Susan E. Andrew
Impact in
- Cellular and Molecular Neuroscience top 0.5%
- Genetic Neurodegenerative Diseases
- Neurology top 1%
- Neurological disorders and treatments
Papers in
-
- DNA Repair Mechanisms 18
- Mitochondrial Function and Pathology 13
- RNA Research and Splicing 6
- CRISPR and Genetic Engineering 4
-
- Genetic factors in colorectal cancer 27
- Co-authors
- Michael R. Hayden (23 shared papers)Håkan Telenius (4 shared papers)Y. Paul Goldberg (14 shared papers)Ferdinando Squitieri (7 shared papers)Jane Theilmann (12 shared papers)Shelin Adam (4 shared papers)Biaoyang Lin (5 shared papers)Jutta Zeisler (5 shared papers)
- Journals
- Human Molecular Genetics (8 papers)Clinical Genetics (6 papers)Carcinogenesis (5 papers)Nature Genetics (4 papers)Mutation research. Fundamental and molecular mechanisms of mutagenesis (3 papers)
- Partner nations
- CanadaUnited StatesSweden
In The Last Decade
Susan E. Andrew
58 papers receiving 3.6k citations
Susan E. Andrew's Hit Papers
Peers
Comparison fields: 5 of 109
- Cellular and Molecular Neuroscience 2.4k
- Neurology 1.2k
- Molecular Biology 2.9k
- Pathology and Forensic Medicine 445
- Cancer Research 313
Countries citing papers authored by Susan E. Andrew
This map shows the geographic impact of Susan E. Andrew'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 Susan E. Andrew with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Susan E. Andrew more than expected).
Fields of papers citing papers by Susan E. Andrew
This network shows the impact of papers produced by Susan E. Andrew. 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 Susan E. Andrew. The network helps show where Susan E. Andrew may publish in the future.
Co-authors
The 25 scholars most cited alongside Susan E. Andrew, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
Showing the 20 most-cited of 59 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | The relationship between trinucleotide (CAG) repeat length and clinical features of Huntington's disease Hit paper breakdown → | 1993 | 821 |
| 2 | 1994 | 428 | |
| 3 | 1994 | 333 | |
| 4 | 1993 | 184 | |
| 5 | 1993 | 163 | |
| 6 | 1994 | 148 | |
| 7 | 1994 | 127 | |
| 8 | A homozygous germ-line mutation in the human MSH2 gene predisposes to hematological malignancy and multiple café-au-lait spots. | 2002 | 113 |
| 9 | 1997 | 108 | |
| 10 | Huntington disease without CAG expansion: phenocopies or errors in assignment? | 1994 | 82 |
| 11 | 2009 | 69 | |
| 12 | 1998 | 69 | |
| 13 | 1993 | 63 | |
| 14 | 1995 | 59 | |
| 15 | 1997 | 57 | |
| 16 | 1993 | 51 | |
| 17 | 1991 | 46 | |
| 18 | 2000 | 44 | |
| 19 | 1993 | 43 | |
| 20 | 1993 | 41 |
About Susan E. Andrew
Susan E. Andrew is a scholar working on Molecular Biology, Pathology and Forensic Medicine, Cellular and Molecular Neuroscience, Cancer Research and Neurology, having authored 59 papers that have together received 3.6k indexed citations. Recurring topics across this work include Genetic factors in colorectal cancer (27 papers), Genetic Neurodegenerative Diseases (25 papers), DNA Repair Mechanisms (18 papers), Mitochondrial Function and Pathology (13 papers), Cancer Genomics and Diagnostics (12 papers), Neurological disorders and treatments (11 papers), RNA Research and Splicing (6 papers) and CRISPR and Genetic Engineering (4 papers). The work is most often cited by research in Cellular and Molecular Neuroscience (2.4k citations), Neurology (1.2k citations), Molecular Biology (2.9k citations), Pathology and Forensic Medicine (445 citations) and Cancer Research (313 citations). Susan E. Andrew has collaborated with scholars based in Canada, United States and Sweden. Frequent co-authors include Michael R. Hayden, Håkan Telenius, Y. Paul Goldberg, Ferdinando Squitieri, Jane Theilmann, Shelin Adam, Biaoyang Lin, Jutta Zeisler, Elizabeth Starr and Rona K. Graham. Their work appears in journals such as Human Molecular Genetics, Clinical Genetics, Carcinogenesis, Nature Genetics and Mutation research. Fundamental and molecular mechanisms of mutagenesis.
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.