the top collaborators of Lorida Llaci 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 Lorida Llaci. Lorida Llaci is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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12 of 12 papers shown

Rubin, Joshua B., et al.. (2024). Epigenetic developmental mechanisms underlying sex differences in cancer. Journal of Clinical Investigation. 134(13). 12 indexed citations

Llaci, Lorida, Joshua B. Rubin, & Robi D. Mitra. (2022). EPCO-22. SINGLE CELL ANALYSIS TO UNDERSTAND SEX DIFFERENCES IN GBM OUTCOME. Neuro-Oncology. 24(Supplement_7). vii120–vii121.

Sakers, Kristina, Yating Liu, Lorida Llaci, et al.. (2021). Loss of Quaking RNA binding protein disrupts the expression of genes associated with astrocyte maturation in mouse brain. Nature Communications. 12(1). 1537–1537. 20 indexed citations

Piras, Ignazio S., Isabelle Schrauwen, Joshua S. Talboom, et al.. (2020). Transcriptional profiling of multiple system atrophy cerebellar tissue highlights differences between the parkinsonian and cerebellar sub-types of the disease. Acta Neuropathologica Communications. 8(1). 76–76. 20 indexed citations

Rangasamy, Sampathkumar, Finny Monickaraj, Christophe Legendre, et al.. (2020). Transcriptomics analysis of pericytes from retinas of diabetic animals reveals novel genes and molecular pathways relevant to blood-retinal barrier alterations in diabetic retinopathy. Experimental Eye Research. 195. 108043–108043. 24 indexed citations

Kari, Elina, Lorida Llaci, John L. Go, et al.. (2020). Genes Implicated in Rare Congenital Inner Ear and Cochleovestibular Nerve Malformations. Ear and Hearing. 41(4). 983–989. 7 indexed citations

Llaci, Lorida, Keri Ramsey, Newell Belnap, et al.. (2019). Compound heterozygous mutations in SNAP29 is associated with Pelizaeus-Merzbacher-like disorder (PMLD). Human Genetics. 138(11-12). 1409–1417. 12 indexed citations

Kari, Elina, Lorida Llaci, John L. Go, et al.. (2019). A de novo SIX1 variant in a patient with a rare nonsyndromic cochleovestibular nerve abnormality, cochlear hypoplasia, and bilateral sensorineural hearing loss. Molecular Genetics & Genomic Medicine. 7(12). e995–e995. 3 indexed citations

Schrauwen, Isabelle, Elina Kari, Lorida Llaci, et al.. (2018). De novo variants in GREB1L are associated with non-syndromic inner ear malformations and deafness. Human Genetics. 137(6-7). 459–470. 28 indexed citations

10.

Llaci, Lorida, et al.. (2018). Methods for CpG Methylation Array Profiling Via Bisulfite Conversion. Methods in molecular biology. 1706. 233–254. 11 indexed citations

11.

Gerhard, Glenn S., Ivana Malenica, Lorida Llaci, et al.. (2018). Differentially methylated loci in NAFLD cirrhosis are associated with key signaling pathways. Clinical Epigenetics. 10(1). 93–93. 28 indexed citations

12.

Kari, Elina, Isabelle Schrauwen, Lorida Llaci, et al.. (2017). Compound heterozygous mutations in MASP1 in a deaf child with absent cochlear nerves. Neurology Genetics. 3(3). e153–e153. 5 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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