Erin Conboy

905 total citations
28 papers, 481 citations indexed

About

Erin Conboy is a scholar working on Genetics, Molecular Biology and Epidemiology. According to data from OpenAlex, Erin Conboy has authored 28 papers receiving a total of 481 indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Genetics, 12 papers in Molecular Biology and 7 papers in Epidemiology. Recurrent topics in Erin Conboy's work include Genomics and Rare Diseases (5 papers), Genetic Syndromes and Imprinting (4 papers) and Genomic variations and chromosomal abnormalities (4 papers). Erin Conboy is often cited by papers focused on Genomics and Rare Diseases (5 papers), Genetic Syndromes and Imprinting (4 papers) and Genomic variations and chromosomal abnormalities (4 papers). Erin Conboy collaborates with scholars based in United States, Germany and Brazil. Erin Conboy's co-authors include Matthew J. Gastinger, Alistair J. Barber, Sarah K. Bronson, Allen R. Kunselman, Dana Kim Reed, Brenda D. Moore, Vijayaraghavan Rangachari, David E. Hartigan, Terrone L. Rosenberry and Filippo Pinto e Vairo and has published in prestigious journals such as SHILAP Revista de lepidopterología, Biochemistry and PEDIATRICS.

In The Last Decade

Erin Conboy

27 papers receiving 475 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Erin Conboy United States 11 241 164 118 62 58 28 481
Anandalakshmi Venkatraman Singapore 12 285 1.2× 78 0.5× 289 2.4× 89 1.4× 27 0.5× 21 743
Junkang Shen China 10 230 1.0× 50 0.3× 85 0.7× 24 0.4× 15 0.3× 19 600
Xu Zha China 9 365 1.5× 51 0.3× 120 1.0× 29 0.5× 33 0.6× 24 644
Arpna Srivastava India 12 261 1.1× 34 0.2× 134 1.1× 73 1.2× 15 0.3× 26 510
Zhenlian Wang China 12 378 1.6× 128 0.8× 27 0.2× 32 0.5× 37 0.6× 19 615
Hyoung Oh Jun South Korea 14 302 1.3× 33 0.2× 171 1.4× 19 0.3× 15 0.3× 19 503
R Y Kim United States 6 293 1.2× 77 0.5× 182 1.5× 41 0.7× 40 0.7× 7 541
Yuriko Minegishi Japan 16 320 1.3× 77 0.5× 126 1.1× 38 0.6× 17 0.3× 32 704
Noboru Satozawa Japan 8 178 0.7× 47 0.3× 53 0.4× 41 0.7× 179 3.1× 8 469

Countries citing papers authored by Erin Conboy

Since Specialization
Citations

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

Fields of papers citing papers by Erin Conboy

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Erin Conboy

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

All Works

20 of 20 papers shown
1.
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Conboy, Erin, et al.. (2024). Further evidence of involvement of ITSN1 in autosomal dominant neurodevelopmental disorder. Clinical Genetics. 105(4). 455–456. 1 indexed citations
3.
Nasır, Abdul, et al.. (2024). Undiagnosed rare disease clinic identifies a novel UBE3A variant in two sisters with Angelman syndrome: The end of a diagnostic odyssey. Congenital Anomalies. 64(3). 155–160. 1 indexed citations
4.
Helm, Benjamin M., Erin Conboy, Gabrielle C. Geddes, et al.. (2024). Performance of Dysmorphology‐Based Screening for Genetic Disorders in Pediatric Congenital Heart Disease Supports Wider Genetic Testing. Molecular Genetics & Genomic Medicine. 12(11). e70040–e70040. 1 indexed citations
5.
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Nasır, Abdul, et al.. (2023). A case of MBTPS1‐related disorder due to compound heterozygous variants in MBTPS1 gene: Genotype–phenotype expansion and the emergence of a novel syndrome. American Journal of Medical Genetics Part A. 194(5). 1 indexed citations
7.
Conboy, Erin, et al.. (2023). A familialSAMD9variant present in pediatric myelodysplastic syndrome. Molecular Case Studies. 9(2). a006256–a006256. 1 indexed citations
8.
9.
Gillespie, Patrick J., Tae‐Hwi Schwantes‐An, Benjamin M. Helm, et al.. (2022). Characterization of a novel deep-intronic variant inDYNC2H1identified by whole-exome sequencing in a patient with a lethal form of a short-rib thoracic dysplasia type III. Molecular Case Studies. 8(7). a006254–a006254. 1 indexed citations
10.
Vance, Gail H., et al.. (2020). An Adolescent with a Rare De Novo Distal Trisomy 6p and Distal Monosomy 6q Chromosomal Combination. SHILAP Revista de lepidopterología. 2020. 1–8. 1 indexed citations
11.
Conboy, Erin, Silvia Tortorelli, Kim K. Nickander, et al.. (2019). Multiplex testing for the screening of lysosomal storage disease in urine: Sulfatides and glycosaminoglycan profiles in 40 cases of sulfatiduria. Molecular Genetics and Metabolism. 129(2). 106–110. 10 indexed citations
12.
Cho, Janice, Joseph C. Y. Chen, Jonas Paludo, et al.. (2019). Hyperammonemic encephalopathy in a patient with fibrolamellar hepatocellular carcinoma: case report and literature review. Journal of Gastrointestinal Oncology. 10(3). 582–588. 12 indexed citations
13.
Conboy, Erin, Filippo Pinto e Vairo, Darrel Waggoner, et al.. (2017). Pathogenic Variant in ACTB, p.Arg183Trp, Causes Juvenile-Onset Dystonia, Hearing Loss, and Developmental Delay without Midline Malformation. SHILAP Revista de lepidopterología. 2017. 1–4. 13 indexed citations
14.
Bazerbachi, Fateh, Erin Conboy, Taofic Mounajjed, et al.. (2017). Cryptogenic Cirrhosis and Sitosterolemia: A Treatable Disease If Identified but Fatal If Missed. Annals of Hepatology. 16(6). 970–978. 15 indexed citations
15.
Vairo, Filippo Pinto e, Nicole J. Boczek, Margot A. Cousin, et al.. (2017). The prevalence of diseases caused by lysosome-related genes in a cohort of undiagnosed patients. Molecular Genetics and Metabolism Reports. 13. 46–51. 17 indexed citations
16.
Conboy, Erin, Filippo Pinto e Vairo, Matthew Schultz, et al.. (2017). Mitochondrial 3-Hydroxy-3-Methylglutaryl-CoA Synthase Deficiency: Unique Presenting Laboratory Values and a Review of Biochemical and Clinical Features. JIMD Reports. 40. 63–69. 29 indexed citations
17.
Conboy, Erin, et al.. (2015). Whole-Exome Sequencing in the Clinic: Lessons from Six Consecutive Cases from the Clinician's Perspective. Molecular Syndromology. 6(1). 23–31. 27 indexed citations
18.
Gastinger, Matthew J., Allen R. Kunselman, Erin Conboy, Sarah K. Bronson, & Alistair J. Barber. (2008). Dendrite Remodeling and Other Abnormalities in the Retinal Ganglion Cells of Ins2AkitaDiabetic Mice. Investigative Ophthalmology & Visual Science. 49(6). 2635–2635. 148 indexed citations
19.
Sauder, Charity L., et al.. (2008). Otolithic activation on visceral circulation in humans: effect of aging. American Journal of Physiology-Renal Physiology. 295(4). F1166–F1169. 7 indexed citations
20.
Rangachari, Vijayaraghavan, Brenda D. Moore, Dana Kim Reed, et al.. (2007). Amyloid-β(1−42) Rapidly Forms Protofibrils and Oligomers by Distinct Pathways in Low Concentrations of Sodium Dodecylsulfate. Biochemistry. 46(43). 12451–12462. 133 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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