Grace E. VanNoy

2.2k total citations
15 papers, 232 citations indexed

About

Grace E. VanNoy is a scholar working on Genetics, Molecular Biology and Cellular and Molecular Neuroscience. According to data from OpenAlex, Grace E. VanNoy has authored 15 papers receiving a total of 232 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Genetics, 8 papers in Molecular Biology and 2 papers in Cellular and Molecular Neuroscience. Recurrent topics in Grace E. VanNoy's work include Genomics and Rare Diseases (8 papers), Genomic variations and chromosomal abnormalities (3 papers) and Mitochondrial Function and Pathology (2 papers). Grace E. VanNoy is often cited by papers focused on Genomics and Rare Diseases (8 papers), Genomic variations and chromosomal abnormalities (3 papers) and Mitochondrial Function and Pathology (2 papers). Grace E. VanNoy collaborates with scholars based in United States, Hong Kong and Netherlands. Grace E. VanNoy's co-authors include Pankaj B. Agrawal, Casie A. Genetti, Monica H. Wojcik, Timothy W. Yu, Jill A. Madden, Cynthia S. Gubbels, Alan H. Beggs, Kira A. Dies, Jane Juusola and Richard B. Parad and has published in prestigious journals such as PEDIATRICS, Genetics in Medicine and Clinical Therapeutics.

In The Last Decade

Grace E. VanNoy

13 papers receiving 226 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Grace E. VanNoy United States	8	155	72	47	36	24	15	232
Quinn Stein United States	9	133 0.9×	72 1.0×	50 1.1×	16 0.4×	27 1.1×	31	214
Sara Caylor United States	4	109 0.7×	44 0.6×	34 0.7×	22 0.6×	16 0.7×	4	139
Helen Dolling United Kingdom	2	130 0.8×	52 0.7×	32 0.7×	28 0.8×	26 1.1×	3	159
Stacey Hume Canada	10	68 0.4×	108 1.5×	30 0.6×	23 0.6×	29 1.2×	19	207
Anastasia L. Wise United States	6	212 1.4×	99 1.4×	13 0.3×	39 1.1×	6 0.3×	8	339
Anna Hurst United States	9	69 0.4×	56 0.8×	34 0.7×	21 0.6×	4 0.2×	30	175
Katrina E. Kotzer United States	9	162 1.0×	54 0.8×	71 1.5×	94 2.6×	6 0.3×	12	271
Mallory Owen United States	5	66 0.4×	27 0.4×	25 0.5×	15 0.4×	10 0.4×	8	103
María Caimari Spain	8	113 0.7×	86 1.2×	11 0.2×	18 0.5×	8 0.3×	14	232

Countries citing papers authored by Grace E. VanNoy

Since Specialization

Citations

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

Fields of papers citing papers by Grace E. VanNoy

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Grace E. VanNoy. 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 Grace E. VanNoy. The network helps show where Grace E. VanNoy may publish in the future.

Co-authorship network of co-authors of Grace E. VanNoy

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

All Works

Sort: Min cites: Since: Top N: Style:

15 of 15 papers shown

Weisburd, Ben, Egor Dolzhenko, Vincent Rubinetti, et al.. (2025). STRchive: a dynamic resource detailing population-level and locus-specific insights at tandem repeat disease loci. Genome Medicine. 17(1). 29–29. 1 indexed citations

Horton, Carolyn, et al.. (2025). Understanding how gene-disease relationships can impact clinical utility: adaptations and challenges in hereditary cancer testing. Genome Medicine. 17(1). 73–73.

Stenton, Sarah L., Grace E. VanNoy, Lynn Pais, et al.. (2025). Male proband with intractable seizures and a de novo start-codon-disrupting variant in GLUL. Human Genetics and Genomics Advances. 6(2). 100419–100419.

O’Leary, Melanie, Grace E. VanNoy, Brian Mangilog, et al.. (2023). Advancing Understanding of Inequities in Rare Disease Genomics. Clinical Therapeutics. 45(8). 745–753. 12 indexed citations

Lemire, Gabrielle, et al.. (2023). DNM1L Variant Presenting as Adolescent-Onset Sensory Neuronopathy, Spasticity, Dystonia, and Ataxia. Journal of Pediatric Neurology. 21(6). 475–478. 2 indexed citations

VanNoy, Grace E., et al.. (2023). Emerging roles and opportunities for rare disease patient advocacy groups. PubMed. 4. 921074185–921074185. 28 indexed citations

VanNoy, Grace E., Monica H. Wojcik, Casie A. Genetti, et al.. (2020). Reconsidering Genetic Testing for Neonatal Polycystic Kidney Disease. Kidney International Reports. 5(8). 1316–1319. 2 indexed citations

D’Gama, Alissa M., William Brucker, Tian Zhang, et al.. (2020). A phenotypically severe, biochemically “silent” case of HIBCH deficiency in a newborn diagnosed by rapid whole exome sequencing and enzymatic testing. American Journal of Medical Genetics Part A. 182(4). 780–784. 5 indexed citations

Gubbels, Cynthia S., Grace E. VanNoy, Jill A. Madden, et al.. (2019). Prospective, phenotype-driven selection of critically ill neonates for rapid exome sequencing is associated with high diagnostic yield. Genetics in Medicine. 22(4). 736–744. 79 indexed citations

10.

VanNoy, Grace E., Casie A. Genetti, Amy L. McGuire, et al.. (2019). Challenging the Current Recommendations for Carrier Testing in Children. PEDIATRICS. 143(Supplement_1). S27–S32. 17 indexed citations

11.

Wojcik, Monica H., Talia S. Schwartz, Thomas E. Mullen, et al.. (2019). Infant mortality: the contribution of genetic disorders. Journal of Perinatology. 39(12). 1611–1619. 49 indexed citations

12.

VanNoy, Grace E., Meghan C. Towne, Yiping Shen, et al.. (2018). Three‐generation family with novel contiguous gene deletion on chromosome 2p22 associated with thoracic aortic aneurysm syndrome. American Journal of Medical Genetics Part A. 176(3). 560–569. 11 indexed citations

13.

Murry, Jaclyn B., Kalotina Machini, Ozge Ceyhan‐Birsoy, et al.. (2018). Reconciling newborn screening and a novel splice variant in BTD associated with partial biotinidase deficiency: a BabySeq Project case report. Molecular Case Studies. 4(4). a002873–a002873. 4 indexed citations

14.

Brownstein, Catherine A., Casie A. Genetti, Kelsey Graber, et al.. (2018). De novo variant of TRRAP in a patient with very early onset psychosis in the context of non-verbal learning disability and obsessive-compulsive disorder: a case report. BMC Medical Genetics. 19(1). 197–197. 8 indexed citations

15.

Lo, Mindy S., Meghan C. Towne, Grace E. VanNoy, et al.. (2017). Monogenic Hashimoto thyroiditis associated with a variant in the thyroglobulin (TG) gene. Journal of Autoimmunity. 86. 116–119. 14 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.

Explore authors with similar magnitude of impact