Susan E. Andrew

4.7k total citations · 1 hit paper
59 papers, 3.6k citations indexed

About

Susan E. Andrew is a scholar working on Molecular Biology, Pathology and Forensic Medicine and Cellular and Molecular Neuroscience. According to data from OpenAlex, Susan E. Andrew has authored 59 papers receiving a total of 3.6k indexed citations (citations by other indexed papers that have themselves been cited), including 40 papers in Molecular Biology, 27 papers in Pathology and Forensic Medicine and 25 papers in Cellular and Molecular Neuroscience. Recurrent topics in Susan E. Andrew's work include Genetic factors in colorectal cancer (27 papers), Genetic Neurodegenerative Diseases (25 papers) and DNA Repair Mechanisms (18 papers). Susan E. Andrew is often cited by papers focused on Genetic factors in colorectal cancer (27 papers), Genetic Neurodegenerative Diseases (25 papers) and DNA Repair Mechanisms (18 papers). Susan E. Andrew collaborates with scholars based in Canada, United States and Sweden. Susan E. Andrew's 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 and has published in prestigious journals such as Nature, New England Journal of Medicine and Proceedings of the National Academy of Sciences.

In The Last Decade

Susan E. Andrew

58 papers receiving 3.6k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

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

1993 821 citations Susan E. Andrew, Berry Kremer et al. Nature Genetics profile →

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
Susan E. Andrew Canada	27	2.9k	2.4k	1.2k	445	408	59	3.6k
N J Scavarda United States	15	1.4k 0.5×	594 0.2×	1.2k 1.0×	89 0.2×	340 0.8×	17	2.3k
Victoria Campuzano Spain	17	2.4k 0.8×	1.7k 0.7×	497 0.4×	53 0.1×	273 0.7×	35	3.1k
Cédric Raoul France	28	1.3k 0.5×	688 0.3×	1.2k 1.0×	151 0.3×	191 0.5×	70	2.7k
Mehrdad Khajavi United States	21	1.5k 0.5×	984 0.4×	517 0.4×	45 0.1×	596 1.5×	31	2.6k
M. Rosario Hernandez United States	42	2.5k 0.8×	532 0.2×	424 0.3×	443 1.0×	323 0.8×	87	5.0k
Anat Bar‐Shira Israel	27	1.6k 0.5×	354 0.1×	1.3k 1.0×	159 0.4×	353 0.9×	86	3.4k
Hiroko Baba Japan	26	1.1k 0.4×	1.3k 0.5×	993 0.8×	147 0.3×	90 0.2×	72	2.6k
Shuying Sun United States	22	2.3k 0.8×	321 0.1×	758 0.6×	84 0.2×	211 0.5×	47	3.0k
Y. Paul Goldberg Canada	31	3.0k 1.0×	2.4k 1.0×	1.0k 0.8×	33 0.1×	353 0.9×	40	3.8k
Lisa Chakrabarti United Kingdom	26	1.2k 0.4×	306 0.1×	628 0.5×	170 0.4×	538 1.3×	55	2.4k

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-authorship network of co-authors of Susan E. Andrew

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

All Works

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20 of 20 papers shown

Young, Leah C., Peng Wang, Fang Wu, et al.. (2011). Fusion Tyrosine Kinase NPM-ALK Deregulates MSH2 and Suppresses DNA Mismatch Repair Function. American Journal Of Pathology. 179(1). 411–421. 11 indexed citations

Parker, Arabesque, et al.. (2009). RNA Silencing of Mcl-1 Enhances ABT-737-Mediated Apoptosis in Melanoma: Role for a Caspase-8-Dependent Pathway. PLoS ONE. 4(8). e6651–e6651. 69 indexed citations

Young, Leah C., et al.. (2007). The associated contributions of p53 and the DNA mismatch repair protein Msh6 to spontaneous tumorigenesis. Carcinogenesis. 28(10). 2131–2138. 19 indexed citations

Honoré, Louis H., Jacky Hanson, & Susan E. Andrew. (2006). Microsatellite instability in endometrioid endometrial carcinoma: correlation with clinically relevant pathologic variables. International Journal of Gynecological Cancer. 16(3). 1386–1392. 34 indexed citations

Campbell, Marcia R., et al.. (2005). Msh2 deficiency leads to chromosomal abnormalities, centrosome amplification, and telomere capping defect. Oncogene. 25(17). 2531–2536. 40 indexed citations

Constantinescu, Gabriela, et al.. (2005). Variable MLH1 promoter methylation patterns in endometrial carcinomas of endometrioid subtype lacking DNA mismatch repair. International Journal of Gynecological Cancer. 15(6). 1089–1096. 7 indexed citations

Andrew, Susan E., et al.. (2002). An Intronic Polymorphism of the hMLH1 Gene Contributes Toward Incomplete Genetic Testing for HNPCC. Genetic Testing. 6(4). 319–322. 3 indexed citations

Benavides, Fernando, Mónica Zamisch, Marcia R. Campbell, et al.. (2002). Application of inter–simple sequence repeat PCR to mouse models: Assessment of genetic alterations in carcinogenesis. Genes Chromosomes and Cancer. 35(4). 299–310. 6 indexed citations

Andrew, Susan E. & Anthea Peters. (2001). DNA Instability and Human Disease. PubMed. 1(1). 21–28. 14 indexed citations

10.

Andrew, Susan E.. (1999). Noncoding germline mutations in p16/CDKN2A in melanoma‐prone families. Clinical Genetics. 56(3). 188–190.

11.

Andrew, Susan E., et al.. (1996). A novel lacI transgenic mutation-detection system and its application to establish baseline mutation frequencies in the scid mouse. Mutation research. Fundamental and molecular mechanisms of mutagenesis. 357(1-2). 57–66. 19 indexed citations

12.

Almqvist, E., Niamh Spence, K. Nichol, et al.. (1995). 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. 4(2). 207–214. 59 indexed citations

13.

Andrew, Susan E., Y. Paul Goldberg, Jane Theilmann, Jutta Zeisler, & Michael R. Hayden. (1994). A CCG repeat polymorphism adjacent to the CAG repeat in the Huntington disease gene: implications for diagnostic accuracy and predictive testing. Human Molecular Genetics. 3(1). 65–67. 127 indexed citations

14.

Kremer, Berry, Paul Goldberg, Susan E. Andrew, et al.. (1994). A Worldwide Study of the Huntington's Disease Mutation: The Sensitivity and Specificity of Measuring CAG Repeats. New England Journal of Medicine. 330(20). 1401–1406. 428 indexed citations

15.

Goldberg, Y. Paul, Susan E. Andrew, Jane Theilmann, et al.. (1993). Familial predisposition to recurrent mutations causing Huntington's disease: genetic risk to sibs of sporadic cases.. Journal of Medical Genetics. 30(12). 987–990. 32 indexed citations

16.

Goldberg, Y. Paul, Susan E. Andrew, Gordon B. Hutchinson, et al.. (1993). Identification of an Alu retrotransposition event in close proximity to a strong candidate gene for Huntington's disease. Nature. 362(6418). 370–373. 41 indexed citations

17.

Goldberg, Y. Paul, Susan E. Andrew, L. Clarke, & Michael R. Hayden. (1993). A PCR method for accurate assessment of trinucleotide repeat expansion in Huntington disease. Human Molecular Genetics. 2(6). 635–636. 63 indexed citations

18.

Andrew, Susan E., Berry Kremer, Håkan Telenius, et al.. (1993). The relationship between trinucleotide (CAG) repeat length and clinical features of Huntington's disease. Nature Genetics. 4(4). 398–403. 821 indexed citations breakdown →

19.

Goldberg, Y. Paul, Berry Kremer, Susan E. Andrew, et al.. (1993). Molecular analysis of new mutations for Huntington's disease: intermediate alleles and sex of origin effects. Nature Genetics. 5(2). 174–179. 184 indexed citations

20.

Goldberg, Y. Paul, Biaoyang Lin, Susan E. Andrew, et al.. (1992). Cloning and mapping of the -adducin gene close to D4S95 and assessment of its relationship to Huntington disease. Human Molecular Genetics. 1(9). 669–675. 20 indexed citations

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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