Elise Valkanas

2.1k total citations
6 papers, 125 citations indexed

About

Elise Valkanas is a scholar working on Genetics, Molecular Biology and Cellular and Molecular Neuroscience. According to data from OpenAlex, Elise Valkanas has authored 6 papers receiving a total of 125 indexed citations (citations by other indexed papers that have themselves been cited), including 4 papers in Genetics, 3 papers in Molecular Biology and 2 papers in Cellular and Molecular Neuroscience. Recurrent topics in Elise Valkanas's work include Genomics and Rare Diseases (3 papers), Muscle Physiology and Disorders (2 papers) and Retinal Development and Disorders (1 paper). Elise Valkanas is often cited by papers focused on Genomics and Rare Diseases (3 papers), Muscle Physiology and Disorders (2 papers) and Retinal Development and Disorders (1 paper). Elise Valkanas collaborates with scholars based in United States, Saudi Arabia and Australia. Elise Valkanas's co-authors include Daniel G. MacArthur, Monkol Lek, Timothy W. Yu, Anthony A. Amato, David Margulies, Mustafa A. Salih, Hart G.W. Lidov, Kyung‐Ah Cho, Elicia Estrella and Peter B. Kang and has published in prestigious journals such as Human Mutation, Genetics in Medicine and Physiological Genomics.

In The Last Decade

Elise Valkanas

6 papers receiving 124 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Elise Valkanas United States	6	89	50	32	29	17	6	125
Katherine R. Chao United States	8	120 1.3×	45 0.9×	16 0.5×	43 1.5×	19 1.1×	16	177
Khanh‐Dung H. Nguyen United States	4	85 1.0×	43 0.9×	33 1.0×	15 0.5×	3 0.2×	4	145
Yannis Duffourd France	10	115 1.3×	132 2.6×	12 0.4×	13 0.4×	8 0.5×	25	221
Sebastian Röner Germany	3	84 0.9×	68 1.4×	13 0.4×	6 0.2×	7 0.4×	5	160
C. Labasse France	5	75 0.8×	18 0.4×	26 0.8×	44 1.5×	15 0.9×	11	101
S. Makri France	5	140 1.6×	23 0.5×	43 1.3×	27 0.9×	12 0.7×	8	156
Dana Marafi United States	8	88 1.0×	70 1.4×	22 0.7×	10 0.3×	15 0.9×	24	171
Jawid M. Fatih United States	8	138 1.6×	88 1.8×	25 0.8×	11 0.4×	9 0.5×	13	217
Lilia Kraoua Tunisia	9	130 1.5×	64 1.3×	14 0.4×	35 1.2×	7 0.4×	23	182
Dmitriy Niyazov United States	7	140 1.6×	99 2.0×	11 0.3×	11 0.4×	12 0.7×	8	208

Countries citing papers authored by Elise Valkanas

Since Specialization

Citations

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

Fields of papers citing papers by Elise Valkanas

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Elise Valkanas

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

All Works

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6 of 6 papers shown

1.

Jamshidi, Farzad, Emily Place, Sudeep Mehrotra, et al.. (2018). Contribution of noncoding pathogenic variants to RPGRIP1-mediated inherited retinal degeneration. Genetics in Medicine. 21(3). 694–704. 17 indexed citations

2.

Arachchi, Harindra, Monica H. Wojcik, Julius O.B. Jacobsen, et al.. (2018). matchbox: An open-source tool for patient matching via the Matchmaker Exchange. Human Mutation. 39(12). 1827–1834. 7 indexed citations

3.

Saha, Madhurima, Hemakumar M. Reddy, Mustafa A. Salih, et al.. (2018). Impact of PYROXD1 deficiency on cellular respiration and correlations with genetic analyses of limb-girdle muscular dystrophy in Saudi Arabia and Sudan. Physiological Genomics. 50(11). 929–939. 15 indexed citations

4.

Xu, Karen, Amanda E. Links, David R. Adams, et al.. (2016). Pharmacogenomic incidental findings in 308 families: The NIH Undiagnosed Diseases Program experience. Genetics in Medicine. 18(12). 1303–1307. 12 indexed citations

5.

Valkanas, Elise, Katherine E. Schaffer, Christopher Dunham, et al.. (2016). Phenotypic evolution of UNC80 loss of function. American Journal of Medical Genetics Part A. 170(12). 3106–3114. 14 indexed citations

6.

Reddy, Hemakumar M., Kyung‐Ah Cho, Monkol Lek, et al.. (2016). The sensitivity of exome sequencing in identifying pathogenic mutations for LGMD in the United States. Journal of Human Genetics. 62(2). 243–252. 60 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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