Ann P. Walker

6.0k total citations · 3 hit papers
61 papers, 4.2k citations indexed

About

Ann P. Walker is a scholar working on Hematology, Genetics and Genetics. According to data from OpenAlex, Ann P. Walker has authored 61 papers receiving a total of 4.2k indexed citations (citations by other indexed papers that have themselves been cited), including 26 papers in Hematology, 25 papers in Genetics and 20 papers in Genetics. Recurrent topics in Ann P. Walker's work include Iron Metabolism and Disorders (26 papers), Hemoglobinopathies and Related Disorders (21 papers) and Trace Elements in Health (14 papers). Ann P. Walker is often cited by papers focused on Iron Metabolism and Disorders (26 papers), Hemoglobinopathies and Related Disorders (21 papers) and Trace Elements in Health (14 papers). Ann P. Walker collaborates with scholars based in United Kingdom, United States and Canada. Ann P. Walker's co-authors include James Dooley, Aftab Ala, Keyoumars Ashkan, Michael L. Schilsky, Anthony P. Monaco, Françoise Muscatelli, Barbara Bardoni, Elena Zanaria, Tim M. Strom and Silvana Guioli and has published in prestigious journals such as Nature, Proceedings of the National Academy of Sciences and The Lancet.

In The Last Decade

Ann P. Walker

59 papers receiving 4.1k 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.

Wilson's disease

2007 881 citations Ann P. Walker, James Dooley et al. profile →
An unusual member of the nuclear hormone receptor superfamily responsible for X-linked adrenal hypoplasia congenita

1994 656 citations Ann P. Walker, Anthony P. Monaco et al. profile →
Mutations in the DAX-1 gene give rise to both X-linked adrenal hypoplasia congenita and hypogonadotropic hypogonadism

1994 549 citations Ann P. Walker, Anthony P. Monaco et al. profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Ann P. Walker United Kingdom	24	1.7k	1.6k	1.2k	872	599	61	4.2k
Antonio Cao Italy	53	4.5k 2.6×	2.6k 1.7×	832 0.7×	3.9k 4.4×	4.9k 8.1×	303	12.1k
Elizabeth J. Cartwright United Kingdom	36	2.7k 1.6×	626 0.4×	847 0.7×	212 0.2×	83 0.1×	147	5.2k
Han‐Wook Yoo South Korea	33	1.8k 1.1×	971 0.6×	344 0.3×	173 0.2×	115 0.2×	300	4.0k
Peter J. Leedman Australia	50	3.8k 2.2×	553 0.4×	384 0.3×	445 0.5×	292 0.5×	128	7.5k
Elizabeth Moore United States	32	1.0k 0.6×	308 0.2×	824 0.7×	1.1k 1.3×	384 0.6×	76	4.0k
Generoso Andria Italy	46	2.9k 1.7×	1.7k 1.1×	226 0.2×	436 0.5×	192 0.3×	215	8.5k
Shunji Tomatsu United States	55	2.1k 1.2×	867 0.5×	1.7k 1.4×	2.2k 2.5×	2.1k 3.6×	311	10.2k
Anne Gompel France	47	1.2k 0.7×	2.4k 1.5×	239 0.2×	274 0.3×	707 1.2×	189	6.5k
Timothy A. Donlon United States	37	2.5k 1.4×	1.1k 0.7×	62 0.1×	610 0.7×	221 0.4×	105	5.3k
Fahri Saatcioglu Norway	41	2.5k 1.4×	1.1k 0.7×	106 0.1×	144 0.2×	268 0.4×	105	4.6k

Countries citing papers authored by Ann P. Walker

Since Specialization

Citations

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

Fields of papers citing papers by Ann P. Walker

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Ann P. Walker. 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 Ann P. Walker. The network helps show where Ann P. Walker may publish in the future.

Co-authorship network of co-authors of Ann P. Walker

This figure shows the co-authorship network connecting the top 25 collaborators of Ann P. Walker. A scholar is included among the top collaborators of Ann P. Walker 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 Ann P. Walker. Ann P. Walker 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

Gill, Dipender, Beben Benyamin, Luke Moore, et al.. (2019). Associations of genetically determined iron status across the phenome: A mendelian randomization study. PLoS Medicine. 16(6). e1002833–e1002833. 41 indexed citations

Yin, Dan, et al.. (2013). Raised serum ferritin concentration in hereditary hyperferritinemia cataract syndrome is not a marker for iron overload. Hepatology. 59(3). 1204–1206. 10 indexed citations

Sewell, Gavin W., Farooq Rahman, Adam P. Levine, et al.. (2012). Defective tumor necrosis factor release from Crohnʼs disease macrophages in response to toll-like receptor activation: Relationship to phenotype and genome-wide association susceptibility loci. Inflammatory Bowel Diseases. 18(11). 2120–2127. 24 indexed citations

Sewell, Gavin W., Yusuf A. Hannun, Xianlin Han, et al.. (2012). Lipidomic profiling in Crohn's disease: Abnormalities in phosphatidylinositols, with preservation of ceramide, phosphatidylcholine and phosphatidylserine composition. The International Journal of Biochemistry & Cell Biology. 44(11). 1839–1846. 41 indexed citations

Smith, Andrew, Farooq Rahman, Bu Hayee, et al.. (2009). Disordered macrophage cytokine secretion underlies impaired acute inflammation and bacterial clearance in Crohn's disease. The Journal of Experimental Medicine. 206(9). 1883–1897. 315 indexed citations

Harrison, Helen, Barbara Harrison, Ann P. Walker, et al.. (2008). Screening for Hemochromatosis and Iron Overload: Satisfaction with Results Notification and Understanding of Mailed Results in Unaffected Participants of the HEIRS Study. Genetic Testing. 12(4). 491–500. 8 indexed citations

Kachman, Maureen, Ann P. Walker, John R. Strahler, et al.. (2008). Microparticle Surface Proteins Are Associated With Experimental Venous Thrombosis: A Preliminary Study. Clinical and Applied Thrombosis/Hemostasis. 15(2). 201–8. 16 indexed citations

Adams, Paul C., James C. Barton, Ronald T. Acton, et al.. (2007). Psychosocial Impact of Genetic Testing for Hemochromatosis in The HEIRS Study: A Comparison of Participants Recruited in Canada And in The United States. Genetic Testing. 11(1). 55–64. 12 indexed citations

Tucker, Diane C., Ronald T. Acton, Nancy Press, et al.. (2006). Predictors of Belief That Genetic Test Information About Hemochromatosis Should Be Shared with Family Members. Genetic Testing. 10(1). 50–59. 8 indexed citations

10.

Anderson, Roger T., Lari Wenzel, Ann P. Walker, et al.. (2006). Impact of hemochromatosis screening in patients with indeterminate results: The hemochromatosis and iron overload screening study. Genetics in Medicine. 8(11). 681–687. 13 indexed citations

11.

Walker, Ann P.. (2004). Hepcidin: what every gastroenterologist should know. Gut. 53(5). 624–627. 23 indexed citations

12.

Browner, Carole H., H. Mabel Preloran, Maria Casado, Harold N. Bass, & Ann P. Walker. (2003). Genetic counseling gone awry: miscommunication between prenatal genetic service providers and Mexican-origin clients. Social Science & Medicine. 56(9). 1933–1946. 91 indexed citations

13.

Adams, Paul C., Ann P. Walker, & Ronald T. Acton. (2001). A Primer for Predicting Risk of Disease in HFE -Linked Hemochromatosis. Genetic Testing. 5(4). 311–316. 13 indexed citations

14.

Dooley, James & Ann P. Walker. (2000). Genetic Hemochromatosis: Detection, Management, and Population Screening. Genetic Testing. 4(2). 97–101. 7 indexed citations

15.

Loke, Kah Yin, et al.. (2000). An Atypical Kindred with X-linked Adrenal Hypoplasia Congenita, Normal Puberty, and Normal Dax-1 Promoter and Coding Sequence. Journal of Pediatric Endocrinology and Metabolism. 13(1). 29–36. 6 indexed citations

16.

Wallace, Daniel F., James Dooley, & Ann P. Walker. (1999). A novel mutation of HFE explains the classical phenotype of genetic hemochromatosis in a C282Y heterozygote. UCL Discovery (University College London). 2 indexed citations

17.

Worwood, Mark, JS Dooley, William Rosenberg, et al.. (1997). A simple genetic test identifies 90% of UK patients with haemochromatosis. Gut. 41(6). 841–844. 179 indexed citations

18.

Monaco, Anthony P., Ann P. Walker, Iona Y. Millwood, Zoia Larin, & Hans Lehrach. (1992). A yeast artificial chromosome contig containing the complete Duchenne muscular dystrophy gene. Genomics. 12(3). 465–473. 59 indexed citations

19.

Bocian, Maureen, et al.. (1987). Interstitial deletion of the long arm of chromosome 3: Case report, review, and definition of a phenotype. American Journal of Medical Genetics. 27(4). 781–786. 38 indexed citations

20.

Bocian, Maureen, M. Anne Spence, Mary L. Marazita, et al.. (1986). Familial diaphragmatic defects. Early prenatal diagnosis and evidence for major gene inheritance. American Journal of Medical Genetics. 25(S2). 163–176. 9 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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