Ann Curtis

2.3k citations
54 papers · 1.6k · h-index 21

Impact in

  • Neurology top 2%
    • Neurological diseases and metabolism
    • Neuroblastoma Research and Treatments
    • Amyotrophic Lateral Sclerosis Research
    • Parkinson's Disease Mechanisms and Treatments
  • Genetics top 5%

Papers in

Ann Curtis

53 papers receiving 1.6k citations

Peers

Ann Curtis
Comparison fields: 5 of 102
  • Neurology 322
  • Neurology 391
  • Genetics 220
  • Hematology 212
  • Cellular and Molecular Neuroscience 349
Replace Brith Otterud with:
Brith Otterud United States
Sara Rollinson United Kingdom
Merja Soilu‐Hänninen Finland
Paola Mandich Italy
Alice Laroni Italy
Daniëlle Majoor‐Krakauer Netherlands
Julia Wanschitz Austria
Jia Nee Foo Singapore
Alessandro Malandrini Italy
Yolanda Espinosa‐Parrilla Spain
Ann Curtis relative to Brith Otterud United States Brith Otterud's profile →
Citations per field
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Brith Otterud · 1×
Citations per year

Countries citing papers authored by Ann Curtis

Since Specialization
Citations

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

Fields of papers citing papers by Ann Curtis

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside Ann Curtis, 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 Ann Curtis Line = papers co-authored together Ann Curtis links everyone, so they are left out of the graph.

All Works

20 of 20 papers shown

Showing the 20 most-cited of 54 papers — load more, or switch the sort, to bring in the rest.

#Work
1 2001389
2 1998122
3 198685
4
Comparative genomic hybridization study of primary neuroblastoma tumors. United Kingdom Children's Cancer Study Group.
199785
5 199376
6 200069
7 199765
8 199458
9 200255
10 199350
11 200136
12 200435
13 200031
14 200027
15 200327
16 198326
17
A submicroscopic translocation, t(4;10), responsible for recurrent Wolf-Hirschhorn syndrome identified by allele loss and fluorescent in situ hybridisation.
199226
18 199325
19 199724
20 199323

About Ann Curtis

Ann Curtis is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience, Pulmonary and Respiratory Medicine, Surgery and Pathology and Forensic Medicine, having authored 54 papers that have together received 1.6k indexed citations. Recurring topics across this work include Genetic Neurodegenerative Diseases (11 papers), Cystic Fibrosis Research Advances (7 papers), Hypothalamic control of reproductive hormones (5 papers), Prenatal Screening and Diagnostics (5 papers), Genetic factors in colorectal cancer (5 papers), Muscle Physiology and Disorders (4 papers), Neonatal Respiratory Health Research (4 papers) and Hematopoietic Stem Cell Transplantation (3 papers). The work is most often cited by research in Neurology (322 citations), Neurology (391 citations), Genetics (220 citations), Hematology (212 citations) and Cellular and Molecular Neuroscience (349 citations). Ann Curtis has collaborated with scholars based in United Kingdom, United States and Belgium. Frequent co-authors include John Burn, Paul G. Ince, Patrick F. Chinnery, George Fink, Margaret Jackson, Christopher M. Morris, Alan Coulthard, Andrew R.J. Curtis, David Bates and Duncan P. McHale. Their work appears in journals such as Journal of Medical Genetics, Human Genetics, Neuroreport, Genes Chromosomes and Cancer and Clinical Genetics.

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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