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Genetics

D-Index
68
Citations
20979
World Ranking
2414
National Ranking
1086

Overview

Nathan Pankratz is affiliated with the University of Minnesota in the United States. Their research spans multiple fields within biomedical science, with a particular emphasis on Medicine and Biochemistry, Genetics, and Molecular Biology. The focus of their work includes several specialized subfields such as Genetics, Molecular Biology, Hematology, Surgery, and Pulmonary and Respiratory Medicine.

The scientist's research covers a broad range of topics, which include:

  • Genetic Associations and Epidemiology
  • Mitochondrial Function and Pathology
  • Blood groups and transfusion
  • Genomics and Rare Diseases
  • Metabolism and Genetic Disorders
  • Epigenetics and DNA Methylation
  • RNA modifications and cancer

Nathan Pankratz has contributed to peer-reviewed journals with papers in high-impact publication venues. Some of the frequent venues for their work are:

  • bioRxiv (Cold Spring Harbor Laboratory)
  • UNC Libraries
  • Nature Communications
  • Journal of the Endocrine Society
  • Cancer Research

Recent notable papers authored or co-authored by Nathan Pankratz include:

  • The Polygenic and Monogenic Basis of Blood Traits and Diseases, 2020, Cell
  • Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations, 2020, Cell
  • Frequency of Pathogenic Germline Variants in Cancer-Susceptibility Genes in Patients With Osteosarcoma, 2020, JAMA Oncology
  • Interleukin-6 Signaling Effects on Ischemic Stroke and Other Cardiovascular Outcomes, 2020, Circulation Genomic and Precision Medicine
  • Evaluation of mitochondrial DNA copy number estimation techniques, 2020, PLoS ONE

Collaboration is a significant aspect of Nathan Pankratz's research career. The scientist has worked frequently with several co-authors, including:

  • Bruce M. Psaty
  • Jerome I. Rotter
  • Laura M. Raffield
  • Stephen S. Rich
  • Eric Boerwinkle

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

  • Large-scale meta-analysis of genome-wide association data identifies six new risk loci for Parkinson's disease

    Mike A Nalls;Nathan Pankratz;Christina M. Lill;Chuong B. Do

  • The polygenic and monogenic basis of blood traits and diseases

    Dragana Vuckovic;Erik L. Bao;Parsa Akbari;Caleb A. Lareau

  • Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations.

    Ming-Huei Chen;Laura M Raffield;Abdou Mousas;Saori Sakaue

  • Comprehensive research synopsis and systematic meta-analyses in Parkinson's disease genetics: the PDGene database.

    Christina M. Lill;Johannes T. Roehr;Johannes T. Roehr;Matthew B. McQueen;Fotini K. Kavvoura;Fotini K. Kavvoura;Fotini K. Kavvoura

  • Genetic screening for a single common LRRK2 mutation in familial Parkinson's disease.

    William C. Nichols;Nathan D Pankratz;Dena Hernandez;Coro Paisán-Ruíz;Coro Paisán-Ruíz

  • Genomewide association study for susceptibility genes contributing to familial Parkinson disease.

    Nathan Pankratz;Jemma B. Wilk;Jeanne C. Latourelle;Anita L. DeStefano

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

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

  • A Multicenter Study of Glucocerebrosidase Mutations in Dementia With Lewy Bodies

    Michael A. Nalls;Raquel Duran;Grisel Lopez;Marzena Kurzawa-Akanbi

  • Whole genome association study of brain-wide imaging phenotypes for identifying quantitative trait loci in MCI and AD: A study of the ADNI cohort

    Li Shen;Sungeun Kim;Shannon L. Risacher;Kwangsik Nho

  • Translation initiator EIF4G1 mutations in familial Parkinson disease

    Marie Christine Chartier-Harlin;Marie Christine Chartier-Harlin;Justus C. Dachsel;Carles Vilariño-Güell;Sarah J. Lincoln

  • Functional variants in the LRRK2 gene confer shared effects on risk for Crohn's disease and Parkinson's disease.

    Ken Y. Hui;Heriberto Fernandez-Hernandez;Jianzhong Hu;Adam Schaffner

  • Meta-analysis of Parkinson's Disease: Identification of a Novel Locus, RIT2

    Nathan Pankratz;Gary W. Beecham;Anita L. Destefano;Ted M. Dawson

  • Large-Scale Gene-Centric Meta-analysis across 32 Studies Identifies Multiple Lipid Loci

    Folkert W. Asselbergs;Yiran Guo;Yiran Guo;Erik P A Van Iperen;Suthesh Sivapalaratnam

  • Voxelwise genome-wide association study (vGWAS)

    Jason L. Stein;Xue Hua;Suh Lee;April J. Ho

  • A commonly carried allele of the obesity-related FTO gene is associated with reduced brain volume in the healthy elderly

    April J. Ho;Jason L. Stein;Xue Hua;Suh Lee

  • Heterozygosity for a mutation in the parkin gene leads to later onset Parkinson disease

    Tatiana Foroud;S. K. Uniacke;L. Liu;Nathan D Pankratz

  • Mutations in GBA are associated with familial Parkinson disease susceptibility and age at onset

    W. C. Nichols;W. C. Nichols;N. Pankratz;D. K. Marek;M. W. Pauciulo

  • Genetics of Parkinson disease.

    Nathan D Pankratz;Tatiana Foroud

  • The Polygenic and Monogenic Basis of Blood Traits and Diseases

    Dragana Vuckovic;Dragana Vuckovic;Erik L. Bao;Erik L. Bao;Parsa Akbari;Caleb A. Lareau;Caleb A. Lareau

Frequent Co-Authors

Eric Boerwinkle
Eric Boerwinkle The University of Texas Health Science Center at Houston
Tatiana Foroud
Tatiana Foroud Indiana University
Alexander P. Reiner
Alexander P. Reiner University of Washington
Nicholas L. Smith
Nicholas L. Smith University of Washington
Bruce M. Psaty
Bruce M. Psaty University of Washington
Kent D. Taylor
Kent D. Taylor David Geffen School of Medicine at UCLA
Jennifer A. Brody
Jennifer A. Brody University of Washington
Myriam Fornage
Myriam Fornage The University of Texas Health Science Center at Houston
James S. Pankow
James S. Pankow University of Minnesota
Jerome I. Rotter
Jerome I. Rotter UCLA Medical Center

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