World's Best Scientists 2026 revealed!
Margaret A. Pericak-Vance

Margaret A. Pericak-Vance

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Best Scientists
2025
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Best Female Scientists
2025

D-Index & Metrics

Best Female Scientists

D-Index
179
Citations
191227
World Ranking
47
National Ranking
31

Best Scientists

D-Index
179
Citations
191227
World Ranking
621
National Ranking
388

Genetics

D-Index
178
Citations
190595
World Ranking
47
National Ranking
29

Medicine

D-Index
180
Citations
199248
World Ranking
361
National Ranking
227

Margaret A. Pericak-Vance publication distribution in Genetics in 2026

The chart shows the distribution of publications by all Research.com ranked scientists in the field of Genetics in 2026. The highlighted bar marks where Margaret A. Pericak-Vance sits on this spectrum.

45–54 publications: 6 scientists 55–64 publications: 10 scientists 65–74 publications: 35 scientists 75–84 publications: 84 scientists 85–94 publications: 102 scientists 95–104 publications: 151 scientists 105–114 publications: 175 scientists 115–124 publications: 203 scientists 125–134 publications: 217 scientists 135–144 publications: 205 scientists 145–154 publications: 193 scientists 155–164 publications: 188 scientists 165–174 publications: 170 scientists 175–184 publications: 178 scientists 185–194 publications: 164 scientists 195–204 publications: 173 scientists 205–214 publications: 159 scientists 215–224 publications: 134 scientists 225–234 publications: 143 scientists 235–244 publications: 105 scientists 245–254 publications: 114 scientists 255–264 publications: 92 scientists 265–274 publications: 88 scientists 275–284 publications: 87 scientists 285–294 publications: 80 scientists 295–304 publications: 62 scientists 305–314 publications: 75 scientists 315–324 publications: 67 scientists 325–334 publications: 60 scientists 335–344 publications: 52 scientists 345–354 publications: 40 scientists 355–364 publications: 48 scientists 365–374 publications: 47 scientists 375–384 publications: 46 scientists 385–394 publications: 31 scientists 395–404 publications: 27 scientists 405–414 publications: 40 scientists 415–424 publications: 30 scientists 425–434 publications: 43 scientists 435–444 publications: 29 scientists 445–454 publications: 14 scientists 455–464 publications: 28 scientists 465–474 publications: 21 scientists 475–484 publications: 21 scientists 485–494 publications: 22 scientists 495–504 publications: 17 scientists 505–514 publications: 12 scientists 515–524 publications: 11 scientists 525–534 publications: 8 scientists 535–544 publications: 8 scientists 545–554 publications: 14 scientists 555–564 publications: 4 scientists 565–574 publications: 11 scientists 575–584 publications: 5 scientists 585–594 publications: 11 scientists 595–604 publications: 12 scientists 605–614 publications: 7 scientists 615–624 publications: 6 scientists 625–634 publications: 10 scientists 635–644 publications: 9 scientists 645–654 publications: 10 scientists 655–664 publications: 6 scientists 665–674 publications: 6 scientists 675–684 publications: 6 scientists 685–694 publications: 4 scientists 695–702 publications: 6 scientists 703+ publications: 100 scientists
45 publications 703+

This scientist: 1,234 publications — 100th percentile

100% of scientists in this discipline score the same or lower.

The last bar groups every scientist with 703 publications or more.

Margaret A. Pericak-Vance D-index placement in Genetics in 2026

The chart shows the D-index (discipline H-index) distribution of Genetics scientists ranked by Research.com in 2026. The highlighted bar marks where Margaret A. Pericak-Vance sits on this spectrum.

40–41 D-Index: 24 scientists 42–43 D-Index: 52 scientists 44–45 D-Index: 84 scientists 46–47 D-Index: 112 scientists 48–49 D-Index: 118 scientists 50–51 D-Index: 141 scientists 52–53 D-Index: 143 scientists 54–55 D-Index: 145 scientists 56–57 D-Index: 179 scientists 58–59 D-Index: 162 scientists 60–61 D-Index: 175 scientists 62–63 D-Index: 191 scientists 64–65 D-Index: 172 scientists 66–67 D-Index: 184 scientists 68–69 D-Index: 164 scientists 70–71 D-Index: 158 scientists 72–73 D-Index: 150 scientists 74–75 D-Index: 136 scientists 76–77 D-Index: 127 scientists 78–79 D-Index: 127 scientists 80–81 D-Index: 111 scientists 82–83 D-Index: 110 scientists 84–85 D-Index: 110 scientists 86–87 D-Index: 84 scientists 88–89 D-Index: 102 scientists 90–91 D-Index: 66 scientists 92–93 D-Index: 72 scientists 94–95 D-Index: 70 scientists 96–97 D-Index: 54 scientists 98–99 D-Index: 60 scientists 100–101 D-Index: 49 scientists 102–103 D-Index: 55 scientists 104–105 D-Index: 45 scientists 106–107 D-Index: 42 scientists 108–109 D-Index: 28 scientists 110–111 D-Index: 39 scientists 112–113 D-Index: 25 scientists 114–115 D-Index: 31 scientists 116–117 D-Index: 29 scientists 118–119 D-Index: 34 scientists 120–121 D-Index: 29 scientists 122–123 D-Index: 29 scientists 124–125 D-Index: 18 scientists 126–127 D-Index: 27 scientists 128–129 D-Index: 22 scientists 130–131 D-Index: 16 scientists 132–133 D-Index: 11 scientists 134–135 D-Index: 17 scientists 136–137 D-Index: 12 scientists 138–139 D-Index: 21 scientists 140–141 D-Index: 4 scientists 142–143 D-Index: 9 scientists 144–145 D-Index: 14 scientists 146–147 D-Index: 6 scientists 148–149 D-Index: 10 scientists 150–151 D-Index: 7 scientists 152–153 D-Index: 9 scientists 154–155 D-Index: 8 scientists 156–157 D-Index: 8 scientists 158–159 D-Index: 9 scientists 160+ D-Index: 96 scientists
40 D-Index 160+

This scientist: 178 D-Index — 99th percentile

99% of scientists in this discipline score the same or lower.

The last bar groups every scientist with 160 D-Index or more.

Research.com Recognitions

  • 2026 - Research.com Genetics in United States Leader Award
  • 2025 - Research.com Best Female Scientists Award
  • 2025 - Research.com Best Scientists Award
  • 2025 - Research.com Genetics in United States Leader Award
  • 2024 - Research.com Genetics in United States Leader Award
  • 2024 - Research.com Genetics and Molecular Biology in United States Leader Award
  • 2023 - Research.com Genetics in United States Leader Award
  • 2011 - Fellow of the American Association for the Advancement of Science (AAAS)
  • 2003 - Member of the National Academy of Medicine (NAM)
  • 2001 - Grand Prix scientifique de la Fondation Louis D., Institut de France

Overview

Margaret A. Pericak-Vance is affiliated with the University of Miami in the United States. Their research spans multiple fields, primarily within biochemistry, genetics, and molecular biology, as well as medicine. The subfields they focus on include molecular biology, genetics, physiology, psychiatry and mental health, and neurology.

The key topics in their work include genetic associations and epidemiology, Alzheimer's disease research and treatments, bioinformatics and genomic networks, dementia and cognitive impairment research, epigenetics and DNA methylation, genomics and rare diseases, and mitochondrial function and pathology.

The scientist has contributed to research published mainly in venues such as Alzheimer's & Dementia, bioRxiv (Cold Spring Harbor Laboratory), International Psychogeriatrics, Alzheimer's Research & Therapy, and Human Molecular Genetics. The distribution of their publications highlights 7 papers in Alzheimer's & Dementia, indicating a significant focus in that journal.

Recent papers by Margaret A. Pericak-Vance include:

  • "Blood-derived mitochondrial DNA copy number is associated with Alzheimer disease, Alzheimer-related biomarkers and serum metabolites" (2024, Alzheimer's Research & Therapy)
  • "Genetic analysis of cognitive preservation in the midwestern Amish reveals a novel locus on chromosome 2" (2024, Alzheimer's & Dementia)
  • "Novel early-onset Alzheimer-associated genes influence risk through dysregulation of glutamate, immune activation, and intracellular signaling pathways" (2025, Alzheimer's & Dementia)
  • "Developing biobanking processes for Alzheimer's disease and related dementia research in Africa: Experience from the Recruitment and Retention for Alzheimer's Disease Diversity in the Alzheimer's Disease Sequencing Project (READD-ADSP)" (2025, Alzheimer's & Dementia)
  • "APOE and Alzheimer's disease and related dementias risk among 12,221 Hispanics/Latinos" (2025, Alzheimer's & Dementia)

Coauthors frequently collaborating with this researcher include Michael L. Cuccaro, Jeffery M. Vance, Anthony J. Griswold, Brian W. Kunkle, and Jonathan L. Haines. These collaborations have contributed to advancing research in their field.

The scientist has received several awards: they were elected a Member of the National Academy of Medicine in 2003, named a Fellow of the American Association for the Advancement of Science (AAAS) in 2011, and were a recipient of the Grand Prix scientifique de la Fondation Louis D., Institut de France in 2001.

Best Publications

  • Gene dose of apolipoprotein E type 4 allele and the risk of Alzheimer's disease in late onset families

    E. H. Corder;A. M. Saunders;W. J. Strittmatter;D. E. Schmechel

  • Segregation of a missense mutation in the amyloid precursor protein gene with familial Alzheimer's disease.

    Alison Goate;Marie-Christine Chartier-Harlin;Mike Mullan;Jeremy Brown

  • Effects of Age, Sex, and Ethnicity on the Association Between Apolipoprotein E Genotype and Alzheimer Disease: A Meta-analysis

    Lindsay A. Farrer;L. Adrienne Cupples;Jonathan L. Haines;Bradley T Hyman

  • Apolipoprotein E: high-avidity binding to beta-amyloid and increased frequency of type 4 allele in late-onset familial Alzheimer disease.

    Warren J. Strittmatter;Ann M. Saunders;Donald Schmechel;Margaret Pericak-Vance

  • Cloning of a gene bearing missense mutations in early-onset familial Alzheimer's disease

    R. Sherrington;E. I. Rogaev;Y. Liang;E. A. Rogaeva

  • Meta-analysis of 74,046 individuals identifies 11 new susceptibility loci for Alzheimer's disease

    Jean-Charles Lambert;Jean-Charles Lambert;Jean-Charles Lambert;Carla A Ibrahim-Verbaas;Denise Harold;Adam C Naj

  • Association of apolipoprotein E allele epsilon 4 with late-onset familial and sporadic Alzheimer's disease.

    A. M. Saunders;W. J. Strittmatter;D. Schmechel;P. H. St. George-Hyslop

  • Mutations in the FUS/TLS gene on chromosome 16 cause familial amyotrophic lateral sclerosis.

    T. J. Kwiatkowski;D. A. Bosco;D. A. Bosco;A. L. LeClerc;A. L. LeClerc;E. Tamrazian

  • Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis

    Stephen Sawcer;Garrett Hellenthal;Matti Pirinen;Chris C. A. Spencer

  • Complement factor H variant increases the risk of age-related macular degeneration.

    Jonathan L. Haines;Michael A. Hauser;Silke Schmidt;William K. Scott

  • Risk alleles for multiple sclerosis identified by a genomewide study.

    David A. Hafler;Alastair Compston;Stephen Sawcer;Mark J. Daly

  • 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

  • Protective effect of apolipoprotein E type 2 allele for late onset Alzheimer disease.

    Corder Eh;Saunders Am;Risch Nj;Strittmatter Wj

  • 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

  • Common variants at MS4A4/MS4A6E, CD2AP, CD33 and EPHA1 are associated with late-onset Alzheimer's disease.

    Adam C. Naj;Gyungah Jun;Gary W. Beecham;Li-San Wang

  • Mutations in the mitochondrial GTPase mitofusin 2 cause Charcot-Marie-Tooth neuropathy type 2A.

    Stephan Züchner;Stephan Züchner;Irina V Mersiyanova;Maria Muglia;Nisrine Bissar-Tadmouri;Nisrine Bissar-Tadmouri

  • Amyotrophic lateral sclerosis and structural defects in Cu,Zn superoxide dismutase

    Han Xiang Deng;Afif Hentati;John A. Tainer;Zafar Iqbal

  • Increased amyloid beta-peptide deposition in cerebral cortex as a consequence of apolipoprotein E genotype in late-onset Alzheimer disease

    D E Schmechel;A M Saunders;W J Strittmatter;B J Crain

  • Binding of human apolipoprotein E to synthetic amyloid beta peptide: isoform-specific effects and implications for late-onset Alzheimer disease

    Warren J. Strittmatter;Karl H. Weisgraber;David Y. Huang;Li Ming Dong

Frequent Co-Authors

Jonathan L. Haines
Jonathan L. Haines Case Western Reserve University
Jeffery M. Vance
Jeffery M. Vance University of Miami
William K. Scott
William K. Scott University of Miami
Eden R. Martin
Eden R. Martin University of Miami
John R. Gilbert
John R. Gilbert University of Miami
Gary W. Beecham
Gary W. Beecham University of Miami
Lindsay A. Farrer
Lindsay A. Farrer Boston University
Gerard D. Schellenberg
Gerard D. Schellenberg University of Pennsylvania
Michael L. Cuccaro
Michael L. Cuccaro University of Miami
Richard Mayeux
Richard Mayeux Columbia University

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