Kenneth Offit

2.9k citations
14 papers · 1.2k indexed · h-index 11
Topics
BRCA gene mutations in cancer (8 papers)Cancer Genomics and Diagnostics (5 papers)Genomic variations and chromosomal abnormalities (4 papers)
Partner nations
United StatesCanadaSpain

In The Last Decade

Kenneth Offit

14 papers receiving 1.1k citations

Peers

Kenneth Offit
Comparison fields: 5 of 65
  • Pathology and Forensic Medicine 663
  • Oncology 453
  • Genetics 444
  • Genetics 334
  • Cancer Research 241
Replace Grzegorz Rymkiewicz with:
Grzegorz Rymkiewicz Poland
Vundavalli V. Murty United States
PM Kluin Netherlands
Brandie Heald United States
Valérie Bonadona France
Fong Chun Chan Canada
L Sánchez‐Verde Spain
Annette Bröcker‐Vriends Netherlands
Fabrizio Tabbò Italy
Michael C. Luce United States
Kenneth Offit relative to Grzegorz Rymkiewicz Poland Grzegorz Rymkiewicz's profile →
Citations per field
00.5×3.0×
Grzegorz Rymkiewicz · 1×
Citations per year

Countries citing papers authored by Kenneth Offit

Since Specialization
Citations

This map shows the geographic impact of Kenneth Offit'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 Kenneth Offit with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Kenneth Offit more than expected).

Fields of papers citing papers by Kenneth Offit

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Kenneth Offit. 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 Kenneth Offit. The network helps show where Kenneth Offit may publish in the future.

Co-authorship network of co-authors of Kenneth Offit

This figure shows the co-authorship network connecting the top 25 collaborators of Kenneth Offit. A scholar is included among the top collaborators of Kenneth Offit 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 Kenneth Offit. Kenneth Offit is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

14 of 14 papers shown
#WorkIndexed citations
1 1
2 10
3 9
4 22
5 39
6 22
7 90
8 64
9
BRCA-associated breast cancer: absence of a characteristic immunophenotype.
66
10 44
11 129
12 304
13 165
14 187

About Kenneth Offit

Kenneth Offit is a scholar working on Genetics, Cancer Research and Pathology and Forensic Medicine, having authored 14 papers that have together received 1.2k indexed citations. Recurring topics across this work include BRCA gene mutations in cancer (8 papers), Cancer Genomics and Diagnostics (5 papers) and Genomic variations and chromosomal abnormalities (4 papers). The work is most often cited by research in Pathology and Forensic Medicine (663 citations), Genetics (334 citations) and Oncology (453 citations). Kenneth Offit has collaborated with scholars based in United States, Canada and Spain. Frequent co-authors include RS Chaganti, Marc Ladanyi, Daniel A. Filippa, Suresh C. Jhanwar, G Wong, DA Filippa, Yu Tao, Karen L. Brown, Heiðdís Valdimarsdóttir and Paul B. Jacobsen. Their work appears in journals such as New England Journal of Medicine, Blood and Cancer.

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.

Explore authors with similar magnitude of impact

Rankless by CCL
2026