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Genetics

D-Index
47
Citations
12713
World Ranking
4092
National Ranking
1766

Overview

Michael A. White is affiliated with Washington University Medical Center in the United States. Their research spans several interconnected fields within the life sciences, primarily focusing on biochemistry, genetics, and molecular biology, with a substantial portion of work also related to medicine.

The main areas of study where Michael A. White has contributed include:

  • Biochemistry, Genetics and Molecular Biology
  • Medicine

Within these fields, their work further specializes in subfields such as molecular biology, genetics, plant science, surgery, and pulmonary and respiratory medicine.

The key topics addressed in their research corpus are diverse, including:

  • Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
  • Chromosomal and Genetic Variations
  • CRISPR and Genetic Engineering
  • Genetic diversity and population structure
  • RNA Research and Splicing
  • Eosinophilic Esophagitis
  • Animal Genetics and Reproduction

Michael A. White has been involved in multiple research publications, frequently collaborating with a group of established co-authors. These key collaborators include Elizabeth A. McMillan, Daniel E. Shaw, Shivangi Nath, Roberto Peraza, and Joshua B. Wechsler, each contributing recurrently to the body of work.

The scientist's publications often appear in well-regarded scholarly venues. Notable frequent publication venues are:

  • bioRxiv (Cold Spring Harbor Laboratory)
  • Gastroenterology
  • Molecular Biology and Evolution
  • Cancer Research
  • PLoS Genetics

Selected recent papers illustrate a range of research topics and publication outlets:

  • "Expanding control of the tumor cell cycle with a CDK2/4/6 inhibitor," 2021, Cancer Cell
  • "Assembly of the threespine stickleback Y chromosome reveals convergent signatures of sex chromosome evolution," 2020, Genome biology
  • "Improved contiguity of the threespine stickleback genome using long-read sequencing," 2021, G3 Genes Genomes Genetics
  • "Long-read RNA sequencing reveals widespread sex-specific alternative splicing in threespine stickleback fish," 2021, Genome Research
  • "An in vivo functional genomics screen of nuclear receptors and their co-regulators identifies FOXA1 as an essential gene in lung tumorigenesis," 2020, Neoplasia

Best Publications

  • Mouse genomic variation and its effect on phenotypes and gene regulation

    T M Keane;L Goodstadt;P Danecek;M A White

  • Whole-exome sequencing of pancreatic cancer defines genetic diversity and therapeutic targets

    Agnieszka Witkiewicz;Elizabeth A. McMillan;Uthra Balaji;GuemHee Baek

  • Correction: Corrigendum: The OncoPPi network of cancer-focused protein–protein interactions to inform biological insights and therapeutic strategies

    Zenggang Li;Andrei A. Ivanov;Rina Su;Valentina Gonzalez-Pecchi

  • Meta- and Orthogonal Integration of Influenza “OMICs” Data Defines a Role for UBR4 in Virus Budding

    Shashank Tripathi;Marie O. Pohl;Yingyao Zhou;Ariel Rodriguez-Frandsen

  • Functional requirement of p23 and Hsp90 in telomerase complexes

    Shawn E. Holt;Shawn E. Holt;Dara L. Aisner;Joseph Baur;Valerie M. Tesmer

  • Synthetic lethal screen identification of chemosensitizer loci in cancer cells

    Angelique W. Whitehurst;Brian O. Bodemann;Jessica Cardenas;Deborah Ferguson

  • The exocyst is a Ral effector complex

    Serge Moskalenko;Dale O. Henry;Carine Rosse;Gladys Mirey

  • Heterozygous TBK1 mutations impair TLR3 immunity and underlie herpes simplex encephalitis of childhood

    Melina Herman;Michael Ciancanelli;Yi Hung Ou;Lazaro Lorenzo

  • A 12-Gene Set Predicts Survival Benefits from Adjuvant Chemotherapy in Non-Small-Cell Lung Cancer Patients

    Hao Tang;Guanghua Xiao;Carmen Behrens;Joan Schiller

  • Ral GTPases and cancer: linchpin support of the tumorigenic platform

    Brian O. Bodemann;Michael A. White

  • RAL GTPases are linchpin modulators of human tumour-cell proliferation and survival.

    Yuchen Chien;Michael A White

  • The OncoPPi network of cancer-focused protein-protein interactions to inform biological insights and therapeutic strategies

    Zenggang Li;Andrei A. Ivanov;Rina Su;Rina Su;Rina Su;Valentina Gonzalez-Pecchi

  • XPO1-dependent nuclear export is a druggable vulnerability in KRAS -mutant lung cancer

    Jimi Kim;Elizabeth McMillan;Hyun Seok Kim;Niranjan Venkateswaran

  • Systematic Identification of Molecular Subtype-Selective Vulnerabilities in Non Small Cell Lung Cancer

    Hyun Seok Kim;Saurabh Mendiratta;Jiyeon Kim;Chad Victor Pecot

  • Ras interaction with two distinct binding domains in Raf-1 may be required for Ras transformation

    Jonelle K. Drugan;Roya Khosravi-Far;Michael A. White;Channing J. Der

  • Genome-Wide siRNA-Based Functional Genomics of Pigmentation Identifies Novel Genes and Pathways That Impact Melanogenesis in Human Cells

    Anand K. Ganesan;Hsiang Ho;Brian Bodemann;Sean Petersen

  • Revealing static and dynamic modular architecture of the eukaryotic protein interaction network

    Kakajan Komurov;Michael White

  • Metabolic Diversity in Human Non-Small Cell Lung Cancer Cells

    Pei Hsuan Chen;Ling Cai;Kenneth Huffman;Chendong Yang

  • Broad Spectrum Identification of Cellular Small Ubiquitin-related Modifier (SUMO) Substrate Proteins

    Yingming Zhao;Sung Won Kwon;Anthony Anselmo;Kiran Kaur

  • Distinct roles of RalA and RalB in the progression of cytokinesis are supported by distinct RalGEFs

    Ilaria Cascone;Rasim Selimoglu;Cafer Ozdemir;Elaine Del Nery

Frequent Co-Authors

Bret A. Payseur
Bret A. Payseur University of Wisconsin–Madison
Catherine L. Peichel
Catherine L. Peichel University of Bern
Tim Wiltshire
Tim Wiltshire University of North Carolina at Chapel Hill
Richard M. Myers
Richard M. Myers HudsonAlpha Institute for Biotechnology
Jeremy Schmutz
Jeremy Schmutz Lawrence Berkeley National Laboratory
David M. Kingsley
David M. Kingsley Stanford University
Jonathan Flint
Jonathan Flint University of California, Los Angeles
Richard Durbin
Richard Durbin University of Cambridge
Detlef Weigel
Detlef Weigel Max Planck Institute for Developmental Biology
David J. Adams
David J. Adams Wellcome Sanger Institute

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