World's Best Scientists 2026 revealed!
Mariza de Andrade

Mariza de Andrade

D-Index & Metrics

Biology and Biochemistry

D-Index
104
Citations
39920
World Ranking
1254
National Ranking
740

Medicine

D-Index
104
Citations
40618
World Ranking
7038
National Ranking
3699

Research.com Recognitions

  • 2017 - Fellow of the American Statistical Association (ASA)

Overview

Mariza de Andrade is affiliated with the Mayo Clinic in the United States and has contributed extensively to the fields of Biochemistry, Genetics and Molecular Biology, as well as Medicine.

The researcher's work encompasses several subfields, including Genetics, Molecular Biology, Surgery, Hematology, and Cancer Research. Their research primarily focuses on topics such as Genetic Associations and Epidemiology, Cancer Genomics and Diagnostics, Acute Myeloid Leukemia Research, Epigenetics and DNA Methylation, Genomics and Rare Diseases, RNA modifications and cancer, and Telomeres, Telomerase, and Senescence.

Their recent publications include:

  • Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program (2021, Nature)
  • Inherited causes of clonal haematopoiesis in 97,691 whole genomes (2020, Nature)
  • Genetic diversity fuels gene discovery for tobacco and alcohol use (2022, Nature)
  • Cerebral small vessel disease genomics and its implications across the lifespan (2020, Nature Communications)
  • An international genome-wide meta-analysis of primary biliary cholangitis: Novel risk loci and candidate drugs (2021, Journal of Hepatology)

Frequent collaborators in their research include Bruce M. Psaty, Joshua C. Bis, Susan R. Heckbert, Ramachandran S. Vasan, and Nicholas L. Smith, reflecting a network of co-authorship across numerous studies.

In terms of publication venues, their work appears often in UNC Libraries, bioRxiv (Cold Spring Harbor Laboratory), Nature, Nature Communications, and Circulation Genomic and Precision Medicine.

Mariza de Andrade was awarded the title Fellow of the American Statistical Association (ASA) in 2017.

Best Publications

  • Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program.

    Daniel Taliun;Daniel N. Harris;Michael D. Kessler;Jedidiah Carlson;Jedidiah Carlson

  • Genome-partitioning of genetic variation for complex traits using common SNPs

    Jian Yang;Teri A. Manolio;Louis R. Pasquale;Eric Boerwinkle

  • GWAS of 126,559 Individuals Identifies Genetic Variants Associated with Educational Attainment

    Cornelius A. Rietveld;Sarah E. Medland;Jaime Lane Derringer;Jian Yang

  • A genome-wide approach accounting for body mass index identifies genetic variants influencing fasting glycemic traits and insulin resistance.

    Alisa K. Manning;Alisa K. Manning;Alisa K. Manning;Robert A. Scott;Jonna L. Grimsby

  • New loci associated with kidney function and chronic kidney disease

    Anna Köttgen;Anna Köttgen;Cristian Pattaro;Carsten A. Böger;Christian Fuchsberger

  • Increased Risk of Cognitive Impairment or Dementia in Women Who Underwent Oophorectomy Before Menopause

    W. A. Rocca;J. H. Bower;D. M. Maraganore;J. E. Ahlskog

  • Genome-wide association study identifies variants in the ABO locus associated with susceptibility to pancreatic cancer

    Laufey Amundadottir;Peter Kraft;Rachael Z. Stolzenberg-Solomon;Charles S. Fuchs

  • A comprehensive 1000 Genomes-based genome-wide association meta-analysis of coronary artery disease

    Majid Nikpay;Anuj Goel;Hong-Hee Won;Leanne M. Hall

  • Inherited causes of clonal haematopoiesis in 97,691 whole genomes.

    Alexander G Bick;Joshua S Weinstock;Satish K Nandakumar;Satish K Nandakumar;Charles P Fulco;Charles P Fulco

  • Lower Cancer Incidence in Amsterdam-I Criteria Families Without Mismatch Repair Deficiency: Familial Colorectal Cancer Type X

    Noralane M. Lindor;Kari Rabe;Gloria M. Petersen;Robert Haile

  • Detectable clonal mosaicism from birth to old age and its relationship to cancer.

    Cathy C. Laurie;Cecelia A Laurie;Kenneth Rice;Kimberly F. Doheny

  • A genome-wide association study identifies pancreatic cancer susceptibility loci on chromosomes 13q22.1, 1q32.1 and 5p15.33

    Gloria M. Petersen;Laufey Amundadottir;Charles S. Fuchs;Peter Kraft

  • Probability of Pancreatic Cancer Following Diabetes: A Population-Based Study

    Suresh T. Chari;Cynthia L. Leibson;Kari G. Rabe;Jeanine Ransom

  • Collaborative analysis of alpha-synuclein gene promoter variability and Parkinson disease.

    Demetrius M. Maraganore;Mariza De Andrade;Alexis Elbaz;Matthew J. Farrer

  • Survival patterns after oophorectomy in premenopausal women: a population-based cohort study

    Walter A Rocca;Brandon R Grossardt;Mariza de Andrade;George D Malkasian

  • High-Resolution Whole-Genome Association Study of Parkinson Disease

    Demetrius M. Maraganore;Mariza de Andrade;Timothy G. Lesnick;Kari J. Strain

  • Pancreatic cancer-associated diabetes mellitus: prevalence and temporal association with diagnosis of cancer.

    Suresh T. Chari;Cynthia L. Leibson;Kari G. Rabe;Lawrence J. Timmons

  • Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function

    Cristian Pattaro;Alexander Teumer;Mathias Gorski;Audrey Y. Chu

  • Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program

    Daniel Taliun;Daniel N. Harris;Michael D. Kessler;Jedidiah Carlson;Jedidiah Carlson

  • A genomic pathway approach to a complex disease: axon guidance and Parkinson disease.

    Timothy G. Lesnick;Spiridon Papapetropoulos;Deborah C. Mash;Jarlath M H Ffrench-Mullen

Frequent Co-Authors

Eric Boerwinkle
Eric Boerwinkle The University of Texas Health Science Center at Houston
Ping Yang
Ping Yang Mayo Clinic
Christopher I. Amos
Christopher I. Amos Baylor College of Medicine
Sharon L.R. Kardia
Sharon L.R. Kardia University of Michigan–Ann Arbor
Nicholas L. Smith
Nicholas L. Smith University of Washington
Marylyn D. Ritchie
Marylyn D. Ritchie University of Pennsylvania
Albert V. Smith
Albert V. Smith University of Michigan–Ann Arbor

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