Cathy M. Tuck‐Müller

1.2k total citations
37 papers, 855 citations indexed

About

Cathy M. Tuck‐Müller is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Cathy M. Tuck‐Müller has authored 37 papers receiving a total of 855 indexed citations (citations by other indexed papers that have themselves been cited), including 25 papers in Molecular Biology, 21 papers in Genetics and 7 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Cathy M. Tuck‐Müller's work include Genomic variations and chromosomal abnormalities (11 papers), Chromosomal and Genetic Variations (7 papers) and Prenatal Screening and Diagnostics (5 papers). Cathy M. Tuck‐Müller is often cited by papers focused on Genomic variations and chromosomal abnormalities (11 papers), Chromosomal and Genetic Variations (7 papers) and Prenatal Screening and Diagnostics (5 papers). Cathy M. Tuck‐Müller collaborates with scholars based in United States, Netherlands and Denmark. Cathy M. Tuck‐Müller's co-authors include Wladimir Wertelecki, Dominique Smeets, Melanie Ehrlich, Harold Chen, Ethylin Wang Jabs, Alison R. H. Narayan, O.S. Sohn, Jeffery R. Sawyer, Emerich S. Fiala and Fern Tsien and has published in prestigious journals such as New England Journal of Medicine, Mutation research. Fundamental and molecular mechanisms of mutagenesis and Human Genetics.

In The Last Decade

Cathy M. Tuck‐Müller

36 papers receiving 797 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Cathy M. Tuck‐Müller United States 17 515 428 167 157 98 37 855
Rita Fischetto Italy 15 486 0.9× 538 1.3× 80 0.5× 219 1.4× 61 0.6× 33 837
Roel Hordijk Netherlands 15 409 0.8× 520 1.2× 100 0.6× 184 1.2× 73 0.7× 22 739
Joseph Shen United States 16 678 1.3× 598 1.4× 193 1.2× 481 3.1× 85 0.9× 26 1.3k
Kutay Taysi United States 17 277 0.5× 440 1.0× 133 0.8× 221 1.4× 111 1.1× 48 710
A. Rodewald Germany 17 218 0.4× 552 1.3× 154 0.9× 170 1.1× 45 0.5× 41 726
Fortunato Lonardo Italy 16 258 0.5× 350 0.8× 53 0.3× 99 0.6× 73 0.7× 52 645
Nicola Vickaryous Australia 10 572 1.1× 273 0.6× 56 0.3× 125 0.8× 37 0.4× 16 769
Gita Akots United States 12 405 0.8× 363 0.8× 62 0.4× 51 0.3× 152 1.6× 14 839
Pilar Magoulas United States 15 383 0.7× 290 0.7× 38 0.2× 132 0.8× 73 0.7× 24 727
Jürgen Kunze Germany 12 337 0.7× 343 0.8× 63 0.4× 61 0.4× 43 0.4× 35 588

Countries citing papers authored by Cathy M. Tuck‐Müller

Since Specialization
Citations

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

Fields of papers citing papers by Cathy M. Tuck‐Müller

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Cathy M. Tuck‐Müller. 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 Cathy M. Tuck‐Müller. The network helps show where Cathy M. Tuck‐Müller may publish in the future.

Co-authorship network of co-authors of Cathy M. Tuck‐Müller

This figure shows the co-authorship network connecting the top 25 collaborators of Cathy M. Tuck‐Müller. A scholar is included among the top collaborators of Cathy M. Tuck‐Müller 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 Cathy M. Tuck‐Müller. Cathy M. Tuck‐Müller 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.
Wang, Yueying, José E. Martínez, Cathy M. Tuck‐Müller, et al.. (2006). A novel RSK2 (RPS6KA3) gene mutation associated with abnormal brain MRI findings in a family with Coffin–Lowry syndrome. American Journal of Medical Genetics Part A. 140A(12). 1274–1279. 12 indexed citations
2.
Gisselsson, David, Chunbo Shao, Cathy M. Tuck‐Müller, et al.. (2005). Interphase chromosomal abnormalities and mitotic missegregation of hypomethylated sequences in ICF syndrome cells. Chromosoma. 114(2). 118–126. 43 indexed citations
3.
4.
Scammell, Jonathan G., J. Allan Tucker, Judy A. King, et al.. (2002). A KIDNEY EPITHELIAL CELL LINE FROM A BOLIVIAN SQUIRREL MONKEY. In Vitro Cellular & Developmental Biology - Animal. 38(5). 258–258. 10 indexed citations
5.
Scammell, Jonathan G., James L. Wright, & Cathy M. Tuck‐Müller. (2001). The origin of four squirrel monkey cell lines established by karyotype analysis. Cytogenetic and Genome Research. 93(3-4). 263–264. 8 indexed citations
6.
Tuck‐Müller, Cathy M., Barbara K. Goodman, Shibo Li, et al.. (2001). Partial trisomy 7p defined by analysis of a complex chromosome rearrangement using a BAC clone panel. Genetics in Medicine. 3(2). 126–131. 4 indexed citations
7.
Tuck‐Müller, Cathy M., et al.. (2001). Molecular characterization of a ring chromosome 16 from a patient with bilateral cataracts. American Journal of Medical Genetics. 107(1). 12–17. 19 indexed citations
8.
Tuck‐Müller, Cathy M., et al.. (1999). 1p microdeletion in sibs with minimal phenotypic manifestations. American Journal of Medical Genetics. 82(2). 107–109. 8 indexed citations
9.
Li, Shibo, et al.. (1998). Prenatal detection of de novo duplication of the short arm of chromosome 18 confirmed by fluorescence in situ hybridization (FISH). American Journal of Medical Genetics. 80(5). 487–490. 22 indexed citations
10.
Tuck‐Müller, Cathy M., Harold Chen, Shibo Li, et al.. (1995). Isodicentric Y chromosome: cytogenetic, molecular and clinical studies and review of the literature. Human Genetics. 96(1). 119–129. 81 indexed citations
11.
Migeon, Barbara R., et al.. (1995). Molecular characterization of a deleted X chromosome (Xq13.3-Xq21.31) exhibiting random X inactivation. Somatic Cell and Molecular Genetics. 21(2). 113–120. 4 indexed citations
12.
Tuck‐Müller, Cathy M., Paul Dyken, Shibo Li, et al.. (1995). Translocation 10;18 in a patient with juvenile neuronal ceroid‐lipofuscinosis (Batten disease). American Journal of Medical Genetics. 57(2). 168–171.
13.
Chen, Harold, Cathy M. Tuck‐Müller, Denise Batista, & Wladimir Wertelecki. (1995). Identification of supernumerary ring chromosome 1 mosaicism using fluorescence in situ hybridization. American Journal of Medical Genetics. 56(2). 219–223. 20 indexed citations
14.
Peterson, Raymond D. A., et al.. (1994). Short Communication: An HLA‐Haplotype Associated With Preeclampsia and Intrauterine Growth Retardation. American Journal of Reproductive Immunology. 31(4). 177–179. 10 indexed citations
15.
Jabs, Ethylin Wang, Cathy M. Tuck‐Müller, Grant J. Anhalt, et al.. (1993). Cytogenetic survey in systemic sclerosis: correlation of aneuploidy with the presence of anticentromere antibodies. Cytogenetic and Genome Research. 63(3). 169–175. 11 indexed citations
16.
Perlman, Elizabeth J., Gail Stetten, Cathy M. Tuck‐Müller, et al.. (1990). Sexual discordance in monozygotic twins. American Journal of Medical Genetics. 37(4). 551–557. 39 indexed citations
17.
Ackerman, Alice D., James C. Fackler, Cathy M. Tuck‐Müller, et al.. (1988). Partial Monosomy 21, Diminished Activity of Superoxide Dismutase, and Pulmonary Oxygen Toxicity. New England Journal of Medicine. 318(25). 1666–1669. 23 indexed citations
18.
Tuck‐Müller, Cathy M., et al.. (1988). Correction of sphingomyelinase deficiency in Niemann‐Pick type C fibroblasts by removal of lipoprotein fraction from culture media. Journal of Inherited Metabolic Disease. 12(2). 139–151. 38 indexed citations
19.
Tuck‐Müller, Cathy M., et al.. (1987). Autosomal Dominant Congenital Cataract Associated With Chromosomal Translocation [t(3;4)(p26.2;p15) ]. Archives of Ophthalmology. 105(10). 1382–1384. 23 indexed citations
20.
Tuck‐Müller, Cathy M., Brenda L. Bordson, Maria Varela, & Joan W. Bennett. (1984). NOR associations with heterochromatin. Cytogenetic and Genome Research. 38(3). 165–170. 11 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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