O. Thomas Mueller

1.1k total citations
30 papers, 743 citations indexed

About

O. Thomas Mueller is a scholar working on Molecular Biology, Genetics and Organic Chemistry. According to data from OpenAlex, O. Thomas Mueller has authored 30 papers receiving a total of 743 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Molecular Biology, 11 papers in Genetics and 9 papers in Organic Chemistry. Recurrent topics in O. Thomas Mueller's work include Lysosomal Storage Disorders Research (9 papers), Carbohydrate Chemistry and Synthesis (9 papers) and Glycosylation and Glycoproteins Research (5 papers). O. Thomas Mueller is often cited by papers focused on Lysosomal Storage Disorders Research (9 papers), Carbohydrate Chemistry and Synthesis (9 papers) and Glycosylation and Glycoproteins Research (5 papers). O. Thomas Mueller collaborates with scholars based in United States, Oman and Poland. O. Thomas Mueller's co-authors include Abraham Rosenberg, Barry B. Bercu, Stephen J. Usala, T.B. Shows, A L Miller, Allen W. Root, I. David Schwartz, David A. Wenger, Thomas B. Shows and Fredric E. Wondisford and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nucleic Acids Research and Journal of Biological Chemistry.

In The Last Decade

O. Thomas Mueller

30 papers receiving 702 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
O. Thomas Mueller United States 16 313 222 221 207 107 30 743
Harold A. Taylor United States 16 324 1.0× 158 0.7× 329 1.5× 21 0.1× 150 1.4× 22 681
N. U. Bosshard Switzerland 18 338 1.1× 163 0.7× 446 2.0× 53 0.3× 164 1.5× 27 972
Alessia Lombardi Italy 13 235 0.8× 81 0.4× 294 1.3× 75 0.4× 183 1.7× 20 705
D. Christie Riddell Canada 15 302 1.0× 106 0.5× 191 0.9× 28 0.1× 48 0.4× 25 656
J Jaeken Belgium 11 421 1.3× 146 0.7× 162 0.7× 20 0.1× 58 0.5× 19 760
Marie‐Thérèse Vanier France 11 335 1.1× 80 0.4× 361 1.6× 25 0.1× 169 1.6× 17 641
I Maire France 17 341 1.1× 146 0.7× 785 3.6× 31 0.1× 188 1.8× 85 1.2k
Tracey Sikora United States 11 202 0.6× 189 0.9× 396 1.8× 27 0.1× 102 1.0× 15 677
Lars Schlotawa Germany 13 215 0.7× 110 0.5× 260 1.2× 31 0.1× 118 1.1× 29 621
Ester Lara Spain 12 803 2.6× 168 0.8× 266 1.2× 52 0.3× 26 0.2× 15 1.3k

Countries citing papers authored by O. Thomas Mueller

Since Specialization
Citations

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

Fields of papers citing papers by O. Thomas Mueller

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of O. Thomas Mueller

This figure shows the co-authorship network connecting the top 25 collaborators of O. Thomas Mueller. A scholar is included among the top collaborators of O. Thomas Mueller 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 O. Thomas Mueller. O. Thomas Mueller 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.
Miller, Jennifer, John H. Kranzler, Yijun Liu, et al.. (2006). Neurocognitive findings in Prader-Willi syndrome and early-onset morbid obesity. The Journal of Pediatrics. 149(2). 192–198.e3. 35 indexed citations
2.
Mueller, O. Thomas, et al.. (2006). Gene symbol: AR. Disease: Androgen insensitivity syndrome.. PubMed. 119(1). 105–1. 7 indexed citations
3.
Quintero, Rubén A., O. Thomas Mueller, J. Martı́nez, et al.. (2003). Twin–twin transfusion syndrome in a dizygotic monochorionic–diamniotic twin pregnancy. The Journal of Maternal-Fetal & Neonatal Medicine. 14(4). 279–281. 35 indexed citations
4.
Sutcliffe, Maxine J., et al.. (2001). Three cell line mosaicism involving structural and numerical abnormalities of chromosome 18 in a 3.5-Year-old girl: 47,XX,+18/47,XX,+del(18)(q22)/46,XX. American Journal of Medical Genetics. 102(2). 192–199. 5 indexed citations
5.
Lacson, Atilano, Maria Gieron‐Korthals, & O. Thomas Mueller. (2001). Peripheral Neuropathy in the First 2 Years of Life: Diagnostic Evaluation Including Molecular Genetics. Advances in Pediatrics. 48(1). 213–243. 2 indexed citations
6.
Papenhausen, Peter, et al.. (1996). Uniparental isodisomy of chromosome 14 in two cases: An abnormal child and a normal adult. American Journal of Medical Genetics. 66(1). 90–90. 8 indexed citations
7.
Mueller, O. Thomas, et al.. (1995). Fragile X syndrome: Discordant levels of CGG repeat mosaicism in two brothers. American Journal of Medical Genetics. 60(4). 302–306. 7 indexed citations
8.
Fan, Yao‐Shan, et al.. (1993). Correction of Mucolipidosis III in Vitro by Gene Transfer. Genomics. 18(2). 236–243. 1 indexed citations
9.
Schwartz, I. David, et al.. (1991). Homozygosity for a Dominant Negative Thyroid Hormone Receptor Gene Responsible for Generalized Resistance to Thyroid Hormone*. The Journal of Clinical Endocrinology & Metabolism. 73(5). 990–994. 93 indexed citations
10.
Usala, Stephen J., J B Menke, Fredric E. Wondisford, et al.. (1991). A Homozygous Deletion in the c-erbAβ Thyroid Hormone Receptor Gene in a Patient with Generalized Thyroid Hormone Resistance: Isolation and Characterization of the Mutant Receptor. Molecular Endocrinology. 5(3). 327–335. 102 indexed citations
11.
Papenhausen, Peter, et al.. (1991). Cell line segregation in a 45,X/46,XY mosaic child with asymmetric leg growth. Clinical Genetics. 40(3). 237–241. 13 indexed citations
12.
Madiyalakan, Ragupathy, O. Thomas Mueller, Thomas B. Shows, & Khushi L. Matta. (1987). UDP-N-Acetylglucosamine: Lysosomal Enzyme Precursor N-Acetylglucosamine-1-Phosphate Transferase Activities in Human Ovarian Tumor Tissue and Some Transformed Cell Lines. Cancer Investigation. 5(6). 553–558. 6 indexed citations
13.
Litt, M., et al.. (1987). A single copy sarbclone, P1–101, from cosmid 3–3B, defines three RFLPs on 10pter–q23[HGM9 no. D10S4]. Nucleic Acids Research. 15(6). 2783–2783. 14 indexed citations
14.
Mueller, O. Thomas, et al.. (1986). Heterogeneity of N-acetylglucosamine 1-phosphotransferase within mucolipidosis III.. Journal of Biological Chemistry. 261(2). 733–738. 22 indexed citations
15.
16.
Mueller, O. Thomas, Thomas B. Shows, John M. Opitz, & James F. Reynolds. (1984). Apparent allelism of the hurler, scheie, and hurler/scheie syndromes. American Journal of Medical Genetics. 18(3). 547–556. 9 indexed citations
17.
Mueller, O. Thomas, et al.. (1983). Mucolipidosis II and III. The genetic relationships between two disorders of lysosomal enzyme biosynthesis.. Journal of Clinical Investigation. 72(3). 1016–1023. 32 indexed citations
18.
Mueller, O. Thomas, et al.. (1982). Mucolipidosis III is genetically heterogeneous.. Proceedings of the National Academy of Sciences. 79(23). 7420–7424. 32 indexed citations
19.
Mueller, O. Thomas & Thomas B. Shows. (1982). Human ?-galactosidase and ?-neuraminidase deficient mucolipidosis: Genetic complementation analysis of the neuraminidase deficiency. Human Genetics. 60(2). 158–162. 15 indexed citations
20.

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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