Brian Hendrich

14.6k total citations · 6 hit papers
59 papers, 10.2k citations indexed

About

Brian Hendrich is a scholar working on Molecular Biology, Genetics and Oncology. According to data from OpenAlex, Brian Hendrich has authored 59 papers receiving a total of 10.2k indexed citations (citations by other indexed papers that have themselves been cited), including 51 papers in Molecular Biology, 25 papers in Genetics and 4 papers in Oncology. Recurrent topics in Brian Hendrich's work include Epigenetics and DNA Methylation (34 papers), Genomics and Chromatin Dynamics (24 papers) and Genetics and Neurodevelopmental Disorders (19 papers). Brian Hendrich is often cited by papers focused on Epigenetics and DNA Methylation (34 papers), Genomics and Chromatin Dynamics (24 papers) and Genetics and Neurodevelopmental Disorders (19 papers). Brian Hendrich collaborates with scholars based in United Kingdom, United States and Germany. Brian Hendrich's co-authors include Adrian Bird, Jacky Guy, Joanne E. Martin, Megan C. Holmes, Wendy Dean, Fátima Santos, Wolf Reik, Huntington F. Willard, Carolyn J. Brown and Huck‐Hui Ng and has published in prestigious journals such as Nature, Science and Cell.

In The Last Decade

Brian Hendrich

59 papers receiving 10.1k citations

Hit Papers

A mouse Mecp2-null mutation causes neurological symptoms ... 1992 2026 2003 2014 2001 1998 1992 2002 1999 400 800 1.2k

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Brian Hendrich United Kingdom 39 8.8k 4.1k 920 854 595 59 10.2k
Hans van Bokhoven Netherlands 64 9.0k 1.0× 4.6k 1.1× 967 1.1× 731 0.9× 534 0.9× 243 13.2k
Caroline Beard United States 30 9.6k 1.1× 3.4k 0.8× 629 0.7× 635 0.7× 776 1.3× 36 12.0k
C. Geoffrey Woods United Kingdom 48 6.8k 0.8× 3.4k 0.8× 537 0.6× 320 0.4× 856 1.4× 97 11.0k
Paul A. Wade United States 61 11.8k 1.3× 3.0k 0.7× 1.1k 1.2× 475 0.6× 506 0.9× 135 14.2k
Albert W. Cheng United States 34 11.4k 1.3× 3.0k 0.7× 881 1.0× 261 0.3× 291 0.5× 51 13.0k
Jean‐Pierre Fryns Belgium 46 4.9k 0.5× 5.7k 1.4× 325 0.4× 1.2k 1.4× 1.3k 2.1× 255 9.1k
Christian Gilissen Netherlands 47 4.6k 0.5× 4.4k 1.1× 944 1.0× 362 0.4× 425 0.7× 135 8.5k
Robert J. Klose United Kingdom 45 10.2k 1.2× 2.2k 0.5× 1.3k 1.4× 261 0.3× 408 0.7× 69 11.7k
Alexandre Reymond Switzerland 48 5.9k 0.7× 2.6k 0.6× 987 1.1× 267 0.3× 355 0.6× 122 8.6k
Vera M. Kalscheuer Germany 45 4.4k 0.5× 3.6k 0.9× 351 0.4× 407 0.5× 704 1.2× 152 6.7k

Countries citing papers authored by Brian Hendrich

Since Specialization
Citations

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

Fields of papers citing papers by Brian Hendrich

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Brian Hendrich

This figure shows the co-authorship network connecting the top 25 collaborators of Brian Hendrich. A scholar is included among the top collaborators of Brian Hendrich 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 Brian Hendrich. Brian Hendrich 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.
Lando, David, Xiaoyan Ma, Tim J. Stevens, et al.. (2024). Enhancer-promoter interactions are reconfigured through the formation of long-range multiway hubs as mouse ES cells exit pluripotency. Molecular Cell. 84(8). 1406–1421.e8. 3 indexed citations
3.
Gharbi, Sarah, Julie Cramard, Susan L. Kloet, et al.. (2020). Differential regulation of lineage commitment in human and mouse primed pluripotent stem cells by the nucleosome remodelling and deacetylation complex. Stem Cell Research. 46. 101867–101867. 6 indexed citations
4.
Link, Stephanie, Mario Torrado, Moritz Völker-Albert, et al.. (2018). PWWP2A binds distinct chromatin moieties and interacts with an MTA1-specific core NuRD complex. Nature Communications. 9(1). 4300–4300. 42 indexed citations
5.
Lando, David, Srinjan Basu, Tim J. Stevens, et al.. (2018). Combining fluorescence imaging with Hi-C to study 3D genome architecture of the same single cell. Nature Protocols. 13(5). 1034–1061. 10 indexed citations
6.
Basu, Srinjan, Lisa-Maria Needham, David Lando, et al.. (2018). FRET-enhanced photostability allows improved single-molecule tracking of proteins and protein complexes in live mammalian cells. Nature Communications. 9(1). 2520–2520. 29 indexed citations
7.
Knock, Erin, João D. Pereira, Patrick Lombard, et al.. (2015). The methyl binding domain 3/nucleosome remodelling and deacetylase complex regulates neural cell fate determination and terminal differentiation in the cerebral cortex. Neural Development. 10(1). 13–13. 36 indexed citations
8.
Reynolds, Nicola, Paulina A. Latos, Antony Hynes-Allen, et al.. (2012). NuRD Suppresses Pluripotency Gene Expression to Promote Transcriptional Heterogeneity and Lineage Commitment. Cell stem cell. 10(5). 583–594. 174 indexed citations
9.
10.
Barr, Helen, Andrea Hermann, Jennifer Berger, et al.. (2007). Mbd2 Contributes to DNA Methylation-Directed Repression of the Xist Gene. Molecular and Cellular Biology. 27(10). 3750–3757. 50 indexed citations
11.
Kaji, Keisuke, Isabel Martín Caballero, Ruth MacLeod, et al.. (2006). The NuRD component Mbd3 is required for pluripotency of embryonic stem cells. Nature Cell Biology. 8(3). 285–292. 286 indexed citations
12.
Hendrich, Brian & Susan Tweedie. (2003). The methyl-CpG binding domain and the evolving role of DNA methylation in animals. Trends in Genetics. 19(5). 269–277. 311 indexed citations
13.
Young, Lorraine, et al.. (2002). Epigenetic Reprogramming: How Now, Cloned Cow?. Current Biology. 12(2). R68–R70. 23 indexed citations
14.
Santos, Fátima, Brian Hendrich, Wolf Reik, & Wendy Dean. (2002). Dynamic Reprogramming of DNA Methylation in the Early Mouse Embryo. Developmental Biology. 241(1). 172–182. 946 indexed citations breakdown →
15.
Hendrich, Brian & Adrian Bird. (2000). Mammalian Methyltransferases and Methyl-CpG-Binding Domains: Proteins Involved in DNA Methylation. Current topics in microbiology and immunology. 249. 55–74. 85 indexed citations
16.
Bader, Scott, Marion Walker, Brian Hendrich, et al.. (1999). Somatic frameshift mutations in the MBD4 gene of sporadic colon cancers with mismatch repair deficiency. Oncogene. 18(56). 8044–8047. 103 indexed citations
17.
Hendrich, Brian, Ulrike Hardeland, Huck‐Hui Ng, Josef Jiricny, & Adrian Bird. (1999). The thymine glycosylase MBD4 can bind to the product of deamination at methylated CpG sites. Nature. 401(6750). 301–304. 511 indexed citations breakdown →
18.
Hendrich, Brian & Adrian Bird. (1998). Identification and Characterization of a Family of Mammalian Methyl-CpG Binding Proteins. Molecular and Cellular Biology. 18(11). 6538–6547. 1057 indexed citations breakdown →
19.
Willard, H.F., Carolyn J. Brown, Laura Carrel, Brian Hendrich, & Andrew P. Miller. (1993). Epigenetic and Chromosomal Control of Gene Expression: Molecular and Genetic Analysis of X Chromosome Inactivation. Cold Spring Harbor Symposia on Quantitative Biology. 58(0). 315–322. 37 indexed citations
20.
Brown, Carolyn J., Brian Hendrich, Jim L. Rupert, et al.. (1992). The human XIST gene: Analysis of a 17 kb inactive X-specific RNA that contains conserved repeats and is highly localized within the nucleus. Cell. 71(3). 527–542. 1021 indexed citations breakdown →

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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