Susan E. Andrew

4.8k citations

59 papers · 3.9k · 1 hit paper · h-index 27

Impact in

Cellular and Molecular Neuroscience top 0.5%
- Genetic Neurodegenerative Diseases
Neurology top 1%
- Neurological disorders and treatments

Papers in

Pathology and Forensic Medicine 27
- Genetic factors in colorectal cancer 27
Cellular and Molecular Neuroscience 25
- Genetic Neurodegenerative Diseases 25

Co-authors: Michael R. Hayden (23 shared papers)Håkan Telenius (4 shared papers)Ferdinando Squitieri (7 shared papers)Y. Paul Goldberg (14 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: Canada United States Sweden

In The Last Decade

Susan E. Andrew

59 papers receiving 3.8k citations

Susan E. Andrew's Hit Papers

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The relationship between trinucleotide (CAG) repeat length and clinical features of Huntington's disease 1993 · 897 citations

What are hit papers?

Paper score: A paper's citations measured against the top-1% bar of its own field and year: the square root of citations ÷ bar, so 1 means right at the bar and 2 means four times its citations. The bar blends the citation counts that enter the top 1% of the paper's subfields in its year (weighted 89.5%), of those subfields over all years (0.5%) and of its year across all fields (10%); a subfield and year with fewer than 400 papers takes its year's bar. Papers from 2026 are not scored yet: in an unfinished year, when a paper appeared matters more than how it is cited.

Hit paper: A paper cited at least 1.5× the top-1% bar of its field and year: a paper score of at least √1.5.

1993 Nature Genetics

Peers

Countries citing papers authored by Susan E. Andrew

Since Specialization

Citations

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

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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.

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

All Works

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20 of 20 papers shown

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 Nature Genetics ·Susan E. Andrew, Y. Paul Goldberg, Berry Kremer, Håkan Telenius, Jane Theilmann, Shelin Adam, Elizabeth M. Starr, Ferdinando Squitieri Hit paper breakdown →	1993	897
2	A Worldwide Study of the Huntington's Disease Mutation: The Sensitivity and Specificity of Measuring CAG Repeats New England Journal of Medicine ·Berry P. H. Kremer, Paul Goldberg, Susan E. Andrew, Jane Theilmann, Håkan Telenius, Jutta Zeisler, Ferdinando Squitieri, Biaoyang Lin	1994	483
3	Somatic and gonadal mosaicism of the Huntington disease gene CAG repeat in brain and sperm Nature Genetics ·Håkan Telenius, Berry P. H. Kremer, Y. Paul Goldberg, Jane Theilmann, Susan E. Andrew, Jutta Zeisler, Shelin Adam, Cheryl R. Greenberg	1994	356
4	Molecular analysis of new mutations for Huntington's disease: intermediate alleles and sex of origin effects Nature Genetics ·Y. Paul Goldberg, Berry P. H. Kremer, Susan E. Andrew, Jane Theilmann, Rona K. Graham, Ferdinando Squitieri, Håkan Telenius, Shelin Adam	1993	207
5	Molecular analysis of juvenile Huntington disease: the major influence on (CAG) n repeat length is the sex of the affected parent Human Molecular Genetics ·H. Telenius, Hannie Kremer, J. Thellmann, Susan E. Andrew, Elisabeth W. Almqvist, Maria Anvret, Cheryl R. Greenberg, Jacquie Greenberg	1993	170
6	DNA haplotype analysis of Huntington disease reveals clues to the origins and mechanisms of CAG expansion and reasons for geographic variations of prevalence Human Molecular Genetics ·Ferdinando Squitieri, Susan E. Andrew, Y. Paul Goldberg, B. P. H. Kremer, Niamh Spence, J. Zelsler, Kerrie Nichol, Jane Theilmann	1994	164
7	A CCG repeat polymorphism adjacent to the CAG repeat in the Huntington disease gene: implications for diagnostic accuracy and predictive testing Human Molecular Genetics ·Susan E. Andrew, Y. Paul Goldberg, Jane Theilmann, Jutta Zeisler, Michael R. Hayden	1994	135
8	A homozygous germ-line mutation in the human MSH2 gene predisposes to hematological malignancy and multiple café-au-lait spots. PubMed ·Darcy Whiteside, Ross McLeod, Gail E. Graham, Jamie L. Steckley, Karen Booth, Martin J. Somerville, Susan E. Andrew	2002	124
9	Rethinking Genotype and Phenotype Correlations in Polyglutamine Expansion Disorders Human Molecular Genetics ·Susan E. Andrew, Y. Paul Goldberg, Michael R. Hayden	1997	114
10	Huntington disease without CAG expansion: phenocopies or errors in assignment? PubMed ·Susan E. Andrew, Y. Paul Goldberg, B. P. H. Kremer, Ferdinando Squitieri, Jane Theilmann, Jutta Zeisler, H. Telenius, Shelin Adam	1994	94
11	RNA Silencing of Mcl-1 Enhances ABT-737-Mediated Apoptosis in Melanoma: Role for a Caspase-8-Dependent Pathway PLoS ONE ·Angela M. Keuling, Kathleen E. A. Felton, Arabesque Parker, Majid Akbari, Susan E. Andrew, Victor A. Tron	2009	72
12	Tissues of MSH2-deficient mice demonstrate hypermutability on exposure to a DNA methylating agent Proceedings of the National Academy of Sciences ·Susan E. Andrew, Margaret L. McKinnon, Benjamin S. Cheng, Agnes Francis, Janice E. Penney, Armin H. Reitmair, Tak W. Mak, Frank Robert Jirik	1998	70
13	A PCR method for accurate assessment of trinucleotide repeat expansion in Huntington disease Human Molecular Genetics ·Y. Paul Goldberg, Susan E. Andrew, Lorne A. Clarke, Michael R. Hayden	1993	66
14	Ancestral differences in the distribution of the Δ2642 glutamic acid polymorphism is associated with varying CAG repeat lengths on normal chromosomes: insights into the genetic evolution of Huntington disease Human Molecular Genetics ·Elisabeth W. Almqvist, Niamh Spence, Kerrie Nichol, Susan E. Andrew, J. Vesa, Leena Peltonen, Maria Anvret, Jun Goto	1995	66
15	Base transitions dominate the mutational spectrum of a transgenic reporter gene in MSH2 deficient mice Oncogene ·Susan E. Andrew, Armin H. Reitmair, Joanne A. Fox, Letticia Hsiao, Agnes Francis, Margaret L. McKinnon, Tak W. Mak, Frank Robert Jirik	1997	61
16	Molecular analysis of late onset Huntington's disease. Journal of Medical Genetics ·B. P. H. Kremer, Ferdinando Squitieri, H. Telenius, Susan E. Andrew, Jane Theilmann, Niamh Spence, Y. Paul Goldberg, Michael R. Hayden	1993	53
17	Genomic organization and complete sequence of the human gene encoding the β-subunit of the cGMP phosphodiesterase and its localisation to 4p16.3 Nucleic Acids Research ·Bernhard H. F. Weber, Olaf Horst Riess, Gordon B. Hutchinson, Colin C. Collins, Biaoyang Lin, David Kowbel, Susan E. Andrew, Keith T. Schappert	1991	52
18	DNA Mismatch Repair Proteins: Potential Guardians Against Genomic Instability and Tumorigenesis Induced by Ultraviolet Photoproducts Journal of Investigative Dermatology ·Leah C. Young, John B. Hays, Victor A. Tron, Susan E. Andrew	2003	44
19	Identification of an Alu retrotransposition event in close proximity to a strong candidate gene for Huntington's disease Nature ·Y. Paul Goldberg, Johanna M. Rommens, Susan E. Andrew, Gordon B. Hutchinson, Biaoyang Lin, Jane Theilmann, Rona Graham, Martha L. Glaves	1993	43
20	Mutagenesis in PMS2- and MSH2-deficient mice indicates differential protection from transversions and frameshifts Carcinogenesis ·Susan E. Andrew, Xiaoxin Xu, Agnes Baross-Francis, Latha Narayanan, Kate Milhausen, R. Michael Liskay, Frank Robert Jirik, Peter M. Glazer	2000	43

About Susan E. Andrew

Susan E. Andrew is a scholar working on Pathology and Forensic Medicine, Cellular and Molecular Neuroscience, Cancer Research, Molecular Biology and Neurology, having authored 59 papers that have together received 3.9k indexed citations. Recurring topics across this work include Genetic factors in colorectal cancer (27 papers), Genetic Neurodegenerative Diseases (25 papers), DNA Repair Mechanisms (17 papers), Mitochondrial Function and Pathology (12 papers), Cancer Genomics and Diagnostics (11 papers), Neurological disorders and treatments (9 papers), RNA Research and Splicing (5 papers) and Genomics and Rare Diseases (4 papers). The work is most often cited by research in Cellular and Molecular Neuroscience (2.6k citations), Neurology (1.2k citations), Molecular Biology (2.8k citations), Pathology and Forensic Medicine (442 citations) and Cancer Research (299 citations). Susan E. Andrew has collaborated with scholars based in Canada, United States and Sweden. Frequent co-authors include Michael R. Hayden, Håkan Telenius, Ferdinando Squitieri, Y. Paul Goldberg, Jane Theilmann, Shelin Adam, Biaoyang Lin, Jutta Zeisler, Elizabeth M. 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.

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Susan E. Andrew

Susan E. Andrew's Hit Papers

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Fields of papers citing papers by Susan E. Andrew

All Works

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