Arthur R. Brothman

10.9k citations

122 papers · 5.1k indexed · 1 hit paper · h-index 39

Molecular Biology top 5%
Genetics top 0.5%
Pulmonary and Respiratory Medicine top 1%
Cancer Research top 2%
Pediatrics, Perinatology and Child Health top 1%

Co-authors: A. John Iafrate Charles Lee John C. Carey Teresa M. Maxwell Xiao Lin Zhu Briana J. Williams L. Ralph Rohr Xue‐Xue Zhu
Topics: Genomic variations and chromosomal abnormalities (46 papers)Prostate Cancer Treatment and Research (24 papers)Prenatal Screening and Diagnostics (23 papers)
Cited by: Genetics Cancer Research Pulmonary and Respiratory Medicine
Journals: Nature Medicine Nature Genetics PLoS ONE
Partner nations: United States United Kingdom Germany

In The Last Decade

Arthur R. Brothman

120 papers receiving 4.9k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

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

2011 548 citations Jack Cuzick, Gregory P. Swanson et al. The Lancet Oncology profile →

Peers

Countries citing papers authored by Arthur R. Brothman

Since Specialization

Citations

This map shows the geographic impact of Arthur R. Brothman's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Arthur R. Brothman with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Arthur R. Brothman more than expected).

Fields of papers citing papers by Arthur R. Brothman

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Arthur R. Brothman. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Arthur R. Brothman. The network helps show where Arthur R. Brothman may publish in the future.

Co-authorship network of co-authors of Arthur R. Brothman

This figure shows the co-authorship network connecting the top 25 collaborators of Arthur R. Brothman. A scholar is included among the top collaborators of Arthur R. Brothman based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Arthur R. Brothman. Arthur R. Brothman is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	Genome-Wide Analysis Reveals the Unique Stem Cell Identity of Human Amniocytes 2013 ·PLoS ONE ·Colin T. Maguire,Bradley L. Demarest,Jonathon T. Hill,James D. Palmer,Arthur R. Brothman,H. Joseph Yost,Maureen L. Condic	46
2	Prognostic value of an RNA expression signature derived from cell cycle proliferation genes in patients with prostate cancer: a retrospective studybreakdown → 2011 ·The Lancet Oncology ·Jack Cuzick,Gregory P. Swanson,Gabrielle Fisher,Arthur R. Brothman,Daniel M. Berney,Julia Reid,David Mesher,V. O. Speights,Elzbieta Stankiewicz,Christopher S. Foster,Henrik Møller,Peter T. Scardino,(unknown),Jimmy Park,Adib Younus,Darl D. Flake,Susanne Wagner,Alexander Gutin,Jerry S. Lanchbury,Steven Stone	548
3	Nomenclature Evolution: Changes in the ISCN from the 2005 to the 2009 Edition 2009 ·Cytogenetic and Genome Research ·Arthur R. Brothman,Diane L. Persons,Lisa G. Shaffer	73
4	Homozygous deletions of a copy number change detected by array CGH: A new cause for mental retardation? 2008 ·American Journal of Medical Genetics Part A ·Cynthia J. Curry,Rong Mao,Emily Aston,(unknown),(unknown),Melinda Procter,(unknown),Heidi Whitby,Sarah T. South,Arthur R. Brothman	10
5	Benign copy number changes in clinical cytogenetic diagnostics by array CGH 2008 ·Cytogenetic and Genome Research ·Heidi Whitby,Anya Tsalenko,(unknown),Peter Tsang,Steven Mitchell,Pınar Bayrak‐Toydemir,Corey R. Hopkins,Greg B. Peters,Dione K. Bailey,Laurakay Bruhn,Arthur R. Brothman	8
6	How physicians use array comparative genomic hybridization results to guide patient management in children with developmental delay 2008 ·Genetics in Medicine ·Jennifer Saam,(unknown),Emily Aston,Arthur R. Brothman	31
7	Section E6 of the ACMG technical standards and guidelines: Chromosome studies for acquired abnormalitie: This updated Section E6 has been incorporated into Section E: Clinical Cytogenetics of the 2005 ACMG Standards and Guidelines for Clinical Genetics Laboratories and supersedes the previous section E6 2005 ·Genetics in Medicine ·(unknown),Arthur R. Brothman,Peter B. Jacky,Kathleen W. Rao,Daynna J. Wolff	2
8	Multiple abnormalities detected by dye reversal genomic microarrays in prostate cancer: a much greater sensitivity than conventional cytogenetics 2004 ·Cancer Genetics and Cytogenetics ·Joseph A. Pettus,(unknown),Teresa M. Maxwell,Brett Milash,Robert A. Stephenson,L. Ralph Rohr,Charles Hoff,Arthur R. Brothman	12
9	Clinical laboratory assays for HER-2/neu amplification and overexpression: Quality assurance, standardization, and proficiency testing 2002 ·Archives of Pathology & Laboratory Medicine ·Raymond B. Nagle,(unknown),Patrick C. Roche,Eric D. Hsi,Michael D. Linden,Adrian Ormsby,Norman M. Pettigrew,Robert R. Rickert,Jonathan Said,Ilene B. Bayer‐Garner,Linda D. Cooley,Arthur R. Brothman,Diane L. Persons,Gail H. Vance,James T. Mascarello,Kathleen W. Rao,Marille E. Herrmann,Gordon W. Dewald,Jonathan P. Park	65
10	Nonrandom Rearrangements of 6p in Malignant Hematological Disorders 2000 ·Cancer Genetics and Cytogenetics ·Zhong Chen,(unknown),Lisa J. Brothman,(unknown),(unknown),Arthur R. Brothman	15
11	Microdissection, DOP-PCR, and comparative genomic hybridization of paraffin-embedded familial prostate cancers 2000 ·Cancer Genetics and Cytogenetics ·Paul C.M.S. Verhagen,Xiao Lin Zhu,L. Ralph Rohr,Lisa Cannon‐Albright,Sean V. Tavtigian,Mark H. Skolnick,Arthur R. Brothman	23
12	Chromosome 7 Abnormalities in Prostate Cancer Detected by Dual-Color Fluorescence In Situ Hybridization 1998 ·Cancer Genetics and Cytogenetics ·Cui Jiang,(unknown),L. Ralph Rohr,Xiao Lin Zhu,Teresa M. Maxwell,(unknown),Arthur R. Brothman	28
13	Assignment of Human Protein Phosphatase 2A Regulatory Subunit Genes B56α, B56β, B56γ, B56δ, and B56ϵ (PPP2R5A–PPP2R5E), Highly Expressed in Muscle and Brain, to Chromosome Regions 1q41, 11q12, 3p21, 6p21.1, and 7p11.2 → p12 1996 ·Genomics ·Brent McCright,Arthur R. Brothman,David M. Virshup	47
14	Mutation of the MXI1 gene in prostate cancer 1995 ·Nature Genetics ·(unknown),Xiaoying Yin,Arthur R. Brothman,Briana J. Williams,Niels B. Atkin,Edward V. Prochownik	160
15	Identification of Neurofibromatosis 1 (NF1) Homologous Loci by Direct Sequencing, Fluorescence in Situ Hybridization, and PCR Amplification of Somatic Cell Hybrids 1995 ·Genomics ·Smita M. Purandare,(unknown),Ying Li,Xiao Lin Zhu,Shunichi Sawada,(unknown),Arthur R. Brothman,R. White,Richard Cawthon,David Viskochil	33
16	Aneusomy of chromosomes 7 and 17 detected by fish in prostate cancer and the effects of selection in vitro 1994 ·Genes Chromosomes and Cancer ·(unknown),Xiao Lin Zhu,L. Ralph Rohr,Robert A. Stephenson,Arthur R. Brothman	42
17	Assignment of Human Xanthine Dehydrogenase Gene to Chromosome 2p22 1994 ·Genomics ·Ping Xu,Xiao Lin Zhu,Thomas P. Huecksteadt,Arthur R. Brothman,John R. Hoidal	24
18	Confirmation of true mosaic trisomy 20 in a phenotypically normal liveborn male 1992 ·Clinical Genetics ·Arthur R. Brothman,(unknown),Patrick D. Storto,(unknown),(unknown)	8
19	Cytogenetic evaluation of 20 cultured primary prostatic tumors 1991 ·Cancer Genetics and Cytogenetics ·Arthur R. Brothman,Donna M. Peehl,(unknown),Gordon R. MacDonald,John E. McNeal,(unknown),(unknown)	46
20	Phenotypic and cytogenetic characterization of a cell line derived from primary prostatic carcinoma 1989 ·International Journal of Cancer ·Arthur R. Brothman,(unknown),Kenneth D. Somers,(unknown),Donald J. Merchant	54

About Arthur R. Brothman

Arthur R. Brothman is a scholar working on Genetics, Cancer Research and Pediatrics, Perinatology and Child Health, having authored 122 papers that have together received 5.1k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (46 papers), Prostate Cancer Treatment and Research (24 papers) and Prenatal Screening and Diagnostics (23 papers). The work is most often cited by research in Genetics (1.9k citations), Cancer Research (990 citations) and Pulmonary and Respiratory Medicine (1.5k citations). Arthur R. Brothman has collaborated with scholars based in United States, United Kingdom and Germany. Frequent co-authors include A. John Iafrate, Charles Lee, John C. Carey, Teresa M. Maxwell, Xiao Lin Zhu, Briana J. Williams, L. Ralph Rohr, Xue‐Xue Zhu, Lisa G. Shaffer and Sarah T. South. Their work appears in journals such as Nature Medicine, Nature Genetics and PLoS ONE.

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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