World's Best Scientists 2026 revealed!

D-Index & Metrics

Genetics

D-Index
103
Citations
86671
World Ranking
658
National Ranking
333

Research.com Recognitions

  • 2012 - Fellow of the American Association for the Advancement of Science (AAAS)

Overview

Lynn B. Jorde is affiliated with the University of Utah in the United States. Their research primarily spans the fields of Biochemistry, Genetics, and Molecular Biology, as well as Medicine. Within these disciplines, their work focuses on several subfields, including Molecular Biology, Genetics, Plant Science, Pediatrics, Perinatology and Child Health, and Pathology and Forensic Medicine.

The scientist's research covers a range of topics, notably:

  • Chromosomal and Genetic Variations
  • Genomics and Rare Diseases
  • Genomics and Phylogenetic Studies
  • Genomic variations and chromosomal abnormalities
  • RNA and protein synthesis mechanisms
  • Genetic factors in colorectal cancer
  • Prenatal Screening and Diagnostics

Lynn B. Jorde has contributed to multiple publications in various venues. Frequent publication platforms include:

  • bioRxiv (Cold Spring Harbor Laboratory)
  • Neurology
  • Scientific Reports
  • G3 Genes Genomes Genetics
  • Human Genetics and Genomics Advances

Among their recent papers are:

  • "De novo structural mutation rates and gamete-of-origin biases revealed through genome sequencing of 2,396 families," published in 2021, The American Journal of Human Genetics
  • "Large-scale Identification of Clonal Hematopoiesis and Mutations Recurrent in Blood Cancers," published in 2021, Blood Cancer Discovery
  • "The Simons Genome Diversity Project: A Global Analysis of Mobile Element Diversity," published in 2020, Genome Biology and Evolution
  • "The mutational dynamics of short tandem repeats in large, multigenerational families," published in 2022, Genome Biology
  • "Human de novo mutation rates from a four-generation pedigree reference," published in 2025, Nature

Frequent co-authors collaborating with Lynn B. Jorde include:

  • Aaron R. Quinlan
  • Cody J. Steely
  • W. Scott Watkins
  • Deborah W. Neklason
  • Julie Feusier

Recognition of their work includes being named a Fellow of the American Association for the Advancement of Science (AAAS) in 2012.

Best Publications

  • A global reference for human genetic variation.

    Adam Auton;Gonçalo R. Abecasis;David M. Altshuler;Richard M. Durbin

  • An integrated map of genetic variation from 1,092 human genomes

    Goncalo R Abecasis;Adam Auton;Lisa D Brooks

  • Table S2: Trans-factors and trinucleotide repeat instability Trans-factor

    Arturo López Castel;John D Cleary;Christopher E Pearson

  • The International HapMap Project

    John W. Belmont;Paul Hardenbol;Thomas D. Willis;Fuli Yu

  • The Simons Genome Diversity Project: 300 genomes from 142 diverse populations

    Swapan Mallick;Swapan Mallick;Swapan Mallick;Heng Li;Mark Lipson;Iain Mathieson

  • Mapping copy number variation by population-scale genome sequencing

    Ryan E. Mills;Klaudia Walter;Chip Stewart;Robert E. Handsaker

  • Genetic Evidence for High-Altitude Adaptation in Tibet

    Tatum S. Simonson;Yingzhong Yang;Chad D. Huff;Haixia Yun

  • Analysis of genetic inheritance in a family quartet by whole-genome sequencing

    Jared C. Roach;Gustavo Glusman;Arian F. A. Smit;Chad D. Huff;Chad D. Huff

  • A global reference for human genetic variation

    Adam Auton;Gonçalo R. Abecasis;David M. Altshuler;Richard M. Durbin

  • Genetic variation, classification and 'race'.

    Lynn B Jorde;Stephen P Wooding

  • Genetic traces of ancient demography

    Henry C. Harpending;Mark A. Batzer;Michael Gurven;Lynn B. Jorde

  • Mutations in human TBX3 alter limb, apocrine and genital development in ulnar-mammary syndrome

    M Bamshad;R C Lin;D J Law;W C Watkins

  • The Distribution of Human Genetic Diversity: A Comparison of Mitochondrial, Autosomal, and Y-Chromosome Data

    Lynn B. Jorde;W. S. Watkins;M. J. Bamshad;M. E. Dixon

  • A map of human genome variation from population-scale sequencing

    Richard M. Durbin;David L. Altshuler;Gonçalo R. Abecasis;David R. Bentley

  • Linkage Disequilibrium and the Search for Complex Disease Genes

    L.B. Jorde

  • Genetic Evidence on the Origins of Indian Caste Populations

    Michael Bamshad;Toomas Kivisild;W. Scott Watkins;Mary E. Dixon

  • De novo mutations in ATP1A3 cause alternating hemiplegia of childhood

    Erin L Heinzen;Kathryn J Swoboda;Yuki Hitomi;Fiorella Gurrieri

  • A genetic mechanism for Tibetan high-altitude adaptation

    Felipe R. Lorenzo;Chad Huff;Chad Huff;Mikko Myllymäki;Benjamin Olenchock

  • Human Population Genetic Structure and Inference of Group Membership

    Michael J. Bamshad;Stephen Wooding;W. Scott Watkins;Christopher T. Ostler

  • High polymorphism at the human melanocortin 1 receptor locus.

    Brinda K. Rana;David Hewett-Emmett;Li Jin;Benny H J Chang

Frequent Co-Authors

Michael J. Bamshad
Michael J. Bamshad University of Washington
Jinchuan Xing
Jinchuan Xing Rutgers, The State University of New Jersey
Chad D. Huff
Chad D. Huff The University of Texas MD Anderson Cancer Center
Mark A. Batzer
Mark A. Batzer Louisiana State University
John C. Carey
John C. Carey University of Utah
Mark Yandell
Mark Yandell University of Utah
Michael W. Varner
Michael W. Varner University of Utah
John F. Bohnsack
John F. Bohnsack University of Utah
Aaron R. Quinlan
Aaron R. Quinlan University of Utah
Bryan J. Mowry
Bryan J. Mowry University of Queensland

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