David Umlauf

2.4k total citations · 1 hit paper
19 papers, 1.9k citations indexed

About

David Umlauf is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, David Umlauf has authored 19 papers receiving a total of 1.9k indexed citations (citations by other indexed papers that have themselves been cited), including 18 papers in Molecular Biology, 6 papers in Genetics and 3 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in David Umlauf's work include Genomics and Chromatin Dynamics (8 papers), Epigenetics and DNA Methylation (6 papers) and Genetic Syndromes and Imprinting (5 papers). David Umlauf is often cited by papers focused on Genomics and Chromatin Dynamics (8 papers), Epigenetics and DNA Methylation (6 papers) and Genetic Syndromes and Imprinting (5 papers). David Umlauf collaborates with scholars based in France, United Kingdom and United States. David Umlauf's co-authors include Robert Feil, Yuji Goto, Peter Fraser, Tom Sexton, Sreenivasulu Kurukuti, Alexandre Wagschal, Ru Cao, Yi Zhang, Frédérique Cerqueira and Jennifer A. Mitchell and has published in prestigious journals such as Nature Genetics, PLoS ONE and Molecular and Cellular Biology.

In The Last Decade

David Umlauf

19 papers receiving 1.9k citations

Hit Papers

Preferential associations between co-regulated genes reve... 2009 2026 2014 2020 2009 100 200 300 400 500

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
David Umlauf France 14 1.7k 630 317 236 190 19 1.9k
Ramaiah Nagaraja United States 20 1.1k 0.7× 609 1.0× 83 0.3× 116 0.5× 211 1.1× 44 1.5k
Ryuichi Ono Japan 17 1.6k 0.9× 1.1k 1.7× 625 2.0× 155 0.7× 363 1.9× 31 2.0k
Florian M. Pauler Austria 23 2.9k 1.7× 871 1.4× 309 1.0× 1.9k 8.0× 227 1.2× 39 3.3k
Judith Singer–Sam United States 24 1.5k 0.9× 918 1.5× 152 0.5× 81 0.3× 126 0.7× 38 1.9k
Nathalie Beaujean France 28 2.6k 1.5× 749 1.2× 473 1.5× 70 0.3× 249 1.3× 69 3.0k
Benjamin E. Powell United States 9 1.6k 0.9× 393 0.6× 166 0.5× 86 0.4× 103 0.5× 12 1.7k
Sandrine Caburet France 23 1.3k 0.7× 686 1.1× 98 0.3× 141 0.6× 229 1.2× 39 1.9k
Hitomi Yatsuki Japan 20 693 0.4× 383 0.6× 209 0.7× 124 0.5× 33 0.2× 51 920
Takashi Sado Japan 28 3.5k 2.1× 2.1k 3.3× 633 2.0× 565 2.4× 402 2.1× 54 4.0k
Lionel A. Sanz United States 17 2.5k 1.4× 543 0.9× 147 0.5× 635 2.7× 241 1.3× 20 2.7k

Countries citing papers authored by David Umlauf

Since Specialization
Citations

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

Fields of papers citing papers by David Umlauf

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of David Umlauf

This figure shows the co-authorship network connecting the top 25 collaborators of David Umlauf. A scholar is included among the top collaborators of David Umlauf 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 David Umlauf. David Umlauf is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

19 of 19 papers shown
1.
Keller, Debora, David Umlauf, Edith Gourbeyre, et al.. (2024). Non-random spatial organization of telomeres varies during the cell cycle and requires LAP2 and BAF. iScience. 27(4). 109343–109343. 1 indexed citations
2.
Umlauf, David, Michal Sobecki, & Laure Crabbé. (2020). Methyl Adenine Identification (MadID): High-Resolution Detection of Protein-DNA Interactions. Methods in molecular biology. 2175. 123–138. 3 indexed citations
3.
Malnou, Cécile E., et al.. (2019). Imprinted MicroRNA Gene Clusters in the Evolution, Development, and Functions of Mammalian Placenta. Frontiers in Genetics. 9. 706–706. 68 indexed citations
4.
Umlauf, David & Raphaël Mourad. (2018). The 3D genome: From fundamental principles to disease and cancer. Seminars in Cell and Developmental Biology. 90. 128–137. 13 indexed citations
5.
Umlauf, David. (2015). Le génome intime… et en trois dimensions. médecine/sciences. 31(3). 304–311. 1 indexed citations
6.
Gyenis, Ákos, David Umlauf, Zsuzsanna Újfaludi, et al.. (2014). UVB Induces a Genome-Wide Acting Negative Regulatory Mechanism That Operates at the Level of Transcription Initiation in Human Cells. PLoS Genetics. 10(7). e1004483–e1004483. 33 indexed citations
7.
Umlauf, David, Jacques Bonnet, François Waharte, et al.. (2013). The human TREX-2 complex is stably associated with the nuclear pore basket. Journal of Cell Science. 126(Pt 12). 2656–67. 100 indexed citations
8.
Mitchell, Jennifer A., Ieuan Clay, David Umlauf, et al.. (2012). Nuclear RNA Sequencing of the Mouse Erythroid Cell Transcriptome. PLoS ONE. 7(11). e49274–e49274. 29 indexed citations
9.
Sexton, Tom, Sreenivasulu Kurukuti, Jennifer A. Mitchell, et al.. (2012). Sensitive detection of chromatin coassociations using enhanced chromosome conformation capture on chip. Nature Protocols. 7(7). 1335–1350. 31 indexed citations
10.
Lang, Guillaume, Jacques Bonnet, David Umlauf, et al.. (2011). The Tightly Controlled Deubiquitination Activity of the Human SAGA Complex Differentially Modifies Distinct Gene Regulatory Elements. Molecular and Cellular Biology. 31(18). 3734–3744. 104 indexed citations
11.
Schoenfelder, Stefan, Tom Sexton, Lyubomira Chakalova, et al.. (2009). Preferential associations between co-regulated genes reveal a transcriptional interactome in erythroid cells. Nature Genetics. 42(1). 53–61. 536 indexed citations breakdown →
12.
Umlauf, David, Peter Fraser, & Takashi Nagano. (2008). The role of long non-coding RNAs in chromatin structure and gene regulation: variations on a theme. Biological Chemistry. 389(4). 323–331. 52 indexed citations
13.
Sexton, Tom, David Umlauf, Sreenivasulu Kurukuti, & Peter Fraser. (2007). The role of transcription factories in large-scale structure and dynamics of interphase chromatin. Seminars in Cell and Developmental Biology. 18(5). 691–697. 54 indexed citations
14.
Umlauf, David, Yuji Goto, Ru Cao, et al.. (2004). Imprinting along the Kcnq1 domain on mouse chromosome 7 involves repressive histone methylation and recruitment of Polycomb group complexes. Nature Genetics. 36(12). 1296–1300. 332 indexed citations
15.
Umlauf, David, Yuji Goto, & Robert Feil. (2004). Site-Specific Analysis of Histone Methylation and Acetylation. Humana Press eBooks. 287. 99–120. 90 indexed citations
16.
Reik, Wolf, Adele Murrell, Annabelle Lewis, et al.. (2004). Chromosome Loops, Insulators, and Histone Methylation: New Insights into Regulation of Imprinting in Clusters. Cold Spring Harbor Symposia on Quantitative Biology. 69(0). 29–38. 17 indexed citations
17.
Lewis, Annabelle, Kohzoh Mitsuya, David Umlauf, et al.. (2004). Imprinting on distal chromosome 7 in the placenta involves repressive histone methylation independent of DNA methylation. Nature Genetics. 36(12). 1291–1295. 347 indexed citations
18.
Reik, Wolf, Adele Murrell, Annabelle Lewis, et al.. (2004). Chromosome Loops, Insulators, and Histone Methylation: New Insights into Regulation of Imprinting in Clusters. Cold Spring Harbor Symposia on Quantitative Biology. 69(1). 1–10. 2 indexed citations
19.
Mangé, Alain, Ollivier Milhavet, David Umlauf, David A. Harris, & Sylvain Lehmann. (2002). PrP‐dependent cell adhesion in N2a neuroblastoma cells. FEBS Letters. 514(2-3). 159–162. 78 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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