Sandra Gill

1.3k total citations
15 papers, 880 citations indexed

About

Sandra Gill is a scholar working on Cellular and Molecular Neuroscience, Molecular Biology and Cell Biology. According to data from OpenAlex, Sandra Gill has authored 15 papers receiving a total of 880 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Cellular and Molecular Neuroscience, 9 papers in Molecular Biology and 4 papers in Cell Biology. Recurrent topics in Sandra Gill's work include Hereditary Neurological Disorders (10 papers), RNA Research and Splicing (4 papers) and Signaling Pathways in Disease (3 papers). Sandra Gill is often cited by papers focused on Hereditary Neurological Disorders (10 papers), RNA Research and Splicing (4 papers) and Signaling Pathways in Disease (3 papers). Sandra Gill collaborates with scholars based in United States, Israel and United Kingdom. Sandra Gill's co-authors include Maire Leyne, Susan A. Slaugenhaupt, James F. Gusella, James Mull, Math P. Cuajungco, Channa Maayan, Felicia B. Axelrod, Anat Blumenfeld, Izabela Makałowska and Christiane M. Robbins and has published in prestigious journals such as The Journal of Clinical Endocrinology & Metabolism, Brain Research and The American Journal of Human Genetics.

In The Last Decade

Sandra Gill

15 papers receiving 854 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Sandra Gill United States	11	481	461	171	117	83	15	880
Maire Leyne United States	15	689 1.4×	613 1.3×	241 1.4×	140 1.2×	92 1.1×	21	1.3k
Ercan Demir Türkiye	11	368 0.8×	237 0.5×	212 1.2×	117 1.0×	87 1.0×	24	732
Erich E. Sirkowski United States	10	491 1.0×	449 1.0×	104 0.6×	128 1.1×	84 1.0×	10	828
Hiroko Ikeshima‐Kataoka Japan	15	554 1.2×	254 0.6×	187 1.1×	244 2.1×	90 1.1×	24	956
David Trisler United States	15	379 0.8×	319 0.7×	86 0.5×	121 1.0×	44 0.5×	28	885
M. C. McCulloch United Kingdom	16	399 0.8×	369 0.8×	94 0.5×	253 2.2×	73 0.9×	28	883
Frédéric Lebrun-Julien Switzerland	11	606 1.3×	433 0.9×	101 0.6×	145 1.2×	52 0.6×	12	1.0k
Edward C. Hurlock United States	8	475 1.0×	252 0.5×	60 0.4×	196 1.7×	47 0.6×	8	888
Brian A. Pierchala United States	16	375 0.8×	364 0.8×	128 0.7×	35 0.3×	44 0.5×	33	780
Laura Davis Keppen United States	14	400 0.8×	419 0.9×	89 0.5×	182 1.6×	118 1.4×	23	887

Countries citing papers authored by Sandra Gill

Since Specialization

Citations

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

Fields of papers citing papers by Sandra Gill

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Sandra Gill

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

All Works

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15 of 15 papers shown

Gill, Sandra & Richard H. Gomer. (2025). Translational Regulators in Pulmonary Fibrosis: MicroRNAs, Long Non-Coding RNAs, and Transcript Modifications. Cells. 14(7). 536–536. 5 indexed citations

Hims, Matthew M., El Chérif Ibrahim, Maire Leyne, et al.. (2007). Therapeutic potential and mechanism of kinetin as a treatment for the human splicing disease familial dysautonomia. Journal of Molecular Medicine. 85(2). 149–161. 48 indexed citations

Cuajungco, Math P., Maire Leyne, James Mull, et al.. (2003). Tissue-Specific Reduction in Splicing Efficiency of IKBKAP Due to the Major Mutation Associated with Familial Dysautonomia. The American Journal of Human Genetics. 72(3). 749–758. 108 indexed citations

Mezey, Éva, Ildikó Szalayova, Sandra Gill, et al.. (2003). Of splice and men: what does the distribution of IKAP mRNA in the rat tell us about the pathogenesis of familial dysautonomia?. Brain Research. 983(1-2). 209–214. 24 indexed citations

Leyne, Maire, James Mull, Sandra Gill, et al.. (2003). Identification of the first non‐Jewish mutation in familial Dysautonomia. American Journal of Medical Genetics Part A. 118A(4). 305–308. 53 indexed citations

Gill, Sandra. (2002). Evidence That GnRH Decreases with Gonadal Steroid Feedback but Increases with Age in Postmenopausal Women. The Journal of Clinical Endocrinology & Metabolism. 87(5). 2290–2296. 15 indexed citations

Cuajungco, Math P., Maire Leyne, James Mull, et al.. (2001). Cloning, Characterization, and Genomic Structure of the Mouse Ikbkap Gene. DNA and Cell Biology. 20(9). 579–586. 23 indexed citations

Slaugenhaupt, Susan A., Anat Blumenfeld, Sandra Gill, et al.. (2001). Tissue-Specific Expression of a Splicing Mutation in the Gene Causes Familial Dysautonomia. The American Journal of Human Genetics. 68(3). 598–605. 448 indexed citations

Filippov, Valery, et al.. (2001). Drosophila RNase H1 is essential for development but not for proliferation. Molecular Genetics and Genomics. 265(5). 771–777. 26 indexed citations

10.

Chadwick, Brian P., Maire Leyne, Sandra Gill, et al.. (2000). Cloning, mapping, and expression of a novel brain-specific transcript in the Familial Dysautonomia candidate region on Chromosome 9q31. Mammalian Genome. 11(1). 81–83. 5 indexed citations

11.

Blumenfeld, Anat, Susan A. Slaugenhaupt, Christopher B. Liebert, et al.. (1999). Precise Genetic Mapping and Haplotype Analysis of the Familial Dysautonomia Gene on Human Chromosome 9q31. The American Journal of Human Genetics. 64(4). 1110–1118. 53 indexed citations

12.

Chadwick, Brian P., James Mull, Sandra Gill, et al.. (1999). Cloning, Mapping, and Expression of Two Novel Actin Genes, Actin-like-7A (ACTL7A) and Actin-like-7B (ACTL7B), from the Familial Dysautonomia Candidate Region on 9q31. Genomics. 58(3). 302–309. 32 indexed citations

13.

Chadwick, Brian P., Sandra Gill, Maire Leyne, et al.. (1999). Cloning, genomic organization and expression of a putative human transmembrane protein related to the Caenorhabditis elegans M01F1.4 gene. Gene. 240(1). 67–73. 3 indexed citations

14.

Patterson, Helen, Sandra Gill, Harry Benjamin, Philip J. Mitchell, & Colin S. Cooper. (1998). Lip, a Human Gene Detected by Transfection of DNA From a Human Liposarcoma Encodes a Protein With Homology to Regulators of Small G Proteins. Sarcoma. 2(1). 35–44. 2 indexed citations

15.

Gill, Sandra, Aidan McManus, A. Jayne Crew, et al.. (1995). Fusion of the EWS Gene to a DNA segment from 9q22‐31 in a human myxoid chondrosarcoma. Genes Chromosomes and Cancer. 12(4). 307–310. 35 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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