Susan M. White

10.0k total citations · 1 hit paper
113 papers, 3.5k citations indexed

About

Susan M. White is a scholar working on Genetics, Molecular Biology and Pathology and Forensic Medicine. According to data from OpenAlex, Susan M. White has authored 113 papers receiving a total of 3.5k indexed citations (citations by other indexed papers that have themselves been cited), including 51 papers in Genetics, 49 papers in Molecular Biology and 15 papers in Pathology and Forensic Medicine. Recurrent topics in Susan M. White's work include Genomics and Rare Diseases (25 papers), Genomic variations and chromosomal abnormalities (22 papers) and Genetic factors in colorectal cancer (11 papers). Susan M. White is often cited by papers focused on Genomics and Rare Diseases (25 papers), Genomic variations and chromosomal abnormalities (22 papers) and Genetic factors in colorectal cancer (11 papers). Susan M. White collaborates with scholars based in Australia, United States and United Kingdom. Susan M. White's co-authors include Zornitza Stark, Tiong Yang Tan, David Dimmock, Stephen F. Kingsmore, Lauge Farnaes, Michelle M. Clark, Clara Gaff, Wyllie Ah, Bird Cc and Sebastian Lunke and has published in prestigious journals such as The Journal of Experimental Medicine, SHILAP Revista de lepidopterología and Journal of the American College of Cardiology.

In The Last Decade

Susan M. White

110 papers receiving 3.4k citations

Hit Papers

align trajectories sort by overperformance

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.

Meta-analysis of the diagnostic and clinical utility of genome and exome sequencing and chromosomal microarray in children with suspected genetic diseases

2018 340 citations Zornitza Stark, Tiong Yang Tan et al. profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Susan M. White Australia	33	1.6k	1.4k	619	541	385	113	3.5k
Graeme Suthers Australia	25	1.2k 0.8×	981 0.7×	718 1.2×	597 1.1×	429 1.1×	57	2.5k
Donald W. Hadley United States	27	1.4k 0.9×	754 0.5×	660 1.1×	530 1.0×	248 0.6×	65	2.7k
Peter Ainsworth Canada	37	2.3k 1.4×	1.6k 1.1×	473 0.8×	941 1.7×	821 2.1×	96	4.1k
Christi J. van Asperen Netherlands	36	2.4k 1.5×	848 0.6×	564 0.9×	818 1.5×	708 1.8×	104	3.4k
Ketil Heimdal Norway	29	1.5k 0.9×	1.2k 0.8×	1.1k 1.8×	1.0k 1.9×	787 2.0×	103	3.6k
Trevor Cole United Kingdom	31	1.7k 1.1×	1.7k 1.2×	321 0.5×	241 0.4×	267 0.7×	62	3.2k
Margreet G.E.M. Ausems Netherlands	35	2.0k 1.3×	744 0.5×	638 1.0×	1.0k 1.9×	769 2.0×	157	3.6k
C. Sue Richards United States	22	2.1k 1.3×	1.4k 1.0×	420 0.7×	185 0.3×	499 1.3×	45	3.8k
Ruth Gershoni‐Baruch Israel	39	1.7k 1.1×	3.1k 2.2×	368 0.6×	812 1.5×	573 1.5×	145	6.1k
Hanne Meijers‐Heijboer Netherlands	40	2.5k 1.6×	1.9k 1.3×	917 1.5×	1.1k 2.0×	1.1k 2.7×	98	4.9k

Countries citing papers authored by Susan M. White

Since Specialization

Citations

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

Fields of papers citing papers by Susan M. White

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Susan M. White. 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 M. White. The network helps show where Susan M. White may publish in the future.

Co-authorship network of co-authors of Susan M. White

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

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

Collins, Felicity, Susan M. White, Mathew Wallis, et al.. (2024). Assessing the unmet needs of genomic testing in Australia: a geospatial exploration. European Journal of Human Genetics. 33(4). 496–503. 1 indexed citations

Best, Stephanie, et al.. (2022). A systematic review of geographical inequities for accessing clinical genomic and genetic services for non-cancer related rare disease. European Journal of Human Genetics. 30(6). 645–652. 27 indexed citations

Helman, Guy, Marzena Walkiewicz, Stefanie Eggers, et al.. (2021). Aberrant splicing and transcriptional activity of TPP1 result in CLN2-like disorder. European Journal of Medical Genetics. 64(8). 104259–104259. 2 indexed citations

Lam, Wayne, Nora Shannon, Karen Knapp, et al.. (2020). Pathogenic variants causing ABL1 malformation syndrome cluster in a myristoyl-binding pocket and increase tyrosine kinase activity. European Journal of Human Genetics. 29(4). 593–603. 10 indexed citations

Akesson, Lauren, David Francis, M. De Silva, et al.. (2020). Microarray diagnosis of autoimmune polyendocrinopathy‐candidiasis‐ectodermal dystrophy caused by a novel homozygous intragenic AIRE deletion. Journal of Paediatrics and Child Health. 57(7). 1109–1112. 1 indexed citations

Apelt, Katja, Susan M. White, Jung-Eun Yeo, et al.. (2020). ERCC1mutations impede DNA damage repair and cause liver and kidney dysfunction in patients. The Journal of Experimental Medicine. 218(3). 24 indexed citations

Tan, Tiong Yang, Sebastian Lunke, Belinda Chong, et al.. (2019). A head-to-head evaluation of the diagnostic efficacy and costs of trio versus singleton exome sequencing analysis. European Journal of Human Genetics. 27(12). 1791–1799. 35 indexed citations

Lunke, Sebastian, Zornitza Stark, Alison Yeung, et al.. (2018). Exome sequencing has higher diagnostic yield compared to simulated disease-specific panels in children with suspected monogenic disorders. European Journal of Human Genetics. 26(5). 644–651. 83 indexed citations

Huq, Aamira, Michael Bogwitz, Alexandra Gorelik, et al.. (2017). Cohort study of Gorlin syndrome with emphasis on standardised phenotyping and quality of life assessment. Internal Medicine Journal. 47(6). 664–673. 12 indexed citations

10.

Stark, Zornitza, Harriet Dashnow, Sebastian Lunke, et al.. (2017). A clinically driven variant prioritization framework outperforms purely computational approaches for the diagnostic analysis of singleton WES data. European Journal of Human Genetics. 25(11). 1268–1272. 13 indexed citations

11.

Roland, Katherine B., Erin L. Milliken, Elizabeth A. Rohan, et al.. (2017). Use of Community Health Workers and Patient Navigators to Improve Cancer Outcomes Among Patients Served by Federally Qualified Health Centers: A Systematic Literature Review. Health Equity. 1(1). 61–76. 159 indexed citations

12.

Wastell, David & Susan M. White. (2017). Blinded by Science. Policy Press eBooks. 12 indexed citations

13.

Harcourt, Brooke E., Denise V. R. Bullen, Kung‐Ting Kao, et al.. (2017). Maternal inheritance of BDNF deletion, with phenotype of obesity and developmental delay in mother and child. American Journal of Medical Genetics Part A. 176(1). 194–200. 7 indexed citations

14.

Wilkins, Ella, Alison D. Archibald, Margaret Sahhar, & Susan M. White. (2016). “It wasn't a disaster or anything”: Parents’ experiences of their child's uncertain chromosomal microarray result. American Journal of Medical Genetics Part A. 170(11). 2895–2904. 42 indexed citations

15.

White, Susan M., et al.. (2015). Evaluation of the Upper Airway Morphology: The Role of Cone Beam Computed Tomography. Journal of the California Dental Association. 43(9). 531–539. 10 indexed citations

16.

Sadedin, Simon, Harriet Dashnow, Paul A. James, et al.. (2015). Cpipe: a shared variant detection pipeline designed for diagnostic settings. Genome Medicine. 7(1). 54 indexed citations

17.

Banka, Siddharth, Damien Lederer, Valérie Benoît, et al.. (2014). Novel KDM6A (UTX) mutations and a clinical and molecular review of the X‐linked Kabuki syndrome (KS2). Clinical Genetics. 87(3). 252–258. 91 indexed citations

18.

Yuan, Rui, Fatemeh Haghighi, Susan M. White, et al.. (2006). A Single Nucleotide Polymorphism Chip-Based Method for Combined Genetic and Epigenetic Profiling: Validation in Decitabine Therapy and Tumor/Normal Comparisons. Cancer Research. 66(7). 3443–3451. 46 indexed citations

19.

Kannus, Pekka, Ravi Savarirayan, Linda Ozoemena, Susan M. White, & John A. McGrath. (2006). Rapp–Hodgkin ectodermal dysplasia syndrome: The clinical and molecular overlap with Hay–Wells syndrome. American Journal of Medical Genetics Part A. 140A(8). 887–891. 13 indexed citations

20.

White, Susan M., Dennis B. DeNicola, Alan H. Rebar, Gordon S. Born, & Wayne V. Kessler. (1988). Effects of Chlorphentermine and Nitrogen Dioxide on Murine Alveolar Macrophages. Experimental Lung Research. 14(5). 619–636. 2 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.

Explore authors with similar magnitude of impact