Scott Bader

1.9k citations
27 papers · 1.5k · h-index 18

Impact in

Papers in

Scott Bader

27 papers receiving 1.4k citations

Peers

Scott Bader
Comparison fields: 5 of 69
  • Cancer Research 263
  • Oncology 379
  • Molecular Biology 1.0k
  • Pathology and Forensic Medicine 216
  • Genetics 291
Replace Maria L. Henriksson with:
Maria L. Henriksson Sweden
Abdellatif Errami Netherlands
Donatella Malanga Italy
Verónica Rodilla Spain
Shin‐ichiro Numata Japan
Yoji Kukita Japan
Joel E. Straughen United States
David Siwarski United States
Kay Minn United States
Sétha Douc‐Rasy France
Scott Bader relative to Maria L. Henriksson Sweden Maria L. Henriksson's profile →
Citations per field
00.5×2.9×
Maria L. Henriksson · 1×
Citations per year

Countries citing papers authored by Scott Bader

Since Specialization
Citations

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

Fields of papers citing papers by Scott Bader

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside Scott Bader, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Scott Bader Line = papers co-authored together Scott Bader links everyone, so they are left out of the graph.

All Works

20 of 20 papers shown

Showing the 20 most-cited of 27 papers — load more, or switch the sort, to bring in the rest.

#Work
1
FHIT and FRA3B 3p14.2 allele loss are common in lung cancer and preneoplastic bronchial lesions and are associated with cancer-related FHIT cDNA splicing aberrations.
1997170
2
Construction of a 600-kilobase cosmid clone contig and generation of a transcriptional map surrounding the lung cancer tumor suppressor gene (TSG) locus on human chromosome 3p21.3: progress toward the isolation of a lung cancer TSG.
1996133
3 1998125
4
Homozygous loss of the interferon genes defines the critical region on 9p that is deleted in lung cancers.
1993123
5 2009113
6 1999104
7 200491
8
Dissociation of suppression of tumorigenicity and differentiation in vitro effected by transfer of single human chromosomes into human neuroblastoma cells.
199191
9 200183
10
Molecular analysis of the von Hippel-Lindau disease tumor suppressor gene in human lung cancer cell lines.
199478
11
K-ras 4A and 4B are co-expressed widely in human tissues, and their ratio is altered in sporadic colorectal cancer.
200663
12 199545
13 199440
14 200231
15 200729
16 200328
17 199726
18 199724
19 200516
20 200412

About Scott Bader

Scott Bader is a scholar working on Molecular Biology, Pathology and Forensic Medicine, Oncology, Genetics and Cancer Research, having authored 27 papers that have together received 1.5k indexed citations. Recurring topics across this work include RNA modifications and cancer (7 papers), Genetic factors in colorectal cancer (6 papers), Epigenetics and DNA Methylation (4 papers), Genomics and Chromatin Dynamics (4 papers), DNA Repair Mechanisms (3 papers), Cancer-related Molecular Pathways (3 papers), Neuroblastoma Research and Treatments (3 papers) and Genetics and Neurodevelopmental Disorders (2 papers). The work is most often cited by research in Cancer Research (263 citations), Oncology (379 citations), Molecular Biology (1.0k citations), Pathology and Forensic Medicine (216 citations) and Genetics (291 citations). Scott Bader has collaborated with scholars based in United States, United Kingdom and Netherlands. Frequent co-authors include John D. Minna, David J. Harrison, Yoshitaka Sekido, Adi F. Gazdar, Farida Latif, Marion Walker, Ignacio I. Wistuba, Mohsen Ahmadian, Michael I. Lerman and Michael S. Donnenberg. Their work appears in journals such as Oncogene, British Journal of Cancer, The Journal of Pathology, Human Genetics and Genes Chromosomes 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.

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