Nadav Ahituv

15.8k citations
142 papers · 8.2k · 2 hit papers · h-index 45

Impact in

Papers in

    • Genomics and Chromatin Dynamics 56
    • RNA and protein synthesis mechanisms 33
    • RNA Research and Splicing 32
    • CRISPR and Genetic Engineering 14
    • Congenital heart defects research 11
    • Epigenetics and DNA Methylation 10

Nadav Ahituv

137 papers receiving 8.2k citations

Nadav Ahituv's Hit Papers

A Genome-wide Framework for Mapping Gene Regulation via Cellular Genetic Screens 2019 · 385 citations
3850+6+13Years since publication250500750

Peers

Nadav Ahituv
Comparison fields: 5 of 156
  • Sensory Systems 569
  • Developmental Biology 201
  • Molecular Biology 6.0k
  • Genetics 1.9k
  • Aging 72
Replace Thomas Haaf with:
Thomas Haaf Germany
C. Geoffrey Woods United Kingdom
Aimee K. Ryan Canada
Stephen C. Ekker United States
Marianne LeMeur France
Lilianna Solnica‐Krezel United States
Bernice E. Morrow United States
Muriel T. Davisson United States
Robert Geisler Germany
Katsuhiko Mikoshiba Japan
Nadav Ahituv relative to Thomas Haaf Germany Thomas Haaf's profile →
Citations per field
00.5×4.0×
Thomas Haaf · 1×
Citations per year

Countries citing papers authored by Nadav Ahituv

Since Specialization
Citations

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

Fields of papers citing papers by Nadav Ahituv

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside Nadav Ahituv, 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 Nadav Ahituv Line = papers co-authored together Nadav Ahituv links everyone, so they are left out of the graph.

All Works

20 of 20 papers shown

Showing the 20 most-cited of 142 papers — load more, or switch the sort, to bring in the rest.

#Work
1
In vivo enhancer analysis of human conserved non-coding sequences
Hit paper breakdown →
2006869
2 2006389
3 2012388
4
A Genome-wide Framework for Mapping Gene Regulation via Cellular Genetic Screens
Hit paper breakdown →
2019385
5 2013333
6 1998258
7 2007229
8 2017225
9 2018221
10 2001182
11 2016181
12 2001179
13 2015174
14 2013173
15 2012169
16 2021163
17 2014151
18 2019135
19 2013129
20 2020117

About Nadav Ahituv

Nadav Ahituv is a scholar working on Molecular Biology, Genetics, Plant Science, Developmental Biology and Surgery, having authored 142 papers that have together received 8.2k indexed citations. Recurring topics across this work include Genomics and Chromatin Dynamics (56 papers), RNA and protein synthesis mechanisms (33 papers), RNA Research and Splicing (32 papers), CRISPR and Genetic Engineering (14 papers), Chromosomal and Genetic Variations (13 papers), Congenital heart defects research (11 papers), Congenital limb and hand anomalies (11 papers) and Epigenetics and DNA Methylation (10 papers). The work is most often cited by research in Sensory Systems (569 citations), Developmental Biology (201 citations), Molecular Biology (6.0k citations), Genetics (1.9k citations) and Aging (72 citations). Nadav Ahituv has collaborated with scholars based in United States, Israel and China. Frequent co-authors include Fumitaka Inoue, Jay Shendure, Edward M. Rubin, L Pennacchio, Nir Oksenberg, Mee J. Kim, Beth Martin, Navneet Matharu, Veena Afzal and Karen B. Avraham. Their work appears in journals such as Nature Communications, Human Molecular Genetics, PLoS Genetics, Nature and Genome biology.

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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