Gail Chuck

4.1k total citations · 1 hit paper
36 papers, 3.0k citations indexed

About

Gail Chuck is a scholar working on Molecular Biology, Physiology and Clinical Biochemistry. According to data from OpenAlex, Gail Chuck has authored 36 papers receiving a total of 3.0k indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Molecular Biology, 11 papers in Physiology and 10 papers in Clinical Biochemistry. Recurrent topics in Gail Chuck's work include Metabolism and Genetic Disorders (10 papers), Glycogen Storage Diseases and Myoclonus (8 papers) and Lysosomal Storage Disorders Research (6 papers). Gail Chuck is often cited by papers focused on Metabolism and Genetic Disorders (10 papers), Glycogen Storage Diseases and Myoclonus (8 papers) and Lysosomal Storage Disorders Research (6 papers). Gail Chuck collaborates with scholars based in United States, Norway and Australia. Gail Chuck's co-authors include Sarah Hake, Jennifer Leonard, David Neal Franz, Cynthia Lincoln, Alan S. Brody, Robert Meeley, John J. Bissler, Francis X. McCormack, George Hug and Judy A. Bean and has published in prestigious journals such as Science, New England Journal of Medicine and Journal of Clinical Investigation.

In The Last Decade

Gail Chuck

36 papers receiving 2.9k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Sirolimus for Angiomyolipoma in Tuberous Sclerosis Complex or Lymphangioleiomyomatosis

2008 888 citations John J. Bissler, Francis X. McCormack et al. New England Journal of Medicine profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Gail Chuck United States	20	1.4k	1.3k	705	515	432	36	3.0k
Philip D. Cotter United States	26	87 0.1×	1.3k 1.0×	318 0.5×	200 0.4×	116 0.3×	95	2.4k
J.M. Rary United States	14	91 0.1×	1.1k 0.8×	229 0.3×	179 0.3×	100 0.2×	25	2.0k
Stephan M. Tanner United States	23	93 0.1×	1.4k 1.1×	35 0.0×	358 0.7×	141 0.3×	44	2.4k
André Lechel Germany	25	755 0.5×	1.3k 1.0×	44 0.1×	595 1.2×	181 0.4×	54	2.5k
Denise P. Muñoz United States	9	1.2k 0.9×	1.5k 1.1×	44 0.1×	427 0.8×	128 0.3×	15	2.7k
Victoriano Baladrón Spain	21	241 0.2×	1.0k 0.8×	86 0.1×	156 0.3×	95 0.2×	34	1.7k
Akira Nabetani Japan	15	894 0.6×	1.6k 1.2×	164 0.2×	165 0.3×	48 0.1×	18	2.2k
Barbara K. Goodman United States	25	71 0.1×	811 0.6×	109 0.2×	193 0.4×	80 0.2×	48	1.5k
Takanori Muto Japan	13	120 0.1×	1.8k 1.3×	23 0.0×	594 1.2×	394 0.9×	16	4.1k

Countries citing papers authored by Gail Chuck

Since Specialization

Citations

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

Fields of papers citing papers by Gail Chuck

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Gail Chuck

This figure shows the co-authorship network connecting the top 25 collaborators of Gail Chuck. A scholar is included among the top collaborators of Gail Chuck 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 Gail Chuck. Gail Chuck 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

Bissler, John J., Francis X. McCormack, Lisa R. Young, et al.. (2008). Sirolimus for Angiomyolipoma in Tuberous Sclerosis Complex or Lymphangioleiomyomatosis. New England Journal of Medicine. 358(2). 140–151. 888 indexed citations breakdown →

Newmeyer, Amy, Ton J. deGrauw, Joseph F. Clark, Gail Chuck, & G. S. Salomons. (2007). Screening of Male Patients with Autism Spectrum Disorder for Creatine Transporter Deficiency. Neuropediatrics. 38(6). 310–312. 12 indexed citations

Kure, Shigeo, Gail Chuck, Ton J. deGrauw, et al.. (2006). Comprehensive mutation analysis ofGLDC,AMT, andGCSHin nonketotic hyperglycinemia. Human Mutation. 27(4). 343–352. 71 indexed citations

Franz, David Neal, Jennifer Leonard, Cynthia Tudor, et al.. (2006). Rapamycin causes regression of astrocytomas in tuberous sclerosis complex. Annals of Neurology. 59(3). 490–498. 430 indexed citations

Pyne‐Geithman, Gail J., Ton J. deGrauw, Kim M. Cecil, et al.. (2004). Presence of normal creatine in the muscle of a patient with a mutation in the creatine transporter: A case study. Molecular and Cellular Biochemistry. 262(1-2). 35–39. 26 indexed citations

deGrauw, Ton J., G. S. Salomons, Kim M. Cecil, et al.. (2002). Congenital Creatine Transporter Deficiency. Neuropediatrics. 33(5). 232–238. 78 indexed citations

Tang, Peter, et al.. (2002). Anticoagulant effects on plasma coenzyme Q10 estimated by HPLC with coulometric detection. Clinica Chimica Acta. 318(1-2). 127–131. 11 indexed citations

Bissler, John J., Harald H.H. Göring, Peter Hug, et al.. (2002). Infantile Dilated X-Linked Cardiomyopathy, G4.5 Mutations, Altered Lipids, and Ultrastructural Malformations of Mitochondria in Heart, Liver, and Skeletal Muscle. Laboratory Investigation. 82(3). 335–344. 55 indexed citations

Franz, David Neal, Alan S. Brody, Cristopher A. Meyer, et al.. (2001). Mutational and Radiographic Analysis of Pulmonary Disease Consistent with Lymphangioleiomyomatosis and Micronodular Pneumocyte Hyperplasia in Women with Tuberous Sclerosis. American Journal of Respiratory and Critical Care Medicine. 164(4). 661–668. 200 indexed citations

10.

Cecil, Kim M., G. S. Salomons, William S. Ball, et al.. (2001). Irreversible brain creatine deficiency with elevated serum and urine creatine: A creatine transporter defect?. Annals of Neurology. 49(3). 401–404. 137 indexed citations

11.

Chuck, Gail, Robert Meeley, & Sarah Hake. (1998). The control of maize spikelet meristem fate by the APETALA2-like gene indeterminate spikelet1. Genes & Development. 12(8). 1145–1154. 268 indexed citations

12.

Thompson, Jerry N., et al.. (1996). Biochemical and molecular analysis in a patient with the severe form of Hunter syndrome after bone marrow transplantation. American Journal of Medical Genetics. 64(4). 531–535. 14 indexed citations

13.

Hake, Sarah, Bharat Char, Gail Chuck, et al.. (1995). Homeobox genes in the functioning of plant meristems. Philosophical Transactions of the Royal Society B Biological Sciences. 350(1331). 45–51. 49 indexed citations

14.

Garcia, Victor F., et al.. (1995). Weanling and adult rats differ in fatty acid and carnitine metabolism during sepsis. Journal of Pediatric Surgery. 30(7). 959–966. 7 indexed citations

15.

Thompson, Jerry N., et al.. (1994). Mutation analysis and carrier detection of Hunter syndrome. The American Journal of Human Genetics. 55. 1 indexed citations

16.

Hug, G., et al.. (1983). Membranoproliferative glomerulonephritis and alpha 1-antitrypsin deficiency in children.. PubMed. 71(1). 88–92. 26 indexed citations

17.

Hug, George, Gail Chuck, & Manley McGill. (1982). Pi<sup>Winneytown</sup>: New Alpha<sub>1</sub>-Antitrypsin Allele in an American Negro Family. Human Heredity. 32(4). 280–284. 6 indexed citations

18.

Hug, George, et al.. (1982). Alpha1-Antitrypsin Phenotype: Transient Cathodal Shift in Serum of Infant Girl with Urinary Cytomegalovirus and Fatty Liver. Pediatric Research. 16(3). 192–198. 19 indexed citations

19.

Hug, G., Gail Chuck, Linda L. Walling, & William K. Schubert. (1974). Liver phosphorylase deficiency in glycogenosis type VI: documentation by biochemical analysis of hepatic biopsy specimens.. PubMed. 84(1). 26–35. 7 indexed citations

20.

Hug, George, William K. Schubert, & Gail Chuck. (1969). Deficient activity of dephosphophosphorylase kinase and accumulation of glycogen in the liver. Journal of Clinical Investigation. 48(4). 704–715. 45 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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