Juliana Helou

1.7k total citations
5 papers, 399 citations indexed

About

Juliana Helou is a scholar working on Molecular Biology, Genetics and Nephrology. According to data from OpenAlex, Juliana Helou has authored 5 papers receiving a total of 399 indexed citations (citations by other indexed papers that have themselves been cited), including 4 papers in Molecular Biology, 4 papers in Genetics and 1 paper in Nephrology. Recurrent topics in Juliana Helou's work include Genetic and Kidney Cyst Diseases (4 papers), Renal and related cancers (4 papers) and Hemoglobinopathies and Related Disorders (1 paper). Juliana Helou is often cited by papers focused on Genetic and Kidney Cyst Diseases (4 papers), Renal and related cancers (4 papers) and Hemoglobinopathies and Related Disorders (1 paper). Juliana Helou collaborates with scholars based in United States, Canada and Germany. Juliana Helou's co-authors include Friedhelm Hildebrandt, Edgar A. Otto, Ulla T. Schultheiß, Lynne M. Quarmby, John F. O’Toole, Massimo Attanasio, Katrin Anlag, N. Henriette Uhlenhaut, Peter Nürnberg and John A. Sayer and has published in prestigious journals such as Nature Genetics, Journal of the American Society of Nephrology and Human Mutation.

In The Last Decade

Juliana Helou

5 papers receiving 395 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Juliana Helou United States	5	329	314	76	36	35	5	399
Valeska Frank Germany	11	389 1.2×	396 1.3×	92 1.2×	51 1.4×	24 0.7×	12	488
Nadina Ortiz Brüchle Germany	9	380 1.2×	333 1.1×	104 1.4×	65 1.8×	19 0.5×	13	475
Simon A. Ramsbottom United Kingdom	13	360 1.1×	209 0.7×	45 0.6×	21 0.6×	82 2.3×	16	432
Marijn F. Stokman Netherlands	10	271 0.8×	222 0.7×	57 0.8×	37 1.0×	35 1.0×	15	360
Veronica Moran United Kingdom	3	344 1.0×	363 1.2×	50 0.7×	16 0.4×	23 0.7×	3	478
Kristen L. Sund United States	9	193 0.6×	171 0.5×	56 0.7×	15 0.4×	28 0.8×	15	326
Sandra Hakim Australia	7	263 0.8×	202 0.6×	24 0.3×	26 0.7×	106 3.0×	7	353
Anna Sowińska‐Seidler Poland	13	254 0.8×	237 0.8×	74 1.0×	17 0.5×	19 0.5×	38	409
M. Cecilia Cirio United States	10	330 1.0×	163 0.5×	122 1.6×	6 0.2×	29 0.8×	15	394
Philip L. Beales United Kingdom	7	102 0.3×	152 0.5×	32 0.4×	18 0.5×	20 0.6×	8	263

Countries citing papers authored by Juliana Helou

Since Specialization

Citations

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

Fields of papers citing papers by Juliana Helou

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Juliana Helou

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

All Works

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5 of 5 papers shown

1.

Lim, Wei Sing, et al.. (2017). Retinal thickness measurements in sickle cell patients with HbSS and HbSC genotype. Canadian Journal of Ophthalmology. 53(4). 420–424. 9 indexed citations

2.

Otto, Edgar A., et al.. (2008). NEK8 Mutations Affect Ciliary and Centrosomal Localization and May Cause Nephronophthisis. Journal of the American Society of Nephrology. 19(3). 587–592. 148 indexed citations

3.

Otto, Edgar A., Juliana Helou, Susan J. Allen, et al.. (2007). Mutation analysis in nephronophthisis using a combined approach of homozygosity mapping, CEL I endonuclease cleavage, and direct sequencing. Human Mutation. 29(3). 418–426. 60 indexed citations

4.

Attanasio, Massimo, N. Henriette Uhlenhaut, Vitor H. Sousa, et al.. (2007). Loss of GLIS2 causes nephronophthisis in humans and mice by increased apoptosis and fibrosis. Nature Genetics. 39(8). 1018–1024. 174 indexed citations

5.

O’Toole, John F., Edgar A. Otto, Julia Hoefele, Juliana Helou, & Friedhelm Hildebrandt. (2006). Mutational analysis in 119 families with nephronophthisis. Pediatric Nephrology. 22(3). 366–370. 8 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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