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Arthur R. Brothman

Arthur R. Brothman

D-Index & Metrics

Biology and Biochemistry

D-Index
54
Citations
13019
World Ranking
15479
National Ranking
6459

Overview

Arthur R. Brothman is affiliated with the University of Utah in the United States. Their professional profile encompasses a career oriented around academic research and scientific inquiry.

This researcher's work does not currently list specific publications, co-authors, or frequent publication venues. Consequently, detailed information on research outputs or collaborative networks is not available.

Similarly, there is no recorded data on their main fields of study, subfields, or central research topics, which limits the scope for describing their specialized areas of expertise or thematic focus within scientific disciplines.

There are no entries indicating awards or recognitions received by Arthur R. Brothman, nor are there records of published books under their name.

Best Publications

  • Consensus Statement : Chromosomal Microarray Is a First-Tier Clinical Diagnostic Test for Individuals with Developmental Disabilities or Congenital Anomalies

    David T. Miller;Margaret P. Adam;Margaret P. Adam;Swaroop Aradhya;Leslie G. Biesecker

  • Prognostic value of an RNA expression signature derived from cell cycle proliferation genes in patients with prostate cancer: a retrospective study.

    Jack Cuzick;Gregory P Swanson;Gabrielle Fisher;Arthur R Brothman

  • Copy number variations and clinical cytogenetic diagnosis of constitutional disorders.

    Charles Lee;A John Iafrate;Arthur R Brothman

  • Progression of metastatic human prostate cancer to androgen independence in immunodeficient SCID mice.

    Karen A. Klein;Robert E. Reiter;James Redula;Hamid Moradi

  • An evidence-based approach to establish the functional and clinical significance of copy number variants in intellectual and developmental disabilities.

    Erin B. Kaminsky;Vineith Kaul;Justin Paschall;Deanna M. Church

  • Strong Correlation of Elastin Deletions, Detected by FISH, With Williams Syndrome: Evaluation of 235 Patients

    M. C. Lowery;C. A. Morris;A. Ewart;L. J. Brothman

  • Deletion 17q12 Is a Recurrent Copy Number Variant that Confers High Risk of Autism and Schizophrenia

    Daniel Moreno-De-Luca;Jennifer Mulle;Erin Baldwin Kaminsky;Stephan J. Sanders

  • Analysis of chromosome breakpoints in neuroblastoma at sub‐kilobase resolution using fine‐tiling oligonucleotide array CGH

    Rebecca R. Selzer;Todd A. Richmond;Nathan J. Pofahl;Roland D. Green

  • Technical Standards and Guidelines for Fragile X: The First of a Series of Disease-Specific Supplements to the Standards and Guidelines for Clinical Genetics Laboratories of the American College of Medical Genetics

    Anne Maddalena;Carolyn Sue Richards;Matthew J McGinniss;Arthur Brothman

  • Mutation of the MXI1 gene in prostate cancer

    Linette R. Eagle;Xiaoying Yin;Arthur R. Brothman;Briana J. Williams

  • RARE TRISOMY MOSAICISM DIAGNOSED IN AMNIOCYTES, INVOLVING AN AUTOSOME OTHER THAN CHROMOSOMES 13, 18, 20, AND 21: KARYOTYPE/PHENOTYPE CORRELATIONS

    Lillian Y.F. Hsu;Ming Tsung Yu;Richard L. Neu;Daniel L. Van Dyke

  • Frequency and pattern of karyotypic abnormalities in human prostate cancer.

    Arthur R. Brothman;Donna M. Peehl;Ankita M. Patel;John E. McNeal

  • Natural history of wolf-hirschhorn syndrome : Experience with 15 cases

    Agatino Battaglia;John C. Carey;Peeches Cederholm;David H. Viskochil

  • Her-2/neu expression in osteosarcoma increases risk of lung metastasis and can be associated with gene amplification.

    Holly Zhou;R Randall;Arthur R. Brothman;Teresa Maxwell

  • Tumorigenicity of SV40 T antigen immortalized human prostate epithelial cells: Association with decreased epidermal growth factor receptor (EGFR) expression

    Bae Vl;Jackson-Cook Ck;Brothman Ar;Maygarden Sj

  • Nomenclature evolution: Changes in the ISCN from the 2005 to the 2009 edition.

    A.R. Brothman;D.L. Persons;L.G. Shaffer

  • Chromosomal clues to the development of prostate tumors.

    Arthur R. Brothman;Teresa M. Maxwell;Jiang Cui;Debra A. Deubler

  • Global hypomethylation is common in prostate cancer cells: a quantitative predictor for clinical outcome?

    Arthur R. Brothman;Gregory P Swanson;Teresa M. Maxwell;Jiang Cui

  • Commonly occurring loss and mutation of the MXI1 gene in prostate cancer

    Edward V. Prochownik;Linette Eagle Grove;Debra Deubler;Xiao Lin Zhu

  • A physical map and candidate genes in the BRCA1 region on chromosome 17q12–21

    H M Albertsen;S A Smith;S Mazoyer;E Fujimoto

Frequent Co-Authors

John C. Carey
John C. Carey University of Utah
Gordon W. Dewald
Gordon W. Dewald Mayo Clinic
Christa Lese Martin
Christa Lese Martin Geisinger Health System
Urvashi Surti
Urvashi Surti University of Pittsburgh
David H. Viskochil
David H. Viskochil University of Utah
David H. Ledbetter
David H. Ledbetter University of Florida
John A. Crolla
John A. Crolla Salisbury District Hospital
Warren G. Sanger
Warren G. Sanger University of Nebraska Medical Center
Lisa G. Shaffer
Lisa G. Shaffer Paw Print Genetics
Stephen T. Warren
Stephen T. Warren Emory University

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