World's Best Scientists 2026 revealed!
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Best Scientists
2025
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Genetics
Netherlands
2026

D-Index & Metrics

Best Scientists

D-Index
177
Citations
138319
World Ranking
668
National Ranking
17

Genetics

D-Index
176
Citations
133899
World Ranking
52
National Ranking
2

Medicine

D-Index
178
Citations
138089
World Ranking
387
National Ranking
11

Research.com Recognitions

  • 2026 - Research.com Genetics in Netherlands Leader Award
  • 2025 - Research.com Best Scientists Award
  • 2025 - Research.com Genetics in Netherlands Leader Award
  • 2024 - Research.com Genetics in Netherlands Leader Award
  • 2024 - Research.com Genetics and Molecular Biology in Netherlands Leader Award
  • 2023 - Research.com Genetics in Netherlands Leader Award
  • 2022 - Research.com Genetics and Molecular Biology in Netherlands Leader Award

Overview

Ben A. Oostra is affiliated with Erasmus University Rotterdam in the Netherlands. Their research contributions focus primarily on the fields of neuroscience, with specific attention to neurology and molecular biology. Oostra's work integrates advanced neuroimaging techniques and applications, often exploring mechanisms and treatments relevant to neurological diseases.

The scientist's publication record includes research on topics such as protein tyrosine phosphatases, brain tumor detection and classification, as well as neurological disease mechanisms and treatments. These areas demonstrate a focus on both molecular and diagnostic aspects of neuroscience research.

Oostra has authored several papers published in the UNC Libraries, indicating a consistent outlet for disseminating their research findings. Recent publications include:

  • Meta-analysis of genome-wide association studies from the CHARGE consortium identifies common variants associated with carotid intima media thickness and plaque (2020, UNC Libraries)
  • Genome-wide Studies of Verbal Declarative Memory in Nondemented Older People: The Cohorts for Heart and Aging Research in Genomic Epidemiology Consortium (2020, UNC Libraries)
  • Multi-Ethnic Genome-Wide Association Study of Cerebral White Matter Hyperintensities on MRI (2020, UNC Libraries)

Frequent co-authors collaborating with Oostra include Joshua C. Bis, Albert V. Smith, Reinhold Schmidt, Susan R. Heckbert, and Caroline Hayward. These collaborations highlight contributions to multi-author studies in genomics and neuroimaging.

Oostra's research intersects multiple subfields of study encompassing neurology, radiology, nuclear medicine, and imaging, which aligns with the neuroimaging and clinical applications evident in their published work.

Best Publications

  • Association of missense and 5′-splice-site mutations in tau with the inherited dementia FTDP-17

    M. Hutton;C. L. Lendon;P. Rizzu;M. Baker

  • Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome

    Annemiske J.M.H. Verkerk;Maura Pieretti;James S. Sutcliffe;Ying-Hui Fu

  • Biological, clinical and population relevance of 95 loci for blood lipids

    Tanya M. Teslovich;Kiran Musunuru;Albert V. Smith;Andrew C. Edmondson

  • Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index

    Elizabeth K. Speliotes;Elizabeth K. Speliotes;Cristen J. Willer;Sonja I. Berndt;Keri L. Monda

  • Mutations in the DJ-1 Gene Associated with Autosomal Recessive Early-Onset Parkinsonism

    Vincenzo Bonifati;Vincenzo Bonifati;Patrizia Rizzu;Marijke J. van Baren;Onno Schaap

  • New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk

    Josée Dupuis;Josée Dupuis;Claudia Langenberg;Inga Prokopenko;Richa Saxena;Richa Saxena

  • Variation of the CGG repeat at the fragile X site results in genetic instability: resolution of the Sherman paradox.

    Ying-Hui Fu;Derek P.A. Kuhl;Antonio Pizzuti;Maura Pieretti

  • Hundreds of variants clustered in genomic loci and biological pathways affect human height

    Hana Lango Allen;Karol Estrada;Guillaume Lettre;Sonja I. Berndt

  • Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk

    Georg B. Ehret;Georg B. Ehret;Georg B. Ehret;Patricia B. Munroe;Kenneth M. Rice;Murielle Bochud

  • Defining the role of common variation in the genomic and biological architecture of adult human height

    Andrew R. Wood;Tonu Esko;Jian Yang;Sailaja Vedantam

  • New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk (vol 42, pg 105, 2010)

    J Dupuis;C Langenberg;I Prokopenko;R Saxena

  • Absence of expression of the FMR-1 gene in fragile X syndrome.

    Maura Pieretti;Fuping Zhang;Ying-Hui Fu;Stephen T. Warren

  • Genetic studies of body mass index yield new insights for obesity biology

    Adam E. Locke;Bratati Kahali;Sonja I. Berndt;Anne E. Justice

  • A mutation in the interferon-gamma-receptor gene and susceptibility to mycobacterial infection.

    Melanie J Newport;Clare M Huxley;Sara Huston;Catherine M Hawrylowicz

  • Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits.

    Evangelos Evangelou;Evangelos Evangelou;Helen R. Warren;Helen R. Warren;David Mosen-Ansorena;Borbala Mifsud

  • A long-range Shh enhancer regulates expression in the developing limb and fin and is associated with preaxial polydactyly

    Laura A Lettice;Simon J H Heaney;Lorna A Purdie;Li Li

  • Genome-wide meta-analysis identifies 56 bone mineral density loci and reveals 14 loci associated with risk of fracture

    Karol Estrada;Unnur Styrkarsdottir;Evangelos Evangelou;Yi-Hsiang Hsu

  • Abnormal dendritic spines in fragile X knockout mice: maturation and pruning deficits.

    Thomas A. Comery;Jennifer B. Harris;Patrick J. Willems;Ben A. Oostra

  • Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution

    Iris M. Heid;Anne U. Jackson;Joshua C. Randall;Tthomas W. Winkler

  • Erratum: New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk (Nature Genetics (2010) 42 (105-116))

    Josée Dupuis;Claudia Langenberg;Inga Prokopenko;Richa Saxena

Frequent Co-Authors

Albert Hofman
Albert Hofman Harvard University
André G. Uitterlinden
André G. Uitterlinden Erasmus University Rotterdam
Najaf Amin
Najaf Amin University of Oxford
Rob Willemsen
Rob Willemsen Erasmus University Rotterdam
Fernando Rivadeneira
Fernando Rivadeneira Erasmus University Rotterdam
Peter Heutink
Peter Heutink German Center for Neurodegenerative Diseases
Yurii S. Aulchenko
Yurii S. Aulchenko University of Edinburgh
Igor Rudan
Igor Rudan University of Edinburgh
Markus Perola
Markus Perola Finnish Institute for Health and Welfare
Tim D. Spector
Tim D. Spector King's College London

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