Sofia Khan

12.0k citations
97 papers · 8.9k · 8 hit papers · h-index 36

Impact in

    • Cancer Genomics and Diagnostics
    • Cancer-related molecular mechanisms research
  • Genetics top 0.5%
    • BRCA gene mutations in cancer
    • Genetic Associations and Epidemiology

Papers in

    • BRCA gene mutations in cancer 30
    • Genetic Associations and Epidemiology 12
    • Genomic variations and chromosomal abnormalities 10
    • Cancer Genomics and Diagnostics 10

Sofia Khan

95 papers receiving 8.7k citations

Sofia Khan's Hit Papers

Genome-wide association study identifies 32 novel breast cancer susceptibility loci from overall and subtype-specific analyses 2020 · 303 citations
3030+5+11Years since publication2505007501000

Peers

Sofia Khan
Comparison fields: 5 of 204
  • Cancer Research 1.8k
  • Genetics 3.0k
  • Oncology 1.2k
  • Molecular Biology 3.3k
  • Pathology and Forensic Medicine 748
Replace Marion Dawn Teare with:
Marion Dawn Teare United Kingdom
Jaana M. Hartikainen Germany
Keith Humphreys Sweden
Tuomas Heikkinen Finland
Henrik Flyger United Kingdom
Yon‐Dschun Ko Germany
Martine Dumont Canada
Nicola Miller United Kingdom
Nichola Johnson United Kingdom
José Ignacio Arias Pérez United Kingdom
Sofia Khan relative to Marion Dawn Teare United Kingdom Marion Dawn Teare's profile →
Citations per field
00.5×1.5×1.9×
Marion Dawn Teare · 1×
Citations per year

Countries citing papers authored by Sofia Khan

Since Specialization
Citations

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

Fields of papers citing papers by Sofia Khan

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside Sofia Khan, 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 Sofia Khan Line = papers co-authored together Sofia Khan links everyone, so they are left out of the graph.

All Works

20 of 20 papers shown

Showing the 20 most-cited of 97 papers — load more, or switch the sort, to bring in the rest.

#Work
1
Association analysis identifies 65 new breast cancer risk loci
Hit paper breakdown →
20171013
2
Breast-Cancer Risk in Families with Mutations in PALB2
Hit paper breakdown →
2014681
3
RAD51B in Familial Breast Cancer
Hit paper breakdown →
2016642
4
MicroRNA Related Polymorphisms and Breast Cancer Risk
Hit paper breakdown →
2014610
5
Copy number analysis indicates monoclonal origin of lethal metastatic prostate cancer
Hit paper breakdown →
2009516
6
Genome-wide association analysis of more than 120,000 individuals identifies 15 new susceptibility loci for breast cancer
Hit paper breakdown →
2015486
7
Association of BRCA1 and BRCA2 Mutations With Survival, Chemotherapy Sensitivity, and Gene Mutator Phenotype in Patients With Ovarian Cancer
Hit paper breakdown →
2011478
8 2007344
9
Genome-wide association study identifies 32 novel breast cancer susceptibility loci from overall and subtype-specific analyses
Hit paper breakdown →
2020303
10 2017298
11 2010257
12 2011247
13 2015210
14 2013176
15 2014157
16 2017139
17 2018125
18 2016124
19 2007115
20 2009108

About Sofia Khan

Sofia Khan is a scholar working on Genetics, Cancer Research, Pathology and Forensic Medicine, Molecular Biology and Oncology, having authored 97 papers that have together received 8.9k indexed citations. Recurring topics across this work include BRCA gene mutations in cancer (30 papers), Genetic factors in colorectal cancer (15 papers), Genetic Associations and Epidemiology (12 papers), Cancer Genomics and Diagnostics (10 papers), Genomic variations and chromosomal abnormalities (10 papers), Genomics and Chromatin Dynamics (10 papers), DNA Repair Mechanisms (9 papers) and RNA modifications and cancer (8 papers). The work is most often cited by research in Cancer Research (1.8k citations), Genetics (3.0k citations), Oncology (1.2k citations), Molecular Biology (3.3k citations) and Pathology and Forensic Medicine (748 citations). Sofia Khan has collaborated with scholars based in Finland, United Kingdom and United States. Frequent co-authors include Mauno Vihinen, Hugh Stephen Markus, Da Yang, Anil K. Sood, Kenneth R. Hess, Ilya Shmulevich, Yan Sun, Wei Zhang, Laura L. Elo and Giosué Gulli. Their work appears in journals such as PLoS ONE, Breast Cancer Research and Treatment, Breast Cancer Research, Nature Genetics and Oncotarget.

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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