Deborah L. Stabley

2.3k total citations
55 papers, 1.5k citations indexed

About

Deborah L. Stabley is a scholar working on Molecular Biology, Immunology and Organic Chemistry. According to data from OpenAlex, Deborah L. Stabley has authored 55 papers receiving a total of 1.5k indexed citations (citations by other indexed papers that have themselves been cited), including 42 papers in Molecular Biology, 13 papers in Immunology and 12 papers in Organic Chemistry. Recurrent topics in Deborah L. Stabley's work include Protein Tyrosine Phosphatases (28 papers), Galectins and Cancer Biology (10 papers) and Carbohydrate Chemistry and Synthesis (6 papers). Deborah L. Stabley is often cited by papers focused on Protein Tyrosine Phosphatases (28 papers), Galectins and Cancer Biology (10 papers) and Carbohydrate Chemistry and Synthesis (6 papers). Deborah L. Stabley collaborates with scholars based in United States, Canada and Germany. Deborah L. Stabley's co-authors include Katia Sol‐Church, Karen W. Gripp, Linda K. Nicholson, Jennifer Holbrook, Angela E. Lin, Marni E. Axelrad, Daniel Doyle, Iris L. Gonzalez, Elizabeth Hopkins and Elaine H. Zackai and has published in prestigious journals such as SHILAP Revista de lepidopterología, Cancer Research and Annals of Neurology.

In The Last Decade

Deborah L. Stabley

54 papers receiving 1.5k citations

Peers

Deborah L. Stabley

IMMUN

GENET

ONCOL

Katia Sol‐Church United States

William E. Tidyman United States

Stefano Regis Italy

Sharon Boast United States

Maria Ringvall Sweden

R.L. Eddy United States

Wouter Korver United States

Jesús Cruces Spain

Lee N. Lawton United States

David George United States

Katia Sol‐Church United States

Deborah L. Stabley

1.4k ×1.2

549 ×1.2

IMMUN

341 ×1.1

GENET

285 ×1.3

ONCOL

155 ×1.1

Citations per year, relative to Deborah L. Stabley Deborah L. Stabley (= 1×) peers Katia Sol‐Church

Countries citing papers authored by Deborah L. Stabley

Since Specialization

Citations

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

Fields of papers citing papers by Deborah L. Stabley

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Deborah L. Stabley. 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 Deborah L. Stabley. The network helps show where Deborah L. Stabley may publish in the future.

Co-authorship network of co-authors of Deborah L. Stabley

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

All Works

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20 of 20 papers shown

Stabley, Deborah L., Jennifer Holbrook, Mena Scavina, et al.. (2021). Detection of SMN1 to SMN2 gene conversion events and partial SMN1 gene deletions using array digital PCR. Neurogenetics. 22(1). 53–64. 12 indexed citations

Morlet, Thierry, et al.. (2021). Mutations in LOXHD1 gene can cause auditory neuropathy spectrum disorder. SHILAP Revista de lepidopterología. 21. 100367–100367.

Stabley, Deborah L., Suhita Gayen Betal, Yan Zhu, et al.. (2021). Pulmonary immune cell transcriptome changes in double-hit model of BPD induced by chorioamnionitis and postnatal hyperoxia. Pediatric Research. 90(3). 565–575. 11 indexed citations

Schwartz, David D., Jennifer M. Katzenstein, Deborah L. Stabley, et al.. (2017). Age‐related differences in prevalence of autism spectrum disorder symptoms in children and adolescents with Costello syndrome. American Journal of Medical Genetics Part A. 173(5). 1294–1300. 12 indexed citations

Stabley, Deborah L., Jennifer Holbrook, Kathryn J. Swoboda, et al.. (2017). Establishing a reference dataset for the authentication of spinal muscular atrophy cell lines using STR profiling and digital PCR. Neuromuscular Disorders. 27(5). 439–446. 12 indexed citations

Gripp, Karen W., Katherine Robbins, Nara Sobreira, et al.. (2014). Truncating mutations in the last exon of NOTCH3 cause lateral meningocele syndrome. American Journal of Medical Genetics Part A. 167(2). 271–281. 59 indexed citations

Gripp, Karen W., Cynthia J. Curry, Ann Haskins Olney, et al.. (2014). Diamond–Blackfan anemia with mandibulofacial dystostosis is heterogeneous, including the novel DBA genes TSR2 and RPS28. American Journal of Medical Genetics Part A. 164(9). 2240–2249. 98 indexed citations

Robbins, Katherine, Deborah L. Stabley, Jennifer Holbrook, Karen W. Gripp, & Katia Sol‐Church. (2013). Uniparental Disomy is Associated with Embryonal Rhabdomyosarcoma in Costello Syndrome and Nonsyndromic Patients: From Core-Side to Bed-Side and Back Again, Impact of Core Laboratories on Biomedical Research. Journal of Biomolecular Techniques JBT. 24. 1 indexed citations

McCormick, Elizabeth M., Elizabeth Hopkins, Laura Conway, et al.. (2013). Assessing genotype–phenotype correlation in Costello syndrome using a severity score. Genetics in Medicine. 15(7). 554–557. 16 indexed citations

10.

Gripp, Karen W., et al.. (2012). Transmission of the rare HRAS mutation (c. 173C > T; p.T58I) further illustrates its attenuated phenotype. American Journal of Medical Genetics Part A. 158A(5). 1095–1101. 14 indexed citations

11.

Hopkins, Elizabeth, Katia Sol‐Church, Deborah L. Stabley, et al.. (2012). Normative growth charts for individuals with Costello syndrome. American Journal of Medical Genetics Part A. 158A(11). 2692–2699. 16 indexed citations

12.

Baratela, Wagner Antonio da Rosa, Michael B. Bober, George E. Tiller, et al.. (2012). A newly recognized syndrome with characteristic facial features, skeletal dysplasia, and developmental delay. American Journal of Medical Genetics Part A. 158A(8). 1815–1822. 10 indexed citations

13.

Gripp, Karen W., Deborah L. Stabley, Elizabeth Hopkins, et al.. (2011). Molecular confirmation of HRAS p.G12S in siblings with Costello syndrome. American Journal of Medical Genetics Part A. 155(9). 2263–2268. 13 indexed citations

14.

Stabley, Deborah L., Davida Kamara, Jennifer Holbrook, et al.. (2010). Digital Gene Expression of miRNA in Osteosarcoma Xenografts: Finding Biological Relevance in miRNA High Throughput Sequencing Data. Journal of Biomolecular Techniques JBT. 21. 2 indexed citations

15.

Sol‐Church, Katia, Deborah L. Stabley, Laurie Demmer, et al.. (2009). Male‐to‐male transmission of Costello syndrome: G12S HRAS germline mutation inherited from a father with somatic mosaicism. American Journal of Medical Genetics Part A. 149A(3). 315–321. 42 indexed citations

16.

Gripp, Karen W., Angela E. Lin, Linda K. Nicholson, et al.. (2007). Further delineation of the phenotype resulting from BRAF or MEK1 germline mutations helps differentiate cardio‐facio‐cutaneous syndrome from Costello syndrome. American Journal of Medical Genetics Part A. 143A(13). 1472–1480. 62 indexed citations

17.

Gripp, Karen W., Angela E. Lin, Deborah L. Stabley, et al.. (2005). HRAS mutation analysis in Costello syndrome: Genotype and phenotype correlation. American Journal of Medical Genetics Part A. 140A(1). 1–7. 133 indexed citations

18.

Devoto, Marcella, Loretta D. Spotila, Deborah L. Stabley, et al.. (2005). Univariate and bivariate variance component linkage analysis of a whole-genome scan for loci contributing to bone mineral density. European Journal of Human Genetics. 13(6). 781–788. 41 indexed citations

19.

Hobson, Grace M., Zhong Huang, Karen Sperle, et al.. (2002). A PLP splicing abnormality is associated with an unusual presentation of PMD. Annals of Neurology. 52(4). 477–488. 44 indexed citations

20.

Hobson, Grace M., Deborah L. Stabley, Vicky L. Funanage, & Harold G. Marks. (2001). A new polymorphism in the proteolipid protein (PLP1) gene and its use for carrier detection ofPLP1 gene duplication in Pelizaeus-Merzbacher disease. Human Mutation. 17(2). 152–152. 3 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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