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Genetics

D-Index
61
Citations
17761
World Ranking
3040
National Ranking
1327

Overview

Michael Lovett is affiliated with Washington University in St. Louis in the United States. Their research spans multiple areas within neuroscience with a particular focus on neurobiology, sensory systems, and aging.

Among the recent publications authored or co-authored by Lovett are the following papers:

  • Homeostatic maintenance and age-related functional decline in the Drosophila ear, 2020, Scientific Reports
  • Transcriptomic change in human utricles after aminoglycoside-induced hair cell ablation: Dynamic alterations to hair cell and supporting cell genes, 2025, Hearing Research
  • Revealing heterogeneity and damage response in the adult human utricle, 2025, Nature Communications

Lovett's work is frequently published in venues such as Scientific Reports, Hearing Research, and Nature Communications, indicating involvement in a broad range of fields related to auditory and sensory biology.

The main fields of study for Lovett include Neuroscience, with subfields covering Cellular and Molecular Neuroscience, Aging, Sensory Systems, Plant Science, and Immunology. This range reflects an interdisciplinary research approach encompassing both human biology and model organisms.

The principal research topics Lovett has contributed to are:

  • Neurobiology and Insect Physiology Research
  • Genetics, Aging, and Longevity in Model Organisms
  • Plant Molecular Biology Research
  • Hearing, Cochlea, Tinnitus, Genetics
  • Immune Cell Function and Interaction

Frequent co-authors in Lovett's work include Jonathan E. Gale, Alyona Keder, Camille Tardieu, Liza Malong, and Anastasia Filia, illustrating collaboration with several researchers in related fields.

Best Publications

  • A SINGLE ATAXIA TELANGIECTASIA GENE WITH A PRODUCT SIMILAR TO PI-3 KINASE

    Kinneret Savitsky;Anat Bar-Shira;Shlomit Gilad;Galit Rotman

  • Fusion of PDGF receptor β to a novel ets-like gene, tel, in chronic myelomonocytic leukemia with t(5;12) chromosomal translocation

    T R Golub;G F Barker;G F Barker;M Lovett;D G Gilliland;D G Gilliland

  • The diastrophic dysplasia gene encodes a novel sulfate transporter: Positional cloning by fine-structure linkage disequilibrium mapping

    Johanna Hästbacka;Albert de la Chapelle;Melanie M. Mahtani;Greg Clines

  • Plasmid ColE1 as a Molecular Vehicle for Cloning and Amplification of DNA

    Vickers Hershfield;Herbert W. Boyer;Charles Yanofsky;Michael A. Lovett

  • Identification of the homologous beige and Chediak–Higashi syndrome genes

    Maria D. F. S. Barbosa;Quan A. Nguyen;Velizar T. Tchernev;Jennifer A. Ashley

  • Transgenic mice with increased Cu/Zn-superoxide dismutase activity: animal model of dosage effects in Down syndrome.

    Charles J. Epstein;Karen B. Avraham;Michael Lovett;Sandra Smith

  • Mutations in CD2BP1 disrupt binding to PTP PEST and are responsible for PAPA syndrome, an autoinflammatory disorder

    Carol A. Wise;Joseph D. Gillum;Christine E. Seidman;Noralane M. Lindor

  • The EXT2 multiple exostoses gene defines a family of putative tumour suppressor genes

    Dominique Stickens;Dominique Stickens;Gregory Clines;David Burbee;Purita Ramos

  • Presenilin 1 interaction in the brain with a novel member of the Armadillo family.

    Jianhua Zhou;Udaya Liyanage;Miguel Medina;Carole Ho

  • Abnormal skin, limb and craniofacial morphogenesis in mice deficient for interferon regulatory factor 6 ( Irf6 )

    Christopher R. Ingraham;Akira Kinoshita;Shinji Kondo;Baoli Yang

  • Direct selection: a method for the isolation of cDNAs encoded by large genomic regions.

    Michael Lovett;Juha Kere;Linda M. Hinton

  • Mutational and haplotype analyses of families with familial partial lipodystrophy (Dunnigan variety) reveal recurrent missense mutations in the globular C-terminal domain of lamin A/C.

    Rebecca A. Speckman;Abhimanyu Garg;Fenghe Du;Lynda Bennett

  • A Human Homologue of Drosophila Minibrain (Mnb) Is Expressed in the Neuronal Regions Affected in Down Syndrome and Maps to the Critical Region

    Jordi Guimerá;Caty Casas;Carles Pucharcòs;Asun Solans

  • Treponema pallidum invades intercellular junctions of endothelial cell monolayers

    D. Denee Thomas;Mahamad Navab;David A. Haake;Alan M. Fogelman

  • CHD7 gene polymorphisms are associated with susceptibility to idiopathic scoliosis

    Carol Wise

  • Orofacial cleft risk is increased with maternal smoking and specific detoxification-gene variants

    Min Shi;Min Shi;Kaare Christensen;Clarice R. Weinberg;Paul Romitti

  • Molecular properties of adult mouse gastric and intestinal epithelial progenitors in their niches.

    Marios Giannakis;Thaddeus S. Stappenbeck;Jason C. Mills;Douglas G. Leip

  • Identification and localization of the gene for EXTL, a third member of the multiple exostoses gene family.

    Carol A. Wise;Gregory A. Clines;Hillary Massa;Barbara J. Trask

  • Localization of susceptibility to familial idiopathic scoliosis.

    Carol A. Wise;Robert Barnes;T. Joseph Gillum;John A. Herring

  • Cleft lip/palate and CDH1/E-cadherin mutations in families with hereditary diffuse gastric cancer.

    T Frebourg;C Oliveira;P Hochain;R Karam

Frequent Co-Authors

James N. Miller
James N. Miller University of California, Los Angeles
Mark E. Warchol
Mark E. Warchol Washington University in St. Louis
Anne M. Bowcock
Anne M. Bowcock Icahn School of Medicine at Mount Sinai
Ethylin Wang Jabs
Ethylin Wang Jabs Icahn School of Medicine at Mount Sinai
Carol A. Wise
Carol A. Wise The University of Texas Southwestern Medical Center
Julian P. Whitelegge
Julian P. Whitelegge University of California, Los Angeles
Francis S. Collins
Francis S. Collins National Institutes of Health
Christine Clayton
Christine Clayton Heidelberg University
John J. Wasmuth
John J. Wasmuth University of California, Irvine
Richard J.H. Smith
Richard J.H. Smith University of Iowa

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