Renee Bend

410 total citations
5 papers, 61 citations indexed

About

Renee Bend is a scholar working on Genetics, Molecular Biology and Cellular and Molecular Neuroscience. According to data from OpenAlex, Renee Bend has authored 5 papers receiving a total of 61 indexed citations (citations by other indexed papers that have themselves been cited), including 3 papers in Genetics, 2 papers in Molecular Biology and 1 paper in Cellular and Molecular Neuroscience. Recurrent topics in Renee Bend's work include Mitochondrial Function and Pathology (2 papers), Genetics and Neurodevelopmental Disorders (2 papers) and Genomic variations and chromosomal abnormalities (2 papers). Renee Bend is often cited by papers focused on Mitochondrial Function and Pathology (2 papers), Genetics and Neurodevelopmental Disorders (2 papers) and Genomic variations and chromosomal abnormalities (2 papers). Renee Bend collaborates with scholars based in United States, Norway and Netherlands. Renee Bend's co-authors include Catherine J. Spellicy, Michael J. Friez, Emil Alexov, Carlos R. Ferreira, Ingrid M. Wentzensen, Lior Cohen, Erin Torti, Tracy Reynolds, Claudia Gonzaga‐Jauregui and Jane H. Dean and has published in prestigious journals such as Molecular Psychiatry, Journal of Medical Genetics and European Journal of Human Genetics.

In The Last Decade

Renee Bend

5 papers receiving 60 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Renee Bend United States	5	43	23	10	6	6	5	61
Catherine L. Mercer United Kingdom	5	41 1.0×	49 2.1×	13 1.3×	9 1.5×	5 0.8×	6	72
Melissa A Dempsey United States	5	63 1.5×	47 2.0×	11 1.1×	6 1.0×	10 1.7×	8	86
Valeria Lo Faro Netherlands	7	36 0.8×	33 1.4×	7 0.7×	3 0.5×	4 0.7×	10	91
Stacy Gabriel United States	1	27 0.6×	40 1.7×	21 2.1×	3 0.5×	9 1.5×	2	60
Anna Wilsdon United Kingdom	3	42 1.0×	40 1.7×	10 1.0×	5 0.8×		6	76
Randa Bassiouni Egypt	4	19 0.4×	15 0.7×	9 0.9×	12 2.0×	6 1.0×	7	36
Nobuhiko Okamoto Japan	4	35 0.8×	34 1.5×	8 0.8×	2 0.3×	7 1.2×	7	68
Christian Marshall Canada	4	27 0.6×	35 1.5×	17 1.7×	6 1.0×	2 0.3×	8	80
Ainhoa García-Ribes Spain	5	21 0.5×	32 1.4×	4 0.4×	5 0.8×	18 3.0×	10	74
Julija Pavaine United Kingdom	5	59 1.4×	15 0.7×	7 0.7×	10 1.7×	7 1.2×	7	98

Countries citing papers authored by Renee Bend

Since Specialization

Citations

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

Fields of papers citing papers by Renee Bend

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Renee Bend

This figure shows the co-authorship network connecting the top 25 collaborators of Renee Bend. A scholar is included among the top collaborators of Renee Bend 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 Renee Bend. Renee Bend 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.

Nia, Fatemeh Hassani, Isabel Bento, Stephan Niebling, et al.. (2022). Structural deficits in key domains of Shank2 lead to alterations in postsynaptic nanoclusters and to a neurodevelopmental disorder in humans. Molecular Psychiatry. 29(6). 1683–1697. 9 indexed citations

2.

Fee, Timothy, Renee Bend, Raymond J. Louie, et al.. (2022). Mosaicism of common pathogenic MECP2 variants identified in two males with a clinical diagnosis of Rett syndrome. American Journal of Medical Genetics Part A. 188(10). 2988–2998. 5 indexed citations

3.

Matalon, Dena R., Brieana Fregeau, Ingvild Aukrust, et al.. (2020). De novo variants in SUPT16H cause neurodevelopmental disorders associated with corpus callosum abnormalities. Journal of Medical Genetics. 57(7). 461–465. 12 indexed citations

4.

Bend, Renee, Lior Cohen, Melissa T. Carter, et al.. (2019). Phenotype and mutation expansion of the PTPN23 associated disorder characterized by neurodevelopmental delay and structural brain abnormalities. European Journal of Human Genetics. 28(1). 76–87. 18 indexed citations

5.

Spellicy, Catherine J., Joy Norris, Renee Bend, et al.. (2018). Key apoptotic genes APAF1 and CASP9 implicated in recurrent folate-resistant neural tube defects. European Journal of Human Genetics. 26(3). 420–427. 17 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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