Ellen Moran

932 total citations
10 papers, 218 citations indexed

About

Ellen Moran is a scholar working on Molecular Biology, Genetics and Cellular and Molecular Neuroscience. According to data from OpenAlex, Ellen Moran has authored 10 papers receiving a total of 218 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Molecular Biology, 4 papers in Genetics and 3 papers in Cellular and Molecular Neuroscience. Recurrent topics in Ellen Moran's work include Genetics and Neurodevelopmental Disorders (2 papers), Congenital heart defects research (2 papers) and Genetic Neurodegenerative Diseases (2 papers). Ellen Moran is often cited by papers focused on Genetics and Neurodevelopmental Disorders (2 papers), Congenital heart defects research (2 papers) and Genetic Neurodegenerative Diseases (2 papers). Ellen Moran collaborates with scholars based in United States, Australia and Belgium. Ellen Moran's co-authors include M. L. Chu, Robert Wallerstein, Rebecca Sutphen, John C. Carey, Lynn B. Jorde, Bridget Kramer, Thanh Le, Lionel Van Maldergem, W. Scott Watkins and Susan Root and has published in prestigious journals such as SHILAP Revista de lepidopterología, The Journal of Clinical Endocrinology & Metabolism and The American Journal of Human Genetics.

In The Last Decade

Ellen Moran

9 papers receiving 212 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Ellen Moran United States	4	193	73	26	23	19	10	218
Siddaramappa J. Patil India	7	89 0.5×	71 1.0×	17 0.7×	8 0.3×	10 0.5×	24	165
Angeline Lai Singapore	10	152 0.8×	133 1.8×	67 2.6×	19 0.8×	12 0.6×	31	349
Thomas Smol France	10	129 0.7×	70 1.0×	13 0.5×	8 0.3×	18 0.9×	34	224
Jennifer McDaid United Kingdom	8	271 1.4×	99 1.4×	22 0.8×	21 0.9×	11 0.6×	8	325
Rosamaria Silipigni Italy	10	144 0.7×	79 1.1×	11 0.4×	20 0.9×	12 0.6×	35	264
María Gabriela Obregón Argentina	10	176 0.9×	124 1.7×	19 0.7×	26 1.1×	9 0.5×	33	256
Neda Zadeh United States	7	152 0.8×	141 1.9×	25 1.0×	6 0.3×	16 0.8×	12	253
Giulia Pascolini Italy	7	69 0.4×	89 1.2×	33 1.3×	16 0.7×	10 0.5×	27	176
Amal Hashem Saudi Arabia	9	236 1.2×	138 1.9×	21 0.8×	32 1.4×	6 0.3×	11	354
Juliane Eckhold Germany	8	116 0.6×	66 0.9×	18 0.7×	6 0.3×	28 1.5×	10	202

Countries citing papers authored by Ellen Moran

Since Specialization

Citations

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

Fields of papers citing papers by Ellen Moran

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ellen Moran

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

All Works

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10 of 10 papers shown

McDonald‐McGinn, Donna M., T. Blaine Crowley, Daniel E. McGinn, et al.. (2024). P217: Abnormalities of TBX1 result in broad overlapping features of 22q11.2 deletion syndrome. SHILAP Revista de lepidopterología. 2. 101114–101114.

Moran, Ellen, John Pappas, M. L. Chu, et al.. (2023). Biochemical characterization of two novel mutations in the human high-affinity choline transporter 1 identified in a patient with congenital myasthenic syndrome. Human Molecular Genetics. 32(9). 1552–1564. 2 indexed citations

Chu, M. L., Ellen Moran, Elizabeth Wohler, et al.. (2022). MRM2 variants in families with complex dystonic syndromes: evidence for phenotypic heterogeneity. Journal of Medical Genetics. 60(4). 352–358. 1 indexed citations

Chu, M. L. & Ellen Moran. (2018). The Limb–Girdle Muscular Dystrophies: Is Treatment on the Horizon?. Neurotherapeutics. 15(4). 849–862. 42 indexed citations

Noch, Evan, Claire Henchcliffe, M. L. Chu, et al.. (2017). Kufor‐Rakeb Syndrome Due to a Novel ATP13A2 Mutation in 2 Chinese‐American Brothers. Movement Disorders Clinical Practice. 5(1). 92–95. 3 indexed citations

Chu, Alice, et al.. (2015). Potocki–Lupski syndrome in conjunction with bilateral clubfoot. Journal of Pediatric Orthopaedics B. 24(4). 373–376. 4 indexed citations

Shah, Bina, Ellen Moran, Andrew R. Zinn, & John Pappas. (2009). Effect of Growth Hormone Therapy on Severe Short Stature and Skeletal Deformities in a Patient with Combined Turner Syndrome and Langer Mesomelic Dysplasia. The Journal of Clinical Endocrinology & Metabolism. 94(12). 5028–5033. 2 indexed citations

Sala, Debra A., et al.. (2002). Tethered cord in a patient with multiple vertebral segmentation defects: a case report.. PubMed. 60(2). 96–9. 2 indexed citations

Stewart, Patricia A., Robert Wallerstein, Ellen Moran, & Minju Lee. (2000). Early prenatal ultrasound diagnosis of cleidocranial dysplasia. Ultrasound in Obstetrics and Gynecology. 15(2). 154–156. 16 indexed citations

10.

Bamshad, Michael J., Thanh Le, W. Scott Watkins, et al.. (1999). The Spectrum of Mutations in TBX3: Genotype/Phenotype Relationship in Ulnar-Mammary Syndrome. The American Journal of Human Genetics. 64(6). 1550–1562. 146 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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