George H. Thomas

4.2k total citations
55 papers, 1.9k citations indexed

About

George H. Thomas is a scholar working on Molecular Biology, Genetics and Clinical Biochemistry. According to data from OpenAlex, George H. Thomas has authored 55 papers receiving a total of 1.9k indexed citations (citations by other indexed papers that have themselves been cited), including 22 papers in Molecular Biology, 17 papers in Genetics and 13 papers in Clinical Biochemistry. Recurrent topics in George H. Thomas's work include Genomic variations and chromosomal abnormalities (15 papers), Metabolism and Genetic Disorders (13 papers) and Lysosomal Storage Disorders Research (8 papers). George H. Thomas is often cited by papers focused on Genomic variations and chromosomal abnormalities (15 papers), Metabolism and Genetic Disorders (13 papers) and Lysosomal Storage Disorders Research (8 papers). George H. Thomas collaborates with scholars based in United States, Denmark and Singapore. George H. Thomas's co-authors include Linda Reynolds, Carol S. Miller, Harold A. Taylor, Saul W. Brusilow, Mark L. Batshaw, Barbara R. Migeon, William J. Mahoney, G. Shashidhar Pai, Yuan Chuan Lee and Yoshihiro Uchida and has published in prestigious journals such as Nature, Science and New England Journal of Medicine.

In The Last Decade

George H. Thomas

53 papers receiving 1.8k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
George H. Thomas United States 28 925 582 411 361 353 55 1.9k
Judith L. Fridovich‐Keil United States 31 1.3k 1.4× 195 0.3× 333 0.8× 1.2k 3.2× 493 1.4× 84 2.6k
Roy A. Gravel Canada 32 1.8k 1.9× 334 0.6× 535 1.3× 741 2.1× 502 1.4× 69 3.4k
Rody P. Cox United States 27 1.3k 1.4× 226 0.4× 193 0.5× 297 0.8× 70 0.2× 70 2.1k
Marcella Camici Italy 25 1.3k 1.4× 213 0.4× 139 0.3× 83 0.2× 210 0.6× 100 2.1k
Margherita Ruoppolo Italy 30 1.5k 1.6× 280 0.5× 344 0.8× 373 1.0× 136 0.4× 116 2.4k
Dina Bellizzi Italy 30 1.8k 1.9× 327 0.6× 732 1.8× 161 0.4× 180 0.5× 75 2.9k
Manuel Schiff France 25 1.3k 1.5× 255 0.4× 380 0.9× 870 2.4× 200 0.6× 115 2.3k
Burton M. Wice United States 23 1.8k 2.0× 385 0.7× 403 1.0× 114 0.3× 139 0.4× 42 3.2k
J. A. Lowden Canada 25 1.2k 1.4× 194 0.3× 1.3k 3.1× 159 0.4× 169 0.5× 77 2.3k
Michael J. Coady Canada 25 1.4k 1.5× 268 0.5× 209 0.5× 140 0.4× 141 0.4× 40 2.5k

Countries citing papers authored by George H. Thomas

Since Specialization
Citations

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

Fields of papers citing papers by George H. Thomas

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by George H. Thomas. 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 George H. Thomas. The network helps show where George H. Thomas may publish in the future.

Co-authorship network of co-authors of George H. Thomas

This figure shows the co-authorship network connecting the top 25 collaborators of George H. Thomas. A scholar is included among the top collaborators of George H. Thomas 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 George H. Thomas. George H. Thomas 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.
Roberson, Elisha, Elizabeth Wohler, Julie Hoover‐Fong, et al.. (2010). Genomic analysis of partial 21q monosomies with variable phenotypes. European Journal of Human Genetics. 19(2). 235–238. 44 indexed citations
2.
Nance, Melonie A., Elizabeth Wohler, Julie Hoover‐Fong, et al.. (2009). Molecular (SNP) analyses of overlapping hemizygous deletions of 10q25.3 to 10qter in four patients: Evidence for HMX2 and HMX3 as candidate genes in hearing and vestibular function. American Journal of Medical Genetics Part A. 149A(4). 669–680. 36 indexed citations
3.
4.
Lisi, Emily C., Ada Hamosh, Kimberly F. Doheny, et al.. (2008). 3q29 interstitial microduplication: A new syndrome in a three‐generation family. American Journal of Medical Genetics Part A. 146A(5). 601–609. 71 indexed citations
5.
Balciuniene, Jorune, Ningping Feng, Betsy Hirsch, et al.. (2007). Recurrent 10q22-q23 Deletions: A Genomic Disorder on 10q Associated with Cognitive and Behavioral Abnormalities. The American Journal of Human Genetics. 80(5). 938–947. 85 indexed citations
6.
Ting, Jason C., Elisha Roberson, Dietrich A. Stephan, et al.. (2007). Visualization of uniparental inheritance, Mendelian inconsistencies, deletions, and parent of origin effects in single nucleotide polymorphism trio data with SNPtrio. Human Mutation. 28(12). 1225–1235. 37 indexed citations
7.
Thomas, George H., et al.. (2006). Optical determination of Cr(VI) using regenerable, functionalized sol–gel monoliths. Analytica Chimica Acta. 581(2). 232–240. 41 indexed citations
8.
Boyadjiev, Simeon A., Sarah T. South, Ankita Patel, et al.. (2005). A reciprocal translocation 46,XY,t(8;9)(p11.2;q13) in a bladder exstrophy patient disrupts CNTNAP3 and presents evidence of a pericentromeric duplication on chromosome 9. Genomics. 85(5). 622–629. 21 indexed citations
9.
Thomas, George H., et al.. (2005). Epitaxial Growth of Strontium Bismuth Tantalate/Niobate on Buffered Magnesium Oxide Substrates. MRS Proceedings. 902. 1 indexed citations
10.
Cargile, Colyn B., Denise Goh, Barbara K. Goodman, et al.. (2002). Molecular cytogenetic characterization of a subtle interstitial del(3)(p25.3p26.2) in a patient with deletion 3p syndrome. American Journal of Medical Genetics. 109(2). 133–138. 50 indexed citations
11.
Li, Shiyong, Rima Couzi, George H. Thomas, Alan D. Friedman, & Michael J. Borowitz. (2001). A novel variant three-way translocation of inversion 16 in a case of AML-M4eo following low dose methotrexate therapy. Cancer Genetics and Cytogenetics. 125(1). 74–77. 5 indexed citations
12.
Cargile, Colyn B., Iain McIntosh, Mark V. Clough, et al.. (2000). Delayed membranous ossification of the cranium associated with familial translocation (2;3)(p15;q12). American Journal of Medical Genetics. 92(5). 328–335. 4 indexed citations
13.
Praphanphoj, Verayuth, Barbara K. Goodman, George H. Thomas, et al.. (2000). Molecular Cytogenetic Evaluation in a Patient with a Translocation (3;21) Associated with Blepharophimosis, Ptosis, Epicanthus Inversus Syndrome (BPES). Genomics. 65(1). 67–69. 44 indexed citations
14.
Goodman, Barbara K., et al.. (1997). Familial tandem duplication of bands q31.1 to q32.3 on chromosome 4 with mild phenotypic effect. American Journal of Medical Genetics. 73(2). 119–124. 26 indexed citations
15.
Thomas, George H., et al.. (1993). Growing up with Patricia. Pediatric Clinics of North America. 40(3). 675–683. 1 indexed citations
16.
Arn, Pamela, Elizabeth R. Hauser, George H. Thomas, et al.. (1990). Hyperammonemia in Women with a Mutation at the Ornithine Carbamoyltransferase Locus. New England Journal of Medicine. 322(23). 1652–1655. 140 indexed citations
17.
Thomas, George H., Morton F. Goldberg, Carol S. Miller, & Linda Reynolds. (1979). Neuraminidase deficiency in the original patient with the Goldberg Syndrome. Clinical Genetics. 16(5). 323–330. 22 indexed citations
18.
Aylsworth, Arthur S., et al.. (1976). Mannosidosis: Phenotype of a severely affected child and characterization of α-mannosidase activity in cultured fibroblasts from the patient and his parents. The Journal of Pediatrics. 88(5). 814–818. 20 indexed citations
19.
Thomas, George H., et al.. (1975). Hyperpipecolic acidemia associated with hepatomegaly, mental retardation, optic nerve dysplasia and progressive neurological disease. Clinical Genetics. 8(5). 376–382. 84 indexed citations
20.
Thomas, George H. & R. Rodney Howell. (1973). Selected Screening Tests for Genetic Metabolic Diseases. Medical Entomology and Zoology. 28 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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