World's Best Scientists 2026 revealed!

D-Index & Metrics

Genetics

D-Index
71
Citations
21399
World Ranking
2173
National Ranking
985

Medicine

D-Index
73
Citations
23056
World Ranking
19586
National Ranking
9754

Overview

Marcella Devoto is affiliated with the University of Pennsylvania in the United States and has an extensive publication record focused on genetics, immunology, and medicine. Their research spans several subfields, including genetics, immunology, pathology and forensic medicine, surgery, and infectious diseases, reflecting a multidisciplinary approach to medical science.

Their work has been published in various prominent venues, with multiple contributions in bioRxiv (Cold Spring Harbor Laboratory), Frontiers in Immunology, Nature Genetics, Gastroenterology, and Nature Communications. These publication venues suggest a focus on both basic and clinical biomedical research.

Among recent papers authored or co-authored by Devoto are:

  • Complex genetic signatures in immune cells underlie autoimmunity and inform therapy (2020, Nature Genetics)
  • Large-scale sequencing identifies multiple genes and rare variants associated with Crohn's disease susceptibility (2022, Nature Genetics)
  • Rare copy number variants in over 100,000 European ancestry subjects reveal multiple disease associations (2020, Nature Communications)
  • Effect of Different Disease-Modifying Therapies on Humoral Response to BNT162b2 Vaccine in Sardinian Multiple Sclerosis Patients (2021, Frontiers in Immunology)
  • Author Correction: Complex genetic signatures in immune cells underlie autoimmunity and inform therapy (2020, Nature Genetics)

Frequent co-authors collaborating with Marcella Devoto include Edoardo Fiorillo, Francesco Cucca, Judith R. Kelsen, Noor Dawany, and Maristella Steri, indicating active research partnerships. These collaborations often coincide with studies in genetics and immunology, as reflected in the co-authored publications.

The primary fields of study for Devoto are medicine and biochemistry, genetics, and molecular biology. Their research topics cover a diverse range, specifically:

  • Inflammatory Bowel Disease
  • SARS-CoV-2 and COVID-19 Research
  • Multiple Sclerosis Research Studies
  • Immunodeficiency and Autoimmune Disorders
  • Immune Cell Function and Interaction
  • Peripheral Neuropathies and Disorders
  • Eosinophilic Esophagitis

This range of topics highlights a focus on complex immune-related conditions and their genetic underpinnings, alongside infectious disease research and neurological disorders. Devoto's work on autoimmunity and genetic susceptibility contributes to a broader understanding of disease mechanisms relevant to both clinical and translational medicine.

Best Publications

  • The Wilson disease gene is a copper transporting ATPase with homology to the Menkes disease gene.

    R E Tanzi;K Petrukhin;I Chernov;J L Pellequer

  • Identification of ALK as a major familial neuroblastoma predisposition gene

    Yaël P. Mossé;Marci Laudenslager;Luca Longo;Kristina A. Cole

  • Cornelia de Lange syndrome is caused by mutations in NIPBL , the human homolog of Drosophila melanogaster Nipped-B

    Ian D. Krantz;Jennifer McCallum;Cheryl DeScipio;Maninder Kaur

  • A common molecular basis for three inherited kidney stone diseases

    Sarah E. Lloyd;Simon H. S. Pearce;Simon E. Fisher;Klaus Steinmeyer

  • Polymorphisms of α-adducin and salt sensitivity in patients with essential hypertension

    Daniele Cusi;Cristina Barlassina;Tiziana Azzani;Giorgio Casari

  • A genome-wide association study identifies KIAA0350 as a type 1 diabetes gene

    Hakon Hakonarson;Struan F A Grant;Jonathan P. Bradfield;Luc Marchand

  • Mapping, Cloning and Genetic Characterization of the Region Containing the Wilson Disease Gene

    K Petrukhin;S G Fischer;M Pirastu;R E Tanzi

  • Rare structural variants found in attention-deficit hyperactivity disorder are preferentially associated with neurodevelopmental genes

    J. Elia;X. Gai;H. M. Xie;J. C. Perin

  • Complex genetic signatures in immune cells underlie autoimmunity and inform therapy.

    Valeria Orrù;Maristella Steri;Carlo Sidore;Michele Marongiu

  • Charcot-Marie-Tooth type 4B is caused by mutations in the gene encoding myotubularin-related protein-2

    Alessandra Bolino;Maria Muglia;Francesca Luisa Conforti;Eric LeGuern

  • Genome-wide copy number variation study associates metabotropic glutamate receptor gene networks with attention deficit hyperactivity disorder

    Josephine Elia;Joseph T. Glessner;Kai Wang;Nagahide Takahashi

  • Copy number variation at 1q21.1 associated with neuroblastoma

    Sharon J. Diskin;Cuiping Hou;Joseph T. Glessner;Edward F. Attiyeh;Edward F. Attiyeh

  • NIPBL Mutational Analysis in 120 Individuals with Cornelia de Lange Syndrome and Evaluation of Genotype-Phenotype Correlations

    Lynette A. Gillis;Jennifer McCallum;Maninder Kaur;Cheryl DeScipio

  • Variants of DENND1B Associated with Asthma in Children

    Patrick M. A. Sleiman;James Flory;Marcin Imielinski;Jonathan P. Bradfield

  • Common variations in BARD1 influence susceptibility to high-risk neuroblastoma

    Mario Capasso;Marcella Devoto;Cuiping Hou;Shahab Asgharzadeh

  • Integrative genomics identifies LMO1 as a neuroblastoma oncogene

    Kai Wang;Kai Wang;Sharon J. Diskin;Haitao Zhang;Edward F. Attiyeh

  • Chromosome 6p22 Locus Associated with Clinically Aggressive Neuroblastoma

    John M. Maris;Yael P. Mosse;Jonathan P. Bradfield;Cuiping Hou

  • A common mutation in Sardinian autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy patients

    M. C. Rosatelli;A. Meloni;M. Devoto;A. Cao

  • Common variation at 6q16 within HACE1 and LIN28B influences susceptibility to neuroblastoma

    Sharon J Diskin;Mario Capasso;Robert W Schnepp;Kristina A Cole;Kristina A Cole

  • New locus for autosomal dominant high myopia maps to the long arm of chromosome 17.

    Prasuna Paluru;Shawn M Ronan;Elise Heon;Marcella Devoto;Marcella Devoto

Frequent Co-Authors

Hakon Hakonarson
Hakon Hakonarson Children's Hospital of Philadelphia
John M. Maris
John M. Maris Children's Hospital of Philadelphia
Nancy B. Spinner
Nancy B. Spinner Children's Hospital of Philadelphia
Struan F.A. Grant
Struan F.A. Grant University of Pennsylvania
Joseph T. Glessner
Joseph T. Glessner Children's Hospital of Philadelphia
Ian D. Krantz
Ian D. Krantz Children's Hospital of Philadelphia
Eric F. Rappaport
Eric F. Rappaport Children's Hospital of Philadelphia
Roberto Ravazzolo
Roberto Ravazzolo University of Genoa
Yael P. Mosse
Yael P. Mosse Children's Hospital of Philadelphia
Bruno Dallapiccola
Bruno Dallapiccola Bambino Gesù Children's Hospital

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