Brian Hendrich

14.7k citations
59 papers · 10.8k · 6 hit papers · h-index 40

Impact in

  • Genetics top 0.2%
    • Genetics and Neurodevelopmental Disorders
    • Epigenetics and DNA Methylation
    • Genomics and Chromatin Dynamics
    • RNA modifications and cancer
    • Cancer-related gene regulation
    • Pluripotent Stem Cells Research
    • CRISPR and Genetic Engineering

Papers in

    • Epigenetics and DNA Methylation 33
    • Genomics and Chromatin Dynamics 24
    • Pluripotent Stem Cells Research 12
    • CRISPR and Genetic Engineering 12
    • Cancer-related gene regulation 8
    • Histone Deacetylase Inhibitors Research 5
    • Genetics and Neurodevelopmental Disorders 18
    • Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 5

Brian Hendrich

59 papers receiving 10.5k citations

Brian Hendrich's Hit Papers

Dynamic Reprogramming of DNA Methylation in the Early Mouse Embryo 2002 · 1.0k citations
1.0k0+11+22Years since publication4008001.2k

Peers

Brian Hendrich
Comparison fields: 5 of 128
  • Genetics 4.2k
  • Molecular Biology 9.0k
  • Cancer Research 882
  • Developmental Neuroscience 186
  • Aging 76
Replace Hans van Bokhoven with:
Hans van Bokhoven Netherlands
Kuniya Abe Japan
Caroline Beard United States
Alexandre Reymond Switzerland
Robert J. Klose United Kingdom
Joan H.M. Knoll United States
C. Geoffrey Woods United Kingdom
Jean‐Pierre Fryns Belgium
Brian J. O’Roak United States
Jonathan Sebat United States
Brian Hendrich relative to Hans van Bokhoven Netherlands Hans van Bokhoven's profile →
Citations per field
00.5×1.5×
Hans van Bokhoven · 1×
Citations per year

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-authors

The 25 scholars most cited alongside Brian Hendrich, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Brian Hendrich Line = papers co-authored together Brian Hendrich links everyone, so they are left out of the graph.

All Works

20 of 20 papers shown

Showing the 20 most-cited of 59 papers — load more, or switch the sort, to bring in the rest.

#Work
1
A mouse Mecp2-null mutation causes neurological symptoms that mimic Rett syndrome
Hit paper breakdown →
20011288
2
Identification and Characterization of a Family of Mammalian Methyl-CpG Binding Proteins
Hit paper breakdown →
19981119
3
The human XIST gene: Analysis of a 17 kb inactive X-specific RNA that contains conserved repeats and is highly localized within the nucleus
Hit paper breakdown →
19921074
4
Dynamic Reprogramming of DNA Methylation in the Early Mouse Embryo
Hit paper breakdown →
20021018
5
MBD2 is a transcriptional repressor belonging to the MeCP1 histone deacetylase complex
Hit paper breakdown →
1999765
6
The thymine glycosylase MBD4 can bind to the product of deamination at methylated CpG sites
Hit paper breakdown →
1999538
7 2001424
8 2001412
9 2003326
10 2006301
11 2002268
12 1997224
13 2011203
14 2012182
15 2002176
16 2003155
17 2007145
18 2014138
19 2005138
20 2018127

About Brian Hendrich

Brian Hendrich is a scholar working on Molecular Biology, Genetics, Oncology, Ecology, Evolution, Behavior and Systematics and Pediatrics, Perinatology and Child Health, having authored 59 papers that have together received 10.8k indexed citations. Recurring topics across this work include Epigenetics and DNA Methylation (33 papers), Genomics and Chromatin Dynamics (24 papers), Genetics and Neurodevelopmental Disorders (18 papers), Pluripotent Stem Cells Research (12 papers), CRISPR and Genetic Engineering (12 papers), Cancer-related gene regulation (8 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (5 papers) and Histone Deacetylase Inhibitors Research (5 papers). The work is most often cited by research in Genetics (4.2k citations), Molecular Biology (9.0k citations), Cancer Research (882 citations), Developmental Neuroscience (186 citations) and Aging (76 citations). Brian Hendrich has collaborated with scholars based in United Kingdom, United States and Germany. Frequent co-authors include Adrian Bird, Jacky Guy, Joanne E. Martin, Megan C. Holmes, Wolf Reik, Wendy Dean, Fátima Santos, Huntington F. Willard, Huck‐Hui Ng and Carolyn J. Brown. Their work appears in journals such as Human Molecular Genetics, Development, Nature Genetics, Molecular and Cellular Biology and Molecular Cell.

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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