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D-Index & Metrics

Biology and Biochemistry

D-Index
44
Citations
16822
World Ranking
19191
National Ranking
7836

Overview

Tim Wiltshire is affiliated with the University of North Carolina at Chapel Hill in the United States. Their research primarily spans the fields of Medicine and Biochemistry, Genetics and Molecular Biology, with notable contributions across several subfields including Oncology, Molecular Biology, Genetics, Pediatrics, Perinatology and Child Health, and Hematology.

Their scholarly output includes work on topics such as Pharmacological Effects and Toxicity Studies, Hematopoietic Stem Cell Transplantation, Renal Transplantation Outcomes and Treatments, Pharmacogenetics and Drug Metabolism, Monoclonal and Polyclonal Antibodies Research, Neutropenia and Cancer Infections, and Glioma Diagnosis and Treatment.

Recent published papers by Wiltshire include:

  • Influence of Germline Genetics on Tacrolimus Pharmacokinetics and Pharmacodynamics in Allogeneic Hematopoietic Stem Cell Transplant Patients (2020) in International Journal of Molecular Sciences
  • Projected Impact of Pharmacogenomic Testing on Medications Beyond Antiplatelet Therapy in Percutaneous Coronary Intervention Patients (2020) in Pharmacogenomics
  • Evaluation of the performance of a prior tacrolimus population pharmacokinetic kidney transplant model among adult allogeneic hematopoietic stem cell transplant patients (2021) in Clinical and Translational Science
  • RYK Gene Expression Associated with Drug Response Variation of Temozolomide and Clinical Outcomes in Glioma Patients (2023) in Pharmaceuticals
  • North Carolina's Multi-Institutional Pharmacogenomics Efforts with the North Carolina Precision Health Collaborative (2021) in Pharmacogenomics

Wiltshire collaborates frequently with several co-authors, including Oscar Suzuki, Daniel J. Crona, George W. Small, Adrian J. Green, and Tammy M. Havener.

They have contributed multiple works published in venues such as UNC Libraries, Pharmacogenomics, Pharmaceuticals, Clinical and Translational Science, and International Journal of Molecular Sciences.

Best Publications

  • A gene atlas of the mouse and human protein-encoding transcriptomes

    Andrew I. Su;Tim Wiltshire;Serge Batalov;Hilmar Lapp

  • Large-scale analysis of the human and mouse transcriptomes

    Andrew I. Su;Michael P. Cooke;Keith A. Ching;Yaron Hakak

  • The Collaborative Cross, a community resource for the genetic analysis of complex traits

    Gary A. Churchill;David C. Airey;Hooman Allayee;Joe M. Angel

  • Melanopsin Is Required for Non-Image-Forming Photic Responses in Blind Mice

    Satchidananda Panda;Ignacio Provencio;Daniel C. Tu;Susana S. Pires

  • The Unc93b1 mutation 3d disrupts exogenous antigen presentation and signaling via Toll-like receptors 3, 7 and 9.

    Koichi Tabeta;Kasper Hoebe;Edith M. Janssen;Xin Du

  • The genome architecture of the collaborative cross mouse genetic reference population

    Fuad A. Iraqi;Mustafa Mahajne;Yasser Salaymah;Hani Sandovski

  • Expression analysis of G Protein-Coupled Receptors in mouse macrophages.

    Jane E Lattin;Kate Schroder;Andrew I Su;John R Walker

  • Uncovering regulatory pathways that affect hematopoietic stem cell function using 'genetical genomics'.

    Leonid Bystrykh;Ellen Weersing;Bert Dontje;Sue Sutton

  • Mutations in the homeodomain of the human SIX3 gene cause holoprosencephaly.

    Deeann E. Wallis;Erich Roessler;Erich Roessler;Ute Hehr;Luisa Nanni

  • Limb-girdle muscular dystrophy type 2G is caused by mutations in the gene encoding the sarcomeric protein telethonin.

    Eloisa S. Moreira;Tim J. Wiltshire;Georgine Faulkner;Antje Nilforoushan

  • c-Myb and p300 regulate hematopoietic stem cell proliferation and differentiation.

    Mark L. Sandberg;Susan E. Sutton;Mathew T. Pletcher;Tim Wiltshire

  • Genome-wide single-nucleotide polymorphism analysis defines haplotype patterns in mouse

    Tim Wiltshire;Mathew T. Pletcher;Serge Batalov;S. Whitney Barnes

  • Use of a dense single nucleotide polymorphism map for in silico mapping in the mouse.

    Mathew T Pletcher;Philip McClurg;Serge Batalov;Andrew I Su

  • Genetical genomics: spotlight on QTL hotspots.

    Rainer Breitling;Yang Li;Bruno M. Tesson;Jingyuan Fu

  • A Forward Genetics Screen in Mice Identifies Recessive Deafness Traits and Reveals That Pejvakin Is Essential for Outer Hair Cell Function

    Martin Schwander;Anna Sczaniecka;Nicolas Grillet;Janice S. Bailey

  • Mouse population-guided resequencing reveals that variants in CD44 contribute to acetaminophen-induced liver injury in humans

    Alison H. Harrill;Paul B. Watkins;Stephen Su;Pamela K. Ross

  • Marked Interindividual Variability in the Response to Selective Inhibitors of Cyclooxygenase-2

    Susanne Fries;Tilo Grosser;Thomas S. Price;John A. Lawson

  • A novel approach to investigate tissue-specific trinucleotide repeat instability

    Jong Min Lee;Jie Zhang;Andrew I. Su;John R. Walker

  • Mutations in LOXHD1, an Evolutionarily Conserved Stereociliary Protein, Disrupt Hair Cell Function in Mice and Cause Progressive Hearing Loss in Humans

    Nicolas Grillet;Martin Schwander;Michael S. Hildebrand;Anna Sczaniecka

  • INDUCED PREMATURE G2/M-PHASE TRANSITION IN PACHYTENE SPERMATOCYTES INCLUDES EVENTS UNIQUE TO MEIOSIS

    Tim Wiltshire;Cynthia Park;Kim A. Caldwell;Mary Ann Handel

Frequent Co-Authors

Andrew I. Su
Andrew I. Su Scripps Research Institute
Steven R. Kleeberger
Steven R. Kleeberger National Institutes of Health
Serge Batalov
Serge Batalov Genomics Institute of the Novartis Research Foundation
Luda Diatchenko
Luda Diatchenko McGill University
Roger H. Reeves
Roger H. Reeves Johns Hopkins University School of Medicine
John B. Hogenesch
John B. Hogenesch Cincinnati Children's Hospital Medical Center
William Maixner
William Maixner Duke University
Joseph S. Takahashi
Joseph S. Takahashi The University of Texas Southwestern Medical Center
Eden R. Martin
Eden R. Martin University of Miami
Ulrich Müller
Ulrich Müller Johns Hopkins University School of Medicine

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