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Michael L. Cuccaro

Michael L. Cuccaro

D-Index & Metrics

Genetics

D-Index
71
Citations
36267
World Ranking
2146
National Ranking
975

Overview

Michael L. Cuccaro is affiliated with the University of Miami in the United States. Their research primarily focuses on biochemistry, genetics, and molecular biology, with significant contributions in medicine. Their work spans several subfields, including genetics, molecular biology, physiology, psychiatry and mental health, and neurology.

The scientist's research interests encompass a range of topics, notably genetic associations and epidemiology, Alzheimer's disease research and treatments, dementia and cognitive impairment research, genomics and rare diseases, bioinformatics and genomic networks, epigenetics and DNA methylation, and genetic mapping and diversity in plants and animals.

Michael L. Cuccaro has published extensively, with frequent publication venues including Alzheimer s & Dementia, bioRxiv (Cold Spring Harbor Laboratory), Neurology, Neurobiology of Aging, and the Journal of Alzheimer s Disease.

Among their recent notable papers are:

  • Large-Scale Exome Sequencing Study Implicates Both Developmental and Functional Changes in the Neurobiology of Autism (2020, Cell)
  • New insights into the genetic etiology of Alzheimer's disease and related dementias (2022, Nature Genetics)
  • Rare coding variation provides insight into the genetic architecture and phenotypic context of autism (2022, Nature Genetics)
  • APOE Genotype and Alzheimer Disease Risk Across Age, Sex, and Population Ancestry (2023, JAMA Neurology)
  • Sex differences in the genetic architecture of cognitive resilience to Alzheimer's disease (2022, Brain)

Frequent collaborators in their research include Jeffery M. Vance, Larry D. Adams, Margaret A. Pericak-Vance, Jonathan L. Haines, and Gary W. Beecham, reflecting extensive co-authorship networks across related fields.

Best Publications

  • Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs

    S. Hong Lee;Stephan Ripke;Stephan Ripke;Benjamin M. Neale;Benjamin M. Neale;Stephen V. Faraone

  • Functional impact of global rare copy number variation in autism spectrum disorders

    Dalila Pinto;Alistair T. Pagnamenta;Lambertus Klei;Richard Anney

  • Large-Scale Exome Sequencing Study Implicates Both Developmental and Functional Changes in the Neurobiology of Autism

    F. Kyle Satterstrom;F. Kyle Satterstrom;Jack A. Kosmicki;Jiebiao Wang;Michael S. Breen

  • Mapping autism risk loci using genetic linkage and chromosomal rearrangements

    Peter Szatmari;Andrew D. Paterson;Lonnie Zwaigenbaum;Wendy Roberts

  • Convergence of Genes and Cellular Pathways Dysregulated in Autism Spectrum Disorders

    Dalila Pinto;Elsa Delaby;Elsa Delaby;Elsa Delaby;Daniele Merico;Mafalda Barbosa

  • Common genetic variants on 5p14.1 associate with autism spectrum disorders

    Kai Wang;Haitao Zhang;Deqiong Ma;Maja Bucan

  • A genome-wide linkage and association scan reveals novel loci for autism

    Lauren A. Weiss;Lauren A. Weiss;Dan E. Arking;Mark J. Daly;Mark J. Daly;Aravinda Chakravarti

  • Meta-analysis of GWAS of over 16,000 individuals with autism spectrum disorder highlights a novel locus at 10q24.32 and a significant overlap with schizophrenia

    Richard J.L. Anney;Richard J.L. Anney;Stephan Ripke;Stephan Ripke;Stephan Ripke;Verneri Anttila;Jakob Grove;Jakob Grove

  • Psychiatric genome-wide association study analyses implicate neuronal, immune and histone pathways

    Colm O'Dushlaine;Lizzy Rossin;Phil H. Lee;Laramie Duncan;Laramie Duncan

  • A genome-wide scan for common alleles affecting risk for autism

    Richard Anney;Lambertus Klei;Dalila Pinto;Regina Regan

  • Genomic and epigenetic evidence for oxytocin receptor deficiency in autism.

    Simon G Gregory;Jessica J Connelly;Aaron J Towers;Jessica Johnson

  • Autism and maternally derived aberrations of chromosome 15q

    Richard J. Schroer;Mary C. Phelan;Ron C. Michaelis;Eric C. Crawford

  • Fine mapping of autistic disorder to chromosome 15q11-q13 by use of phenotypic subtypes

    Yujun Shao;M. L. Cuccaro;E. R. Hauser;K. L. Raiford

  • Individual common variants exert weak effects on the risk for autism spectrum disorders.

    Richard Anney;Lambertus Klei;Dalila Pinto;Dalila Pinto;Joana Almeida

  • Identification of significant association and gene-gene interaction of GABA receptor subunit genes in autism

    D. Q. Ma;P. L. Whitehead;M. M. Menold;E. R. Martin

  • Reconstructing the population genetic history of the Caribbean.

    Andrés Moreno-Estrada;Simon Gravel;Simon Gravel;Fouad Zakharia;Jacob L. McCauley

  • Factor analysis of restricted and repetitive behaviors in autism using the autism diagnostic interview-R

    Michael L. Cuccaro;Yujan Shao;Janet Grubber;Michael Slifer

  • Genomic screen and follow-up analysis for autistic disorder

    Yujun Shao;Chantelle M. Wolpert;Kimberly L. Raiford;Marisa M. Menold

  • Exome sequencing of extended families with autism reveals genes shared across neurodevelopmental and neuropsychiatric disorders

    Holly N Cukier;Nicole D Dueker;Susan H Slifer;Joycelyn M Lee

  • Convergence of genes and cellular pathways dysregulated in autism spectrum disorders

    Dalila Pinto;Elsa Delaby;Daniele Merico;Mafalda Barbosa

Frequent Co-Authors

Margaret A. Pericak-Vance
Margaret A. Pericak-Vance University of Miami
Jeffery M. Vance
Jeffery M. Vance University of Miami
John R. Gilbert
John R. Gilbert University of Miami
Eden R. Martin
Eden R. Martin University of Miami
Harry H. Wright
Harry H. Wright University of South Carolina
Gary W. Beecham
Gary W. Beecham University of Miami
Jonathan L. Haines
Jonathan L. Haines Case Western Reserve University
Gerard D. Schellenberg
Gerard D. Schellenberg University of Pennsylvania
Catalina Betancur
Catalina Betancur Sorbonne University
Joseph D. Buxbaum
Joseph D. Buxbaum Icahn School of Medicine at Mount Sinai

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