World's Best Scientists 2026 revealed!

D-Index & Metrics

Genetics

D-Index
62
Citations
15940
World Ranking
2963
National Ranking
1296

Overview

Nadav Ahituv is affiliated with the University of California, San Francisco in the United States. Their research spans primarily within the fields of Biochemistry, Genetics and Molecular Biology, including extensive work in the subfields of Molecular Biology, Genetics, Surgery, Plant Science, and Infectious Diseases.

The focus of Ahituv's research centers on several main topics related to genomics and molecular function. These include Genomics and Chromatin Dynamics, RNA Research and Splicing, RNA and protein synthesis mechanisms, Single-cell and spatial transcriptomics, Epigenetics and DNA Methylation, Genomics and Phylogenetic Studies, and Chromosomal and Genetic Variations.

Ahituv has contributed to numerous academic publications, with frequent appearances in a variety of venues. Key publication outlets include ENCODE Datasets, bioRxiv (Cold Spring Harbor Laboratory), Nature Communications, Nature, and Science.

Notable recent papers authored or coauthored by Ahituv include:

  • Single-cell epigenomics reveals mechanisms of human cortical development, 2021, Nature
  • A systematic evaluation of the design and context dependencies of massively parallel reporter assays, 2020, Nature Methods
  • Chromatin compartmentalization regulates the response to DNA damage, 2023, Nature
  • lentiMPRA and MPRAflow for high-throughput functional characterization of gene regulatory elements, 2020, Nature Protocols
  • Oestrogen engages brain MC4R signalling to drive physical activity in female mice, 2021, Nature

Ahituv collaborates regularly with several frequent coauthors, including Fumitaka Inoue, Ilias Georgakopoulos-Soares, Jingjing Zhao, Chengyu Deng, and Martin Hemberg. These partnerships reflect a consistent pattern of collaborative research across related molecular biology and genetics disciplines.

Best Publications

  • In vivo enhancer analysis of human conserved non-coding sequences

    Len A. Pennacchio;Len A. Pennacchio;Nadav Ahituv;Alan M. Moses;Shyam Prabhakar

  • Massively parallel functional dissection of mammalian enhancers in vivo

    Rupali P. Patwardhan;Joseph B. Hiatt;Daniela M. Witten;Mee J. Kim

  • A distal enhancer and an ultraconserved exon are derived from a novel retroposon

    Gill Bejerano;Craig B. Lowe;Nadav Ahituv;Nadav Ahituv;Bryan King

  • Chromatin connectivity maps reveal dynamic promoter–enhancer long-range associations

    Yubo Zhang;Chee-Hong Wong;Ramon Y. Birnbaum;Guoliang Li

  • Mutations in DMRT3 affect locomotion in horses and spinal circuit function in mice

    Lisa S. Andersson;Martin Larhammar;Fatima Memic;Hanna Wootz

  • A Genome-wide Framework for Mapping Gene Regulation via Cellular Genetic Screens.

    Molly Gasperini;Andrew J. Hill;José L. McFaline-Figueroa;Beth Martin

  • Mutation in transcription factor POU4F3 associated with inherited progressive hearing loss in humans.

    Oz Vahava;Robert Morell;Eric D. Lynch;Sigal Weiss

  • Deletion of Ultraconserved Elements Yields Viable Mice

    Nadav Ahituv;Yiwen Zhu;Axel Visel;Amy Holt

  • A systematic comparison reveals substantial differences in chromosomal versus episomal encoding of enhancer activity

    Fumitaka Inoue;Martin Kircher;Beth Martin;Gregory M. Cooper

  • Variant Interpretation: Functional Assays to the Rescue

    Lea M. Starita;Nadav Ahituv;Maitreya J. Dunham;Jacob O. Kitzman

  • Genome-wide de novo risk score implicates promoter variation in autism spectrum disorder

    Joon Yong An;Kevin Lin;Lingxue Zhu;Donna M. Werling

  • MYO6, the human homologue of the gene responsible for deafness in Snell's waltzer mice, is mutated in autosomal dominant nonsyndromic hearing loss

    Salvatore Melchionda;Nadav Ahituv;Luigi Bisceglia;Tama Sobe

  • CRISPR-mediated activation of a promoter or enhancer rescues obesity caused by haploinsufficiency

    Navneet Matharu;Sawitree Rattanasopha;Sawitree Rattanasopha;Serena Tamura;Lenka Maliskova

  • Massively parallel decoding of mammalian regulatory sequences supports a flexible organizational model

    Robin P Smith;Leila Taher;Rupali P Patwardhan;Mee J Kim

  • Medical sequencing at the extremes of human body mass.

    Nadav Ahituv;Nihan Kavaslar;Wendy Schackwitz;Wendy Schackwitz;Anna Ustaszewska

  • Decoding enhancers using massively parallel reporter assays.

    Fumitaka Inoue;Nadav Ahituv

  • Coding exons function as tissue-specific enhancers of nearby genes

    Ramon Y. Birnbaum;E. Josephine Clowney;Orly Agamy;Mee J. Kim

  • The Notch ligand Jagged1 is required for inner ear sensory development

    A. E. Kiernan;N. Ahituv;H. Fuchs;Rudi Balling

  • Single-cell epigenomics reveals mechanisms of human cortical development.

    Ryan S. Ziffra;Chang N. Kim;Jayden M. Ross;Amy Wilfert

  • Enhancer interaction networks as a means for singular olfactory receptor expression.

    Eirene Markenscoff-Papadimitriou;William E. Allen;Bradley M. Colquitt;Tracie Goh

Frequent Co-Authors

Jay Shendure
Jay Shendure University of Washington
Nir Yosef
Nir Yosef University of California, Berkeley
Len A. Pennacchio
Len A. Pennacchio Lawrence Berkeley National Laboratory
Katherine S. Pollard
Katherine S. Pollard University of California, San Francisco
Martin Kircher
Martin Kircher Charité - University Medicine Berlin
Edward M. Rubin
Edward M. Rubin Joint Genome Institute
Carol A. Wise
Carol A. Wise The University of Texas Southwestern Medical Center
Kathleen M. Giacomini
Kathleen M. Giacomini University of California, San Francisco
Pui-Yan Kwok
Pui-Yan Kwok University of California, San Francisco
Karen B. Avraham
Karen B. Avraham Tel Aviv University

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