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Genetics

D-Index
53
Citations
17494
World Ranking
3694
National Ranking
1599

Research.com Recognitions

  • 2018 - Fellow of the American Association for the Advancement of Science (AAAS)

Overview

Andreas D. Baxevanis is affiliated with the National Institutes of Health in the United States. Their research spans multiple areas within biochemistry, genetics, molecular biology, and environmental science. The scientist has contributed to a variety of fields including molecular biology, paleontology, ecology, global and planetary change, and genetics.

Their work frequently addresses topics such as marine invertebrate physiology and ecology, marine ecology and invasive species, protist diversity and phylogeny, planarian biology and electrostimulation, developmental biology and gene regulation, genomics and phylogenetic studies, and coastal wetland ecosystem dynamics.

Recent notable publications by Andreas D. Baxevanis include:

  • Transcription factor AP2 controls cnidarian germ cell induction, 2020, Science
  • A chromosome-scale epigenetic map of the Hydra genome reveals conserved regulators of cell state, 2023, Genome Research
  • Senescence-induced cellular reprogramming drives cnidarian whole-body regeneration, 2023, Cell Reports
  • A cellular and molecular analysis of SoxB-driven neurogenesis in a cnidarian, 2022, eLife
  • Mapping the cortico-striatal transcriptome in attention deficit hyperactivity disorder, 2022, Molecular Psychiatry

Andreas D. Baxevanis commonly collaborates with several researchers including Christine E. Schnitzler, Steven M. Sanders, Matthew L. Nicotra, Uri Frank, and R. Travis Moreland. These collaborations have resulted in multiple joint publications across various research topics.

The scientist's work is often published in prominent venues such as bioRxiv (Cold Spring Harbor Laboratory), Zenodo (CERN European Organization for Nuclear Research), Genome Research, Science, and Cell Reports. The distribution of publications shows a significant presence in preprint and open-access repositories alongside peer-reviewed journals.

Andreas D. Baxevanis was recognized as a Fellow of the American Association for the Advancement of Science (AAAS) in 2018, reflecting engagement with the scientific community and contributions to their fields of study.

Best Publications

  • The ENCODE (ENCyclopedia of DNA elements) Project

    E. A. Feingold;P. J. Good;M. S. Guyer;S. Kamholz

  • Ancient missense mutations in a new member of the RoRet gene family are likely to cause familial Mediterranean fever

    I. Aksentijevich;M. Centola;Z. M. Deng;R. Sood

  • Pendred syndrome is caused by mutations in a putative sulphate transporter gene (PDS)

    Lorraine A. Everett;Benjamin Glaser;John C. Beck;Jacquelyn R. Idol

  • Ancient missense mutations in a new member of the RoRet gene family are likely to cause familial Mediterranean fever. The International FMF Consortium.

    N Zaks;JE Balow;E Mansfield;M. E. Mangelsdorf

  • The Genome of the Ctenophore Mnemiopsis leidyi and Its Implications for Cell Type Evolution

    Joseph F. Ryan;Joseph F. Ryan;Kevin Pang;Christine E. Schnitzler;Anh Dao Nguyen

  • Characterization of the CHD family of proteins.

    Trevor Woodage;Munira A. Basrai;Andreas D. Baxevanis;Philip Hieter

  • MLH3: a DNA mismatch repair gene associated with mammalian microsatellite instability.

    Steven M. Lipkin;Victoria Wang;Russell Jacoby;Sharmila Banerjee-Basu

  • The Molecular Biology Database Collection: 2002 update.

    Andreas D. Baxevanis

  • The HMG-1 box protein family: classification and functional relationships

    Andreas D. Baxevanis;David Landsman

  • A variety of DNA-binding and multimeric proteins contain the histone fold motif

    Andreas D. Baxevanis;Gina Arents;Evangelos N. Moudrianakis;David Landsman

  • The Molecular Biology Database Collection: 2003 update.

    Andreas D. Baxevanis

  • Pre-bilaterian origins of the Hox cluster and the Hox code: evidence from the sea anemone, Nematostella vectensis.

    Joseph F. Ryan;Joseph F. Ryan;Maureen E. Mazza;Kevin Pang;David Q. Matus

  • Interactions of coiled coils in transcription factors: where is the specificity?

    Andreas D. Baxevanis;Charles R. Vinson

  • Progressive juvenile-onset punctate cataracts caused by mutation of the γD-crystallin gene

    Dietrich A. Stephan;Elizabeth Gillanders;Deborah Vanderveen;Diana Freas-Lutz

  • Mutation of a gene encoding a putative chaperonin causes McKusick-Kaufman syndrome.

    Deborah L. Stone;Anne Slavotinek;Gerard G. Bouffard;Sharmila Banerjee-Basu

  • The Molecular Biology Database Collection: an online compilation of relevant database resources

    Andreas D. Baxevanis

  • Molecular evolution of the homeodomain family of transcription factors

    Sharmila Banerjee-Basu;Andreas D. Baxevanis

  • The Sox10Dom Mouse: Modeling the Genetic Variation of Waardenburg-Shah (WS4) Syndrome

    E. Michelle Southard-Smith;Misha Angrist;Jane S. Ellison;Richa Agarwala

  • Loss-of-Function Mutations in Growth Differentiation Factor-1 (GDF1) Are Associated with Congenital Heart Defects in Humans

    J.D. Karkera;J.S. Lee;E. Roessler;S. Banerjee-Basu

  • The homeodomain complement of the ctenophore Mnemiopsis leidyi suggests that Ctenophora and Porifera diverged prior to the ParaHoxozoa

    Joseph F. Ryan;Kevin C.H. Pang;James C. Mullikin;Mark Q. Martindale

Frequent Co-Authors

David Landsman
David Landsman National Institutes of Health
Mark Q. Martindale
Mark Q. Martindale University of Florida
Francis S. Collins
Francis S. Collins National Institutes of Health
Jeffrey M. Trent
Jeffrey M. Trent Translational Genomics Research Institute
Lawrence C. Brody
Lawrence C. Brody National Institutes of Health
Dietrich A. Stephan
Dietrich A. Stephan NeuBase Therapeutics
James C. Mullikin
James C. Mullikin National Institutes of Health
Colleen M. McBride
Colleen M. McBride Emory University
John D. Carpten
John D. Carpten University of Southern California
Michael A. Walter
Michael A. Walter University of Alberta

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