Rena A. Godfrey

2.7k total citations
8 papers, 96 citations indexed

About

Rena A. Godfrey is a scholar working on Molecular Biology, Clinical Biochemistry and Neurology. According to data from OpenAlex, Rena A. Godfrey has authored 8 papers receiving a total of 96 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Molecular Biology, 2 papers in Clinical Biochemistry and 2 papers in Neurology. Recurrent topics in Rena A. Godfrey's work include Genomics and Rare Diseases (2 papers), Neurological diseases and metabolism (2 papers) and Metabolism and Genetic Disorders (2 papers). Rena A. Godfrey is often cited by papers focused on Genomics and Rare Diseases (2 papers), Neurological diseases and metabolism (2 papers) and Metabolism and Genetic Disorders (2 papers). Rena A. Godfrey collaborates with scholars based in United States and Italy. Rena A. Godfrey's co-authors include William A. Gahl, Camilo Toro, Colleen E. Wahl, May Christine V. Malicdan, Catherine Groden, Gretchen Golas, Lynne A. Wolfe, Dennis M.D. Landis, David R. Adams and Cornelius F. Boerkoel and has published in prestigious journals such as Developmental Medicine & Child Neurology, Genetics in Medicine and Molecular Genetics and Metabolism.

In The Last Decade

Rena A. Godfrey

8 papers receiving 96 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Rena A. Godfrey United States	4	54	30	18	12	11	8	96
James J. O’Byrne Ireland	8	81 1.5×	95 3.2×	7 0.4×	13 1.1×	8 0.7×	24	174
Mona Mohammad Almramhi United Kingdom	8	58 1.1×	117 3.9×	13 0.7×	9 0.8×	8 0.7×	13	189
Judith D. Ranells United States	7	72 1.3×	58 1.9×	20 1.1×	4 0.3×	13 1.2×	10	195
Lynette Rives United States	4	52 1.0×	33 1.1×	14 0.8×	12 1.0×	7 0.6×	7	97
Christel Thauvin France	6	37 0.7×	81 2.7×	9 0.5×	6 0.5×	7 0.6×	11	146
Natalie B. Tan Australia	6	69 1.3×	50 1.7×	9 0.5×	8 0.7×	10 0.9×	8	131
Naomi Meeks United States	8	50 0.9×	86 2.9×	9 0.5×	5 0.4×	3 0.3×	16	169
Eva Maria Christina Schwaibold Germany	7	57 1.1×	66 2.2×	20 1.1×	7 0.6×	3 0.3×	11	124
Christine Shieh United States	6	78 1.4×	71 2.4×	46 2.6×	5 0.4×	9 0.8×	12	178
Mary Koziura United States	4	70 1.3×	51 1.7×	13 0.7×	14 1.2×	3 0.3×	5	114

Countries citing papers authored by Rena A. Godfrey

Since Specialization

Citations

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

Fields of papers citing papers by Rena A. Godfrey

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Rena A. Godfrey. 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 Rena A. Godfrey. The network helps show where Rena A. Godfrey may publish in the future.

Co-authorship network of co-authors of Rena A. Godfrey

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

All Works

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8 of 8 papers shown

Malicdan, May Christine V., Ellen F. Macnamara, Tanya Lehky, et al.. (2022). MYH2-associated myopathy caused by a novel splice-site variant. Neuromuscular Disorders. 33(3). 257–262. 3 indexed citations

Zein, Wadih M., Robert B. Hufnagel, Rena A. Godfrey, et al.. (2022). A de novo hexokinase 1 (HK1) variant presenting as Boucher–Neuhäuser syndrome. American Journal of Medical Genetics Part A. 191(2). 624–629. 1 indexed citations

Wang, Jennifer, Nicholas Balanda, Yan Huang, et al.. (2020). Biallelic variants in two complex I genes cause abnormal splicing defects in probands with mild Leigh syndrome. Molecular Genetics and Metabolism. 131(1-2). 98–106. 3 indexed citations

Shanbhag, Niraj M., Michael D. Geschwind, John J. DiGiovanna, et al.. (2018). Neurodegeneration as the presenting symptom in 2 adults with xeroderma pigmentosum complementation group F. Neurology Genetics. 4(3). e240–e240. 13 indexed citations

Goheen, Mitchell, Rena A. Godfrey, Colleen E. Wahl, et al.. (2017). Late diagnosis and atypical brain imaging of Aicardi–Goutières syndrome: are we failing to diagnose Aicardi–Goutières syndrome‐2?. Developmental Medicine & Child Neurology. 59(12). 1307–1311. 15 indexed citations

Sincan, Murat, Thomas C. Markello, David R. Adams, et al.. (2014). The implications of familial incidental findings from exome sequencing: the NIH Undiagnosed Diseases Program experience. Genetics in Medicine. 16(10). 741–750. 49 indexed citations

Brady, Jacqueline M., Aditi Trehan, Rena A. Godfrey, et al.. (2013). Mucopolysaccharidosis IIIB (Sanfilippo syndrome type B) masquerading as a behavioral disorder. Molecular Genetics and Metabolism. 108(2). S26–S26. 1 indexed citations

Vanderver, Adeline, Davide Tonduti, Sarah Auerbach, et al.. (2012). Neurotransmitter abnormalities and response to supplementation in SPG11. Molecular Genetics and Metabolism. 107(1-2). 229–233. 11 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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