Sue M. White

505 total citations
7 papers, 169 citations indexed

About

Sue M. White is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Sue M. White has authored 7 papers receiving a total of 169 indexed citations (citations by other indexed papers that have themselves been cited), including 3 papers in Molecular Biology, 3 papers in Genetics and 2 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Sue M. White's work include PI3K/AKT/mTOR signaling in cancer (2 papers), Tracheal and airway disorders (1 paper) and Genetic Syndromes and Imprinting (1 paper). Sue M. White is often cited by papers focused on PI3K/AKT/mTOR signaling in cancer (2 papers), Tracheal and airway disorders (1 paper) and Genetic Syndromes and Imprinting (1 paper). Sue M. White collaborates with scholars based in Australia, United Kingdom and United States. Sue M. White's co-authors include Peter Sullivan, R. Hitchcock, Patricia A. Boyd, P. Chamberlain, Zornitza Stark, Bronwyn Kerr, Rachel Conyers, Angela E. Lin, Daniel Doyle and Marni E. Axelrad and has published in prestigious journals such as American Journal of Medical Genetics, Prenatal Diagnosis and The Journal of Allergy and Clinical Immunology In Practice.

In The Last Decade

Sue M. White

7 papers receiving 154 citations

Peers

Sue M. White

MB

IMMUN

GENET

PPCH

SURGE

Florian Fronhoffs Germany

Esen Özkaya‐Bayazit Türkiye

Irit Tirosh Israel

Rita Consolini Italy

Shiho Nishimura Japan

Dana Pueschl United States

Forough Parhizkar Iran

Alison Maclean United Kingdom

C Herbelin France

Colin Y.C. Lee United Kingdom

Florian Fronhoffs Germany

Sue M. White

108 ×1.4

MB

40 ×0.9

IMMUN

17 ×0.5

GENET

13 ×0.4

PPCH

36 ×1.6

SURGE

Citations per year, relative to Sue M. White Sue M. White (= 1×) peers Florian Fronhoffs

Countries citing papers authored by Sue M. White

Since Specialization

Citations

This map shows the geographic impact of Sue 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 Sue 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 Sue M. White more than expected).

Fields of papers citing papers by Sue M. White

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

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

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

All Works

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7 of 7 papers shown

1.

Gripp, Karen W., Marni E. Axelrad, Kathryn C. Chatfield, et al.. (2019). Costello syndrome: Clinical phenotype, genotype, and management guidelines. American Journal of Medical Genetics Part A. 179(9). 1725–1744. 72 indexed citations

2.

Stutterd, Chloe, George McGillivray, Zornitza Stark, et al.. (2018). Polymicrogyria in association with hypoglycemia points to mutation in the mTOR pathway. European Journal of Medical Genetics. 61(12). 738–740. 11 indexed citations

3.

Burns, Charlotte, Zornitza Stark, Sharon Choo, et al.. (2016). A novel presentation of homozygous loss-of-function STAT-1 mutation in an infant with hyperinflammation—A case report and review of the literature. The Journal of Allergy and Clinical Immunology In Practice. 4(4). 777–779. 29 indexed citations

4.

Canún, Sonia, Martin B. Delatycki, Gabriele Gillessen‐Kaesbach, et al.. (2008). No mutation in genes of the WNT signaling pathway in patients with Zimmermann–Laband syndrome. Clinical Dysmorphology. 17(3). 181–185. 10 indexed citations

5.

Perry, Jo K., Sue M. White, Sara Nouri, et al.. (2005). Unstable Robertsonian translocations der(13;15)(q10;q10): Heritable chromosome fission without phenotypic effect in two kindreds. American Journal of Medical Genetics Part A. 136A(1). 25–30. 14 indexed citations

6.

White, Sue M., Anneke Lucassen, & Gail Norbury. (2001). Cystic fibrosis: A further case of an asymptomatic compound heterozygote. American Journal of Medical Genetics. 103(4). 342–343. 5 indexed citations

7.

White, Sue M., P. Chamberlain, R. Hitchcock, Peter Sullivan, & Patricia A. Boyd. (2000). Megacystis-microcolon-intestinal hypoperistalsis syndrome: the difficulties with antenatal diagnosis. Case report and review of the literature. Prenatal Diagnosis. 20(9). 697–700. 28 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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