Thomas C. Schulz

4.7k total citations
30 papers, 2.5k citations indexed

About

Thomas C. Schulz is a scholar working on Molecular Biology, Genetics and Biomedical Engineering. According to data from OpenAlex, Thomas C. Schulz has authored 30 papers receiving a total of 2.5k indexed citations (citations by other indexed papers that have themselves been cited), including 26 papers in Molecular Biology, 7 papers in Genetics and 6 papers in Biomedical Engineering. Recurrent topics in Thomas C. Schulz's work include Pluripotent Stem Cells Research (17 papers), CRISPR and Genetic Engineering (12 papers) and Epigenetics and DNA Methylation (6 papers). Thomas C. Schulz is often cited by papers focused on Pluripotent Stem Cells Research (17 papers), CRISPR and Genetic Engineering (12 papers) and Epigenetics and DNA Methylation (6 papers). Thomas C. Schulz collaborates with scholars based in United States, Japan and Australia. Thomas C. Schulz's co-authors include Allan J. Robins, Ian Lyons, Peter D. Rathjen, Scott Noggle, Sandii N. Brimble, Stephen Dalton, David M. Gilbert, Michael Kulik, Mahendra S. Rao and Junjie Lu and has published in prestigious journals such as Blood, Current Biology and Biochemical Journal.

In The Last Decade

Thomas C. Schulz

30 papers receiving 2.5k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Thomas C. Schulz United States 21 2.3k 384 362 291 198 30 2.5k
Joy Rathjen Australia 22 2.1k 0.9× 334 0.9× 244 0.7× 263 0.9× 146 0.7× 43 2.2k
Effie Apostolou United States 24 4.0k 1.8× 346 0.9× 518 1.4× 400 1.4× 202 1.0× 45 4.3k
Peter J. Rugg‐Gunn United Kingdom 29 4.4k 1.9× 419 1.1× 703 1.9× 498 1.7× 163 0.8× 58 4.7k
Kazuhiro Aiba Japan 19 1.2k 0.5× 206 0.5× 175 0.5× 191 0.7× 27 0.1× 56 1.4k
Ido Sagi Israel 12 1.3k 0.6× 162 0.4× 292 0.8× 110 0.4× 52 0.3× 20 1.6k
Alice E. Chen United States 6 1.9k 0.8× 300 0.8× 231 0.6× 463 1.6× 17 0.1× 9 2.0k
Ignacio Sancho-Martinez United States 18 1.8k 0.8× 194 0.5× 154 0.4× 272 0.9× 23 0.1× 31 2.0k
Abdolrahman S. Nateri United Kingdom 20 1.6k 0.7× 92 0.2× 195 0.5× 96 0.3× 44 0.2× 41 2.4k
Dina A. Faddah United States 9 1.9k 0.8× 171 0.4× 180 0.5× 132 0.5× 26 0.1× 12 2.0k
Salah Mahmoudi United States 12 1.4k 0.6× 64 0.2× 122 0.3× 89 0.3× 70 0.4× 13 2.0k

Countries citing papers authored by Thomas C. Schulz

Since Specialization
Citations

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

Fields of papers citing papers by Thomas C. Schulz

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Thomas C. Schulz

This figure shows the co-authorship network connecting the top 25 collaborators of Thomas C. Schulz. A scholar is included among the top collaborators of Thomas C. Schulz 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 Thomas C. Schulz. Thomas C. Schulz 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.
Dileep, Vishnu, Korey A. Wilson, Claire Marchal, et al.. (2019). Rapid Irreversible Transcriptional Reprogramming in Human Stem Cells Accompanied by Discordance between Replication Timing and Chromatin Compartment. Stem Cell Reports. 13(1). 193–206. 22 indexed citations
2.
Rivera‐Mulia, Juan Carlos, Takayo Sasaki, Ruth Didier, et al.. (2015). Dynamic changes in replication timing and gene expression during lineage specification of human pluripotent stem cells. Genome Research. 25(8). 1091–1103. 110 indexed citations
3.
Schulz, Thomas C.. (2015). Concise Review: Manufacturing of Pancreatic Endoderm Cells for Clinical Trials in Type 1 Diabetes. Stem Cells Translational Medicine. 4(8). 927–931. 82 indexed citations
4.
Takehara, Shoko, Thomas C. Schulz, Satoshi Abe, et al.. (2014). A novel transchromosomic system: stable maintenance of an engineered Mb-sized human genomic fragment translocated to a mouse chromosome terminal region. Transgenic Research. 23(3). 441–453. 3 indexed citations
5.
Zhao, Peng, Thomas C. Schulz, Eric S. Sherrer, et al.. (2014). The human embryonic stem cell proteome revealed by multidimensional fractionation followed by tandem mass spectrometry. PROTEOMICS. 15(2-3). 554–566. 9 indexed citations
6.
Gupta, Prasoon, Thomas C. Schulz, Eric S. Sherrer, et al.. (2011). Bioactive Diterpenoid Containing a Reversible “Spring-Loaded” (E,Z)-Dieneone Michael Acceptor. Organic Letters. 13(15). 3920–3923. 22 indexed citations
7.
Ryba, Tyrone, Ichiro Hiratani, Junjie Lu, et al.. (2010). Evolutionarily conserved replication timing profiles predict long-range chromatin interactions and distinguish closely related cell types. Genome Research. 20(6). 761–770. 440 indexed citations
8.
Wang, Linlin, Thomas C. Schulz, Eric S. Sherrer, et al.. (2007). Self-renewal of human embryonic stem cells requires insulin-like growth factor-1 receptor and ERBB2 receptor signaling. Blood. 110(12). 4111–4119. 237 indexed citations
9.
Schulz, Thomas C., Anna Maria Swistowska, Ying Liu, et al.. (2007). A large-scale proteomic analysis of human embryonic stem cells. BMC Genomics. 8(1). 478–478. 26 indexed citations
10.
Bhattacharya, Bhaskar, Jingli Cai, Takumi Miura, et al.. (2005). Comparison of the gene expression profile of undifferentiated human embryonic stem cell lines and differentiating embryoid bodies. BMC Developmental Biology. 5(1). 22–22. 91 indexed citations
11.
Brimble, Sandii N., Xianmin Zeng, Deborah A. Weiler, et al.. (2004). Karyotypic Stability, Genotyping, Differentiation, Feeder-Free Maintenance, and Gene Expression Sampling in Three Human Embryonic Stem Cell Lines Derived Prior to August 9, 2001. Stem Cells and Development. 13(6). 585–597. 151 indexed citations
12.
Zeng, Xianmin, Jia Chen, Ying Liu, et al.. (2004). BG01V: A variant human embryonic stem cell line which exhibits rapid growth after passaging and reliable dopaminergic differentiation. Restorative Neurology and Neuroscience. 22(6). 421–428. 45 indexed citations
13.
Kazuki, Yasuhiro, Ryuichi Nishigaki, Satoshi Abe, et al.. (2004). Human chromosome 21q22.2-qter carries a gene(s) responsible for downregulation of mlc2a and PEBP in Down syndrome model mice. Biochemical and Biophysical Research Communications. 317(2). 491–499. 9 indexed citations
14.
Kazuki, Yasuhiro, Thomas C. Schulz, Mitsutaka Kadota, et al.. (2003). A new mouse model for Down syndrome. Journal of neural transmission. Supplementum. 1–20. 9 indexed citations
15.
Schulz, Thomas C., Gail Palmarini, Scott Noggle, et al.. (2003). Directed neuronal differentiation of human embryonic stem cells. BMC Neuroscience. 4(1). 27–27. 116 indexed citations
16.
Faast, Renate, Varaporn Thonglairoam, Thomas C. Schulz, et al.. (2001). Histone variant H2A.Z is required for early mammalian development. Current Biology. 11(15). 1183–1187. 308 indexed citations
17.
Inoue, Jun‐ichiro, Kohzoh Mitsuya, Shinji Maegawa, et al.. (2001). Construction of 700 human/mouse A9 monochromosomal hybrids and analysis of imprinted genes on human chromosome 6. Journal of Human Genetics. 46(3). 137–145. 30 indexed citations
18.
Kugoh, Hiroyuki, Mutsunori Fujiwara, Kazunori Kihara, et al.. (2000). Cellular Senescence of a Human Bladder Carcinoma Cell Line (JTC-32) Induced by a Normal Chromosome 11. Cancer Genetics and Cytogenetics. 116(2). 158–163. 6 indexed citations
19.
Mitsuya, Kohzoh, Makiko Meguro, Hajime Sui, et al.. (1998). Epigenetic reprogramming of the human H19 gene in mouse embryonic cells does not erase the primary parental imprint. Genes to Cells. 3(4). 245–255. 14 indexed citations
20.
Chapman, Gavin, et al.. (1997). The Mouse Homeobox Gene,Gbx2:Genomic Organization and Expression in Pluripotent Cellsin Vitroandin Vivo. Genomics. 46(2). 223–233. 37 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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